Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23229 |
| ensemblid | ENSG00000131089.17 |
| hgncid | 14561 |
| symbol | ARHGEF9 |
| name | Cdc42 guanine nucleotide exchange factor 9 |
| refseq_nuc | NM_001353921.2 |
| refseq_prot | NP_001340850.1 |
| ensembl_nuc | ENST00000671741.2 |
| ensembl_prot | ENSP00000500715.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 63634967 |
| end | 63785214 |
| strand | - |
| ver | v1.2 |
| region | chrX:63634967-63785214 |
| region5000 | chrX:63629967-63790214 |
| regionname0 | ARHGEF9_chrX_63634967_63785214 |
| regionname5000 | ARHGEF9_chrX_63629967_63790214 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 523 | 167 | 47 | 29 | 68 | 5 | 16 | 53 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | MQWIR others(518): Show |
chrX | 63629967 | 63790214 |
| a0002 | 0/0 | 523 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | MQWIR others(518): Show |
chrX | 63629967 | 63790214 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1569 | 167 | 47 | 29 | 68 | 5 | 16 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | ATGCA others(1564): Show |
chrX | 63629967 | 63790214 | ||
| a0002c0002 | 0/0 | 1569 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | ATGCA others(1564): Show |
chrX | 63629967 | 63790214 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4702 | 99 | 4 | 17 | 61 | 4 | 11 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4697): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0002 | 0/0 | 4700 | 29 | 21 | 2 | 5 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4695): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0003 | 0/0 | 4698 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4693): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0004 | 0/0 | 4704 | 5 | 1 | 3 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4699): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0005 | 0/0 | 4699 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4694): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0006 | 0/0 | 4693 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4688): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0007 | 0/0 | 4704 | 3 | 0 | 1 | 1 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4699): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0008 | 0/0 | 4701 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4696): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0009 | 0/0 | 4701 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4696): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0010 | 0/0 | 4701 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4696): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0011 | 0/0 | 4702 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4697): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0012 | 0/0 | 4702 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4697): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0013 | 0/0 | 4702 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4697): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0014 | 0/0 | 4686 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4681): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0015 | 0/0 | 4700 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4695): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0016 | 0/0 | 4698 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4693): Show |
chrX | 63629967 | 63790214 |
| a0001c0001t0017 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4693): Show |
chrX | 63629967 | 63790214 |
| a0002c0002t0018 | 0/0 | 4699 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | CCTTC others(4694): Show |
chrX | 63629967 | 63790214 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0010g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0011g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0012g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0013g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0015g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0016g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0001c0001t0017g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| a0002c0002t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | CHS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0106 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00735 | hp1 | a0001 | c0001 | t0008 | g0006 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG00738 | hp1 | a0001 | c0001 | t0016 | g0152 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0083 | AMR | PEL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0031 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02809 | hp2 | a0002 | c0002 | t0018 | g0138 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0002 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0097 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03492 | hp1 | a0001 | c0001 | t0012 | g0088 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03688 | hp1 | a0001 | c0001 | t0011 | g0121 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04115 | hp1 | a0001 | c0001 | t0013 | g0081 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0145 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0089 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19076 | hp1 | a0001 | c0001 | t0014 | g0109 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0053 | EUR | TSI | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG02486 | hp1 | a0001 | c0001 | t0017 | g0094 | AFR | ACB | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0137 | AFR | MSL | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | USA | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | USA | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0085 | REF | REF | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0076 | REF | REF | ARHGEF9_chrX_63629967_63790214 | ARHGEF9 | chrX | 63629967 | 63790214 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:63724693 | T | C | 1 | a0002 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.49A>G | p.Ile17Val | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/10 | 118/4702 | 49/1572 | 17/523 | chrX | 63724693 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:63635290 | G | GA | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(3): Show |
15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2737dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 2737 | chrX | 63635290 | ||||||
| chrX:63636103 | G | T | 1 | a0001c0001t0017 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1925C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1925 | chrX | 63636103 | ||||||
| chrX:63636431 | G | T | 1 | a0001c0001t0013 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1597C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1597 | chrX | 63636431 | ||||||
| chrX:63636504 | C | T | 1 | a0001c0001t0012 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1524G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1524 | chrX | 63636504 | ||||||
| chrX:63636576 | T | C | 1 | a0001c0001t0009 | 2 | HG02647.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1452 | chrX | 63636576 | ||||||
| chrX:63636604 | C | T | 1 | a0001c0001t0016 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 1424 | chrX | 63636604 | ||||||
| chrX:63637161 | C | T | 1 | a0001c0001t0011 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*867G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 867 | chrX | 63637161 | ||||||
| chrX:63637250 | CATCATCA others(9): Show |
C | 1 | a0001c0001t0014 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*762_*777delATCAGA others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 762 | chrX | 63637250 | ||||||
| chrX:63637744 | T | G | 1 | a0001c0001t0010 | 2 | HG02280.hp1 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*284A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 284 | chrX | 63637744 | ||||||
| chrX:63637816 | C | A | 1 | a0002c0002t0018 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*212G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 212 | chrX | 63637816 | ||||||
| chrX:63637846 | C | CTG | 1 | a0001c0001t0007 | 3 | HG00621.hp1 HG00642.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*180_*181dupCA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 181 | chrX | 63637846 | ||||||
| chrX:63637846 | CTG | C | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(2): Show |
36 | HG00735.hp1 HG01167.hp1 HG01255.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*180_*181delCA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 180 | chrX | 63637846 | ||||||
| chrX:63637846 | CTGTG | C | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(2): Show |
18 | HG00738.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*178_*181delCACA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 178 | chrX | 63637846 | ||||||
| chrX:63637850 | G | C | 1 | a0001c0001t0015 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 178 | chrX | 63637850 | ||||||
| chrX:63637872 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0006 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*146_*155delGACACA others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 146 | chrX | 63637872 | ||||||
| chrX:63637918 | C | CTG | 1 | a0001c0001t0004 | 5 | HG01928.hp1 HG01934.hp1 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*108_*109dupCA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 10/10 | 109 | chrX | 63637918 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:63638625 | G | A | 2 | a0001c0001t0009g0007 a0001c0001t0009g0008 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1391-416C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63638625 | |||||||
| chrX:63638998 | A | C | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1391-789T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63638998 | |||||||
| chrX:63639442 | T | C | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0019 |
3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1391-1233A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63639442 | |||||||
| chrX:63640902 | T | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1391-2693A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63640902 | |||||||
| chrX:63641117 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1390+2863G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641117 | |||||||
| chrX:63641356 | G | GA | 6 | a0001c0001t0001g0108 a0001c0001t0001g0162 a0001c0001t0002g0145 others(3): Show |
6 | HG01358.hp1 HG02055.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1390+2623dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641356 | |||||||
| chrX:63641357 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1390+2623T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641357 | |||||||
| chrX:63641380 | AAGAC | A | 2 | a0001c0001t0002g0034 a0001c0001t0015g0031 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1390+2596_1390+259 others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641380 | |||||||
| chrX:63641952 | C | T | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1390+2028G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63641952 | |||||||
| chrX:63642093 | C | CAT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0112 others(5): Show |
10 | HG00621.hp1 HG02056.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1390+1885_1390+188 others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642093 | |||||||
| chrX:63642112 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1390+1868G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642112 | |||||||
| chrX:63642392 | T | C | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1390+1588A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642392 | |||||||
| chrX:63642411 | A | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1390+1569T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642411 | |||||||
| chrX:63642579 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1390+1401G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642579 | |||||||
| chrX:63642806 | C | G | 1 | a0001c0001t0001g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1390+1174G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642806 | |||||||
| chrX:63642934 | T | G | 1 | a0001c0001t0002g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1390+1046A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63642934 | |||||||
| chrX:63643360 | C | CTT | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1390+618_1390+619d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643360 | |||||||
| chrX:63643360 | CT | C | 5 | a0001c0001t0001g0111 a0001c0001t0002g0062 a0001c0001t0003g0037 others(2): Show |
5 | HG01167.hp1 HG02109.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390+619delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643360 | |||||||
| chrX:63643461 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1390+519G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643461 | |||||||
| chrX:63643717 | T | TA | 5 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0087 others(2): Show |
5 | HG02647.hp1 NA18940.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390+262dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643717 | |||||||
| chrX:63643717 | T | TAA | 11 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(8): Show |
