Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84986 |
| ensemblid | ENSG00000213390.11 |
| hgncid | 23724 |
| symbol | ARHGAP19 |
| name | Rho GTPase activating protein 19 |
| refseq_nuc | NM_032900.6 |
| refseq_prot | NP_116289.4 |
| ensembl_nuc | ENST00000358531.9 |
| ensembl_prot | ENSP00000351333.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 97222179 |
| end | 97292637 |
| strand | - |
| ver | v1.2 |
| region | chr10:97222179-97292637 |
| region5000 | chr10:97217179-97297637 |
| regionname0 | ARHGAP19_chr10_97222179_97292637 |
| regionname5000 | ARHGAP19_chr10_97217179_97297637 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 494 | 217 | 52 | 41 | 82 | 14 | 26 | 51 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | MATEA others(489): Show |
chr10 | 97217179 | 97297637 |
| a0002 | 0/0 | 494 | 20 | 1 | 1 | 10 | 0 | 8 | 4 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | MATEA others(489): Show |
chr10 | 97217179 | 97297637 |
| a0003 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | MATEA others(489): Show |
chr10 | 97217179 | 97297637 |
| a0004 | 0/0 | 494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | MATEA others(489): Show |
chr10 | 97217179 | 97297637 |
| a0005 | 0/0 | 494 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | MATEA others(489): Show |
chr10 | 97217179 | 97297637 |
| a0006 | 0/0 | 494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | MATEA others(489): Show |
chr10 | 97217179 | 97297637 |
| a0007 | 0/0 | 494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | MATEA others(489): Show |
chr10 | 97217179 | 97297637 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1482 | 130 | 24 | 24 | 60 | 7 | 15 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0001c0002 | 0/1 | 1482 | 54 | 16 | 17 | 4 | 6 | 10 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0001c0003 | 1/0 | 1482 | 33 | 12 | 0 | 18 | 1 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0002c0004 | 0/0 | 1482 | 20 | 1 | 1 | 10 | 0 | 8 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0003c0005 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0004c0006 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0005c0007 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0006c0009 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 | ||
| a0007c0008 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | ATGGC others(1477): Show |
chr10 | 97217179 | 97297637 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5438 | 104 | 13 | 15 | 55 | 7 | 14 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0002 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0005 | 0/0 | 5438 | 8 | 7 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0006 | 0/0 | 5438 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0007 | 0/0 | 5438 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0009 | 0/0 | 5438 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0011 | 0/0 | 5438 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0012 | 0/0 | 5438 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0014 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0017 | 0/0 | 5438 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0018 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0019 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0020 | 0/0 | 5438 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0001t0021 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0002t0001 | 0/0 | 5438 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0002t0002 | 0/1 | 5438 | 45 | 10 | 16 | 4 | 4 | 10 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0002t0008 | 0/0 | 5438 | 2 | 0 | 0 | 0 | 2 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0002t0016 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0003t0002 | 0/0 | 5438 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0003t0003 | 0/0 | 5438 | 19 | 0 | 0 | 18 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0003t0004 | 1/0 | 5438 | 9 | 8 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0003t0010 | 0/0 | 5438 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0003t0013 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0001c0003t0015 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0002c0004t0002 | 0/0 | 5438 | 20 | 1 | 1 | 10 | 0 | 8 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0003c0005t0001 | 0/0 | 5438 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0004c0006t0001 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0005c0007t0006 | 0/0 | 5438 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0006c0009t0001 | 0/0 | 5438 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| a0007c0008t0001 | 0/0 | 5438 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | GCTGA others(5433): Show |
chr10 | 97217179 | 97297637 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0006g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0007g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0012g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0017g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0018g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0019g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0020g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0001t0021g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0008g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0008g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0002t0016g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0093 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0010g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0013g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0001c0003t0015g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0002c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0003c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0004c0006t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0005c0007t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0006c0009t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| a0007c0008t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0042 | EUR | GBR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00140 | hp2 | a0001 | c0002 | t0008 | g0052 | EUR | GBR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00280 | hp1 | a0001 | c0003 | t0003 | g0088 | EUR | FIN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00423 | hp2 | a0003 | c0005 | t0001 | g0114 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00438 | hp1 | a0002 | c0004 | t0002 | g0066 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00558 | hp2 | a0002 | c0004 | t0002 | g0072 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00597 | hp2 | a0002 | c0004 | t0002 | g0065 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00609 | hp1 | a0001 | c0001 | t0012 | g0128 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00639 | hp2 | a0004 | c0006 | t0001 | g0195 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00673 | hp2 | a0001 | c0003 | t0003 | g0103 | EAS | CHS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0007 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0048 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01081 | hp1 | a0001 | c0002 | t0016 | g0005 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0039 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01175 | hp2 | a0001 | c0001 | t0018 | g0122 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01346 | hp1 | a0001 | c0001 | t0019 | g0136 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01358 | hp1 | a0001 | c0001 | t0014 | g0013 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01358 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0043 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0024 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0040 | EUR | IBS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01516 | hp1 | a0001 | c0002 | t0008 | g0053 | EUR | IBS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0050 | EUR | IBS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0097 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0037 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0045 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02004 | hp1 | a0002 | c0004 | t0002 | g0073 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02015 | hp1 | a0001 | c0003 | t0003 | g0100 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0080 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02074 | hp1 | a0002 | c0004 | t0002 | g0074 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02074 | hp2 | a0001 | c0001 | t0009 | g0145 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02135 | hp1 | a0002 | c0004 | t0002 | g0089 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02135 | hp2 | a0001 | c0003 | t0003 | g0083 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0022 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0081 | EAS | CDX | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CDX | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02257 | hp2 | a0006 | c0009 | t0001 | g0208 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0229 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02280 | hp2 | a0001 | c0003 | t0013 | g0078 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02523 | hp2 | a0001 | c0003 | t0003 | g0101 | EAS | KHV | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0027 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0236 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0023 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02738 | hp2 | a0001 | c0001 | t0020 | g0234 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02809 | hp2 | a0001 | c0001 | t0021 | g0219 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0092 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0109 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02922 | hp1 | a0001 | c0003 | t0004 | g0091 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02922 | hp2 | a0001 | c0003 | t0004 | g0090 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0006 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03017 | hp1 | a0002 | c0004 | t0002 | g0149 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0096 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | ESN | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | MSL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03490 | hp2 | a0002 | c0004 | t0002 | g0151 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03492 | hp2 | a0002 | c0004 | t0002 | g0176 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | MSL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0063 | AFR | MSL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03654 | hp1 | a0002 | c0004 | t0002 | g0150 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03669 | hp2 | a0001 | c0003 | t0010 | g0082 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0015 | SAS | PJL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03834 | hp1 | a0002 | c0004 | t0002 | g0068 | SAS | BEB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0032 | SAS | BEB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03927 | hp2 | a0002 | c0004 | t0002 | g0178 | SAS | BEB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG04184 | hp1 | a0002 | c0004 | t0002 | g0148 | SAS | BEB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG04204 | hp1 | a0002 | c0004 | t0002 | g0069 | SAS | STU | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18612 | hp2 | a0001 | c0003 | t0003 | g0099 | EAS | CHB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18747 | hp2 | a0002 | c0004 | t0002 | g0070 | EAS | CHB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18943 | hp2 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18946 | hp2 | a0001 | c0003 | t0003 | g0085 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0105 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18952 | hp2 | a0001 | c0003 | t0003 | g0079 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18954 | hp1 | a0002 | c0004 | t0002 | g0071 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0133 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18962 | hp1 | a0001 | c0001 | t0017 | g0159 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18962 | hp2 | a0007 | c0008 | t0001 | g0186 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18965 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18970 | hp2 | a0001 | c0003 | t0003 | g0104 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18975 | hp2 | a0002 | c0004 | t0002 | g0060 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18978 | hp1 | a0001 | c0003 | t0003 | g0106 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0077 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19000 | hp1 | a0001 | c0001 | t0011 | g0117 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0098 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19005 | hp1 | a0001 | c0003 | t0003 | g0102 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19007 | hp2 | a0002 | c0004 | t0002 | g0064 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19057 | hp2 | a0002 | c0004 | t0002 | g0067 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19064 | hp1 | a0001 | c0003 | t0003 | g0086 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0110 | AFR | YRI | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ASW | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20129 | hp2 | a0001 | c0003 | t0004 | g0094 | AFR | ASW | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0058 | EUR | TSI | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0059 | SAS | GIH | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01123 | hp1 | a0005 | c0007 | t0006 | g0008 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0049 | AMR | CLM | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0237 | AFR | MSL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0095 | AFR | MSL | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG06807 | hp1 | a0001 | c0003 | t0015 | g0061 | AFR | USA | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | USA | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20300 | hp1 | a0002 | c0004 | t0002 | g0075 | AFR | USA | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0038 | AFR | USA | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0076 | AFR | LWK | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| NA21309 | hp2 | a0001 | c0003 | t0004 | g0062 | AFR | LWK | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0033 | REF | REF | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0093 | REF | REF | ARHGAP19_chr10_97217179_97297637 | ARHGAP19 | chr10 | 97217179 | 97297637 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:97235242 | G | A | 1 | a0004 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1259C>T | p.Ser420Leu | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/12 | 1269/5438 | 1259/1485 | 420/494 | chr10 | 97235242 | |||
| chr10:97246304 | G | A | 1 | a0005 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.961C>T | p.His321Tyr | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/12 | 971/5438 | 961/1485 | 321/494 | chr10 | 97246304 | |||
| chr10:97256331 | T | C | 1 | a0002 | 20 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(17): Show |
missense_variant | MODERATE | c.914A>G | p.Gln305Arg | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/12 | 924/5438 | 914/1485 | 305/494 | chr10 | 97256331 | |||
| chr10:97259530 | G | A | 1 | a0007 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.712C>T | p.Pro238Ser | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/12 | 722/5438 | 712/1485 | 238/494 | chr10 | 97259530 | |||
| chr10:97263446 | T | C | 1 | a0006 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.587A>G | p.His196Arg | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/12 | 597/5438 | 587/1485 | 196/494 | chr10 | 97263446 | |||
| chr10:97265886 | C | T | 1 | a0003 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.296G>A | p.Arg99Gln | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/12 | 306/5438 | 296/1485 | 99/494 | chr10 | 97265886 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:97246326 | G | A | 1 | a0001c0002 | 53 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(50): Show |
synonymous_variant | LOW | c.939C>T | p.Tyr313Tyr | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/12 | 949/5438 | 939/1485 | 313/494 | chr10 | 97246326 | |||
| chr10:97259420 | A | G | 7 | a0001c0001 a0001c0002 a0003c0005 others(4): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
synonymous_variant | LOW | c.822T>C | p.His274His | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/12 | 832/5438 | 822/1485 | 274/494 | chr10 | 97259420 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:97222470 | C | A | 1 | a0001c0001t0014 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3652G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3652 | chr10 | 97222470 | ||||||
| chr10:97222527 | C | T | 2 | a0001c0001t0006 a0005c0007t0006 |
5 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3595G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3595 | chr10 | 97222527 | ||||||
| chr10:97222599 | C | T | 1 | a0001c0001t0019 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3523G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3523 | chr10 | 97222599 | ||||||
| chr10:97222638 | T | C | 1 | a0001c0001t0007 | 3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3484A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3484 | chr10 | 97222638 | ||||||
| chr10:97222701 | T | C | 1 | a0001c0001t0020 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3421A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3421 | chr10 | 97222701 | ||||||
| chr10:97222813 | C | G | 1 | a0001c0003t0010 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3309G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3309 | chr10 | 97222813 | ||||||
| chr10:97222992 | G | A | 15 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(12): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*3130C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3130 | chr10 | 97222992 | ||||||
| chr10:97223113 | C | T | 1 | a0001c0001t0018 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3009G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 3009 | chr10 | 97223113 | ||||||
| chr10:97223166 | C | T | 1 | a0001c0001t0017 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2956G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 2956 | chr10 | 97223166 | ||||||
| chr10:97223200 | C | T | 1 | a0001c0002t0016 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2922G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 2922 | chr10 | 97223200 | ||||||
| chr10:97223275 | G | A | 1 | a0001c0001t0021 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2847C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 2847 | chr10 | 97223275 | ||||||
| chr10:97223423 | T | C | 1 | a0001c0001t0009 | 2 | HG02074.hp2 NA18957.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2699A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 2699 | chr10 | 97223423 | ||||||
| chr10:97223597 | A | G | 1 | a0001c0003t0013 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2525T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 2525 | chr10 | 97223597 | ||||||
| chr10:97223627 | T | A | 1 | a0001c0002t0008 | 2 | HG00140.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2495A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 2495 | chr10 | 97223627 | ||||||
| chr10:97223797 | G | C | 1 | a0001c0003t0015 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2325C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 2325 | chr10 | 97223797 | ||||||
| chr10:97224198 | G | A | 15 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(12): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1924C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 1924 | chr10 | 97224198 | ||||||
| chr10:97224540 | G | C | 1 | a0001c0001t0005 | 8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1582C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 1582 | chr10 | 97224540 | ||||||
| chr10:97224555 | G | A | 1 | a0001c0001t0005 | 8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1567C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 1567 | chr10 | 97224555 | ||||||
| chr10:97224820 | C | G | 1 | a0001c0001t0005 | 8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1302G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 1302 | chr10 | 97224820 | ||||||
| chr10:97225021 | T | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(25): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1101A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 1101 | chr10 | 97225021 | ||||||
| chr10:97225299 | A | G | 1 | a0001c0001t0005 | 8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*823T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 823 | chr10 | 97225299 | ||||||
| chr10:97225482 | C | G | 1 | a0001c0001t0005 | 8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*640G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 640 | chr10 | 97225482 | ||||||
| chr10:97225667 | A | G | 1 | a0001c0001t0012 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 455 | chr10 | 97225667 | ||||||
| chr10:97225677 | A | C | 1 | a0001c0001t0011 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 445 | chr10 | 97225677 | ||||||
| chr10:97225855 | C | T | 2 | a0001c0003t0003 a0001c0003t0010 |
20 | HG00280.hp1 HG00673.hp2 HG02015.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 267 | chr10 | 97225855 | ||||||
| chr10:97225982 | C | T | 1 | a0001c0001t0007 | 3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*140G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 140 | chr10 | 97225982 | ||||||
| chr10:97225986 | T | G | 1 | a0001c0001t0007 | 3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*136A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 12/12 | 136 | chr10 | 97225986 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:97226343 | G | A | 1 | a0001c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1475-211C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226343 | |||||||
| chr10:97226432 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1475-300A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226432 | |||||||
| chr10:97226559 | C | A | 47 | a0001c0001t0002g0011 a0001c0002t0002g0014 a0001c0002t0002g0015 others(44): Show |
47 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1475-427G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226559 | |||||||
| chr10:97226594 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0200 |
2 | HG02132.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1475-462C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226594 | |||||||
| chr10:97226604 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1475-472T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226604 | |||||||
| chr10:97226625 | A | G | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1475-493T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226625 | |||||||
| chr10:97226715 | T | C | 179 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1475-583A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226715 | |||||||
| chr10:97226769 | A | G | 1 | a0001c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1475-637T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226769 | |||||||
| chr10:97226867 | A | G | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1475-735T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226867 | |||||||
| chr10:97226909 | A | G | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1475-777T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226909 | |||||||
| chr10:97226997 | A | G | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1475-865T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97226997 | |||||||
| chr10:97227040 | G | T | 3 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0038 |
3 | HG02809.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1475-908C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227040 | |||||||
| chr10:97227150 | T | C | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1475-1018A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227150 | |||||||
| chr10:97227213 | C | T | 39 | a0001c0001t0002g0011 a0001c0002t0002g0022 a0001c0002t0002g0023 others(36): Show |
39 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1475-1081G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227213 | |||||||
| chr10:97227231 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1475-1099G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227231 | |||||||
| chr10:97227284 | C | T | 1 | a0001c0002t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1475-1152G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227284 | |||||||
| chr10:97227537 | G | T | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1475-1405C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227537 | |||||||
| chr10:97227731 | C | T | 2 | a0001c0002t0008g0052 a0001c0002t0008g0053 |
2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1474+1416G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227731 | |||||||
| chr10:97227765 | T | C | 47 | a0001c0001t0002g0011 a0001c0002t0002g0014 a0001c0002t0002g0015 others(44): Show |
47 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1474+1382A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227765 | |||||||
| chr10:97227828 | C | T | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474+1319G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227828 | |||||||
| chr10:97227964 | T | C | 4 | a0001c0003t0004g0091 a0001c0003t0004g0092 a0001c0003t0004g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1474+1183A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97227964 | |||||||
| chr10:97228015 | T | C | 6 | a0001c0001t0006g0007 a0001c0001t0006g0009 a0001c0001t0006g0010 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1474+1132A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228015 | |||||||
| chr10:97228228 | G | T | 47 | a0001c0001t0002g0011 a0001c0002t0002g0014 a0001c0002t0002g0015 others(44): Show |
47 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.1474+919C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228228 | |||||||
| chr10:97228486 | A | T | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1474+661T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228486 | |||||||
| chr10:97228568 | T | C | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1474+579A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228568 | |||||||
| chr10:97228585 | T | C | 5 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(2): Show |
5 | HG01175.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1474+562A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228585 | |||||||
| chr10:97228635 | A | G | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1474+512T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228635 | |||||||
| chr10:97228712 | A | C | 39 | a0001c0001t0002g0011 a0001c0002t0002g0022 a0001c0002t0002g0023 others(36): Show |
39 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1474+435T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228712 | |||||||
| chr10:97228750 | A | G | 1 | a0001c0002t0002g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1474+397T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228750 | |||||||
| chr10:97228795 | T | A | 1 | a0001c0002t0002g0036 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1474+352A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97228795 | |||||||
| chr10:97229002 | A | C | 130 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(127): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1474+145T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 11/11 | chr10 | 97229002 | |||||||
| chr10:97229242 | G | A | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1396-17C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 10/11 | chr10 | 97229242 | |||||||
| chr10:97229426 | C | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1396-201G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 10/11 | chr10 | 97229426 | |||||||
| chr10:97229494 | T | C | 189 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1396-269A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 10/11 | chr10 | 97229494 | |||||||
| chr10:97229697 | A | G | 138 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(135): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1395+67T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 10/11 | chr10 | 97229697 | |||||||
| chr10:97229937 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1285-63G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97229937 | |||||||
| chr10:97229957 | G | T | 1 | a0001c0002t0001g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1285-83C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97229957 | |||||||
| chr10:97230006 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1285-132A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230006 | |||||||
| chr10:97230008 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1285-134A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230008 | |||||||
| chr10:97230046 | CA | C | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-173delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230046 | |||||||
| chr10:97230053 | A | C | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-179T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230053 | |||||||
| chr10:97230054 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1285-180G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230054 | |||||||
| chr10:97230264 | A | G | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1285-390T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230264 | |||||||
| chr10:97230335 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1285-461G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230335 | |||||||
| chr10:97230382 | G | C | 117 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1285-508C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230382 | |||||||
| chr10:97230512 | C | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1285-638G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230512 | |||||||
| chr10:97230958 | G | A | 1 | a0001c0002t0002g0051 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1285-1084C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97230958 | |||||||
| chr10:97231025 | C | T | 67 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(64): Show |
67 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285-1151G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231025 | |||||||
| chr10:97231035 | C | CA | 189 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1285-1162dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231035 | |||||||
| chr10:97231038 | C | A | 189 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1285-1164G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231038 | |||||||
| chr10:97231039 | T | C | 189 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(186): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1285-1165A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231039 | |||||||
| chr10:97231059 | C | CA | 38 | a0001c0001t0002g0011 a0001c0002t0002g0024 a0001c0002t0002g0026 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1285-1186dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | C | CAA | 24 | a0001c0002t0002g0023 a0001c0002t0002g0028 a0001c0002t0002g0034 others(21): Show |
24 | HG00673.hp2 HG00738.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1285-1187_1285-118 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | C | CAAA | 11 | a0001c0001t0007g0110 a0001c0002t0002g0025 a0001c0002t0002g0032 others(8): Show |
11 | HG00438.hp1 HG00597.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1285-1188_1285-118 others(7): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0006g0009 a0001c0001t0014g0013 a0005c0007t0006g0008 |
3 | HG01123.hp1 HG01358.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1285-1195_1285-118 others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | C | CAAAAAAA others(6): Show |
3 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0038 |
3 | HG02809.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1285-1198_1285-118 others(17): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | C | CAAAAAAA others(18): Show |
1 | a0001c0002t0002g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1285-1210_1285-118 others(29): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | CAAAAAAA | C | 67 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(64): Show |
67 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285-1192_1285-118 others(11): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | CAAAAAAA others(1): Show |
C | 44 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1285-1193_1285-118 others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(6): Show |
