Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 93663 |
| ensemblid | ENSG00000146376.11 |
| hgncid | 21035 |
| symbol | ARHGAP18 |
| name | Rho GTPase activating protein 18 |
| refseq_nuc | NM_033515.3 |
| refseq_prot | NP_277050.2 |
| ensembl_nuc | ENST00000368149.3 |
| ensembl_prot | ENSP00000357131.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 129576132 |
| end | 129710177 |
| strand | - |
| ver | v1.2 |
| region | chr6:129576132-129710177 |
| region5000 | chr6:129571132-129715177 |
| regionname0 | ARHGAP18_chr6_129576132_129710177 |
| regionname5000 | ARHGAP18_chr6_129571132_129715177 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 663 | 179 | 50 | 40 | 65 | 9 | 15 | 40 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0002 | 1/1 | 663 | 51 | 8 | 10 | 28 | 1 | 2 | 17 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0003 | 0/0 | 663 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0004 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0005 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0006 | 0/0 | 663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0007 | 0/0 | 663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0008 | 0/0 | 663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| a0009 | 0/0 | 663 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | MSWLS others(658): Show |
chr6 | 129571132 | 129715177 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1989 | 174 | 48 | 39 | 65 | 8 | 14 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0001c0003 | 0/0 | 1989 | 3 | 1 | 0 | 0 | 1 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0001c0009 | 0/0 | 1989 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0001c0011 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0002c0002 | 1/1 | 1989 | 50 | 8 | 10 | 27 | 1 | 2 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0002c0006 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0003c0004 | 0/0 | 1989 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0004c0008 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0005c0005 | 0/0 | 1989 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0006c0010 | 0/0 | 1989 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0007c0012 | 0/0 | 1989 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0008c0013 | 0/0 | 1989 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 | ||
| a0009c0007 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | ATGAG others(1984): Show |
chr6 | 129571132 | 129715177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4414 | 105 | 15 | 33 | 44 | 7 | 6 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0002 | 0/0 | 4413 | 35 | 11 | 6 | 11 | 1 | 6 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4408): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0003 | 0/0 | 4414 | 14 | 10 | 0 | 4 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0004 | 0/0 | 4411 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4406): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0005 | 0/0 | 4416 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4411): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0006 | 0/0 | 4411 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4406): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0007 | 0/0 | 4414 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0008 | 0/0 | 4414 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0009 | 0/0 | 4416 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4411): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0010 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4406): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0011 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4406): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0013 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4408): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0015 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0016 | 0/0 | 4414 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0017 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0001t0019 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0003t0002 | 0/0 | 4413 | 3 | 1 | 0 | 0 | 1 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4408): Show |
chr6 | 129571132 | 129715177 |
| a0001c0009t0001 | 0/0 | 4414 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0001c0011t0001 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0002c0002t0001 | 1/1 | 4414 | 32 | 4 | 6 | 18 | 1 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0002c0002t0002 | 0/0 | 4413 | 8 | 1 | 2 | 5 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4408): Show |
chr6 | 129571132 | 129715177 |
| a0002c0002t0003 | 0/0 | 4414 | 6 | 2 | 1 | 3 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0002c0002t0005 | 0/0 | 4416 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4411): Show |
chr6 | 129571132 | 129715177 |
| a0002c0002t0006 | 0/0 | 4411 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4406): Show |
chr6 | 129571132 | 129715177 |
| a0002c0002t0014 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0002c0002t0018 | 0/0 | 4414 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0002c0006t0012 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4408): Show |
chr6 | 129571132 | 129715177 |
| a0003c0004t0001 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0003c0004t0005 | 0/0 | 4416 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4411): Show |
chr6 | 129571132 | 129715177 |
| a0004c0008t0004 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4406): Show |
chr6 | 129571132 | 129715177 |
| a0005c0005t0003 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0006c0010t0001 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0007c0012t0002 | 0/0 | 4413 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4408): Show |
chr6 | 129571132 | 129715177 |
| a0008c0013t0001 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| a0009c0007t0001 | 0/0 | 4414 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | CTCTG others(4409): Show |
chr6 | 129571132 | 129715177 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0013g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0016g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0017g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0019g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0003t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0009t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0011t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0006g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0018g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0006t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0003c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0003c0004t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0004c0008t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0005c0005t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0006c0010t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0007c0012t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0008c0013t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0009c0007t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0190 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00733 | hp2 | a0002 | c0002 | t0018 | g0009 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01099 | hp2 | a0001 | c0009 | t0001 | g0122 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0031 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02027 | hp2 | a0001 | c0001 | t0016 | g0149 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CDX | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | CDX | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0043 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02615 | hp2 | a0004 | c0008 | t0004 | g0055 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0110 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0118 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02965 | hp1 | a0005 | c0005 | t0003 | g0002 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0151 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0174 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0136 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03209 | hp2 | a0001 | c0011 | t0001 | g0056 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03491 | hp1 | a0002 | c0002 | t0006 | g0028 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03540 | hp2 | a0002 | c0002 | t0014 | g0045 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0211 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03704 | hp2 | a0006 | c0010 | t0001 | g0197 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0060 | SAS | BEB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04115 | hp1 | a0007 | c0012 | t0002 | g0095 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04115 | hp2 | a0008 | c0013 | t0001 | g0208 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0029 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0198 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0033 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18612 | hp1 | a0001 | c0001 | t0009 | g0069 | EAS | CHB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18983 | hp1 | a0001 | c0001 | t0013 | g0119 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19004 | hp1 | a0002 | c0002 | t0005 | g0024 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0233 | AFR | LWK | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | LWK | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19056 | hp2 | a0002 | c0006 | t0012 | g0034 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19070 | hp2 | a0009 | c0007 | t0001 | g0027 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19090 | hp2 | a0001 | c0001 | t0009 | g0070 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0228 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0175 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20300 | hp1 | a0003 | c0004 | t0005 | g0088 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0005 | REF | REF | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0003 | REF | REF | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129584076 | G | A | 1 | a0007 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1750C>T | p.Pro584Ser | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/15 | 1791/4414 | 1750/1992 | 584/663 | chr6 | 129584076 | |||
| chr6:129599221 | T | C | 1 | a0009 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.1708A>G | p.Asn570Asp | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/15 | 1749/4414 | 1708/1992 | 570/663 | chr6 | 129599221 | |||
| chr6:129608031 | C | T | 1 | a0006 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1144G>A | p.Ala382Thr | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/15 | 1185/4414 | 1144/1992 | 382/663 | chr6 | 129608031 | |||
| chr6:129629396 | T | C | 1 | a0003 | 2 | HG03098.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.743A>G | p.Lys248Arg | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/15 | 784/4414 | 743/1992 | 248/663 | chr6 | 129629396 | |||
| chr6:129634101 | G | A | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.557C>T | p.Pro186Leu | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/15 | 598/4414 | 557/1992 | 186/663 | chr6 | 129634101 | |||
| chr6:129710043 | C | T | 1 | a0004 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.94G>A | p.Gly32Arg | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 135/4414 | 94/1992 | 32/663 | chr6 | 129710043 | |||
| chr6:129710066 | A | G | 1 | a0005 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.71T>C | p.Val24Ala | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 112/4414 | 71/1992 | 24/663 | chr6 | 129710066 | |||
| chr6:129710070 | T | C | 6 | a0001 a0003 a0004 others(3): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
missense_variant | MODERATE | c.67A>G | p.Thr23Ala | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 108/4414 | 67/1992 | 23/663 | chr6 | 129710070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129584104 | A | G | 2 | a0001c0003 a0002c0006 |
4 | HG00099.hp1 HG03669.hp2 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.1722T>C | p.Val574Val | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/15 | 1763/4414 | 1722/1992 | 574/663 | chr6 | 129584104 | |||
| chr6:129600648 | C | G | 1 | a0001c0011 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1566G>C | p.Leu522Leu | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/15 | 1607/4414 | 1566/1992 | 522/663 | chr6 | 129600648 | |||
| chr6:129638484 | C | T | 1 | a0001c0009 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.462G>A | p.Thr154Thr | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/15 | 503/4414 | 462/1992 | 154/663 | chr6 | 129638484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129576195 | A | T | 1 | a0001c0001t0013 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2318T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2318 | chr6 | 129576195 | ||||||
| chr6:129576206 | C | G | 4 | a0001c0001t0003 a0001c0001t0008 a0002c0002t0003 others(1): Show |
23 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2307G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2307 | chr6 | 129576206 | ||||||
| chr6:129576390 | G | T | 1 | a0002c0006t0012 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2123 | chr6 | 129576390 | ||||||
| chr6:129576411 | C | T | 1 | a0001c0001t0016 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2102G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2102 | chr6 | 129576411 | ||||||
| chr6:129576554 | G | C | 1 | a0001c0001t0011 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1959C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1959 | chr6 | 129576554 | ||||||
| chr6:129576665 | G | A | 2 | a0001c0001t0010 a0001c0001t0011 |
2 | HG02615.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1848C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1848 | chr6 | 129576665 | ||||||
| chr6:129576700 | C | T | 1 | a0001c0001t0015 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1813G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1813 | chr6 | 129576700 | ||||||
| chr6:129576725 | T | C | 1 | a0001c0001t0017 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1788A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1788 | chr6 | 129576725 | ||||||
| chr6:129576783 | T | C | 1 | a0002c0002t0018 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1730A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1730 | chr6 | 129576783 | ||||||
| chr6:129576922 | A | G | 1 | a0002c0002t0014 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1591T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1591 | chr6 | 129576922 | ||||||
| chr6:129577023 | T | G | 1 | a0001c0001t0008 | 2 | HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1490A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1490 | chr6 | 129577023 | ||||||
| chr6:129577033 | TA | T | 6 | a0001c0001t0002 a0001c0001t0013 a0001c0003t0002 others(3): Show |
49 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1479delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1479 | chr6 | 129577033 | ||||||
| chr6:129577037 | A | G | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(5): Show |
12 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1476T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1476 | chr6 | 129577037 | ||||||
| chr6:129577169 | C | T | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(3): Show |
9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1344G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1344 | chr6 | 129577169 | ||||||
| chr6:129577195 | G | T | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(3): Show |
9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1318C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1318 | chr6 | 129577195 | ||||||
| chr6:129577508 | C | T | 2 | a0001c0001t0010 a0001c0001t0011 |
2 | HG02615.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1005G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1005 | chr6 | 129577508 | ||||||
| chr6:129577586 | T | TAA | 4 | a0001c0001t0005 a0001c0001t0009 a0002c0002t0005 others(1): Show |
6 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*926dupTT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 926 | chr6 | 129577586 | ||||||
| chr6:129577621 | C | A | 1 | a0001c0001t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 892 | chr6 | 129577621 | ||||||
| chr6:129577869 | G | A | 2 | a0001c0001t0004 a0004c0008t0004 |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*644C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 644 | chr6 | 129577869 | ||||||
| chr6:129577982 | A | G | 1 | a0001c0001t0009 | 2 | NA18612.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*531T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 531 | chr6 | 129577982 | ||||||
| chr6:129578141 | G | A | 4 | a0001c0001t0005 a0001c0001t0009 a0002c0002t0005 others(1): Show |
6 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*372C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 372 | chr6 | 129578141 | ||||||
| chr6:129578291 | C | T | 2 | a0001c0001t0006 a0002c0002t0006 |
3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*222G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 222 | chr6 | 129578291 | ||||||
| chr6:129578314 | CTAA | C | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(3): Show |
9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*196_*198delTTA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 196 | chr6 | 129578314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129578990 | A | T | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1901-386T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129578990 | |||||||
| chr6:129579003 | C | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1901-399G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579003 | |||||||
| chr6:129579229 | G | C | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-625C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579229 | |||||||
| chr6:129579275 | T | C | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-671A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579275 | |||||||
| chr6:129579326 | C | G | 19 | a0001c0001t0003g0073 a0001c0001t0003g0128 a0001c0001t0003g0133 others(16): Show |
19 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1901-722G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579326 | |||||||
| chr6:129579464 | T | A | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1900+606A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579464 | |||||||
| chr6:129579505 | A | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0002c0002t0001g0025 |
3 | HG02257.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1900+565T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579505 | |||||||
| chr6:129579822 | A | C | 2 | a0001c0001t0001g0199 a0002c0002t0001g0004 |
2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1900+248T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579822 | |||||||
| chr6:129580016 | C | G | 1 | a0001c0001t0001g0218 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1900+54G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129580016 | |||||||
| chr6:129580237 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1839-106A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580237 | |||||||
| chr6:129580261 | G | A | 1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1839-130C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580261 | |||||||
| chr6:129580293 | A | G | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1839-162T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580293 | |||||||
| chr6:129580322 | TTAAAA | T | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1839-196_1839-192d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580322 | |||||||
| chr6:129580335 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1839-204T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580335 | |||||||
| chr6:129580687 | A | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1839-556T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580687 | |||||||
| chr6:129580998 | C | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0146 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp2 HG02523.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839-867G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580998 | |||||||
| chr6:129581187 | T | G | 2 | a0002c0002t0001g0021 a0002c0002t0001g0051 |
2 | NA18977.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1839-1056A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581187 | |||||||
| chr6:129581355 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1839-1224G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581355 | |||||||
| chr6:129581369 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0154 a0001c0001t0001g0196 |
3 | HG00558.hp2 NA18987.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1839-1238G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581369 | |||||||
| chr6:129581376 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1839-1245C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581376 | |||||||
| chr6:129581448 | AACT | A | 9 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(6): Show |
9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1839-1320_1839-131 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581448 | |||||||
| chr6:129581494 | T | G | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1839-1363A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581494 | |||||||
| chr6:129581608 | T | A | 47 | a0001c0001t0002g0057 a0001c0001t0002g0066 a0001c0001t0002g0067 others(44): Show |
47 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1839-1477A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581608 | |||||||
| chr6:129581660 | C | T | 1 | a0002c0002t0002g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1839-1529G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581660 | |||||||
| chr6:129581879 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0131 a0001c0001t0001g0194 |
3 | HG02896.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1839-1748G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581879 | |||||||
| chr6:129581907 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1839-1776G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581907 | |||||||
| chr6:129581965 | A | G | 3 | a0001c0001t0006g0060 a0001c0001t0006g0198 a0002c0002t0006g0028 |
3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1839-1834T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581965 | |||||||
| chr6:129582131 | G | GAAGGAAT others(8): Show |
9 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(6): Show |
9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1838+1842_1838+185 others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582131 | |||||||
| chr6:129582232 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1838+1756G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582232 | |||||||
| chr6:129582358 | T | C | 5 | a0001c0001t0006g0060 a0001c0001t0006g0198 a0001c0001t0010g0136 others(2): Show |
5 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+1630A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582358 | |||||||
| chr6:129582373 | A | G | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1838+1615T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582373 | |||||||
| chr6:129582533 | T | C | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1838+1455A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582533 | |||||||
| chr6:129582626 | G | C | 9 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(6): Show |
9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1838+1362C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582626 | |||||||
| chr6:129582633 | C | G | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1838+1355G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582633 | |||||||
| chr6:129582840 | C | T | 1 | a0001c0001t0003g0219 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1838+1148G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582840 | |||||||
| chr6:129583107 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1838+881C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583107 | |||||||
| chr6:129583159 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1838+829C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583159 | |||||||
| chr6:129583170 | C | G | 10 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1838+818G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583170 | |||||||
| chr6:129583507 | C | T | 5 | a0001c0001t0006g0060 a0001c0001t0006g0198 a0001c0001t0010g0136 others(2): Show |
5 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+481G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583507 | |||||||
| chr6:129583553 | C | A | 17 | a0001c0001t0001g0074 a0001c0001t0001g0086 a0001c0001t0001g0105 others(14): Show |
17 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1838+435G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583553 | |||||||
| chr6:129583890 | CA | C | 12 | a0001c0001t0001g0193 a0001c0001t0002g0097 a0001c0001t0002g0217 others(9): Show |
12 | HG00597.hp2 HG02258.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1838+97delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583890 | |||||||
| chr6:129583913 | A | C | 1 | a0001c0001t0002g0185 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1838+75T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583913 | |||||||
| chr6:129583922 | C | T | 3 | a0001c0001t0006g0060 a0001c0001t0006g0198 a0002c0002t0006g0028 |
3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1838+66G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583922 | |||||||
| chr6:129583923 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1838+65C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583923 | |||||||
| chr6:129583975 | A | C | 7 | a0001c0001t0001g0161 a0001c0001t0001g0186 a0001c0001t0001g0201 others(4): Show |
7 | HG00544.hp2 HG01358.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1838+13T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583975 | |||||||
| chr6:129584445 | G | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1714-333C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584445 | |||||||
| chr6:129584503 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1714-391A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584503 | |||||||
| chr6:129584667 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1714-555T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584667 | |||||||
| chr6:129584749 | G | T | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-637C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584749 | |||||||
| chr6:129584858 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-746C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584858 | |||||||
| chr6:129584877 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1714-765T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584877 | |||||||
| chr6:129584932 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1714-820A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584932 | |||||||
| chr6:129585020 | C | CT | 37 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0083 others(34): Show |
37 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1714-909dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585020 | |||||||
| chr6:129585020 | CT | C | 66 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1714-909delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585020 | |||||||
| chr6:129585020 | CTT | C | 67 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0080 others(64): Show |
67 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1714-910_1714-909d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585020 | |||||||
| chr6:129585027 | T | A | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-915A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585027 | |||||||
| chr6:129585064 | T | A | 3 | a0001c0001t0006g0060 a0001c0001t0006g0198 a0002c0002t0006g0028 |
3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1714-952A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585064 | |||||||
| chr6:129585196 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1714-1084C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585196 | |||||||
| chr6:129585277 | C | T | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-1165G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585277 | |||||||
| chr6:129585301 | AAAAAT | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-1194_1714-119 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585301 | |||||||
| chr6:129585508 | T | C | 43 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0080 others(40): Show |
43 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.1714-1396A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585508 | |||||||
| chr6:129585620 | G | A | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1714-1508C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585620 | |||||||
| chr6:129585719 | A | T | 10 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-1607T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585719 | |||||||
| chr6:129585772 | T | C | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-1660A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585772 | |||||||
| chr6:129586127 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1714-2015T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586127 | |||||||
| chr6:129586268 | G | T | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-2156C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586268 | |||||||
| chr6:129586369 | T | C | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1714-2257A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586369 | |||||||
| chr6:129586442 | G | T | 48 | a0001c0001t0002g0057 a0001c0001t0002g0066 a0001c0001t0002g0067 others(45): Show |
48 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1714-2330C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586442 | |||||||
| chr6:129586452 | G | T | 48 | a0001c0001t0002g0057 a0001c0001t0002g0066 a0001c0001t0002g0067 others(45): Show |
48 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1714-2340C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586452 | |||||||
| chr6:129586792 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1714-2680G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586792 | |||||||
| chr6:129586841 | C | T | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1714-2729G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586841 | |||||||
| chr6:129586851 | G | A | 5 | a0001c0001t0006g0060 a0001c0001t0006g0198 a0001c0001t0010g0136 others(2): Show |
5 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714-2739C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586851 | |||||||
| chr6:129587446 | T | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0041 |
2 | HG02155.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1714-3334A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587446 | |||||||
| chr6:129587485 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1714-3373T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587485 | |||||||
| chr6:129587597 | C | T | 10 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-3485G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587597 | |||||||
| chr6:129587634 | C | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0223 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1714-3522G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587634 | |||||||
| chr6:129587967 | G | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1714-3855C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587967 | |||||||
| chr6:129587984 | C | T | 48 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0083 others(45): Show |
48 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1714-3872G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587984 | |||||||
| chr6:129588087 | A | G | 141 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(138): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1714-3975T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588087 | |||||||
| chr6:129588095 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1714-3983C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588095 | |||||||
| chr6:129588121 | C | CT | 47 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0083 others(44): Show |
47 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1714-4010dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588121 | |||||||
| chr6:129588121 | C | CTTT | 78 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0071 others(75): Show |
78 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1714-4012_1714-401 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588121 | |||||||
| chr6:129588195 | A | G | 71 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(68): Show |
71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1714-4083T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588195 | |||||||
| chr6:129588213 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1714-4101C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588213 | |||||||
| chr6:129588225 | C | A | 4 | a0001c0001t0001g0126 a0001c0001t0002g0125 a0001c0001t0002g0223 others(1): Show |
4 | HG02257.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-4113G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588225 | |||||||
| chr6:129588242 | C | T | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1714-4130G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588242 | |||||||
| chr6:129588263 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1714-4151C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588263 | |||||||
| chr6:129588371 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1714-4259G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588371 | |||||||
| chr6:129588383 | T | C | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1714-4271A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588383 | |||||||
| chr6:129588409 | C | T | 30 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(27): Show |
30 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1714-4297G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588409 | |||||||
| chr6:129588454 | T | TCCA | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714-4345_1714-434 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588454 | |||||||
| chr6:129588558 | C | T | 69 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(66): Show |
69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1714-4446G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588558 | |||||||
| chr6:129588567 | G | A | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1714-4455C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588567 | |||||||
| chr6:129588634 | G | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1714-4522C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588634 | |||||||
| chr6:129588675 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1714-4563C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588675 | |||||||
| chr6:129588826 | G | A | 2 | a0001c0001t0010g0136 a0001c0011t0001g0056 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1714-4714C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588826 | |||||||
| chr6:129589223 | T | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714-5111A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589223 | |||||||
| chr6:129589245 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1714-5133T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589245 | |||||||
| chr6:129589535 | G | A | 128 | a0001c0001t0001g0065 a0001c0001t0001g0071 a0001c0001t0001g0072 others(125): Show |
128 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1714-5423C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589535 | |||||||
| chr6:129589677 | T | C | 47 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0083 others(44): Show |
47 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1714-5565A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589677 | |||||||
| chr6:129589943 | G | C | 1 | a0001c0001t0002g0181 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1714-5831C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589943 | |||||||
| chr6:129589997 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1714-5885G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589997 | |||||||
| chr6:129590024 | T | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1714-5912A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590024 | |||||||
| chr6:129590276 | C | G | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1714-6164G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590276 | |||||||
| chr6:129590379 | A | C | 1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1714-6267T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590379 | |||||||
| chr6:129590393 | A | C | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1714-6281T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590393 | |||||||
| chr6:129590394 | T | C | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1714-6282A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590394 | |||||||
| chr6:129590491 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1714-6379C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590491 | |||||||
| chr6:129590644 | C | T | 1 | a0002c0002t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1714-6532G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590644 | |||||||
| chr6:129590657 | G | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1714-6545C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590657 | |||||||
| chr6:129590693 | T | G | 1 | a0001c0003t0002g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1714-6581A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590693 | |||||||
| chr6:129590775 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1714-6663G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590775 | |||||||
| chr6:129590786 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1714-6674G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590786 | |||||||
| chr6:129590860 | T | C | 19 | a0001c0001t0003g0073 a0001c0001t0003g0128 a0001c0001t0003g0133 others(16): Show |
19 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1714-6748A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590860 | |||||||
| chr6:129590916 | A | G | 5 | a0001c0001t0001g0102 a0001c0001t0001g0147 a0001c0001t0001g0193 others(2): Show |
5 | NA18950.hp2 NA18956.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714-6804T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590916 | |||||||
| chr6:129590917 | A | G | 2 | a0001c0001t0010g0136 a0001c0011t0001g0056 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1714-6805T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590917 | |||||||
| chr6:129590920 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1714-6808A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590920 | |||||||
| chr6:129590928 | C | A | 9 | a0001c0001t0003g0073 a0001c0001t0003g0219 a0001c0001t0003g0222 others(6): Show |
9 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1714-6816G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590928 | |||||||
| chr6:129591067 | A | G | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1714-6955T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591067 | |||||||
| chr6:129591142 | G | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1714-7030C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591142 | |||||||
| chr6:129591268 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1714-7156A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591268 | |||||||
| chr6:129591318 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1714-7206G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591318 | |||||||
| chr6:129591369 | G | C | 67 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1714-7257C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591369 | |||||||
| chr6:129591636 | C | T | 69 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(66): Show |
69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1714-7524G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591636 | |||||||
| chr6:129591654 | A | G | 10 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-7542T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591654 | |||||||
| chr6:129591685 | G | A | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1713+7531C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591685 | |||||||
| chr6:129591917 | G | T | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1713+7299C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591917 | |||||||
| chr6:129591942 | G | A | 69 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(66): Show |
69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1713+7274C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591942 | |||||||
| chr6:129592100 | AT | A | 47 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0086 others(44): Show |
47 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1713+7115delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592100 | |||||||
| chr6:129592282 | A | G | 69 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(66): Show |
69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1713+6934T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592282 | |||||||
| chr6:129592349 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1713+6867C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592349 | |||||||
| chr6:129592390 | C | G | 2 | a0001c0001t0010g0136 a0001c0011t0001g0056 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1713+6826G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592390 | |||||||
| chr6:129592503 | G | T | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1713+6713C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592503 | |||||||
| chr6:129592923 | G | A | 67 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1713+6293C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592923 | |||||||
| chr6:129593239 | C | T | 65 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(62): Show |
65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1713+5977G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593239 | |||||||
| chr6:129593697 | T | C | 2 | a0001c0001t0010g0136 a0001c0011t0001g0056 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1713+5519A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593697 | |||||||
| chr6:129593749 | T | C | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+5467A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593749 | |||||||
| chr6:129593780 | T | G | 2 | a0001c0001t0010g0136 a0001c0011t0001g0056 |
2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1713+5436A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593780 | |||||||
| chr6:129593859 | C | T | 1 | a0001c0001t0005g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1713+5357G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593859 | |||||||
| chr6:129594262 | T | C | 139 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1713+4954A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594262 | |||||||
| chr6:129594726 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1713+4490A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594726 | |||||||
| chr6:129594775 | T | C | 1 | a0002c0002t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1713+4441A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594775 | |||||||
| chr6:129594800 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1713+4416C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594800 | |||||||
| chr6:129594869 | C | A | 19 | a0001c0001t0003g0073 a0001c0001t0003g0128 a0001c0001t0003g0133 others(16): Show |
19 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1713+4347G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594869 | |||||||
| chr6:129595138 | C | CAT | 142 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(139): Show |
142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1713+4077_1713+407 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595138 | |||||||
| chr6:129595198 | T | C | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1713+4018A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595198 | |||||||
| chr6:129595325 | G | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1713+3891C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595325 | |||||||
| chr6:129595459 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1713+3757C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595459 | |||||||
| chr6:129595541 | T | G | 20 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0080 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1713+3675A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595541 | |||||||
| chr6:129595597 | T | G | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1713+3619A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595597 | |||||||
| chr6:129596026 | T | C | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1713+3190A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596026 | |||||||
| chr6:129596117 | T | C | 3 | a0001c0001t0001g0159 a0001c0001t0002g0180 a0001c0001t0002g0220 |
3 | HG02071.hp1 NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1713+3099A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596117 | |||||||
| chr6:129596279 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1713+2937T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596279 | |||||||