12 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1390+261_1390+262d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643717 | |||||||
| chrX:63643756 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1390+224G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643756 | |||||||
| chrX:63643799 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1390+181A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643799 | |||||||
| chrX:63643817 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1390+163C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 9/9 | chrX | 63643817 | |||||||
| chrX:63644097 | A | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1322-49T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644097 | |||||||
| chrX:63644167 | C | CA | 6 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0005g0012 others(3): Show |
6 | HG01243.hp1 HG02738.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1322-120dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644167 | |||||||
| chrX:63644167 | C | CAA | 9 | a0001c0001t0005g0014 a0001c0001t0005g0015 a0001c0001t0006g0016 others(6): Show |
10 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1322-121_1322-120d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644167 | |||||||
| chrX:63644238 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1322-190G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644238 | |||||||
| chrX:63644762 | A | T | 1 | a0001c0001t0012g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1322-714T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644762 | |||||||
| chrX:63644762 | AT | A | 20 | a0001c0001t0001g0027 a0001c0001t0001g0119 a0001c0001t0001g0139 others(17): Show |
20 | HG01167.hp1 HG01255.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.1322-715delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644762 | |||||||
| chrX:63644762 | ATT | A | 7 | a0001c0001t0001g0024 a0001c0001t0002g0023 a0001c0001t0002g0025 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1322-716_1322-715d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644762 | |||||||
| chrX:63644765 | T | A | 8 | a0001c0001t0001g0067 a0001c0001t0001g0117 a0001c0001t0001g0120 others(5): Show |
9 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1322-717A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644765 | |||||||
| chrX:63644871 | T | A | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-823A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63644871 | |||||||
| chrX:63645012 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1322-964G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645012 | |||||||
| chrX:63645054 | A | C | 15 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(12): Show |
16 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1322-1006T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645054 | |||||||
| chrX:63645214 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1322-1166A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645214 | |||||||
| chrX:63645221 | AT | A | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1322-1174delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645221 | |||||||
| chrX:63645464 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1322-1416G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645464 | |||||||
| chrX:63645471 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1322-1423C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645471 | |||||||
| chrX:63645605 | C | G | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1322-1557G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645605 | |||||||
| chrX:63645677 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0002g0072 |
2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1322-1629G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645677 | |||||||
| chrX:63645678 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1322-1630C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645678 | |||||||
| chrX:63645884 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1322-1836G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645884 | |||||||
| chrX:63645951 | G | A | 1 | a0001c0001t0008g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1322-1903C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63645951 | |||||||
| chrX:63646116 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1322-2068T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646116 | |||||||
| chrX:63646130 | G | C | 16 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(13): Show |
17 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1322-2082C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646130 | |||||||
| chrX:63646278 | A | G | 16 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0002g0010 others(13): Show |
16 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.1322-2230T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646278 | |||||||
| chrX:63646361 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1322-2313T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646361 | |||||||
| chrX:63646593 | C | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0061 a0001c0001t0002g0062 |
3 | HG01167.hp1 HG02896.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1322-2545G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646593 | |||||||
| chrX:63646608 | T | A | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1322-2560A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646608 | |||||||
| chrX:63646992 | A | C | 1 | a0001c0001t0001g0003 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1322-2944T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63646992 | |||||||
| chrX:63647345 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1322-3297G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647345 | |||||||
| chrX:63647412 | T | C | 28 | a0001c0001t0002g0010 a0001c0001t0002g0032 a0001c0001t0003g0037 others(25): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1322-3364A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647412 | |||||||
| chrX:63647413 | G | C | 28 | a0001c0001t0002g0010 a0001c0001t0002g0032 a0001c0001t0003g0037 others(25): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1322-3365C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647413 | |||||||
| chrX:63647443 | G | T | 1 | a0001c0001t0004g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1322-3395C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63647443 | |||||||
| chrX:63648283 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1322-4235C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63648283 | |||||||
| chrX:63648314 | T | G | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1322-4266A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63648314 | |||||||
| chrX:63648475 | T | G | 28 | a0001c0001t0002g0010 a0001c0001t0002g0032 a0001c0001t0003g0037 others(25): Show |
29 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1322-4427A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63648475 | |||||||
| chrX:63649018 | C | A | 1 | a0001c0001t0002g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1322-4970G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649018 | |||||||
| chrX:63649030 | T | C | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1322-4982A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649030 | |||||||
| chrX:63649042 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1322-4994G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649042 | |||||||
| chrX:63649353 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1322-5305C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649353 | |||||||
| chrX:63649410 | T | C | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1322-5362A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63649410 | |||||||
| chrX:63650063 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1321+5431C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650063 | |||||||
| chrX:63650206 | T | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321+5288A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650206 | |||||||
| chrX:63650342 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1321+5152G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650342 | |||||||
| chrX:63650677 | A | G | 1 | a0001c0001t0001g0003 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1321+4817T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63650677 | |||||||
| chrX:63651868 | A | C | 1 | a0001c0001t0003g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1321+3626T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63651868 | |||||||
| chrX:63652170 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1321+3324T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652170 | |||||||
| chrX:63652492 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1321+3002T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652492 | |||||||
| chrX:63652917 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1321+2577G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63652917 | |||||||
| chrX:63653215 | C | A | 1 | a0001c0001t0002g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1321+2279G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653215 | |||||||
| chrX:63653351 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1321+2143C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653351 | |||||||
| chrX:63653776 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1321+1718C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653776 | |||||||
| chrX:63653928 | C | T | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1321+1566G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63653928 | |||||||
| chrX:63654078 | GT | G | 10 | a0001c0001t0001g0040 a0001c0001t0005g0012 a0001c0001t0005g0013 others(7): Show |
11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321+1415delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654078 | |||||||
| chrX:63654159 | C | CA | 6 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG00735.hp2 HG01109.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1321+1334dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654159 | |||||||
| chrX:63654545 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1321+949G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63654545 | |||||||
| chrX:63655171 | T | G | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1321+323A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63655171 | |||||||
| chrX:63655311 | T | C | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1321+183A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 8/9 | chrX | 63655311 | |||||||
| chrX:63655835 | T | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1078-98A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63655835 | |||||||
| chrX:63656061 | G | T | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1078-324C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63656061 | |||||||
| chrX:63656519 | T | A | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1078-782A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63656519 | |||||||
| chrX:63656868 | A | G | 5 | a0001c0001t0008g0006 a0001c0001t0008g0137 a0001c0001t0009g0007 others(2): Show |
6 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-1131T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63656868 | |||||||
| chrX:63657135 | C | T | 4 | a0001c0001t0003g0039 a0001c0001t0003g0071 a0001c0001t0003g0099 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-1398G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657135 | |||||||
| chrX:63657345 | T | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1078-1608A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657345 | |||||||
| chrX:63657637 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1078-1900G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657637 | |||||||
| chrX:63657849 | C | T | 7 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1078-2112G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63657849 | |||||||
| chrX:63658194 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1078-2457C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63658194 | |||||||
| chrX:63660089 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1078-4352G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660089 | |||||||
| chrX:63660765 | G | T | 1 | a0001c0001t0008g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1078-5028C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660765 | |||||||
| chrX:63660901 | A | G | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+4985T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660901 | |||||||
| chrX:63660906 | A | T | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1077+4980T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660906 | |||||||
| chrX:63660993 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1077+4893G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63660993 | |||||||
| chrX:63661279 | A | G | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+4607T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661279 | |||||||
| chrX:63661497 | C | T | 1 | a0001c0001t0004g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1077+4389G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661497 | |||||||