9 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1195_1285-118 others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | CAAAAAAA others(6): Show |
C | 2 | a0002c0004t0002g0072 a0002c0004t0002g0089 |
2 | HG00558.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1285-1198_1285-118 others(17): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | CAAAAAAA others(7): Show |
C | 7 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(4): Show |
7 | HG01081.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1285-1199_1285-118 others(18): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231059 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0003t0002g0076 |
3 | NA18951.hp1 NA18984.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1285-1200_1285-118 others(19): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231059 | |||||||
| chr10:97231105 | G | A | 188 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.1285-1231C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231105 | |||||||
| chr10:97231217 | G | A | 1 | a0001c0003t0003g0087 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1285-1343C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231217 | |||||||
| chr10:97231449 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1285-1575T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231449 | |||||||
| chr10:97231614 | G | T | 1 | a0001c0002t0002g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1285-1740C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231614 | |||||||
| chr10:97231615 | C | T | 1 | a0001c0002t0002g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1285-1741G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231615 | |||||||
| chr10:97231870 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1285-1996C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231870 | |||||||
| chr10:97231979 | G | GT | 44 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0137 others(41): Show |
44 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1285-2106dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231979 | |||||||
| chr10:97231979 | GT | G | 21 | a0001c0001t0001g0116 a0001c0001t0001g0131 a0001c0001t0001g0164 others(18): Show |
21 | HG00423.hp2 HG00609.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1285-2106delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97231979 | |||||||
| chr10:97232090 | A | C | 20 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(17): Show |
20 | HG00280.hp1 HG00673.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1285-2216T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97232090 | |||||||
| chr10:97232154 | A | AT | 78 | a0001c0001t0001g0107 a0001c0001t0001g0112 a0001c0001t0001g0115 others(75): Show |
78 | HG00280.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1285-2281dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97232154 | |||||||
| chr10:97232154 | A | ATT | 14 | a0001c0001t0006g0009 a0001c0001t0014g0013 a0001c0002t0001g0004 others(11): Show |
14 | HG00438.hp1 HG01358.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.1285-2282_1285-228 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97232154 | |||||||
| chr10:97232154 | AT | A | 8 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0233 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1285-2281delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97232154 | |||||||
| chr10:97232194 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1285-2320G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97232194 | |||||||
| chr10:97232356 | A | G | 1 | a0001c0003t0003g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1285-2482T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97232356 | |||||||
| chr10:97232747 | C | T | 1 | a0005c0007t0006g0008 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1284+2470G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97232747 | |||||||
| chr10:97233105 | C | T | 1 | a0001c0003t0003g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1284+2112G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233105 | |||||||
| chr10:97233344 | CCT | C | 39 | a0001c0001t0002g0011 a0001c0002t0002g0022 a0001c0002t0002g0023 others(36): Show |
39 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.1284+1871_1284+187 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233344 | |||||||
| chr10:97233353 | A | AAAAT | 185 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1284+1860_1284+186 others(8): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233353 | |||||||
| chr10:97233466 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG02486.hp2 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1284+1751T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233466 | |||||||
| chr10:97233573 | G | A | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1284+1644C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233573 | |||||||
| chr10:97233575 | G | A | 3 | a0001c0003t0003g0084 a0001c0003t0003g0085 a0001c0003t0003g0086 |
3 | NA18943.hp2 NA18946.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1284+1642C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233575 | |||||||
| chr10:97233621 | A | T | 132 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1284+1596T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233621 | |||||||
| chr10:97233739 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1284+1478T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233739 | |||||||
| chr10:97233741 | G | A | 38 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1284+1476C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233741 | |||||||
| chr10:97233847 | G | A | 1 | a0001c0003t0003g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1284+1370C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97233847 | |||||||
| chr10:97234056 | C | T | 117 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1284+1161G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97234056 | |||||||
| chr10:97234382 | G | A | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1284+835C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97234382 | |||||||
| chr10:97234386 | A | G | 46 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(43): Show |
46 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.1284+831T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97234386 | |||||||
| chr10:97234415 | TA | T | 57 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(54): Show |
57 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.1284+801delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97234415 | |||||||
| chr10:97234415 | TAA | T | 55 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(52): Show |
55 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1284+800_1284+801d others(4): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97234415 | |||||||
| chr10:97234415 | TAAA | T | 106 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(103): Show |
106 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1284+799_1284+801d others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97234415 | |||||||
| chr10:97234415 | TAAAA | T | 14 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0134 others(11): Show |
14 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.1284+798_1284+801d others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | 97234415 | |||||||
| chr10:97235319 | A | G | 46 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(43): Show |
46 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(43): Show |
splice_region_variant&intron_variant | LOW | c.1186-4T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235319 | |||||||
| chr10:97235336 | C | T | 1 | a0001c0002t0002g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1186-21G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235336 | |||||||
| chr10:97235604 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0174 |
2 | NA18951.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1186-289C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235604 | |||||||
| chr10:97235652 | CCA | C | 20 | a0002c0004t0002g0060 a0002c0004t0002g0064 a0002c0004t0002g0065 others(17): Show |
20 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1186-339_1186-338d others(4): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235652 | |||||||
| chr10:97235688 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1186-373T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235688 | |||||||
| chr10:97235705 | T | C | 1 | a0007c0008t0001g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1186-390A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235705 | |||||||
| chr10:97235868 | T | C | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1186-553A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235868 | |||||||
| chr10:97235944 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0232 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1186-629G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235944 | |||||||
| chr10:97235997 | G | A | 1 | a0001c0002t0002g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1186-682C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97235997 | |||||||
| chr10:97236338 | C | T | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1186-1023G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97236338 | |||||||
| chr10:97236773 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1186-1458G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97236773 | |||||||
| chr10:97236803 | G | GA | 35 | a0001c0001t0001g0116 a0001c0002t0002g0022 a0001c0002t0002g0024 others(32): Show |
35 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.1186-1489dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97236803 | |||||||
| chr10:97236803 | GA | G | 159 | a0001c0001t0001g0107 a0001c0001t0001g0118 a0001c0001t0001g0119 others(156): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1186-1489delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97236803 | |||||||
| chr10:97236803 | GAA | G | 8 | a0001c0001t0001g0139 a0001c0001t0001g0192 a0001c0001t0001g0213 others(5): Show |
8 | HG01255.hp2 HG02071.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.1186-1490_1186-148 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97236803 | |||||||
| chr10:97237046 | C | T | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1186-1731G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237046 | |||||||
| chr10:97237158 | AG | A | 3 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0038 |
3 | HG02809.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1186-1844delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237158 | |||||||
| chr10:97237216 | GATCA | G | 185 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1186-1905_1186-190 others(8): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237216 | |||||||
| chr10:97237263 | C | CA | 203 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0113 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.1186-1949dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237263 | |||||||
| chr10:97237263 | C | CAA | 19 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0001t0001g0142 others(16): Show |
19 | HG00280.hp2 HG00438.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1186-1950_1186-194 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237263 | |||||||
| chr10:97237343 | C | T | 2 | a0001c0002t0002g0022 a0001c0002t0002g0055 |
2 | HG01346.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1186-2028G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237343 | |||||||
| chr10:97237380 | T | C | 1 | a0001c0002t0001g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1186-2065A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237380 | |||||||
| chr10:97237623 | C | G | 1 | a0001c0003t0004g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1186-2308G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237623 | |||||||
| chr10:97237731 | C | T | 1 | a0001c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1186-2416G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237731 | |||||||
| chr10:97237918 | G | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1186-2603C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237918 | |||||||
| chr10:97237947 | T | C | 7 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(4): Show |
7 | HG01081.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-2632A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97237947 | |||||||
| chr10:97238229 | G | A | 7 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(4): Show |
7 | HG01081.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-2914C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238229 | |||||||
| chr10:97238284 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1186-2969C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238284 | |||||||
| chr10:97238309 | C | T | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1186-2994G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238309 | |||||||
| chr10:97238438 | G | A | 124 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.1186-3123C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238438 | |||||||
| chr10:97238509 | C | T | 53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1186-3194G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238509 | |||||||
| chr10:97238598 | T | C | 53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1186-3283A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238598 | |||||||
| chr10:97238803 | C | T | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | NA18966.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186-3488G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238803 | |||||||
| chr10:97238804 | G | A | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1186-3489C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238804 | |||||||
| chr10:97238995 | T | C | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1186-3680A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97238995 | |||||||
| chr10:97239068 | C | T | 7 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(4): Show |
7 | HG01081.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-3753G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239068 | |||||||
| chr10:97239217 | G | A | 38 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.1186-3902C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239217 | |||||||
| chr10:97239322 | G | A | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1186-4007C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239322 | |||||||
| chr10:97239324 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1186-4009G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239324 | |||||||
| chr10:97239456 | T | C | 53 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.1186-4141A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239456 | |||||||
| chr10:97239501 | CA | C | 183 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(180): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1186-4187delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239501 | |||||||
| chr10:97239546 | GAGAGGGT others(2): Show |
G | 7 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0238 others(4): Show |
7 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-4240_1186-423 others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239546 | |||||||
| chr10:97239547 | AGAGG | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0177 a0001c0001t0001g0223 |
3 | HG00597.hp1 HG02486.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1186-4236_1186-423 others(8): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGT | A | 5 | a0001c0001t0001g0143 a0001c0002t0002g0017 a0001c0002t0002g0019 others(2): Show |
5 | HG01496.hp2 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1186-4238_1186-423 others(10): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(1): Show |
A | 12 | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0158 others(9): Show |
12 | HG01175.hp1 HG02074.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1186-4240_1186-423 others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(3): Show |
A | 25 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0138 others(22): Show |
25 | HG00673.hp1 HG01071.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1186-4242_1186-423 others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(4): Show |
A | 1 | a0001c0001t0001g0135 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1186-4243_1186-423 others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(5): Show |
A | 58 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0123 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1186-4244_1186-423 others(16): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(6): Show |
A | 1 | a0001c0001t0001g0212 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1186-4245_1186-423 others(17): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(7): Show |
A | 8 | a0001c0001t0001g0116 a0001c0001t0001g0171 a0001c0002t0001g0001 others(5): Show |
8 | HG01071.hp2 HG01081.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1186-4246_1186-423 others(18): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(9): Show |
A | 3 | a0001c0001t0001g0162 a0001c0002t0002g0025 a0001c0002t0002g0029 |
3 | HG02630.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1186-4248_1186-423 others(20): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(11): Show |
A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0185 others(4): Show |
7 | HG00438.hp2 HG02071.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.1186-4250_1186-423 others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239547 | AGAGGGTG others(13): Show |
A | 44 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1186-4252_1186-423 others(24): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239547 | |||||||
| chr10:97239548 | GAGGGTGT others(4): Show |
G | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1186-4244_1186-423 others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239548 | |||||||
| chr10:97239548 | GAGGGTGT others(6): Show |
G | 1 | a0001c0001t0001g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1186-4246_1186-423 others(17): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239548 | |||||||
| chr10:97239549 | A | G | 5 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0014g0013 others(2): Show |
5 | HG01358.hp1 HG02280.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1186-4234T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239549 | |||||||
| chr10:97239549 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1186-4234T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239549 | |||||||
| chr10:97239551 | G | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0152 a0001c0001t0014g0013 others(1): Show |
4 | HG01358.hp1 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186-4236C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239551 | |||||||
| chr10:97239551 | GGT | G | 4 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0003t0003g0085 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1186-4238_1186-423 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239551 | |||||||
| chr10:97239551 | GGTGT | G | 7 | a0001c0001t0007g0110 a0001c0003t0003g0079 a0001c0003t0003g0080 others(4): Show |
7 | HG02056.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-4240_1186-423 others(8): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239551 | |||||||
| chr10:97239551 | GGTGTGT | G | 19 | a0001c0002t0002g0020 a0001c0003t0002g0063 a0001c0003t0003g0077 others(16): Show |
19 | HG00280.hp1 HG00673.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.1186-4242_1186-423 others(10): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239551 | |||||||
| chr10:97239551 | GGTGTGTG others(1): Show |
G | 7 | a0001c0003t0003g0081 a0001c0003t0003g0084 a0001c0003t0004g0097 others(4): Show |
7 | HG01884.hp2 HG02155.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.1186-4244_1186-423 others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239551 | |||||||
| chr10:97239551 | GGTGTGTG others(3): Show |
G | 14 | a0001c0001t0001g0172 a0001c0003t0003g0099 a0002c0004t0002g0064 others(11): Show |
14 | HG00438.hp1 HG00597.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.1186-4246_1186-423 others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239551 | |||||||
| chr10:97239551 | GGTGTGTG others(5): Show |
G | 2 | a0001c0003t0002g0076 a0002c0004t0002g0072 |
2 | HG00558.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1186-4248_1186-423 others(16): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239551 | |||||||
| chr10:97239553 | T | G | 4 | a0001c0001t0001g0142 a0001c0001t0001g0177 a0001c0001t0001g0223 others(1): Show |
4 | HG00597.hp1 HG02135.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186-4238A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239553 | |||||||
| chr10:97239555 | T | G | 6 | a0001c0001t0001g0143 a0001c0002t0002g0017 a0001c0002t0002g0019 others(3): Show |
6 | HG01496.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1186-4240A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239555 | |||||||
| chr10:97239557 | T | G | 17 | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0158 others(14): Show |
17 | HG01175.hp1 HG02056.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1186-4242A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239557 | |||||||
| chr10:97239557 | TG | T | 7 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0238 others(4): Show |
7 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-4243delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239557 | |||||||
| chr10:97239559 | T | G | 37 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0138 others(34): Show |
37 | HG00280.hp1 HG00673.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.1186-4244A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239559 | |||||||
| chr10:97239561 | T | G | 60 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0123 others(57): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1186-4246A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239561 | |||||||
| chr10:97239563 | T | G | 9 | a0001c0001t0001g0116 a0001c0001t0001g0171 a0001c0002t0001g0001 others(6): Show |
9 | HG01071.hp2 HG01081.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.1186-4248A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239563 | |||||||
| chr10:97239565 | T | G | 3 | a0001c0001t0001g0162 a0001c0002t0002g0025 a0001c0002t0002g0029 |
3 | HG02630.hp1 HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1186-4250A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239565 | |||||||
| chr10:97239567 | T | G | 6 | a0001c0001t0001g0139 a0001c0001t0001g0185 a0001c0001t0001g0202 others(3): Show |
6 | HG00438.hp2 HG02071.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1186-4252A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239567 | |||||||
| chr10:97239569 | T | G | 44 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1186-4254A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239569 | |||||||
| chr10:97239693 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1185+4275A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239693 | |||||||
| chr10:97239743 | T | C | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185+4225A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239743 | |||||||
| chr10:97239852 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1185+4116G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97239852 | |||||||
| chr10:97240026 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1185+3942A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240026 | |||||||
| chr10:97240127 | G | A | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1185+3841C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240127 | |||||||
| chr10:97240262 | AT | A | 117 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1185+3705delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240262 | |||||||
| chr10:97240334 | T | C | 2 | a0001c0002t0002g0040 a0001c0002t0002g0050 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1185+3634A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240334 | |||||||
| chr10:97240539 | T | C | 5 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(2): Show |
5 | HG01071.hp1 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185+3429A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240539 | |||||||
| chr10:97240638 | A | G | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1185+3330T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240638 | |||||||
| chr10:97240696 | A | C | 1 | a0001c0002t0002g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1185+3272T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240696 | |||||||
| chr10:97240919 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0166 |
2 | HG03669.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1185+3049A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97240919 | |||||||
| chr10:97241013 | T | C | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185+2955A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241013 | |||||||
| chr10:97241106 | G | A | 186 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(183): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1185+2862C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241106 | |||||||
| chr10:97241299 | T | C | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1185+2669A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241299 | |||||||
| chr10:97241304 | T | TTTTACTT others(9): Show |
1 | a0001c0001t0005g0236 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1185+2648_1185+266 others(20): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241304 | |||||||
| chr10:97241481 | G | A | 2 | a0001c0002t0002g0026 a0001c0002t0002g0057 |
2 | HG03490.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1185+2487C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241481 | |||||||
| chr10:97241500 | G | A | 1 | a0001c0001t0007g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1185+2468C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241500 | |||||||
| chr10:97241501 | G | A | 132 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(129): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1185+2467C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241501 | |||||||
| chr10:97241616 | G | A | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185+2352C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241616 | |||||||
| chr10:97241668 | G | A | 20 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(17): Show |
20 | HG00280.hp1 HG00673.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.1185+2300C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241668 | |||||||
| chr10:97241730 | C | T | 5 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(2): Show |
5 | HG01071.hp1 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185+2238G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241730 | |||||||
| chr10:97241867 | G | A | 185 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1185+2101C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241867 | |||||||
| chr10:97241967 | G | A | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1185+2001C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97241967 | |||||||
| chr10:97242009 | CA | C | 14 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(11): Show |
14 | HG00639.hp1 HG01081.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1185+1958delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242009 | |||||||
| chr10:97242019 | A | T | 3 | a0001c0001t0001g0199 a0001c0002t0002g0027 a0001c0002t0002g0037 |
3 | HG01952.hp1 HG01952.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1185+1949T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242019 | |||||||
| chr10:97242022 | A | T | 118 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0131 others(115): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1185+1946T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242022 | |||||||
| chr10:97242025 | T | A | 1 | a0001c0001t0001g0158 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1185+1943A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242025 | |||||||
| chr10:97242251 | C | T | 1 | a0001c0001t0006g0007 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1185+1717G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242251 | |||||||
| chr10:97242324 | C | CT | 73 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0116 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1185+1643dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242324 | |||||||
| chr10:97242324 | C | CTT | 10 | a0001c0001t0005g0237 a0001c0002t0002g0014 a0001c0002t0002g0018 others(7): Show |
10 | HG00423.hp1 HG01175.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.1185+1642_1185+164 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242324 | |||||||
| chr10:97242324 | CT | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0222 a0001c0002t0001g0001 others(5): Show |
8 | HG01081.hp1 HG02735.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185+1643delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242324 | |||||||
| chr10:97242324 | CTT | C | 7 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0238 others(4): Show |
7 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185+1642_1185+164 others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242324 | |||||||
| chr10:97242356 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1185+1612C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242356 | |||||||
| chr10:97242358 | G | T | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1185+1610C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242358 | |||||||
| chr10:97242421 | C | T | 1 | a0002c0004t0002g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1185+1547G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242421 | |||||||
| chr10:97242534 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0232 |
2 | HG02040.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1185+1434G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242534 | |||||||
| chr10:97242761 | A | G | 151 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(148): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1185+1207T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242761 | |||||||
| chr10:97242901 | A | G | 2 | a0002c0004t0002g0067 a0002c0004t0002g0068 |
2 | HG03834.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1185+1067T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97242901 | |||||||
| chr10:97243321 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0001g0165 |
2 | HG02683.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1185+647C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243321 | |||||||
| chr10:97243375 | C | T | 1 | a0001c0002t0002g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1185+593G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243375 | |||||||
| chr10:97243552 | G | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1185+416C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243552 | |||||||
| chr10:97243618 | A | C | 47 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(44): Show |
47 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1185+350T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243618 | |||||||
| chr10:97243661 | C | G | 7 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(4): Show |
7 | HG01081.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185+307G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243661 | |||||||
| chr10:97243679 | G | A | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1185+289C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243679 | |||||||
| chr10:97243707 | C | T | 2 | a0001c0002t0002g0041 a0001c0002t0002g0046 |
2 | HG01071.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1185+261G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243707 | |||||||
| chr10:97243799 | C | T | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1185+169G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243799 | |||||||
| chr10:97243856 | A | C | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1185+112T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243856 | |||||||
| chr10:97243928 | A | G | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1185+40T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243928 | |||||||
| chr10:97243959 | T | TTTAGGCA others(4): Show |
1 | a0001c0001t0001g0142 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.1183_1185+8dupCAGG others(7): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | 97243959 | |||||||
| chr10:97244182 | G | A | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.994-23C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244182 | |||||||
