Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54848 |
| ensemblid | ENSG00000236699.9 |
| hgncid | 25968 |
| symbol | ARHGEF38 |
| name | Rho guanine nucleotide exchange factor 38 |
| refseq_nuc | NM_001242729.2 |
| refseq_prot | NP_001229658.1 |
| ensembl_nuc | ENST00000420470.3 |
| ensembl_prot | ENSP00000416125.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 105552620 |
| end | 105680914 |
| strand | + |
| ver | v1.2 |
| region | chr4:105552620-105680914 |
| region5000 | chr4:105547620-105685914 |
| regionname0 | ARHGEF38_chr4_105552620_105680914 |
| regionname5000 | ARHGEF38_chr4_105547620_105685914 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 777 | 152 | 56 | 34 | 44 | 6 | 11 | 24 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0002 | 0/0 | 777 | 17 | 8 | 4 | 2 | 2 | 1 | 2 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0003 | 0/0 | 777 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0004 | 0/0 | 777 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0005 | 0/0 | 777 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0006 | 0/0 | 777 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0007 | 0/0 | 673 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(668): Show |
chr4 | 105547620 | 105685914 |
| a0008 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0009 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| a0010 | 0/1 | 777 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | MEPKE others(772): Show |
chr4 | 105547620 | 105685914 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2331 | 113 | 32 | 24 | 41 | 4 | 11 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0002 | 0/0 | 2331 | 19 | 18 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0004 | 0/0 | 2331 | 8 | 0 | 8 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0007 | 0/0 | 2331 | 4 | 2 | 1 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0008 | 0/0 | 2331 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0013 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0018 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0019 | 0/0 | 2331 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0020 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0001c0022 | 0/0 | 2331 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0002c0003 | 0/0 | 2331 | 11 | 2 | 4 | 2 | 2 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0002c0005 | 0/0 | 2331 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0002c0012 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0003c0006 | 0/0 | 2331 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0003c0015 | 0/0 | 2331 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0003c0023 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0004c0011 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0004c0021 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0005c0009 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0006c0010 | 0/0 | 2331 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0007c0014 | 0/0 | 2019 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2014): Show |
chr4 | 105547620 | 105685914 | ||
| a0008c0017 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0009c0016 | 0/0 | 2331 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 | ||
| a0010c0024 | 0/1 | 2331 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | ATGGA others(2326): Show |
chr4 | 105547620 | 105685914 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5457 | 59 | 6 | 16 | 29 | 2 | 5 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0002 | 0/0 | 5456 | 26 | 9 | 4 | 10 | 0 | 3 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0003 | 0/0 | 5452 | 14 | 11 | 2 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0004 | 0/0 | 5452 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0005 | 0/0 | 5457 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0007 | 0/0 | 5452 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0011 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0012 | 0/0 | 5455 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5450): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0014 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0016 | 0/0 | 5457 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0017 | 0/0 | 5457 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0018 | 0/0 | 5457 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0001t0019 | 0/0 | 5457 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0002t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0002t0002 | 0/0 | 5456 | 6 | 5 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0001c0002t0003 | 0/0 | 5452 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0002t0007 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0002t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0002t0009 | 0/0 | 5449 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5444): Show |
chr4 | 105547620 | 105685914 |
| a0001c0002t0011 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0004t0005 | 0/0 | 5457 | 6 | 0 | 6 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0004t0009 | 0/0 | 5449 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5444): Show |
chr4 | 105547620 | 105685914 |
| a0001c0007t0002 | 0/0 | 5456 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0001c0007t0007 | 0/0 | 5452 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0007t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0007t0015 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0008t0006 | 0/0 | 5457 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0013t0006 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0018t0001 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0001c0019t0004 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0020t0004 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0001c0022t0001 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0002c0003t0001 | 0/0 | 5457 | 4 | 0 | 3 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0002c0003t0004 | 0/0 | 5452 | 4 | 0 | 0 | 1 | 2 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0002c0003t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0002c0003t0010 | 0/0 | 5454 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5449): Show |
chr4 | 105547620 | 105685914 |
| a0002c0003t0012 | 0/0 | 5455 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5450): Show |
chr4 | 105547620 | 105685914 |
| a0002c0005t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0002c0005t0002 | 0/0 | 5456 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0002c0012t0006 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0002c0012t0010 | 0/0 | 5454 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5449): Show |
chr4 | 105547620 | 105685914 |
| a0003c0006t0001 | 0/0 | 5457 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0003c0006t0003 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0003c0015t0003 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0003c0023t0020 | 0/0 | 5450 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5445): Show |
chr4 | 105547620 | 105685914 |
| a0004c0011t0002 | 0/0 | 5456 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0004c0021t0002 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0005c0009t0013 | 0/0 | 5456 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5451): Show |
chr4 | 105547620 | 105685914 |
| a0006c0010t0021 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0006c0010t0022 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| a0007c0014t0005 | 0/0 | 5145 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5140): Show |
chr4 | 105547620 | 105685914 |
| a0008c0017t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0009c0016t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5452): Show |
chr4 | 105547620 | 105685914 |
| a0010c0024t0004 | 0/1 | 5452 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | AGTCA others(5447): Show |
chr4 | 105547620 | 105685914 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0012g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0014g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0016g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0017g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0018g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0001t0019g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0011g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0009g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0009g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0007t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0007t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0007t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0007t0015g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0008t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0008t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0008t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0013t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0018t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0019t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0020t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0022t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0010g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0003t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0005t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0005t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0005t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0012t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0012t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0006t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0006t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0015t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0023t0020g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0011t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0011t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0021t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0005c0009t0013g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0006c0010t0021g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0006c0010t0022g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0007c0014t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0008c0017t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0009c0016t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0010c0024t0004g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0007 | t0007 | g0087 | EUR | FIN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0085 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0036 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00735 | hp2 | a0001 | c0004 | t0009 | g0105 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00741 | hp2 | a0001 | c0004 | t0005 | g0086 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01070 | hp1 | a0003 | c0015 | t0003 | g0019 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0094 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01074 | hp2 | a0001 | c0001 | t0016 | g0168 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01109 | hp1 | a0001 | c0004 | t0005 | g0043 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01109 | hp2 | a0001 | c0007 | t0002 | g0093 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01167 | hp1 | a0001 | c0004 | t0005 | g0034 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01175 | hp2 | a0001 | c0004 | t0005 | g0042 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01243 | hp1 | a0001 | c0004 | t0009 | g0103 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01243 | hp2 | a0002 | c0003 | t0010 | g0139 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01346 | hp2 | a0001 | c0004 | t0005 | g0038 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01516 | hp1 | a0002 | c0003 | t0004 | g0136 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01517 | hp1 | a0002 | c0003 | t0004 | g0137 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01517 | hp2 | a0001 | c0001 | t0018 | g0037 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01884 | hp2 | a0001 | c0013 | t0006 | g0022 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01981 | hp1 | a0001 | c0004 | t0005 | g0035 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0159 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02004 | hp1 | a0007 | c0014 | t0005 | g0005 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02027 | hp1 | a0001 | c0022 | t0001 | g0053 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02071 | hp1 | a0001 | c0020 | t0004 | g0061 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02145 | hp1 | a0008 | c0017 | t0001 | g0131 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02145 | hp2 | a0002 | c0005 | t0002 | g0027 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CDX | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CDX | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02257 | hp2 | a0003 | c0023 | t0020 | g0114 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02300 | hp2 | a0001 | c0019 | t0004 | g0041 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02451 | hp2 | a0002 | c0003 | t0012 | g0129 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02523 | hp1 | a0001 | c0018 | t0001 | g0162 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02615 | hp1 | a0002 | c0003 | t0008 | g0102 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02622 | hp1 | a0003 | c0006 | t0001 | g0144 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0107 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02717 | hp2 | a0002 | c0005 | t0001 | g0008 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02723 | hp2 | a0001 | c0008 | t0006 | g0157 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02818 | hp1 | a0001 | c0007 | t0008 | g0045 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02818 | hp2 | a0003 | c0006 | t0003 | g0143 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02886 | hp2 | a0001 | c0001 | t0011 | g0091 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02896 | hp1 | a0004 | c0011 | t0002 | g0004 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0033 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02897 | hp1 | a0004 | c0011 | t0002 | g0003 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0032 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02922 | hp2 | a0005 | c0009 | t0013 | g0001 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02965 | hp1 | a0009 | c0016 | t0001 | g0021 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02965 | hp2 | a0002 | c0005 | t0002 | g0013 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0020 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03130 | hp2 | a0006 | c0010 | t0021 | g0012 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03139 | hp1 | a0004 | c0021 | t0002 | g0089 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0030 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03195 | hp1 | a0001 | c0001 | t0012 | g0092 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0025 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0029 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03453 | hp2 | a0001 | c0002 | t0009 | g0184 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03486 | hp1 | a0003 | c0006 | t0001 | g0175 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03516 | hp1 | a0003 | c0006 | t0001 | g0150 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0023 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03579 | hp1 | a0006 | c0010 | t0022 | g0006 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03710 | hp1 | a0001 | c0001 | t0017 | g0133 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03834 | hp1 | a0002 | c0003 | t0004 | g0054 | SAS | BEB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03834 | hp2 | a0001 | c0001 | t0019 | g0062 | SAS | BEB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0109 | SAS | STU | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18522 | hp1 | a0001 | c0008 | t0006 | g0076 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0178 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18990 | hp2 | a0002 | c0003 | t0004 | g0098 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19030 | hp1 | a0001 | c0002 | t0009 | g0016 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19030 | hp2 | a0005 | c0009 | t0013 | g0001 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19043 | hp1 | a0002 | c0005 | t0002 | g0007 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20129 | hp1 | a0002 | c0012 | t0006 | g0015 | AFR | ASW | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | ASW | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0099 | EUR | TSI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | GIH | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0026 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02559 | hp1 | a0001 | c0008 | t0006 | g0077 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02559 | hp2 | a0002 | c0012 | t0010 | g0024 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03471 | hp2 | a0001 | c0007 | t0015 | g0106 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG06807 | hp1 | a0001 | c0002 | t0011 | g0028 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| homoSapiens | chm13v2 | a0010 | c0024 | t0004 | g0160 | REF | REF | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0126 | REF | REF | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105552826 | T | C | 2 | a0005 a0006 |
4 | HG02922.hp2 HG03130.hp2 HG03579.hp1 others(1): Show |
missense_variant | MODERATE | c.61T>C | p.Phe21Leu | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/14 | 207/5457 | 61/2334 | 21/777 | chr4 | 105552826 | |||
| chr4:105589313 | A | G | 1 | a0002 | 17 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(14): Show |
missense_variant | MODERATE | c.262A>G | p.Met88Val | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/14 | 408/5457 | 262/2334 | 88/777 | chr4 | 105589313 | |||
| chr4:105645214 | G | T | 1 | a0004 | 3 | HG02896.hp1 HG02897.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.701G>T | p.Gly234Val | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/14 | 847/5457 | 701/2334 | 234/777 | chr4 | 105645214 | |||
| chr4:105645321 | G | C | 4 | a0003 a0005 a0008 others(1): Show |
10 | HG01070.hp1 HG02145.hp1 HG02257.hp2 others(7): Show |
missense_variant | MODERATE | c.808G>C | p.Asp270His | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/14 | 954/5457 | 808/2334 | 270/777 | chr4 | 105645321 | |||
| chr4:105656685 | ATTATAGG others(5274): Show |
A | 1 | a0007 | 1 | HG02004.hp1 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1233+970_1545+2607 others(3): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr4 | 105656685 | ||||||
| chr4:105659073 | T | A | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1253T>A | p.Leu418His | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/14 | 1399/5457 | 1253/2334 | 418/777 | chr4 | 105659073 | |||
| chr4:105659183 | A | G | 7 | a0001 a0002 a0003 others(4): Show |
112 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(109): Show |
missense_variant | MODERATE | c.1363A>G | p.Thr455Ala | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/14 | 1509/5457 | 1363/2334 | 455/777 | chr4 | 105659183 | |||
| chr4:105667456 | A | G | 1 | a0008 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.1901A>G | p.Tyr634Cys | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/14 | 2047/5457 | 1901/2334 | 634/777 | chr4 | 105667456 | |||
| chr4:105667692 | G | C | 1 | a0009 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2137G>C | p.Val713Leu | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/14 | 2283/5457 | 2137/2334 | 713/777 | chr4 | 105667692 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105552921 | G | A | 10 | a0001c0002 a0001c0013 a0002c0005 others(7): Show |
35 | HG01070.hp1 HG01884.hp2 HG02004.hp1 others(32): Show |
synonymous_variant | LOW | c.156G>A | p.Arg52Arg | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/14 | 302/5457 | 156/2334 | 52/777 | chr4 | 105552921 | |||
| chr4:105552942 | A | G | 1 | a0009c0016 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.177A>G | p.Glu59Glu | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/14 | 323/5457 | 177/2334 | 59/777 | chr4 | 105552942 | |||
| chr4:105613443 | A | G | 4 | a0001c0007 a0002c0005 a0003c0015 others(1): Show |
10 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(7): Show |
synonymous_variant | LOW | c.444A>G | p.Ser148Ser | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/14 | 590/5457 | 444/2334 | 148/777 | chr4 | 105613443 | |||
| chr4:105631010 | G | T | 1 | a0001c0022 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.621G>T | p.Leu207Leu | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/14 | 767/5457 | 621/2334 | 207/777 | chr4 | 105631010 | |||
| chr4:105645269 | C | T | 1 | a0001c0020 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.756C>T | p.Cys252Cys | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/14 | 902/5457 | 756/2334 | 252/777 | chr4 | 105645269 | |||
| chr4:105648653 | C | T | 1 | a0001c0019 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.979C>T | p.Leu327Leu | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/14 | 1125/5457 | 979/2334 | 327/777 | chr4 | 105648653 | |||
| chr4:105654112 | A | G | 2 | a0001c0004 a0007c0014 |
9 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(6): Show |
synonymous_variant | LOW | c.1056A>G | p.Leu352Leu | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/14 | 1202/5457 | 1056/2334 | 352/777 | chr4 | 105654112 | |||
| chr4:105667302 | A | C | 2 | a0001c0008 a0001c0013 |
4 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
synonymous_variant | LOW | c.1863A>C | p.Thr621Thr | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 12/14 | 2009/5457 | 1863/2334 | 621/777 | chr4 | 105667302 | |||
| chr4:105667559 | C | T | 1 | a0001c0018 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.2004C>T | p.Phe668Phe | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/14 | 2150/5457 | 2004/2334 | 668/777 | chr4 | 105667559 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105552705 | C | T | 3 | a0005c0009t0013 a0006c0010t0021 a0006c0010t0022 |