| chr6:129596320 | C | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0194 |
2 | HG02896.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1713+2896G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596320 | |||||||
| chr6:129596506 | C | T | 2 | a0001c0001t0001g0102 a0002c0002t0001g0048 |
2 | NA18969.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1713+2710G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596506 | |||||||
| chr6:129597058 | T | A | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1713+2158A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597058 | |||||||
| chr6:129597094 | C | T | 34 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0142 others(31): Show |
34 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1713+2122G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597094 | |||||||
| chr6:129597126 | T | A | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1713+2090A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597126 | |||||||
| chr6:129597127 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1713+2089T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597127 | |||||||
| chr6:129597135 | G | A | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1713+2081C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597135 | |||||||
| chr6:129597148 | A | AT | 16 | a0001c0001t0001g0090 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): Show |
16 | HG01192.hp2 HG01361.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1713+2067dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597148 | |||||||
| chr6:129597207 | G | A | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+2009C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597207 | |||||||
| chr6:129597239 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0002g0125 a0001c0001t0002g0223 others(1): Show |
4 | HG02257.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+1977G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597239 | |||||||
| chr6:129597293 | G | A | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+1923C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597293 | |||||||
| chr6:129597400 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1713+1816A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597400 | |||||||
| chr6:129597527 | C | T | 1 | a0002c0002t0018g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1713+1689G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597527 | |||||||
| chr6:129597543 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0002g0145 |
2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1713+1673G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597543 | |||||||
| chr6:129597598 | C | T | 44 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0086 others(41): Show |
44 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1713+1618G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597598 | |||||||
| chr6:129597711 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1713+1505A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597711 | |||||||
| chr6:129597721 | A | G | 33 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(30): Show |
33 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+1495T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597721 | |||||||
| chr6:129597730 | G | GA | 30 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0098 others(27): Show |
30 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+1485dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597730 | |||||||
| chr6:129597782 | A | G | 33 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(30): Show |
33 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+1434T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597782 | |||||||
| chr6:129597865 | T | C | 31 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(28): Show |
31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1713+1351A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597865 | |||||||
| chr6:129597905 | A | C | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1713+1311T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597905 | |||||||
| chr6:129597908 | A | T | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+1308T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597908 | |||||||
| chr6:129598161 | C | CA | 11 | a0001c0001t0001g0231 a0001c0001t0002g0145 a0001c0001t0003g0225 others(8): Show |
11 | HG00597.hp2 HG01106.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+1054dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598161 | |||||||
| chr6:129598188 | T | C | 7 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(4): Show |
7 | HG00597.hp2 HG03130.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1713+1028A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598188 | |||||||
| chr6:129598281 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1713+935A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598281 | |||||||
| chr6:129598378 | C | T | 30 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(27): Show |
30 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+838G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598378 | |||||||
| chr6:129598630 | A | G | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+586T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598630 | |||||||
| chr6:129598941 | G | GGTGTGT | 30 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(27): Show |
30 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+269_1713+274d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598941 | |||||||
| chr6:129598946 | G | C | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1713+270C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598946 | |||||||
| chr6:129599153 | AAATTTTG others(16): Show |
A | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1713+40_1713+62del others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129599153 | |||||||
| chr6:129599360 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.1573-4A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599360 | |||||||
| chr6:129599399 | C | T | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1573-43G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599399 | |||||||
| chr6:129599431 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1573-75A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599431 | |||||||
| chr6:129599632 | G | A | 12 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0098 others(9): Show |
12 | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1573-276C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599632 | |||||||
| chr6:129599639 | A | G | 31 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(28): Show |
31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1573-283T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599639 | |||||||
| chr6:129600034 | T | C | 1 | a0002c0002t0001g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1572+608A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600034 | |||||||
| chr6:129600071 | G | A | 58 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1572+571C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600071 | |||||||
| chr6:129600172 | T | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1572+470A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600172 | |||||||
| chr6:129600203 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1572+439G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600203 | |||||||
| chr6:129600220 | C | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1572+422G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600220 | |||||||
| chr6:129600433 | G | A | 8 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0007g0077 others(5): Show |
8 | HG00597.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+209C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600433 | |||||||
| chr6:129600534 | T | C | 2 | a0001c0001t0002g0229 a0001c0001t0002g0230 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1572+108A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600534 | |||||||
| chr6:129600626 | T | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+16A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600626 | |||||||
| chr6:129601088 | C | A | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-240G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601088 | |||||||
| chr6:129601098 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1366-250C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601098 | |||||||
| chr6:129601105 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1366-257C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601105 | |||||||
| chr6:129601107 | G | C | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-259C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601107 | |||||||
| chr6:129601190 | C | A | 3 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0002c0002t0001g0004 |
3 | HG00642.hp2 HG01074.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1366-342G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601190 | |||||||
| chr6:129601368 | G | C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366-520C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601368 | |||||||
| chr6:129601469 | A | C | 1 | a0009c0007t0001g0027 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1366-621T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601469 | |||||||
| chr6:129601506 | AAGAGAAA others(9): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1366-674_1366-659d others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601506 | |||||||
| chr6:129601535 | GAAGAAAA others(5): Show |
G | 5 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-699_1366-688d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601535 | |||||||
| chr6:129601598 | C | T | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-750G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601598 | |||||||
| chr6:129601631 | C | CT | 59 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1366-784dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601631 | |||||||
| chr6:129601721 | G | A | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366-873C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601721 | |||||||
| chr6:129601754 | G | A | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366-906C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601754 | |||||||
| chr6:129601808 | CAT | C | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-962_1366-961d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601808 | |||||||
| chr6:129601810 | T | C | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1366-962A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601810 | |||||||
| chr6:129601824 | C | T | 57 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1366-976G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601824 | |||||||
| chr6:129601942 | T | A | 1 | a0001c0001t0003g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1366-1094A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601942 | |||||||
| chr6:129602036 | C | G | 2 | a0001c0001t0001g0160 a0001c0001t0001g0221 |
2 | HG02056.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1366-1188G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602036 | |||||||
| chr6:129602159 | G | A | 1 | a0001c0001t0010g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1366-1311C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602159 | |||||||
| chr6:129602276 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1366-1428T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602276 | |||||||
| chr6:129602311 | T | C | 10 | a0001c0001t0002g0125 a0001c0001t0002g0223 a0001c0001t0003g0128 others(7): Show |
10 | HG02257.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1366-1463A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602311 | |||||||
| chr6:129602407 | A | C | 59 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(56): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1366-1559T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602407 | |||||||
| chr6:129602419 | C | G | 2 | a0001c0001t0001g0105 a0009c0007t0001g0027 |
2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1366-1571G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602419 | |||||||
| chr6:129602495 | G | GA | 46 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(43): Show |
46 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1366-1648dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602495 | |||||||
| chr6:129602517 | C | T | 1 | a0001c0001t0005g0212 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1366-1669G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602517 | |||||||
| chr6:129602608 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1366-1760T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602608 | |||||||
| chr6:129602709 | T | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1366-1861A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602709 | |||||||
| chr6:129602964 | T | C | 31 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(28): Show |
31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1366-2116A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602964 | |||||||
| chr6:129602987 | T | TTA | 86 | a0001c0001t0001g0065 a0001c0001t0001g0071 a0001c0001t0001g0072 others(83): Show |
86 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1366-2141_1366-214 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | |||||||
| chr6:129602987 | T | TTATA | 22 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(19): Show |
22 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1366-2143_1366-214 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | |||||||
| chr6:129602987 | T | TTATATAT others(1): Show |
7 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(4): Show |
7 | HG00597.hp2 HG02615.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-2147_1366-214 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | |||||||
| chr6:129602987 | T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1366-2149_1366-214 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | |||||||
| chr6:129602987 | T | TTATATAT others(5): Show |
7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(4): Show |
7 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-2151_1366-214 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | |||||||
| chr6:129602987 | T | TTATATAT others(7): Show |
2 | a0001c0001t0006g0060 a0003c0004t0001g0151 |
2 | HG03098.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1366-2153_1366-214 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | |||||||
| chr6:129603032 | G | A | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1366-2184C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603032 | |||||||
| chr6:129603058 | T | C | 2 | a0001c0001t0002g0125 a0001c0001t0002g0223 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1366-2210A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603058 | |||||||
| chr6:129603062 | C | T | 58 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1366-2214G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603062 | |||||||
| chr6:129603161 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1366-2313C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603161 | |||||||
| chr6:129603261 | G | C | 31 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(28): Show |
31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1366-2413C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603261 | |||||||
| chr6:129603326 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1366-2478A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603326 | |||||||
| chr6:129603574 | T | C | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+2303A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603574 | |||||||
| chr6:129603717 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1365+2160G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603717 | |||||||
| chr6:129603858 | A | G | 23 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0080 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+2019T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603858 | |||||||
| chr6:129603945 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1365+1932C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603945 | |||||||
| chr6:129603998 | A | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1365+1879T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603998 | |||||||
| chr6:129604202 | TC | T | 93 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(90): Show |
93 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1365+1674delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604202 | |||||||
| chr6:129604303 | A | G | 10 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0003g0219 others(7): Show |
10 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1365+1574T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604303 | |||||||
| chr6:129604334 | C | T | 64 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1365+1543G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604334 | |||||||
| chr6:129604833 | C | T | 29 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1365+1044G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604833 | |||||||
| chr6:129605395 | T | G | 1 | a0001c0001t0004g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1365+482A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605395 | |||||||
| chr6:129605572 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1365+305T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605572 | |||||||
| chr6:129605578 | A | G | 1 | a0001c0001t0017g0174 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1365+299T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605578 | |||||||
| chr6:129605619 | C | T | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1365+258G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605619 | |||||||
| chr6:129605620 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1365+257C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605620 | |||||||
| chr6:129605624 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1365+253T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605624 | |||||||
| chr6:129605625 | A | T | 2 | a0001c0001t0003g0225 a0001c0001t0010g0136 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1365+252T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605625 | |||||||
| chr6:129605657 | T | C | 30 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(27): Show |
30 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1365+220A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605657 | |||||||
| chr6:129605719 | A | G | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1365+158T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605719 | |||||||
| chr6:129605764 | T | C | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+113A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605764 | |||||||
| chr6:129605766 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1365+111A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605766 | |||||||
| chr6:129605869 | A | G | 123 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.1365+8T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605869 | |||||||
| chr6:129606065 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1283-106C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606065 | |||||||
| chr6:129606200 | G | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1283-241C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606200 | |||||||
| chr6:129606296 | T | G | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1283-337A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606296 | |||||||
| chr6:129606459 | C | T | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1283-500G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606459 | |||||||
| chr6:129606493 | ATTATCAT others(5): Show |
A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1283-546_1283-535d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606493 | |||||||
| chr6:129606774 | C | T | 7 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(4): Show |
7 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1283-815G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606774 | |||||||
| chr6:129606865 | C | CT | 39 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(36): Show |
39 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1283-907dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606865 | |||||||
| chr6:129607116 | T | C | 17 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(14): Show |
17 | HG00099.hp2 HG00597.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1282+777A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607116 | |||||||
| chr6:129607373 | A | G | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1282+520T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607373 | |||||||
| chr6:129607407 | C | G | 29 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282+486G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607407 | |||||||
| chr6:129607450 | A | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0004g0123 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+443T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607450 | |||||||
| chr6:129607593 | CTATTA | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282+295_1282+299d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607593 | |||||||
| chr6:129608063 | C | A | 2 | a0001c0001t0006g0198 a0002c0002t0006g0028 |
2 | HG03491.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1123-11G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608063 | |||||||
| chr6:129608064 | G | GA | 13 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0075 others(10): Show |
13 | HG00140.hp1 HG00544.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1123-13dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | |||||||
| chr6:129608064 | G | GAAAA | 10 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1123-16_1123-13dup others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | |||||||
| chr6:129608064 | GA | G | 56 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0079 others(53): Show |
56 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1123-13delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | |||||||
| chr6:129608064 | GAA | G | 27 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(24): Show |
27 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1123-14_1123-13del others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | |||||||
| chr6:129608068 | AAAAAAAA others(26): Show |
A | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1123-49_1123-17del others(33): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608068 | |||||||
| chr6:129608084 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1123-32T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608084 | |||||||
| chr6:129608088 | A | C | 7 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(4): Show |
7 | HG00597.hp2 HG01261.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1123-36T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608088 | |||||||
| chr6:129608124 | T | C | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1123-72A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608124 | |||||||
| chr6:129608319 | T | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1123-267A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608319 | |||||||
| chr6:129608376 | C | T | 24 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0102 others(21): Show |
24 | HG00544.hp2 HG01071.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1123-324G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608376 | |||||||
| chr6:129608401 | G | A | 24 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0102 others(21): Show |
24 | HG00544.hp2 HG01071.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1123-349C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608401 | |||||||
| chr6:129608417 | A | C | 1 | a0002c0002t0001g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1123-365T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608417 | |||||||
| chr6:129608433 | G | A | 1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1123-381C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608433 | |||||||
| chr6:129608743 | A | G | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1123-691T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608743 | |||||||
| chr6:129608898 | C | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 |
3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1123-846G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608898 | |||||||
| chr6:129608966 | TAGAG | T | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1123-918_1123-915d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608966 | |||||||
| chr6:129609005 | GA | G | 24 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(21): Show |
24 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1123-954delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609005 | |||||||
| chr6:129609071 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1123-1019C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609071 | |||||||
| chr6:129609104 | GGGGAAAG others(8): Show |
G | 1 | a0001c0001t0002g0173 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1123-1067_1123-105 others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609104 | |||||||
| chr6:129609202 | T | C | 1 | a0001c0001t0002g0181 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1123-1150A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609202 | |||||||
| chr6:129609451 | G | A | 58 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1123-1399C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609451 | |||||||
| chr6:129609459 | T | C | 18 | a0001c0001t0001g0074 a0001c0001t0001g0083 a0001c0001t0001g0086 others(15): Show |
18 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1123-1407A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609459 | |||||||
| chr6:129609501 | T | C | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1123-1449A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609501 | |||||||
| chr6:129609509 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1123-1457G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609509 | |||||||
| chr6:129609573 | TGTTACCT others(407): Show |
T | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1122+1546_1123-152 others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609573 | |||||||
| chr6:129609599 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0139 |
2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1123-1547G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609599 | |||||||
| chr6:129609629 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0178 a0002c0002t0001g0010 |
3 | HG00733.hp1 HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1123-1577C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609629 | |||||||
| chr6:129609654 | A | G | 1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1123-1602T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609654 | |||||||
| chr6:129609734 | G | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0003c0004t0001g0151 others(1): Show |
4 | HG02486.hp1 HG03098.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1123-1682C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609734 | |||||||
| chr6:129609765 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1123-1713G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609765 | |||||||
| chr6:129609964 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1122+1569C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609964 | |||||||
| chr6:129610057 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1122+1476G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610057 | |||||||
| chr6:129610201 | C | T | 1 | a0007c0012t0002g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1122+1332G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610201 | |||||||
| chr6:129610236 | C | G | 13 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(10): Show |
13 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122+1297G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610236 | |||||||
| chr6:129610334 | C | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122+1199G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610334 | |||||||
| chr6:129610442 | C | T | 1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1122+1091G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610442 | |||||||
| chr6:129610494 | T | C | 1 | a0002c0002t0002g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1122+1039A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610494 | |||||||
| chr6:129610727 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1122+806T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610727 | |||||||
| chr6:129610788 | T | C | 38 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0079 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1122+745A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610788 | |||||||
| chr6:129610962 | T | C | 29 | a0001c0001t0001g0065 a0001c0001t0001g0094 a0001c0001t0001g0096 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1122+571A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610962 | |||||||
| chr6:129611058 | G | A | 13 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122+475C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129611058 | |||||||
| chr6:129611503 | A | C | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1122+30T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129611503 | |||||||
| chr6:129611642 | C | T | 1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1045-32G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611642 | |||||||
| chr6:129611643 | G | A | 3 | a0001c0001t0002g0145 a0001c0001t0010g0136 a0003c0004t0005g0088 |
3 | HG02451.hp1 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1045-33C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611643 | |||||||
| chr6:129611703 | T | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0004g0123 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045-93A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611703 | |||||||
| chr6:129611749 | T | C | 100 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(97): Show |
100 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1045-139A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611749 | |||||||
| chr6:129611839 | T | C | 62 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(59): Show |
62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1045-229A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611839 | |||||||
| chr6:129612438 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1045-828T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612438 | |||||||
| chr6:129612661 | T | C | 2 | a0001c0001t0002g0185 a0001c0001t0003g0184 |
2 | NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1045-1051A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612661 | |||||||
| chr6:129612727 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1045-1117T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612727 | |||||||
| chr6:129612736 | T | C | 4 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0002g0145 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-1126A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612736 | |||||||
| chr6:129612944 | C | G | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1045-1334G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612944 | |||||||
| chr6:129612998 | G | C | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1045-1388C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612998 | |||||||
| chr6:129613004 | C | T | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1045-1394G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613004 | |||||||
| chr6:129613005 | G | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-1395C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613005 | |||||||
| chr6:129613032 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1045-1422C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613032 | |||||||
| chr6:129613042 | G | C | 2 | a0001c0001t0001g0126 a0002c0002t0001g0025 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1045-1432C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613042 | |||||||
| chr6:129613158 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1045-1548G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613158 | |||||||
| chr6:129613159 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(126): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1045-1549T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613159 | |||||||
| chr6:129613164 | C | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1045-1554G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613164 | |||||||
| chr6:129613182 | A | G | 1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1045-1572T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613182 | |||||||
| chr6:129613194 | G | C | 25 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(22): Show |
25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1045-1584C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613194 | |||||||
| chr6:129613232 | C | CA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0090 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1045-1623dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613232 | |||||||
| chr6:129613232 | CA | C | 27 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0089 others(24): Show |
27 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1045-1623delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613232 | |||||||
| chr6:129613280 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1045-1670G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613280 | |||||||
| chr6:129613335 | C | T | 10 | a0001c0001t0002g0145 a0001c0001t0005g0207 a0001c0001t0005g0212 others(7): Show |
10 | HG00597.hp2 HG02451.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.1045-1725G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613335 | |||||||
| chr6:129613493 | T | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1045-1883A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613493 | |||||||
| chr6:129613650 | C | T | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-2040G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613650 | |||||||
| chr6:129613790 | G | T | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1045-2180C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613790 | |||||||
| chr6:129613825 | C | T | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1045-2215G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613825 | |||||||
| chr6:129613844 | G | GTTT | 25 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(22): Show |
25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1045-2235_1045-223 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613844 | |||||||
| chr6:129613952 | CTT | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0191 a0002c0002t0018g0009 |
3 | HG00140.hp2 HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1044+2258_1044+225 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613952 | |||||||
| chr6:129614177 | G | A | 5 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(2): Show |
5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+2035C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614177 | |||||||
| chr6:129614230 | C | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0007g0077 others(1): Show |
4 | HG02486.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+1982G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614230 | |||||||
| chr6:129614291 | T | C | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1044+1921A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614291 | |||||||
| chr6:129614417 | T | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+1795A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614417 | |||||||
| chr6:129614465 | T | C | 25 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(22): Show |
25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1044+1747A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614465 | |||||||
| chr6:129614468 | A | G | 2 | a0003c0004t0001g0151 a0003c0004t0005g0088 |
2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1044+1744T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614468 | |||||||
| chr6:129614748 | A | AT | 13 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(10): Show |
13 | HG00609.hp1 HG01081.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1044+1463dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | |||||||
| chr6:129614748 | AT | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(67): Show |
71 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1044+1463delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | |||||||
| chr6:129614748 | ATT | A | 27 | a0001c0001t0001g0112 a0001c0001t0001g0142 a0001c0001t0001g0216 others(24): Show |
27 | HG00408.hp2 HG00558.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1044+1462_1044+146 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | |||||||
| chr6:129614748 | ATTT | A | 6 | a0001c0001t0003g0224 a0001c0001t0005g0207 a0001c0001t0005g0212 others(3): Show |
6 | HG00597.hp2 HG02630.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+1461_1044+146 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | |||||||
| chr6:129614816 | T | C | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1044+1396A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614816 | |||||||
| chr6:129614880 | G | A | 26 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0091 others(23): Show |
26 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1044+1332C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614880 | |||||||
| chr6:129615007 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1044+1205T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615007 | |||||||
| chr6:129615078 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1044+1134A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615078 | |||||||
| chr6:129615245 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1044+967C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615245 | |||||||
| chr6:129615417 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | NA18950.hp1 NA18977.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+795G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615417 | |||||||
| chr6:129615433 | G | C | 13 | a0001c0001t0001g0065 a0001c0001t0001g0129 a0001c0001t0001g0155 others(10): Show |
13 | HG00544.hp2 HG01071.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1044+779C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615433 | |||||||
| chr6:129615470 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1044+742T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615470 | |||||||
| chr6:129615532 | G | C | 1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1044+680C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615532 | |||||||
| chr6:129615595 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1044+617T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615595 | |||||||
| chr6:129615617 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1044+595G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615617 | |||||||
| chr6:129615630 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0079 others(98): Show |
102 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1044+582G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615630 | |||||||
| chr6:129615668 | G | A | 5 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(2): Show |
5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+544C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615668 | |||||||
| chr6:129615686 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0079 others(98): Show |
102 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.1044+526G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615686 | |||||||
| chr6:129615881 | G | A | 1 | a0002c0002t0002g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1044+331C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615881 | |||||||
| chr6:129615892 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1044+320C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615892 | |||||||
| chr6:129615968 | A | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1044+244T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615968 | |||||||
| chr6:129615997 | G | T | 1 | a0001c0001t0002g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1044+215C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615997 | |||||||
| chr6:129616086 | T | C | 1 | a0001c0001t0010g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1044+126A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129616086 | |||||||
| chr6:129616144 | T | C | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1044+68A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129616144 | |||||||
| chr6:129616311 | A | G | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.953-8T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616311 | |||||||
| chr6:129616752 | A | T | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.953-449T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616752 | |||||||
| chr6:129616803 | A | G | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.953-500T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616803 | |||||||
| chr6:129616886 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0157 |
2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.953-583C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616886 | |||||||
| chr6:129617050 | G | A | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.953-747C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617050 | |||||||
| chr6:129617083 | A | G | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.953-780T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617083 | |||||||
| chr6:129617091 | C | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.953-788G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617091 | |||||||
| chr6:129617459 | AATTCGGA others(13): Show |
A | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.953-1176_953-1157d others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617459 | |||||||
| chr6:129617635 | G | C | 25 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(22): Show |
25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.952+1052C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617635 | |||||||
| chr6:129617867 | G | T | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.952+820C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617867 | |||||||
| chr6:129618113 | C | A | 1 | a0002c0002t0003g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.952+574G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618113 | |||||||
| chr6:129618113 | CA | C | 43 | a0001c0001t0001g0080 a0001c0001t0001g0089 a0001c0001t0001g0108 others(40): Show |
43 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.952+573delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618113 | |||||||
| chr6:129618114 | A | C | 1 | a0002c0002t0003g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.952+573T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618114 | |||||||
| chr6:129618117 | A | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(13): Show |
17 | HG00099.hp2 HG00597.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.952+570T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618117 | |||||||
| chr6:129618220 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.952+467A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618220 | |||||||
| chr6:129619118 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(57): Show |
61 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.787-266T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619118 | |||||||
| chr6:129619257 | GA | G | 3 | a0001c0001t0003g0128 a0001c0001t0003g0237 a0002c0002t0014g0045 |
3 | HG02257.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.787-406delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619257 | |||||||
| chr6:129619336 | A | G | 1 | a0001c0001t0016g0149 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.787-484T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619336 | |||||||
| chr6:129619345 | C | CAGGGGGA others(19): Show |
1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.787-519_787-494dup others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619345 | |||||||
| chr6:129619345 | CAGGGGGA others(6): Show |
C | 4 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-506_787-494del others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619345 | |||||||
| chr6:129619368 | GA | G | 9 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0112 others(6): Show |
9 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-517delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619368 | |||||||
| chr6:129619369 | A | AAAAGGGG others(5): Show |
9 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0002g0180 others(6): Show |
9 | HG00544.hp1 HG02027.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-529_787-518dup others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619369 | |||||||
| chr6:129619369 | AAAAGGGG others(5): Show |
A | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.787-529_787-518del others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619369 | |||||||
| chr6:129619372 | A | AGGGGGAG others(6): Show |