| chr10:97244212 | T | TG | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.994-54dupC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244212 | |||||||
| chr10:97244322 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.994-163A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244322 | |||||||
| chr10:97244409 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.994-250A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244409 | |||||||
| chr10:97244414 | G | A | 185 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.994-255C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244414 | |||||||
| chr10:97244463 | C | T | 45 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(42): Show |
45 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.994-304G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244463 | |||||||
| chr10:97244517 | A | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.994-358T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244517 | |||||||
| chr10:97244525 | G | A | 1 | a0001c0002t0002g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.994-366C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244525 | |||||||
| chr10:97244557 | C | A | 1 | a0001c0001t0020g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.994-398G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244557 | |||||||
| chr10:97244607 | T | C | 1 | a0005c0007t0006g0008 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.994-448A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244607 | |||||||
| chr10:97244687 | C | A | 4 | a0001c0003t0004g0091 a0001c0003t0004g0092 a0001c0003t0004g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.994-528G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244687 | |||||||
| chr10:97244851 | C | T | 117 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.994-692G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244851 | |||||||
| chr10:97244885 | CT | C | 15 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0130 others(12): Show |
15 | HG00597.hp1 HG01346.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.994-727delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97244885 | |||||||
| chr10:97245130 | C | T | 1 | a0001c0003t0004g0095 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.994-971G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245130 | |||||||
| chr10:97245272 | G | A | 4 | a0001c0003t0004g0091 a0001c0003t0004g0092 a0001c0003t0004g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+1000C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245272 | |||||||
| chr10:97245499 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.993+773A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245499 | |||||||
| chr10:97245575 | A | G | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.993+697T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245575 | |||||||
| chr10:97245595 | C | CA | 5 | a0001c0002t0002g0014 a0001c0002t0002g0021 a0001c0002t0002g0022 others(2): Show |
5 | HG01175.hp1 HG02148.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.993+676dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245595 | |||||||
| chr10:97245595 | CA | C | 57 | a0001c0001t0001g0154 a0001c0001t0001g0185 a0001c0001t0001g0223 others(54): Show |
57 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.993+676delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245595 | |||||||
| chr10:97245595 | CAA | C | 107 | a0001c0001t0001g0107 a0001c0001t0001g0112 a0001c0001t0001g0113 others(104): Show |
107 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.993+675_993+676del others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245595 | |||||||
| chr10:97245595 | CAAA | C | 13 | a0001c0001t0001g0111 a0001c0001t0001g0142 a0001c0001t0001g0165 others(10): Show |
13 | HG00099.hp1 HG00639.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.993+674_993+676del others(3): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245595 | |||||||
| chr10:97245651 | ATTATACA others(7): Show |
A | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.993+607_993+620del others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245651 | |||||||
| chr10:97245674 | A | C | 1 | a0001c0002t0002g0034 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.993+598T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245674 | |||||||
| chr10:97245960 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0161 |
2 | HG01975.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.993+312G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97245960 | |||||||
| chr10:97246011 | T | C | 1 | a0001c0003t0003g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.993+261A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97246011 | |||||||
| chr10:97246066 | A | ATACCTCA others(20): Show |
1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.993+179_993+205dup others(27): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97246066 | |||||||
| chr10:97246085 | T | C | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.993+187A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 7/11 | chr10 | 97246085 | |||||||
| chr10:97246455 | C | CAAAGATC others(85): Show |
1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928-210_928-119dup others(92): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97246455 | |||||||
| chr10:97246857 | G | A | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.928-520C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97246857 | |||||||
| chr10:97246900 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.928-563C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97246900 | |||||||
| chr10:97246994 | GGGTGTGG others(8): Show |
G | 1 | a0001c0001t0005g0236 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.928-672_928-658del others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97246994 | |||||||
| chr10:97247006 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928-669C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247006 | |||||||
| chr10:97247124 | C | T | 1 | a0001c0003t0004g0095 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.928-787G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247124 | |||||||
| chr10:97247137 | CA | C | 7 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0001g0223 others(4): Show |
7 | HG00558.hp1 HG00597.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-801delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247137 | |||||||
| chr10:97247166 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.928-829G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247166 | |||||||
| chr10:97247214 | G | C | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.928-877C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247214 | |||||||
| chr10:97247399 | ATAATACA others(24): Show |
A | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.928-1093_928-1063d others(33): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247399 | |||||||
| chr10:97247440 | T | C | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-1103A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247440 | |||||||
| chr10:97247473 | C | T | 1 | a0001c0001t0007g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.928-1136G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247473 | |||||||
| chr10:97247534 | C | T | 184 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(181): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.928-1197G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247534 | |||||||
| chr10:97247619 | A | G | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-1282T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247619 | |||||||
| chr10:97247723 | T | C | 176 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(173): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.928-1386A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247723 | |||||||
| chr10:97247731 | AG | A | 67 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(64): Show |
67 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.928-1395delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247731 | |||||||
| chr10:97247966 | C | CT | 161 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(158): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.928-1630dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247966 | |||||||
| chr10:97247966 | C | CTT | 14 | a0001c0001t0001g0119 a0001c0001t0001g0124 a0001c0001t0001g0125 others(11): Show |
14 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.928-1631_928-1630d others(4): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247966 | |||||||
| chr10:97247989 | G | A | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.928-1652C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97247989 | |||||||
| chr10:97248126 | C | T | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-1789G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248126 | |||||||
| chr10:97248185 | C | T | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-1848G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248185 | |||||||
| chr10:97248187 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.928-1850C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248187 | |||||||
| chr10:97248311 | G | A | 116 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(113): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.928-1974C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248311 | |||||||
| chr10:97248418 | GA | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0002t0002g0028 others(3): Show |
6 | HG01516.hp1 HG02300.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.928-2082delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248418 | |||||||
| chr10:97248475 | C | A | 187 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.928-2138G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248475 | |||||||
| chr10:97248603 | C | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.928-2266G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248603 | |||||||
| chr10:97248697 | C | G | 21 | a0001c0001t0001g0225 a0002c0004t0002g0060 a0002c0004t0002g0064 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-2360G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248697 | |||||||
| chr10:97248786 | CGGCCAAA others(4): Show |
C | 1 | a0001c0001t0017g0159 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.928-2460_928-2450d others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248786 | |||||||
| chr10:97248816 | T | TTTTG | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-2483_928-2480d others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248816 | |||||||
| chr10:97248825 | T | TTTGTTTG others(50): Show |
1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.928-2545_928-2489d others(59): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248825 | |||||||
| chr10:97248844 | G | T | 1 | a0001c0002t0002g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.928-2507C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248844 | |||||||
| chr10:97248858 | C | T | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.928-2521G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248858 | |||||||
| chr10:97248958 | A | T | 1 | a0001c0003t0003g0079 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.928-2621T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248958 | |||||||
| chr10:97248963 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-2626A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97248963 | |||||||
| chr10:97249194 | T | C | 123 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(120): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.928-2857A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249194 | |||||||
| chr10:97249196 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.928-2859A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249196 | |||||||
| chr10:97249275 | TATTTACT others(15): Show |
T | 1 | a0001c0003t0003g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.928-2960_928-2939d others(24): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249275 | |||||||
| chr10:97249287 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-2950C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249287 | |||||||
| chr10:97249307 | C | A | 1 | a0001c0003t0010g0082 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.928-2970G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249307 | |||||||
| chr10:97249322 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-2985C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249322 | |||||||
| chr10:97249336 | C | A | 1 | a0001c0001t0011g0117 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.928-2999G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249336 | |||||||
| chr10:97249400 | C | T | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.928-3063G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249400 | |||||||
| chr10:97249453 | C | CTGATTAA others(105): Show |
1 | a0001c0003t0003g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.928-3228_928-3117d others(114): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249453 | |||||||
| chr10:97249473 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-3136C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249473 | |||||||
| chr10:97249507 | T | C | 21 | a0001c0001t0001g0225 a0002c0004t0002g0060 a0002c0004t0002g0064 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-3170A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249507 | |||||||
| chr10:97249618 | G | A | 1 | a0002c0004t0002g0074 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.928-3281C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249618 | |||||||
| chr10:97249649 | AAAACCAG others(5): Show |
A | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.928-3324_928-3313d others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249649 | |||||||
| chr10:97249765 | A | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-3428T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249765 | |||||||
| chr10:97249797 | C | CT | 12 | a0001c0001t0001g0116 a0001c0001t0006g0007 a0001c0001t0006g0009 others(9): Show |
12 | HG00423.hp1 HG01071.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.928-3461dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249797 | |||||||
| chr10:97249797 | CT | C | 167 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(164): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.928-3461delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249797 | |||||||
| chr10:97249972 | G | T | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-3635C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249972 | |||||||
| chr10:97249978 | G | T | 1 | a0001c0002t0002g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-3641C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249978 | |||||||
| chr10:97249998 | ATGGTCTC others(28): Show |
A | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.928-3696_928-3662d others(37): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97249998 | |||||||
| chr10:97250061 | G | A | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.928-3724C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250061 | |||||||
| chr10:97250073 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-3736G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250073 | |||||||
| chr10:97250212 | G | T | 181 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.928-3875C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250212 | |||||||
| chr10:97250280 | ATTCACTG others(3): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.928-3953_928-3944d others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250280 | |||||||
| chr10:97250310 | T | A | 124 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.928-3973A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250310 | |||||||
| chr10:97250316 | TGAAATTT others(10): Show |
T | 1 | a0001c0003t0003g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.928-3996_928-3980d others(19): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250316 | |||||||
| chr10:97250338 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-4001G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250338 | |||||||
| chr10:97250383 | T | C | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.928-4046A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250383 | |||||||
| chr10:97250390 | CT | C | 218 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.928-4054delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250390 | |||||||
| chr10:97250425 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-4088C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250425 | |||||||
| chr10:97250527 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.928-4190C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250527 | |||||||
| chr10:97250533 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-4196T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250533 | |||||||
| chr10:97250535 | C | G | 38 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.928-4198G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250535 | |||||||
| chr10:97250564 | G | A | 1 | a0001c0001t0020g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.928-4227C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250564 | |||||||
| chr10:97250578 | G | A | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.928-4241C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250578 | |||||||
| chr10:97250597 | T | TATTTTTT others(21): Show |
1 | a0001c0002t0002g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.928-4261_928-4260i others(30): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250597 | |||||||
| chr10:97250598 | G | A | 1 | a0001c0002t0002g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.928-4261C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250598 | |||||||
| chr10:97250669 | C | T | 21 | a0001c0001t0001g0225 a0002c0004t0002g0060 a0002c0004t0002g0064 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.928-4332G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250669 | |||||||
| chr10:97250696 | AAAAACTA others(51): Show |
A | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.928-4417_928-4360d others(60): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250696 | |||||||
| chr10:97250737 | CCAAACAA others(5): Show |
C | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4412_928-4401d others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250737 | |||||||
| chr10:97250747 | A | ATAACACA others(67): Show |
1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928-4411_928-4410i others(76): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250747 | |||||||
| chr10:97250747 | A | ATATAT | 228 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.928-4415_928-4411d others(7): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250747 | |||||||
| chr10:97250768 | TA | T | 7 | a0001c0001t0001g0230 a0001c0001t0005g0236 a0001c0002t0002g0039 others(4): Show |
7 | HG01081.hp1 HG01081.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.928-4432delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250768 | |||||||
| chr10:97250852 | GC | G | 4 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0002t0002g0024 others(1): Show |
4 | HG01496.hp2 HG02602.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-4516delG | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250852 | |||||||
| chr10:97250887 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.928-4550T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250887 | |||||||
| chr10:97250929 | G | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-4592C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250929 | |||||||
| chr10:97250936 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.928-4599G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97250936 | |||||||
| chr10:97251002 | G | T | 1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928-4665C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251002 | |||||||
| chr10:97251047 | T | TGAGACCC others(71): Show |
1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.928-4788_928-4711d others(80): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251047 | |||||||
| chr10:97251072 | T | TAAGG | 3 | a0001c0002t0002g0016 a0001c0002t0002g0017 a0001c0002t0002g0018 |
3 | HG02486.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.928-4739_928-4736d others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251072 | |||||||
| chr10:97251085 | G | C | 1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928-4748C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251085 | |||||||
| chr10:97251090 | G | GGGAAGGG others(9): Show |
1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.928-4769_928-4754d others(18): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251090 | |||||||
| chr10:97251128 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0211 |
2 | HG02132.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.928-4791C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251128 | |||||||
| chr10:97251138 | G | A | 2 | a0001c0001t0007g0109 a0001c0002t0002g0021 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.928-4801C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251138 | |||||||
| chr10:97251139 | A | G | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.928-4802T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251139 | |||||||
| chr10:97251155 | C | T | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4818G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251155 | |||||||
| chr10:97251159 | G | GAGGAAGG others(19): Show |
1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4823_928-4822i others(28): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251159 | |||||||
| chr10:97251164 | G | GGGAAGGG others(5): Show |
7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-4828_928-4827i others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251164 | |||||||
| chr10:97251176 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.928-4839C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251176 | |||||||
| chr10:97251178 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4841T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251178 | |||||||
| chr10:97251186 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4849T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251186 | |||||||
| chr10:97251192 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4855C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251192 | |||||||
| chr10:97251204 | G | C | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4867C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251204 | |||||||
| chr10:97251205 | G | C | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4868C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251205 | |||||||
| chr10:97251208 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.928-4871C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251208 | |||||||
| chr10:97251208 | G | GGGAGAAG others(6): Show |
1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.928-4872_928-4871i others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251208 | |||||||
| chr10:97251209 | G | GGAAGGGG others(3): Show |
1 | a0001c0002t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.928-4873_928-4872i others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251209 | |||||||
| chr10:97251209 | G | GGGAAGGG others(4): Show |
164 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.928-4883_928-4873d others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251209 | |||||||
| chr10:97251209 | G | GGGGAAGG others(5): Show |
1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.928-4873_928-4872i others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251209 | |||||||
| chr10:97251210 | G | GGAAGGGG others(4): Show |
2 | a0001c0001t0001g0129 a0001c0001t0001g0156 |
2 | HG01074.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.928-4874_928-4873i others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251210 | |||||||
| chr10:97251214 | G | GGGGAATG others(3): Show |
1 | a0001c0002t0002g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.928-4887_928-4878d others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251214 | |||||||
| chr10:97251217 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4880C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251217 | |||||||
| chr10:97251219 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4882T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251219 | |||||||
| chr10:97251220 | T | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4883A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251220 | |||||||
| chr10:97251231 | G | T | 13 | a0001c0001t0001g0118 a0001c0001t0001g0139 a0001c0001t0001g0155 others(10): Show |
13 | HG00438.hp2 HG00558.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.928-4894C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251231 | |||||||
| chr10:97251232 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.928-4895C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251232 | |||||||
| chr10:97251246 | A | AGGGGAAG others(5): Show |
1 | a0001c0001t0001g0139 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.928-4910_928-4909i others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251246 | |||||||
| chr10:97251247 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4910C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251247 | |||||||
| chr10:97251247 | G | GGGGAAGG others(3): Show |
1 | a0001c0001t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.928-4911_928-4910i others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251247 | |||||||
| chr10:97251251 | G | A | 11 | a0001c0001t0001g0118 a0001c0001t0001g0157 a0001c0001t0001g0226 others(8): Show |
11 | HG00558.hp1 HG01071.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.928-4914C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251251 | |||||||
| chr10:97251258 | G | GGGAAGGG others(3): Show |
1 | a0001c0002t0008g0053 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.928-4922_928-4921i others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251258 | |||||||
| chr10:97251258 | G | GGGGAAGG others(4): Show |
32 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(29): Show |
32 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.928-4932_928-4922d others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251258 | |||||||
| chr10:97251258 | G | GGGGAAGG others(5): Show |
1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.928-4922_928-4921i others(14): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251258 | |||||||
| chr10:97251258 | G | GGGGGAGG others(16): Show |
1 | a0001c0002t0002g0056 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.928-4922_928-4921i others(25): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251258 | |||||||
| chr10:97251259 | G | GGGAAGGG others(3): Show |
1 | a0001c0002t0002g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.928-4932_928-4923d others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251259 | |||||||
| chr10:97251261 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4924C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251261 | |||||||
| chr10:97251262 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.928-4925T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251262 | |||||||
| chr10:97251263 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4926T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251263 | |||||||
| chr10:97251264 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.928-4927C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251264 | |||||||
| chr10:97251269 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.928-4932A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251269 | |||||||
| chr10:97251275 | G | GGGAATGG others(3): Show |
1 | a0001c0002t0002g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.928-4939_928-4938i others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251275 | |||||||
| chr10:97251283 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4946T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251283 | |||||||
| chr10:97251291 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4954T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251291 | |||||||
| chr10:97251296 | AG | A | 3 | a0001c0001t0001g0180 a0001c0002t0002g0027 a0001c0002t0002g0029 |
3 | HG01517.hp2 HG02602.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.928-4960delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251296 | |||||||
| chr10:97251322 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4985C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251322 | |||||||
| chr10:97251327 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.928-4990C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251327 | |||||||
| chr10:97251331 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4987T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251331 | |||||||
| chr10:97251353 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4965T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251353 | |||||||
| chr10:97251358 | AG | A | 3 | a0001c0001t0001g0218 a0001c0002t0002g0021 a0001c0002t0002g0048 |
3 | HG01074.hp1 HG03579.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.927+4959delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251358 | |||||||
| chr10:97251365 | A | G | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4953T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251365 | |||||||
| chr10:97251376 | T | A | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4942A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251376 | |||||||
| chr10:97251376 | TGGAAGGG others(4): Show |
T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4931_927+4941d others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251376 | |||||||
| chr10:97251385 | A | AG | 4 | a0001c0001t0007g0108 a0001c0002t0002g0021 a0001c0003t0003g0106 others(1): Show |
4 | HG00423.hp2 HG02630.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+4932dupC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251385 | |||||||
| chr10:97251390 | A | AAGGAAGG others(896): Show |
1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4927_927+4928i others(905): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251390 | |||||||
| chr10:97251391 | AG | A | 3 | a0001c0001t0001g0142 a0001c0003t0003g0079 a0002c0004t0002g0071 |
3 | HG02486.hp2 NA18952.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.927+4926delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251391 | |||||||
| chr10:97251397 | G | A | 1 | a0001c0002t0002g0048 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.927+4921C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251397 | |||||||
| chr10:97251398 | G | GGAAAGGA others(518): Show |
1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.927+4919_927+4920i others(527): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251398 | |||||||
| chr10:97251398 | G | GGAAAGGA others(489): Show |
1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+4919_927+4920i others(498): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251398 | |||||||
| chr10:97251398 | G | GGAAAGGA others(501): Show |
1 | a0001c0002t0001g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+4919_927+4920i others(510): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251398 | |||||||
| chr10:97251409 | G | A | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4909C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251409 | |||||||
| chr10:97251411 | A | G | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4907T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251411 | |||||||
| chr10:97251429 | G | GGGGGAAG others(511): Show |
1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4888_927+4889i others(520): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251429 | |||||||
| chr10:97251431 | G | A | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4887C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251431 | |||||||
| chr10:97251442 | A | G | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4876T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251442 | |||||||
| chr10:97251445 | C | A | 5 | a0001c0001t0001g0131 a0001c0001t0007g0109 a0001c0002t0001g0001 others(2): Show |
5 | HG01952.hp2 HG02071.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+4873G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251445 | |||||||
| chr10:97251445 | CGGGGAA | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4867_927+4872d others(8): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251445 | |||||||
| chr10:97251448 | G | GGAAGGCG others(1113): Show |