| chrX:63661679 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1077+4207T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661679 | |||||||
| chrX:63661758 | T | TTC | 7 | a0001c0001t0002g0060 a0001c0001t0002g0118 a0001c0001t0002g0126 others(4): Show |
8 | HG00735.hp1 HG02132.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+4126_1077+412 others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661758 | |||||||
| chrX:63661871 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1077+4015A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63661871 | |||||||
| chrX:63662493 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1077+3393A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63662493 | |||||||
| chrX:63662724 | T | C | 6 | a0001c0001t0001g0090 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | HG02015.hp1 HG02074.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+3162A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63662724 | |||||||
| chrX:63662932 | G | C | 1 | a0001c0001t0007g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1077+2954C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63662932 | |||||||
| chrX:63663141 | C | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0012g0088 |
3 | HG00280.hp1 HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1077+2745G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663141 | |||||||
| chrX:63663341 | C | A | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+2545G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663341 | |||||||
| chrX:63663355 | G | A | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077+2531C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663355 | |||||||
| chrX:63663710 | A | G | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1077+2176T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63663710 | |||||||
| chrX:63664920 | G | A | 26 | a0001c0001t0003g0037 a0001c0001t0003g0039 a0001c0001t0003g0069 others(23): Show |
27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1077+966C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63664920 | |||||||
| chrX:63665107 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1077+779A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665107 | |||||||
| chrX:63665198 | G | A | 1 | a0001c0001t0008g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1077+688C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665198 | |||||||
| chrX:63665341 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1077+545C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665341 | |||||||
| chrX:63665536 | T | C | 1 | a0001c0001t0002g0020 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1077+350A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665536 | |||||||
| chrX:63665558 | T | G | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1077+328A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665558 | |||||||
| chrX:63665827 | G | T | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1077+59C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665827 | |||||||
| chrX:63665834 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1077+52G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 7/9 | chrX | 63665834 | |||||||
| chrX:63666115 | A | G | 1 | a0001c0001t0007g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.946-98T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666115 | |||||||
| chrX:63666326 | C | CCT | 2 | a0001c0001t0001g0080 a0001c0001t0002g0096 |
2 | HG01952.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.946-311_946-310dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666326 | |||||||
| chrX:63666417 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.946-400A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666417 | |||||||
| chrX:63666417 | T | TAC | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-402_946-401dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666417 | |||||||
| chrX:63666449 | T | TACACACA others(3): Show |
2 | a0001c0001t0002g0034 a0001c0001t0015g0031 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.946-433_946-432ins others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666449 | |||||||
| chrX:63666453 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0015g0031 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.946-436A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.946-436A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TAC | 3 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 |
3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.946-438_946-437dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACAC | 9 | a0001c0001t0001g0035 a0001c0001t0002g0063 a0001c0001t0002g0096 others(6): Show |
9 | HG02055.hp1 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.946-440_946-437dup others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACACAC | 5 | a0001c0001t0001g0068 a0001c0001t0001g0108 a0001c0001t0002g0021 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.946-442_946-437dup others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACACACA others(1): Show |
81 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(78): Show |
83 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.946-444_946-437dup others(8): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACACACA others(3): Show |
38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(35): Show |
41 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.946-446_946-437dup others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACACACA others(5): Show |
5 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0116 others(2): Show |
5 | HG03490.hp1 HG04115.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-448_946-437dup others(12): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACACACA others(7): Show |
5 | a0001c0001t0001g0124 a0001c0001t0001g0135 a0001c0001t0002g0060 others(2): Show |
5 | HG00642.hp1 HG01099.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-450_946-437dup others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACACACA others(9): Show |
2 | a0001c0001t0002g0032 a0001c0001t0017g0094 |
2 | HG02486.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.946-452_946-437dup others(16): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | T | TACACACA others(19): Show |
1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.946-462_946-437dup others(26): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | TAC | T | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.946-438_946-437del others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666453 | TACAC | T | 3 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 |
3 | HG00735.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.946-440_946-437del others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666453 | |||||||
| chrX:63666489 | T | C | 1 | a0001c0001t0013g0081 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.946-472A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666489 | |||||||
| chrX:63666552 | T | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-535A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666552 | |||||||
| chrX:63666700 | T | G | 1 | a0001c0001t0003g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.946-683A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63666700 | |||||||
| chrX:63667760 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.946-1743G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63667760 | |||||||
| chrX:63668197 | G | A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-2180C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668197 | |||||||
| chrX:63668262 | T | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-2245A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668262 | |||||||
| chrX:63668366 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.946-2349C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668366 | |||||||
| chrX:63668383 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.946-2366G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668383 | |||||||
| chrX:63668911 | C | G | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-2894G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63668911 | |||||||
| chrX:63669012 | C | T | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-2995G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669012 | |||||||
| chrX:63669128 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.946-3111C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669128 | |||||||
| chrX:63669173 | G | T | 1 | a0001c0001t0008g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.946-3156C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669173 | |||||||
| chrX:63669391 | T | A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.946-3374A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669391 | |||||||
| chrX:63669538 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.946-3521G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63669538 | |||||||
| chrX:63670136 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.945+3902C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63670136 | |||||||
| chrX:63670286 | T | C | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.945+3752A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63670286 | |||||||
| chrX:63671200 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.945+2838C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63671200 | |||||||
| chrX:63671545 | G | A | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.945+2493C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63671545 | |||||||
| chrX:63671909 | G | A | 7 | a0001c0001t0001g0024 a0001c0001t0002g0023 a0001c0001t0002g0025 others(4): Show |
7 | HG02622.hp2 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.945+2129C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63671909 | |||||||
| chrX:63673109 | A | G | 26 | a0001c0001t0003g0037 a0001c0001t0003g0039 a0001c0001t0003g0069 others(23): Show |
27 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.945+929T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63673109 | |||||||
| chrX:63673686 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.945+352C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 6/9 | chrX | 63673686 | |||||||
| chrX:63674725 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.816-558C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63674725 | |||||||
| chrX:63676125 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.816-1958G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676125 | |||||||
| chrX:63676308 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.815+2032A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676308 | |||||||
| chrX:63676435 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.815+1905G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676435 | |||||||
| chrX:63676478 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.815+1862A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676478 | |||||||
| chrX:63676560 | G | A | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.815+1780C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676560 | |||||||
| chrX:63676806 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.815+1534T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63676806 | |||||||
| chrX:63677242 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.815+1098A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677242 | |||||||
| chrX:63677582 | G | A | 4 | a0001c0001t0003g0039 a0001c0001t0003g0071 a0001c0001t0003g0099 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+758C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677582 | |||||||
| chrX:63677616 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.815+724G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677616 | |||||||
| chrX:63677853 | A | C | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+487T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63677853 | |||||||
| chrX:63678031 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.815+309C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63678031 | |||||||
| chrX:63678038 | G | A | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.815+302C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63678038 | |||||||
| chrX:63678105 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.815+235A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 5/9 | chrX | 63678105 | |||||||
| chrX:63678704 | G | T | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.583-132C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63678704 | |||||||
| chrX:63678763 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.583-191C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63678763 | |||||||
| chrX:63678934 | A | G | 2 | a0001c0001t0002g0025 a0001c0001t0002g0028 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.583-362T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63678934 | |||||||
| chrX:63679748 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.583-1176T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63679748 | |||||||
| chrX:63680559 | T | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-1987A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63680559 | |||||||
| chrX:63680787 | C | T | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-2215G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63680787 | |||||||