1 | a0001c0001t0001g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.787-533_787-521dup others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619372 | |||||||
| chr6:129619397 | G | GGGGGAGG others(4): Show |
1 | a0001c0001t0001g0086 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.787-546_787-545ins others(11): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619397 | |||||||
| chr6:129619467 | A | AGGGGGAG others(1046): Show |
1 | a0001c0001t0002g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.787-616_787-615ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619467 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1068): Show |
1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1020): Show |
1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1027): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1082): Show |
1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1089): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1051): Show |
2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1045): Show |
1 | a0001c0001t0003g0219 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1097): Show |
1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1104): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1058): Show |
10 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0002g0223 others(7): Show |
10 | HG00408.hp2 HG00558.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1044): Show |
2 | a0001c0001t0003g0128 a0002c0002t0014g0045 |
2 | HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1051): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1058): Show |
1 | a0002c0002t0003g0031 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1045): Show |
1 | a0001c0001t0003g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1071): Show |
2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1078): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1084): Show |
2 | a0001c0001t0001g0142 a0005c0005t0003g0002 |
2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1091): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1078): Show |
1 | a0001c0001t0003g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1085): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1078): Show |
1 | a0001c0001t0002g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1085): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1069): Show |
1 | a0001c0001t0001g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1076): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1024): Show |
1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1031): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1064): Show |
1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1071): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1028): Show |
1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1035): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1045): Show |
3 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0210 |
3 | NA18954.hp2 NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(997): Show |
1 | a0008c0013t0001g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1004): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1065): Show |
1 | a0001c0001t0004g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1072): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1045): Show |
3 | a0001c0001t0001g0124 a0002c0002t0002g0032 a0002c0002t0003g0033 |
3 | HG03041.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1069): Show |
1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1076): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1032): Show |
1 | a0001c0001t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1068): Show |
1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1079): Show |
3 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0002c0002t0001g0004 |
3 | HG00642.hp2 HG01074.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1086): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1059): Show |
1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1066): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1068): Show |
1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1081): Show |
1 | a0001c0001t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1088): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1068): Show |
1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1066): Show |
1 | a0002c0002t0001g0021 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1073): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1086): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1093): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1068): Show |
32 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0001g0096 others(29): Show |
32 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1050): Show |
1 | a0001c0001t0001g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1057): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1082): Show |
1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1089): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1066): Show |
1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1073): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1067): Show |
1 | a0001c0001t0004g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1074): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1068): Show |
1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1028): Show |
1 | a0001c0001t0002g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1035): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1078): Show |
1 | a0002c0002t0001g0035 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1085): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1103): Show |
3 | a0001c0001t0001g0105 a0002c0006t0012g0034 a0009c0007t0001g0027 |
3 | NA19056.hp1 NA19056.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1110): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1172): Show |
1 | a0002c0002t0001g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1179): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1051): Show |
1 | a0002c0002t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1024): Show |
1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1031): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1032): Show |
1 | a0001c0001t0001g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1019): Show |
2 | a0001c0001t0002g0092 a0001c0001t0002g0176 |
2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1026): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1044): Show |
1 | a0001c0001t0001g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1051): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1070): Show |
1 | a0002c0002t0002g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1077): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1045): Show |
26 | a0001c0001t0001g0085 a0001c0001t0001g0111 a0001c0001t0001g0126 others(23): Show |
26 | HG00558.hp2 HG01106.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1045): Show |
5 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0163 others(2): Show |
5 | HG00438.hp2 NA18942.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1058): Show |
1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1050): Show |
1 | a0001c0001t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1057): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1077): Show |
1 | a0001c0001t0001g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1084): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1007): Show |
1 | a0001c0001t0002g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1014): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1032): Show |
12 | a0001c0001t0001g0201 a0001c0001t0001g0206 a0001c0001t0001g0213 others(9): Show |
12 | HG00438.hp1 HG01358.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1057): Show |
2 | a0001c0001t0002g0143 a0001c0001t0002g0170 |
2 | HG02004.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1064): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1051): Show |
1 | a0001c0001t0002g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1037): Show |
1 | a0002c0002t0001g0017 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1044): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1038): Show |
1 | a0001c0003t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1045): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1038): Show |
11 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0002g0082 others(8): Show |
11 | HG00544.hp1 HG02027.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1045): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1051): Show |
1 | a0002c0002t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0001g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1052): Show |
1 | a0002c0002t0001g0007 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1059): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0001g0062 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1058): Show |
3 | a0001c0001t0002g0185 a0001c0001t0003g0184 a0002c0002t0002g0039 |
3 | NA18964.hp2 NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(999): Show |
7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(4): Show |
7 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1006): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1058): Show |
2 | a0001c0001t0001g0071 a0001c0001t0002g0093 |
2 | HG00609.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1006): Show |
1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1013): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1062): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0139 a0001c0001t0011g0141 |
3 | HG02615.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1069): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1051): Show |
1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0001g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1055): Show |
1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1062): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1060): Show |
1 | a0002c0002t0001g0036 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1067): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1048): Show |
1 | a0001c0001t0016g0149 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1055): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1013): Show |
1 | a0001c0001t0001g0202 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1020): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1069): Show |
1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1076): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1043): Show |
1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1050): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1033): Show |
1 | a0001c0001t0001g0065 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1040): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1000): Show |
1 | a0001c0001t0001g0177 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1007): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1052): Show |
1 | a0001c0001t0002g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1059): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(918): Show |
1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(925): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(777): Show |
1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(784): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0010g0136 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0002g0113 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(778): Show |
3 | a0001c0001t0005g0207 a0001c0011t0001g0056 a0002c0002t0005g0024 |
3 | HG00597.hp2 HG03209.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(785): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(907): Show |
1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(914): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(920): Show |
7 | a0001c0001t0001g0080 a0001c0001t0001g0109 a0001c0001t0001g0157 others(4): Show |
7 | HG00639.hp1 HG00642.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(927): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1088): Show |
1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1095): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(765): Show |
2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(772): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(779): Show |
1 | a0001c0001t0005g0212 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(786): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1101): Show |
1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1108): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0196 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(935): Show |
1 | a0002c0002t0001g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(942): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(936): Show |
1 | a0002c0002t0018g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(943): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1032): Show |
1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1008): Show |
1 | a0001c0001t0002g0181 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1015): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(775): Show |
1 | a0001c0001t0009g0070 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(782): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1431): Show |
1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1438): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1044): Show |
1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1051): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1074): Show |
1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1081): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(1064): Show |
1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1071): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(945): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(952): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGAGG others(946): Show |
1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(953): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGGAG others(1040): Show |
1 | a0001c0009t0001g0122 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1047): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619468 | G | GGGGGGAG others(1051): Show |
1 | a0001c0001t0001g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | |||||||
| chr6:129619469 | G | GGGGAGGG others(1031): Show |
1 | a0001c0001t0001g0086 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.787-618_787-617ins others(1038): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619469 | |||||||
| chr6:129619479 | A | AG | 6 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0096 others(3): Show |
6 | HG00438.hp2 HG00597.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-628dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619479 | |||||||
| chr6:129619482 | G | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.787-630C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619482 | |||||||
| chr6:129619488 | C | CAG | 50 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(47): Show |
50 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.787-637_787-636ins others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619488 | |||||||
| chr6:129619509 | G | A | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(8): Show |
11 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-657C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619509 | |||||||
| chr6:129619635 | G | A | 2 | a0003c0004t0001g0151 a0003c0004t0005g0088 |
2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.787-783C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619635 | |||||||
| chr6:129619665 | A | C | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-813T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619665 | |||||||
| chr6:129619689 | G | C | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-837C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619689 | |||||||
| chr6:129619979 | A | AGAAG | 15 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.787-1131_787-1128d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619979 | |||||||
| chr6:129620027 | C | T | 2 | a0001c0001t0001g0126 a0002c0002t0001g0025 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.787-1175G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620027 | |||||||
| chr6:129620052 | G | A | 1 | a0001c0003t0002g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.787-1200C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620052 | |||||||
| chr6:129620702 | C | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.787-1850G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620702 | |||||||
| chr6:129620749 | T | C | 5 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(2): Show |
5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-1897A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620749 | |||||||
| chr6:129620809 | T | C | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.787-1957A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620809 | |||||||
| chr6:129620989 | A | G | 8 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0007g0077 others(5): Show |
8 | HG00597.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.787-2137T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620989 | |||||||
| chr6:129621018 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(55): Show |
59 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.787-2166A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621018 | |||||||
| chr6:129621084 | T | C | 1 | a0002c0002t0001g0017 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.787-2232A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621084 | |||||||
| chr6:129621085 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.787-2233T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621085 | |||||||
| chr6:129621278 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.787-2426C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621278 | |||||||
| chr6:129621322 | C | G | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-2470G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621322 | |||||||
| chr6:129621328 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.787-2476T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621328 | |||||||
| chr6:129621363 | G | A | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.787-2511C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621363 | |||||||
| chr6:129621374 | G | GT | 8 | a0001c0001t0001g0064 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG00597.hp1 HG01433.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.787-2523dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621374 | |||||||
| chr6:129621403 | A | T | 1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.787-2551T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621403 | |||||||
| chr6:129621478 | G | T | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2626C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621478 | |||||||
| chr6:129621625 | T | C | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2773A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621625 | |||||||
| chr6:129621672 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.787-2820A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621672 | |||||||
| chr6:129621696 | A | G | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.787-2844T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621696 | |||||||
| chr6:129621764 | T | C | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-2912A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621764 | |||||||
| chr6:129621775 | A | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(53): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.787-2923T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621775 | |||||||
| chr6:129621796 | T | A | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(7): Show |
10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.787-2944A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621796 | |||||||
| chr6:129621931 | G | GT | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.787-3080dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621931 | |||||||
| chr6:129622043 | G | T | 13 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(10): Show |
13 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.787-3191C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622043 | |||||||
| chr6:129622159 | T | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(48): Show |
52 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.787-3307A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622159 | |||||||
| chr6:129622181 | G | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.787-3329C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622181 | |||||||
| chr6:129622250 | A | G | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-3398T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622250 | |||||||
| chr6:129622329 | T | C | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3477A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622329 | |||||||
| chr6:129622716 | T | TAAG | 56 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(53): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.787-3867_787-3865d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622716 | |||||||
| chr6:129622852 | C | G | 1 | a0002c0002t0002g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.787-4000G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622852 | |||||||
| chr6:129622958 | G | C | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.787-4106C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622958 | |||||||
| chr6:129623001 | CAAAACAA others(9): Show |
C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG00621.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.787-4165_787-4150d others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623001 | |||||||
| chr6:129623003 | AAAC | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0096 others(41): Show |
45 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.787-4154_787-4152d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623003 | |||||||
| chr6:129623006 | CA | C | 40 | a0001c0001t0001g0127 a0001c0001t0001g0142 a0001c0001t0001g0150 others(37): Show |
40 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.787-4155delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623006 | |||||||
| chr6:129623006 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787-4165_787-4155d others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623006 | |||||||
| chr6:129623036 | A | G | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.787-4184T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623036 | |||||||
| chr6:129623053 | C | CA | 26 | a0001c0001t0001g0065 a0001c0001t0001g0142 a0001c0001t0001g0216 others(23): Show |
26 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.787-4202dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623053 | |||||||
| chr6:129623082 | T | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.787-4230A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623082 | |||||||
| chr6:129623239 | A | T | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-4387T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623239 | |||||||
| chr6:129623711 | C | CAATGAGT others(4): Show |
1 | a0001c0001t0002g0113 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787-4870_787-4860d others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623711 | |||||||
| chr6:129623979 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.787-5127A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623979 | |||||||
| chr6:129624032 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.787-5180C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624032 | |||||||
| chr6:129624080 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.787-5228C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624080 | |||||||
| chr6:129624148 | C | T | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.786+5205G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624148 | |||||||
| chr6:129624372 | T | C | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+4981A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624372 | |||||||
| chr6:129624374 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(53): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.786+4979A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624374 | |||||||
| chr6:129624440 | G | A | 1 | a0007c0012t0002g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.786+4913C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624440 | |||||||
| chr6:129624455 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4898T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624455 | |||||||
| chr6:129624466 | G | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+4887C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624466 | |||||||
| chr6:129624515 | C | T | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+4838G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624515 | |||||||
| chr6:129624545 | A | T | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.786+4808T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624545 | |||||||
| chr6:129624592 | T | C | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+4761A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624592 | |||||||
| chr6:129624610 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.786+4743A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624610 | |||||||
| chr6:129624637 | C | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4716G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624637 | |||||||
| chr6:129624673 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0079 a0001c0001t0001g0080 others(97): Show |
101 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.786+4680T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624673 | |||||||
| chr6:129624735 | A | T | 1 | a0001c0001t0002g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.786+4618T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624735 | |||||||
| chr6:129624736 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.786+4617C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624736 | |||||||
| chr6:129624736 | G | T | 1 | a0001c0001t0002g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.786+4617C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624736 | |||||||
| chr6:129624806 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4547C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624806 | |||||||
| chr6:129624825 | A | T | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+4528T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624825 | |||||||
| chr6:129624877 | G | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+4476C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624877 | |||||||
| chr6:129624948 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+4405T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624948 | |||||||
| chr6:129624949 | A | AAT | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4402_786+4403d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624949 | |||||||
| chr6:129624956 | A | ATATATAT others(26): Show |
1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.786+4364_786+4396d others(35): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624956 | |||||||
| chr6:129624976 | T | A | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+4377A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624976 | |||||||
| chr6:129624990 | T | G | 19 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(16): Show |
19 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+4363A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624990 | |||||||
| chr6:129624990 | T | TATATATG | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+4356_786+4362d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624990 | |||||||
| chr6:129624990 | T | TATATATG others(24): Show |
3 | a0001c0001t0003g0225 a0002c0002t0001g0029 a0002c0002t0006g0028 |
3 | HG03130.hp1 HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.786+4332_786+4362d others(33): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624990 | |||||||
| chr6:129625002 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+4351T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625002 | |||||||
| chr6:129625006 | T | TTA | 15 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(12): Show |
15 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4345_786+4346d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625006 | |||||||
| chr6:129625006 | T | TTATATAT others(2): Show |
50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+4346_786+4347i others(11): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625006 | |||||||
| chr6:129625006 | T | TTATATAT others(28): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+4346_786+4347i others(37): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625006 | |||||||
| chr6:129625013 | A | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+4340T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625013 | |||||||
| chr6:129625021 | G | T | 15 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0079 others(12): Show |
15 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4332C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625021 | |||||||
| chr6:129625037 | T | TTA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0075 a0001c0001t0001g0084 others(90): Show |
94 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.786+4314_786+4315d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625037 | |||||||
| chr6:129625044 | A | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4309T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625044 | |||||||
| chr6:129625054 | T | TATA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(91): Show |
95 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.786+4298_786+4299i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625054 | |||||||
| chr6:129625054 | T | TATATGAT others(29): Show |
12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4298_786+4299i others(38): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625054 | |||||||
| chr6:129625055 | T | A | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4298A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625055 | |||||||
| chr6:129625056 | G | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4297C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625056 | |||||||
| chr6:129625057 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+4296T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625057 | |||||||
| chr6:129625058 | T | TG | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4294_786+4295i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625058 | |||||||
| chr6:129625066 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786+4287A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625066 | |||||||
| chr6:129625066 | T | G | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4287A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625066 | |||||||
| chr6:129625072 | TAA | T | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.786+4279_786+4280d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625072 | |||||||
| chr6:129625073 | A | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0096 others(29): Show |
33 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.786+4280T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625073 | |||||||
| chr6:129625074 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4279T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625074 | |||||||
| chr6:129625075 | TATATATG | T | 7 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(4): Show |
7 | HG00597.hp2 HG02818.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+4271_786+4277d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625075 | |||||||
| chr6:129625082 | G | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4271C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625082 | |||||||
| chr6:129625084 | TATATGAT others(3): Show |
T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4259_786+4268d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625084 | |||||||
| chr6:129625087 | AT | A | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4265delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625087 | |||||||
| chr6:129625090 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4263T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625090 | |||||||
| chr6:129625091 | TATATG | T | 20 | a0001c0001t0001g0142 a0001c0001t0001g0188 a0001c0001t0001g0189 others(17): Show |
20 | HG01071.hp1 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.786+4257_786+4261d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625091 | |||||||
| chr6:129625094 | A | ATAT | 8 | a0001c0001t0003g0219 a0001c0001t0003g0222 a0001c0001t0008g0118 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4258_786+4259i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625094 | |||||||
| chr6:129625096 | G | A | 15 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4257C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625096 | |||||||
| chr6:129625096 | G | T | 8 | a0001c0001t0003g0219 a0001c0001t0003g0222 a0001c0001t0008g0118 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4257C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625096 | |||||||
| chr6:129625097 | A | T | 15 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(12): Show |
15 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4256T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625097 | |||||||
| chr6:129625098 | T | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+4255A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625098 | |||||||
| chr6:129625098 | T | TTATATAT others(1): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4254_786+4255i others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625098 | |||||||
| chr6:129625102 | TA | T | 20 | a0001c0001t0001g0142 a0001c0001t0001g0188 a0001c0001t0001g0189 others(17): Show |
20 | HG01071.hp1 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.786+4250delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625102 | |||||||
| chr6:129625103 | A | AT | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4249dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625103 | |||||||
| chr6:129625104 | T | A | 8 | a0001c0001t0003g0219 a0001c0001t0003g0222 a0001c0001t0008g0118 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4249A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625104 | |||||||
| chr6:129625105 | T | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0002g0145 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4248A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625105 | |||||||
| chr6:129625111 | TTATATAG others(1): Show |
T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(35): Show |
39 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.786+4234_786+4241d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625111 | |||||||
| chr6:129625112 | T | A | 28 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(25): Show |
28 | HG00099.hp2 HG00735.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.786+4241A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625112 | |||||||
| chr6:129625112 | T | G | 12 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0002g0145 others(9): Show |
12 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4241A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625112 | |||||||
| chr6:129625117 | A | AT | 22 | a0001c0001t0001g0079 a0001c0001t0001g0129 a0001c0001t0001g0137 others(19): Show |
22 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.786+4235_786+4236i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625117 | |||||||
| chr6:129625118 | G | T | 30 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(27): Show |
30 | HG00099.hp2 HG00735.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786+4235C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625118 | |||||||
| chr6:129625120 | T | TG | 28 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(25): Show |
28 | HG00099.hp2 HG00735.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.786+4232_786+4233i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625120 | |||||||
| chr6:129625125 | A | AT | 8 | a0001c0001t0003g0219 a0001c0001t0003g0222 a0001c0001t0008g0118 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4227dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625125 | |||||||
| chr6:129625125 | A | G | 10 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
10 | HG00544.hp2 HG01952.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4228T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625125 | |||||||
| chr6:129625126 | T | A | 10 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
10 | HG00544.hp2 HG01952.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4227A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625126 | |||||||
| chr6:129625127 | T | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(75): Show |
79 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.786+4226A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625127 | |||||||
| chr6:129625133 | T | TTATATA | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4219_786+4220i others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625133 | |||||||
| chr6:129625133 | TGA | T | 10 | a0001c0001t0001g0129 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
10 | HG00544.hp2 HG01952.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4218_786+4219d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625133 | |||||||
| chr6:129625134 | G | A | 8 | a0001c0001t0003g0219 a0001c0001t0003g0222 a0001c0001t0008g0118 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4219C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625134 | |||||||
| chr6:129625134 | GAT | G | 14 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(11): Show |
14 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+4217_786+4218d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625134 | |||||||
| chr6:129625136 | T | TATATG | 4 | a0001c0001t0002g0145 a0001c0001t0007g0077 a0001c0001t0010g0136 others(1): Show |
4 | HG02451.hp1 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4216_786+4217i others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625136 | |||||||
| chr6:129625138 | TATATTAT others(25): Show |
T | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+4183_786+4214d others(34): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625138 | |||||||
| chr6:129625141 | A | G | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4212T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625141 | |||||||
| chr6:129625141 | A | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(7): Show |
10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4212T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625141 | |||||||
| chr6:129625142 | T | A | 16 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(13): Show |
16 | HG00423.hp1 HG00597.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.786+4211A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625142 | |||||||
| chr6:129625143 | T | G | 22 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(19): Show |
22 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.786+4210A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625143 | |||||||
| chr6:129625143 | TATATATT others(6): Show |
T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.786+4197_786+4209d others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625143 | |||||||
| chr6:129625146 | ATAT | A | 108 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(105): Show |
108 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.786+4204_786+4206d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625146 | |||||||
| chr6:129625148 | A | AT | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4204dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625148 | |||||||
| chr6:129625149 | T | TATGATA | 2 | a0001c0001t0007g0077 a0003c0004t0005g0088 |
2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+4203_786+4204i others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625149 | |||||||
| chr6:129625149 | TTATATAG others(1): Show |
T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(7): Show |
10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4196_786+4203d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625149 | |||||||
| chr6:129625150 | T | A | 5 | a0001c0001t0002g0093 a0001c0001t0002g0172 a0002c0002t0002g0019 others(2): Show |
5 | HG00609.hp2 HG01261.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4203A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625150 | |||||||
| chr6:129625150 | T | G | 10 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0003g0219 others(7): Show |
10 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4203A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625150 | |||||||
| chr6:129625151 | A | T | 5 | a0001c0001t0002g0093 a0001c0001t0002g0172 a0002c0002t0002g0019 others(2): Show |
5 | HG00609.hp2 HG01261.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4202T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625151 | |||||||
| chr6:129625152 | T | G | 5 | a0001c0001t0002g0093 a0001c0001t0002g0172 a0002c0002t0002g0019 others(2): Show |
5 | HG00609.hp2 HG01261.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4201A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625152 | |||||||
| chr6:129625152 | T | TG | 2 | a0001c0001t0007g0077 a0003c0004t0005g0088 |
2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+4200_786+4201i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625152 | |||||||
| chr6:129625154 | T | TG | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4198_786+4199i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625154 | |||||||
| chr6:129625154 | TAGA | T | 108 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(105): Show |
108 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.786+4196_786+4198d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625154 | |||||||
| chr6:129625155 | A | AT | 13 | a0001c0001t0001g0079 a0001c0001t0001g0107 a0001c0001t0001g0137 others(10): Show |
13 | HG00408.hp2 HG00558.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+4197_786+4198i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625155 | |||||||
| chr6:129625155 | A | T | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4198T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625155 | |||||||
| chr6:129625156 | G | A | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4197C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625156 | |||||||
| chr6:129625156 | G | T | 22 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(19): Show |
22 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.786+4197C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625156 | |||||||
| chr6:129625158 | T | G | 118 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.786+4195A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625158 | |||||||
| chr6:129625158 | T | TATG | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4194_786+4195i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625158 | |||||||
| chr6:129625158 | T | TG | 19 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(16): Show |
19 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+4194_786+4195i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625158 | |||||||
| chr6:129625163 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4190T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625163 | |||||||
| chr6:129625163 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4190T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625163 | |||||||
| chr6:129625164 | T | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0001g0188 others(1): Show |
4 | HG01071.hp1 HG01169.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+4189A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625164 | |||||||
| chr6:129625165 | T | G | 146 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(143): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.786+4188A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625165 | |||||||
| chr6:129625165 | T | TATATATG | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4181_786+4187d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625165 | |||||||
| chr6:129625165 | TATATATG | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0096 others(41): Show |
45 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.786+4181_786+4187d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625165 | |||||||
| chr6:129625172 | G | T | 37 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0084 others(34): Show |
37 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.786+4181C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625172 | |||||||
| chr6:129625177 | A | AG | 8 | a0001c0001t0003g0219 a0001c0001t0003g0222 a0001c0001t0008g0118 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4175_786+4176i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625177 | |||||||
| chr6:129625178 | T | A | 8 | a0001c0001t0003g0219 a0001c0001t0003g0222 a0001c0001t0008g0118 others(5): Show |
8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4175A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625178 | |||||||
| chr6:129625178 | T | TATTTA | 5 | a0001c0001t0005g0212 a0001c0001t0009g0069 a0001c0001t0009g0070 others(2): Show |
5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4174_786+4175i others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625178 | |||||||