1 | a0001c0002t0001g0003 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1122): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(583): Show |
1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(592): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(594): Show |
1 | a0001c0002t0001g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(603): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1079): Show |
1 | a0001c0002t0002g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1088): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1135): Show |
1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1144): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1092): Show |
1 | a0001c0001t0021g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1101): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1081): Show |
1 | a0001c0001t0001g0209 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1090): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1136): Show |
1 | a0001c0002t0001g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1145): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1089): Show |
1 | a0001c0002t0002g0016 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1098): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1089): Show |
1 | a0001c0002t0002g0017 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1098): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1090): Show |
2 | a0001c0002t0002g0015 a0001c0002t0002g0020 |
2 | HG02280.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.927+4869_927+4870i others(1099): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1117): Show |
1 | a0001c0002t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1126): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1148): Show |
1 | a0001c0002t0016g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1157): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1091): Show |
1 | a0001c0002t0002g0018 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1100): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1176): Show |
1 | a0002c0004t0002g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1185): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251448 | G | GGAAGGGG others(1187): Show |
1 | a0001c0003t0003g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.927+4869_927+4870i others(1196): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251448 | |||||||
| chr10:97251452 | G | GGGAAAAG others(139): Show |
1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4865_927+4866i others(148): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251452 | |||||||
| chr10:97251467 | A | C | 19 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(16): Show |
19 | HG00280.hp1 HG00673.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.927+4851T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251467 | |||||||
| chr10:97251471 | A | G | 2 | a0002c0004t0002g0148 a0002c0004t0002g0151 |
2 | HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.927+4847T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251471 | |||||||
| chr10:97251476 | A | G | 2 | a0002c0004t0002g0148 a0002c0004t0002g0151 |
2 | HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.927+4842T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251476 | |||||||
| chr10:97251477 | G | T | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+4841C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251477 | |||||||
| chr10:97251478 | G | GAAGGGAA others(733): Show |
1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.927+4839_927+4840i others(742): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251478 | |||||||
| chr10:97251478 | G | GAGGGGAA others(1196): Show |
1 | a0002c0004t0002g0060 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.927+4839_927+4840i others(1205): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251478 | |||||||
| chr10:97251478 | G | GAGGGGAA others(1210): Show |
1 | a0001c0003t0003g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.927+4839_927+4840i others(1219): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251478 | |||||||
| chr10:97251480 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4838C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251480 | |||||||
| chr10:97251489 | G | A | 3 | a0001c0001t0001g0230 a0002c0004t0002g0148 a0002c0004t0002g0151 |
3 | HG01255.hp1 HG03490.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.927+4829C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251489 | |||||||
| chr10:97251495 | A | AAGGGAAG others(1094): Show |
1 | a0001c0001t0001g0218 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.927+4822_927+4823i others(1103): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251495 | |||||||
| chr10:97251495 | A | AAGGGAAG others(1091): Show |
1 | a0001c0001t0001g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.927+4822_927+4823i others(1100): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251495 | |||||||
| chr10:97251497 | A | G | 208 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.927+4821T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251497 | |||||||
| chr10:97251499 | G | C | 1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4819C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251499 | |||||||
| chr10:97251500 | A | AAGGAAGG others(1206): Show |
1 | a0002c0004t0002g0151 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1215): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGAAGG others(1218): Show |
1 | a0002c0004t0002g0148 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1227): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGAAA others(1225): Show |
1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1234): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1099): Show |
1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1108): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1091): Show |
1 | a0001c0001t0001g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1100): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1125): Show |
1 | a0001c0002t0002g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1134): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1092): Show |
1 | a0001c0001t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1101): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1194): Show |
1 | a0001c0003t0003g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1203): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1183): Show |
1 | a0001c0003t0003g0100 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1192): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1228): Show |
1 | a0002c0004t0002g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1237): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1206): Show |
1 | a0002c0004t0002g0074 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1215): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1195): Show |
3 | a0001c0001t0001g0225 a0002c0004t0002g0067 a0002c0004t0002g0068 |
3 | HG03834.hp1 NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1204): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1196): Show |
1 | a0002c0004t0002g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1205): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1207): Show |
6 | a0002c0004t0002g0064 a0002c0004t0002g0065 a0002c0004t0002g0066 others(3): Show |
6 | HG00438.hp1 HG00597.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1216): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1206): Show |
1 | a0002c0004t0002g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1215): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1220): Show |
1 | a0002c0004t0002g0150 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1229): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1221): Show |
1 | a0002c0004t0002g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1230): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1212): Show |
1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1221): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1230): Show |
1 | a0001c0003t0003g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1239): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1185): Show |
1 | a0002c0004t0002g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1194): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1209): Show |
1 | a0001c0003t0003g0079 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1218): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1219): Show |
1 | a0001c0003t0010g0082 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1228): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1230): Show |
1 | a0001c0003t0003g0087 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1239): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1228): Show |
1 | a0001c0003t0003g0086 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1237): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1243): Show |
1 | a0001c0003t0003g0084 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1252): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1207): Show |
1 | a0001c0003t0003g0081 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1216): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1207): Show |
1 | a0001c0003t0003g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1216): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1114): Show |
1 | a0001c0001t0001g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1123): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1126): Show |
1 | a0001c0001t0001g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1135): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1184): Show |
1 | a0001c0003t0003g0101 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1193): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1194): Show |
1 | a0001c0003t0003g0105 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1203): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1195): Show |
1 | a0001c0003t0003g0077 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1204): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1185): Show |
1 | a0001c0003t0003g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1194): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1196): Show |
1 | a0001c0003t0003g0104 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1205): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1114): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0183 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1123): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1079): Show |
1 | a0001c0001t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1088): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1133): Show |
1 | a0001c0001t0001g0170 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1142): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1124): Show |
1 | a0001c0001t0001g0233 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1133): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1218): Show |
1 | a0001c0003t0003g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1227): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1115): Show |
1 | a0001c0001t0001g0227 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1124): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1096): Show |
1 | a0001c0001t0001g0185 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1105): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1047): Show |
1 | a0001c0001t0001g0111 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1056): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1093): Show |
1 | a0001c0001t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1102): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1063): Show |
1 | a0001c0001t0001g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1072): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1109): Show |
1 | a0001c0001t0001g0142 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1118): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0004c0006t0001g0195 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0001c0001t0017g0159 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1092): Show |
1 | a0001c0001t0001g0205 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1101): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1102): Show |
1 | a0001c0001t0001g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1111): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1092): Show |
9 | a0001c0001t0001g0123 a0001c0001t0001g0160 a0001c0001t0001g0168 others(6): Show |
9 | HG00140.hp1 HG00280.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1101): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0001c0001t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
25 | a0001c0001t0001g0119 a0001c0001t0001g0138 a0001c0001t0001g0154 others(22): Show |
25 | HG01074.hp2 HG01515.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1114): Show |
17 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0129 others(14): Show |
17 | HG01192.hp1 HG01978.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1123): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1125): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0169 |
2 | HG02523.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1134): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1136): Show |
1 | a0001c0001t0001g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1145): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0001c0001t0001g0177 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1113): Show |
1 | a0001c0001t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1122): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1102): Show |
1 | a0001c0001t0001g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1111): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1115): Show |
1 | a0001c0001t0018g0122 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1124): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1101): Show |
1 | a0001c0001t0001g0222 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1110): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1122): Show |
1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1131): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1113): Show |
1 | a0001c0001t0001g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1122): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1113): Show |
1 | a0001c0001t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1122): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1114): Show |
1 | a0001c0001t0001g0141 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1123): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1136): Show |
1 | a0001c0001t0001g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1145): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1126): Show |
1 | a0001c0001t0001g0127 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1135): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1115): Show |
3 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0192 |
3 | NA18951.hp1 NA18966.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1124): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1126): Show |
1 | a0001c0001t0001g0164 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1135): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1137): Show |
1 | a0001c0001t0001g0163 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1146): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1105): Show |
1 | a0001c0001t0012g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1114): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1115): Show |
1 | a0001c0001t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1124): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0001c0001t0001g0181 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0001c0001t0001g0182 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0001c0001t0001g0194 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1111): Show |
1 | a0001c0001t0001g0174 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1120): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0006c0009t0001g0208 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1110): Show |
1 | a0001c0001t0001g0191 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1119): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1100): Show |
1 | a0001c0001t0001g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1109): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1114): Show |
1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1123): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1115): Show |
1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1124): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1218): Show |
1 | a0001c0001t0001g0173 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1227): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1116): Show |
1 | a0001c0001t0007g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1125): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1099): Show |
1 | a0001c0001t0005g0239 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1108): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1081): Show |
2 | a0001c0001t0005g0236 a0001c0001t0005g0241 |
2 | HG02615.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1090): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1093): Show |
3 | a0001c0001t0005g0238 a0001c0001t0005g0240 a0001c0001t0005g0242 |
3 | HG00639.hp1 HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1102): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1103): Show |
1 | a0001c0001t0019g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1112): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1122): Show |
1 | a0001c0002t0002g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1131): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1044): Show |
1 | a0001c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1053): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1081): Show |
1 | a0001c0002t0002g0014 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1090): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1152): Show |
1 | a0001c0002t0002g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1161): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1128): Show |
1 | a0001c0002t0002g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1137): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1125): Show |
1 | a0001c0002t0002g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1134): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1111): Show |
4 | a0001c0002t0002g0034 a0001c0002t0002g0044 a0001c0002t0002g0045 others(1): Show |
4 | HG01934.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1120): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1122): Show |
12 | a0001c0002t0002g0026 a0001c0002t0002g0030 a0001c0002t0002g0031 others(9): Show |
12 | HG01071.hp2 HG01346.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.927+4817_927+4818i others(1131): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1123): Show |
1 | a0001c0002t0002g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1132): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1137): Show |
1 | a0001c0002t0008g0053 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1146): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1140): Show |
1 | a0001c0002t0008g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1149): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1123): Show |
1 | a0001c0002t0002g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1132): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1128): Show |
1 | a0001c0002t0002g0058 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1137): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1110): Show |
1 | a0001c0002t0002g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1119): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1101): Show |
1 | a0001c0002t0002g0028 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1110): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1207): Show |
1 | a0001c0003t0003g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1216): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1123): Show |
1 | a0001c0002t0002g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1132): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1204): Show |
1 | a0002c0004t0002g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1213): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1122): Show |
1 | a0001c0002t0002g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1131): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGAA others(1080): Show |
1 | a0001c0001t0005g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1089): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AAGGGGGA others(1094): Show |
1 | a0003c0005t0001g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1103): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | AGGGGAAA others(1122): Show |
1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+4817_927+4818i others(1131): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251500 | A | G | 5 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0218 others(2): Show |
5 | HG02071.hp2 HG03704.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+4818T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251500 | |||||||
| chr10:97251501 | A | AGGGGAAA others(1107): Show |
1 | a0001c0001t0007g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.927+4816_927+4817i others(1116): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251501 | |||||||
| chr10:97251501 | A | AGGGGGAA others(1135): Show |
1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4816_927+4817i others(1144): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251501 | |||||||
| chr10:97251505 | T | A | 2 | a0001c0002t0002g0024 a0001c0002t0002g0048 |
2 | HG01074.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.927+4813A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251505 | |||||||
| chr10:97251505 | T | G | 228 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.927+4813A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251505 | |||||||
| chr10:97251505 | TAAGGGGA others(4): Show |
T | 1 | a0001c0003t0004g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.927+4802_927+4812d others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251505 | |||||||
| chr10:97251506 | A | AAAGG | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4811_927+4812i others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251506 | |||||||
| chr10:97251507 | A | AAGGAAGA others(451): Show |
1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4810_927+4811i others(460): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251507 | |||||||
| chr10:97251507 | A | AAGGAAGG others(3): Show |
6 | a0001c0001t0001g0112 a0001c0001t0001g0161 a0001c0001t0001g0197 others(3): Show |
6 | HG00597.hp1 HG01433.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4810_927+4811i others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251507 | |||||||
| chr10:97251507 | A | AAGGAAGG others(1202): Show |
1 | a0001c0003t0003g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.927+4810_927+4811i others(1211): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251507 | |||||||
| chr10:97251507 | A | AAGGAAGG others(1016): Show |
1 | a0001c0002t0002g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+4810_927+4811i others(1025): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251507 | |||||||
| chr10:97251507 | A | AAGGAAGG others(1122): Show |
1 | a0001c0001t0009g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.927+4810_927+4811i others(1131): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251507 | |||||||
| chr10:97251508 | G | A | 43 | a0001c0001t0002g0011 a0001c0001t0005g0235 a0001c0001t0005g0236 others(40): Show |
43 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.927+4810C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251508 | |||||||
| chr10:97251508 | G | GGAAGGAA others(1100): Show |
1 | a0001c0002t0002g0048 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.927+4809_927+4810i others(1109): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251508 | |||||||
| chr10:97251508 | G | GGGGGAGG others(1086): Show |
1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+4809_927+4810i others(1095): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251508 | |||||||
| chr10:97251509 | G | GGAAGGAA others(1068): Show |
1 | a0001c0001t0005g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.927+4808_927+4809i others(1077): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251509 | |||||||
| chr10:97251509 | G | GGAAGGAA others(1125): Show |
1 | a0001c0002t0002g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.927+4808_927+4809i others(1134): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251509 | |||||||
| chr10:97251510 | G | GAAGGAAG others(1118): Show |
1 | a0001c0002t0002g0056 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.927+4807_927+4808i others(1127): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251510 | |||||||
| chr10:97251511 | G | A | 41 | a0001c0001t0002g0011 a0001c0001t0005g0236 a0001c0001t0005g0237 others(38): Show |
41 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.927+4807C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251511 | |||||||
| chr10:97251511 | G | T | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4807C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251511 | |||||||
| chr10:97251513 | G | A | 2 | a0001c0001t0005g0235 a0001c0002t0002g0038 |
2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.927+4805C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251513 | |||||||
| chr10:97251514 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0153 |
2 | HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.927+4804C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251514 | |||||||
| chr10:97251517 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4801T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251517 | |||||||
| chr10:97251519 | G | A | 9 | a0001c0001t0001g0111 a0001c0001t0005g0239 a0001c0002t0002g0025 others(6): Show |
9 | HG00099.hp1 HG01884.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.927+4799C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251519 | |||||||
| chr10:97251522 | G | A | 14 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0161 others(11): Show |
14 | HG00099.hp1 HG00597.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.927+4796C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251522 | |||||||
| chr10:97251524 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4794C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251524 | |||||||
| chr10:97251530 | G | GGGGAGGG others(13): Show |
1 | a0002c0004t0002g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+4787_927+4788i others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251530 | |||||||
| chr10:97251532 | G | T | 1 | a0001c0001t0009g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.927+4786C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251532 | |||||||
| chr10:97251533 | G | A | 13 | a0001c0001t0001g0112 a0001c0001t0001g0161 a0001c0001t0001g0197 others(10): Show |
13 | HG00597.hp1 HG01071.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.927+4785C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251533 | |||||||
| chr10:97251539 | A | AAGGGG | 2 | a0001c0001t0001g0189 a0001c0001t0001g0198 |
2 | NA19012.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.927+4774_927+4778d others(7): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251539 | |||||||
| chr10:97251541 | G | GGGGAGGG others(13): Show |
1 | a0001c0003t0003g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.927+4776_927+4777i others(22): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251541 | |||||||
| chr10:97251544 | G | A | 13 | a0001c0001t0001g0112 a0001c0001t0001g0161 a0001c0001t0001g0197 others(10): Show |
13 | HG00597.hp1 HG01071.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.927+4774C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251544 | |||||||
| chr10:97251550 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+4768T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251550 | |||||||
| chr10:97251551 | A | AG | 3 | a0001c0001t0001g0130 a0001c0002t0002g0022 a0001c0002t0002g0056 |
3 | HG00558.hp1 HG02148.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.927+4766dupC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251551 | |||||||
| chr10:97251555 | A | AAAGGGAA others(106): Show |
1 | a0001c0002t0002g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+4762_927+4763i others(115): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251555 | |||||||
| chr10:97251555 | A | AAGGGAAA others(73): Show |
5 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(2): Show |
5 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+4762_927+4763i others(82): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251555 | |||||||
| chr10:97251555 | A | AAGGGAAA others(73): Show |
1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.927+4762_927+4763i others(82): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251555 | |||||||
| chr10:97251555 | A | AAGGGGAA others(835): Show |
1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.927+4762_927+4763i others(844): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251555 | |||||||
| chr10:97251555 | A | G | 170 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0113 others(167): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.927+4763T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251555 | |||||||
| chr10:97251556 | A | G | 2 | a0001c0001t0001g0130 a0001c0002t0002g0056 |
2 | HG00558.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.927+4762T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251556 | |||||||
| chr10:97251560 | G | A | 1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4758C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251560 | |||||||
| chr10:97251561 | A | AAGGGAAG others(1090): Show |
1 | a0001c0001t0001g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.927+4756_927+4757i others(1099): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251561 | |||||||
| chr10:97251562 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+4756T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251562 | |||||||
| chr10:97251566 | G | A | 50 | a0001c0001t0001g0161 a0001c0001t0001g0192 a0001c0001t0001g0197 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.927+4752C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251566 | |||||||
| chr10:97251566 | G | GAAGATGA others(95): Show |
1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4751_927+4752i others(104): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251566 | |||||||
| chr10:97251568 | G | A | 3 | a0001c0001t0007g0110 a0001c0002t0001g0002 a0001c0002t0002g0029 |
3 | HG02257.hp1 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.927+4750C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251568 | |||||||
| chr10:97251571 | G | A | 1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4747C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251571 | |||||||
| chr10:97251573 | A | G | 1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4745T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251573 | |||||||
| chr10:97251575 | G | A | 1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4743C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251575 | |||||||
| chr10:97251575 | G | C | 4 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0006 others(1): Show |
4 | HG01081.hp1 HG02717.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+4743C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251575 | |||||||
| chr10:97251577 | A | AAGGGGAA others(4): Show |
1 | a0001c0002t0001g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+4740_927+4741i others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251577 | |||||||
| chr10:97251577 | A | G | 59 | a0001c0001t0001g0111 a0001c0001t0001g0160 a0001c0001t0001g0161 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.927+4741T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251577 | |||||||
| chr10:97251579 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0001c0001t0006g0012 others(2): Show |
5 | HG01255.hp2 HG01975.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+4739C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251579 | |||||||
| chr10:97251580 | G | A | 3 | a0001c0001t0006g0012 a0001c0002t0001g0002 a0001c0002t0002g0029 |
3 | HG01255.hp2 HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.927+4738C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251580 | |||||||
| chr10:97251581 | G | GGAAGGGG others(22): Show |