| chrX:63680866 | A | AAAC | 3 | a0001c0001t0001g0104 a0001c0001t0002g0072 a0001c0001t0002g0098 |
3 | HG03540.hp1 HG03579.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.583-2297_583-2295d others(5): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63680866 | |||||||
| chrX:63681174 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.583-2602C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681174 | |||||||
| chrX:63681326 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.583-2754C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681326 | |||||||
| chrX:63681451 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00639.hp1 HG01070.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-2879G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681451 | |||||||
| chrX:63681923 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.583-3351G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63681923 | |||||||
| chrX:63682133 | C | CAATA | 8 | a0001c0001t0001g0093 a0001c0001t0001g0115 a0001c0001t0001g0131 others(5): Show |
8 | HG00621.hp1 HG01106.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.583-3565_583-3562d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682133 | |||||||
| chrX:63682133 | CAATA | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0080 a0001c0001t0001g0102 others(10): Show |
15 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.583-3565_583-3562d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682133 | |||||||
| chrX:63682133 | CAATAAAT others(1): Show |
C | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0019 |
3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.583-3569_583-3562d others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682133 | |||||||
| chrX:63682461 | G | A | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.583-3889C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63682461 | |||||||
| chrX:63683092 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.583-4520G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63683092 | |||||||
| chrX:63684202 | G | A | 1 | a0001c0001t0005g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.583-5630C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63684202 | |||||||
| chrX:63685361 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.583-6789G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63685361 | |||||||
| chrX:63685379 | C | T | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-6807G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63685379 | |||||||
| chrX:63685868 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.583-7296C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63685868 | |||||||
| chrX:63686202 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.583-7630A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686202 | |||||||
| chrX:63686283 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.583-7711G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686283 | |||||||
| chrX:63686301 | G | A | 21 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0139 others(18): Show |
22 | HG01255.hp1 HG02280.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.583-7729C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686301 | |||||||
| chrX:63686355 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.583-7783G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686355 | |||||||
| chrX:63686553 | T | C | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.583-7981A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63686553 | |||||||
| chrX:63687295 | G | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0129 |
5 | NA18960.hp1 NA18984.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-8723C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63687295 | |||||||
| chrX:63687312 | A | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0101 a0001c0001t0001g0129 |
5 | NA18960.hp1 NA18984.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.583-8740T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63687312 | |||||||
| chrX:63687846 | C | T | 10 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(7): Show |
10 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.583-9274G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63687846 | |||||||
| chrX:63688211 | T | C | 2 | a0001c0001t0002g0118 a0001c0001t0002g0126 |
2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.582+8914A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63688211 | |||||||
| chrX:63688251 | A | C | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.582+8874T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63688251 | |||||||
| chrX:63688475 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582+8650T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63688475 | |||||||
| chrX:63689311 | C | T | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+7814G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689311 | |||||||
| chrX:63689462 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.582+7663G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689462 | |||||||
| chrX:63689610 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.582+7515C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689610 | |||||||
| chrX:63689625 | A | C | 1 | a0001c0001t0002g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.582+7500T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63689625 | |||||||
| chrX:63690529 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.582+6596C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63690529 | |||||||
| chrX:63690575 | T | C | 10 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(7): Show |
11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+6550A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63690575 | |||||||
| chrX:63690847 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0015g0031 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.582+6278G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63690847 | |||||||
| chrX:63691312 | T | A | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.582+5813A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63691312 | |||||||
| chrX:63691703 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.582+5422T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63691703 | |||||||
| chrX:63692106 | G | A | 2 | a0001c0001t0009g0007 a0001c0001t0009g0008 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.582+5019C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63692106 | |||||||
| chrX:63692141 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.582+4984A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63692141 | |||||||
| chrX:63692243 | G | A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+4882C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63692243 | |||||||
| chrX:63693092 | T | G | 10 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(7): Show |
11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+4033A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693092 | |||||||
| chrX:63693611 | C | CA | 27 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0027 others(24): Show |
28 | HG00735.hp1 HG00735.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.582+3513dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693611 | |||||||
| chrX:63693611 | C | CAA | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+3512_582+3513d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693611 | |||||||
| chrX:63693630 | C | A | 3 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 |
3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.582+3495G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693630 | |||||||
| chrX:63693643 | A | G | 5 | a0001c0001t0002g0032 a0001c0001t0002g0061 a0001c0001t0002g0062 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.582+3482T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693643 | |||||||
| chrX:63693687 | AAAACT | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0136 a0001c0001t0002g0145 others(1): Show |
4 | HG02602.hp1 HG02735.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+3433_582+3437d others(7): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693687 | |||||||
| chrX:63693725 | C | T | 10 | a0001c0001t0001g0051 a0001c0001t0005g0012 a0001c0001t0005g0013 others(7): Show |
11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+3400G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693725 | |||||||
| chrX:63693952 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.582+3173C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63693952 | |||||||
| chrX:63694183 | C | CA | 12 | a0001c0001t0001g0043 a0001c0001t0001g0068 a0001c0001t0001g0091 others(9): Show |
12 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.582+2941dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694183 | |||||||
| chrX:63694575 | T | C | 1 | a0001c0001t0005g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.582+2550A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694575 | |||||||
| chrX:63694638 | C | T | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.582+2487G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694638 | |||||||
| chrX:63694695 | T | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0157 |
3 | NA18971.hp1 NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.582+2430A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694695 | |||||||
| chrX:63694868 | T | C | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.582+2257A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63694868 | |||||||
| chrX:63695235 | G | A | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.582+1890C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63695235 | |||||||
| chrX:63695530 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.582+1595A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63695530 | |||||||
| chrX:63695624 | C | G | 2 | a0001c0001t0001g0108 a0001c0001t0014g0109 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.582+1501G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63695624 | |||||||
| chrX:63696450 | C | A | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.582+675G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63696450 | |||||||
| chrX:63697018 | T | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.582+107A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 4/9 | chrX | 63697018 | |||||||
| chrX:63697395 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.403-91G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63697395 | |||||||
| chrX:63697796 | T | C | 13 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(10): Show |
14 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.403-492A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63697796 | |||||||
| chrX:63697903 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.403-599T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63697903 | |||||||
| chrX:63698609 | G | A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.403-1305C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63698609 | |||||||
| chrX:63699052 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.403-1748A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699052 | |||||||
| chrX:63699078 | G | C | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.403-1774C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699078 | |||||||
| chrX:63699521 | A | G | 15 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(12): Show |
16 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.403-2217T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699521 | |||||||
| chrX:63699804 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.403-2500T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63699804 | |||||||
| chrX:63700045 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.403-2741C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63700045 | |||||||
| chrX:63700873 | C | G | 2 | a0001c0001t0002g0034 a0001c0001t0015g0031 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.403-3569G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63700873 | |||||||
| chrX:63701092 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.403-3788G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701092 | |||||||
| chrX:63701553 | T | C | 1 | a0001c0001t0008g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.403-4249A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701553 | |||||||
| chrX:63701628 | G | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-4324C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701628 | |||||||
| chrX:63701719 | G | A | 1 | a0001c0001t0002g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.403-4415C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701719 | |||||||
| chrX:63701842 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.402+4416C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63701842 | |||||||
| chrX:63702222 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.402+4036A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63702222 | |||||||
| chrX:63702956 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.402+3302C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63702956 | |||||||
| chrX:63703394 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.402+2864G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63703394 | |||||||