| chr6:129625178 | T | TATTTATA others(5): Show |
2 | a0001c0001t0005g0207 a0001c0001t0007g0077 |
2 | HG00597.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.786+4174_786+4175i others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625178 | |||||||
| chr6:129625179 | T | G | 26 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0101 others(23): Show |
26 | HG00741.hp2 HG01192.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.786+4174A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625179 | |||||||
| chr6:129625182 | A | G | 5 | a0001c0001t0005g0212 a0001c0001t0009g0069 a0001c0001t0009g0070 others(2): Show |
5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4171T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625182 | |||||||
| chr6:129625182 | ATAT | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0002c0002t0001g0038 |
3 | NA18943.hp2 NA18963.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.786+4168_786+4170d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625182 | |||||||
| chr6:129625185 | T | A | 5 | a0001c0001t0005g0212 a0001c0001t0009g0069 a0001c0001t0009g0070 others(2): Show |
5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4168A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625185 | |||||||
| chr6:129625186 | T | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0079 a0001c0001t0001g0090 others(52): Show |
56 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.786+4167A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625186 | |||||||
| chr6:129625186 | T | TATATATG others(66): Show |
1 | a0001c0001t0007g0078 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.786+4166_786+4167i others(75): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625186 | |||||||
| chr6:129625186 | TATATATG others(17): Show |
T | 13 | a0001c0001t0001g0142 a0001c0001t0002g0125 a0001c0001t0002g0223 others(10): Show |
13 | HG01192.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.786+4143_786+4166d others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625186 | |||||||
| chr6:129625191 | A | G | 1 | a0002c0002t0001g0017 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.786+4162T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625191 | |||||||
| chr6:129625191 | AT | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4161delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625191 | |||||||
| chr6:129625193 | G | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0155 others(2): Show |
5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4160C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625193 | |||||||
| chr6:129625194 | A | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0155 others(2): Show |
5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4159T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625194 | |||||||
| chr6:129625194 | ATATATAT others(1): Show |
A | 3 | a0001c0001t0003g0219 a0002c0002t0003g0022 a0002c0002t0003g0023 |
3 | HG00558.hp1 HG02129.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.786+4151_786+4158d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625194 | |||||||
| chr6:129625195 | T | G | 1 | a0002c0002t0003g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.786+4158A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625195 | |||||||
| chr6:129625198 | ATAT | A | 3 | a0001c0001t0008g0118 a0001c0001t0008g0228 a0002c0002t0014g0045 |
3 | HG02922.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.786+4152_786+4154d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625198 | |||||||
| chr6:129625198 | ATATTTAT others(3): Show |
A | 2 | a0001c0001t0003g0222 a0002c0002t0003g0037 |
2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.786+4145_786+4154d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625198 | |||||||
| chr6:129625199 | T | TG | 5 | a0001c0001t0005g0212 a0001c0001t0009g0069 a0001c0001t0009g0070 others(2): Show |
5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4153_786+4154i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625199 | |||||||
| chr6:129625199 | TA | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0002c0002t0001g0038 |
3 | NA18943.hp2 NA18963.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.786+4153delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625199 | |||||||
| chr6:129625201 | T | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0002c0002t0001g0038 |
3 | NA18943.hp2 NA18963.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.786+4152A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625201 | |||||||
| chr6:129625201 | TTTATATG others(3): Show |
T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0096 others(43): Show |
47 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.786+4142_786+4151d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625201 | |||||||
| chr6:129625202 | T | A | 9 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0005g0212 others(6): Show |
9 | HG02451.hp2 HG03209.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+4151A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625202 | |||||||
| chr6:129625202 | T | TA | 4 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0155 others(1): Show |
4 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4150_786+4151i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625202 | |||||||
| chr6:129625203 | T | G | 3 | a0001c0001t0008g0118 a0001c0001t0008g0228 a0002c0002t0014g0045 |
3 | HG02922.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.786+4150A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625203 | |||||||
| chr6:129625207 | TG | T | 5 | a0001c0001t0005g0212 a0001c0001t0009g0069 a0001c0001t0009g0070 others(2): Show |
5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4145delC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625207 | |||||||
| chr6:129625208 | G | A | 4 | a0001c0001t0008g0118 a0001c0001t0008g0228 a0002c0002t0014g0045 others(1): Show |
4 | HG02922.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4145C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625208 | |||||||
| chr6:129625208 | G | GATA | 3 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0232 |
3 | HG00741.hp2 HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.786+4144_786+4145i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625208 | |||||||
| chr6:129625208 | GTAAT | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0218 others(2): Show |
5 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4141_786+4144d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625208 | |||||||
| chr6:129625209 | T | A | 3 | a0001c0001t0003g0219 a0002c0002t0003g0022 a0002c0002t0003g0023 |
3 | HG00558.hp1 HG02129.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.786+4144A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625209 | |||||||
| chr6:129625210 | A | G | 2 | a0001c0001t0003g0222 a0002c0002t0003g0037 |
2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.786+4143T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625210 | |||||||
| chr6:129625210 | A | T | 12 | a0001c0001t0003g0219 a0001c0001t0005g0212 a0001c0001t0008g0118 others(9): Show |
12 | HG00558.hp1 HG02129.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4143T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625210 | |||||||
| chr6:129625211 | A | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0232 others(1): Show |
4 | HG00597.hp2 HG00741.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4142T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625211 | |||||||
| chr6:129625212 | T | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0232 |
3 | HG00741.hp2 HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.786+4141A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625212 | |||||||
| chr6:129625215 | A | G | 5 | a0001c0001t0005g0212 a0001c0001t0009g0069 a0001c0001t0009g0070 others(2): Show |
5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4138T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625215 | |||||||
| chr6:129625219 | G | GATATATG others(19): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+4133_786+4134i others(28): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | |||||||
| chr6:129625219 | G | GATATATG others(52): Show |
1 | a0001c0001t0005g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.786+4133_786+4134i others(61): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | |||||||
| chr6:129625219 | G | GATATATG others(26): Show |
3 | a0001c0001t0001g0164 a0001c0001t0002g0185 a0001c0001t0003g0184 |
3 | NA18969.hp2 NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.786+4101_786+4133d others(35): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | |||||||
| chr6:129625219 | G | GATATATG others(59): Show |
1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+4068_786+4133d others(68): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | |||||||
| chr6:129625219 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(52): Show |
56 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.786+4134C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | |||||||
| chr6:129625219 | GATATATG others(26): Show |
G | 2 | a0001c0001t0001g0065 a0001c0001t0002g0067 |
2 | HG00438.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.786+4101_786+4133d others(35): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | |||||||
| chr6:129625219 | GATATATG others(59): Show |
G | 2 | a0001c0001t0002g0093 a0002c0002t0002g0019 |
2 | HG00609.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.786+4068_786+4133d others(68): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | |||||||
| chr6:129625226 | G | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0155 others(2): Show |
5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4127C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625226 | |||||||
| chr6:129625233 | G | T | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.786+4120C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625233 | |||||||
| chr6:129625233 | GATATATA others(10): Show |
G | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.786+4103_786+4119d others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625233 | |||||||
| chr6:129625239 | TATTTATA others(5): Show |
T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0096 others(61): Show |
65 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.786+4102_786+4113d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625239 | |||||||
| chr6:129625241 | TTTA | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0188 others(2): Show |
5 | HG00741.hp2 HG01071.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4109_786+4111d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625241 | |||||||
| chr6:129625242 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.786+4111A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625242 | |||||||
| chr6:129625248 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG01071.hp1 HG01169.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.786+4105C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625248 | |||||||
| chr6:129625251 | A | T | 6 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0155 others(3): Show |
6 | HG00741.hp2 HG01071.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4102T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625251 | |||||||
| chr6:129625252 | T | TATATATG | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4094_786+4100d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625252 | |||||||
| chr6:129625259 | G | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0096 others(41): Show |
45 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.786+4094C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625259 | |||||||
| chr6:129625268 | T | TATATGAT others(36): Show |
1 | a0001c0001t0007g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.786+4084_786+4085i others(45): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625268 | |||||||
| chr6:129625272 | TATTTATA others(5): Show |
T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4069_786+4080d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625272 | |||||||
| chr6:129625274 | TTTA | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0096 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+4076_786+4078d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625274 | |||||||
| chr6:129625284 | A | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0096 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+4069T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625284 | |||||||
| chr6:129625285 | TATATATG | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4061_786+4067d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625285 | |||||||
| chr6:129625292 | G | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4061C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625292 | |||||||
| chr6:129625292 | GATATATG others(19): Show |
G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0001g0232 |
3 | HG00741.hp2 HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.786+4035_786+4060d others(28): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625292 | |||||||
| chr6:129625299 | G | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4054C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625299 | |||||||
| chr6:129625311 | TATGTA | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4037_786+4041d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625311 | |||||||
| chr6:129625316 | AAT | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+4035_786+4036d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625316 | |||||||
| chr6:129625317 | A | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4036T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625317 | |||||||
| chr6:129625318 | T | TATATATG | 45 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0096 others(42): Show |
46 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+4028_786+4034d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625318 | |||||||
| chr6:129625325 | G | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4028C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625325 | |||||||
| chr6:129625327 | TATATG | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4021_786+4025d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625327 | |||||||
| chr6:129625331 | TG | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0002c0002t0001g0038 others(1): Show |
4 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+4021delC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625331 | |||||||
| chr6:129625335 | A | T | 4 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0002c0002t0001g0038 others(1): Show |
4 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+4018T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625335 | |||||||
| chr6:129625337 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4016T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625337 | |||||||
| chr6:129625337 | ATATTTAT others(136): Show |
A | 4 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0002c0002t0001g0038 others(1): Show |
4 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+3873_786+4015d others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625337 | |||||||
| chr6:129625341 | T | A | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4012A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625341 | |||||||
| chr6:129625342 | T | C | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4011A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625342 | |||||||
| chr6:129625350 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4003T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625350 | |||||||
| chr6:129625356 | ATT | A | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(7): Show |
10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+3995_786+3996d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625356 | |||||||
| chr6:129625357 | T | TGATA | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3995_786+3996i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625357 | |||||||
| chr6:129625357 | TTATGTAT others(5): Show |
T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3984_786+3995d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625357 | |||||||
| chr6:129625358 | T | G | 24 | a0001c0001t0001g0137 a0001c0001t0001g0142 a0001c0001t0002g0125 others(21): Show |
24 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.786+3995A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625358 | |||||||
| chr6:129625359 | A | ATATATGA others(83): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+3993_786+3994i others(92): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625359 | |||||||
| chr6:129625361 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.786+3992C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625361 | |||||||
| chr6:129625361 | G | GATA | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3991_786+3992i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625361 | |||||||
| chr6:129625364 | TATTTA | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3984_786+3988d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625364 | |||||||
| chr6:129625367 | T | A | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3986A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625367 | |||||||
| chr6:129625369 | A | ATATATAT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(44): Show |
48 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.786+3977_786+3983d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625369 | |||||||
| chr6:129625369 | ATATATAT others(104): Show |
A | 21 | a0001c0001t0001g0142 a0001c0001t0002g0125 a0001c0001t0002g0223 others(18): Show |
21 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.786+3873_786+3983d others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625369 | |||||||
| chr6:129625370 | T | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3983A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625370 | |||||||
| chr6:129625373 | A | G | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3980T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625373 | |||||||
| chr6:129625373 | A | T | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3980T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625373 | |||||||
| chr6:129625375 | A | T | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3978T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625375 | |||||||
| chr6:129625376 | T | A | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3977A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625376 | |||||||
| chr6:129625377 | T | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3976A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625377 | |||||||
| chr6:129625380 | A | G | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3973T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625380 | |||||||
| chr6:129625383 | T | A | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3970A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625383 | |||||||
| chr6:129625384 | T | G | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0005g0212 others(2): Show |
5 | HG01071.hp1 HG01169.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3969A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625384 | |||||||
| chr6:129625385 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3968T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625385 | |||||||
| chr6:129625386 | T | TATATG | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3966_786+3967i others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625386 | |||||||
| chr6:129625391 | T | A | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3962A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625391 | |||||||
| chr6:129625391 | T | TA | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3961_786+3962i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625391 | |||||||
| chr6:129625395 | A | T | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0005g0212 others(2): Show |
5 | HG01071.hp1 HG01169.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3958T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625395 | |||||||
| chr6:129625395 | AC | A | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3957delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625395 | |||||||
| chr6:129625396 | C | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG01071.hp1 HG01169.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+3957G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625396 | |||||||
| chr6:129625397 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3956T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625397 | |||||||
| chr6:129625401 | G | A | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3952C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625401 | |||||||
| chr6:129625401 | G | T | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3952C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625401 | |||||||
| chr6:129625404 | T | A | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0005g0212 others(2): Show |
5 | HG01071.hp1 HG01169.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3949A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625404 | |||||||
| chr6:129625408 | A | G | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3945T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625408 | |||||||
| chr6:129625413 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3940T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625413 | |||||||
| chr6:129625415 | A | ATATTATA others(14): Show |
1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.786+3937_786+3938i others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625415 | |||||||
| chr6:129625415 | A | ATATTATA others(152): Show |
1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3937_786+3938i others(161): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625415 | |||||||
| chr6:129625417 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+3936T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625417 | |||||||
| chr6:129625418 | TAA | T | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3933_786+3934d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625418 | |||||||
| chr6:129625419 | A | ATTT | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3933_786+3934i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | |||||||
| chr6:129625419 | A | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3934T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | |||||||
| chr6:129625419 | A | T | 2 | a0001c0001t0009g0069 a0003c0004t0005g0088 |
2 | NA18612.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3934T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | |||||||
| chr6:129625419 | AATATAT | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3928_786+3933d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | |||||||
| chr6:129625420 | A | ATATATAT others(21): Show |
1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.786+3932_786+3933i others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | |||||||
| chr6:129625420 | A | ATATATAT others(23): Show |
12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02155.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.786+3903_786+3932d others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | |||||||
| chr6:129625420 | A | ATATATAT others(53): Show |
4 | a0001c0001t0001g0139 a0001c0001t0001g0221 a0001c0001t0003g0140 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+3873_786+3932d others(62): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | |||||||
| chr6:129625420 | A | ATATATAT others(67): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+3932_786+3933i others(76): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | |||||||
| chr6:129625420 | A | G | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3933T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | |||||||
| chr6:129625420 | A | T | 3 | a0001c0001t0001g0079 a0001c0011t0001g0056 a0003c0004t0001g0151 |
3 | HG03098.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3933T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | |||||||
| chr6:129625420 | ATATATAT others(23): Show |
A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0111 others(2): Show |
5 | HG00140.hp1 HG01433.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3903_786+3932d others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | |||||||
| chr6:129625426 | A | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3927T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625426 | |||||||
| chr6:129625427 | T | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3926A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625427 | |||||||
| chr6:129625429 | A | ATAAATTT others(116): Show |
1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.786+3923_786+3924i others(125): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625429 | |||||||
| chr6:129625434 | TAATATAT others(57): Show |
T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3855_786+3918d others(66): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625434 | |||||||
| chr6:129625435 | A | C | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3918T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625435 | |||||||
| chr6:129625435 | A | T | 3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3918T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625435 | |||||||
| chr6:129625436 | A | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3917T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625436 | |||||||
| chr6:129625440 | A | ATTTATAC others(5): Show |
3 | a0001c0001t0005g0212 a0001c0001t0009g0070 a0002c0002t0005g0024 |
3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3912_786+3913i others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625440 | |||||||
| chr6:129625440 | A | G | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3913T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625440 | |||||||
| chr6:129625445 | T | A | 6 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0005g0212 others(3): Show |
6 | HG01071.hp1 HG01169.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+3908A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625445 | |||||||
| chr6:129625451 | T | A | 2 | a0001c0001t0005g0207 a0001c0011t0001g0056 |
2 | HG00597.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.786+3902A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625451 | |||||||
| chr6:129625458 | TA | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3894delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625458 | |||||||
| chr6:129625463 | AT | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0002g0113 |
3 | HG01071.hp1 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.786+3889delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625463 | |||||||
| chr6:129625465 | A | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3888T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625465 | |||||||
| chr6:129625465 | A | T | 2 | a0001c0001t0001g0137 a0002c0002t0001g0040 |
2 | HG02486.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.786+3888T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625465 | |||||||
| chr6:129625470 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG01071.hp1 HG01169.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.786+3883T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625470 | |||||||
| chr6:129625472 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+3881T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625472 | |||||||
| chr6:129625473 | T | TTTTATAT others(21): Show |
1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+3879_786+3880i others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625473 | |||||||
| chr6:129625475 | T | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3878A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625475 | |||||||
| chr6:129625479 | A | ATAATATA others(127): Show |
11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3873_786+3874i others(136): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625479 | |||||||
| chr6:129625488 | T | A | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3865A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625488 | |||||||
| chr6:129625488 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3865A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625488 | |||||||
| chr6:129625500 | A | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3853T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625500 | |||||||
| chr6:129625504 | T | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3849A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625504 | |||||||
| chr6:129625509 | A | ATTATATA others(199): Show |
2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3843_786+3844i others(208): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625509 | |||||||
| chr6:129625513 | C | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3840G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625513 | |||||||
| chr6:129625514 | A | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3839T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625514 | |||||||
| chr6:129625527 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3826G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625527 | |||||||
| chr6:129625542 | T | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3811A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625542 | |||||||
| chr6:129625551 | T | TTATA | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3801_786+3802i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625551 | |||||||
| chr6:129625569 | C | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3784G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625569 | |||||||
| chr6:129625585 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.786+3768A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625585 | |||||||
| chr6:129625594 | T | G | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+3759A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625594 | |||||||
| chr6:129625606 | A | C | 12 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+3747T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625606 | |||||||
| chr6:129625607 | T | TTATTATA others(23): Show |
11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3716_786+3745d others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625607 | |||||||
| chr6:129625607 | TTATTATA others(8): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.786+3731_786+3745d others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625607 | |||||||
| chr6:129625616 | AT | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3736delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625616 | |||||||
| chr6:129625633 | AT | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3719delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625633 | |||||||
| chr6:129625637 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3716T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625637 | |||||||
| chr6:129625639 | A | G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+3714T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625639 | |||||||
| chr6:129625658 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3695A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625658 | |||||||
| chr6:129625670 | TTATATTA others(25): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3651_786+3682d others(34): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625670 | |||||||
| chr6:129625675 | TTA | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3676_786+3677d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625675 | |||||||
| chr6:129625677 | A | ATATATAT others(51): Show |
1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.786+3618_786+3675d others(60): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625677 | |||||||
| chr6:129625681 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+3672T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625681 | |||||||
| chr6:129625693 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.786+3660A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625693 | |||||||
| chr6:129625700 | T | A | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3653A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625700 | |||||||
| chr6:129625702 | A | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3651T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625702 | |||||||
| chr6:129625704 | A | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3649T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625704 | |||||||
| chr6:129625728 | A | ATATTAAT others(29): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3624_786+3625i others(38): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625728 | |||||||
| chr6:129625728 | A | ATATTAAT others(61): Show |
2 | a0003c0004t0001g0151 a0003c0004t0005g0088 |
2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3624_786+3625i others(70): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625728 | |||||||
| chr6:129625729 | TATTTA | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3619_786+3623d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625729 | |||||||
| chr6:129625732 | T | TAATA | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3620_786+3621i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625732 | |||||||
| chr6:129625732 | T | TTATA | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+3620_786+3621i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625732 | |||||||
| chr6:129625732 | TTATTATA others(8): Show |
T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0215 a0001c0001t0003g0237 |
3 | HG02074.hp2 HG02257.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.786+3606_786+3620d others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625732 | |||||||
| chr6:129625739 | ATATT | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3610_786+3613d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625739 | |||||||
| chr6:129625746 | T | A | 1 | a0002c0002t0001g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.786+3607A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625746 | |||||||
| chr6:129625750 | T | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3603A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625750 | |||||||
| chr6:129625750 | T | TTA | 7 | a0001c0001t0002g0145 a0001c0001t0005g0207 a0001c0001t0005g0212 others(4): Show |
7 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+3601_786+3602d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625750 | |||||||
| chr6:129625760 | A | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(46): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3593T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625760 | |||||||
| chr6:129625762 | A | T | 7 | a0001c0001t0002g0145 a0001c0001t0005g0207 a0001c0001t0005g0212 others(4): Show |
7 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+3591T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625762 | |||||||
| chr6:129625766 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3587A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625766 | |||||||
| chr6:129625771 | A | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3582T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625771 | |||||||
| chr6:129625772 | TATTTATA others(7): Show |
T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(45): Show |
49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3567_786+3580d others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625772 | |||||||
| chr6:129625773 | A | T | 5 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(2): Show |
5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3580T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625773 | |||||||
| chr6:129625775 | T | A | 8 | a0001c0001t0002g0145 a0001c0001t0005g0207 a0001c0001t0005g0212 others(5): Show |
8 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3578A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625775 | |||||||
| chr6:129625777 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3576T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625777 | |||||||
| chr6:129625778 | TATATATA | T | 27 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0074 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.786+3568_786+3574d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625778 | |||||||
| chr6:129625779 | A | AT | 5 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(2): Show |
5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3573dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625779 | |||||||
| chr6:129625779 | A | ATATATAT others(8): Show |
1 | a0001c0003t0002g0175 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.786+3573_786+3574i others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625779 | |||||||
| chr6:129625779 | A | T | 3 | a0001c0001t0002g0145 a0001c0001t0010g0136 a0001c0011t0001g0056 |
3 | HG02451.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.786+3574T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625779 | |||||||
| chr6:129625781 | ATATAATA others(6): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+3559_786+3571d others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625781 | |||||||
| chr6:129625785 | A | AT | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG00733.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+3567_786+3568i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625785 | |||||||
| chr6:129625785 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3568T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625785 | |||||||
| chr6:129625786 | A | T | 11 | a0001c0001t0001g0146 a0001c0001t0001g0178 a0001c0001t0002g0145 others(8): Show |
11 | HG00597.hp2 HG00733.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3567T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625786 | |||||||
| chr6:129625792 | A | T | 1 | a0002c0002t0001g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.786+3561T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625792 | |||||||
| chr6:129625794 | T | A | 3 | a0001c0001t0002g0145 a0001c0001t0010g0136 a0001c0011t0001g0056 |
3 | HG02451.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.786+3559A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625794 | |||||||
| chr6:129625794 | T | TA | 5 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(2): Show |
5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3558_786+3559i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625794 | |||||||
| chr6:129625796 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(52): Show |
56 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.786+3557A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625796 | |||||||
| chr6:129625800 | AT | A | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3552delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625800 | |||||||
| chr6:129625801 | T | G | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3552A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625801 | |||||||
| chr6:129625801 | T | TTTA | 5 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(2): Show |
5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3551_786+3552i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625801 | |||||||
| chr6:129625802 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+3551A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625802 | |||||||
| chr6:129625803 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+3550T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625803 | |||||||
| chr6:129625804 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.786+3549A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625804 | |||||||
| chr6:129625808 | T | A | 8 | a0001c0001t0002g0145 a0001c0001t0005g0207 a0001c0001t0005g0212 others(5): Show |
8 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3545A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625808 | |||||||
| chr6:129625813 | T | C | 3 | a0001c0003t0002g0175 a0003c0004t0001g0151 a0003c0004t0005g0088 |
3 | HG03098.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3540A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625813 | |||||||
| chr6:129625818 | A | T | 8 | a0001c0001t0002g0145 a0001c0001t0005g0207 a0001c0001t0005g0212 others(5): Show |
8 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3535T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625818 | |||||||
| chr6:129625820 | A | G | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+3533T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625820 | |||||||
| chr6:129625835 | C | T | 19 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(16): Show |
19 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+3518G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625835 | |||||||
| chr6:129625849 | ATAT | A | 3 | a0001c0001t0002g0171 a0001c0001t0002g0217 a0002c0002t0001g0026 |
3 | HG02056.hp2 HG02523.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.786+3501_786+3503d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625849 | |||||||
| chr6:129625852 | T | TTATACAT others(37): Show |
2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3500_786+3501i others(46): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625852 | |||||||
| chr6:129625853 | T | TATATTTA others(54): Show |
8 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(5): Show |
8 | HG00423.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+3499_786+3500i others(63): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625853 | |||||||
| chr6:129625855 | T | TAC | 19 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(16): Show |
19 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+3497_786+3498i others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625855 | |||||||
| chr6:129625857 | TTTATATA | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3489_786+3495d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625857 | |||||||
| chr6:129625867 | A | ATATATTA others(59): Show |
1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+3420_786+3485d others(68): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625867 | |||||||
| chr6:129625872 | TTA | T | 19 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(16): Show |
19 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+3479_786+3480d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625872 | |||||||
| chr6:129625876 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.786+3477T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625876 | |||||||
| chr6:129625894 | T | TTTATATA others(78): Show |
2 | a0001c0001t0003g0140 a0001c0001t0011g0141 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.786+3458_786+3459i others(87): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625894 | |||||||
| chr6:129625897 | T | G | 2 | a0001c0001t0003g0140 a0001c0001t0011g0141 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.786+3456A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625897 | |||||||
| chr6:129625902 | TTA | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3449_786+3450d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625902 | |||||||
| chr6:129625904 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.786+3449T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625904 | |||||||
| chr6:129625908 | A | ATTATATA others(8): Show |
11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3444_786+3445i others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625908 | |||||||
| chr6:129625919 | TAG | T | 3 | a0001c0001t0001g0079 a0001c0001t0003g0140 a0001c0001t0011g0141 |
3 | HG02615.hp1 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3432_786+3433d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625919 | |||||||
| chr6:129625921 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(58): Show |
62 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.786+3432C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625921 | |||||||
| chr6:129625932 | A | G | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.786+3421T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625932 | |||||||
| chr6:129625935 | ATATAT | A | 4 | a0001c0001t0002g0145 a0001c0001t0010g0136 a0003c0004t0001g0151 others(1): Show |
4 | HG02451.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+3413_786+3417d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625935 | |||||||
| chr6:129625942 | ATATATTT others(6): Show |
A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3398_786+3410d others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625942 | |||||||
| chr6:129625957 | ATATATT | A | 13 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(10): Show |
13 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+3390_786+3395d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625957 | |||||||
| chr6:129625970 | TTA | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3381_786+3382d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625970 | |||||||
| chr6:129626039 | T | TAC | 2 | a0001c0001t0001g0072 a0001c0001t0001g0201 |
2 | HG01081.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.786+3312_786+3313d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626039 | |||||||
| chr6:129626041 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3312G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626041 | |||||||
| chr6:129626065 | T | C | 3 | a0001c0001t0001g0203 a0003c0004t0001g0151 a0003c0004t0005g0088 |
3 | HG01517.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3288A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TAC | 32 | a0001c0001t0001g0065 a0001c0001t0001g0109 a0001c0001t0001g0126 others(29): Show |