1 | a0001c0001t0021g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+4736_927+4737i others(31): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251581 | |||||||
| chr10:97251583 | A | G | 2 | a0001c0002t0001g0002 a0001c0002t0002g0029 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.927+4735T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251583 | |||||||
| chr10:97251585 | A | C | 1 | a0001c0001t0009g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.927+4733T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251585 | |||||||
| chr10:97251585 | A | G | 12 | a0001c0001t0001g0146 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.927+4733T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251585 | |||||||
| chr10:97251587 | G | GGAAAGAA others(202): Show |
6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4730_927+4731i others(211): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251587 | |||||||
| chr10:97251588 | AAG | A | 2 | a0001c0002t0001g0002 a0001c0002t0002g0029 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.927+4728_927+4729d others(4): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251588 | |||||||
| chr10:97251589 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.927+4729T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251589 | |||||||
| chr10:97251592 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.927+4726T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251592 | |||||||
| chr10:97251593 | A | AGGGGGAG others(240): Show |
1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.927+4724_927+4725i others(249): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251593 | |||||||
| chr10:97251594 | G | A | 3 | a0001c0001t0006g0012 a0001c0002t0001g0002 a0001c0002t0002g0029 |
3 | HG01255.hp2 HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.927+4724C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251594 | |||||||
| chr10:97251595 | G | A | 2 | a0001c0002t0001g0002 a0001c0002t0002g0029 |
2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.927+4723C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251595 | |||||||
| chr10:97251595 | G | GAGAAAA | 2 | a0001c0001t0001g0161 a0001c0001t0001g0197 |
2 | HG01975.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.927+4722_927+4723i others(8): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251595 | |||||||
| chr10:97251598 | A | G | 1 | a0001c0001t0009g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.927+4720T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251598 | |||||||
| chr10:97251601 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.927+4717C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251601 | |||||||
| chr10:97251605 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.927+4713C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251605 | |||||||
| chr10:97251608 | G | A | 1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4710C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251608 | |||||||
| chr10:97251609 | A | AAGGGGAA others(4): Show |
1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.927+4708_927+4709i others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251609 | |||||||
| chr10:97251610 | AG | A | 4 | a0001c0001t0001g0153 a0001c0001t0007g0109 a0001c0001t0007g0110 others(1): Show |
4 | HG02258.hp2 HG02895.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+4707delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251610 | |||||||
| chr10:97251614 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4704T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251614 | |||||||
| chr10:97251618 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4700C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251618 | |||||||
| chr10:97251621 | A | T | 1 | a0001c0003t0003g0100 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.927+4697T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251621 | |||||||
| chr10:97251623 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4695T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251623 | |||||||
| chr10:97251624 | T | G | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4694A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251624 | |||||||
| chr10:97251627 | AG | A | 4 | a0001c0001t0021g0219 a0001c0002t0002g0024 a0001c0002t0002g0049 others(1): Show |
4 | HG01123.hp2 HG01496.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+4690delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251627 | |||||||
| chr10:97251631 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0001c0001t0006g0012 others(2): Show |
5 | HG01255.hp2 HG01975.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+4687C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251631 | |||||||
| chr10:97251636 | GA | G | 3 | a0001c0001t0001g0124 a0001c0001t0007g0109 a0002c0004t0002g0074 |
3 | HG02074.hp1 HG02683.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.927+4681delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251636 | |||||||
| chr10:97251641 | G | T | 1 | a0002c0004t0002g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+4677C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251641 | |||||||
| chr10:97251643 | A | AAGG | 11 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0001c0001t0002g0011 others(8): Show |
11 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.927+4674_927+4675i others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251643 | |||||||
| chr10:97251652 | AG | A | 4 | a0001c0001t0001g0174 a0001c0001t0001g0226 a0001c0002t0002g0037 others(1): Show |
4 | HG01952.hp2 NA18951.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+4665delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251652 | |||||||
| chr10:97251653 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4665C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251653 | |||||||
| chr10:97251659 | A | G | 11 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0001c0001t0002g0011 others(8): Show |
11 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.927+4659T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251659 | |||||||
| chr10:97251659 | AG | A | 3 | a0001c0001t0007g0109 a0001c0002t0002g0048 a0003c0005t0001g0114 |
3 | HG00423.hp2 HG01074.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.927+4658delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251659 | |||||||
| chr10:97251669 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.927+4649T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251669 | |||||||
| chr10:97251670 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.927+4648C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251670 | |||||||
| chr10:97251672 | G | C | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4646C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251672 | |||||||
| chr10:97251679 | A | G | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+4639T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251679 | |||||||
| chr10:97251680 | A | AAGGAAGG others(3): Show |
6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4637_927+4638i others(12): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251680 | |||||||
| chr10:97251680 | AG | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0194 a0001c0001t0001g0230 |
3 | HG00738.hp2 HG01255.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.927+4637delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251680 | |||||||
| chr10:97251681 | G | A | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+4637C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251681 | |||||||
| chr10:97251685 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.927+4633T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251685 | |||||||
| chr10:97251686 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4632T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251686 | |||||||
| chr10:97251687 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4631T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251687 | |||||||
| chr10:97251689 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0001c0001t0006g0012 others(2): Show |
5 | HG01255.hp2 HG01975.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.927+4629C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251689 | |||||||
| chr10:97251691 | AG | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0217 a0001c0001t0001g0226 |
3 | HG02083.hp1 HG02897.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.927+4626delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251691 | |||||||
| chr10:97251694 | G | A | 20 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(17): Show |
20 | HG00280.hp1 HG00673.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.927+4624C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251694 | |||||||
| chr10:97251696 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4622C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251696 | |||||||
| chr10:97251696 | G | GAGGGAGG others(936): Show |
1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+4621_927+4622i others(945): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251696 | |||||||
| chr10:97251696 | G | GAGGGAGG others(954): Show |
1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.927+4621_927+4622i others(963): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251696 | |||||||
| chr10:97251697 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0006g0012 a0001c0002t0001g0002 |
3 | HG01255.hp2 HG01975.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.927+4621C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251697 | |||||||
| chr10:97251698 | G | GA | 2 | a0001c0001t0007g0109 a0002c0004t0002g0178 |
2 | HG02895.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.927+4619_927+4620i others(3): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251698 | |||||||
| chr10:97251700 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+4618C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251700 | |||||||
| chr10:97251701 | A | C | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4617T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251701 | |||||||
| chr10:97251701 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.927+4617T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251701 | |||||||
| chr10:97251704 | G | A | 53 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.927+4614C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251704 | |||||||
| chr10:97251707 | A | AG | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4610dupC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251707 | |||||||
| chr10:97251707 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.927+4611T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251707 | |||||||
| chr10:97251711 | A | G | 1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.927+4607T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251711 | |||||||
| chr10:97251716 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4602C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251716 | |||||||
| chr10:97251718 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4600T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251718 | |||||||
| chr10:97251718 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.927+4600T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251718 | |||||||
| chr10:97251719 | G | T | 2 | a0001c0001t0001g0161 a0001c0002t0001g0002 |
2 | HG01975.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.927+4599C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251719 | |||||||
| chr10:97251722 | A | G | 1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.927+4596T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251722 | |||||||
| chr10:97251725 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0001c0002t0001g0002 |
3 | HG01975.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.927+4593C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251725 | |||||||
| chr10:97251727 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4591C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251727 | |||||||
| chr10:97251728 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+4590T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251728 | |||||||
| chr10:97251729 | A | ATGGAAGA others(323): Show |
1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4588_927+4589i others(332): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251729 | |||||||
| chr10:97251729 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+4589T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251729 | |||||||
| chr10:97251731 | G | A | 1 | a0001c0002t0002g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.927+4587C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251731 | |||||||
| chr10:97251731 | GA | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0223 a0001c0001t0001g0226 others(2): Show |
5 | HG00558.hp1 HG00597.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+4586delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251731 | |||||||
| chr10:97251732 | A | AAGGGTTG others(87): Show |
1 | a0001c0001t0001g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.927+4585_927+4586i others(96): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251732 | |||||||
| chr10:97251732 | A | G | 8 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(5): Show |
8 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+4586T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251732 | |||||||
| chr10:97251734 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0197 a0001c0002t0001g0002 others(1): Show |
4 | HG01975.hp2 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+4584T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251734 | |||||||
| chr10:97251738 | A | G | 2 | a0001c0001t0001g0230 a0001c0002t0002g0031 |
2 | HG01255.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.927+4580T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251738 | |||||||
| chr10:97251740 | G | A | 8 | a0001c0001t0001g0217 a0001c0001t0002g0011 a0001c0001t0006g0007 others(5): Show |
8 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+4578C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251740 | |||||||
| chr10:97251740 | G | GGAAGGGG others(513): Show |
1 | a0001c0001t0001g0161 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.927+4577_927+4578i others(522): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251740 | |||||||
| chr10:97251740 | G | GGAAGGGG others(1219): Show |
1 | a0001c0002t0001g0002 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+4577_927+4578i others(1228): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251740 | |||||||
| chr10:97251743 | G | A | 1 | a0001c0002t0002g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.927+4575C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251743 | |||||||
| chr10:97251745 | A | G | 2 | a0001c0001t0001g0112 a0001c0002t0002g0029 |
2 | HG01433.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.927+4573T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251745 | |||||||
| chr10:97251745 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.927+4573T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251745 | |||||||
| chr10:97251745 | AG | A | 3 | a0001c0001t0001g0124 a0001c0001t0005g0237 a0001c0003t0002g0063 |
3 | HG02683.hp2 HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.927+4572delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251745 | |||||||
| chr10:97251749 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.927+4569T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251749 | |||||||
| chr10:97251750 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.927+4568T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251750 | |||||||
| chr10:97251751 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4567C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251751 | |||||||
| chr10:97251752 | GA | G | 2 | a0001c0001t0001g0197 a0001c0002t0001g0002 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.927+4565delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251752 | |||||||
| chr10:97251753 | A | AGAAGGGA others(39): Show |
1 | a0001c0002t0002g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.927+4564_927+4565i others(48): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251753 | |||||||
| chr10:97251753 | A | G | 10 | a0001c0001t0001g0161 a0001c0001t0001g0217 a0001c0001t0002g0011 others(7): Show |
10 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.927+4565T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251753 | |||||||
| chr10:97251753 | AGAAGG | A | 30 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0025 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.927+4560_927+4564d others(7): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251753 | |||||||
| chr10:97251754 | G | A | 1 | a0001c0003t0003g0104 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.927+4564C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251754 | |||||||
| chr10:97251754 | G | GAAGGGAA others(170): Show |
1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4563_927+4564i others(179): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251754 | |||||||
| chr10:97251756 | A | AG | 8 | a0001c0001t0001g0161 a0001c0001t0002g0011 a0001c0001t0006g0007 others(5): Show |
8 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.927+4561dupC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251756 | |||||||
| chr10:97251756 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.927+4562T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251756 | |||||||
| chr10:97251761 | A | AG | 3 | a0001c0001t0006g0012 a0001c0001t0021g0219 a0001c0002t0002g0027 |
3 | HG01255.hp2 HG02602.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.927+4556dupC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251761 | |||||||
| chr10:97251761 | AG | A | 4 | a0001c0001t0001g0118 a0001c0002t0002g0021 a0002c0004t0002g0176 others(1): Show |
4 | HG00423.hp2 HG02735.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+4556delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251761 | |||||||
| chr10:97251763 | G | C | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+4555C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251763 | |||||||
| chr10:97251765 | A | G | 3 | a0001c0001t0007g0110 a0001c0002t0002g0035 a0001c0002t0002g0043 |
3 | HG00738.hp1 HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.927+4553T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251765 | |||||||
| chr10:97251765 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+4553T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251765 | |||||||
| chr10:97251766 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+4552T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251766 | |||||||
| chr10:97251767 | G | A | 4 | a0001c0001t0006g0012 a0001c0001t0007g0110 a0001c0002t0002g0035 others(1): Show |
4 | HG00738.hp1 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+4551C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251767 | |||||||
| chr10:97251768 | G | A | 1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4550C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251768 | |||||||
| chr10:97251772 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+4546T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251772 | |||||||
| chr10:97251777 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+4541T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251777 | |||||||
| chr10:97251777 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.927+4541T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251777 | |||||||
| chr10:97251778 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.927+4540C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251778 | |||||||
| chr10:97251782 | A | AAGATGAA others(834): Show |
1 | a0001c0002t0002g0029 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.927+4535_927+4536i others(843): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251782 | |||||||
| chr10:97251782 | A | AAGGGAAG others(493): Show |
1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.927+4535_927+4536i others(502): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251782 | |||||||
| chr10:97251782 | A | AAGGGTTG others(633): Show |
1 | a0001c0001t0001g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.927+4535_927+4536i others(642): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251782 | |||||||
| chr10:97251782 | A | ATGGGAAG others(794): Show |
1 | a0001c0001t0001g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.927+4535_927+4536i others(803): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251782 | |||||||
| chr10:97251783 | A | AGGG | 4 | a0001c0001t0001g0223 a0001c0002t0002g0027 a0001c0002t0002g0035 others(1): Show |
4 | HG00597.hp1 HG00738.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+4534_927+4535i others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251783 | |||||||
| chr10:97251784 | A | AAAGGGGA others(745): Show |
1 | a0001c0001t0001g0185 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.927+4533_927+4534i others(754): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AAGGAAGG others(510): Show |
6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.927+4533_927+4534i others(519): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AAGGGAAG others(729): Show |
1 | a0001c0001t0007g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.927+4533_927+4534i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AAGGGAAG others(737): Show |
1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.927+4533_927+4534i others(746): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AAGGGAAG others(719): Show |
1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.927+4533_927+4534i others(728): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AAGGGAAG others(727): Show |
1 | a0001c0001t0021g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+4533_927+4534i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AGGGAAGG others(612): Show |
1 | a0001c0002t0001g0002 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.927+4533_927+4534i others(621): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AGGGAAGG others(1311): Show |
1 | a0001c0001t0001g0161 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.927+4533_927+4534i others(1320): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AGGGGAAG others(732): Show |
1 | a0001c0003t0003g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.927+4533_927+4534i others(741): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AGGGGAAG others(726): Show |
1 | a0001c0001t0001g0184 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.927+4533_927+4534i others(735): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | AGGGGAAG others(727): Show |
1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.927+4533_927+4534i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | ATGGGGAA others(738): Show |
1 | a0001c0001t0001g0112 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.927+4533_927+4534i others(747): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251784 | A | G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0217 a0001c0001t0006g0012 others(1): Show |
4 | HG01255.hp2 HG02083.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+4534T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251784 | |||||||
| chr10:97251785 | A | AAGGGGAA others(721): Show |
1 | a0001c0001t0001g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.927+4532_927+4533i others(730): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251785 | |||||||
| chr10:97251786 | G | GGAAGGGC others(582): Show |
1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4531_927+4532i others(591): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251786 | |||||||
| chr10:97251789 | G | A | 22 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0001c0001t0001g0161 others(19): Show |
22 | HG00438.hp2 HG00673.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.927+4529C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGAAG others(723): Show |
1 | a0002c0004t0002g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(732): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGAAG others(725): Show |
1 | a0001c0001t0001g0155 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(734): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(733): Show |
1 | a0001c0003t0003g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(742): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(721): Show |
1 | a0001c0002t0001g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(730): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(731): Show |
1 | a0001c0001t0001g0218 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(740): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(747): Show |
1 | a0001c0002t0002g0027 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(756): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(735): Show |
1 | a0001c0002t0002g0043 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(744): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(736): Show |
1 | a0001c0002t0002g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(745): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(683): Show |
1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(692): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(734): Show |
1 | a0001c0001t0001g0230 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(743): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(747): Show |
1 | a0001c0001t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(756): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(721): Show |
1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(730): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(705): Show |
1 | a0001c0003t0004g0097 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(714): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(727): Show |
1 | a0001c0001t0001g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(735): Show |
1 | a0001c0001t0001g0194 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(744): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(751): Show |
1 | a0001c0002t0002g0038 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(760): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(720): Show |
1 | a0002c0004t0002g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(729): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(720): Show |
1 | a0002c0004t0002g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(729): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(720): Show |
1 | a0002c0004t0002g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(729): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(721): Show |
9 | a0002c0004t0002g0064 a0002c0004t0002g0065 a0002c0004t0002g0066 others(6): Show |
9 | HG00438.hp1 HG00597.hp2 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(730): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(725): Show |
1 | a0002c0004t0002g0070 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(734): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(718): Show |
1 | a0002c0004t0002g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(727): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(731): Show |
1 | a0001c0001t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(740): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(720): Show |
1 | a0002c0004t0002g0073 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(729): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(723): Show |
1 | a0002c0004t0002g0060 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(732): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(719): Show |
1 | a0002c0004t0002g0151 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(728): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(724): Show |
1 | a0001c0001t0001g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(733): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(728): Show |
1 | a0001c0001t0001g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(737): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(709): Show |
1 | a0002c0004t0002g0176 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(718): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(724): Show |
1 | a0001c0003t0003g0085 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(733): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(733): Show |
1 | a0001c0003t0003g0100 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(742): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(732): Show |
1 | a0001c0003t0003g0077 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(741): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(734): Show |
4 | a0001c0003t0003g0081 a0001c0003t0003g0101 a0001c0003t0003g0105 others(1): Show |
4 | HG02155.hp2 HG02523.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(743): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(738): Show |
9 | a0001c0003t0003g0084 a0001c0003t0003g0088 a0001c0003t0004g0062 others(6): Show |
9 | HG00280.hp1 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(747): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(737): Show |
1 | a0001c0003t0003g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(746): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(731): Show |
1 | a0001c0003t0003g0086 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(740): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(745): Show |
1 | a0001c0003t0003g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(754): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(754): Show |
1 | a0001c0003t0004g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(763): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0001c0003t0003g0079 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(712): Show |
1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(721): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(723): Show |
1 | a0001c0003t0003g0104 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(732): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(733): Show |
1 | a0001c0003t0003g0098 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(742): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(728): Show |
1 | a0001c0001t0001g0192 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(737): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(736): Show |
1 | a0001c0002t0002g0048 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(745): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(748): Show |
1 | a0001c0002t0002g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(757): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(758): Show |
1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(767): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(750): Show |
1 | a0001c0001t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(759): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(752): Show |
1 | a0001c0002t0002g0049 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(761): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(740): Show |
1 | a0001c0002t0002g0025 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(749): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(758): Show |
1 | a0001c0002t0002g0030 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(767): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(733): Show |
1 | a0001c0002t0001g0001 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(742): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(758): Show |
1 | a0001c0002t0002g0042 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(767): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(746): Show |
1 | a0001c0002t0002g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(755): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(741): Show |
1 | a0001c0002t0008g0053 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(750): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(746): Show |
1 | a0001c0002t0002g0037 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(755): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(747): Show |
13 | a0001c0002t0002g0028 a0001c0002t0002g0031 a0001c0002t0002g0032 others(10): Show |
13 | HG00140.hp2 HG01071.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(756): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(751): Show |
1 | a0001c0002t0002g0055 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(760): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(748): Show |
1 | a0001c0002t0002g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(757): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(752): Show |
1 | a0001c0002t0002g0022 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(761): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(734): Show |