4 | HG02922.hp2 HG03130.hp2 HG03579.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-61C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/14 | 61 | chr4 | 105552705 | ||||||
| chr4:105678470 | TACC | T | 2 | a0002c0003t0010 a0002c0012t0010 |
2 | HG01243.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*538_*540delCCA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 538 | INFO_REALIGN_3_PRIME | chr4 | 105678470 | |||||
| chr4:105678517 | TTA | T | 3 | a0001c0001t0012 a0002c0003t0012 a0003c0023t0020 |
3 | HG02257.hp2 HG02451.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*584_*585delAT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 584 | INFO_REALIGN_3_PRIME | chr4 | 105678517 | |||||
| chr4:105678657 | C | T | 5 | a0001c0001t0005 a0001c0002t0009 a0001c0004t0005 others(2): Show |
12 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 720 | chr4 | 105678657 | ||||||
| chr4:105678816 | GT | G | 8 | a0001c0001t0002 a0001c0001t0014 a0001c0002t0002 others(5): Show |
42 | HG00408.hp2 HG00438.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*894delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 894 | INFO_REALIGN_3_PRIME | chr4 | 105678816 | |||||
| chr4:105678945 | A | C | 1 | a0001c0001t0019 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1008A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 1008 | chr4 | 105678945 | ||||||
| chr4:105679126 | T | A | 1 | a0001c0007t0015 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1189T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 1189 | chr4 | 105679126 | ||||||
| chr4:105679181 | A | C | 5 | a0001c0001t0005 a0001c0002t0009 a0001c0004t0005 others(2): Show |
12 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1244A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 1244 | chr4 | 105679181 | ||||||
| chr4:105679465 | T | A | 4 | a0001c0001t0007 a0001c0002t0007 a0001c0007t0007 others(1): Show |
5 | HG00280.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1528T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 1528 | chr4 | 105679465 | ||||||
| chr4:105679681 | G | A | 9 | a0001c0001t0002 a0001c0001t0011 a0001c0002t0002 others(6): Show |
43 | HG00408.hp2 HG00438.hp2 HG01109.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1744G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 1744 | chr4 | 105679681 | ||||||
| chr4:105679737 | T | C | 3 | a0001c0008t0006 a0001c0013t0006 a0002c0012t0006 |
5 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1800T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 1800 | chr4 | 105679737 | ||||||
| chr4:105679902 | T | C | 1 | a0001c0001t0016 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1965T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 1965 | chr4 | 105679902 | ||||||
| chr4:105680012 | A | C | 4 | a0001c0001t0008 a0001c0002t0008 a0001c0007t0008 others(1): Show |
4 | HG02615.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2075A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2075 | chr4 | 105680012 | ||||||
| chr4:105680183 | CCTTT | C | 2 | a0001c0002t0009 a0001c0004t0009 |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2251_*2254delCTTT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2251 | INFO_REALIGN_3_PRIME | chr4 | 105680183 | |||||
| chr4:105680479 | C | T | 4 | a0001c0001t0004 a0001c0019t0004 a0001c0020t0004 others(1): Show |
9 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2542C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2542 | chr4 | 105680479 | ||||||
| chr4:105680548 | CAGTT | C | 2 | a0001c0002t0009 a0001c0004t0009 |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2613_*2616delGTTA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2613 | INFO_REALIGN_3_PRIME | chr4 | 105680548 | |||||
| chr4:105680767 | CCTAAA | C | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(11): Show |
39 | HG00280.hp1 HG01069.hp1 HG01070.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2836_*2840delCTAA others(1): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2836 | INFO_REALIGN_3_PRIME | chr4 | 105680767 | |||||
| chr4:105680796 | C | G | 1 | a0001c0001t0018 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2859C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2859 | chr4 | 105680796 | ||||||
| chr4:105680832 | T | C | 10 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0017 others(7): Show |
44 | HG00408.hp2 HG00438.hp2 HG01109.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2895T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2895 | chr4 | 105680832 | ||||||
| chr4:105680903 | T | C | 4 | a0001c0001t0004 a0001c0019t0004 a0001c0020t0004 others(1): Show |
9 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2966T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2966 | chr4 | 105680903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:105553068 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.196+107C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553068 | |||||||
| chr4:105553169 | C | T | 1 | a0001c0002t0009g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196+208C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553169 | |||||||
| chr4:105553216 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.196+255A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553216 | |||||||
| chr4:105553419 | A | C | 20 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(17): Show |
20 | HG00408.hp2 HG00609.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.196+458A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553419 | |||||||
| chr4:105553442 | A | T | 2 | a0001c0001t0001g0161 a0001c0018t0001g0162 |
2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.196+481A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553442 | |||||||
| chr4:105553569 | G | C | 16 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(13): Show |
17 | HG02004.hp1 HG02451.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+608G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553569 | |||||||
| chr4:105553687 | C | T | 37 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0163 others(34): Show |
37 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.196+726C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553687 | |||||||
| chr4:105553818 | C | A | 155 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.196+857C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553818 | |||||||
| chr4:105553886 | G | A | 155 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.196+925G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553886 | |||||||
| chr4:105553920 | A | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196+959A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553920 | |||||||
| chr4:105553935 | C | T | 20 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(17): Show |
20 | HG00408.hp2 HG00609.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.196+974C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553935 | |||||||
| chr4:105554070 | G | A | 1 | a0003c0006t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.196+1109G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554070 | |||||||
| chr4:105554120 | A | T | 2 | a0001c0002t0002g0113 a0002c0003t0001g0159 |
2 | HG01981.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+1159A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554120 | |||||||
| chr4:105554378 | T | C | 155 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.196+1417T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554378 | |||||||
| chr4:105554465 | G | T | 155 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.196+1504G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554465 | |||||||
| chr4:105554491 | A | T | 120 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(117): Show |
120 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.196+1530A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554491 | |||||||
| chr4:105554756 | C | CAT | 155 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(152): Show |
156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.196+1796_196+1797i others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105554756 | ||||||
| chr4:105554760 | A | C | 4 | a0001c0002t0003g0030 a0001c0002t0003g0031 a0001c0002t0003g0032 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+1799A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554760 | |||||||
| chr4:105554837 | C | A | 120 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(117): Show |
120 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.196+1876C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554837 | |||||||
| chr4:105554942 | A | G | 120 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(117): Show |
120 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.196+1981A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554942 | |||||||
| chr4:105554944 | G | GT | 39 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0001t0001g0163 others(36): Show |
39 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.196+1989dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105554944 | ||||||
| chr4:105554953 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+1992G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554953 | |||||||
| chr4:105554986 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.196+2025T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554986 | |||||||
| chr4:105555105 | T | C | 157 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(154): Show |
158 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.196+2144T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105555105 | |||||||
| chr4:105555108 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.196+2147G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105555108 | |||||||
| chr4:105555246 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196+2285G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105555246 | |||||||
| chr4:105555379 | C | G | 1 | a0001c0001t0003g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196+2418C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105555379 | |||||||
| chr4:105555613 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196+2652C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105555613 | |||||||
| chr4:105555866 | A | G | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+2905A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105555866 | |||||||
| chr4:105555890 | T | G | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+2929T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105555890 | |||||||
| chr4:105556144 | A | G | 1 | a0001c0001t0004g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.196+3183A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105556144 | |||||||
| chr4:105556236 | C | T | 1 | a0001c0001t0004g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.196+3275C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105556236 | |||||||
| chr4:105556260 | C | T | 16 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0010 others(13): Show |
17 | HG02004.hp1 HG02451.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+3299C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105556260 | |||||||
| chr4:105556443 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.196+3482G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105556443 | |||||||
| chr4:105556488 | T | G | 3 | a0001c0002t0002g0113 a0001c0002t0003g0018 a0003c0015t0003g0019 |
3 | HG01070.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+3527T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105556488 | |||||||
| chr4:105556598 | T | A | 3 | a0001c0001t0002g0146 a0001c0001t0007g0147 a0001c0001t0007g0148 |
3 | HG02622.hp2 HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.196+3637T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105556598 | |||||||
| chr4:105556654 | C | T | 1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+3693C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105556654 | |||||||
| chr4:105557092 | T | A | 120 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(117): Show |
120 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.196+4131T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557092 | |||||||
| chr4:105557158 | A | G | 8 | a0001c0001t0002g0108 a0001c0001t0014g0107 a0001c0002t0003g0030 others(5): Show |
8 | HG02257.hp2 HG02630.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+4197A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557158 | |||||||
| chr4:105557268 | A | G | 1 | a0001c0002t0009g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196+4307A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557268 | |||||||
| chr4:105557272 | G | A | 6 | a0001c0001t0002g0108 a0001c0001t0014g0107 a0001c0002t0003g0030 others(3): Show |
6 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.196+4311G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557272 | |||||||
| chr4:105557445 | C | T | 9 | a0001c0001t0002g0156 a0001c0002t0003g0025 a0001c0002t0003g0026 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+4484C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557445 | |||||||
| chr4:105557598 | TA | T | 96 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(93): Show |
96 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.196+4653delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105557598 | ||||||
| chr4:105557706 | A | T | 22 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(19): Show |
22 | HG00408.hp2 HG00609.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.196+4745A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557706 | |||||||
| chr4:105557764 | G | A | 1 | a0001c0002t0002g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.196+4803G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557764 | |||||||
| chr4:105557853 | A | G | 154 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(151): Show |
155 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.196+4892A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557853 | |||||||
| chr4:105557857 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.196+4896C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557857 | |||||||
| chr4:105557957 | A | G | 1 | a0001c0007t0015g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.196+4996A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105557957 | |||||||
| chr4:105558035 | C | T | 22 | a0001c0001t0001g0104 a0001c0001t0001g0154 a0001c0001t0001g0158 others(19): Show |
22 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.196+5074C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558035 | |||||||
| chr4:105558215 | C | T | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+5254C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558215 | |||||||
| chr4:105558268 | G | A | 11 | a0001c0001t0001g0183 a0001c0001t0002g0039 a0001c0001t0002g0040 others(8): Show |
11 | HG00639.hp2 HG01106.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+5307G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558268 | |||||||
| chr4:105558468 | A | G | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.196+5507A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558468 | |||||||
| chr4:105558656 | AG | A | 22 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(19): Show |
22 | HG00408.hp2 HG00609.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.196+5697delG | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105558656 | ||||||
| chr4:105558658 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.196+5697G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558658 | |||||||
| chr4:105558816 | CT | C | 79 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(76): Show |
79 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.196+5866delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105558816 | ||||||
| chr4:105558831 | T | C | 3 | a0001c0002t0002g0113 a0001c0002t0003g0018 a0003c0015t0003g0019 |
3 | HG01070.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.196+5870T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558831 | |||||||
| chr4:105558832 | A | G | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.196+5871A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558832 | |||||||
| chr4:105558914 | A | G | 3 | a0001c0001t0002g0156 a0001c0002t0011g0028 a0001c0008t0006g0157 |
3 | HG02572.hp2 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.196+5953A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558914 | |||||||
| chr4:105558916 | A | G | 3 | a0001c0001t0002g0156 a0001c0002t0011g0028 a0001c0008t0006g0157 |
3 | HG02572.hp2 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.196+5955A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558916 | |||||||
| chr4:105558919 | C | G | 3 | a0001c0001t0002g0156 a0001c0002t0011g0028 a0001c0008t0006g0157 |
3 | HG02572.hp2 HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.196+5958C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105558919 | |||||||
| chr4:105559009 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.196+6048C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105559009 | |||||||
| chr4:105559050 | G | GA | 95 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(92): Show |
96 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.196+6100dupA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105559050 | ||||||
| chr4:105559111 | C | T | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+6150C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105559111 | |||||||
| chr4:105559517 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.196+6556C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105559517 | |||||||
| chr4:105559580 | A | G | 22 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0166 others(19): Show |
22 | HG00408.hp2 HG00609.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.196+6619A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105559580 | |||||||
| chr4:105559676 | C | T | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0002c0003t0010g0139 |
3 | HG01243.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.196+6715C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105559676 | |||||||
| chr4:105559728 | G | A | 2 | a0004c0011t0002g0003 a0004c0011t0002g0004 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.196+6767G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105559728 | |||||||
| chr4:105560018 | A | T | 2 | a0001c0002t0008g0029 a0003c0023t0020g0114 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.196+7057A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105560018 | |||||||
| chr4:105560037 | G | T | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+7076G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105560037 | |||||||
| chr4:105560115 | C | T | 2 | a0004c0011t0002g0003 a0004c0011t0002g0004 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.196+7154C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105560115 | |||||||
| chr4:105560166 | T | A | 1 | a0001c0001t0002g0116 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.196+7205T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105560166 | |||||||
| chr4:105560244 | T | C | 2 | a0001c0002t0008g0029 a0003c0023t0020g0114 |
2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.196+7283T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105560244 | |||||||
| chr4:105560336 | T | C | 1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196+7375T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105560336 | |||||||
| chr4:105560516 | T | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0007c0014t0005g0005 |
3 | HG01070.hp2 HG01106.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.196+7555T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105560516 | |||||||
| chr4:105561028 | G | C | 27 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0079 others(24): Show |
27 | HG00280.hp1 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.196+8067G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561028 | |||||||
| chr4:105561054 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0007c0014t0005g0005 |
3 | HG01070.hp2 HG01106.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.196+8093C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561054 | |||||||
| chr4:105561063 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.196+8102T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561063 | |||||||
| chr4:105561078 | G | T | 63 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(60): Show |
63 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.196+8117G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561078 | |||||||
| chr4:105561101 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196+8140A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561101 | |||||||
| chr4:105561245 | A | G | 2 | a0001c0001t0003g0096 a0003c0023t0020g0114 |
2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.196+8284A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561245 | |||||||
| chr4:105561329 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.196+8368G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561329 | |||||||
| chr4:105561394 | GTAGAATA others(1): Show |
G | 10 | a0001c0001t0001g0046 a0001c0001t0002g0040 a0001c0001t0005g0085 others(7): Show |
10 | HG00639.hp1 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+8441_196+8448d others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561394 | ||||||
| chr4:105561394 | GTAGAATA others(6): Show |
G | 11 | a0001c0001t0001g0073 a0001c0001t0001g0095 a0001c0001t0002g0072 others(8): Show |
11 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+8441_196+8453d others(15): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561394 | ||||||
| chr4:105561394 | GTAGAATA others(56): Show |
G | 1 | a0002c0003t0001g0178 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.196+8441_196+8503d others(65): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561394 | ||||||
| chr4:105561394 | GTAGAATA others(76): Show |
G | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.196+8441_196+8523d others(85): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561394 | ||||||
| chr4:105561396 | AGAATAAT others(21): Show |
A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0066 a0001c0001t0001g0067 others(12): Show |