32 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.786+3286_786+3287d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TACAC | 29 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0071 others(26): Show |
29 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.786+3284_786+3287d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TACACAC | 51 | a0001c0001t0001g0074 a0001c0001t0001g0086 a0001c0001t0001g0089 others(48): Show |
51 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.786+3282_786+3287d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TACACACA others(1): Show |
14 | a0001c0001t0001g0064 a0001c0001t0001g0075 a0001c0001t0001g0083 others(11): Show |
14 | HG00099.hp2 HG00423.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+3280_786+3287d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TACACACA others(3): Show |
8 | a0001c0001t0001g0063 a0001c0001t0001g0130 a0001c0001t0001g0148 others(5): Show |
8 | HG00423.hp2 HG01928.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3278_786+3287d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TACACACA others(5): Show |
3 | a0001c0001t0001g0091 a0001c0001t0001g0210 a0001c0001t0011g0141 |
3 | HG02615.hp1 HG02976.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.786+3276_786+3287d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TACACACA others(7): Show |
1 | a0001c0001t0006g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.786+3274_786+3287d others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | T | TACACACA others(9): Show |
1 | a0002c0002t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.786+3272_786+3287d others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | TAC | T | 9 | a0001c0001t0001g0216 a0001c0001t0003g0219 a0001c0001t0003g0222 others(6): Show |
9 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+3286_786+3287d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | TACAC | T | 16 | a0001c0001t0001g0142 a0001c0001t0001g0218 a0001c0001t0002g0125 others(13): Show |
16 | HG01192.hp2 HG02451.hp2 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.786+3284_786+3287d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | TACACACA others(1): Show |
T | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.786+3280_786+3287d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | TACACACA others(3): Show |
T | 1 | a0001c0001t0004g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.786+3278_786+3287d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | TACACACA others(5): Show |
T | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+3276_786+3287d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626065 | TACACACA others(17): Show |
T | 1 | a0001c0001t0002g0181 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.786+3264_786+3287d others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | |||||||
| chr6:129626073 | C | CACACACA others(7): Show |
1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3279_786+3280i others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626073 | |||||||
| chr6:129626075 | C | CACACACA others(9): Show |
1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.786+3277_786+3278i others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626075 | |||||||
| chr6:129626101 | CACACAT | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3246_786+3251d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626101 | |||||||
| chr6:129626103 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.786+3250G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626103 | |||||||
| chr6:129626105 | C | CACACACA others(9): Show |
4 | a0001c0001t0001g0096 a0001c0001t0001g0131 a0001c0001t0002g0162 others(1): Show |
4 | HG01081.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | |||||||
| chr6:129626105 | C | CACACACA others(7): Show |
8 | a0001c0001t0001g0102 a0001c0001t0001g0129 a0001c0001t0001g0155 others(5): Show |
8 | HG00738.hp1 HG03516.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | |||||||
| chr6:129626105 | C | CACACACA others(3): Show |
1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.786+3247_786+3248i others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | |||||||
| chr6:129626105 | C | CACACACA others(5): Show |
14 | a0001c0001t0001g0090 a0001c0001t0001g0098 a0001c0001t0001g0101 others(11): Show |
14 | HG00544.hp2 HG00733.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | |||||||
| chr6:129626105 | C | CACACACA others(3): Show |
9 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
9 | HG00621.hp1 HG00741.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | |||||||
| chr6:129626105 | C | CACACATA others(1): Show |
12 | a0001c0001t0001g0094 a0001c0001t0001g0106 a0001c0001t0001g0116 others(9): Show |
12 | HG00642.hp2 HG01074.hp1 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | |||||||
| chr6:129626105 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0005g0207 a0001c0001t0009g0069 others(3): Show |
7 | HG00597.hp2 HG00738.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+3248G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | |||||||
| chr6:129626107 | T | C | 2 | a0001c0001t0011g0141 a0003c0004t0005g0088 |
2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3246A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626107 | |||||||
| chr6:129626297 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.786+3056C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626297 | |||||||
| chr6:129626378 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.786+2975T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626378 | |||||||
| chr6:129626441 | T | A | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+2912A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626441 | |||||||
| chr6:129626455 | A | G | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.786+2898T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626455 | |||||||
| chr6:129626650 | G | A | 11 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+2703C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626650 | |||||||
| chr6:129626655 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.786+2698G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626655 | |||||||
| chr6:129626672 | T | TAC | 53 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0071 others(50): Show |
53 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.786+2679_786+2680d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | |||||||
| chr6:129626672 | TAC | T | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0075 others(15): Show |
18 | HG00099.hp2 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.786+2679_786+2680d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | |||||||
| chr6:129626672 | TACAC | T | 46 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(43): Show |
46 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.786+2677_786+2680d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | |||||||
| chr6:129626672 | TACACACA others(1): Show |
T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(49): Show |
53 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.786+2673_786+2680d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | |||||||
| chr6:129626702 | C | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+2651G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626702 | |||||||
| chr6:129626706 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+2647A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626706 | |||||||
| chr6:129627024 | A | G | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+2329T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627024 | |||||||
| chr6:129627042 | AACAGAAA others(7): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+2297_786+2310d others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627042 | |||||||
| chr6:129627053 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0079 a0001c0001t0001g0080 others(96): Show |
100 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.786+2300A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627053 | |||||||
| chr6:129627112 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.786+2241C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627112 | |||||||
| chr6:129627174 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+2179T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627174 | |||||||
| chr6:129627331 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(47): Show |
51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+2022C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627331 | |||||||
| chr6:129627343 | A | G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+2010T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627343 | |||||||
| chr6:129627382 | C | CA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0079 a0001c0001t0001g0090 others(59): Show |
63 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.786+1970dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627382 | |||||||
| chr6:129627446 | G | A | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+1907C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627446 | |||||||
| chr6:129627485 | G | A | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.786+1868C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627485 | |||||||
| chr6:129627588 | T | G | 1 | a0002c0002t0002g0042 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.786+1765A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627588 | |||||||
| chr6:129627715 | A | G | 2 | a0001c0001t0002g0145 a0001c0001t0010g0136 |
2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+1638T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627715 | |||||||
| chr6:129627867 | T | A | 25 | a0001c0001t0001g0142 a0001c0001t0001g0216 a0001c0001t0001g0218 others(22): Show |
25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+1486A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627867 | |||||||
| chr6:129627910 | C | T | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+1443G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627910 | |||||||
| chr6:129627913 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+1440A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627913 | |||||||
| chr6:129627986 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+1367G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627986 | |||||||
| chr6:129628106 | A | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+1247T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628106 | |||||||
| chr6:129628560 | C | A | 1 | a0001c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.786+793G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628560 | |||||||
| chr6:129628560 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(53): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.786+793G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628560 | |||||||
| chr6:129628864 | G | A | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.786+489C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628864 | |||||||
| chr6:129628926 | A | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(53): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.786+427T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628926 | |||||||
| chr6:129628976 | G | A | 1 | a0001c0001t0016g0149 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.786+377C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628976 | |||||||
| chr6:129629199 | C | T | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.786+154G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629199 | |||||||
| chr6:129629221 | C | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0137 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+132G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629221 | |||||||
| chr6:129629233 | G | GTC | 7 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0002g0145 others(4): Show |
7 | HG02451.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+118_786+119dup others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629233 | |||||||
| chr6:129629247 | C | A | 3 | a0001c0001t0002g0125 a0001c0001t0002g0223 a0002c0002t0003g0023 |
3 | HG00558.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.786+106G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629247 | |||||||
| chr6:129629247 | CTA | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(53): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.786+104_786+105del others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629247 | |||||||
| chr6:129629249 | A | C | 140 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0065 others(137): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.786+104T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629249 | |||||||
| chr6:129629251 | A | C | 37 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0090 others(34): Show |
37 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.786+102T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629251 | |||||||
| chr6:129629253 | A | C | 11 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(8): Show |
11 | HG00423.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.786+100T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629253 | |||||||
| chr6:129629255 | A | C | 2 | a0001c0001t0003g0140 a0001c0001t0011g0141 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.786+98T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629255 | |||||||
| chr6:129629261 | A | G | 36 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0079 others(33): Show |
36 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.786+92T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629261 | |||||||
| chr6:129629268 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.786+85A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629268 | |||||||
| chr6:129629581 | T | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.617-59A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129629581 | |||||||
| chr6:129629619 | T | C | 10 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(7): Show |
10 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.617-97A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129629619 | |||||||
| chr6:129629646 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0177 |
3 | HG01433.hp1 HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.617-124G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129629646 | |||||||
| chr6:129630064 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(56): Show |
60 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.617-542C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630064 | |||||||
| chr6:129630077 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0002c0002t0001g0044 |
3 | HG02486.hp1 HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.617-555C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630077 | |||||||
| chr6:129630095 | C | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(54): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.617-573G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630095 | |||||||
| chr6:129630312 | T | C | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.617-790A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630312 | |||||||
| chr6:129630386 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(54): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.617-864T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630386 | |||||||
| chr6:129630403 | T | A | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.617-881A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630403 | |||||||
| chr6:129630434 | A | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(6): Show |
9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.617-912T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630434 | |||||||
| chr6:129630505 | G | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.617-983C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630505 | |||||||
| chr6:129630662 | A | G | 1 | a0001c0001t0002g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.617-1140T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630662 | |||||||
| chr6:129630714 | T | A | 57 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(54): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.617-1192A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630714 | |||||||
| chr6:129630716 | C | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0090 a0001c0001t0001g0094 others(54): Show |
58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.617-1194G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630716 | |||||||
| chr6:129630763 | G | T | 1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.617-1241C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630763 | |||||||
| chr6:129630767 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.617-1245G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630767 | |||||||
| chr6:129630856 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(124): Show |
128 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.617-1334G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630856 | |||||||
| chr6:129630869 | T | C | 6 | a0001c0001t0005g0207 a0001c0001t0005g0212 a0001c0001t0009g0069 others(3): Show |
6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.617-1347A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630869 | |||||||
| chr6:129630983 | T | C | 10 | a0001c0001t0002g0082 a0001c0001t0005g0207 a0001c0001t0005g0212 others(7): Show |
10 | HG00099.hp1 HG00597.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.617-1461A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630983 | |||||||
| chr6:129631217 | G | C | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.617-1695C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631217 | |||||||
| chr6:129631267 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(60): Show |
64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.617-1745A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631267 | |||||||
| chr6:129631334 | G | A | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0099 others(5): Show |
8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-1812C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631334 | |||||||
| chr6:129631358 | A | C | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.617-1836T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631358 | |||||||
| chr6:129631366 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0132 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.617-1844G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631366 | |||||||
| chr6:129631392 | C | CAA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(59): Show |
63 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.617-1872_617-1871d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631392 | |||||||
| chr6:129631485 | G | C | 2 | a0001c0001t0003g0128 a0002c0002t0003g0043 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.617-1963C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631485 | |||||||
| chr6:129631530 | T | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
66 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.617-2008A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631530 | |||||||
| chr6:129631761 | TTA | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
66 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.617-2241_617-2240d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631761 | |||||||
| chr6:129631762 | T | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.617-2240A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631762 | |||||||
| chr6:129631762 | T | TA | 33 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0075 others(30): Show |
33 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.617-2241dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631762 | |||||||
| chr6:129631762 | T | TAA | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0153 others(5): Show |
8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-2242_617-2241d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631762 | |||||||
| chr6:129631785 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.616+2257A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631785 | |||||||
| chr6:129631863 | T | G | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.616+2179A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631863 | |||||||
| chr6:129631896 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(61): Show |
65 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.616+2146G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631896 | |||||||
| chr6:129631941 | G | GAATT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
67 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.616+2097_616+2100d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631941 | |||||||
| chr6:129631972 | C | A | 1 | a0002c0002t0001g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.616+2070G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631972 | |||||||
| chr6:129632130 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(59): Show |
63 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.616+1912G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632130 | |||||||
| chr6:129632230 | T | C | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.616+1812A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632230 | |||||||
| chr6:129632291 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.616+1751G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632291 | |||||||
| chr6:129632439 | T | C | 1 | a0001c0001t0002g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.616+1603A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632439 | |||||||
| chr6:129632698 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.616+1344G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632698 | |||||||
| chr6:129632766 | A | G | 1 | a0002c0002t0001g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.616+1276T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632766 | |||||||
| chr6:129632781 | G | C | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.616+1261C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632781 | |||||||
| chr6:129632808 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0132 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.616+1234T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632808 | |||||||
| chr6:129633124 | T | C | 31 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(28): Show |
31 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.616+918A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633124 | |||||||
| chr6:129633136 | A | G | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.616+906T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633136 | |||||||
| chr6:129633231 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0132 a0001c0001t0007g0077 others(3): Show |
6 | HG02280.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.616+811G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633231 | |||||||
| chr6:129633266 | TA | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.616+775delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633266 | |||||||
| chr6:129633268 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.616+774T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633268 | |||||||
| chr6:129633285 | A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.616+757T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633285 | |||||||
| chr6:129633371 | G | A | 19 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(16): Show |
19 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.616+671C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633371 | |||||||
| chr6:129633431 | C | T | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.616+611G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633431 | |||||||
| chr6:129633434 | C | CAA | 83 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.616+606_616+607dup others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633434 | |||||||
| chr6:129633434 | C | CAAA | 38 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(35): Show |
39 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.616+605_616+607dup others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633434 | |||||||
| chr6:129633772 | G | A | 3 | a0001c0001t0002g0145 a0001c0001t0010g0136 a0003c0004t0001g0151 |
3 | HG02451.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.616+270C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633772 | |||||||
| chr6:129633829 | C | T | 2 | a0001c0011t0001g0056 a0003c0004t0005g0088 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.616+213G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633829 | |||||||
| chr6:129633908 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.616+134G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633908 | |||||||
| chr6:129633972 | A | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.616+70T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633972 | |||||||
| chr6:129633989 | A | C | 1 | a0001c0001t0002g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.616+53T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633989 | |||||||
| chr6:129634006 | G | GA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(70): Show |
74 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.616+35dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129634006 | |||||||
| chr6:129634006 | GA | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(2): Show |
5 | HG00609.hp1 HG01081.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.616+35delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129634006 | |||||||
| chr6:129634026 | A | G | 10 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.616+16T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129634026 | |||||||
| chr6:129634159 | T | C | 1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.553-54A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634159 | |||||||
| chr6:129634182 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(69): Show |
73 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.553-77A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634182 | |||||||
| chr6:129634342 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(67): Show |
71 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.553-237G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634342 | |||||||
| chr6:129634368 | C | T | 2 | a0001c0001t0002g0125 a0001c0001t0002g0223 |
2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.553-263G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634368 | |||||||
| chr6:129634379 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.553-274C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634379 | |||||||
| chr6:129634679 | T | A | 1 | a0001c0001t0002g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.553-574A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634679 | |||||||
| chr6:129634681 | T | C | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-576A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634681 | |||||||
| chr6:129634781 | T | C | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.553-676A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634781 | |||||||
| chr6:129634847 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0002g0113 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.553-742T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634847 | |||||||
| chr6:129634888 | T | TA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(59): Show |
63 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.553-784dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634888 | |||||||
| chr6:129634888 | TA | T | 31 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0108 others(28): Show |
31 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.553-784delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634888 | |||||||
| chr6:129634926 | AC | A | 3 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0009c0007t0001g0027 |
3 | HG00408.hp1 HG02132.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.553-822delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634926 | |||||||
| chr6:129634974 | C | T | 30 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(27): Show |
30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-869G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634974 | |||||||
| chr6:129634992 | G | A | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-887C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634992 | |||||||
| chr6:129635011 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-906G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635011 | |||||||
| chr6:129635246 | A | G | 2 | a0001c0011t0001g0056 a0003c0004t0005g0088 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.553-1141T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635246 | |||||||
| chr6:129635331 | G | A | 2 | a0001c0011t0001g0056 a0003c0004t0005g0088 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.553-1226C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635331 | |||||||
| chr6:129635485 | C | T | 3 | a0001c0001t0007g0077 a0001c0001t0007g0078 a0001c0011t0001g0056 |
3 | HG02896.hp1 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.553-1380G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635485 | |||||||
| chr6:129635709 | C | T | 2 | a0001c0001t0001g0164 a0001c0011t0001g0056 |
2 | HG03209.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.553-1604G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635709 | |||||||
| chr6:129635835 | T | C | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-1730A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635835 | |||||||
| chr6:129635900 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.553-1795G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635900 | |||||||
| chr6:129636185 | GTAAGCAA others(10): Show |
G | 1 | a0001c0001t0001g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.553-2097_553-2081d others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636185 | |||||||
| chr6:129636208 | AAG | A | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.553-2105_553-2104d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636208 | |||||||
| chr6:129636408 | A | G | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.552+1986T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636408 | |||||||
| chr6:129636488 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.552+1906G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636488 | |||||||
| chr6:129636586 | T | C | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0153 others(5): Show |
8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+1808A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636586 | |||||||
| chr6:129636605 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.552+1789C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636605 | |||||||
| chr6:129636771 | C | T | 2 | a0001c0011t0001g0056 a0003c0004t0005g0088 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.552+1623G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636771 | |||||||
| chr6:129636808 | G | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.552+1586C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636808 | |||||||
| chr6:129636809 | G | A | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.552+1585C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636809 | |||||||
| chr6:129636907 | T | C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(2): Show |
5 | HG00609.hp1 HG01081.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+1487A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636907 | |||||||
| chr6:129636977 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+1417G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636977 | |||||||
| chr6:129637188 | G | A | 1 | a0002c0002t0006g0028 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.552+1206C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637188 | |||||||
| chr6:129637210 | A | G | 3 | a0001c0001t0001g0209 a0002c0002t0001g0007 a0002c0002t0001g0018 |
3 | HG00621.hp2 NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.552+1184T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637210 | |||||||
| chr6:129637257 | G | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.552+1137C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637257 | |||||||
| chr6:129637345 | G | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.552+1049C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637345 | |||||||
| chr6:129637524 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+870G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637524 | |||||||
| chr6:129637550 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.552+844T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637550 | |||||||
| chr6:129637620 | C | A | 2 | a0001c0001t0001g0126 a0002c0002t0001g0025 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.552+774G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637620 | |||||||
| chr6:129637676 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.552+718T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637676 | |||||||
| chr6:129637952 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(49): Show |
53 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.552+442G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637952 | |||||||
| chr6:129638130 | C | G | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.552+264G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129638130 | |||||||
| chr6:129638141 | C | A | 2 | a0001c0001t0001g0112 a0001c0001t0002g0113 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.552+253G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129638141 | |||||||
| chr6:129638272 | G | T | 2 | a0001c0001t0002g0145 a0003c0004t0001g0151 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.552+122C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129638272 | |||||||
| chr6:129638742 | C | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317-113G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129638742 | |||||||
| chr6:129638868 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.317-239T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129638868 | |||||||
| chr6:129639161 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.317-532C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639161 | |||||||
| chr6:129639192 | GT | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.317-564delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639192 | |||||||
| chr6:129639223 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.317-594T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639223 | |||||||
| chr6:129639231 | A | C | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.317-602T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639231 | |||||||
| chr6:129639236 | G | T | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.317-607C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639236 | |||||||
| chr6:129639351 | T | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.317-722A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639351 | |||||||
| chr6:129639389 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.317-760C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639389 | |||||||
| chr6:129639470 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.317-841C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639470 | |||||||
| chr6:129639555 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.317-926A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639555 | |||||||
| chr6:129639630 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.317-1001A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639630 | |||||||
| chr6:129639649 | G | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0132 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.317-1020C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639649 | |||||||
| chr6:129639714 | C | T | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.317-1085G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639714 | |||||||
| chr6:129639716 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.317-1087G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639716 | |||||||
| chr6:129639732 | C | G | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-1103G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639732 | |||||||
| chr6:129639994 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.317-1365C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639994 | |||||||
| chr6:129639999 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.317-1370A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639999 | |||||||
| chr6:129640023 | C | T | 24 | a0001c0001t0001g0080 a0001c0001t0001g0137 a0001c0001t0001g0206 others(21): Show |
24 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.317-1394G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640023 | |||||||
| chr6:129640042 | C | CA | 39 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0079 others(36): Show |
39 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.317-1414dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640042 | |||||||
| chr6:129640042 | C | CAA | 10 | a0001c0001t0001g0064 a0001c0001t0001g0099 a0001c0001t0001g0179 others(7): Show |
10 | HG00735.hp2 HG01433.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-1415_317-1414d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640042 | |||||||
| chr6:129640042 | CAAAA | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(45): Show |
49 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.317-1417_317-1414d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640042 | |||||||
| chr6:129640059 | A | C | 2 | a0001c0011t0001g0056 a0003c0004t0005g0088 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.317-1430T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640059 | |||||||
| chr6:129640065 | C | A | 49 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(46): Show |
49 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.317-1436G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640065 | |||||||
| chr6:129640069 | C | A | 10 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(7): Show |
10 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-1440G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640069 | |||||||
| chr6:129640104 | A | G | 49 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(46): Show |
49 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.317-1475T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640104 | |||||||
| chr6:129640287 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0132 |
2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.316+1529A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640287 | |||||||
| chr6:129640398 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.316+1418T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640398 | |||||||
| chr6:129640605 | C | T | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.316+1211G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640605 | |||||||
| chr6:129640618 | T | C | 2 | a0001c0001t0002g0145 a0003c0004t0001g0151 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.316+1198A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640618 | |||||||
| chr6:129640693 | G | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.316+1123C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640693 | |||||||
| chr6:129640829 | A | C | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.316+987T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640829 | |||||||
| chr6:129640831 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.316+985C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640831 | |||||||
| chr6:129640986 | T | C | 14 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(11): Show |
14 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.316+830A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640986 | |||||||
| chr6:129640991 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316+825C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640991 | |||||||
| chr6:129641156 | G | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.316+660C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641156 | |||||||
| chr6:129641247 | T | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.316+569A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641247 | |||||||
| chr6:129641322 | T | C | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.316+494A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641322 | |||||||
| chr6:129641338 | A | G | 2 | a0001c0001t0001g0126 a0002c0002t0001g0025 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316+478T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641338 | |||||||
| chr6:129641445 | C | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.316+371G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641445 | |||||||
| chr6:129641488 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.316+328A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641488 | |||||||
| chr6:129641612 | T | C | 3 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 |
3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.316+204A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641612 | |||||||
| chr6:129641728 | A | AT | 21 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0079 others(18): Show |
21 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.316+87dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641728 | |||||||
| chr6:129641786 | C | A | 20 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(17): Show |
20 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+30G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641786 | |||||||
| chr6:129642574 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(49): Show |
53 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.114-556C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642574 | |||||||
| chr6:129642577 | T | C | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-559A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642577 | |||||||
| chr6:129642702 | A | G | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.114-684T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642702 | |||||||
| chr6:129642825 | C | T | 2 | a0001c0011t0001g0056 a0003c0004t0005g0088 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.114-807G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642825 | |||||||
| chr6:129642827 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.114-809C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642827 | |||||||
| chr6:129642907 | C | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.114-889G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642907 | |||||||
| chr6:129642917 | A | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(73): Show |
77 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.114-899T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642917 | |||||||
| chr6:129643155 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.114-1137A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643155 | |||||||
| chr6:129643226 | G | A | 5 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(2): Show |
5 | HG02622.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-1208C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643226 | |||||||
| chr6:129643293 | C | A | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114-1275G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643293 | |||||||
| chr6:129643297 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.114-1279G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643297 | |||||||
| chr6:129643303 | G | T | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-1285C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643303 | |||||||
| chr6:129643857 | C | G | 2 | a0001c0001t0007g0077 a0001c0001t0007g0078 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.114-1839G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643857 | |||||||
| chr6:129643861 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.114-1843C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643861 | |||||||
| chr6:129643931 | A | T | 2 | a0001c0011t0001g0056 a0003c0004t0005g0088 |
2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.114-1913T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643931 | |||||||
| chr6:129643998 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG00735.hp2 HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.114-1980A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643998 | |||||||
| chr6:129644209 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(52): Show |
56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.114-2191C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644209 | |||||||
| chr6:129644287 | A | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0101 a0001c0001t0007g0077 others(1): Show |
4 | HG01361.hp2 HG01981.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-2269T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644287 | |||||||
| chr6:129644359 | A | G | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.114-2341T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644359 | |||||||
| chr6:129644388 | T | A | 17 | a0001c0001t0001g0098 a0001c0001t0001g0129 a0001c0001t0001g0155 others(14): Show |
17 | HG00544.hp2 HG00609.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.114-2370A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644388 | |||||||
| chr6:129644388 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114-2370A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644388 | |||||||