| chrX:63703635 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.402+2623G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63703635 | |||||||
| chrX:63704074 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.402+2184T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704074 | |||||||
| chrX:63704397 | C | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.402+1861G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704397 | |||||||
| chrX:63704514 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.402+1744C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704514 | |||||||
| chrX:63704525 | T | A | 5 | a0001c0001t0002g0030 a0001c0001t0002g0061 a0001c0001t0002g0062 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.402+1733A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704525 | |||||||
| chrX:63704608 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.402+1650C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704608 | |||||||
| chrX:63704695 | T | C | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.402+1563A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704695 | |||||||
| chrX:63704857 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.402+1401C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704857 | |||||||
| chrX:63704858 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.402+1400G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63704858 | |||||||
| chrX:63705357 | A | ATG | 3 | a0001c0001t0001g0036 a0001c0001t0001g0111 a0001c0001t0016g0152 |
3 | HG00673.hp1 HG00738.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.402+899_402+900dup others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | |||||||
| chrX:63705357 | A | ATGTG | 3 | a0001c0001t0001g0035 a0001c0001t0006g0016 a0001c0001t0006g0018 |
3 | HG00639.hp2 HG01070.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.402+897_402+900dup others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | |||||||
| chrX:63705357 | ATG | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(104): Show |
113 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.402+899_402+900del others(2): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | |||||||
| chrX:63705357 | ATGTG | A | 9 | a0001c0001t0001g0049 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00735.hp1 HG01943.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.402+897_402+900del others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | |||||||
| chrX:63705357 | ATGTGTG | A | 2 | a0001c0001t0002g0148 a0002c0002t0018g0138 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.402+895_402+900del others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | |||||||
| chrX:63705357 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.402+885_402+900del others(16): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705357 | |||||||
| chrX:63705374 | T | C | 7 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.402+884A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705374 | |||||||
| chrX:63705401 | GT | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0095 |
2 | HG00639.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.402+856delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705401 | |||||||
| chrX:63705706 | A | T | 1 | a0001c0001t0012g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.402+552T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705706 | |||||||
| chrX:63705717 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.402+541G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705717 | |||||||
| chrX:63705742 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.402+516A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 3/9 | chrX | 63705742 | |||||||
| chrX:63706668 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.211-219C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63706668 | |||||||
| chrX:63706792 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211-343G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63706792 | |||||||
| chrX:63707360 | T | TA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0036 others(20): Show |
24 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.211-912dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707360 | |||||||
| chrX:63707360 | T | TG | 2 | a0001c0001t0001g0157 a0001c0001t0002g0107 |
2 | NA19082.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.211-912_211-911ins others(1): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707360 | |||||||
| chrX:63707360 | TA | T | 8 | a0001c0001t0001g0136 a0001c0001t0005g0012 a0001c0001t0005g0013 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.211-912delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707360 | |||||||
| chrX:63707361 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0075 a0001c0001t0001g0110 |
4 | NA18971.hp1 NA18986.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-912T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63707361 | |||||||
| chrX:63708178 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.211-1729T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708178 | |||||||
| chrX:63708266 | T | C | 10 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(7): Show |
11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.211-1817A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708266 | |||||||
| chrX:63708745 | A | C | 1 | a0001c0001t0003g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.211-2296T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708745 | |||||||
| chrX:63708760 | T | C | 11 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(8): Show |
12 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.211-2311A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63708760 | |||||||
| chrX:63709057 | C | T | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.211-2608G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709057 | |||||||
| chrX:63709193 | G | T | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-2744C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709193 | |||||||
| chrX:63709195 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.211-2746A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709195 | |||||||
| chrX:63709474 | T | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-3025A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709474 | |||||||
| chrX:63709770 | G | A | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-3321C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709770 | |||||||
| chrX:63709944 | G | A | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.211-3495C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63709944 | |||||||
| chrX:63710296 | G | GA | 46 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0024 others(43): Show |
48 | HG00609.hp1 HG00735.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.211-3848dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710296 | |||||||
| chrX:63710296 | GA | G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0047 others(6): Show |
10 | HG00621.hp1 HG00673.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.211-3848delT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710296 | |||||||
| chrX:63710499 | G | A | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-4050C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710499 | |||||||
| chrX:63710722 | A | G | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-4273T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710722 | |||||||
| chrX:63710817 | C | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0019 |
3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.211-4368G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63710817 | |||||||
| chrX:63711677 | T | C | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-5228A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63711677 | |||||||
| chrX:63712502 | G | A | 2 | a0001c0001t0009g0007 a0001c0001t0009g0008 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.211-6053C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63712502 | |||||||
| chrX:63712789 | T | C | 10 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(7): Show |
11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.211-6340A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63712789 | |||||||
| chrX:63712992 | T | A | 1 | a0001c0001t0002g0061 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.211-6543A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63712992 | |||||||
| chrX:63713312 | C | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.211-6863G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713312 | |||||||
| chrX:63713387 | T | A | 1 | a0001c0001t0009g0008 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211-6938A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713387 | |||||||
| chrX:63713494 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.211-7045G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713494 | |||||||
| chrX:63713701 | T | TAC | 2 | a0001c0001t0001g0050 a0001c0001t0002g0098 |
2 | HG03579.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.211-7254_211-7253d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | |||||||
| chrX:63713701 | T | TACAC | 41 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0086 others(38): Show |
41 | HG00642.hp1 HG01167.hp1 HG01255.hp1 others(38): Show |
intron_variant | MODIFIER | c.211-7256_211-7253d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | |||||||
| chrX:63713701 | T | TACACACA others(1): Show |
7 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.211-7260_211-7253d others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | |||||||
| chrX:63713701 | T | TACACACA others(3): Show |
3 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 |
3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.211-7262_211-7253d others(12): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | |||||||
| chrX:63713701 | T | TACACACA others(5): Show |
1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.211-7264_211-7253d others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | |||||||
| chrX:63713701 | T | TACACACA others(7): Show |
1 | a0001c0001t0008g0006 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.211-7266_211-7253d others(16): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | |||||||
| chrX:63713701 | TAC | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-7254_211-7253d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63713701 | |||||||
| chrX:63714700 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.211-8251G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63714700 | |||||||
| chrX:63715341 | C | T | 6 | a0001c0001t0001g0090 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | HG02015.hp1 HG02074.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-8892G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715341 | |||||||
| chrX:63715385 | GCT | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0068 a0001c0001t0001g0141 |
3 | NA18953.hp1 NA18955.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.211-8938_211-8937d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715385 | |||||||
| chrX:63715388 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0068 a0001c0001t0001g0141 |
3 | NA18953.hp1 NA18955.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.211-8939C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715388 | |||||||
| chrX:63715445 | G | GA | 5 | a0001c0001t0001g0057 a0001c0001t0001g0127 a0001c0001t0006g0016 others(2): Show |
5 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-8997dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715445 | |||||||
| chrX:63715621 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.210+8911A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715621 | |||||||
| chrX:63715765 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.210+8767G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715765 | |||||||
| chrX:63715769 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.210+8763T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715769 | |||||||
| chrX:63715776 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.210+8756T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715776 | |||||||
| chrX:63715867 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.210+8665A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63715867 | |||||||
| chrX:63716292 | G | T | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+8240C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63716292 | |||||||
| chrX:63716293 | A | T | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+8239T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63716293 | |||||||
| chrX:63716536 | T | C | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+7996A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63716536 | |||||||
| chrX:63717422 | T | C | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210+7110A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717422 | |||||||
| chrX:63717452 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.210+7080C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717452 | |||||||
| chrX:63717884 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.210+6648T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717884 | |||||||