2 | a0001c0002t0001g0003 a0001c0002t0016g0005 |
2 | HG01081.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.927+4528_927+4529i others(743): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(736): Show |
1 | a0001c0002t0002g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(745): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(716): Show |
1 | a0001c0002t0002g0021 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(725): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0001c0003t0003g0080 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(718): Show |
4 | a0001c0002t0002g0014 a0001c0002t0002g0016 a0001c0002t0002g0018 others(1): Show |
4 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(727): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(728): Show |
1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(737): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(717): Show |
1 | a0001c0002t0002g0017 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(726): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(724): Show |
1 | a0001c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(733): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(706): Show |
1 | a0001c0002t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(715): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(735): Show |
1 | a0001c0002t0002g0047 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(744): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(730): Show |
1 | a0001c0001t0001g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(739): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(739): Show |
1 | a0004c0006t0001g0195 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(748): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0001c0001t0001g0139 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(740): Show |
1 | a0001c0001t0001g0222 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(749): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(730): Show |
1 | a0001c0001t0001g0166 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(739): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(742): Show |
1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(751): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(730): Show |
1 | a0001c0001t0001g0115 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(739): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(731): Show |
1 | a0001c0001t0001g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(740): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0001c0001t0001g0224 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(739): Show |
1 | a0001c0001t0001g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(748): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(738): Show |
1 | a0001c0001t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(747): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(739): Show |
1 | a0007c0008t0001g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(748): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0001c0001t0001g0157 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0001c0001t0001g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(732): Show |
1 | a0001c0001t0001g0174 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(741): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(739): Show |
1 | a0001c0001t0001g0231 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(748): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(739): Show |
1 | a0001c0001t0001g0119 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(748): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(740): Show |
22 | a0001c0001t0001g0111 a0001c0001t0001g0187 a0001c0001t0001g0189 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(749): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(744): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0232 |
2 | HG02040.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.927+4528_927+4529i others(753): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(739): Show |
1 | a0001c0001t0001g0188 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(748): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(739): Show |
1 | a0001c0001t0001g0196 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(748): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(738): Show |
1 | a0001c0001t0017g0159 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(747): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(720): Show |
1 | a0001c0001t0001g0126 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(729): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(728): Show |
1 | a0001c0001t0001g0154 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(737): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(730): Show |
1 | a0001c0001t0001g0169 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(739): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(727): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0183 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.927+4528_927+4529i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(731): Show |
19 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0129 others(16): Show |
19 | HG00280.hp2 HG01074.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(740): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(735): Show |
1 | a0001c0001t0019g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(744): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(731): Show |
7 | a0001c0001t0001g0144 a0001c0001t0001g0152 a0001c0001t0001g0172 others(4): Show |
7 | HG01934.hp1 HG02074.hp2 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4528_927+4529i others(740): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(735): Show |
1 | a0001c0001t0001g0135 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(744): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(727): Show |
1 | a0001c0001t0001g0181 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(749): Show |
1 | a0001c0001t0001g0171 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(758): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(733): Show |
1 | a0001c0001t0001g0233 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(742): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(741): Show |
1 | a0001c0001t0001g0207 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(750): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(718): Show |
1 | a0001c0001t0001g0141 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(727): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(726): Show |
1 | a0001c0001t0001g0182 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(735): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(720): Show |
1 | a0001c0001t0001g0162 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(729): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(734): Show |
1 | a0001c0001t0001g0212 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(743): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(733): Show |
1 | a0001c0001t0009g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(742): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(727): Show |
1 | a0001c0001t0012g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(727): Show |
1 | a0001c0001t0001g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(727): Show |
1 | a0001c0001t0001g0190 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(736): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0001c0001t0001g0191 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(729): Show |
1 | a0003c0005t0001g0114 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(738): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(744): Show |
1 | a0001c0002t0002g0051 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(753): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(734): Show |
1 | a0001c0001t0001g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(743): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(726): Show |
1 | a0001c0002t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(735): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(742): Show |
1 | a0001c0002t0002g0057 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(751): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(724): Show |
1 | a0001c0003t0003g0087 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(733): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(713): Show |
1 | a0001c0001t0007g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(722): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(750): Show |
1 | a0001c0001t0005g0240 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(759): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(746): Show |
1 | a0001c0001t0005g0242 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(755): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(743): Show |
3 | a0001c0001t0005g0238 a0001c0001t0005g0239 a0001c0001t0005g0241 |
3 | HG00639.hp1 HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.927+4528_927+4529i others(752): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(738): Show |
1 | a0001c0001t0005g0235 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(747): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(738): Show |
1 | a0001c0001t0005g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(747): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(734): Show |
1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(743): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(688): Show |
1 | a0001c0002t0002g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(697): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(746): Show |
1 | a0001c0001t0005g0236 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(755): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGAA others(737): Show |
1 | a0001c0002t0002g0056 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(746): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GAAGGGGA others(730): Show |
1 | a0001c0001t0001g0142 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.927+4528_927+4529i others(739): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251789 | G | GTAGGGTT others(718): Show |
1 | a0002c0004t0002g0074 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.927+4528_927+4529i others(727): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251789 | |||||||
| chr10:97251792 | G | A | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4526C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251792 | |||||||
| chr10:97251792 | G | GGGAAGGG others(528): Show |
1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4525_927+4526i others(537): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251792 | |||||||
| chr10:97251793 | A | G | 2 | a0001c0001t0001g0226 a0001c0002t0002g0024 |
2 | HG01496.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.927+4525T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251793 | |||||||
| chr10:97251794 | A | AGGGGAAG others(645): Show |
1 | a0001c0003t0003g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.927+4523_927+4524i others(654): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251794 | |||||||
| chr10:97251794 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.927+4524T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251794 | |||||||
| chr10:97251796 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4522T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251796 | |||||||
| chr10:97251798 | G | GGAAGGGA others(712): Show |
1 | a0001c0001t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.927+4519_927+4520i others(721): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251798 | |||||||
| chr10:97251801 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.927+4517T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251801 | |||||||
| chr10:97251806 | C | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0226 |
2 | HG02622.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.927+4512G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251806 | |||||||
| chr10:97251807 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4511T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251807 | |||||||
| chr10:97251809 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4509G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251809 | |||||||
| chr10:97251809 | CA | C | 4 | a0001c0001t0001g0155 a0001c0002t0002g0024 a0001c0002t0002g0220 others(1): Show |
4 | HG01496.hp2 NA18965.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+4508delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251809 | |||||||
| chr10:97251814 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4504T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251814 | |||||||
| chr10:97251815 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4503G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251815 | |||||||
| chr10:97251816 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4502G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251816 | |||||||
| chr10:97251817 | A | T | 1 | a0001c0001t0001g0226 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.927+4501T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251817 | |||||||
| chr10:97251818 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4500G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251818 | |||||||
| chr10:97251819 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4499G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251819 | |||||||
| chr10:97251821 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4497A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251821 | |||||||
| chr10:97251822 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4496G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251822 | |||||||
| chr10:97251823 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4495G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251823 | |||||||
| chr10:97251824 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4494G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251824 | |||||||
| chr10:97251825 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4493G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251825 | |||||||
| chr10:97251826 | A | C | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.927+4492T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251826 | |||||||
| chr10:97251827 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4491T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251827 | |||||||
| chr10:97251828 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4490T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251828 | |||||||
| chr10:97251831 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4487A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251831 | |||||||
| chr10:97251833 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4485G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251833 | |||||||
| chr10:97251834 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4484A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251834 | |||||||
| chr10:97251835 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4483T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251835 | |||||||
| chr10:97251836 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4482A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251836 | |||||||
| chr10:97251841 | T | C | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4477A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251841 | |||||||
| chr10:97251842 | G | T | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4476C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251842 | |||||||
| chr10:97251842 | GA | G | 3 | a0001c0001t0001g0185 a0001c0001t0001g0223 a0001c0002t0002g0039 |
3 | HG00438.hp2 HG00597.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.927+4475delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251842 | |||||||
| chr10:97251843 | A | G | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4475T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251843 | |||||||
| chr10:97251845 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4473T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251845 | |||||||
| chr10:97251846 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4472T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251846 | |||||||
| chr10:97251849 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4469A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251849 | |||||||
| chr10:97251850 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4468T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251850 | |||||||
| chr10:97251851 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4467A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251851 | |||||||
| chr10:97251856 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4462T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251856 | |||||||
| chr10:97251858 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4460T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251858 | |||||||
| chr10:97251861 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4457C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251861 | |||||||
| chr10:97251863 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4455T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251863 | |||||||
| chr10:97251864 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4454G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251864 | |||||||
| chr10:97251869 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4449G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251869 | |||||||
| chr10:97251870 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4448A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251870 | |||||||
| chr10:97251871 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4447A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251871 | |||||||
| chr10:97251873 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4445C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251873 | |||||||
| chr10:97251874 | ACAAATAG others(20): Show |
A | 1 | a0001c0003t0003g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.927+4417_927+4443d others(29): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251874 | |||||||
| chr10:97251875 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4443G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251875 | |||||||
| chr10:97251879 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4439A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251879 | |||||||
| chr10:97251886 | AC | A | 2 | a0001c0002t0002g0024 a0001c0002t0002g0039 |
2 | HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.927+4431delG | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251886 | |||||||
| chr10:97251887 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4431G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251887 | |||||||
| chr10:97251888 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4430T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251888 | |||||||
| chr10:97251889 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4429A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251889 | |||||||
| chr10:97251890 | GA | G | 3 | a0001c0001t0001g0124 a0001c0002t0002g0024 a0001c0002t0002g0039 |
3 | HG01081.hp2 HG01496.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.927+4427delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251890 | |||||||
| chr10:97251892 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4426T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251892 | |||||||
| chr10:97251893 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4425T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251893 | |||||||
| chr10:97251895 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4423A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251895 | |||||||
| chr10:97251896 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4422G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251896 | |||||||
| chr10:97251897 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4421A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251897 | |||||||
| chr10:97251900 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4418C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251900 | |||||||
| chr10:97251904 | T | TTTCCGCT others(188): Show |
1 | a0001c0001t0001g0140 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927+4413_927+4414i others(197): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251904 | |||||||
| chr10:97251912 | T | A | 1 | a0001c0003t0003g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.927+4406A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251912 | |||||||
| chr10:97251997 | A | C | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.927+4321T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97251997 | |||||||
| chr10:97252013 | C | T | 1 | a0001c0002t0002g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.927+4305G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252013 | |||||||
| chr10:97252139 | GA | G | 3 | a0001c0001t0001g0156 a0001c0002t0002g0024 a0001c0002t0002g0039 |
3 | HG01074.hp2 HG01081.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.927+4178delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252139 | |||||||
| chr10:97252153 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4165G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252153 | |||||||
| chr10:97252266 | T | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+4052A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252266 | |||||||
| chr10:97252315 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.927+4003T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252315 | |||||||
| chr10:97252324 | C | CA | 39 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0205 others(36): Show |
39 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.927+3993dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252324 | |||||||
| chr10:97252324 | CA | C | 9 | a0001c0001t0001g0141 a0001c0001t0001g0187 a0001c0001t0001g0206 others(6): Show |
9 | HG00597.hp1 HG00673.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.927+3993delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252324 | |||||||
| chr10:97252344 | C | CG | 4 | a0001c0001t0001g0226 a0001c0002t0002g0220 a0002c0004t0002g0069 others(1): Show |
4 | HG04204.hp1 NA18954.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+3973dupC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252344 | |||||||
| chr10:97252351 | G | A | 1 | a0001c0002t0008g0052 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.927+3967C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252351 | |||||||
| chr10:97252353 | T | C | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.927+3965A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252353 | |||||||
| chr10:97252377 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+3941A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252377 | |||||||
| chr10:97252485 | G | A | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.927+3833C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252485 | |||||||
| chr10:97252643 | A | T | 1 | a0001c0001t0018g0122 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.927+3675T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252643 | |||||||
| chr10:97252644 | T | A | 1 | a0001c0001t0018g0122 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.927+3674A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252644 | |||||||
| chr10:97252748 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+3570G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252748 | |||||||
| chr10:97252834 | C | T | 1 | a0001c0001t0012g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.927+3484G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252834 | |||||||
| chr10:97252896 | T | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+3422A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252896 | |||||||
| chr10:97252962 | T | G | 1 | a0001c0001t0005g0236 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.927+3356A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252962 | |||||||
| chr10:97252997 | A | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+3321T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97252997 | |||||||
| chr10:97253184 | C | T | 8 | a0001c0001t0001g0225 a0001c0002t0001g0001 a0001c0002t0001g0002 others(5): Show |
8 | HG01081.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.927+3134G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253184 | |||||||
| chr10:97253379 | C | CAAAAAAA | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+2932_927+2938d others(9): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253379 | |||||||
| chr10:97253379 | CA | C | 22 | a0001c0001t0001g0124 a0001c0001t0001g0130 a0001c0001t0001g0134 others(19): Show |
22 | HG01074.hp1 HG01515.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.927+2938delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253379 | |||||||
| chr10:97253380 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.927+2938T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253380 | |||||||
| chr10:97253441 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+2877T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253441 | |||||||
| chr10:97253452 | A | G | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.927+2866T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253452 | |||||||
| chr10:97253504 | G | C | 1 | a0001c0001t0001g0233 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.927+2814C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253504 | |||||||
| chr10:97253513 | T | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+2805A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253513 | |||||||
| chr10:97253555 | A | G | 115 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.927+2763T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253555 | |||||||
| chr10:97253566 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.927+2752G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253566 | |||||||
| chr10:97253611 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+2707C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253611 | |||||||
| chr10:97253745 | T | A | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.927+2573A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253745 | |||||||
| chr10:97253825 | C | T | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.927+2493G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253825 | |||||||
| chr10:97253829 | T | C | 41 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(38): Show |
41 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.927+2489A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253829 | |||||||
| chr10:97253848 | A | G | 188 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.927+2470T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97253848 | |||||||
| chr10:97254347 | A | G | 2 | a0001c0002t0002g0020 a0001c0002t0002g0021 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.927+1971T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97254347 | |||||||
| chr10:97254515 | C | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1803G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97254515 | |||||||
| chr10:97254561 | G | T | 42 | a0001c0003t0002g0076 a0001c0003t0003g0077 a0001c0003t0003g0079 others(39): Show |
42 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.927+1757C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97254561 | |||||||
| chr10:97254818 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1500T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97254818 | |||||||
| chr10:97254968 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.927+1350T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97254968 | |||||||
| chr10:97255061 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+1257C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255061 | |||||||
| chr10:97255393 | G | A | 1 | a0001c0001t0020g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.927+925C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255393 | |||||||
| chr10:97255607 | A | G | 66 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(63): Show |
66 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.927+711T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255607 | |||||||
| chr10:97255630 | A | G | 1 | a0001c0001t0021g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.927+688T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255630 | |||||||
| chr10:97255659 | G | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.927+659C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255659 | |||||||
| chr10:97255817 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.927+501T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255817 | |||||||
| chr10:97255818 | C | A | 1 | a0001c0001t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.927+500G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255818 | |||||||
| chr10:97255873 | T | C | 1 | a0001c0002t0002g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.927+445A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97255873 | |||||||
| chr10:97256047 | T | C | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.927+271A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97256047 | |||||||
| chr10:97256048 | A | G | 1 | a0001c0002t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.927+270T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | 97256048 | |||||||
| chr10:97256426 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.841-22T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256426 | |||||||
| chr10:97256833 | G | A | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-429C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256833 | |||||||
| chr10:97256843 | C | G | 1 | a0004c0006t0001g0195 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.841-439G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256843 | |||||||
| chr10:97256849 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.841-445A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256849 | |||||||
| chr10:97256893 | G | A | 3 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0007g0108 |
3 | HG01496.hp1 HG02630.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.841-489C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256893 | |||||||
| chr10:97256903 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.841-499G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256903 | |||||||
| chr10:97256917 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0206 |
2 | HG02602.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.841-513A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256917 | |||||||
| chr10:97256922 | C | T | 226 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(223): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.841-518G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256922 | |||||||
| chr10:97256923 | C | T | 226 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(223): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.841-519G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256923 | |||||||
| chr10:97256933 | A | G | 1 | a0001c0002t0002g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.841-529T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97256933 | |||||||
| chr10:97257002 | T | C | 7 | a0001c0002t0002g0028 a0001c0002t0002g0034 a0001c0002t0002g0037 others(4): Show |
7 | HG01934.hp2 HG01952.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.841-598A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257002 | |||||||
| chr10:97257013 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.841-609G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257013 | |||||||
| chr10:97257038 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0171 |
2 | HG00673.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.841-634T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257038 | |||||||
| chr10:97257282 | CT | C | 198 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0113 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.841-879delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257282 | |||||||
| chr10:97257282 | CTT | C | 16 | a0001c0001t0001g0112 a0001c0001t0001g0174 a0001c0001t0001g0182 others(13): Show |
16 | HG00639.hp1 HG01433.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.841-880_841-879del others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257282 | |||||||
| chr10:97257335 | T | C | 1 | a0002c0004t0002g0067 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.841-931A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257335 | |||||||