| chr6:129644421 | A | G | 6 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(3): Show |
6 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-2403T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644421 | |||||||
| chr6:129644547 | TTC | T | 18 | a0001c0001t0001g0079 a0001c0001t0001g0142 a0001c0001t0002g0145 others(15): Show |
18 | HG01192.hp2 HG02451.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.114-2531_114-2530d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644547 | |||||||
| chr6:129644983 | A | G | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.114-2965T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644983 | |||||||
| chr6:129645021 | T | C | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.114-3003A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645021 | |||||||
| chr6:129645202 | G | T | 11 | a0001c0001t0001g0079 a0001c0001t0002g0145 a0001c0001t0003g0225 others(8): Show |
11 | HG02451.hp1 HG02622.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-3184C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645202 | |||||||
| chr6:129645205 | ACTT | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | NA18986.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.114-3190_114-3188d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645205 | |||||||
| chr6:129645260 | A | G | 20 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(17): Show |
20 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-3242T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645260 | |||||||
| chr6:129645268 | G | A | 22 | a0001c0001t0001g0080 a0001c0001t0001g0137 a0001c0001t0001g0206 others(19): Show |
22 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.114-3250C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645268 | |||||||
| chr6:129645300 | A | G | 3 | a0001c0001t0003g0237 a0002c0002t0001g0044 a0002c0002t0014g0045 |
3 | HG02257.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.114-3282T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645300 | |||||||
| chr6:129645391 | T | C | 22 | a0001c0001t0001g0080 a0001c0001t0001g0137 a0001c0001t0001g0206 others(19): Show |
22 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.114-3373A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645391 | |||||||
| chr6:129645457 | T | A | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.114-3439A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645457 | |||||||
| chr6:129645515 | C | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(86): Show |
90 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.114-3497G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645515 | |||||||
| chr6:129645542 | C | T | 5 | a0001c0001t0002g0145 a0001c0001t0004g0123 a0001c0001t0004g0134 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-3524G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645542 | |||||||
| chr6:129645570 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.114-3552T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645570 | |||||||
| chr6:129645637 | G | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(99): Show |
103 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.114-3619C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645637 | |||||||
| chr6:129645762 | C | CT | 26 | a0001c0001t0001g0080 a0001c0001t0001g0137 a0001c0001t0001g0206 others(23): Show |
26 | HG00408.hp2 HG00642.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.114-3745dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645762 | |||||||
| chr6:129645775 | G | A | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0153 others(5): Show |
8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-3757C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645775 | |||||||
| chr6:129646078 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG00099.hp2 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-4060T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646078 | |||||||
| chr6:129646088 | C | T | 4 | a0001c0001t0008g0118 a0001c0001t0008g0228 a0002c0002t0001g0006 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-4070G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646088 | |||||||
| chr6:129646368 | G | C | 2 | a0002c0002t0001g0006 a0004c0008t0004g0055 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-4350C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646368 | |||||||
| chr6:129646460 | C | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-4442G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646460 | |||||||
| chr6:129646555 | A | T | 58 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.114-4537T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646555 | |||||||
| chr6:129646823 | C | T | 44 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0084 others(41): Show |
44 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.114-4805G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646823 | |||||||
| chr6:129646929 | A | G | 2 | a0001c0011t0001g0056 a0003c0004t0001g0151 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114-4911T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646929 | |||||||
| chr6:129646971 | T | C | 2 | a0001c0011t0001g0056 a0003c0004t0001g0151 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114-4953A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646971 | |||||||
| chr6:129647085 | C | G | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114-5067G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647085 | |||||||
| chr6:129647221 | T | A | 1 | a0002c0002t0014g0045 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114-5203A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647221 | |||||||
| chr6:129647335 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.114-5317A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647335 | |||||||
| chr6:129647338 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(125): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.114-5320T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647338 | |||||||
| chr6:129647347 | A | G | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-5329T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647347 | |||||||
| chr6:129647487 | T | C | 5 | a0001c0001t0002g0145 a0001c0001t0004g0123 a0001c0001t0004g0134 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-5469A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647487 | |||||||
| chr6:129647673 | TA | T | 26 | a0001c0001t0001g0080 a0001c0001t0001g0103 a0001c0001t0001g0132 others(23): Show |
26 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.114-5656delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647673 | |||||||
| chr6:129647770 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114-5752T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647770 | |||||||
| chr6:129647996 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.114-5978A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647996 | |||||||
| chr6:129648012 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.114-5994G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648012 | |||||||
| chr6:129648164 | T | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0202 |
3 | HG00423.hp1 NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.114-6146A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648164 | |||||||
| chr6:129648231 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114-6213G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648231 | |||||||
| chr6:129648265 | G | A | 2 | a0002c0002t0001g0006 a0004c0008t0004g0055 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-6247C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648265 | |||||||
| chr6:129648284 | A | G | 2 | a0002c0002t0001g0006 a0004c0008t0004g0055 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-6266T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648284 | |||||||
| chr6:129648445 | T | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG00099.hp2 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-6427A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648445 | |||||||
| chr6:129648583 | G | A | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-6565C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648583 | |||||||
| chr6:129648610 | TA | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.114-6593delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648610 | |||||||
| chr6:129648719 | TTATCTC | T | 2 | a0002c0002t0001g0006 a0004c0008t0004g0055 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-6707_114-6702d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648719 | |||||||
| chr6:129648733 | GA | G | 59 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.114-6716delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648733 | |||||||
| chr6:129648766 | A | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(120): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(121): Show |
intron_variant | MODIFIER | c.114-6748T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648766 | |||||||
| chr6:129648779 | C | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-6761G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648779 | |||||||
| chr6:129649065 | G | A | 60 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(57): Show |
60 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.114-7047C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649065 | |||||||
| chr6:129649079 | C | A | 1 | a0002c0002t0006g0028 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.114-7061G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649079 | |||||||
| chr6:129649137 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.114-7119T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649137 | |||||||
| chr6:129649187 | T | G | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-7169A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649187 | |||||||
| chr6:129649269 | G | A | 20 | a0001c0001t0001g0098 a0001c0001t0001g0155 a0001c0001t0001g0156 others(17): Show |
20 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-7251C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649269 | |||||||
| chr6:129649422 | C | T | 25 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(22): Show |
25 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.114-7404G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649422 | |||||||
| chr6:129649427 | G | A | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-7409C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649427 | |||||||
| chr6:129649462 | G | A | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(7): Show |
10 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-7444C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649462 | |||||||
| chr6:129649553 | C | CA | 41 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0074 others(38): Show |
41 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.114-7536dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | |||||||
| chr6:129649553 | C | CAA | 24 | a0001c0001t0001g0132 a0001c0001t0001g0158 a0001c0001t0001g0177 others(21): Show |
24 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.114-7537_114-7536d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | |||||||
| chr6:129649553 | C | CAAA | 15 | a0001c0001t0001g0080 a0001c0001t0001g0216 a0001c0001t0001g0218 others(12): Show |
15 | HG00597.hp2 HG00642.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-7538_114-7536d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | |||||||
| chr6:129649553 | CAA | C | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7537_114-7536d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | |||||||
| chr6:129649817 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(116): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.114-7799G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649817 | |||||||
| chr6:129649882 | G | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.114-7864C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649882 | |||||||
| chr6:129649904 | CT | C | 5 | a0001c0001t0004g0123 a0001c0001t0004g0134 a0001c0001t0004g0138 others(2): Show |
5 | HG02622.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7887delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649904 | |||||||
| chr6:129649913 | T | G | 21 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(18): Show |
21 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.114-7895A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649913 | |||||||
| chr6:129649914 | G | GT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0090 others(58): Show |
62 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.114-7897dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | |||||||
| chr6:129649914 | G | GTT | 33 | a0001c0001t0001g0062 a0001c0001t0001g0080 a0001c0001t0001g0132 others(30): Show |
33 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.114-7898_114-7897d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | |||||||
| chr6:129649914 | G | GTTT | 5 | a0001c0001t0001g0206 a0001c0001t0001g0221 a0001c0001t0002g0180 others(2): Show |
5 | HG02071.hp1 NA18944.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7899_114-7897d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | |||||||
| chr6:129649914 | G | T | 21 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(18): Show |
21 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.114-7896C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | |||||||
| chr6:129649981 | C | T | 3 | a0001c0001t0008g0118 a0001c0001t0008g0228 a0004c0008t0004g0055 |
3 | HG02615.hp2 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-7963G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649981 | |||||||
| chr6:129650079 | A | AT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(89): Show |
93 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.114-8062dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650079 | |||||||
| chr6:129650079 | AT | A | 26 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(23): Show |
26 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.114-8062delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650079 | |||||||
| chr6:129650151 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.114-8133G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650151 | |||||||
| chr6:129650316 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.114-8298G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650316 | |||||||
| chr6:129650343 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.114-8325C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650343 | |||||||
| chr6:129650399 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.114-8381C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650399 | |||||||
| chr6:129650631 | T | TA | 3 | a0001c0001t0019g0233 a0002c0002t0001g0006 a0004c0008t0004g0055 |
3 | HG02615.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-8614dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650631 | |||||||
| chr6:129650717 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-8699G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650717 | |||||||
| chr6:129650784 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(49): Show |
53 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.114-8766G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650784 | |||||||
| chr6:129650915 | C | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(57): Show |
61 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.114-8897G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650915 | |||||||
| chr6:129650931 | T | C | 2 | a0002c0002t0001g0052 a0002c0002t0001g0053 |
2 | HG02622.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.114-8913A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650931 | |||||||
| chr6:129651170 | T | TAA | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(7): Show |
10 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-9154_114-9153d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651170 | |||||||
| chr6:129651171 | A | AAG | 16 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(13): Show |
16 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.114-9155_114-9154d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651171 | |||||||
| chr6:129651271 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.114-9253C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651271 | |||||||
| chr6:129651463 | C | T | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.114-9445G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651463 | |||||||
| chr6:129651780 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(49): Show |
53 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.114-9762T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651780 | |||||||
| chr6:129651832 | T | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0150 a0001c0001t0001g0154 others(1): Show |
4 | HG00558.hp2 NA18942.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-9814A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651832 | |||||||
| chr6:129651884 | GA | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.114-9867delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651884 | |||||||
| chr6:129651920 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.114-9902A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651920 | |||||||
| chr6:129651985 | C | T | 1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.114-9967G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651985 | |||||||
| chr6:129652003 | G | A | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(15): Show |
18 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-9985C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652003 | |||||||
| chr6:129652073 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-10055G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652073 | |||||||
| chr6:129652102 | G | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.114-10084C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652102 | |||||||
| chr6:129652179 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.114-10161A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652179 | |||||||
| chr6:129652344 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114-10326T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652344 | |||||||
| chr6:129652698 | T | C | 44 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0142 others(41): Show |
44 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.114-10680A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652698 | |||||||
| chr6:129652735 | C | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.114-10717G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652735 | |||||||
| chr6:129652800 | C | G | 2 | a0001c0001t0019g0233 a0002c0002t0001g0006 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-10782G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652800 | |||||||
| chr6:129652817 | A | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.114-10799T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652817 | |||||||
| chr6:129652935 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114-10917A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652935 | |||||||
| chr6:129652969 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.114-10951A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652969 | |||||||
| chr6:129653037 | A | T | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(15): Show |
18 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-11019T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653037 | |||||||
| chr6:129653112 | C | A | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.114-11094G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653112 | |||||||
| chr6:129653286 | A | C | 1 | a0002c0002t0001g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114-11268T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653286 | |||||||
| chr6:129653550 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(57): Show |
61 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.114-11532C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653550 | |||||||
| chr6:129653622 | A | G | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-11604T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653622 | |||||||
| chr6:129653701 | G | A | 36 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0206 others(33): Show |
36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-11683C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653701 | |||||||
| chr6:129653817 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114-11799A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653817 | |||||||
| chr6:129653822 | A | AG | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.114-11805dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653822 | |||||||
| chr6:129653823 | G | GA | 24 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(21): Show |
24 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.114-11806dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653823 | |||||||
| chr6:129654703 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.114-12685C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129654703 | |||||||
| chr6:129655045 | G | A | 1 | a0002c0002t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.114-13027C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655045 | |||||||
| chr6:129655091 | C | T | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-13073G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655091 | |||||||
| chr6:129655119 | G | A | 10 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-13101C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655119 | |||||||
| chr6:129655123 | C | T | 1 | a0001c0001t0006g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114-13105G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655123 | |||||||
| chr6:129655159 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.114-13141T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655159 | |||||||
| chr6:129655211 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.114-13193G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655211 | |||||||
| chr6:129655235 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.114-13217G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655235 | |||||||
| chr6:129655317 | CA | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0090 others(44): Show |
48 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.114-13300delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655317 | |||||||
| chr6:129655317 | CAA | C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0194 a0001c0001t0017g0174 others(2): Show |
5 | HG00558.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-13301_114-1330 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655317 | |||||||
| chr6:129655332 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0090 others(23): Show |
27 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.114-13314T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655332 | |||||||
| chr6:129655332 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0009g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.114-13324_114-1331 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655332 | |||||||
| chr6:129655333 | AAAAAAAA others(2): Show |
A | 34 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0206 others(31): Show |
34 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.114-13324_114-1331 others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655333 | |||||||
| chr6:129655337 | A | AG | 2 | a0001c0001t0019g0233 a0002c0002t0001g0006 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-13320_114-1331 others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655337 | |||||||
| chr6:129655337 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(59): Show |
63 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.114-13319T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655337 | |||||||
| chr6:129655337 | AAAAAG | A | 8 | a0001c0001t0001g0063 a0001c0001t0001g0084 a0001c0001t0001g0091 others(5): Show |
8 | HG02004.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-13324_114-1332 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655337 | |||||||
| chr6:129655338 | AAAAG | A | 9 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0199 others(6): Show |
9 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-13324_114-1332 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655338 | |||||||
| chr6:129655353 | AAAAG | A | 8 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(5): Show |
8 | HG01192.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-13339_114-1333 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655353 | |||||||
| chr6:129655373 | C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-13355G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655373 | |||||||
| chr6:129655649 | C | CATG | 36 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0206 others(33): Show |
36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-13632_114-1363 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655649 | |||||||
| chr6:129655932 | C | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-13914G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655932 | |||||||
| chr6:129655943 | T | G | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0153 others(5): Show |
8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-13925A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655943 | |||||||
| chr6:129655956 | G | A | 1 | a0002c0002t0001g0047 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.114-13938C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655956 | |||||||
| chr6:129656004 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.114-13986A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656004 | |||||||
| chr6:129656415 | G | A | 6 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(3): Show |
6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-14397C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656415 | |||||||
| chr6:129656510 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.114-14492T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656510 | |||||||
| chr6:129656512 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0187 a0001c0001t0001g0196 others(1): Show |
4 | NA18979.hp2 NA18999.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-14494C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656512 | |||||||
| chr6:129656622 | C | T | 36 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0206 others(33): Show |
36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-14604G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656622 | |||||||
| chr6:129656642 | TC | T | 18 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(15): Show |
18 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-14625delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656642 | |||||||
| chr6:129656668 | TA | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.114-14651delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656668 | |||||||
| chr6:129656668 | TAA | T | 10 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(7): Show |
10 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-14652_114-1465 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656668 | |||||||
| chr6:129656764 | C | G | 36 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0206 others(33): Show |
36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-14746G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656764 | |||||||
| chr6:129656774 | C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-14756G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656774 | |||||||
| chr6:129656783 | T | C | 2 | a0001c0001t0019g0233 a0002c0002t0001g0006 |
2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-14765A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656783 | |||||||
| chr6:129656813 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.114-14795T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656813 | |||||||
| chr6:129656938 | T | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(51): Show |
55 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.114-14920A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656938 | |||||||
| chr6:129657123 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.114-15105A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657123 | |||||||
| chr6:129657145 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-15127G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657145 | |||||||
| chr6:129657251 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.114-15233A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657251 | |||||||
| chr6:129657260 | T | C | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.114-15242A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657260 | |||||||
| chr6:129657378 | T | C | 2 | a0001c0001t0001g0126 a0002c0002t0001g0025 |
2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.114-15360A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657378 | |||||||
| chr6:129657429 | T | TAA | 20 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(17): Show |
20 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.114-15413_114-1541 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657429 | |||||||
| chr6:129657429 | T | TAAA | 57 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(54): Show |
58 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.114-15414_114-1541 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657429 | |||||||
| chr6:129657430 | A | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0201 a0001c0001t0001g0213 |
3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.114-15412T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657430 | |||||||
| chr6:129657446 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114-15428G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657446 | |||||||
| chr6:129657447 | A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-15429T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657447 | |||||||
| chr6:129658009 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.114-15991A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658009 | |||||||
| chr6:129658422 | G | GA | 22 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(19): Show |
22 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.114-16405dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658422 | |||||||
| chr6:129658422 | GA | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(112): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.114-16405delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658422 | |||||||
| chr6:129658593 | A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-16575T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658593 | |||||||
| chr6:129658617 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(57): Show |
61 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.114-16599G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658617 | |||||||
| chr6:129658771 | TAG | T | 2 | a0003c0004t0001g0151 a0009c0007t0001g0027 |
2 | HG03098.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.114-16755_114-1675 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658771 | |||||||
| chr6:129658804 | A | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-16786T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658804 | |||||||
| chr6:129658931 | G | T | 2 | a0001c0001t0009g0069 a0001c0001t0009g0070 |
2 | NA18612.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.114-16913C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658931 | |||||||
| chr6:129659065 | C | G | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-17047G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659065 | |||||||
| chr6:129659180 | C | A | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17162G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659180 | |||||||
| chr6:129659291 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.114-17273A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659291 | |||||||
| chr6:129659307 | T | C | 2 | a0001c0001t0003g0140 a0001c0001t0011g0141 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.114-17289A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659307 | |||||||
| chr6:129659456 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114-17438A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659456 | |||||||
| chr6:129659456 | TTTTTA | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.114-17443_114-1743 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659456 | |||||||
| chr6:129659482 | T | A | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17464A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659482 | |||||||
| chr6:129659483 | A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17465T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659483 | |||||||
| chr6:129659545 | T | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.114-17527A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659545 | |||||||
| chr6:129659660 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.114-17642A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659660 | |||||||
| chr6:129659660 | T | G | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17642A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659660 | |||||||
| chr6:129659846 | T | G | 4 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-17828A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659846 | |||||||
| chr6:129659919 | C | T | 35 | a0001c0001t0001g0132 a0001c0001t0001g0144 a0001c0001t0001g0186 others(32): Show |
35 | HG00408.hp2 HG00597.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.114-17901G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659919 | |||||||
| chr6:129659986 | T | TG | 10 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0153 others(7): Show |
10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-17969dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659986 | |||||||
| chr6:129660068 | A | G | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-18050T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660068 | |||||||
| chr6:129660167 | C | T | 1 | a0002c0002t0001g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114-18149G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660167 | |||||||
| chr6:129660170 | CA | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0178 |
2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.114-18153delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660170 | |||||||
| chr6:129660368 | A | C | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.114-18350T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660368 | |||||||
| chr6:129660428 | A | G | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-18410T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660428 | |||||||
| chr6:129660497 | GA | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.114-18480delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660497 | |||||||
| chr6:129660499 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-18481T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660499 | |||||||
| chr6:129660752 | T | A | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.114-18734A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660752 | |||||||
| chr6:129660825 | T | C | 5 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-18807A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660825 | |||||||
| chr6:129660861 | G | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(82): Show |
intron_variant | MODIFIER | c.114-18843C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660861 | |||||||
| chr6:129660893 | T | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-18875A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660893 | |||||||
| chr6:129660894 | A | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.114-18876T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660894 | |||||||
| chr6:129661021 | TA | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-19004delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661021 | |||||||
| chr6:129661108 | C | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-19090G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661108 | |||||||
| chr6:129661140 | A | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.114-19122T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661140 | |||||||
| chr6:129661256 | C | G | 15 | a0001c0001t0001g0079 a0001c0001t0001g0142 a0001c0001t0001g0144 others(12): Show |
15 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-19238G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661256 | |||||||
| chr6:129661298 | T | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.114-19280A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661298 | |||||||
| chr6:129661309 | T | TA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0071 others(127): Show |
131 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.114-19292dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661309 | |||||||
| chr6:129661309 | T | TAA | 10 | a0001c0001t0001g0108 a0001c0001t0001g0157 a0001c0001t0001g0179 others(7): Show |
10 | HG00140.hp2 HG00544.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.114-19293_114-1929 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661309 | |||||||
| chr6:129661309 | TA | T | 9 | a0001c0001t0001g0186 a0001c0001t0001g0199 a0001c0001t0001g0210 others(6): Show |
9 | HG01074.hp1 HG02615.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-19292delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661309 | |||||||
| chr6:129661512 | G | GA | 10 | a0001c0001t0001g0080 a0001c0001t0001g0144 a0001c0001t0002g0145 others(7): Show |
10 | HG00642.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-19495dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | |||||||
| chr6:129661512 | G | GAA | 20 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(17): Show |
20 | HG00423.hp1 HG02074.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.114-19496_114-1949 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | |||||||
| chr6:129661512 | G | GAAA | 101 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(98): Show |
102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.114-19497_114-1949 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | |||||||
| chr6:129661512 | G | GAAAA | 10 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(7): Show |
10 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-19498_114-1949 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | |||||||
| chr6:129661769 | C | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(63): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.114-19751G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661769 | |||||||
| chr6:129661972 | C | CCA | 3 | a0001c0011t0001g0056 a0003c0004t0001g0151 a0003c0004t0005g0088 |
3 | HG03098.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.114-19956_114-1995 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661972 | |||||||
| chr6:129661972 | CCA | C | 50 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(47): Show |
50 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.114-19956_114-1995 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661972 | |||||||
| chr6:129662223 | A | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0202 |
3 | HG00423.hp1 NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.114-20205T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662223 | |||||||
| chr6:129662229 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0007g0077 a0001c0001t0007g0078 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114-20211G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662229 | |||||||
| chr6:129662385 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-20367A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662385 | |||||||
| chr6:129662489 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.114-20471G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662489 | |||||||
| chr6:129662498 | G | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-20480C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662498 | |||||||
| chr6:129662727 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-20709A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662727 | |||||||
| chr6:129662733 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-20715T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662733 | |||||||
| chr6:129663078 | T | G | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-21060A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663078 | |||||||
| chr6:129663155 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-21137G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663155 | |||||||
| chr6:129663210 | A | G | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-21192T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663210 | |||||||
| chr6:129663217 | T | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.114-21199A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663217 | |||||||
| chr6:129663450 | A | G | 4 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-21432T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663450 | |||||||
| chr6:129663451 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.114-21433G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663451 | |||||||
| chr6:129663670 | C | A | 2 | a0001c0001t0004g0123 a0001c0001t0004g0134 |
2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.114-21652G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663670 | |||||||
| chr6:129663748 | A | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-21730T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663748 | |||||||
| chr6:129663775 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.114-21757C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663775 | |||||||
| chr6:129664002 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.114-21984A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664002 | |||||||
| chr6:129664025 | A | T | 1 | a0002c0002t0001g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.114-22007T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664025 | |||||||
| chr6:129664079 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-22061A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664079 | |||||||
| chr6:129664388 | A | C | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-22370T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664388 | |||||||
| chr6:129664505 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-22487C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664505 | |||||||
| chr6:129664776 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-22758C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664776 | |||||||
| chr6:129665219 | A | G | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-23201T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665219 | |||||||
| chr6:129665283 | G | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-23265C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665283 | |||||||
| chr6:129665308 | C | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.114-23290G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665308 | |||||||
| chr6:129665325 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.114-23307C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665325 | |||||||
| chr6:129665344 | G | A | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-23326C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665344 | |||||||
| chr6:129665443 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-23425T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665443 | |||||||
| chr6:129665570 | T | A | 5 | a0001c0001t0002g0125 a0001c0001t0002g0223 a0001c0001t0003g0224 others(2): Show |
5 | HG02451.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-23552A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665570 | |||||||
| chr6:129665619 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-23601G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665619 | |||||||
| chr6:129665647 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-23629A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665647 | |||||||
| chr6:129665660 | G | A | 3 | a0001c0001t0003g0237 a0002c0002t0001g0044 a0002c0002t0014g0045 |
3 | HG02257.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.114-23642C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665660 | |||||||
| chr6:129665661 | G | T | 15 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0084 others(12): Show |
15 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-23643C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665661 | |||||||
| chr6:129665803 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.114-23785A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665803 | |||||||
| chr6:129666216 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-24198T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666216 | |||||||
| chr6:129666247 | A | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-24229T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666247 | |||||||
| chr6:129666259 | A | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.114-24241T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666259 | |||||||
| chr6:129666319 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.114-24301G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666319 | |||||||
| chr6:129666347 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(55): Show |