15 | HG00438.hp1 HG01106.hp1 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.196+8441_196+8468d others(30): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561396 | ||||||
| chr4:105561396 | AGAATAAT others(46): Show |
A | 1 | a0001c0001t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.196+8441_196+8493d others(55): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561396 | ||||||
| chr4:105561397 | GAAT | G | 70 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(67): Show |
70 | HG00408.hp2 HG00438.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.196+8441_196+8443d others(5): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561397 | ||||||
| chr4:105561398 | A | AAGAATAG others(28): Show |
1 | a0001c0001t0002g0078 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.196+8438_196+8439i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561398 | ||||||
| chr4:105561398 | A | AAGAATAG others(88): Show |
1 | a0001c0001t0002g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.196+8438_196+8439i others(97): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561398 | ||||||
| chr4:105561398 | AATAATAG others(3): Show |
A | 3 | a0001c0008t0006g0077 a0005c0009t0013g0001 a0006c0010t0022g0006 |
3 | HG02559.hp1 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.196+8439_196+8448d others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561398 | ||||||
| chr4:105561398 | AATAATAG others(8): Show |
A | 1 | a0001c0001t0003g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.196+8439_196+8453d others(17): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561398 | ||||||
| chr4:105561398 | AATAATAG others(13): Show |
A | 1 | a0005c0009t0013g0001 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.196+8439_196+8458d others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561398 | ||||||
| chr4:105561400 | T | G | 3 | a0001c0001t0002g0078 a0001c0001t0002g0149 a0001c0008t0006g0076 |
3 | HG01175.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.196+8439T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561400 | |||||||
| chr4:105561400 | T | TAATAG | 2 | a0001c0002t0007g0023 a0002c0012t0010g0024 |
2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.196+8458_196+8462d others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAG | 25 | a0001c0001t0001g0068 a0001c0001t0001g0082 a0001c0001t0001g0083 others(22): Show |
25 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.196+8440_196+8441i others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAAAAT others(27): Show |
1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196+8440_196+8441i others(36): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAAAAT others(67): Show |
1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.196+8440_196+8441i others(76): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAAAAT others(62): Show |
1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.196+8440_196+8441i others(71): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG | 9 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(6): Show |
9 | HG01978.hp1 HG02004.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.196+8440_196+8441i others(9): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(5): Show |
1 | a0002c0003t0001g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.196+8440_196+8441i others(14): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(10): Show |
2 | a0001c0001t0001g0161 a0001c0001t0001g0181 |
2 | HG02080.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.196+8440_196+8441i others(19): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(20): Show |
1 | a0001c0001t0002g0116 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(29): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(25): Show |
1 | a0003c0006t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(34): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(30): Show |
1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(39): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(140): Show |
1 | a0001c0001t0001g0120 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(149): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(25): Show |
1 | a0001c0001t0002g0039 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(34): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(20): Show |
1 | a0001c0001t0002g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(29): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(30): Show |
1 | a0001c0001t0003g0112 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.196+8440_196+8441i others(39): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(35): Show |
1 | a0001c0001t0002g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(44): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(5): Show |
4 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0004g0132 others(1): Show |
4 | HG01109.hp2 HG02015.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+8440_196+8441i others(14): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | T | TAGAATAG others(10): Show |
1 | a0001c0001t0002g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.196+8440_196+8441i others(19): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | TAATAGAA others(18): Show |
T | 1 | a0001c0001t0003g0088 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.196+8488_196+8512d others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | TAATAGAA others(53): Show |
T | 1 | a0001c0002t0003g0026 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196+8463_196+8522d others(62): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561400 | TAATAGAA others(58): Show |
T | 1 | a0001c0002t0003g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.196+8463_196+8527d others(67): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561400 | ||||||
| chr4:105561401 | AATAGAAT others(16): Show |
A | 1 | a0001c0001t0003g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+8441_196+8463d others(25): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561401 | |||||||
| chr4:105561401 | AATAGAAT others(41): Show |
A | 3 | a0001c0001t0001g0169 a0001c0001t0016g0168 a0002c0003t0012g0129 |
3 | HG01074.hp2 HG02451.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.196+8441_196+8488d others(50): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561401 | |||||||
| chr4:105561404 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0181 a0001c0002t0008g0029 |
3 | HG02080.hp2 HG03209.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.196+8443A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561404 | |||||||
| chr4:105561409 | A | G | 12 | a0001c0001t0001g0115 a0001c0001t0001g0135 a0001c0001t0001g0177 others(9): Show |
12 | HG00408.hp1 HG01069.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+8448A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561409 | |||||||
| chr4:105561414 | A | AGAATGGA others(3): Show |
3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0007t0002g0093 |
3 | HG01109.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.196+8457_196+8458i others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561414 | ||||||
| chr4:105561414 | A | G | 10 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(7): Show |
10 | HG01516.hp2 HG01978.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+8453A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561414 | |||||||
| chr4:105561419 | A | AGAATAGA others(23): Show |
1 | a0001c0001t0018g0037 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.196+8462_196+8463i others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561419 | ||||||
| chr4:105561419 | A | AGAATAGA others(23): Show |
1 | a0001c0001t0003g0084 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.196+8462_196+8463i others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561419 | ||||||
| chr4:105561419 | A | AGAATGGA others(8): Show |
1 | a0001c0001t0004g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.196+8467_196+8468i others(17): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561419 | ||||||
| chr4:105561419 | A | AGAATGGA others(28): Show |
1 | a0002c0005t0002g0027 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.196+8467_196+8468i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561419 | ||||||
| chr4:105561419 | A | G | 14 | a0001c0001t0001g0068 a0001c0001t0001g0154 a0001c0001t0001g0176 others(11): Show |
14 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.196+8458A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561419 | |||||||
| chr4:105561419 | AGAATGGA others(23): Show |
A | 1 | a0001c0013t0006g0022 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.196+8463_196+8492d others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561419 | ||||||
| chr4:105561424 | G | A | 53 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(50): Show |
54 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.196+8463G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561424 | |||||||
| chr4:105561424 | G | GGAATAGA others(28): Show |
1 | a0001c0001t0001g0049 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.196+8487_196+8488i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | G | GGAATAGA others(33): Show |
1 | a0001c0001t0004g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.196+8487_196+8488i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | G | GGAATAGA others(8): Show |
1 | a0001c0001t0001g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.196+8472_196+8473i others(17): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | G | GGAATGGA others(18): Show |
1 | a0001c0002t0002g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.196+8467_196+8468i others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | G | GGAATGGA others(33): Show |
1 | a0001c0007t0015g0106 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.196+8467_196+8468i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | G | GGAATGGA others(28): Show |
1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196+8467_196+8468i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | GGAATAGA others(23): Show |
G | 2 | a0002c0003t0004g0136 a0008c0017t0001g0131 |
2 | HG01516.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.196+8488_196+8517d others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | GGAATAGA others(28): Show |
G | 2 | a0001c0001t0001g0121 a0001c0001t0003g0153 |
2 | HG01167.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.196+8488_196+8522d others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | GGAATAGA others(33): Show |
G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0164 a0001c0001t0001g0180 |
3 | HG02015.hp2 HG02040.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.196+8488_196+8527d others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561424 | GGAATAGA others(58): Show |
G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0097 |
2 | HG01361.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.196+8488_196+8552d others(67): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561424 | ||||||
| chr4:105561429 | A | G | 9 | a0001c0001t0002g0081 a0001c0001t0002g0140 a0001c0001t0002g0141 others(6): Show |
9 | HG01069.hp1 HG01109.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+8468A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561429 | |||||||
| chr4:105561434 | A | AGAATGGA others(18): Show |
1 | a0001c0004t0009g0103 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.196+8477_196+8478i others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561434 | ||||||
| chr4:105561434 | A | AGAATGGA others(23): Show |
3 | a0001c0001t0002g0108 a0001c0002t0003g0030 a0002c0005t0002g0013 |
3 | HG02965.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.196+8477_196+8478i others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561434 | ||||||
| chr4:105561434 | A | AGAATGGA others(28): Show |
3 | a0001c0002t0003g0031 a0001c0002t0003g0032 a0002c0005t0002g0007 |
3 | HG02897.hp2 HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.196+8477_196+8478i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561434 | ||||||
| chr4:105561434 | A | AGAATGGA others(38): Show |
2 | a0001c0001t0001g0104 a0002c0005t0001g0008 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.196+8477_196+8478i others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561434 | ||||||
| chr4:105561434 | A | AGAATGGA others(43): Show |
1 | a0001c0004t0009g0105 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.196+8477_196+8478i others(52): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561434 | ||||||
| chr4:105561434 | A | AGAATGGA others(58): Show |
1 | a0001c0002t0003g0033 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.196+8477_196+8478i others(67): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561434 | ||||||
| chr4:105561434 | A | AGAATGGA others(83): Show |
1 | a0001c0001t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.196+8477_196+8478i others(92): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561434 | ||||||
| chr4:105561434 | A | G | 10 | a0001c0001t0001g0158 a0001c0001t0002g0081 a0001c0001t0002g0140 others(7): Show |
10 | HG00735.hp1 HG01069.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+8473A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561434 | |||||||
| chr4:105561439 | A | AGAATGGA others(18): Show |
1 | a0001c0001t0001g0170 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.196+8482_196+8483i others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(33): Show |
1 | a0001c0001t0003g0171 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.196+8482_196+8483i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(38): Show |
1 | a0001c0001t0003g0172 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.196+8482_196+8483i others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(23): Show |
1 | a0001c0007t0007g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.196+8482_196+8483i others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(33): Show |
1 | a0001c0001t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.196+8482_196+8483i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(38): Show |
2 | a0001c0001t0003g0090 a0004c0021t0002g0089 |
2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.196+8482_196+8483i others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(43): Show |
7 | a0001c0001t0002g0138 a0001c0001t0002g0155 a0001c0001t0002g0173 others(4): Show |
7 | HG01884.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+8482_196+8483i others(52): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(53): Show |
1 | a0001c0001t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.196+8482_196+8483i others(62): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(63): Show |
1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.196+8482_196+8483i others(72): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | AGAATGGA others(83): Show |
1 | a0001c0001t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.196+8482_196+8483i others(92): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561439 | A | G | 22 | a0001c0001t0001g0104 a0001c0001t0001g0130 a0001c0001t0001g0158 others(19): Show |
22 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.196+8478A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561439 | |||||||
| chr4:105561439 | AGAATAGA others(3): Show |
A | 1 | a0001c0001t0002g0165 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.196+8488_196+8497d others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561439 | ||||||
| chr4:105561444 | A | AGAATAGA others(38): Show |
1 | a0001c0001t0005g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.196+8487_196+8488i others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATAGA others(33): Show |
1 | a0001c0001t0002g0040 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.196+8487_196+8488i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATAGA others(28): Show |
1 | a0002c0003t0004g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.196+8487_196+8488i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATAGA others(18): Show |
1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.196+8487_196+8488i others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATAGA others(38): Show |
1 | a0002c0012t0006g0015 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.196+8487_196+8488i others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATAGA others(18): Show |
1 | a0002c0003t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.196+8487_196+8488i others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATAGA others(63): Show |
1 | a0001c0001t0001g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.196+8487_196+8488i others(72): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATAGA others(73): Show |
1 | a0003c0006t0003g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.196+8487_196+8488i others(82): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATGGA others(13): Show |
3 | a0001c0001t0002g0072 a0001c0001t0004g0109 a0001c0001t0007g0147 |
3 | HG02622.hp2 HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.196+8492_196+8493i others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATGGA others(18): Show |
2 | a0001c0004t0005g0034 a0001c0004t0005g0038 |
2 | HG01167.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.196+8492_196+8493i others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATGGA others(23): Show |
1 | a0001c0001t0007g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.196+8492_196+8493i others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATGGA others(28): Show |
2 | a0001c0004t0005g0086 a0002c0003t0001g0036 |
2 | HG00639.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.196+8492_196+8493i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATGGA others(43): Show |
1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.196+8492_196+8493i others(52): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATGGA others(48): Show |
1 | a0001c0001t0002g0156 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.196+8492_196+8493i others(57): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | AGAATGGA others(63): Show |
1 | a0001c0008t0006g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.196+8492_196+8493i others(72): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561444 | A | G | 40 | a0001c0001t0001g0104 a0001c0001t0001g0115 a0001c0001t0001g0120 others(37): Show |
40 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.196+8483A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561444 | |||||||
| chr4:105561444 | AGAATG | A | 5 | a0001c0001t0001g0064 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG02300.hp1 HG02615.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+8488_196+8492d others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561444 | ||||||
| chr4:105561449 | G | A | 77 | a0001c0001t0001g0046 a0001c0001t0001g0048 a0001c0001t0001g0050 others(74): Show |
78 | HG00280.hp2 HG00438.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.196+8488G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561449 | |||||||
| chr4:105561449 | GGAATA | G | 5 | a0001c0001t0002g0149 a0001c0001t0008g0017 a0001c0002t0003g0018 others(2): Show |
5 | HG01517.hp1 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+8577_196+8581d others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561449 | ||||||
| chr4:105561449 | GGAATAGA others(3): Show |
G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0003g0112 |
3 | NA19007.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.196+8572_196+8581d others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561449 | ||||||
| chr4:105561449 | GGAATAGA others(13): Show |
G | 4 | a0001c0001t0001g0067 a0001c0002t0002g0010 a0001c0002t0002g0011 others(1): Show |
4 | HG00438.hp1 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+8562_196+8581d others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561449 | ||||||
| chr4:105561449 | GGAATAGA others(28): Show |
G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0080 |
2 | HG01106.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.196+8547_196+8581d others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561449 | ||||||
| chr4:105561454 | A | AGAATAGA others(18): Show |
1 | a0001c0022t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.196+8517_196+8518i others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561454 | ||||||
| chr4:105561454 | A | AGAATAGA others(13): Show |
1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.196+8512_196+8513i others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561454 | ||||||
| chr4:105561454 | A | AGAATGGA others(8): Show |
1 | a0001c0001t0001g0065 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.196+8497_196+8498i others(17): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561454 | ||||||
| chr4:105561454 | A | G | 58 | a0001c0001t0001g0083 a0001c0001t0001g0095 a0001c0001t0001g0104 others(55): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.196+8493A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561454 | |||||||
| chr4:105561459 | A | AGAATAGA others(13): Show |
2 | a0001c0001t0001g0052 a0001c0018t0001g0162 |
2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.196+8517_196+8518i others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561459 | ||||||
| chr4:105561459 | A | AGAATAGA others(8): Show |
2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01978.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.196+8512_196+8513i others(17): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561459 | ||||||
| chr4:105561459 | A | AGAATAGA others(33): Show |
1 | a0001c0004t0005g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.196+8512_196+8513i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561459 | ||||||
| chr4:105561459 | A | AGAATGGA others(3): Show |
1 | a0001c0001t0003g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.196+8502_196+8503i others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561459 | ||||||
| chr4:105561459 | A | AGAATGGA others(58): Show |
1 | a0001c0001t0001g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.196+8502_196+8503i others(67): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561459 | ||||||
| chr4:105561459 | A | AGAATGGA others(63): Show |