| chrX:63717947 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01433.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.210+6585C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63717947 | |||||||
| chrX:63718123 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.210+6409G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63718123 | |||||||
| chrX:63718919 | T | C | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+5613A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63718919 | |||||||
| chrX:63718929 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0015g0031 |
2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.210+5603C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63718929 | |||||||
| chrX:63719459 | G | T | 1 | a0001c0001t0002g0060 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.210+5073C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63719459 | |||||||
| chrX:63719812 | C | T | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+4720G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63719812 | |||||||
| chrX:63720142 | A | T | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.210+4390T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720142 | |||||||
| chrX:63720367 | A | G | 5 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(2): Show |
6 | HG00735.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+4165T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720367 | |||||||
| chrX:63720388 | C | T | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.210+4144G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720388 | |||||||
| chrX:63720919 | T | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.210+3613A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63720919 | |||||||
| chrX:63722410 | G | GT | 10 | a0001c0001t0001g0049 a0001c0001t0001g0065 a0001c0001t0001g0101 others(7): Show |
11 | HG01074.hp1 HG02074.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.210+2121dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722410 | |||||||
| chrX:63722459 | G | T | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+2073C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722459 | |||||||
| chrX:63722772 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.210+1760G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722772 | |||||||
| chrX:63722884 | T | G | 32 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0043 others(29): Show |
32 | HG00280.hp1 HG01099.hp1 HG01258.hp1 others(29): Show |
intron_variant | MODIFIER | c.210+1648A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722884 | |||||||
| chrX:63722981 | C | T | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.210+1551G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63722981 | |||||||
| chrX:63723144 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | HG02738.hp1 NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.210+1388T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63723144 | |||||||
| chrX:63723599 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.210+933C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63723599 | |||||||
| chrX:63724159 | T | C | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.210+373A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 2/9 | chrX | 63724159 | |||||||
| chrX:63724871 | G | A | 8 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(5): Show |
8 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-160C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63724871 | |||||||
| chrX:63725229 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.31-518T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63725229 | |||||||
| chrX:63725425 | A | G | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31-714T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63725425 | |||||||
| chrX:63726067 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-1356C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726067 | |||||||
| chrX:63726191 | T | TA | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-1481dupT | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726191 | |||||||
| chrX:63726441 | C | T | 1 | a0001c0001t0007g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.31-1730G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726441 | |||||||
| chrX:63726524 | A | C | 2 | a0001c0001t0009g0007 a0001c0001t0009g0008 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.31-1813T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726524 | |||||||
| chrX:63726704 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.31-1993A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726704 | |||||||
| chrX:63726769 | G | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2058C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726769 | |||||||
| chrX:63726975 | A | G | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2264T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63726975 | |||||||
| chrX:63727602 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31-2891C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63727602 | |||||||
| chrX:63727906 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31-3195A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63727906 | |||||||
| chrX:63728452 | G | A | 7 | a0001c0001t0003g0039 a0001c0001t0003g0069 a0001c0001t0003g0070 others(4): Show |
7 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-3741C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63728452 | |||||||
| chrX:63728481 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.31-3770A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63728481 | |||||||
| chrX:63728749 | A | T | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.31-4038T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63728749 | |||||||
| chrX:63729376 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.31-4665A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729376 | |||||||
| chrX:63729673 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.31-4962G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729673 | |||||||
| chrX:63729911 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.31-5200G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729911 | |||||||
| chrX:63729981 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31-5270A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63729981 | |||||||
| chrX:63730211 | G | T | 1 | a0001c0001t0002g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31-5500C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63730211 | |||||||
| chrX:63730372 | G | T | 1 | a0001c0001t0001g0011 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.31-5661C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63730372 | |||||||
| chrX:63731333 | CTAGATTC others(241): Show |
C | 2 | a0001c0001t0001g0027 a0001c0001t0002g0026 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.31-6870_31-6623del | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731333 | |||||||
| chrX:63731552 | G | GT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0041 a0001c0001t0001g0044 others(21): Show |
24 | HG00639.hp2 HG01071.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.31-6842dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731552 | |||||||
| chrX:63731669 | C | T | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-6958G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731669 | |||||||
| chrX:63731725 | A | G | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-7014T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731725 | |||||||
| chrX:63731859 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0014g0109 |
2 | NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.31-7148G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731859 | |||||||
| chrX:63731898 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-7187T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731898 | |||||||
| chrX:63731975 | G | A | 2 | a0001c0001t0002g0118 a0001c0001t0002g0126 |
2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.31-7264C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63731975 | |||||||
| chrX:63732006 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.31-7295G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732006 | |||||||
| chrX:63732264 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-7553A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732264 | |||||||
| chrX:63732769 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0157 |
3 | NA18971.hp1 NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.31-8058C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732769 | |||||||
| chrX:63732854 | T | C | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0019 |
3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.31-8143A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63732854 | |||||||
| chrX:63733087 | T | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-8376A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63733087 | |||||||
| chrX:63733216 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.31-8505C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63733216 | |||||||
| chrX:63733583 | T | C | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-8872A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63733583 | |||||||
| chrX:63734252 | C | A | 1 | a0001c0001t0002g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.31-9541G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63734252 | |||||||
| chrX:63734447 | C | T | 1 | a0001c0001t0003g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.31-9736G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63734447 | |||||||
| chrX:63734571 | T | C | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-9860A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63734571 | |||||||
| chrX:63735460 | A | G | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-10749T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63735460 | |||||||
| chrX:63735578 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.31-10867C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63735578 | |||||||
| chrX:63736131 | C | T | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-11420G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63736131 | |||||||
| chrX:63737634 | C | G | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-12923G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63737634 | |||||||
| chrX:63737923 | T | C | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-13212A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63737923 | |||||||
| chrX:63737978 | A | T | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-13267T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63737978 | |||||||
| chrX:63738160 | A | T | 1 | a0001c0001t0002g0154 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.31-13449T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63738160 | |||||||
| chrX:63738563 | C | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-13852G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63738563 | |||||||
| chrX:63738880 | T | C | 1 | a0001c0001t0002g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.31-14169A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63738880 | |||||||
| chrX:63739094 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.31-14383A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739094 | |||||||
| chrX:63739174 | G | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0154 |
2 | HG02257.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.31-14463C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739174 | |||||||
| chrX:63739368 | A | T | 56 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0086 others(53): Show |
57 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.31-14657T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739368 | |||||||
| chrX:63739514 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.31-14803C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739514 | |||||||
| chrX:63739963 | C | T | 1 | a0001c0001t0005g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.31-15252G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739963 | |||||||
| chrX:63739979 | T | A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-15268A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63739979 | |||||||
| chrX:63740335 | G | C | 2 | a0001c0001t0009g0007 a0001c0001t0009g0008 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.31-15624C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63740335 | |||||||
| chrX:63740696 | A | C | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-15985T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63740696 | |||||||
| chrX:63741088 | A | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.31-16377T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63741088 | |||||||
| chrX:63741668 | C | T | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-16957G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63741668 | |||||||
| chrX:63742207 | A | G | 3 | a0001c0001t0006g0016 a0001c0001t0006g0017 a0001c0001t0006g0018 |
3 | HG00639.hp2 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.31-17496T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63742207 | |||||||