59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.114-24329G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666347 | |||||||
| chr6:129666396 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0007g0077 a0001c0001t0007g0078 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114-24378G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666396 | |||||||
| chr6:129666585 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.114-24567G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666585 | |||||||
| chr6:129666699 | C | T | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-24681G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666699 | |||||||
| chr6:129666842 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.114-24824T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666842 | |||||||
| chr6:129666885 | G | GC | 140 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.114-24868dupG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666885 | |||||||
| chr6:129666944 | T | C | 4 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-24926A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666944 | |||||||
| chr6:129666990 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.114-24972G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666990 | |||||||
| chr6:129666999 | TA | T | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-24982delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666999 | |||||||
| chr6:129667032 | A | T | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-25014T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667032 | |||||||
| chr6:129667054 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.114-25036A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667054 | |||||||
| chr6:129667055 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.114-25037A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667055 | |||||||
| chr6:129667056 | C | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.114-25038G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667056 | |||||||
| chr6:129667198 | AT | A | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-25181delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667198 | |||||||
| chr6:129667200 | T | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-25182A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667200 | |||||||
| chr6:129667408 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.114-25390A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667408 | |||||||
| chr6:129667469 | A | ATG | 14 | a0001c0001t0001g0086 a0001c0001t0001g0111 a0001c0001t0001g0124 others(11): Show |
14 | HG00438.hp1 HG00639.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.114-25453_114-2545 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | |||||||
| chr6:129667469 | A | ATGTG | 5 | a0001c0001t0001g0188 a0001c0001t0002g0081 a0001c0001t0013g0119 others(2): Show |
5 | HG01169.hp1 HG01169.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-25455_114-2545 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | |||||||
| chr6:129667469 | A | ATGTGTG | 2 | a0001c0001t0001g0127 a0002c0002t0001g0040 |
2 | HG01175.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.114-25457_114-2545 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | |||||||
| chr6:129667469 | A | G | 6 | a0001c0001t0003g0128 a0001c0001t0003g0133 a0001c0011t0001g0056 others(3): Show |
6 | HG01261.hp1 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-25451T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | |||||||
| chr6:129667469 | ATG | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0147 a0001c0001t0001g0158 others(3): Show |
6 | HG00438.hp2 HG01358.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-25453_114-2545 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | |||||||
| chr6:129667469 | ATGTG | A | 25 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(22): Show |
25 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.114-25455_114-2545 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | |||||||
| chr6:129667469 | ATGTGTG | A | 2 | a0001c0001t0001g0214 a0001c0001t0002g0162 |
2 | HG00544.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.114-25457_114-2545 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | |||||||
| chr6:129667492 | T | C | 1 | a0001c0001t0004g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.114-25474A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667492 | |||||||
| chr6:129667503 | G | A | 25 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(22): Show |
25 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.114-25485C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667503 | G | GTA | 4 | a0001c0001t0002g0068 a0001c0001t0008g0118 a0001c0001t0008g0228 others(1): Show |
4 | HG02717.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667503 | G | GTGTA | 14 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(11): Show |
14 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667503 | G | GTGTGTA | 11 | a0001c0001t0001g0096 a0001c0001t0001g0121 a0001c0001t0001g0132 others(8): Show |
11 | HG00733.hp1 HG01081.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667503 | G | GTGTGTGT others(1): Show |
22 | a0001c0001t0001g0079 a0001c0001t0001g0101 a0001c0001t0001g0109 others(19): Show |
22 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667503 | G | GTGTGTGT others(3): Show |
29 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(26): Show |
30 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667503 | G | GTGTGTGT others(5): Show |
29 | a0001c0001t0001g0106 a0001c0001t0001g0126 a0001c0001t0001g0166 others(26): Show |
29 | HG00408.hp2 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667503 | G | GTGTGTGT others(7): Show |
7 | a0001c0001t0001g0094 a0001c0001t0001g0108 a0001c0001t0001g0216 others(4): Show |
7 | HG00140.hp2 HG00741.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | |||||||
| chr6:129667536 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114-25518G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667536 | |||||||
| chr6:129667747 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.114-25729C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667747 | |||||||
| chr6:129667905 | G | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-25887C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667905 | |||||||
| chr6:129668188 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.114-26170G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668188 | |||||||
| chr6:129668287 | T | C | 3 | a0001c0011t0001g0056 a0002c0002t0001g0006 a0003c0004t0001g0151 |
3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-26269A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668287 | |||||||
| chr6:129668362 | T | TCA | 18 | a0001c0001t0001g0085 a0001c0001t0001g0137 a0001c0001t0001g0139 others(15): Show |
18 | HG00558.hp1 HG00639.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-26346_114-2634 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACA | 30 | a0001c0001t0001g0076 a0001c0001t0001g0089 a0001c0001t0001g0099 others(27): Show |
30 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.114-26348_114-2634 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACACA | 32 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0124 others(29): Show |
32 | HG00558.hp2 HG00621.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.114-26350_114-2634 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACACAC others(1): Show |
16 | a0001c0001t0001g0074 a0001c0001t0001g0080 a0001c0001t0001g0127 others(13): Show |
16 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.114-26352_114-2634 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACACAC others(3): Show |
8 | a0001c0001t0001g0086 a0001c0001t0001g0193 a0001c0001t0001g0201 others(5): Show |
8 | HG00408.hp1 HG02027.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.114-26354_114-2634 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACACAC others(7): Show |
3 | a0001c0001t0002g0172 a0002c0002t0002g0019 a0002c0002t0002g0020 |
3 | HG01261.hp2 HG02273.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.114-26345_114-2634 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACACAC others(11): Show |
1 | a0002c0002t0002g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.114-26345_114-2634 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACACAC others(5): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0146 |
2 | HG02523.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.114-26356_114-2634 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | T | TCACACAC others(7): Show |
3 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0003c0004t0005g0088 |
3 | HG02280.hp2 HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.114-26358_114-2634 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | TCA | T | 25 | a0001c0001t0001g0091 a0001c0001t0001g0132 a0001c0001t0001g0135 others(22): Show |
25 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.114-26346_114-2634 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668362 | TCACA | T | 5 | a0001c0001t0001g0079 a0001c0001t0001g0216 a0001c0001t0007g0077 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-26348_114-2634 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | |||||||
| chr6:129668377 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114-26359G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668377 | |||||||
| chr6:129668378 | A | T | 59 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(56): Show |
60 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.114-26360T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668378 | |||||||
| chr6:129668391 | CACACACA others(3): Show |
C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0002g0143 others(2): Show |
5 | HG00099.hp2 HG01074.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-26383_114-2637 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668391 | |||||||
| chr6:129668393 | CACACACA others(1): Show |
C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG01433.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.114-26383_114-2637 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668393 | |||||||
| chr6:129668395 | CACACAG | C | 3 | a0001c0001t0001g0195 a0002c0002t0001g0016 a0002c0002t0001g0017 |
3 | HG01175.hp2 HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.114-26383_114-2637 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668395 | |||||||
| chr6:129668401 | G | C | 38 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(35): Show |
38 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.114-26383C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668401 | |||||||
| chr6:129668403 | C | G | 1 | a0001c0001t0005g0212 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.114-26385G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668403 | |||||||
| chr6:129668427 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-26409T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668427 | |||||||
| chr6:129668481 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.114-26463T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668481 | |||||||
| chr6:129668687 | G | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-26669C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668687 | |||||||
| chr6:129668784 | C | G | 3 | a0001c0001t0001g0079 a0001c0001t0007g0077 a0001c0001t0007g0078 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114-26766G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668784 | |||||||
| chr6:129668828 | C | T | 15 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0084 others(12): Show |
15 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-26810G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668828 | |||||||
| chr6:129669132 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.114-27114A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669132 | |||||||
| chr6:129669172 | C | CTT | 33 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0186 others(30): Show |
33 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.114-27156_114-2715 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669172 | |||||||
| chr6:129669172 | C | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-27154G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669172 | |||||||
| chr6:129669208 | C | G | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-27190G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669208 | |||||||
| chr6:129669233 | G | C | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-27215C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669233 | |||||||
| chr6:129669526 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-27508G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669526 | |||||||
| chr6:129669548 | G | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(55): Show |
59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.114-27530C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669548 | |||||||
| chr6:129669603 | C | G | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.114-27585G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669603 | |||||||
| chr6:129669692 | G | A | 8 | a0001c0001t0001g0108 a0001c0001t0001g0179 a0001c0001t0001g0204 others(5): Show |
8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-27674C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669692 | |||||||
| chr6:129669782 | C | CA | 12 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(9): Show |
12 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-27765dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669782 | |||||||
| chr6:129669782 | CA | C | 36 | a0001c0001t0001g0079 a0001c0001t0001g0132 a0001c0001t0001g0135 others(33): Show |
36 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-27765delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669782 | |||||||
| chr6:129669795 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.114-27777T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669795 | |||||||
| chr6:129670114 | A | C | 3 | a0001c0011t0001g0056 a0002c0002t0001g0006 a0003c0004t0001g0151 |
3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-28096T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670114 | |||||||
| chr6:129670118 | C | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0201 a0001c0001t0001g0213 |
3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.114-28100G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670118 | |||||||
| chr6:129670221 | C | T | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-28203G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670221 | |||||||
| chr6:129670586 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-28568G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670586 | |||||||
| chr6:129670636 | G | A | 8 | a0001c0001t0002g0067 a0001c0001t0002g0171 a0001c0001t0002g0185 others(5): Show |
8 | HG00438.hp1 HG02056.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.114-28618C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670636 | |||||||
| chr6:129670688 | C | CT | 6 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0127 others(3): Show |
6 | HG01175.hp1 HG02056.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-28671dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670688 | |||||||
| chr6:129670688 | CT | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(101): Show |
105 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.114-28671delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670688 | |||||||
| chr6:129670688 | CTT | C | 34 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(31): Show |
34 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.114-28672_114-2867 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670688 | |||||||
| chr6:129670725 | A | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.114-28707T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670725 | |||||||
| chr6:129670990 | A | T | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-28972T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670990 | |||||||
| chr6:129671332 | A | G | 1 | a0002c0002t0018g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.114-29314T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671332 | |||||||
| chr6:129671424 | C | A | 23 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(20): Show |
23 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.114-29406G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671424 | |||||||
| chr6:129671425 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.114-29407C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671425 | |||||||
| chr6:129671591 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.114-29573A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671591 | |||||||
| chr6:129671599 | C | T | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-29581G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671599 | |||||||
| chr6:129671807 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0127 |
2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.114-29789G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671807 | |||||||
| chr6:129672017 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-29999G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672017 | |||||||
| chr6:129672054 | G | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-30036C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672054 | |||||||
| chr6:129672089 | G | A | 55 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(52): Show |
55 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.114-30071C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672089 | |||||||
| chr6:129672097 | G | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-30079C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672097 | |||||||
| chr6:129672109 | G | A | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-30091C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672109 | |||||||
| chr6:129672172 | G | A | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-30154C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672172 | |||||||
| chr6:129672188 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0173 |
2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.114-30170G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672188 | |||||||
| chr6:129672219 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.114-30201C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672219 | |||||||
| chr6:129672378 | G | A | 3 | a0001c0011t0001g0056 a0002c0002t0001g0006 a0003c0004t0001g0151 |
3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-30360C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672378 | |||||||
| chr6:129672555 | A | C | 35 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0186 others(32): Show |
35 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.114-30537T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672555 | |||||||
| chr6:129672656 | C | A | 8 | a0001c0001t0001g0108 a0001c0001t0001g0179 a0001c0001t0001g0204 others(5): Show |
8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-30638G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672656 | |||||||
| chr6:129672750 | G | T | 7 | a0001c0001t0001g0108 a0001c0001t0001g0179 a0001c0001t0001g0204 others(4): Show |
7 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-30732C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672750 | |||||||
| chr6:129673129 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114-31111A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673129 | |||||||
| chr6:129673222 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31204G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673222 | |||||||
| chr6:129673223 | G | A | 3 | a0001c0011t0001g0056 a0002c0002t0001g0006 a0003c0004t0001g0151 |
3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-31205C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673223 | |||||||
| chr6:129673353 | C | CA | 5 | a0001c0001t0001g0084 a0001c0001t0019g0233 a0001c0003t0002g0211 others(2): Show |
5 | HG00621.hp2 HG03669.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31336dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673353 | |||||||
| chr6:129673353 | C | CAA | 13 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(10): Show |
13 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.114-31337_114-3133 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673353 | |||||||
| chr6:129673429 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.114-31411C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673429 | |||||||
| chr6:129673438 | C | G | 1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114-31420G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673438 | |||||||
| chr6:129673510 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.114-31492G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673510 | |||||||
| chr6:129673667 | T | C | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31649A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673667 | |||||||
| chr6:129673701 | G | T | 1 | a0002c0002t0001g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.114-31683C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673701 | |||||||
| chr6:129673795 | T | C | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31777A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673795 | |||||||
| chr6:129673910 | T | C | 1 | a0002c0002t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.114-31892A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673910 | |||||||
| chr6:129674267 | G | T | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-32249C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674267 | |||||||
| chr6:129674398 | A | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-32380T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674398 | |||||||
| chr6:129674468 | C | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-32450G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674468 | |||||||
| chr6:129674679 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0101 |
2 | HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.114-32661T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674679 | |||||||
| chr6:129674865 | C | T | 1 | a0001c0001t0002g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.114-32847G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674865 | |||||||
| chr6:129674880 | T | C | 81 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(78): Show |
81 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.114-32862A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674880 | |||||||
| chr6:129674901 | T | G | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114-32883A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674901 | |||||||
| chr6:129674932 | C | T | 4 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-32914G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674932 | |||||||
| chr6:129675057 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.114-33039G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675057 | |||||||
| chr6:129675157 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.114-33139G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675157 | |||||||
| chr6:129675371 | G | A | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-33353C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675371 | |||||||
| chr6:129675383 | C | CA | 10 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-33366dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675383 | |||||||
| chr6:129675383 | CA | C | 42 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0144 others(39): Show |
42 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.114-33366delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675383 | |||||||
| chr6:129675537 | C | A | 24 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0084 others(21): Show |
24 | HG00423.hp1 HG02280.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.114-33519G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675537 | |||||||
| chr6:129675634 | CCTG | C | 3 | a0001c0001t0001g0129 a0001c0001t0001g0150 a0001c0001t0001g0154 |
3 | HG00558.hp2 NA18942.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.114-33619_114-3361 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675634 | |||||||
| chr6:129675764 | G | C | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.114-33746C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675764 | |||||||
| chr6:129675919 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.114-33901C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675919 | |||||||
| chr6:129676370 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(76): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.113+33654T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676370 | |||||||
| chr6:129676371 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.113+33653A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676371 | |||||||
| chr6:129676740 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.113+33284G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676740 | |||||||
| chr6:129676912 | CCTCT | C | 4 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+33108_113+3311 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | |||||||
| chr6:129676912 | CCTCTTTT others(1): Show |
C | 27 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.113+33104_113+3311 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | |||||||
| chr6:129676912 | CCTCTTTT others(2): Show |
C | 26 | a0001c0001t0001g0094 a0001c0001t0001g0098 a0001c0001t0001g0103 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.113+33103_113+3311 others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | |||||||
| chr6:129676912 | CCTCTTTT others(3): Show |
C | 4 | a0001c0001t0001g0164 a0001c0001t0019g0233 a0002c0002t0001g0052 others(1): Show |
4 | HG02622.hp2 NA18969.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+33102_113+3311 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | |||||||
| chr6:129676912 | CCTCTTTT others(4): Show |
C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0179 a0001c0001t0001g0204 others(2): Show |
5 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+33101_113+3311 others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | |||||||
| chr6:129676912 | CCTCTTTT others(9): Show |
C | 1 | a0001c0001t0003g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.113+33096_113+3311 others(20): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | |||||||
| chr6:129676912 | CCTCTTTT others(13): Show |
C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.113+33092_113+3311 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | |||||||
| chr6:129676915 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113+33099_113+3310 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.113+33098_113+3310 others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0139 a0001c0001t0004g0138 a0001c0001t0010g0136 |
3 | HG02965.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.113+33096_113+3310 others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113+33095_113+3310 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113+33091_113+3310 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.113+33086_113+3310 others(27): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | CT | C | 38 | a0001c0001t0001g0076 a0001c0001t0001g0085 a0001c0001t0001g0089 others(35): Show |
38 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.113+33108delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | CTT | C | 40 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0083 others(37): Show |
40 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.113+33107_113+3310 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | CTTTTTT | C | 30 | a0001c0001t0001g0132 a0001c0001t0001g0206 a0001c0001t0001g0209 others(27): Show |
30 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.113+33103_113+3310 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0003g0073 a0001c0001t0003g0224 a0001c0001t0011g0141 others(1): Show |
4 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+33096_113+3310 others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676915 | CTTTTTTT others(13): Show |
C | 5 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0004g0123 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+33089_113+3310 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | |||||||
| chr6:129676948 | T | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(76): Show |
80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.113+33076A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676948 | |||||||
| chr6:129676950 | A | G | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+33074T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676950 | |||||||
| chr6:129677103 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.113+32921G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677103 | |||||||
| chr6:129677122 | G | A | 7 | a0001c0001t0001g0108 a0001c0001t0001g0179 a0001c0001t0001g0204 others(4): Show |
7 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.113+32902C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677122 | |||||||
| chr6:129677134 | T | C | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+32890A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677134 | |||||||
| chr6:129677351 | C | T | 2 | a0001c0001t0003g0128 a0001c0001t0003g0133 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+32673G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677351 | |||||||
| chr6:129677361 | C | T | 8 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+32663G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677361 | |||||||
| chr6:129677392 | CA | C | 44 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0084 others(41): Show |
44 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.113+32631delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677392 | |||||||
| chr6:129677407 | A | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(62): Show |
66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.113+32617T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677407 | |||||||
| chr6:129677511 | A | G | 1 | a0006c0010t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.113+32513T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677511 | |||||||
| chr6:129677530 | A | G | 3 | a0001c0001t0001g0177 a0001c0001t0001g0201 a0001c0001t0001g0213 |
3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.113+32494T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677530 | |||||||
| chr6:129677934 | A | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.113+32090T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677934 | |||||||
| chr6:129678125 | G | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(134): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.113+31899C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678125 | |||||||
| chr6:129678311 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.113+31713C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678311 | |||||||
| chr6:129678400 | T | C | 12 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0231 others(9): Show |
12 | HG00597.hp2 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+31624A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678400 | |||||||
| chr6:129678412 | AACGGATG others(15): Show |
A | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+31590_113+3161 others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678412 | |||||||
| chr6:129678981 | C | G | 7 | a0001c0001t0001g0108 a0001c0001t0001g0179 a0001c0001t0001g0204 others(4): Show |
7 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.113+31043G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678981 | |||||||
| chr6:129679083 | T | C | 58 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(55): Show |
59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.113+30941A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679083 | |||||||
| chr6:129679170 | TACTA | T | 10 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0002g0082 others(7): Show |
10 | HG00597.hp2 HG03669.hp2 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.113+30850_113+3085 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679170 | |||||||
| chr6:129679356 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113+30668C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679356 | |||||||
| chr6:129679902 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.113+30122C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679902 | |||||||
| chr6:129679991 | C | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+30033G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679991 | |||||||
| chr6:129680162 | C | G | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.113+29862G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680162 | |||||||
| chr6:129680168 | T | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+29856A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680168 | |||||||
| chr6:129680218 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.113+29806T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680218 | |||||||
| chr6:129680242 | G | T | 2 | a0001c0011t0001g0056 a0003c0004t0001g0151 |
2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.113+29782C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680242 | |||||||
| chr6:129680348 | C | T | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.113+29676G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680348 | |||||||
| chr6:129680428 | T | C | 14 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(11): Show |
14 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.113+29596A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680428 | |||||||
| chr6:129680503 | C | T | 3 | a0001c0001t0001g0079 a0001c0001t0007g0077 a0001c0001t0007g0078 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.113+29521G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680503 | |||||||
| chr6:129680665 | C | T | 14 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(11): Show |
14 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.113+29359G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680665 | |||||||
| chr6:129680699 | C | G | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113+29325G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680699 | |||||||
| chr6:129680732 | A | G | 6 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(3): Show |
6 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.113+29292T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680732 | |||||||
| chr6:129680992 | G | A | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+29032C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680992 | |||||||
| chr6:129681067 | A | C | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.113+28957T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681067 | |||||||
| chr6:129681077 | G | A | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+28947C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681077 | |||||||
| chr6:129681327 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.113+28697G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681327 | |||||||
| chr6:129681335 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0002g0145 |
2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.113+28689G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681335 | |||||||
| chr6:129681398 | A | G | 12 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+28626T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681398 | |||||||
| chr6:129681457 | A | T | 2 | a0001c0001t0008g0118 a0001c0001t0008g0228 |
2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.113+28567T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681457 | |||||||
| chr6:129681877 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.113+28147C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681877 | |||||||
| chr6:129682428 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113+27596G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682428 | |||||||
| chr6:129682436 | T | C | 5 | a0001c0001t0002g0172 a0002c0002t0002g0019 a0002c0002t0002g0020 others(2): Show |
5 | HG01261.hp2 HG01952.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+27588A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682436 | |||||||
| chr6:129682470 | CT | C | 3 | a0001c0001t0019g0233 a0001c0011t0001g0056 a0003c0004t0001g0151 |
3 | HG03098.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.113+27553delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682470 | |||||||
| chr6:129682476 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.113+27548G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682476 | |||||||
| chr6:129682922 | T | C | 4 | a0001c0001t0001g0142 a0001c0001t0003g0058 a0001c0001t0003g0059 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+27102A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682922 | |||||||
| chr6:129683050 | TTTTTC | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG01433.hp1 HG01928.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+26969_113+2697 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683050 | |||||||
| chr6:129683055 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(97): Show |
101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.113+26968delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683055 | |||||||
| chr6:129683055 | CTT | C | 5 | a0001c0001t0001g0131 a0001c0001t0003g0128 a0001c0001t0003g0133 others(2): Show |
5 | HG02970.hp2 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+26967_113+2696 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683055 | |||||||
| chr6:129683056 | T | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG01433.hp1 HG01928.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+26968A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683056 | |||||||
| chr6:129683069 | G | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+26955C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683069 | |||||||
| chr6:129683075 | T | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(115): Show |
119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.113+26949A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683075 | |||||||
| chr6:129683173 | A | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+26851T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683173 | |||||||
| chr6:129683232 | C | T | 43 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+26792G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683232 | |||||||
| chr6:129683340 | G | T | 1 | a0001c0003t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.113+26684C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683340 | |||||||
| chr6:129683454 | C | T | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.113+26570G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683454 | |||||||
| chr6:129683658 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.113+26366C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683658 | |||||||
| chr6:129683839 | G | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(65): Show |
69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.113+26185C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683839 | |||||||
| chr6:129683866 | C | T | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+26158G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683866 | |||||||
| chr6:129684204 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+25820C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684204 | |||||||
| chr6:129684373 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113+25651A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684373 | |||||||
| chr6:129684513 | T | C | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+25511A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684513 | |||||||
| chr6:129684522 | G | T | 85 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0079 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.113+25502C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684522 | |||||||
| chr6:129684571 | T | G | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+25453A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684571 | |||||||
| chr6:129684602 | C | T | 2 | a0002c0002t0003g0022 a0002c0002t0003g0023 |
2 | HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.113+25422G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684602 | |||||||
| chr6:129684603 | G | A | 5 | a0001c0001t0001g0079 a0001c0001t0001g0144 a0001c0001t0002g0145 others(2): Show |
5 | HG02280.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+25421C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684603 | |||||||
| chr6:129684845 | T | C | 1 | a0002c0002t0002g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.113+25179A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684845 | |||||||
| chr6:129685092 | G | T | 12 | a0001c0001t0001g0177 a0001c0001t0001g0201 a0001c0001t0001g0209 others(9): Show |
12 | HG00597.hp2 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+24932C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685092 | |||||||
| chr6:129685173 | T | G | 3 | a0001c0001t0001g0131 a0001c0001t0003g0128 a0001c0001t0003g0133 |
3 | HG02970.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+24851A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685173 | |||||||
| chr6:129685237 | T | G | 20 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0215 others(17): Show |
20 | HG00408.hp2 HG00544.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+24787A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685237 | |||||||
| chr6:129685282 | G | A | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+24742C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685282 | |||||||
| chr6:129685352 | C | A | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+24672G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685352 | |||||||
| chr6:129685374 | G | GCAGGCAC others(5): Show |
39 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0177 others(36): Show |
39 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.113+24638_113+2464 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685374 | |||||||
| chr6:129685570 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.113+24454G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685570 | |||||||
| chr6:129685584 | T | C | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.113+24440A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685584 | |||||||
| chr6:129685602 | G | GGTTA | 44 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(41): Show |
44 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.113+24418_113+2442 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685602 | |||||||
| chr6:129685725 | T | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(170): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.113+24299A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685725 | |||||||
| chr6:129685750 | CT | C | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+24273delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685750 | |||||||
| chr6:129685839 | G | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0002g0066 others(2): Show |
6 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+24185C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685839 | |||||||
| chr6:129686079 | T | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113+23945A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686079 | |||||||
| chr6:129686108 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.113+23916C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686108 | |||||||
| chr6:129686239 | CCACGCTC others(5): Show |
C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(17): Show |
21 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.113+23773_113+2378 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686239 | |||||||
| chr6:129686271 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.113+23753G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686271 | |||||||
| chr6:129686289 | T | A | 33 | a0001c0001t0001g0094 a0001c0001t0001g0098 a0001c0001t0001g0132 others(30): Show |
33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.113+23735A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686289 | |||||||
| chr6:129686332 | T | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.113+23692A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686332 | |||||||
| chr6:129686452 | C | A | 34 | a0001c0001t0001g0135 a0001c0001t0001g0201 a0001c0001t0001g0206 others(31): Show |
34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+23572G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686452 | |||||||
| chr6:129686619 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.113+23405T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686619 | |||||||
| chr6:129686788 | C | CT | 38 | a0001c0001t0001g0001 a0001c0001t0001g0080 a0001c0001t0001g0096 others(35): Show |
39 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.113+23235dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686788 | |||||||
| chr6:129686788 | CT | C | 8 | a0001c0001t0001g0150 a0001c0001t0002g0117 a0001c0001t0002g0167 others(5): Show |
8 | HG02004.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+23235delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686788 | |||||||
| chr6:129686788 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+23226_113+2323 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686788 | |||||||
| chr6:129686839 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.113+23185C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686839 | |||||||