1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.196+8502_196+8503i others(72): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561459 | ||||||
| chr4:105561459 | A | AGAATGGA others(98): Show |
1 | a0002c0003t0010g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+8502_196+8503i others(107): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561459 | ||||||
| chr4:105561459 | A | G | 61 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0083 others(58): Show |
61 | HG00280.hp1 HG00408.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.196+8498A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561459 | |||||||
| chr4:105561464 | A | AGAATAGA others(33): Show |
1 | a0001c0001t0001g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+8522_196+8523i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561464 | ||||||
| chr4:105561464 | A | AGAATAGA others(28): Show |
2 | a0001c0004t0005g0042 a0001c0004t0005g0043 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.196+8517_196+8518i others(37): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561464 | ||||||
| chr4:105561464 | A | AGAATAGA others(3): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0128 a0001c0001t0002g0127 |
3 | HG00741.hp1 NA18963.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.196+8512_196+8513i others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561464 | ||||||
| chr4:105561464 | A | AGAATG | 2 | a0001c0001t0001g0060 a0001c0020t0004g0061 |
2 | HG01346.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.196+8507_196+8508i others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561464 | ||||||
| chr4:105561464 | A | AGAATGGA others(318): Show |
1 | a0001c0001t0019g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.196+8507_196+8508i others(327): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561464 | ||||||
| chr4:105561464 | A | AGAATGGA others(88): Show |
1 | a0001c0001t0001g0182 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.196+8507_196+8508i others(97): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561464 | ||||||
| chr4:105561464 | A | G | 64 | a0001c0001t0001g0064 a0001c0001t0001g0068 a0001c0001t0001g0069 others(61): Show |
64 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.196+8503A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561464 | |||||||
| chr4:105561467 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.196+8506A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561467 | |||||||
| chr4:105561469 | A | AGAATAGA others(33): Show |
1 | a0001c0002t0009g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.196+8522_196+8523i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561469 | ||||||
| chr4:105561469 | A | AGAATAGA others(3): Show |
2 | a0001c0001t0001g0051 a0001c0001t0002g0047 |
2 | HG04115.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.196+8517_196+8518i others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561469 | ||||||
| chr4:105561469 | A | AGAATAGA others(23): Show |
1 | a0001c0019t0004g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.196+8517_196+8518i others(32): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561469 | ||||||
| chr4:105561469 | A | AGAATGGA others(3): Show |
1 | a0001c0001t0001g0082 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.196+8512_196+8513i others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561469 | ||||||
| chr4:105561469 | A | AGAATGGA others(68): Show |
1 | a0001c0001t0014g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.196+8512_196+8513i others(77): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561469 | ||||||
| chr4:105561469 | A | AGAATGGA others(73): Show |
1 | a0001c0002t0002g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.196+8512_196+8513i others(82): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561469 | ||||||
| chr4:105561469 | A | G | 56 | a0001c0001t0001g0095 a0001c0001t0001g0104 a0001c0001t0001g0115 others(53): Show |
56 | HG00280.hp1 HG00408.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.196+8508A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561469 | |||||||
| chr4:105561474 | A | AGAATAGA others(13): Show |
1 | a0001c0002t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.196+8527_196+8528i others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561474 | ||||||
| chr4:105561474 | A | AGAATAGA others(33): Show |
1 | a0001c0001t0017g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.196+8522_196+8523i others(42): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561474 | ||||||
| chr4:105561474 | A | AGAATGGA others(98): Show |
2 | a0004c0011t0002g0003 a0004c0011t0002g0004 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.196+8517_196+8518i others(107): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561474 | ||||||
| chr4:105561474 | A | AGAATGGA others(63): Show |
1 | a0001c0001t0002g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.196+8517_196+8518i others(72): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561474 | ||||||
| chr4:105561474 | A | AGAATGGA others(88): Show |
1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+8517_196+8518i others(97): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561474 | ||||||
| chr4:105561474 | A | G | 40 | a0001c0001t0001g0064 a0001c0001t0001g0095 a0001c0001t0001g0115 others(37): Show |
40 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.196+8513A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561474 | |||||||
| chr4:105561479 | A | AGAATAGA others(158): Show |
1 | a0001c0001t0001g0124 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.196+8532_196+8533i others(167): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561479 | ||||||
| chr4:105561479 | A | AGAATAGA others(3): Show |
1 | a0001c0002t0001g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.196+8527_196+8528i others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561479 | ||||||
| chr4:105561479 | A | AGAATAGA others(8): Show |
1 | a0001c0001t0002g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.196+8527_196+8528i others(17): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561479 | ||||||
| chr4:105561479 | A | AGAATGGA others(68): Show |
2 | a0001c0001t0001g0167 a0003c0006t0001g0144 |
2 | HG02622.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.196+8522_196+8523i others(77): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561479 | ||||||
| chr4:105561479 | A | G | 32 | a0001c0001t0001g0050 a0001c0001t0001g0115 a0001c0001t0001g0166 others(29): Show |
32 | HG00280.hp1 HG00408.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.196+8518A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561479 | |||||||
| chr4:105561484 | A | G | 22 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0170 others(19): Show |
22 | HG00408.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.196+8523A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561484 | |||||||
| chr4:105561489 | A | AGAATGGA others(53): Show |
1 | a0001c0002t0011g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.196+8532_196+8533i others(62): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561489 | ||||||
| chr4:105561489 | A | G | 7 | a0001c0001t0001g0166 a0001c0004t0005g0034 a0002c0005t0001g0008 others(4): Show |
7 | HG01069.hp2 HG01167.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.196+8528A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561489 | |||||||
| chr4:105561494 | A | AGAATAGA others(113): Show |
1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.196+8560_196+8561i others(122): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561494 | ||||||
| chr4:105561494 | A | G | 4 | a0001c0001t0001g0166 a0001c0002t0011g0028 a0001c0004t0005g0034 others(1): Show |
4 | HG01069.hp2 HG01167.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+8533A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561494 | |||||||
| chr4:105561499 | A | G | 2 | a0001c0002t0011g0028 a0002c0005t0002g0027 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.196+8538A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561499 | |||||||
| chr4:105561539 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0002c0003t0001g0036 |
3 | HG00639.hp2 HG01070.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.196+8578A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561539 | |||||||
| chr4:105561558 | G | A | 37 | a0001c0001t0001g0104 a0001c0001t0001g0183 a0001c0001t0001g0185 others(34): Show |
37 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.196+8597G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561558 | |||||||
| chr4:105561600 | G | A | 33 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0057 others(30): Show |
33 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.196+8639G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561600 | |||||||
| chr4:105561602 | C | CT | 3 | a0001c0001t0003g0090 a0001c0001t0011g0091 a0001c0001t0012g0092 |
3 | HG02615.hp2 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.196+8647dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105561602 | ||||||
| chr4:105561617 | C | T | 2 | a0001c0001t0003g0145 a0009c0016t0001g0021 |
2 | HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.196+8656C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561617 | |||||||
| chr4:105561623 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.196+8662G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561623 | |||||||
| chr4:105561730 | A | G | 63 | a0001c0001t0001g0066 a0001c0001t0001g0079 a0001c0001t0001g0080 others(60): Show |
63 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.196+8769A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561730 | |||||||
| chr4:105561732 | A | G | 1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.196+8771A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561732 | |||||||
| chr4:105561749 | T | A | 34 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(31): Show |
34 | HG00408.hp2 HG00438.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.196+8788T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561749 | |||||||
| chr4:105561877 | T | C | 4 | a0001c0001t0008g0017 a0001c0002t0008g0029 a0001c0013t0006g0022 others(1): Show |
4 | HG01884.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.196+8916T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105561877 | |||||||
| chr4:105562170 | G | A | 152 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(149): Show |
153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.196+9209G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562170 | |||||||
| chr4:105562198 | G | A | 7 | a0001c0001t0002g0146 a0001c0001t0003g0075 a0001c0001t0003g0084 others(4): Show |
7 | HG01069.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+9237G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562198 | |||||||
| chr4:105562242 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0163 |
3 | HG02027.hp2 NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.196+9281C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562242 | |||||||
| chr4:105562379 | T | C | 1 | a0001c0001t0003g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+9418T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562379 | |||||||
| chr4:105562458 | A | T | 177 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(174): Show |
178 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.196+9497A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562458 | |||||||
| chr4:105562694 | C | G | 17 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(14): Show |
17 | HG01981.hp1 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+9733C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562694 | |||||||
| chr4:105562741 | A | G | 17 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(14): Show |
17 | HG01981.hp1 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+9780A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562741 | |||||||
| chr4:105562772 | C | T | 1 | a0002c0003t0001g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.196+9811C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562772 | |||||||
| chr4:105562776 | C | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.196+9815C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105562776 | |||||||
| chr4:105562833 | GACC | G | 3 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0002t0002g0014 |
3 | HG01069.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.196+9879_196+9881d others(5): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105562833 | ||||||
| chr4:105563363 | A | G | 8 | a0001c0001t0003g0090 a0001c0001t0003g0101 a0001c0001t0011g0091 others(5): Show |
8 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+10402A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105563363 | |||||||
| chr4:105563468 | C | A | 2 | a0005c0009t0013g0001 a0006c0010t0022g0006 |
3 | HG02922.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.196+10507C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105563468 | |||||||
| chr4:105563669 | GT | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+10713delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105563669 | ||||||
| chr4:105563676 | G | A | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+10715G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105563676 | |||||||
| chr4:105563685 | C | A | 1 | a0001c0004t0005g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.196+10724C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105563685 | |||||||
| chr4:105563694 | T | A | 1 | a0001c0001t0003g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.196+10733T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105563694 | |||||||
| chr4:105563718 | G | A | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+10757G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105563718 | |||||||
| chr4:105564037 | A | G | 159 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(156): Show |
160 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.196+11076A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564037 | |||||||
| chr4:105564238 | C | T | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+11277C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564238 | |||||||
| chr4:105564317 | T | C | 101 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(98): Show |
101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.196+11356T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564317 | |||||||
| chr4:105564335 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.196+11374A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564335 | |||||||
| chr4:105564345 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.196+11384C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564345 | |||||||
| chr4:105564348 | T | C | 1 | a0001c0001t0003g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+11387T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564348 | |||||||
| chr4:105564412 | C | T | 17 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(14): Show |
17 | HG01981.hp1 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+11451C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564412 | |||||||
| chr4:105564588 | T | C | 54 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(51): Show |
54 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.196+11627T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564588 | |||||||
| chr4:105564653 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.196+11692C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564653 | |||||||
| chr4:105564679 | C | T | 158 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.196+11718C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564679 | |||||||
| chr4:105564831 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.196+11870A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564831 | |||||||
| chr4:105564922 | G | C | 1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+11961G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105564922 | |||||||
| chr4:105565010 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196+12049A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565010 | |||||||
| chr4:105565060 | C | G | 101 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(98): Show |
101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.196+12099C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565060 | |||||||
| chr4:105565180 | T | A | 1 | a0002c0003t0010g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+12219T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565180 | |||||||
| chr4:105565234 | G | C | 1 | a0002c0003t0010g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.196+12273G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565234 | |||||||
| chr4:105565427 | C | A | 145 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(142): Show |
146 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.196+12466C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565427 | |||||||
| chr4:105565427 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.196+12466C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565427 | |||||||
| chr4:105565455 | T | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.196+12494T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565455 | |||||||
| chr4:105565460 | T | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+12499T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565460 | |||||||
| chr4:105565866 | A | G | 2 | a0001c0013t0006g0022 a0002c0012t0010g0024 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.196+12905A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565866 | |||||||
| chr4:105565900 | C | G | 17 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(14): Show |
17 | HG01981.hp1 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+12939C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565900 | |||||||
| chr4:105565999 | C | G | 158 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.196+13038C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105565999 | |||||||
| chr4:105566125 | A | G | 5 | a0001c0002t0003g0025 a0001c0002t0003g0026 a0001c0002t0007g0023 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+13164A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566125 | |||||||
| chr4:105566131 | G | A | 6 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0135 others(3): Show |
6 | HG02080.hp2 HG02523.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+13170G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566131 | |||||||
| chr4:105566198 | G | C | 158 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.196+13237G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566198 | |||||||
| chr4:105566218 | C | T | 2 | a0001c0001t0003g0171 a0001c0001t0003g0172 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.196+13257C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566218 | |||||||
| chr4:105566229 | G | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0095 |
2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.196+13268G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566229 | |||||||
| chr4:105566230 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0095 |
2 | HG03490.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.196+13269C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566230 | |||||||
| chr4:105566387 | C | A | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+13426C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566387 | |||||||
| chr4:105566446 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.196+13485G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566446 | |||||||
| chr4:105566498 | A | G | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+13537A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566498 | |||||||
| chr4:105566567 | C | A | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+13606C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566567 | |||||||
| chr4:105566585 | A | G | 2 | a0005c0009t0013g0001 a0006c0010t0022g0006 |
3 | HG02922.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.196+13624A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566585 | |||||||
| chr4:105566752 | C | CT | 145 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(142): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.196+13807dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105566752 | ||||||
| chr4:105566752 | C | CTT | 11 | a0001c0001t0002g0146 a0001c0001t0003g0075 a0001c0001t0003g0084 others(8): Show |
12 | HG01069.hp1 HG02572.hp1 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+13806_196+1380 others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105566752 | ||||||
| chr4:105566758 | T | C | 17 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(14): Show |
17 | HG01981.hp1 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+13797T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566758 | |||||||
| chr4:105566831 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0071 others(2): Show |
5 | HG01346.hp1 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.196+13870G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566831 | |||||||
| chr4:105566910 | C | T | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196+13949C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105566910 | |||||||
| chr4:105567035 | C | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+14074C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567035 | |||||||
| chr4:105567052 | C | A | 3 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.196+14091C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567052 | |||||||
| chr4:105567100 | T | A | 2 | a0001c0001t0018g0037 a0001c0004t0005g0086 |
2 | HG00741.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.196+14139T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567100 | |||||||
| chr4:105567238 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196+14277C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567238 | |||||||
| chr4:105567252 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.196+14291C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567252 | |||||||
| chr4:105567339 | C | T | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196+14378C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567339 | |||||||