| chrX:63742304 | C | T | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-17593G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63742304 | |||||||
| chrX:63742785 | A | T | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.31-18074T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63742785 | |||||||
| chrX:63743065 | G | A | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.31-18354C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743065 | |||||||
| chrX:63743854 | G | A | 54 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0086 others(51): Show |
55 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.31-19143C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743854 | |||||||
| chrX:63743872 | G | A | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-19161C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63743872 | |||||||
| chrX:63744712 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.31-20001T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63744712 | |||||||
| chrX:63744843 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG00735.hp2 HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.31-20132A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63744843 | |||||||
| chrX:63745710 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.31-20999G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63745710 | |||||||
| chrX:63746145 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0158 |
2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.31-21434G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63746145 | |||||||
| chrX:63746610 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.31-21899G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63746610 | |||||||
| chrX:63746738 | C | T | 1 | a0001c0001t0005g0015 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.31-22027G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63746738 | |||||||
| chrX:63748168 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.31-23457G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63748168 | |||||||
| chrX:63748329 | T | C | 1 | a0001c0001t0007g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.31-23618A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63748329 | |||||||
| chrX:63749254 | C | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0002g0020 others(12): Show |
15 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.31-24543G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749254 | |||||||
| chrX:63749337 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.31-24626G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749337 | |||||||
| chrX:63749835 | T | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-25124A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749835 | |||||||
| chrX:63749864 | C | T | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-25153G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63749864 | |||||||
| chrX:63750129 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0087 |
3 | NA18961.hp1 NA18990.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.31-25418C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750129 | |||||||
| chrX:63750706 | C | T | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.31-25995G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750706 | |||||||
| chrX:63750866 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.31-26155C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750866 | |||||||
| chrX:63750936 | A | G | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-26225T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63750936 | |||||||
| chrX:63751007 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.31-26296A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63751007 | |||||||
| chrX:63753349 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.31-28638T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753349 | |||||||
| chrX:63753543 | G | GTT | 9 | a0001c0001t0001g0009 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG00639.hp2 HG00735.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-28834_31-28833d others(4): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753543 | |||||||
| chrX:63753543 | G | T | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.31-28832C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753543 | |||||||
| chrX:63753543 | GT | G | 5 | a0001c0001t0001g0122 a0001c0001t0001g0136 a0001c0001t0002g0096 others(2): Show |
5 | HG02257.hp2 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-28833delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63753543 | |||||||
| chrX:63754408 | A | AT | 9 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0130 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-29698dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63754408 | |||||||
| chrX:63755249 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+29867G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63755249 | |||||||
| chrX:63755284 | A | G | 1 | a0001c0001t0002g0073 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.30+29832T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63755284 | |||||||
| chrX:63755862 | A | T | 5 | a0001c0001t0008g0137 a0001c0001t0009g0007 a0001c0001t0009g0008 others(2): Show |
6 | HG02280.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+29254T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63755862 | |||||||
| chrX:63756290 | T | C | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+28826A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63756290 | |||||||
| chrX:63756442 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.30+28674T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63756442 | |||||||
| chrX:63756557 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.30+28559T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63756557 | |||||||
| chrX:63757515 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0012g0088 |
3 | HG00280.hp1 HG01099.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.30+27601C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63757515 | |||||||
| chrX:63757822 | A | T | 1 | a0001c0001t0002g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.30+27294T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63757822 | |||||||
| chrX:63758054 | T | A | 2 | a0001c0001t0009g0007 a0001c0001t0009g0008 |
2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.30+27062A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758054 | |||||||
| chrX:63758391 | C | G | 1 | a0001c0001t0002g0020 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.30+26725G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758391 | |||||||
| chrX:63758414 | T | G | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.30+26702A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758414 | |||||||
| chrX:63758437 | A | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+26679T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758437 | |||||||
| chrX:63758913 | G | A | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+26203C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63758913 | |||||||
| chrX:63759218 | C | A | 4 | a0001c0001t0002g0010 a0001c0001t0003g0037 a0001c0001t0003g0100 others(1): Show |
4 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+25898G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63759218 | |||||||
| chrX:63759275 | T | A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+25841A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63759275 | |||||||
| chrX:63759854 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.30+25262T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63759854 | |||||||
| chrX:63760024 | C | G | 9 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(6): Show |
10 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+25092G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760024 | |||||||
| chrX:63760304 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.30+24812A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760304 | |||||||
| chrX:63760579 | A | C | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+24537T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760579 | |||||||
| chrX:63760704 | G | T | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+24412C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760704 | |||||||
| chrX:63760753 | G | T | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+24363C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760753 | |||||||
| chrX:63760880 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.30+24236G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63760880 | |||||||
| chrX:63761439 | A | G | 1 | a0001c0001t0004g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+23677T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63761439 | |||||||
| chrX:63761565 | C | G | 1 | a0001c0001t0001g0003 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.30+23551G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63761565 | |||||||
| chrX:63762046 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.30+23070C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762046 | |||||||
| chrX:63762068 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.30+23048G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762068 | |||||||
| chrX:63762147 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.30+22969C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762147 | |||||||
| chrX:63762735 | T | G | 1 | a0001c0001t0007g0089 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.30+22381A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762735 | |||||||
| chrX:63762787 | C | G | 1 | a0001c0001t0010g0002 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.30+22329G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63762787 | |||||||
| chrX:63764052 | T | C | 1 | a0001c0001t0002g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.30+21064A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764052 | |||||||
| chrX:63764592 | G | A | 2 | a0001c0001t0003g0037 a0001c0001t0003g0149 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.30+20524C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764592 | |||||||
| chrX:63764621 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0129 |
2 | NA19000.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.30+20495T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764621 | |||||||
| chrX:63764947 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.30+20169G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764947 | |||||||
| chrX:63764948 | G | A | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+20168C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63764948 | |||||||
| chrX:63765363 | A | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
4 | HG02738.hp1 NA18966.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+19753T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63765363 | |||||||
| chrX:63765799 | G | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | HG02015.hp1 HG02074.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+19317C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63765799 | |||||||
| chrX:63766058 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.30+19058A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766058 | |||||||
| chrX:63766061 | A | C | 11 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(8): Show |
12 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+19055T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766061 | |||||||
| chrX:63766454 | T | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+18662A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766454 | |||||||
| chrX:63766961 | A | C | 2 | a0001c0001t0006g0016 a0001c0001t0006g0017 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.30+18155T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63766961 | |||||||
| chrX:63767545 | A | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0002g0020 others(12): Show |
15 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.30+17571T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767545 | |||||||
| chrX:63767790 | C | T | 52 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0002g0010 others(49): Show |
53 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.30+17326G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767790 | |||||||
| chrX:63767801 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.30+17315C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767801 | |||||||
| chrX:63767860 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+17256A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63767860 | |||||||
| chrX:63768070 | T | A | 1 | a0001c0001t0001g0003 | 2 | NA18961.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.30+17046A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768070 | |||||||
| chrX:63768205 | C | T | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30+16911G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768205 | |||||||
| chrX:63768223 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.30+16893G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768223 | |||||||
| chrX:63768475 | C | A | 2 | a0001c0001t0005g0014 a0001c0001t0005g0015 |
2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.30+16641G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768475 | |||||||