| chr10:97257426 | T | A | 1 | a0001c0003t0004g0091 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.841-1022A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257426 | |||||||
| chr10:97257466 | C | T | 6 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(3): Show |
6 | HG00423.hp2 HG00609.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-1062G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257466 | |||||||
| chr10:97257496 | A | C | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.841-1092T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257496 | |||||||
| chr10:97257707 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0141 |
2 | HG00609.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.841-1303C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257707 | |||||||
| chr10:97257811 | CT | C | 117 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.841-1408delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257811 | |||||||
| chr10:97257817 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.841-1413A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257817 | |||||||
| chr10:97257850 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.841-1446T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257850 | |||||||
| chr10:97257952 | A | G | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.840+1450T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257952 | |||||||
| chr10:97257972 | G | A | 43 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(40): Show |
43 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.840+1430C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97257972 | |||||||
| chr10:97258082 | T | A | 1 | a0001c0002t0002g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.840+1320A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258082 | |||||||
| chr10:97258112 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.840+1290G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258112 | |||||||
| chr10:97258268 | G | T | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.840+1134C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258268 | |||||||
| chr10:97258390 | C | T | 1 | a0001c0001t0007g0108 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.840+1012G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258390 | |||||||
| chr10:97258434 | T | C | 2 | a0001c0002t0008g0052 a0001c0002t0008g0053 |
2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.840+968A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258434 | |||||||
| chr10:97258476 | C | T | 1 | a0001c0003t0003g0099 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.840+926G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258476 | |||||||
| chr10:97258616 | T | G | 1 | a0001c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.840+786A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258616 | |||||||
| chr10:97258749 | GAGACCCT others(21): Show |
G | 1 | a0001c0001t0019g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.840+625_840+652del others(28): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258749 | |||||||
| chr10:97258824 | T | TA | 20 | a0002c0004t0002g0060 a0002c0004t0002g0064 a0002c0004t0002g0065 others(17): Show |
20 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.840+577dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258824 | |||||||
| chr10:97258824 | TA | T | 10 | a0001c0001t0001g0184 a0001c0001t0001g0225 a0001c0001t0002g0011 others(7): Show |
10 | HG01071.hp1 HG01081.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.840+577delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258824 | |||||||
| chr10:97258834 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.840+568T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258834 | |||||||
| chr10:97258839 | A | G | 1 | a0002c0004t0002g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.840+563T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97258839 | |||||||
| chr10:97259001 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.840+401C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97259001 | |||||||
| chr10:97259084 | A | G | 1 | a0001c0002t0002g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.840+318T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97259084 | |||||||
| chr10:97259387 | C | T | 117 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.840+15G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 5/11 | chr10 | 97259387 | |||||||
| chr10:97259731 | G | GA | 41 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(38): Show |
41 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.614-104dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259731 | |||||||
| chr10:97259792 | T | C | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.614-164A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259792 | |||||||
| chr10:97259828 | C | CTGTTT | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-205_614-201dup others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259828 | |||||||
| chr10:97259828 | C | CTGTTTTG others(3): Show |
45 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(42): Show |
45 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.614-210_614-201dup others(10): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259828 | |||||||
| chr10:97259828 | C | CTGTTTTG others(8): Show |
127 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(124): Show |
127 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.614-215_614-201dup others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259828 | |||||||
| chr10:97259828 | CTGTTT | C | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.614-205_614-201del others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259828 | |||||||
| chr10:97259845 | G | GTTTTGTT others(9): Show |
1 | a0001c0001t0001g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.614-218_614-217ins others(16): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259845 | |||||||
| chr10:97259850 | T | G | 7 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(4): Show |
7 | HG01081.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.614-222A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259850 | |||||||
| chr10:97259928 | C | T | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.614-300G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97259928 | |||||||
| chr10:97260126 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.614-498G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260126 | |||||||
| chr10:97260139 | T | C | 181 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.614-511A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260139 | |||||||
| chr10:97260306 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18954.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.614-678C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260306 | |||||||
| chr10:97260314 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.614-686T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260314 | |||||||
| chr10:97260620 | C | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | NA18966.hp2 NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.614-992G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260620 | |||||||
| chr10:97260661 | A | G | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-1033T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260661 | |||||||
| chr10:97260824 | T | C | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.614-1196A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260824 | |||||||
| chr10:97260934 | T | TA | 9 | a0001c0001t0001g0207 a0001c0001t0001g0222 a0001c0001t0002g0011 others(6): Show |
9 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.614-1307dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260934 | |||||||
| chr10:97260934 | TA | T | 23 | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0125 others(20): Show |
23 | HG00140.hp1 HG00280.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.614-1307delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260934 | |||||||
| chr10:97260935 | A | T | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG02257.hp1 HG02258.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.614-1307T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260935 | |||||||
| chr10:97260936 | A | T | 1 | a0001c0002t0016g0005 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.614-1308T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97260936 | |||||||
| chr10:97261024 | A | AGAAAAAT others(6): Show |
7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1409_614-1397d others(15): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261024 | |||||||
| chr10:97261144 | A | C | 3 | a0001c0002t0002g0029 a0001c0002t0002g0030 a0001c0002t0002g0038 |
3 | HG02809.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.614-1516T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261144 | |||||||
| chr10:97261295 | AG | A | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.614-1668delC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261295 | |||||||
| chr10:97261306 | T | C | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.614-1678A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261306 | |||||||
| chr10:97261335 | TA | T | 45 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(42): Show |
45 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.614-1708delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261335 | |||||||
| chr10:97261478 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.614-1850G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261478 | |||||||
| chr10:97261817 | C | T | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+1603G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261817 | |||||||
| chr10:97261868 | A | G | 1 | a0001c0001t0006g0007 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.613+1552T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261868 | |||||||
| chr10:97261992 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.613+1428T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97261992 | |||||||
| chr10:97262037 | T | A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0042 a0001c0002t0002g0059 |
3 | HG00099.hp2 HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.613+1383A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262037 | |||||||
| chr10:97262091 | C | A | 1 | a0001c0002t0002g0031 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.613+1329G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262091 | |||||||
| chr10:97262111 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.613+1309C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262111 | |||||||
| chr10:97262179 | TA | T | 41 | a0001c0003t0002g0063 a0001c0003t0002g0076 a0001c0003t0003g0079 others(38): Show |
41 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.613+1240delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262179 | |||||||
| chr10:97262179 | TAA | T | 5 | a0001c0002t0002g0031 a0001c0003t0003g0077 a0001c0003t0003g0088 others(2): Show |
5 | HG00280.hp1 HG00558.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.613+1239_613+1240d others(4): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262179 | |||||||
| chr10:97262195 | AAAT | A | 42 | a0001c0001t0001g0130 a0001c0001t0001g0168 a0001c0001t0001g0184 others(39): Show |
42 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(39): Show |
intron_variant | MODIFIER | c.613+1222_613+1224d others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262195 | |||||||
| chr10:97262196 | AAT | A | 135 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(132): Show |
135 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.613+1222_613+1223d others(4): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262196 | |||||||
| chr10:97262196 | AATT | A | 6 | a0001c0001t0001g0154 a0001c0002t0002g0015 a0001c0002t0002g0017 others(3): Show |
6 | HG01515.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.613+1221_613+1223d others(5): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262196 | |||||||
| chr10:97262197 | A | T | 1 | a0001c0003t0003g0106 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.613+1223T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262197 | |||||||
| chr10:97262236 | C | T | 1 | a0001c0002t0002g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.613+1184G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262236 | |||||||
| chr10:97262356 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01255.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.613+1064T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262356 | |||||||
| chr10:97262684 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.613+736A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262684 | |||||||
| chr10:97262857 | T | G | 38 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.613+563A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262857 | |||||||
| chr10:97262865 | C | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.613+555G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262865 | |||||||
| chr10:97262977 | G | A | 20 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(17): Show |
20 | HG00280.hp1 HG00673.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.613+443C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97262977 | |||||||
| chr10:97263000 | C | G | 1 | a0001c0001t0005g0236 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.613+420G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97263000 | |||||||
| chr10:97263078 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0154 |
2 | HG01515.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.613+342T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97263078 | |||||||
| chr10:97263319 | A | G | 1 | a0002c0004t0002g0178 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.613+101T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 4/11 | chr10 | 97263319 | |||||||
| chr10:97263700 | C | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-71G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97263700 | |||||||
| chr10:97263789 | G | T | 181 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(178): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.404-160C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97263789 | |||||||
| chr10:97264038 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.404-409C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264038 | |||||||
| chr10:97264099 | C | T | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.404-470G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264099 | |||||||
| chr10:97264142 | G | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-513C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264142 | |||||||
| chr10:97264225 | A | G | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.404-596T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264225 | |||||||
| chr10:97264310 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+516C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264310 | |||||||
| chr10:97264397 | G | A | 56 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.403+429C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264397 | |||||||
| chr10:97264452 | CA | C | 185 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.403+373delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264452 | |||||||
| chr10:97264726 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.403+100A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264726 | |||||||
| chr10:97264815 | A | G | 56 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.403+11T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264815 | |||||||
| chr10:97264817 | T | C | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.403+9A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3/11 | chr10 | 97264817 | |||||||
| chr10:97265066 | G | A | 20 | a0002c0004t0002g0060 a0002c0004t0002g0064 a0002c0004t0002g0065 others(17): Show |
20 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.323-160C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/11 | chr10 | 97265066 | |||||||
| chr10:97265187 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.323-281G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/11 | chr10 | 97265187 | |||||||
| chr10:97265392 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.322+468C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/11 | chr10 | 97265392 | |||||||
| chr10:97265462 | A | G | 188 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(185): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.322+398T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/11 | chr10 | 97265462 | |||||||
| chr10:97265498 | C | T | 1 | a0002c0004t0002g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.322+362G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/11 | chr10 | 97265498 | |||||||
| chr10:97265854 | T | A | 117 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(114): Show |
splice_region_variant&intron_variant | LOW | c.322+6A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2/11 | chr10 | 97265854 | |||||||
| chr10:97266138 | G | A | 1 | a0001c0002t0002g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.57-13C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266138 | |||||||
| chr10:97266355 | T | C | 136 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(133): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.57-230A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266355 | |||||||
| chr10:97266395 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.57-270C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266395 | |||||||
| chr10:97266430 | A | G | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-305T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266430 | |||||||
| chr10:97266752 | G | A | 125 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(122): Show |
125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.57-627C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266752 | |||||||
| chr10:97266852 | G | A | 8 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(5): Show |
8 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.57-727C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266852 | |||||||
| chr10:97266880 | T | C | 1 | a0001c0003t0003g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.57-755A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266880 | |||||||
| chr10:97266943 | G | A | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57-818C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266943 | |||||||
| chr10:97266969 | C | T | 1 | a0001c0002t0002g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57-844G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97266969 | |||||||
| chr10:97267338 | T | C | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.57-1213A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97267338 | |||||||
| chr10:97267472 | C | T | 1 | a0001c0002t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.57-1347G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97267472 | |||||||
| chr10:97267603 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-1478G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97267603 | |||||||
| chr10:97267824 | T | C | 38 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.57-1699A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97267824 | |||||||
| chr10:97267924 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-1799A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97267924 | |||||||
| chr10:97267962 | T | A | 42 | a0001c0003t0002g0076 a0001c0003t0003g0077 a0001c0003t0003g0079 others(39): Show |
42 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.57-1837A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97267962 | |||||||
| chr10:97268053 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-1928C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268053 | |||||||
| chr10:97268066 | ACT | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.57-1943_57-1942del others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268066 | |||||||
| chr10:97268374 | C | T | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-2249G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268374 | |||||||
| chr10:97268637 | G | A | 79 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(76): Show |
79 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.57-2512C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268637 | |||||||
| chr10:97268642 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-2517A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268642 | |||||||
| chr10:97268738 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.57-2613G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268738 | |||||||
| chr10:97268763 | C | T | 4 | a0001c0002t0002g0028 a0001c0002t0002g0037 a0001c0002t0002g0044 others(1): Show |
4 | HG01952.hp2 HG01975.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-2638G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268763 | |||||||
| chr10:97268793 | C | T | 35 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(32): Show |
35 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.57-2668G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268793 | |||||||
| chr10:97268970 | T | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-2845A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97268970 | |||||||
| chr10:97269038 | G | T | 7 | a0001c0001t0005g0236 a0001c0001t0005g0237 a0001c0001t0005g0238 others(4): Show |
7 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.57-2913C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97269038 | |||||||
| chr10:97269255 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.57-3130C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97269255 | |||||||
| chr10:97269463 | G | A | 230 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.57-3338C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97269463 | |||||||
| chr10:97269521 | A | G | 143 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(140): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.57-3396T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97269521 | |||||||
| chr10:97269857 | T | G | 1 | a0001c0002t0002g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57-3732A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97269857 | |||||||
| chr10:97269860 | A | G | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.57-3735T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97269860 | |||||||
| chr10:97270125 | CTAACACA | C | 14 | a0001c0001t0001g0130 a0001c0001t0001g0134 a0001c0001t0001g0135 others(11): Show |
14 | HG00597.hp1 HG01934.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-4007_57-4001del others(7): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97270125 | |||||||
| chr10:97270721 | G | A | 7 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0238 others(4): Show |
7 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.57-4596C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97270721 | |||||||
| chr10:97270797 | C | G | 37 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.57-4672G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97270797 | |||||||
| chr10:97271235 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.57-5110C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97271235 | |||||||
| chr10:97271827 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.57-5702C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97271827 | |||||||
| chr10:97271830 | G | A | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57-5705C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97271830 | |||||||
| chr10:97271928 | T | C | 142 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(139): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.57-5803A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97271928 | |||||||
| chr10:97271990 | T | A | 1 | a0001c0002t0002g0032 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.57-5865A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97271990 | |||||||
| chr10:97272131 | C | CT | 169 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(166): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.57-6007dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272131 | |||||||
| chr10:97272131 | C | CTT | 18 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0221 others(15): Show |
18 | HG00609.hp1 HG00639.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.57-6008_57-6007dup others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272131 | |||||||
| chr10:97272131 | C | CTTTTTTT others(21): Show |
2 | a0001c0001t0002g0011 a0001c0001t0006g0007 |
2 | HG01071.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.57-6007_57-6006ins others(28): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272131 | |||||||
| chr10:97272131 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0006g0010 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.57-6007_57-6006ins others(29): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272131 | |||||||
| chr10:97272131 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0006g0009 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.57-6007_57-6006ins others(31): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272131 | |||||||
| chr10:97272198 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.57-6073G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272198 | |||||||
| chr10:97272412 | C | T | 1 | a0001c0001t0021g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.57-6287G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272412 | |||||||
| chr10:97272414 | C | T | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.57-6289G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272414 | |||||||
| chr10:97272575 | T | A | 1 | a0001c0001t0005g0237 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.57-6450A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272575 | |||||||
| chr10:97272618 | G | A | 56 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.57-6493C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272618 | |||||||
| chr10:97272832 | T | G | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.57-6707A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272832 | |||||||
| chr10:97272842 | G | GT | 5 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(2): Show |
5 | HG01175.hp2 HG02630.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-6718dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97272842 | |||||||
| chr10:97273003 | G | A | 1 | a0002c0004t0002g0068 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.57-6878C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273003 | |||||||
| chr10:97273030 | C | T | 38 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.57-6905G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273030 | |||||||
| chr10:97273082 | C | T | 1 | a0001c0003t0010g0082 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.57-6957G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273082 | |||||||
| chr10:97273086 | C | T | 131 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(128): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.57-6961G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273086 | |||||||
| chr10:97273120 | G | A | 7 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0238 others(4): Show |
7 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.57-6995C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273120 | |||||||
| chr10:97273132 | G | A | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57-7007C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273132 | |||||||
| chr10:97273211 | G | A | 56 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(53): Show |
56 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.57-7086C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273211 | |||||||
| chr10:97273256 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-7131T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273256 | |||||||
| chr10:97273368 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-7243T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273368 | |||||||
| chr10:97273383 | G | A | 1 | a0001c0002t0002g0014 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.57-7258C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273383 | |||||||
| chr10:97273390 | T | C | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57-7265A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273390 | |||||||
| chr10:97273446 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-7321T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273446 | |||||||
| chr10:97273483 | TC | T | 5 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(2): Show |
5 | HG01071.hp1 HG01192.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-7359delG | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273483 | |||||||
| chr10:97273484 | C | CT | 124 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.57-7360dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273484 | |||||||
| chr10:97273484 | C | CTT | 9 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0001t0001g0166 others(6): Show |
9 | HG00423.hp2 HG00609.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.57-7361_57-7360dup others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273484 | |||||||
| chr10:97273484 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0014g0013 a0005c0007t0006g0008 |
3 | HG01123.hp1 HG01358.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.57-7359G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273484 | |||||||
| chr10:97273484 | CT | C | 37 | a0001c0002t0001g0006 a0001c0002t0002g0022 a0001c0002t0002g0023 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.57-7360delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273484 | |||||||
| chr10:97273962 | T | TAC | 54 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(51): Show |
54 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.57-7839_57-7838dup others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97273962 | |||||||
| chr10:97274151 | T | C | 14 | a0002c0004t0002g0060 a0002c0004t0002g0064 a0002c0004t0002g0065 others(11): Show |
14 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.57-8026A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274151 | |||||||
| chr10:97274323 | G | A | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-8198C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274323 | |||||||
| chr10:97274464 | T | TA | 19 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(16): Show |
19 | HG01081.hp1 HG01175.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.57-8340dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274464 | |||||||
| chr10:97274464 | TA | T | 8 | a0001c0001t0001g0189 a0001c0001t0002g0011 a0001c0001t0006g0007 others(5): Show |
8 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.57-8340delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274464 | |||||||
| chr10:97274482 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.57-8357A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274482 | |||||||
| chr10:97274500 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.57-8375C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274500 | |||||||
| chr10:97274528 | C | G | 194 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.57-8403G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274528 | |||||||
| chr10:97274535 | G | C | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-8410C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274535 | |||||||
| chr10:97274592 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-8467C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274592 | |||||||
| chr10:97274651 | A | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0232 |
3 | HG02040.hp2 NA18954.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.57-8526T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274651 | |||||||
| chr10:97274807 | T | C | 1 | a0001c0002t0001g0004 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.57-8682A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274807 | |||||||
| chr10:97274825 | A | C | 1 | a0001c0001t0007g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.57-8700T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97274825 | |||||||
| chr10:97275005 | C | T | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57-8880G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97275005 | |||||||
| chr10:97275066 | C | A | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57-8941G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97275066 | |||||||
| chr10:97275078 | G | A | 37 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.57-8953C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97275078 | |||||||