| chr4:105567402 | G | C | 144 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(141): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.196+14441G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567402 | |||||||
| chr4:105567506 | A | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+14545A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567506 | |||||||
| chr4:105567517 | G | A | 1 | a0002c0003t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.196+14556G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567517 | |||||||
| chr4:105567593 | A | T | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+14632A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567593 | |||||||
| chr4:105567799 | A | C | 1 | a0002c0003t0001g0178 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.196+14838A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567799 | |||||||
| chr4:105567834 | A | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+14873A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567834 | |||||||
| chr4:105567847 | C | T | 17 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(14): Show |
17 | HG01981.hp1 HG02080.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.196+14886C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567847 | |||||||
| chr4:105567870 | C | T | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+14909C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567870 | |||||||
| chr4:105567931 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02015.hp2 NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.196+14970C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567931 | |||||||
| chr4:105568051 | C | T | 9 | a0001c0001t0002g0078 a0001c0001t0002g0156 a0001c0001t0003g0075 others(6): Show |
9 | HG01069.hp1 HG01070.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+15090C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568051 | |||||||
| chr4:105568107 | C | T | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+15146C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568107 | |||||||
| chr4:105568132 | A | G | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196+15171A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568132 | |||||||
| chr4:105568143 | T | C | 5 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0152 others(2): Show |
5 | HG02922.hp1 HG02976.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.196+15182T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568143 | |||||||
| chr4:105568399 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.196+15438A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568399 | |||||||
| chr4:105568411 | C | T | 4 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.196+15450C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568411 | |||||||
| chr4:105568581 | A | G | 1 | a0001c0007t0002g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.196+15620A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568581 | |||||||
| chr4:105568649 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.196+15688A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568649 | |||||||
| chr4:105568730 | G | C | 158 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.196+15769G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568730 | |||||||
| chr4:105568813 | T | C | 3 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0002t0002g0014 |
3 | HG01069.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.196+15852T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568813 | |||||||
| chr4:105568944 | A | G | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.196+15983A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568944 | |||||||
| chr4:105568958 | T | C | 1 | a0001c0001t0004g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.196+15997T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568958 | |||||||
| chr4:105568975 | A | G | 158 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(155): Show |
159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.196+16014A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105568975 | |||||||
| chr4:105569022 | A | G | 7 | a0001c0001t0002g0078 a0001c0001t0002g0156 a0001c0002t0002g0113 others(4): Show |
7 | HG01070.hp1 HG01175.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.196+16061A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105569022 | |||||||
| chr4:105569139 | T | C | 1 | a0007c0014t0005g0005 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.196+16178T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105569139 | |||||||
| chr4:105569420 | G | C | 11 | a0001c0001t0001g0170 a0001c0001t0003g0090 a0001c0001t0003g0101 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.196+16459G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105569420 | |||||||
| chr4:105569498 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0002g0063 |
2 | NA18942.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.196+16537A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105569498 | |||||||
| chr4:105569790 | T | C | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.196+16829T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105569790 | |||||||
| chr4:105569857 | T | G | 8 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0008g0017 others(5): Show |
9 | HG01069.hp1 HG02572.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.196+16896T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105569857 | |||||||
| chr4:105570046 | T | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.196+17085T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570046 | |||||||
| chr4:105570051 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.196+17090G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570051 | |||||||
| chr4:105570060 | G | C | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.196+17099G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570060 | |||||||
| chr4:105570354 | T | C | 10 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(7): Show |
10 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.196+17393T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570354 | |||||||
| chr4:105570356 | G | A | 6 | a0001c0001t0002g0078 a0001c0001t0002g0156 a0001c0008t0006g0076 others(3): Show |
6 | HG01070.hp1 HG01175.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.196+17395G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570356 | |||||||
| chr4:105570484 | G | C | 144 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(141): Show |
145 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.196+17523G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570484 | |||||||
| chr4:105570797 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.196+17836C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570797 | |||||||
| chr4:105570915 | C | T | 1 | a0006c0010t0021g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.196+17954C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570915 | |||||||
| chr4:105570983 | A | G | 1 | a0002c0003t0004g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.196+18022A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105570983 | |||||||
| chr4:105571071 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0005g0085 |
2 | HG00639.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.196+18110A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571071 | |||||||
| chr4:105571171 | A | G | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.197-18077A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571171 | |||||||
| chr4:105571321 | CTT | C | 16 | a0001c0001t0001g0046 a0001c0001t0002g0078 a0001c0001t0002g0156 others(13): Show |
16 | HG01070.hp1 HG01175.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.197-17909_197-1790 others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105571321 | ||||||
| chr4:105571321 | CTTT | C | 146 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(143): Show |
147 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.197-17910_197-1790 others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105571321 | ||||||
| chr4:105571321 | CTTTT | C | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-17911_197-1790 others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105571321 | ||||||
| chr4:105571509 | A | T | 3 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.197-17739A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571509 | |||||||
| chr4:105571553 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.197-17695C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571553 | |||||||
| chr4:105571612 | C | T | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-17636C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571612 | |||||||
| chr4:105571651 | A | G | 1 | a0001c0002t0001g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.197-17597A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571651 | |||||||
| chr4:105571659 | C | T | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-17589C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571659 | |||||||
| chr4:105571849 | C | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0156 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.197-17399C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571849 | |||||||
| chr4:105571911 | T | A | 94 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(91): Show |
94 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.197-17337T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571911 | |||||||
| chr4:105571926 | C | T | 1 | a0002c0003t0001g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.197-17322C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105571926 | |||||||
| chr4:105572184 | C | CCAAATT | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.197-17059_197-1705 others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105572184 | ||||||
| chr4:105572238 | C | T | 132 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(129): Show |
133 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.197-17010C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572238 | |||||||
| chr4:105572245 | T | C | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.197-17003T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572245 | |||||||
| chr4:105572352 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0177 |
2 | HG01258.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.197-16896G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572352 | |||||||
| chr4:105572401 | A | G | 1 | a0001c0002t0001g0020 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.197-16847A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572401 | |||||||
| chr4:105572515 | C | T | 2 | a0001c0004t0005g0042 a0001c0004t0005g0043 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.197-16733C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572515 | |||||||
| chr4:105572537 | C | T | 3 | a0001c0001t0001g0170 a0001c0001t0003g0171 a0001c0001t0003g0172 |
3 | HG02809.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.197-16711C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572537 | |||||||
| chr4:105572812 | A | G | 167 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(164): Show |
168 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.197-16436A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572812 | |||||||
| chr4:105572992 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.197-16256G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105572992 | |||||||
| chr4:105573059 | GC | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.197-16187delC | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105573059 | ||||||
| chr4:105573143 | A | G | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-16105A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105573143 | |||||||
| chr4:105573176 | T | C | 94 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(91): Show |
94 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.197-16072T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105573176 | |||||||
| chr4:105573249 | C | A | 3 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0002t0002g0014 |
3 | HG01069.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.197-15999C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105573249 | |||||||
| chr4:105573572 | T | A | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-15676T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105573572 | |||||||
| chr4:105573738 | G | GT | 17 | a0001c0001t0001g0170 a0001c0001t0002g0078 a0001c0001t0002g0156 others(14): Show |
17 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.197-15499dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105573738 | ||||||
| chr4:105573738 | GT | G | 15 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(12): Show |
15 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.197-15499delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105573738 | ||||||
| chr4:105573757 | CA | C | 12 | a0001c0001t0002g0146 a0001c0001t0003g0075 a0001c0001t0003g0084 others(9): Show |
13 | HG01069.hp1 HG02572.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.197-15482delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105573757 | ||||||
| chr4:105573763 | A | C | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-15485A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105573763 | |||||||
| chr4:105573853 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-15395G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105573853 | |||||||
| chr4:105574565 | AAAG | A | 19 | a0001c0001t0001g0170 a0001c0001t0002g0146 a0001c0001t0002g0151 others(16): Show |
20 | HG01069.hp1 HG01109.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.197-14679_197-1467 others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105574565 | ||||||
| chr4:105574566 | AAG | A | 16 | a0001c0001t0001g0064 a0001c0001t0001g0083 a0001c0001t0001g0154 others(13): Show |
16 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.197-14680_197-1467 others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105574566 | ||||||
| chr4:105574567 | AG | A | 92 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(89): Show |
92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.197-14680delG | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574567 | |||||||
| chr4:105574568 | G | A | 1 | a0001c0020t0004g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.197-14680G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574568 | |||||||
| chr4:105574659 | T | C | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-14589T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574659 | |||||||
| chr4:105574728 | T | A | 11 | a0001c0001t0001g0170 a0001c0001t0003g0090 a0001c0001t0003g0101 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-14520T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574728 | |||||||
| chr4:105574733 | T | C | 11 | a0001c0001t0001g0170 a0001c0001t0003g0090 a0001c0001t0003g0101 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-14515T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574733 | |||||||
| chr4:105574761 | T | G | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.197-14487T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574761 | |||||||
| chr4:105574777 | A | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA18963.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.197-14471A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574777 | |||||||
| chr4:105574778 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.197-14470T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574778 | |||||||
| chr4:105574831 | C | T | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-14417C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574831 | |||||||
| chr4:105574999 | T | C | 153 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(150): Show |
154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.197-14249T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574999 | |||||||
| chr4:105574999 | T | G | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-14249T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105574999 | |||||||
| chr4:105575009 | T | C | 2 | a0001c0001t0002g0134 a0001c0001t0003g0142 |
2 | HG02723.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.197-14239T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575009 | |||||||
| chr4:105575013 | T | TAC | 3 | a0001c0001t0003g0145 a0001c0002t0002g0113 a0002c0003t0010g0139 |
3 | HG01243.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-14212_197-1421 others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105575013 | ||||||
| chr4:105575013 | TAC | T | 118 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(115): Show |
119 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.197-14212_197-1421 others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105575013 | ||||||
| chr4:105575013 | TACAC | T | 4 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 others(1): Show |
4 | HG02559.hp1 HG02622.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-14214_197-1421 others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105575013 | ||||||
| chr4:105575015 | C | T | 2 | a0001c0001t0002g0134 a0001c0001t0003g0142 |
2 | HG02723.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.197-14233C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575015 | |||||||
| chr4:105575017 | C | T | 2 | a0001c0001t0008g0017 a0001c0002t0008g0029 |
2 | HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.197-14231C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575017 | |||||||
| chr4:105575210 | T | C | 1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-14038T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575210 | |||||||
| chr4:105575544 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.197-13704G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575544 | |||||||
| chr4:105575732 | C | T | 2 | a0001c0002t0002g0113 a0003c0023t0020g0114 |
2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-13516C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575732 | |||||||
| chr4:105575776 | C | T | 2 | a0001c0002t0002g0113 a0003c0023t0020g0114 |
2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-13472C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575776 | |||||||
| chr4:105575792 | T | G | 3 | a0001c0001t0008g0017 a0001c0002t0008g0029 a0009c0016t0001g0021 |
3 | HG02965.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.197-13456T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575792 | |||||||
| chr4:105575823 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-13425G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575823 | |||||||
| chr4:105575828 | AGGTGAGA others(2261): Show |
A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-13419_197-1115 others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105575828 | |||||||
| chr4:105576020 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-13228G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105576020 | |||||||
| chr4:105576280 | C | T | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.197-12968C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105576280 | |||||||
| chr4:105576407 | C | CT | 5 | a0001c0001t0001g0083 a0001c0002t0009g0016 a0001c0008t0006g0076 others(2): Show |
5 | HG01516.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-12825dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105576407 | ||||||
| chr4:105576407 | CT | C | 115 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(112): Show |
116 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.197-12825delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105576407 | ||||||
| chr4:105576597 | A | G | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-12651A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105576597 | |||||||
| chr4:105576760 | G | A | 2 | a0001c0004t0005g0042 a0001c0004t0005g0043 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.197-12488G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105576760 | |||||||
| chr4:105576874 | C | T | 5 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0002t0002g0014 others(2): Show |
6 | HG01069.hp1 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-12374C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105576874 | |||||||
| chr4:105577010 | A | G | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-12238A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577010 | |||||||
| chr4:105577099 | A | AT | 172 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(169): Show |
173 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.197-12141dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105577099 | ||||||
| chr4:105577099 | A | T | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.197-12149A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577099 | |||||||
| chr4:105577232 | C | G | 7 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0152 others(4): Show |
7 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-12016C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577232 | |||||||
| chr4:105577491 | A | G | 8 | a0001c0001t0003g0090 a0001c0001t0003g0101 a0001c0001t0011g0091 others(5): Show |
8 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.197-11757A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577491 | |||||||
| chr4:105577513 | C | T | 7 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0152 others(4): Show |
7 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-11735C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577513 | |||||||
| chr4:105577561 | G | A | 97 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(94): Show |
97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.197-11687G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577561 | |||||||
| chr4:105577574 | T | G | 1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-11674T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577574 | |||||||
| chr4:105577575 | T | C | 1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-11673T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577575 | |||||||
| chr4:105577670 | T | C | 1 | a0002c0003t0001g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.197-11578T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577670 | |||||||