| chr6:129686859 | C | T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0051 |
2 | NA18977.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.113+23165G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686859 | |||||||
| chr6:129686893 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0004c0008t0004g0055 |
3 | HG02280.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.113+23131G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686893 | |||||||
| chr6:129686949 | C | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.113+23075G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686949 | |||||||
| chr6:129686973 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(91): Show |
95 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.113+23051A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686973 | |||||||
| chr6:129686974 | TTTTC | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(22): Show |
26 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+23046_113+2304 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686974 | |||||||
| chr6:129686975 | TTTC | T | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(8): Show |
11 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.113+23046_113+2304 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686975 | |||||||
| chr6:129686977 | TC | T | 23 | a0001c0001t0001g0096 a0001c0001t0001g0146 a0001c0001t0001g0178 others(20): Show |
23 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.113+23046delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686977 | |||||||
| chr6:129686978 | C | CT | 37 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0001g0098 others(34): Show |
37 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.113+23045dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | |||||||
| chr6:129686978 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.113+23046G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | |||||||
| chr6:129686978 | CTTTT | C | 34 | a0001c0001t0001g0135 a0001c0001t0001g0201 a0001c0001t0001g0206 others(31): Show |
34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+23042_113+2304 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | |||||||
| chr6:129686978 | CTTTTTTT others(1): Show |
C | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+23038_113+2304 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | |||||||
| chr6:129686978 | CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.113+23035_113+2304 others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | |||||||
| chr6:129687069 | A | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+22955T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687069 | |||||||
| chr6:129687146 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+22878G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687146 | |||||||
| chr6:129687173 | G | A | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+22851C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687173 | |||||||
| chr6:129687273 | C | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+22751G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687273 | |||||||
| chr6:129687297 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.113+22727A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687297 | |||||||
| chr6:129687300 | A | C | 46 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(43): Show |
46 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.113+22724T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687300 | |||||||
| chr6:129687383 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+22641A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687383 | |||||||
| chr6:129687398 | G | A | 32 | a0001c0001t0001g0094 a0001c0001t0001g0098 a0001c0001t0001g0148 others(29): Show |
32 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.113+22626C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687398 | |||||||
| chr6:129687430 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+22594T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687430 | |||||||
| chr6:129687735 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(20): Show |
24 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.113+22289G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687735 | |||||||
| chr6:129687758 | G | T | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+22266C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687758 | |||||||
| chr6:129687787 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+22237T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687787 | |||||||
| chr6:129687789 | A | AT | 95 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(92): Show |
96 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.113+22234dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687789 | |||||||
| chr6:129687789 | AT | A | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+22234delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687789 | |||||||
| chr6:129687965 | A | G | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+22059T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687965 | |||||||
| chr6:129688167 | C | A | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+21857G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688167 | |||||||
| chr6:129688359 | G | GTT | 96 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+21664_113+2166 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688359 | |||||||
| chr6:129688522 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(21): Show |
25 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+21502C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688522 | |||||||
| chr6:129688545 | C | A | 26 | a0001c0001t0001g0096 a0001c0001t0001g0146 a0001c0001t0001g0178 others(23): Show |
26 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+21479G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688545 | |||||||
| chr6:129688593 | G | T | 1 | a0001c0001t0003g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.113+21431C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688593 | |||||||
| chr6:129688652 | C | A | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+21372G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688652 | |||||||
| chr6:129688689 | G | A | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113+21335C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688689 | |||||||
| chr6:129688753 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0090 |
2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.113+21271A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688753 | |||||||
| chr6:129688792 | C | CA | 111 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.113+21231dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688792 | |||||||
| chr6:129688803 | A | AT | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.113+21220_113+2122 others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688803 | |||||||
| chr6:129688965 | C | T | 2 | a0001c0001t0006g0198 a0006c0010t0001g0197 |
2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.113+21059G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688965 | |||||||
| chr6:129688996 | G | C | 21 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(18): Show |
22 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.113+21028C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688996 | |||||||
| chr6:129689031 | C | T | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.113+20993G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689031 | |||||||
| chr6:129689136 | C | A | 1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.113+20888G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689136 | |||||||
| chr6:129689227 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.113+20797A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689227 | |||||||
| chr6:129689354 | C | T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+20670G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689354 | |||||||
| chr6:129689440 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+20584C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689440 | |||||||
| chr6:129689454 | G | A | 1 | a0008c0013t0001g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.113+20570C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689454 | |||||||
| chr6:129689994 | C | T | 31 | a0001c0001t0001g0094 a0001c0001t0001g0148 a0001c0001t0001g0150 others(28): Show |
31 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.113+20030G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689994 | |||||||
| chr6:129689997 | C | A | 178 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(175): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.113+20027G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689997 | |||||||
| chr6:129690059 | CCAAA | C | 4 | a0001c0001t0002g0172 a0002c0002t0002g0019 a0002c0002t0002g0020 others(1): Show |
4 | HG01261.hp2 HG01952.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+19961_113+1996 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690059 | |||||||
| chr6:129690124 | C | CGT | 24 | a0001c0001t0001g0096 a0001c0001t0001g0146 a0001c0001t0001g0178 others(21): Show |
24 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.113+19898_113+1989 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690124 | |||||||
| chr6:129690124 | C | CGTGT | 34 | a0001c0001t0001g0135 a0001c0001t0001g0201 a0001c0001t0001g0206 others(31): Show |
34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+19896_113+1989 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690124 | |||||||
| chr6:129690521 | A | G | 45 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(42): Show |
45 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.113+19503T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690521 | |||||||
| chr6:129690753 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.113+19271A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690753 | |||||||
| chr6:129690774 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0001g0064 others(70): Show |
74 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.113+19250A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690774 | |||||||
| chr6:129690908 | G | A | 37 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0135 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.113+19116C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690908 | |||||||
| chr6:129690980 | C | T | 1 | a0001c0001t0002g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.113+19044G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690980 | |||||||
| chr6:129691051 | C | A | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113+18973G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691051 | |||||||
| chr6:129691080 | C | T | 24 | a0001c0001t0001g0096 a0001c0001t0001g0146 a0001c0001t0001g0178 others(21): Show |
24 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.113+18944G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691080 | |||||||
| chr6:129691125 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0108 |
3 | HG00140.hp2 HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.113+18899T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691125 | |||||||
| chr6:129691213 | A | T | 6 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | NA18950.hp1 NA18983.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+18811T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691213 | |||||||
| chr6:129691228 | C | T | 32 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(29): Show |
32 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.113+18796G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691228 | |||||||
| chr6:129691500 | C | T | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(38): Show |
41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+18524G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691500 | |||||||
| chr6:129691698 | C | T | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.113+18326G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691698 | |||||||
| chr6:129691876 | G | A | 1 | a0002c0002t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.113+18148C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691876 | |||||||
| chr6:129691904 | C | T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+18120G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691904 | |||||||
| chr6:129691924 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0007g0077 a0001c0001t0007g0078 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.113+18100T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691924 | |||||||
| chr6:129692010 | C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+18014G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692010 | |||||||
| chr6:129692038 | G | A | 2 | a0001c0001t0004g0134 a0003c0004t0005g0088 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.113+17986C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692038 | |||||||
| chr6:129692487 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113+17537G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692487 | |||||||
| chr6:129692699 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG00621.hp1 NA18986.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.113+17325G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692699 | |||||||
| chr6:129692889 | T | C | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+17135A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692889 | |||||||
| chr6:129693007 | TTTATTTT others(3): Show |
T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+17007_113+1701 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693007 | |||||||
| chr6:129693039 | C | G | 2 | a0002c0002t0001g0007 a0002c0002t0001g0018 |
2 | HG00621.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.113+16985G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693039 | |||||||
| chr6:129693053 | C | T | 2 | a0002c0002t0001g0016 a0002c0002t0001g0017 |
2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.113+16971G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693053 | |||||||
| chr6:129693081 | G | A | 38 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0135 others(35): Show |
38 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.113+16943C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693081 | |||||||
| chr6:129693108 | A | G | 31 | a0001c0001t0001g0094 a0001c0001t0001g0148 a0001c0001t0001g0150 others(28): Show |
31 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.113+16916T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693108 | |||||||
| chr6:129693355 | G | A | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.113+16669C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693355 | |||||||
| chr6:129693546 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(21): Show |
25 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+16478C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693546 | |||||||
| chr6:129693769 | A | AC | 42 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.113+16254dupG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693769 | |||||||
| chr6:129693814 | T | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0178 |
2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.113+16210A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693814 | |||||||
| chr6:129693843 | A | C | 7 | a0001c0001t0001g0094 a0001c0001t0001g0194 a0001c0001t0002g0057 others(4): Show |
7 | HG02257.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+16181T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693843 | |||||||
| chr6:129693894 | C | G | 1 | a0001c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.113+16130G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693894 | |||||||
| chr6:129693908 | CAGCTGAC others(3): Show |
C | 25 | a0001c0001t0001g0096 a0001c0001t0001g0146 a0001c0001t0001g0178 others(22): Show |
25 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+16106_113+1611 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693908 | |||||||
| chr6:129694186 | T | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.113+15838A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694186 | |||||||
| chr6:129694264 | G | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+15760C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694264 | |||||||
| chr6:129694272 | C | G | 2 | a0002c0002t0001g0015 a0002c0002t0001g0049 |
2 | HG02027.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.113+15752G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694272 | |||||||
| chr6:129694428 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.113+15596C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694428 | |||||||
| chr6:129694564 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG00735.hp2 HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.113+15460A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694564 | |||||||
| chr6:129694619 | G | A | 33 | a0001c0001t0001g0094 a0001c0001t0001g0148 a0001c0001t0001g0150 others(30): Show |
33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.113+15405C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694619 | |||||||
| chr6:129694925 | G | C | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+15099C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694925 | |||||||
| chr6:129694926 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.113+15098A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694926 | |||||||
| chr6:129695004 | A | C | 50 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+15020T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695004 | |||||||
| chr6:129695065 | C | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+14959G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695065 | |||||||
| chr6:129695135 | A | C | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+14889T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695135 | |||||||
| chr6:129695263 | A | AT | 65 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(62): Show |
66 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.113+14760dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695263 | |||||||
| chr6:129695313 | T | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+14711A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695313 | |||||||
| chr6:129695382 | T | TG | 65 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(62): Show |
66 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.113+14641dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695382 | |||||||
| chr6:129695553 | G | T | 1 | a0005c0005t0003g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.113+14471C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695553 | |||||||
| chr6:129695676 | G | A | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0128 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+14348C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695676 | |||||||
| chr6:129695684 | A | G | 42 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(39): Show |
42 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.113+14340T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695684 | |||||||
| chr6:129695821 | TAAAAG | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(63): Show |
67 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.113+14198_113+1420 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695821 | |||||||
| chr6:129695904 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.113+14120G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695904 | |||||||
| chr6:129695948 | T | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.113+14076A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695948 | |||||||
| chr6:129696132 | C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+13892G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696132 | |||||||
| chr6:129696395 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113+13629A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696395 | |||||||
| chr6:129696417 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(62): Show |
66 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.113+13607A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696417 | |||||||
| chr6:129696514 | G | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+13510C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696514 | |||||||
| chr6:129696639 | C | T | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+13385G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696639 | |||||||
| chr6:129696650 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.113+13374T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696650 | |||||||
| chr6:129696685 | A | C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0128 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+13339T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696685 | |||||||
| chr6:129696725 | AATGCACA others(1): Show |
A | 57 | a0001c0001t0001g0096 a0001c0001t0001g0135 a0001c0001t0001g0146 others(54): Show |
57 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.113+13291_113+1329 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696725 | |||||||
| chr6:129696885 | G | A | 25 | a0001c0001t0001g0096 a0001c0001t0001g0146 a0001c0001t0001g0178 others(22): Show |
25 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+13139C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696885 | |||||||
| chr6:129696910 | T | G | 3 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0019g0233 |
3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+13114A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696910 | |||||||
| chr6:129696957 | C | A | 2 | a0002c0002t0001g0044 a0002c0002t0014g0045 |
2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.113+13067G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696957 | |||||||
| chr6:129697221 | T | C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0128 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+12803A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697221 | |||||||
| chr6:129697242 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.113+12782G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697242 | |||||||
| chr6:129697372 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0007c0012t0002g0095 |
3 | HG00099.hp2 HG01074.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.113+12652G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697372 | |||||||
| chr6:129697442 | AT | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(164): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.113+12581delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697442 | |||||||
| chr6:129697442 | ATT | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+12580_113+1258 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697442 | |||||||
| chr6:129697455 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(64): Show |
68 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.113+12569A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697455 | |||||||
| chr6:129697762 | A | G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0128 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+12262T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697762 | |||||||
| chr6:129698096 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.113+11928A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698096 | |||||||
| chr6:129698181 | G | T | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.113+11843C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698181 | |||||||
| chr6:129698209 | T | C | 41 | a0001c0001t0001g0094 a0001c0001t0001g0131 a0001c0001t0001g0132 others(38): Show |
41 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.113+11815A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698209 | |||||||
| chr6:129698471 | T | G | 3 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0019g0233 |
3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+11553A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698471 | |||||||
| chr6:129698503 | C | G | 5 | a0001c0001t0001g0099 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG00735.hp2 HG01106.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+11521G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698503 | |||||||
| chr6:129698533 | CT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(80): Show |
84 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.113+11490delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698533 | |||||||
| chr6:129698533 | CTT | C | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0188 others(3): Show |
6 | HG01071.hp1 HG01169.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.113+11489_113+1149 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698533 | |||||||
| chr6:129698549 | T | G | 43 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0076 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+11475A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698549 | |||||||
| chr6:129698588 | G | A | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+11436C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698588 | |||||||
| chr6:129698605 | A | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(64): Show |
68 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.113+11419T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698605 | |||||||
| chr6:129698691 | G | GT | 5 | a0001c0001t0001g0137 a0001c0001t0010g0136 a0002c0002t0001g0012 others(2): Show |
5 | HG02486.hp1 HG03195.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+11332dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698691 | |||||||
| chr6:129698691 | GT | G | 139 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(136): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.113+11332delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698691 | |||||||
| chr6:129698691 | GTT | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(22): Show |
26 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+11331_113+1133 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698691 | |||||||
| chr6:129698795 | T | G | 3 | a0001c0001t0001g0099 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG00735.hp2 HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.113+11229A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698795 | |||||||
| chr6:129698831 | T | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+11193A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698831 | |||||||
| chr6:129698841 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.113+11183G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698841 | |||||||
| chr6:129698843 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+11181G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698843 | |||||||
| chr6:129698905 | C | T | 1 | a0001c0001t0005g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.113+11119G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698905 | |||||||
| chr6:129698987 | C | T | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+11037G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698987 | |||||||
| chr6:129699110 | T | A | 58 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0146 others(55): Show |
58 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.113+10914A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699110 | |||||||
| chr6:129699127 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.113+10897G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699127 | |||||||
| chr6:129699202 | A | C | 58 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0146 others(55): Show |
58 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.113+10822T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699202 | |||||||
| chr6:129699312 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0178 |
2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.113+10712G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699312 | |||||||
| chr6:129699593 | G | T | 25 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+10431C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699593 | |||||||
| chr6:129699666 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(64): Show |
68 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.113+10358G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699666 | |||||||
| chr6:129699738 | G | C | 1 | a0001c0009t0001g0122 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.113+10286C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699738 | |||||||
| chr6:129699805 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.113+10219A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699805 | |||||||
| chr6:129699830 | C | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+10194G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699830 | |||||||
| chr6:129699983 | A | G | 37 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0135 others(34): Show |
37 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.113+10041T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699983 | |||||||
| chr6:129700023 | T | G | 1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+10001A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700023 | |||||||
| chr6:129700063 | T | C | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+9961A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700063 | |||||||
| chr6:129700120 | G | A | 26 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0153 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.113+9904C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700120 | |||||||
| chr6:129700312 | AGAT | A | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+9709_113+9711d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700312 | |||||||
| chr6:129700473 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(96): Show |
100 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.113+9551C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700473 | |||||||
| chr6:129700936 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0019g0233 |
3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+9088C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700936 | |||||||
| chr6:129700989 | A | G | 16 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0074 others(13): Show |
16 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.113+9035T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700989 | |||||||
| chr6:129700999 | T | TA | 71 | a0001c0001t0001g0094 a0001c0001t0001g0131 a0001c0001t0001g0132 others(68): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.113+9024dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700999 | |||||||
| chr6:129701245 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.113+8779G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701245 | |||||||
| chr6:129701493 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(63): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+8531G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701493 | |||||||
| chr6:129701523 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.113+8501T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701523 | |||||||
| chr6:129701695 | G | A | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.113+8329C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701695 | |||||||
| chr6:129701773 | T | TA | 10 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0142 others(7): Show |
10 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.113+8250dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701773 | |||||||
| chr6:129702068 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(22): Show |
26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+7956T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702068 | |||||||
| chr6:129702161 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(121): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.113+7863C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702161 | |||||||
| chr6:129702206 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.113+7818G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702206 | |||||||
| chr6:129702364 | C | A | 1 | a0002c0002t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.113+7660G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702364 | |||||||
| chr6:129702473 | T | A | 1 | a0002c0002t0001g0047 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.113+7551A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702473 | |||||||
| chr6:129702603 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0002g0170 |
2 | HG01361.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.113+7421A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702603 | |||||||
| chr6:129702740 | C | T | 26 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0153 others(23): Show |
26 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.113+7284G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702740 | |||||||
| chr6:129702771 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0002g0145 a0001c0001t0019g0233 |
3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+7253C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702771 | |||||||
| chr6:129702873 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(63): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+7151C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702873 | |||||||
| chr6:129702881 | T | A | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+7143A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702881 | |||||||
| chr6:129703003 | CA | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.113+7020delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703003 | |||||||
| chr6:129703055 | G | A | 73 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.113+6969C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703055 | |||||||
| chr6:129703309 | C | G | 5 | a0001c0001t0001g0099 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG00735.hp2 HG01106.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+6715G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703309 | |||||||
| chr6:129703442 | C | A | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+6582G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703442 | |||||||
| chr6:129703461 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+6563C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703461 | |||||||
| chr6:129703484 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(98): Show |
102 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.113+6540T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703484 | |||||||
| chr6:129703882 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.113+6142G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703882 | |||||||
| chr6:129703925 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.113+6099G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703925 | |||||||
| chr6:129703996 | GTAA | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.113+6025_113+6027d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703996 | |||||||
| chr6:129704006 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+6018T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704006 | |||||||
| chr6:129704106 | G | A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+5918C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704106 | |||||||
| chr6:129704113 | TCTTA | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(61): Show |
65 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.113+5907_113+5910d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704113 | |||||||
| chr6:129704170 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG01358.hp1 HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.113+5854G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704170 | |||||||
| chr6:129704286 | T | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0072 others(63): Show |
67 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+5738A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704286 | |||||||
| chr6:129704360 | G | A | 1 | a0001c0001t0006g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113+5664C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704360 | |||||||
| chr6:129704369 | T | C | 1 | a0001c0001t0008g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.113+5655A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704369 | |||||||
| chr6:129704520 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0002g0125 |
3 | HG02257.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.113+5504A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704520 | |||||||
| chr6:129704535 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.113+5489A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704535 | |||||||
| chr6:129704640 | T | C | 174 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(171): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.113+5384A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704640 | |||||||
| chr6:129704701 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.113+5323G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704701 | |||||||
| chr6:129704800 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113+5224G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704800 | |||||||
| chr6:129704927 | T | C | 3 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0004c0008t0004g0055 |
3 | HG02615.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.113+5097A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704927 | |||||||
| chr6:129705097 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.113+4927C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705097 | |||||||
| chr6:129705253 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.113+4771T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705253 | |||||||
| chr6:129705298 | C | G | 47 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(44): Show |
47 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.113+4726G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705298 | |||||||
| chr6:129705320 | G | C | 1 | a0004c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+4704C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705320 | |||||||
| chr6:129705664 | G | T | 27 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0150 others(24): Show |
27 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.113+4360C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705664 | |||||||
| chr6:129706015 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113+4009G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706015 | |||||||
| chr6:129706076 | A | C | 1 | a0002c0002t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.113+3948T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706076 | |||||||
| chr6:129706175 | G | A | 154 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(151): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.113+3849C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706175 | |||||||
| chr6:129706218 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0003g0058 a0001c0001t0003g0059 |
3 | HG00639.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+3806C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706218 | |||||||
| chr6:129706227 | C | A | 1 | a0002c0002t0001g0048 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.113+3797G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706227 | |||||||
| chr6:129706619 | G | C | 36 | a0001c0001t0001g0135 a0001c0001t0001g0144 a0001c0001t0001g0201 others(33): Show |
36 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.113+3405C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706619 | |||||||
| chr6:129706739 | T | C | 36 | a0001c0001t0001g0135 a0001c0001t0001g0144 a0001c0001t0001g0201 others(33): Show |
36 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.113+3285A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706739 | |||||||
| chr6:129706841 | G | A | 35 | a0001c0001t0001g0135 a0001c0001t0001g0144 a0001c0001t0001g0201 others(32): Show |
35 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.113+3183C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706841 | |||||||
| chr6:129706885 | C | CA | 9 | a0001c0001t0001g0096 a0001c0001t0001g0192 a0001c0001t0001g0193 others(6): Show |
9 | HG01081.hp2 HG01433.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.113+3138dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706885 | |||||||
| chr6:129706885 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(98): Show |
102 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.113+3138delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706885 | |||||||
| chr6:129706889 | A | C | 1 | a0002c0002t0001g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.113+3135T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706889 | |||||||
| chr6:129706935 | A | G | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0003g0128 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+3089T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706935 | |||||||
| chr6:129706952 | C | T | 48 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(45): Show |
48 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.113+3072G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706952 | |||||||
| chr6:129707017 | G | A | 2 | a0001c0001t0006g0198 a0006c0010t0001g0197 |
2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.113+3007C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707017 | |||||||
| chr6:129707025 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00099.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.113+2999C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707025 | |||||||
| chr6:129707115 | C | T | 40 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(37): Show |
40 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.113+2909G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707115 | |||||||
| chr6:129707125 | A | G | 1 | a0002c0002t0001g0007 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.113+2899T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707125 | |||||||
| chr6:129707245 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.113+2779C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707245 | |||||||
| chr6:129707397 | T | G | 50 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+2627A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707397 | |||||||
| chr6:129707406 | A | C | 149 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(146): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.113+2618T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707406 | |||||||
| chr6:129707530 | G | A | 64 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0001g0146 others(61): Show |
64 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.113+2494C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707530 | |||||||
| chr6:129707557 | T | C | 50 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+2467A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707557 | |||||||
| chr6:129707619 | A | G | 50 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0089 others(47): Show |
50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+2405T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707619 | |||||||
| chr6:129707650 | GT | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(219): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.113+2373delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707650 | |||||||
| chr6:129707656 | T | G | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.113+2368A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707656 | |||||||
| chr6:129708548 | G | A | 3 | a0001c0001t0002g0057 a0001c0001t0003g0058 a0001c0001t0003g0059 |
3 | HG02818.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+1476C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708548 | |||||||
| chr6:129708694 | G | A | 34 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(31): Show |
34 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+1330C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708694 | |||||||
| chr6:129708742 | T | C | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113+1282A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708742 | |||||||
| chr6:129708805 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+1219G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708805 | |||||||
| chr6:129708824 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+1200A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708824 | |||||||
| chr6:129708868 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.113+1156A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708868 | |||||||
| chr6:129708969 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0061 a0001c0001t0001g0062 others(25): Show |
29 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.113+1055G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708969 | |||||||
| chr6:129709287 | GA | G | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(2): Show |
5 | HG00140.hp1 HG00735.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+736delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709287 | |||||||
| chr6:129709417 | C | T | 1 | a0001c0001t0006g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113+607G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709417 | |||||||
| chr6:129709572 | GA | G | 4 | a0001c0001t0002g0057 a0001c0001t0003g0058 a0001c0001t0003g0059 others(1): Show |
4 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+451delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709572 | |||||||
| chr6:129709712 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.113+312A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709712 |