| chrX:63768759 | T | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+16357A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63768759 | |||||||
| chrX:63769890 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.30+15226C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63769890 | |||||||
| chrX:63769998 | G | A | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+15118C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63769998 | |||||||
| chrX:63770172 | A | G | 12 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(9): Show |
13 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.30+14944T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770172 | |||||||
| chrX:63770173 | T | C | 15 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(12): Show |
16 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+14943A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770173 | |||||||
| chrX:63770516 | C | T | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30+14600G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770516 | |||||||
| chrX:63770598 | C | G | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.30+14518G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770598 | |||||||
| chrX:63770958 | C | T | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+14158G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63770958 | |||||||
| chrX:63771573 | C | CT | 9 | a0001c0001t0001g0044 a0001c0001t0005g0012 a0001c0001t0005g0013 others(6): Show |
9 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+13542dupA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771573 | |||||||
| chrX:63771659 | T | C | 14 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(11): Show |
15 | HG00639.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+13457A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771659 | |||||||
| chrX:63771719 | A | T | 1 | a0001c0001t0003g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.30+13397T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771719 | |||||||
| chrX:63771748 | GTAGA | G | 2 | a0001c0001t0003g0069 a0001c0001t0003g0070 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.30+13364_30+13367d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771748 | |||||||
| chrX:63771936 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0146 |
2 | NA18944.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.30+13180A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63771936 | |||||||
| chrX:63772277 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.30+12839C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772277 | |||||||
| chrX:63772358 | A | G | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+12758T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772358 | |||||||
| chrX:63772409 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0131 a0001c0001t0001g0132 others(3): Show |
6 | HG00735.hp2 HG01109.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+12707A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772409 | |||||||
| chrX:63772416 | C | T | 1 | a0001c0001t0003g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.30+12700G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772416 | |||||||
| chrX:63772906 | C | T | 4 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | NA18953.hp1 NA18955.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+12210G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63772906 | |||||||
| chrX:63773116 | C | T | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+12000G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63773116 | |||||||
| chrX:63773117 | A | G | 1 | a0001c0001t0017g0094 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.30+11999T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63773117 | |||||||
| chrX:63773866 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG00639.hp1 HG01070.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+11250T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63773866 | |||||||
| chrX:63774045 | ATATC | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
83 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.30+11067_30+11070d others(6): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774045 | |||||||
| chrX:63774045 | ATATCTAT others(1): Show |
A | 15 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(12): Show |
15 | HG00621.hp1 HG00639.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+11063_30+11070d others(10): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774045 | |||||||
| chrX:63774045 | ATATCTAT others(5): Show |
A | 1 | a0001c0001t0005g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.30+11059_30+11070d others(14): Show |
ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774045 | |||||||
| chrX:63774518 | C | G | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+10598G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774518 | |||||||
| chrX:63774537 | T | C | 1 | a0001c0001t0002g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.30+10579A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63774537 | |||||||
| chrX:63775059 | G | C | 11 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(8): Show |
12 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+10057C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775059 | |||||||
| chrX:63775102 | A | C | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+10014T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775102 | |||||||
| chrX:63775130 | A | T | 4 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | HG01167.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9986T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775130 | |||||||
| chrX:63775148 | T | A | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+9968A>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775148 | |||||||
| chrX:63775407 | C | T | 19 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0044 others(16): Show |
19 | HG01258.hp1 HG01261.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+9709G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775407 | |||||||
| chrX:63775504 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.30+9612G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775504 | |||||||
| chrX:63775522 | G | A | 1 | a0001c0001t0008g0137 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9594C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775522 | |||||||
| chrX:63775529 | T | C | 1 | a0001c0001t0005g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+9587A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775529 | |||||||
| chrX:63775726 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.30+9390T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775726 | |||||||
| chrX:63775792 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | NA18945.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.30+9324T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775792 | |||||||
| chrX:63775859 | C | A | 1 | a0002c0002t0018g0138 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.30+9257G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775859 | |||||||
| chrX:63775931 | G | T | 1 | a0001c0001t0005g0012 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.30+9185C>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63775931 | |||||||
| chrX:63776005 | C | T | 5 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(2): Show |
5 | HG01243.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+9111G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63776005 | |||||||
| chrX:63776239 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.30+8877G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63776239 | |||||||
| chrX:63776402 | G | C | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+8714C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63776402 | |||||||
| chrX:63777212 | A | G | 1 | a0001c0001t0003g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.30+7904T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777212 | |||||||
| chrX:63777315 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+7801G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777315 | |||||||
| chrX:63777444 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.30+7672G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777444 | |||||||
| chrX:63777537 | C | G | 2 | a0001c0001t0003g0037 a0001c0001t0003g0149 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.30+7579G>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777537 | |||||||
| chrX:63777659 | T | C | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0019 |
3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.30+7457A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777659 | |||||||
| chrX:63777685 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.30+7431C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777685 | |||||||
| chrX:63777743 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00673.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.30+7373G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63777743 | |||||||
| chrX:63778171 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.30+6945A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778171 | |||||||
| chrX:63778380 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.30+6736A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778380 | |||||||
| chrX:63778748 | A | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0002g0020 others(12): Show |
15 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(12): Show |
intron_variant | MODIFIER | c.30+6368T>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778748 | |||||||
| chrX:63778811 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18983.hp1 NA18994.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.30+6305C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63778811 | |||||||
| chrX:63779059 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.30+6057C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779059 | |||||||
| chrX:63779161 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+5955G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779161 | |||||||
| chrX:63779285 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.30+5831C>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779285 | |||||||
| chrX:63779311 | A | C | 1 | a0001c0001t0005g0014 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.30+5805T>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779311 | |||||||
| chrX:63779955 | C | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0019 |
3 | HG01243.hp1 HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.30+5161G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63779955 | |||||||
| chrX:63780342 | T | C | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.30+4774A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63780342 | |||||||
| chrX:63780731 | C | A | 1 | a0001c0001t0003g0149 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.30+4385G>T | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63780731 | |||||||
| chrX:63781795 | T | C | 1 | a0001c0001t0005g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+3321A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63781795 | |||||||
| chrX:63781827 | T | C | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02027.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.30+3289A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63781827 | |||||||
| chrX:63782264 | A | G | 8 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0005g0014 others(5): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+2852T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782264 | |||||||
| chrX:63782325 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.30+2791G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782325 | |||||||
| chrX:63782844 | A | G | 1 | a0001c0001t0002g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.30+2272T>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63782844 | |||||||
| chrX:63783144 | T | G | 1 | a0001c0001t0016g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.30+1972A>C | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783144 | |||||||
| chrX:63783179 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.30+1937A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783179 | |||||||
| chrX:63783273 | AT | A | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG00140.hp1 HG01515.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+1842delA | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63783273 | |||||||
| chrX:63784036 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+1080G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784036 | |||||||
| chrX:63784418 | C | T | 4 | a0001c0001t0008g0006 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
5 | HG00735.hp1 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.30+698G>A | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784418 | |||||||
| chrX:63784423 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+693A>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784423 | |||||||
| chrX:63784538 | G | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.30+578C>G | ARHGEF9 | ENSG00000131089.17 | transcript | ENST00000671741.2 | protein_coding | 1/9 | chrX | 63784538 |