| chr4:105577678 | T | C | 34 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(31): Show |
34 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.197-11570T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577678 | |||||||
| chr4:105577685 | A | G | 1 | a0003c0006t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.197-11563A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577685 | |||||||
| chr4:105577781 | A | G | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-11467A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105577781 | |||||||
| chr4:105578111 | G | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11137G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578111 | |||||||
| chr4:105578112 | A | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11136A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578112 | |||||||
| chr4:105578113 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11135T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578113 | |||||||
| chr4:105578114 | A | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11134A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578114 | |||||||
| chr4:105578116 | C | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11132C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578116 | |||||||
| chr4:105578125 | T | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11123T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578125 | |||||||
| chr4:105578126 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11122T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578126 | |||||||
| chr4:105578128 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11120T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578128 | |||||||
| chr4:105578132 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11116C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578132 | |||||||
| chr4:105578135 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11113T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578135 | |||||||
| chr4:105578144 | A | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11104A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578144 | |||||||
| chr4:105578146 | A | C | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11102A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578146 | |||||||
| chr4:105578150 | C | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11098C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578150 | |||||||
| chr4:105578152 | T | C | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-11096T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578152 | |||||||
| chr4:105578153 | A | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11095A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578153 | |||||||
| chr4:105578156 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11092T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578156 | |||||||
| chr4:105578157 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11091T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578157 | |||||||
| chr4:105578158 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11090T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578158 | |||||||
| chr4:105578160 | TATCTTGA others(2261): Show |
T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-11087_197-8820 others(3): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578160 | |||||||
| chr4:105578279 | C | T | 1 | a0001c0001t0002g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.197-10969C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578279 | |||||||
| chr4:105578360 | G | A | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-10888G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578360 | |||||||
| chr4:105578390 | A | C | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-10858A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578390 | |||||||
| chr4:105578855 | A | G | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-10393A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578855 | |||||||
| chr4:105578902 | G | T | 174 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(171): Show |
175 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-10346G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578902 | |||||||
| chr4:105578984 | T | A | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-10264T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105578984 | |||||||
| chr4:105579268 | A | T | 174 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(171): Show |
175 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-9980A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579268 | |||||||
| chr4:105579386 | T | C | 138 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(135): Show |
139 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.197-9862T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579386 | |||||||
| chr4:105579435 | C | T | 1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-9813C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579435 | |||||||
| chr4:105579454 | G | A | 140 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(137): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.197-9794G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579454 | |||||||
| chr4:105579655 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0065 a0001c0001t0001g0128 others(1): Show |
4 | HG02071.hp2 NA18939.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-9593G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579655 | |||||||
| chr4:105579766 | G | T | 174 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(171): Show |
175 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-9482G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579766 | |||||||
| chr4:105579894 | T | A | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.197-9354T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579894 | |||||||
| chr4:105580014 | T | C | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-9234T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580014 | |||||||
| chr4:105580015 | G | A | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-9233G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580015 | |||||||
| chr4:105580019 | T | A | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-9229T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580019 | |||||||
| chr4:105580022 | G | A | 21 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0058 others(18): Show |
21 | HG00438.hp1 HG00609.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.197-9226G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580022 | |||||||
| chr4:105580110 | T | TTTCTC | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-9136_197-9135i others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105580110 | ||||||
| chr4:105580189 | T | G | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-9059T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580189 | |||||||
| chr4:105580414 | G | A | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-8834G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580414 | |||||||
| chr4:105580432 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8816T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580432 | |||||||
| chr4:105580433 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8815T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580433 | |||||||
| chr4:105580434 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8814C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580434 | |||||||
| chr4:105580435 | A | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8813A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580435 | |||||||
| chr4:105580437 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8811C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580437 | |||||||
| chr4:105580441 | C | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8807C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580441 | |||||||
| chr4:105580451 | T | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8797T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580451 | |||||||
| chr4:105580455 | C | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8793C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580455 | |||||||
| chr4:105580456 | C | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8792C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580456 | |||||||
| chr4:105580457 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8791T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580457 | |||||||
| chr4:105580459 | A | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8789A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580459 | |||||||
| chr4:105580462 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8786T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580462 | |||||||
| chr4:105580463 | T | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8785T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580463 | |||||||
| chr4:105580464 | C | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8784C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580464 | |||||||
| chr4:105580465 | A | C | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8783A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580465 | |||||||
| chr4:105580477 | A | C | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8771A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580477 | |||||||
| chr4:105580480 | G | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8768G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580480 | |||||||
| chr4:105580481 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8767T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580481 | |||||||
| chr4:105580489 | G | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8759G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580489 | |||||||
| chr4:105580491 | A | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8757A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580491 | |||||||
| chr4:105580498 | G | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8750G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580498 | |||||||
| chr4:105580500 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8748T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580500 | |||||||
| chr4:105580502 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8746C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580502 | |||||||
| chr4:105580506 | T | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8742T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580506 | |||||||
| chr4:105580510 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8738T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580510 | |||||||
| chr4:105580516 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8732T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580516 | |||||||
| chr4:105580519 | GTGGTTCT others(908): Show |
G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-8727_197-7813d others(2): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105580519 | ||||||
| chr4:105580541 | G | A | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-8707G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580541 | |||||||
| chr4:105580544 | A | G | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-8704A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580544 | |||||||
| chr4:105580573 | TGAGA | T | 3 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02922.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.197-8671_197-8668d others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105580573 | ||||||
| chr4:105580587 | G | C | 16 | a0001c0001t0001g0083 a0001c0001t0001g0154 a0001c0001t0002g0039 others(13): Show |
16 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.197-8661G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580587 | |||||||
| chr4:105580695 | GTTTTTTT others(9): Show |
G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-8549_197-8534d others(18): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105580695 | ||||||
| chr4:105580806 | T | C | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-8442T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580806 | |||||||
| chr4:105580816 | A | G | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-8432A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580816 | |||||||
| chr4:105580867 | G | A | 1 | a0001c0001t0017g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.197-8381G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580867 | |||||||
| chr4:105581036 | A | C | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-8212A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581036 | |||||||
| chr4:105581120 | G | T | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-8128G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581120 | |||||||
| chr4:105581191 | TC | T | 94 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(91): Show |
94 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.197-8053delC | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105581191 | ||||||
| chr4:105581269 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.197-7979A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581269 | |||||||
| chr4:105581324 | T | G | 16 | a0001c0001t0001g0083 a0001c0001t0001g0154 a0001c0001t0002g0039 others(13): Show |
16 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.197-7924T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581324 | |||||||
| chr4:105581352 | C | G | 7 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0152 others(4): Show |
7 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-7896C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581352 | |||||||
| chr4:105581356 | G | T | 174 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(171): Show |
175 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.197-7892G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581356 | |||||||
| chr4:105581404 | G | C | 1 | a0001c0001t0003g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.197-7844G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581404 | |||||||
| chr4:105581438 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-7810T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581438 | |||||||
| chr4:105581442 | T | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-7806T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581442 | |||||||
| chr4:105581443 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-7805C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581443 | |||||||
| chr4:105581444 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-7804C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581444 | |||||||
| chr4:105581446 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-7802C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581446 | |||||||
| chr4:105581461 | T | C | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-7787T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581461 | |||||||
| chr4:105581529 | A | G | 1 | a0001c0019t0004g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.197-7719A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581529 | |||||||
| chr4:105581720 | C | T | 1 | a0001c0001t0019g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.197-7528C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581720 | |||||||
| chr4:105581741 | G | A | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.197-7507G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581741 | |||||||
| chr4:105581832 | G | T | 2 | a0001c0001t0001g0161 a0001c0018t0001g0162 |
2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.197-7416G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581832 | |||||||
| chr4:105581912 | T | C | 72 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(69): Show |
72 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.197-7336T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581912 | |||||||
| chr4:105581991 | C | G | 1 | a0001c0001t0001g0167 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.197-7257C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105581991 | |||||||
| chr4:105582034 | G | A | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-7214G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582034 | |||||||
| chr4:105582037 | C | A | 11 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0014g0107 others(8): Show |
11 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-7211C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582037 | |||||||
| chr4:105582042 | G | C | 16 | a0001c0001t0001g0083 a0001c0001t0001g0154 a0001c0001t0002g0039 others(13): Show |
16 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.197-7206G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582042 | |||||||
| chr4:105582131 | C | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.197-7117C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582131 | |||||||
| chr4:105582164 | C | CA | 35 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(32): Show |
35 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-7067dupA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105582164 | ||||||
| chr4:105582164 | C | CAAA | 53 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0058 others(50): Show |
54 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.197-7069_197-7067d others(5): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105582164 | ||||||
| chr4:105582164 | C | CAAAA | 77 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0050 others(74): Show |
77 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.197-7070_197-7067d others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105582164 | ||||||
| chr4:105582164 | C | CAAAAA | 9 | a0001c0001t0001g0051 a0001c0001t0001g0080 a0001c0001t0001g0124 others(6): Show |
9 | HG00609.hp2 HG01106.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.197-7071_197-7067d others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105582164 | ||||||
| chr4:105582300 | A | AT | 9 | a0001c0001t0001g0044 a0001c0001t0002g0039 a0001c0001t0002g0040 others(6): Show |
10 | HG01256.hp1 HG01258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-6935dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105582300 | ||||||
| chr4:105582300 | AT | A | 35 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(32): Show |
35 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.197-6935delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105582300 | ||||||
| chr4:105582383 | A | C | 1 | a0002c0003t0008g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.197-6865A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582383 | |||||||
| chr4:105582502 | ATTTTGTA others(2): Show |
A | 3 | a0001c0001t0001g0170 a0001c0001t0003g0171 a0001c0001t0003g0172 |
3 | HG02809.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.197-6740_197-6732d others(11): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105582502 | ||||||
| chr4:105582566 | A | G | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.197-6682A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582566 | |||||||
| chr4:105582653 | T | A | 151 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(148): Show |
152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.197-6595T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582653 | |||||||
| chr4:105582836 | A | C | 3 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.197-6412A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582836 | |||||||
| chr4:105582918 | A | G | 12 | a0001c0001t0001g0104 a0001c0001t0002g0108 a0001c0001t0003g0096 others(9): Show |
12 | HG00735.hp2 HG01243.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-6330A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582918 | |||||||
| chr4:105582990 | T | G | 11 | a0001c0001t0001g0082 a0001c0001t0001g0095 a0001c0001t0001g0135 others(8): Show |
11 | HG01884.hp2 HG02080.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-6258T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105582990 | |||||||
| chr4:105583002 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.197-6246T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583002 | |||||||
| chr4:105583228 | T | A | 2 | a0001c0002t0002g0113 a0003c0023t0020g0114 |
2 | HG02257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.197-6020T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583228 | |||||||
| chr4:105583333 | C | T | 150 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(147): Show |
151 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.197-5915C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583333 | |||||||
| chr4:105583385 | G | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-5863G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583385 | |||||||
| chr4:105583406 | C | T | 3 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.197-5842C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583406 | |||||||
| chr4:105583411 | C | T | 22 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(19): Show |
22 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-5837C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583411 | |||||||
| chr4:105583432 | T | C | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-5816T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583432 | |||||||
| chr4:105583445 | C | T | 137 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(134): Show |
138 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.197-5803C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583445 | |||||||
| chr4:105583473 | G | A | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.197-5775G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583473 | |||||||
| chr4:105583554 | T | C | 3 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.197-5694T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583554 | |||||||
| chr4:105583683 | A | C | 1 | a0001c0001t0002g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.197-5565A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583683 | |||||||