| chr10:97275106 | TTAAAGCA others(2527): Show |
T | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.57-11515_57-8982de others(1): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97275106 | |||||||
| chr10:97275808 | C | T | 1 | a0001c0003t0004g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.57-9683G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97275808 | |||||||
| chr10:97276521 | C | A | 1 | a0001c0003t0004g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.57-10396G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97276521 | |||||||
| chr10:97276679 | A | G | 6 | a0001c0003t0004g0062 a0001c0003t0004g0091 a0001c0003t0004g0092 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.57-10554T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97276679 | |||||||
| chr10:97277627 | T | A | 6 | a0001c0003t0004g0062 a0001c0003t0004g0091 a0001c0003t0004g0092 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.57-11502A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97277627 | |||||||
| chr10:97277829 | T | G | 18 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 others(15): Show |
18 | HG01081.hp1 HG01175.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.57-11704A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97277829 | |||||||
| chr10:97277948 | A | T | 1 | a0001c0001t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.57-11823T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97277948 | |||||||
| chr10:97278199 | C | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02486.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.57-12074G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278199 | |||||||
| chr10:97278422 | T | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-12297A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278422 | |||||||
| chr10:97278457 | T | G | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.57-12332A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278457 | |||||||
| chr10:97278591 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.57-12466T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278591 | |||||||
| chr10:97278603 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.57-12478A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278603 | |||||||
| chr10:97278741 | T | C | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-12616A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278741 | |||||||
| chr10:97278805 | G | A | 37 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.57-12680C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278805 | |||||||
| chr10:97278811 | TA | T | 199 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.57-12687delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278811 | |||||||
| chr10:97278856 | C | G | 6 | a0002c0004t0002g0148 a0002c0004t0002g0149 a0002c0004t0002g0150 others(3): Show |
6 | HG03017.hp1 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-12731G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97278856 | |||||||
| chr10:97279142 | T | C | 2 | a0001c0002t0002g0022 a0001c0002t0002g0055 |
2 | HG01346.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.57-13017A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279142 | |||||||
| chr10:97279170 | T | C | 1 | a0001c0002t0002g0036 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57-13045A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279170 | |||||||
| chr10:97279176 | C | T | 195 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.57-13051G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279176 | |||||||
| chr10:97279415 | G | A | 1 | a0001c0002t0002g0036 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.56+13157C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279415 | |||||||
| chr10:97279494 | G | A | 1 | a0001c0002t0002g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56+13078C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279494 | |||||||
| chr10:97279495 | T | TTTTG | 194 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.56+13073_56+13076d others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279495 | |||||||
| chr10:97279578 | A | G | 1 | a0001c0002t0001g0002 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.56+12994T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279578 | |||||||
| chr10:97279667 | T | C | 1 | a0001c0003t0004g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.56+12905A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279667 | |||||||
| chr10:97279670 | T | A | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.56+12902A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279670 | |||||||
| chr10:97279673 | T | C | 8 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0001g0172 others(5): Show |
8 | HG01934.hp1 HG02074.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.56+12899A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279673 | |||||||
| chr10:97279706 | T | C | 1 | a0001c0003t0004g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.56+12866A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279706 | |||||||
| chr10:97279979 | C | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+12593G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97279979 | |||||||
| chr10:97280212 | C | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+12360G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97280212 | |||||||
| chr10:97280334 | G | A | 4 | a0002c0004t0002g0072 a0002c0004t0002g0073 a0002c0004t0002g0075 others(1): Show |
4 | HG00558.hp2 HG02004.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+12238C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97280334 | |||||||
| chr10:97280596 | T | C | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.56+11976A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97280596 | |||||||
| chr10:97280696 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+11876A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97280696 | |||||||
| chr10:97280823 | G | A | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+11749C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97280823 | |||||||
| chr10:97281036 | T | C | 4 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(1): Show |
4 | NA18966.hp2 NA18978.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+11536A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97281036 | |||||||
| chr10:97281219 | C | CA | 34 | a0001c0002t0002g0027 a0001c0003t0002g0063 a0001c0003t0003g0077 others(31): Show |
34 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.56+11352dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97281219 | |||||||
| chr10:97281219 | CAAAAAA | C | 121 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(118): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.56+11347_56+11352d others(8): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97281219 | |||||||
| chr10:97281219 | CAAAAAAA | C | 21 | a0001c0001t0002g0011 a0001c0001t0005g0235 a0001c0001t0005g0236 others(18): Show |
21 | HG00639.hp1 HG01071.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.56+11346_56+11352d others(9): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97281219 | |||||||
| chr10:97281307 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+11265T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97281307 | |||||||
| chr10:97281410 | G | T | 38 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.56+11162C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97281410 | |||||||
| chr10:97281604 | C | A | 194 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.56+10968G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97281604 | |||||||
| chr10:97282114 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+10458G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282114 | |||||||
| chr10:97282377 | A | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+10195T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282377 | |||||||
| chr10:97282386 | A | G | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.56+10186T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282386 | |||||||
| chr10:97282450 | T | C | 1 | a0001c0001t0006g0012 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.56+10122A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282450 | |||||||
| chr10:97282506 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG00597.hp1 HG02015.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.56+10066A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282506 | |||||||
| chr10:97282520 | G | GA | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+10051dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282520 | |||||||
| chr10:97282551 | CTGTT | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+10017_56+10020d others(6): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282551 | |||||||
| chr10:97282709 | G | A | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+9863C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282709 | |||||||
| chr10:97282822 | T | TTTTTTTA others(6): Show |
8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+9749_56+9750ins others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282822 | |||||||
| chr10:97282823 | A | C | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+9749T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282823 | |||||||
| chr10:97282825 | G | T | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+9747C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282825 | |||||||
| chr10:97282839 | CT | C | 168 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(165): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.56+9732delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282839 | |||||||
| chr10:97282839 | CTTT | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+9730_56+9732del others(3): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282839 | |||||||
| chr10:97282844 | T | C | 1 | a0001c0003t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56+9728A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282844 | |||||||
| chr10:97282845 | T | C | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.56+9727A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282845 | |||||||
| chr10:97282870 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.56+9702G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97282870 | |||||||
| chr10:97283288 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.56+9284G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283288 | |||||||
| chr10:97283334 | A | G | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56+9238T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283334 | |||||||
| chr10:97283435 | T | G | 2 | a0001c0002t0002g0020 a0001c0002t0002g0021 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.56+9137A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283435 | |||||||
| chr10:97283440 | G | C | 37 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.56+9132C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283440 | |||||||
| chr10:97283568 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.56+9004A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283568 | |||||||
| chr10:97283831 | T | TA | 47 | a0001c0001t0001g0146 a0001c0001t0007g0109 a0001c0001t0019g0136 others(44): Show |
47 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.56+8740dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283831 | |||||||
| chr10:97283831 | T | TAA | 128 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(125): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.56+8739_56+8740dup others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283831 | |||||||
| chr10:97283831 | T | TAAA | 12 | a0001c0001t0001g0130 a0001c0001t0001g0179 a0001c0001t0001g0214 others(9): Show |
12 | HG00639.hp1 HG01884.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.56+8738_56+8740dup others(3): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283831 | |||||||
| chr10:97283831 | TA | T | 8 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(5): Show |
8 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.56+8740delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283831 | |||||||
| chr10:97283869 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+8703A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283869 | |||||||
| chr10:97283932 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+8640G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283932 | |||||||
| chr10:97283940 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+8632A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283940 | |||||||
| chr10:97283998 | A | C | 1 | a0001c0001t0001g0135 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.56+8574T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97283998 | |||||||
| chr10:97284047 | C | A | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+8525G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284047 | |||||||
| chr10:97284208 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+8364A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284208 | |||||||
| chr10:97284248 | A | G | 231 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(228): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.56+8324T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284248 | |||||||
| chr10:97284272 | G | A | 1 | a0001c0003t0003g0105 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.56+8300C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284272 | |||||||
| chr10:97284282 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.56+8290G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284282 | |||||||
| chr10:97284291 | T | A | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+8281A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284291 | |||||||
| chr10:97284316 | T | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+8256A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284316 | |||||||
| chr10:97284451 | C | T | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+8121G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284451 | |||||||
| chr10:97284469 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0183 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.56+8103A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284469 | |||||||
| chr10:97284470 | A | G | 1 | a0001c0001t0012g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.56+8102T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284470 | |||||||
| chr10:97284623 | G | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+7949C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284623 | |||||||
| chr10:97284855 | C | CT | 28 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0138 others(25): Show |
28 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.56+7716dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284855 | |||||||
| chr10:97284855 | CT | C | 16 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(13): Show |
16 | HG00558.hp1 HG00639.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.56+7716delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284855 | |||||||
| chr10:97284855 | CTT | C | 5 | a0001c0001t0002g0011 a0001c0001t0006g0009 a0001c0001t0006g0010 others(2): Show |
5 | HG01192.hp2 HG01255.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+7715_56+7716del others(2): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97284855 | |||||||
| chr10:97285165 | G | A | 1 | a0001c0001t0020g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.56+7407C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285165 | |||||||
| chr10:97285190 | A | G | 1 | a0001c0002t0002g0036 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.56+7382T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285190 | |||||||
| chr10:97285310 | T | A | 2 | a0001c0002t0001g0001 a0001c0002t0016g0005 |
2 | HG01081.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.56+7262A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285310 | |||||||
| chr10:97285400 | C | T | 1 | a0001c0002t0002g0035 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56+7172G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285400 | |||||||
| chr10:97285473 | C | T | 44 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.56+7099G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285473 | |||||||
| chr10:97285506 | C | CA | 124 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.56+7065_56+7066ins others(1): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285506 | |||||||
| chr10:97285519 | C | CT | 38 | a0001c0001t0001g0134 a0001c0001t0018g0122 a0001c0002t0001g0001 others(35): Show |
38 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.56+7052dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285519 | |||||||
| chr10:97285519 | CT | C | 11 | a0001c0001t0001g0184 a0001c0001t0001g0231 a0001c0001t0002g0011 others(8): Show |
11 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+7052delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285519 | |||||||
| chr10:97285631 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+6941G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285631 | |||||||
| chr10:97285668 | A | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+6904T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285668 | |||||||
| chr10:97285799 | C | T | 37 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.56+6773G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285799 | |||||||
| chr10:97285880 | C | T | 195 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.56+6692G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285880 | |||||||
| chr10:97285955 | G | A | 1 | a0002c0004t0002g0075 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.56+6617C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97285955 | |||||||
| chr10:97286119 | C | T | 69 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(66): Show |
69 | HG00280.hp2 HG00597.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.56+6453G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286119 | |||||||
| chr10:97286133 | A | G | 124 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.56+6439T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286133 | |||||||
| chr10:97286134 | G | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+6438C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286134 | |||||||
| chr10:97286168 | T | TCAGATAT others(6): Show |
7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+6403_56+6404ins others(13): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286168 | |||||||
| chr10:97286186 | C | CT | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+6385dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286186 | |||||||
| chr10:97286424 | T | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+6148A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286424 | |||||||
| chr10:97286647 | T | C | 1 | a0001c0002t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.56+5925A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286647 | |||||||
| chr10:97286695 | C | T | 1 | a0001c0001t0009g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.56+5877G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286695 | |||||||
| chr10:97286765 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.56+5807C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286765 | |||||||
| chr10:97286816 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02040.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.56+5756G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286816 | |||||||
| chr10:97286853 | T | C | 5 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(2): Show |
5 | HG01175.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+5719A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286853 | |||||||
| chr10:97286936 | G | GT | 15 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(12): Show |
15 | HG01071.hp1 HG01123.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+5635dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286936 | |||||||
| chr10:97286954 | G | A | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.56+5618C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97286954 | |||||||
| chr10:97287233 | G | C | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+5339C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97287233 | |||||||
| chr10:97287284 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.56+5288T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97287284 | |||||||
| chr10:97287402 | C | T | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+5170G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97287402 | |||||||
| chr10:97287612 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02083.hp1 NA18994.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.56+4960C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97287612 | |||||||
| chr10:97287756 | A | G | 35 | a0001c0003t0003g0077 a0001c0003t0003g0079 a0001c0003t0003g0080 others(32): Show |
35 | HG00280.hp1 HG00438.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.56+4816T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97287756 | |||||||
| chr10:97287906 | T | C | 15 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(12): Show |
15 | HG01071.hp1 HG01123.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+4666A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97287906 | |||||||
| chr10:97287955 | G | A | 135 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(132): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.56+4617C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97287955 | |||||||
| chr10:97288010 | C | T | 1 | a0001c0003t0002g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.56+4562G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288010 | |||||||
| chr10:97288355 | G | A | 1 | a0001c0001t0021g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56+4217C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288355 | |||||||
| chr10:97288405 | C | A | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+4167G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288405 | |||||||
| chr10:97288409 | G | A | 1 | a0001c0002t0002g0220 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.56+4163C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288409 | |||||||
| chr10:97288435 | T | C | 15 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(12): Show |
15 | HG01071.hp1 HG01123.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+4137A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288435 | |||||||
| chr10:97288450 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+4122G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288450 | |||||||
| chr10:97288505 | G | A | 143 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(140): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.56+4067C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288505 | |||||||
| chr10:97288506 | G | A | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+4066C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288506 | |||||||
| chr10:97288559 | G | A | 1 | a0001c0002t0001g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.56+4013C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288559 | |||||||
| chr10:97288561 | C | G | 1 | a0001c0002t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.56+4011G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288561 | |||||||
| chr10:97288608 | A | C | 16 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(13): Show |
16 | HG00639.hp1 HG01175.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.56+3964T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288608 | |||||||
| chr10:97288670 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.56+3902G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288670 | |||||||
| chr10:97288809 | C | CT | 20 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(17): Show |
20 | HG00423.hp2 HG00609.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.56+3762dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288809 | |||||||
| chr10:97288809 | C | CTTT | 6 | a0001c0002t0002g0015 a0001c0002t0002g0016 a0001c0002t0002g0017 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+3760_56+3762dup others(3): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288809 | |||||||
| chr10:97288809 | CT | C | 12 | a0001c0001t0001g0107 a0001c0001t0001g0221 a0001c0001t0001g0222 others(9): Show |
12 | HG00639.hp1 HG01358.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.56+3762delA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288809 | |||||||
| chr10:97288809 | CTTT | C | 9 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0100 others(6): Show |
9 | HG00673.hp2 HG02015.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.56+3760_56+3762del others(3): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288809 | |||||||
| chr10:97288835 | G | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+3737C>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97288835 | |||||||
| chr10:97289115 | C | CT | 16 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0118 others(13): Show |
16 | HG00423.hp2 HG01175.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.56+3456dupA | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289115 | |||||||
| chr10:97289140 | A | G | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56+3432T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289140 | |||||||
| chr10:97289217 | C | T | 1 | a0001c0003t0015g0061 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56+3355G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289217 | |||||||
| chr10:97289253 | T | G | 143 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(140): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.56+3319A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289253 | |||||||
| chr10:97289478 | C | A | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+3094G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289478 | |||||||
| chr10:97289656 | A | G | 194 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(191): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.56+2916T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289656 | |||||||
| chr10:97289660 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+2912G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289660 | |||||||
| chr10:97289789 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.56+2783C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289789 | |||||||
| chr10:97289809 | G | A | 37 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.56+2763C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289809 | |||||||
| chr10:97289852 | T | TA | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0002t0002g0016 others(3): Show |
6 | HG00597.hp1 HG02015.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.56+2719dupT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289852 | |||||||
| chr10:97289852 | TA | T | 39 | a0001c0001t0002g0011 a0001c0001t0005g0235 a0001c0001t0005g0236 others(36): Show |
39 | HG00438.hp1 HG00558.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.56+2719delT | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289852 | |||||||
| chr10:97289905 | T | G | 11 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
11 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+2667A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97289905 | |||||||
| chr10:97290000 | T | G | 6 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(3): Show |
6 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+2572A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97290000 | |||||||
| chr10:97290045 | A | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG00099.hp1 HG01433.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.56+2527T>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97290045 | |||||||
| chr10:97290257 | CGCTGACT others(11): Show |
C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+2297_56+2314del others(18): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97290257 | |||||||
| chr10:97290407 | T | C | 1 | a0001c0002t0002g0058 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.56+2165A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97290407 | |||||||
| chr10:97290513 | G | A | 44 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.56+2059C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97290513 | |||||||
| chr10:97290591 | G | A | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.56+1981C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97290591 | |||||||
| chr10:97290767 | C | T | 3 | a0001c0001t0007g0108 a0001c0001t0007g0109 a0001c0001t0007g0110 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.56+1805G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97290767 | |||||||
| chr10:97291001 | T | G | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01175.hp1 HG02280.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+1571A>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291001 | |||||||
| chr10:97291052 | A | C | 1 | a0002c0004t0002g0060 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.56+1520T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291052 | |||||||
| chr10:97291077 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.56+1495G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291077 | |||||||
| chr10:97291138 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG01255.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.56+1434C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291138 | |||||||
| chr10:97291194 | A | C | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+1378T>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291194 | |||||||
| chr10:97291574 | G | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+998C>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291574 | |||||||
| chr10:97291755 | G | A | 1 | a0001c0002t0002g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.56+817C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291755 | |||||||
| chr10:97291778 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.56+794A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97291778 | |||||||
| chr10:97292003 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.56+569A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292003 | |||||||
| chr10:97292065 | T | A | 187 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0112 others(184): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.56+507A>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292065 | |||||||
| chr10:97292083 | C | T | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+489G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292083 | |||||||
| chr10:97292112 | CGA | C | 37 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0024 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.56+458_56+459delTC | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292112 | |||||||
| chr10:97292149 | T | C | 15 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(12): Show |
15 | HG01071.hp1 HG01123.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+423A>G | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292149 | |||||||
| chr10:97292231 | A | G | 15 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(12): Show |
15 | HG01071.hp1 HG01123.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.56+341T>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292231 | |||||||
| chr10:97292253 | C | T | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.56+319G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292253 | |||||||
| chr10:97292328 | G | A | 1 | a0001c0001t0020g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.56+244C>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292328 | |||||||
| chr10:97292340 | C | G | 5 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(2): Show |
5 | HG01175.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+232G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292340 | |||||||
| chr10:97292375 | C | A | 1 | a0001c0001t0014g0013 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.56+197G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292375 | |||||||
| chr10:97292407 | C | G | 7 | a0001c0001t0002g0011 a0001c0001t0006g0007 a0001c0001t0006g0009 others(4): Show |
7 | HG01071.hp1 HG01123.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+165G>C | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292407 | |||||||
| chr10:97292413 | C | A | 8 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+159G>T | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292413 | |||||||
| chr10:97292479 | C | T | 6 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(3): Show |
6 | HG01081.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.56+93G>A | ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 1/11 | chr10 | 97292479 |