| chr4:105583692 | A | T | 175 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(172): Show |
176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.197-5556A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583692 | |||||||
| chr4:105583786 | T | C | 96 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(93): Show |
96 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.197-5462T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583786 | |||||||
| chr4:105584196 | G | A | 21 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0058 others(18): Show |
21 | HG00438.hp1 HG00609.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.197-5052G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105584196 | |||||||
| chr4:105584470 | G | A | 1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-4778G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105584470 | |||||||
| chr4:105584497 | T | C | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-4751T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105584497 | |||||||
| chr4:105584646 | T | C | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-4602T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105584646 | |||||||
| chr4:105584761 | T | A | 17 | a0001c0001t0001g0083 a0001c0001t0001g0154 a0001c0001t0002g0039 others(14): Show |
17 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.197-4487T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105584761 | |||||||
| chr4:105585015 | C | T | 23 | a0001c0001t0001g0046 a0001c0001t0001g0082 a0001c0001t0001g0095 others(20): Show |
23 | HG01884.hp2 HG01981.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.197-4233C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585015 | |||||||
| chr4:105585087 | A | G | 46 | a0001c0001t0001g0083 a0001c0001t0001g0154 a0001c0001t0001g0170 others(43): Show |
47 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.197-4161A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585087 | |||||||
| chr4:105585167 | C | T | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.197-4081C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585167 | |||||||
| chr4:105585169 | AT | A | 95 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(92): Show |
95 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.197-4074delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585169 | ||||||
| chr4:105585324 | G | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-3924G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585324 | |||||||
| chr4:105585483 | A | G | 11 | a0001c0001t0001g0170 a0001c0001t0003g0090 a0001c0001t0003g0101 others(8): Show |
11 | HG01109.hp2 HG02145.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-3765A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585483 | |||||||
| chr4:105585497 | ACAT | A | 95 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0049 others(92): Show |
95 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.197-3748_197-3746d others(5): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585497 | ||||||
| chr4:105585648 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.197-3600T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585648 | |||||||
| chr4:105585693 | T | A | 17 | a0001c0001t0001g0170 a0001c0001t0003g0090 a0001c0001t0003g0101 others(14): Show |
17 | HG01109.hp2 HG01884.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.197-3555T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585693 | |||||||
| chr4:105585721 | C | T | 4 | a0001c0001t0003g0090 a0001c0001t0011g0091 a0001c0007t0002g0093 others(1): Show |
4 | HG01109.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-3527C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585721 | |||||||
| chr4:105585726 | C | CTTT | 17 | a0001c0001t0001g0046 a0001c0001t0001g0095 a0001c0001t0001g0161 others(14): Show |
17 | HG01070.hp1 HG01981.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.197-3501_197-3499d others(5): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585726 | ||||||
| chr4:105585726 | C | CTTTT | 31 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0050 others(28): Show |
32 | HG00280.hp1 HG00639.hp1 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.197-3502_197-3499d others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585726 | ||||||
| chr4:105585726 | C | CTTTTT | 24 | a0001c0001t0001g0051 a0001c0001t0001g0073 a0001c0001t0001g0166 others(21): Show |
24 | HG00741.hp2 HG01069.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.197-3503_197-3499d others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585726 | ||||||
| chr4:105585726 | C | CTTTTTT | 62 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0001g0065 others(59): Show |
62 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.197-3504_197-3499d others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585726 | ||||||
| chr4:105585726 | C | CTTTTTTT | 37 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(34): Show |
37 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.197-3505_197-3499d others(9): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585726 | ||||||
| chr4:105585726 | C | CTTTTTTT others(1): Show |
5 | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0083 others(2): Show |
5 | HG00438.hp2 HG01516.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-3506_197-3499d others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105585726 | ||||||
| chr4:105585822 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.197-3426G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585822 | |||||||
| chr4:105585880 | T | C | 2 | a0001c0001t0002g0078 a0001c0001t0002g0156 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.197-3368T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585880 | |||||||
| chr4:105585942 | G | A | 15 | a0001c0001t0001g0083 a0001c0001t0001g0095 a0001c0001t0002g0039 others(12): Show |
15 | HG01109.hp1 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.197-3306G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585942 | |||||||
| chr4:105585981 | T | C | 49 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0051 others(46): Show |
49 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.197-3267T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585981 | |||||||
| chr4:105585983 | G | A | 3 | a0001c0001t0004g0109 a0002c0003t0004g0136 a0002c0003t0004g0137 |
3 | HG01516.hp1 HG01517.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.197-3265G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105585983 | |||||||
| chr4:105586029 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-3219C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586029 | |||||||
| chr4:105586062 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.197-3186G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586062 | |||||||
| chr4:105586231 | T | TAAGAAAT others(457): Show |
1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197-3003_197-3002i others(466): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(321): Show |
2 | a0001c0001t0003g0111 a0001c0001t0003g0145 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.197-3003_197-3002i others(330): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(322): Show |
20 | a0001c0001t0001g0161 a0001c0001t0002g0072 a0001c0001t0002g0140 others(17): Show |
20 | HG01069.hp1 HG02080.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.197-3003_197-3002i others(331): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(323): Show |
8 | a0001c0001t0002g0081 a0001c0001t0012g0092 a0001c0002t0002g0010 others(5): Show |
8 | HG01361.hp1 HG02145.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-3003_197-3002i others(332): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(322): Show |
1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.197-3003_197-3002i others(331): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(325): Show |
1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.197-3003_197-3002i others(334): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(322): Show |
2 | a0001c0001t0001g0046 a0001c0004t0005g0035 |
2 | HG01981.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.197-3003_197-3002i others(331): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(322): Show |
1 | a0001c0001t0003g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.197-3003_197-3002i others(331): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(323): Show |
1 | a0001c0001t0007g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197-3003_197-3002i others(332): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586231 | T | TAAGAAAT others(321): Show |
1 | a0001c0002t0003g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197-3003_197-3002i others(330): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | 105586231 | ||||||
| chr4:105586379 | C | T | 7 | a0001c0001t0002g0146 a0001c0001t0002g0149 a0001c0001t0002g0151 others(4): Show |
7 | HG01070.hp1 HG01884.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-2869C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586379 | |||||||
| chr4:105586438 | C | A | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.197-2810C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586438 | |||||||
| chr4:105586442 | T | C | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.197-2806T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586442 | |||||||
| chr4:105586462 | G | A | 5 | a0001c0001t0011g0091 a0001c0008t0006g0076 a0001c0008t0006g0077 others(2): Show |
5 | HG02559.hp1 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.197-2786G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586462 | |||||||
| chr4:105586471 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.197-2777T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586471 | |||||||
| chr4:105586569 | G | T | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.197-2679G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586569 | |||||||
| chr4:105586829 | G | A | 1 | a0001c0001t0019g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.197-2419G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586829 | |||||||
| chr4:105586850 | T | C | 1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.197-2398T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586850 | |||||||
| chr4:105586858 | A | C | 1 | a0001c0001t0002g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.197-2390A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586858 | |||||||
| chr4:105586876 | G | C | 54 | a0001c0001t0001g0044 a0001c0001t0001g0158 a0001c0001t0002g0039 others(51): Show |
54 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.197-2372G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586876 | |||||||
| chr4:105586943 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.197-2305T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105586943 | |||||||
| chr4:105587022 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.197-2226C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587022 | |||||||
| chr4:105587369 | G | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1879G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587369 | |||||||
| chr4:105587500 | G | A | 4 | a0001c0001t0001g0079 a0001c0001t0001g0177 a0001c0001t0001g0183 others(1): Show |
4 | HG00639.hp1 HG01106.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-1748G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587500 | |||||||
| chr4:105587512 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.197-1736G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587512 | |||||||
| chr4:105587524 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.197-1724G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587524 | |||||||
| chr4:105587580 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.197-1668C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587580 | |||||||
| chr4:105587617 | C | T | 5 | a0001c0001t0012g0092 a0001c0002t0003g0032 a0001c0004t0009g0103 others(2): Show |
5 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-1631C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587617 | |||||||
| chr4:105587621 | C | T | 30 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0146 others(27): Show |
30 | HG01109.hp2 HG01884.hp2 HG01975.hp2 others(27): Show |
intron_variant | MODIFIER | c.197-1627C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587621 | |||||||
| chr4:105587693 | C | G | 1 | a0002c0003t0008g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.197-1555C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587693 | |||||||
| chr4:105587709 | C | T | 6 | a0001c0002t0001g0020 a0003c0006t0003g0143 a0004c0011t0002g0003 others(3): Show |
6 | HG02145.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1539C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587709 | |||||||
| chr4:105587711 | C | T | 10 | a0002c0003t0001g0036 a0002c0003t0001g0094 a0002c0003t0001g0159 others(7): Show |
10 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-1537C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587711 | |||||||
| chr4:105587712 | G | A | 2 | a0004c0011t0002g0003 a0004c0011t0002g0004 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.197-1536G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587712 | |||||||
| chr4:105587780 | G | A | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.197-1468G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587780 | |||||||
| chr4:105587935 | G | T | 6 | a0001c0002t0001g0020 a0003c0006t0003g0143 a0004c0011t0002g0003 others(3): Show |
6 | HG02145.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-1313G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587935 | |||||||
| chr4:105587936 | C | T | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1312C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587936 | |||||||
| chr4:105587938 | T | C | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-1310T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587938 | |||||||
| chr4:105587953 | G | T | 10 | a0002c0003t0001g0036 a0002c0003t0001g0094 a0002c0003t0001g0159 others(7): Show |
10 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-1295G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105587953 | |||||||
| chr4:105588014 | C | T | 1 | a0002c0003t0010g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.197-1234C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588014 | |||||||
| chr4:105588304 | T | G | 2 | a0002c0005t0002g0007 a0002c0005t0002g0013 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.197-944T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588304 | |||||||
| chr4:105588428 | C | T | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.197-820C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588428 | |||||||
| chr4:105588429 | G | A | 1 | a0002c0005t0001g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.197-819G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588429 | |||||||
| chr4:105588487 | C | G | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.197-761C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588487 | |||||||
| chr4:105588489 | G | T | 2 | a0002c0005t0002g0007 a0002c0005t0002g0013 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.197-759G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588489 | |||||||
| chr4:105588633 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.197-615A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588633 | |||||||
| chr4:105588773 | T | C | 1 | a0006c0010t0021g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.197-475T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588773 | |||||||
| chr4:105588817 | A | C | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.197-431A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588817 | |||||||
| chr4:105588920 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.197-328G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588920 | |||||||
| chr4:105588973 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.197-275C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105588973 | |||||||
| chr4:105589062 | G | A | 10 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0047 others(7): Show |
10 | HG00408.hp2 HG00438.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.197-186G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105589062 | |||||||
| chr4:105589158 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.197-90G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105589158 | |||||||
| chr4:105589472 | A | G | 5 | a0001c0001t0012g0092 a0001c0002t0003g0032 a0001c0004t0009g0103 others(2): Show |
5 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+37A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105589472 | |||||||
| chr4:105589525 | G | A | 6 | a0001c0002t0001g0020 a0003c0006t0003g0143 a0004c0011t0002g0003 others(3): Show |
6 | HG02145.hp1 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.384+90G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105589525 | |||||||
| chr4:105589565 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.384+130G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105589565 | |||||||
| chr4:105589704 | T | C | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.384+269T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105589704 | |||||||
| chr4:105589965 | G | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+530G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105589965 | |||||||
| chr4:105589989 | A | AG | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+554_384+555ins others(1): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105589989 | |||||||
| chr4:105590037 | C | CA | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+613dupA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590037 | ||||||
| chr4:105590074 | A | AGAAG | 20 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0073 others(17): Show |
20 | HG00438.hp1 HG00639.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.384+691_384+694dup others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | A | AGAAGGAA others(1): Show |
10 | a0001c0001t0002g0146 a0001c0001t0002g0149 a0001c0001t0003g0111 others(7): Show |
10 | HG01243.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.384+687_384+694dup others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | A | AGAAGGAA others(5): Show |
6 | a0001c0001t0002g0152 a0001c0001t0003g0075 a0001c0001t0003g0084 others(3): Show |
6 | HG01069.hp1 HG01981.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.384+683_384+694dup others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | A | AGAAGGAA others(9): Show |
1 | a0001c0001t0003g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.384+679_384+694dup others(16): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | AGAAG | A | 47 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(44): Show |
47 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.384+691_384+694del others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | AGAAGGAA others(1): Show |
A | 20 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0080 others(17): Show |
21 | HG00280.hp1 HG00639.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.384+687_384+694del others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | AGAAGGAA others(5): Show |
A | 5 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0001t0018g0037 others(2): Show |
5 | HG01517.hp2 HG01981.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+683_384+694del others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | AGAAGGAA others(9): Show |
A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0158 others(1): Show |
4 | HG00735.hp1 HG00741.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+679_384+694del others(16): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | AGAAGGAA others(13): Show |
A | 5 | a0001c0001t0012g0092 a0001c0002t0001g0020 a0003c0006t0003g0143 others(2): Show |
5 | HG01070.hp1 HG02145.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+675_384+694del others(20): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590074 | AGAAGGAA others(17): Show |
A | 5 | a0001c0004t0009g0103 a0001c0004t0009g0105 a0004c0011t0002g0003 others(2): Show |
5 | HG00735.hp2 HG01243.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+671_384+694del others(24): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590074 | ||||||
| chr4:105590126 | G | A | 21 | a0001c0001t0001g0104 a0001c0001t0001g0169 a0001c0001t0001g0170 others(18): Show |
21 | HG01109.hp2 HG01975.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.384+691G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590126 | |||||||
| chr4:105590130 | A | G | 2 | a0001c0001t0003g0153 a0001c0002t0003g0018 |
2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.384+695A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590130 | |||||||
| chr4:105590134 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.384+699A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590134 | |||||||
| chr4:105590135 | G | A | 19 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(16): Show |
19 | HG01109.hp2 HG01975.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.384+700G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590135 | |||||||
| chr4:105590140 | A | AAAAG | 21 | a0001c0001t0001g0044 a0001c0001t0002g0146 a0001c0001t0003g0090 others(18): Show |
21 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.384+719_384+722dup others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105590140 | ||||||
| chr4:105590140 | A | G | 19 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(16): Show |
19 | HG01109.hp2 HG01975.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.384+705A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590140 | |||||||
| chr4:105590158 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.384+723G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590158 | |||||||
| chr4:105590325 | A | T | 2 | a0001c0002t0008g0029 a0009c0016t0001g0021 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.384+890A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590325 | |||||||
| chr4:105590331 | G | T | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+896G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590331 | |||||||
| chr4:105590468 | A | G | 10 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0003g0088 others(7): Show |
10 | HG01975.hp2 HG02257.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.384+1033A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590468 | |||||||
| chr4:105590747 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.384+1312A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590747 | |||||||
| chr4:105590829 | T | C | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.384+1394T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105590829 | |||||||
| chr4:105591024 | CT | C | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+1593delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105591024 | ||||||
| chr4:105591137 | TA | T | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+1706delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105591137 | ||||||
| chr4:105591259 | C | T | 1 | a0003c0006t0003g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.384+1824C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105591259 | |||||||
| chr4:105591315 | G | A | 10 | a0002c0003t0001g0036 a0002c0003t0001g0094 a0002c0003t0001g0159 others(7): Show |
10 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.384+1880G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105591315 | |||||||
| chr4:105591475 | C | T | 2 | a0001c0001t0002g0100 a0001c0001t0011g0091 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.384+2040C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105591475 | |||||||
| chr4:105591675 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.384+2240A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105591675 | |||||||
| chr4:105591744 | G | A | 7 | a0001c0002t0001g0020 a0002c0003t0001g0036 a0002c0003t0001g0094 others(4): Show |
7 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.384+2309G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105591744 | |||||||
| chr4:105591771 | C | A | 1 | a0003c0006t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.384+2336C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105591771 | |||||||
| chr4:105591865 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.384+2430G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105591865 | |||||||
| chr4:105592012 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.384+2577A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592012 | |||||||
| chr4:105592013 | T | C | 11 | a0001c0001t0003g0090 a0001c0001t0003g0142 a0001c0001t0014g0107 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.384+2578T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592013 | |||||||
| chr4:105592046 | G | A | 1 | a0001c0002t0007g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.384+2611G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592046 | |||||||
| chr4:105592053 | A | G | 1 | a0002c0003t0008g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.384+2618A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592053 | |||||||
| chr4:105592113 | A | T | 10 | a0001c0001t0003g0090 a0001c0001t0003g0142 a0001c0001t0014g0107 others(7): Show |
10 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.384+2678A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592113 | |||||||
| chr4:105592411 | C | A | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.384+2976C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592411 | |||||||
| chr4:105592415 | C | T | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.384+2980C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592415 | |||||||
| chr4:105592432 | T | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0067 a0001c0001t0001g0120 others(2): Show |
5 | HG00438.hp1 HG00609.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+2997T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592432 | |||||||
| chr4:105592460 | T | A | 142 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0050 others(139): Show |
143 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.384+3025T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592460 | |||||||
| chr4:105592526 | C | T | 1 | a0007c0014t0005g0005 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.384+3091C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592526 | |||||||
| chr4:105592804 | A | C | 1 | a0001c0001t0018g0037 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.384+3369A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592804 | |||||||
| chr4:105592817 | A | G | 8 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(5): Show |
8 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+3382A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592817 | |||||||
| chr4:105592831 | C | T | 13 | a0001c0001t0003g0145 a0001c0002t0001g0020 a0001c0004t0009g0103 others(10): Show |
13 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.384+3396C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105592831 | |||||||
| chr4:105593188 | G | A | 1 | a0002c0003t0008g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.384+3753G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593188 | |||||||
| chr4:105593254 | C | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.384+3819C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593254 | |||||||
| chr4:105593270 | C | T | 15 | a0001c0001t0001g0083 a0001c0001t0001g0135 a0001c0001t0001g0161 others(12): Show |
15 | HG00280.hp1 HG01109.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.384+3835C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593270 | |||||||
| chr4:105593286 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.384+3851C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593286 | |||||||
| chr4:105593380 | T | TAA | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+3953_384+3954d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105593380 | ||||||
| chr4:105593384 | A | T | 4 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+3949A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593384 | |||||||
| chr4:105593406 | C | T | 30 | a0001c0001t0001g0083 a0001c0001t0001g0135 a0001c0001t0001g0161 others(27): Show |
30 | HG00280.hp1 HG00639.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.384+3971C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593406 | |||||||
| chr4:105593554 | A | G | 16 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(13): Show |
16 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.384+4119A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593554 | |||||||
| chr4:105593625 | T | C | 1 | a0001c0022t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.384+4190T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593625 | |||||||
| chr4:105593640 | T | C | 59 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(56): Show |
60 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.384+4205T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593640 | |||||||
| chr4:105593781 | T | C | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.384+4346T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105593781 | |||||||
| chr4:105593820 | GT | G | 1 | a0005c0009t0013g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.384+4387delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105593820 | ||||||
| chr4:105594082 | T | A | 52 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(49): Show |
52 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.384+4647T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594082 | |||||||
| chr4:105594136 | T | A | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+4701T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594136 | |||||||
| chr4:105594245 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0005c0009t0013g0001 |
4 | HG02922.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+4810A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594245 | |||||||
| chr4:105594251 | T | C | 1 | a0005c0009t0013g0001 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.384+4816T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594251 | |||||||
| chr4:105594267 | A | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.384+4832A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594267 | |||||||
| chr4:105594324 | T | A | 16 | a0001c0001t0001g0083 a0001c0001t0001g0135 a0001c0001t0001g0161 others(13): Show |
16 | HG00280.hp1 HG01109.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.384+4889T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594324 | |||||||
| chr4:105594411 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0005c0009t0013g0001 |
4 | HG02922.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+4976A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594411 | |||||||
| chr4:105594501 | G | A | 2 | a0001c0001t0003g0145 a0003c0015t0003g0019 |
2 | HG01070.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.384+5066G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594501 | |||||||
| chr4:105594597 | A | G | 1 | a0001c0002t0007g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.384+5162A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594597 | |||||||
| chr4:105594631 | C | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0128 |
2 | NA18939.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.384+5196C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594631 | |||||||
| chr4:105594656 | C | G | 47 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.384+5221C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594656 | |||||||
| chr4:105594731 | C | T | 3 | a0004c0011t0002g0003 a0004c0011t0002g0004 a0004c0021t0002g0089 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.384+5296C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594731 | |||||||
| chr4:105594760 | G | A | 1 | a0001c0002t0007g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.384+5325G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594760 | |||||||
| chr4:105594827 | A | G | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.384+5392A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594827 | |||||||
| chr4:105594871 | C | T | 54 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(51): Show |
55 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.384+5436C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594871 | |||||||
| chr4:105594950 | C | A | 1 | a0001c0002t0002g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.384+5515C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594950 | |||||||
| chr4:105594956 | G | A | 3 | a0004c0011t0002g0003 a0004c0011t0002g0004 a0004c0021t0002g0089 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.384+5521G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105594956 | |||||||
| chr4:105595058 | T | C | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+5623T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105595058 | |||||||
| chr4:105595105 | A | G | 13 | a0001c0001t0001g0083 a0001c0001t0001g0135 a0001c0001t0001g0161 others(10): Show |
13 | HG00280.hp1 HG01109.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.384+5670A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105595105 | |||||||
| chr4:105595165 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.384+5730C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105595165 | |||||||
| chr4:105595529 | A | G | 29 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(26): Show |
29 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.384+6094A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105595529 | |||||||
| chr4:105595567 | A | G | 29 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(26): Show |
29 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.384+6132A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105595567 | |||||||
| chr4:105595813 | AATAATGA others(1): Show |
A | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+6380_384+6387d others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105595813 | ||||||
| chr4:105595893 | G | C | 1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.384+6458G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105595893 | |||||||
| chr4:105595960 | C | G | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+6525C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105595960 | |||||||
| chr4:105596140 | G | A | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+6705G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596140 | |||||||
| chr4:105596181 | T | C | 2 | a0001c0001t0012g0092 a0002c0003t0012g0129 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.384+6746T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596181 | |||||||
| chr4:105596292 | G | A | 25 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0146 others(22): Show |
26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.384+6857G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596292 | |||||||
| chr4:105596491 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.384+7056G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596491 | |||||||
| chr4:105596602 | T | C | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+7167T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596602 | |||||||
| chr4:105596607 | T | G | 2 | a0001c0002t0002g0113 a0006c0010t0021g0012 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.384+7172T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596607 | |||||||
| chr4:105596709 | G | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+7274G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596709 | |||||||
| chr4:105596806 | T | C | 1 | a0001c0002t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.384+7371T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596806 | |||||||
| chr4:105596842 | C | G | 57 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(54): Show |
58 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.384+7407C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105596842 | |||||||
| chr4:105597040 | T | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+7605T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105597040 | |||||||
| chr4:105597041 | C | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+7606C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105597041 | |||||||
| chr4:105597156 | A | G | 4 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+7721A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105597156 | |||||||
| chr4:105597360 | A | G | 3 | a0004c0011t0002g0003 a0004c0011t0002g0004 a0004c0021t0002g0089 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.384+7925A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105597360 | |||||||
| chr4:105597759 | G | A | 31 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(28): Show |
31 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+8324G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105597759 | |||||||
| chr4:105597813 | A | T | 31 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(28): Show |
31 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+8378A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105597813 | |||||||
| chr4:105598249 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.384+8814T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598249 | |||||||
| chr4:105598330 | G | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0166 |
2 | HG01069.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.384+8895G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598330 | |||||||
| chr4:105598360 | A | G | 1 | a0001c0001t0019g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.384+8925A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598360 | |||||||
| chr4:105598470 | G | T | 8 | a0001c0002t0007g0023 a0001c0004t0005g0034 a0001c0004t0005g0035 others(5): Show |
8 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+9035G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598470 | |||||||
| chr4:105598506 | G | A | 14 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(11): Show |
14 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.384+9071G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598506 | |||||||
| chr4:105598604 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.384+9169C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598604 | |||||||
| chr4:105598674 | A | AT | 5 | a0001c0001t0003g0172 a0001c0002t0002g0002 a0001c0002t0002g0010 others(2): Show |
5 | HG03453.hp2 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+9249dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105598674 | ||||||
| chr4:105598787 | A | T | 44 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0071 others(41): Show |
44 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.384+9352A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598787 | |||||||
| chr4:105598904 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.384+9469G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105598904 | |||||||
| chr4:105599168 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0018g0037 |
2 | HG01517.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.384+9733A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105599168 | |||||||
| chr4:105599278 | T | A | 29 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(26): Show |
29 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.384+9843T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105599278 | |||||||
| chr4:105599523 | AT | A | 3 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0005c0009t0013g0001 |
4 | HG02922.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+10089delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105599523 | |||||||
| chr4:105599585 | C | T | 17 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(14): Show |
17 | HG00735.hp2 HG00741.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.384+10150C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105599585 | |||||||
| chr4:105599695 | C | T | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+10260C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105599695 | |||||||
| chr4:105599697 | A | G | 4 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.384+10262A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105599697 | |||||||
| chr4:105600357 | A | G | 25 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(22): Show |
25 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.384+10922A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600357 | |||||||
| chr4:105600546 | A | G | 2 | a0001c0001t0012g0092 a0002c0003t0012g0129 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.384+11111A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600546 | |||||||
| chr4:105600681 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.384+11246C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600681 | |||||||
| chr4:105600689 | A | G | 25 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(22): Show |
25 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.384+11254A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600689 | |||||||
| chr4:105600702 | C | G | 25 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(22): Show |
25 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.384+11267C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600702 | |||||||
| chr4:105600709 | C | T | 25 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(22): Show |
25 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.384+11274C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600709 | |||||||
| chr4:105600713 | T | A | 25 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(22): Show |
25 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.384+11278T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600713 | |||||||
| chr4:105600760 | C | T | 1 | a0001c0001t0003g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.384+11325C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600760 | |||||||
| chr4:105600980 | G | A | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+11545G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600980 | |||||||
| chr4:105601020 | A | G | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.384+11585A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601020 | |||||||
| chr4:105601322 | C | G | 14 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(11): Show |
14 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.384+11887C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601322 | |||||||
| chr4:105601611 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.385-11773C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601611 | |||||||
| chr4:105601613 | C | G | 4 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-11771C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601613 | |||||||
| chr4:105601646 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-11738C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601646 | |||||||
| chr4:105601845 | C | T | 2 | a0001c0002t0002g0113 a0006c0010t0021g0012 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.385-11539C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601845 | |||||||
| chr4:105601853 | T | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.385-11531T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601853 | |||||||
| chr4:105601891 | A | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.385-11493A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105601891 | |||||||
| chr4:105602132 | T | C | 28 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(25): Show |
28 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.385-11252T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602132 | |||||||
| chr4:105602162 | G | A | 25 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(22): Show |
25 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.385-11222G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602162 | |||||||
| chr4:105602244 | T | A | 1 | a0001c0001t0002g0127 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.385-11140T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602244 | |||||||
| chr4:105602279 | C | G | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-11105C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602279 | |||||||
| chr4:105602406 | G | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-10978G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602406 | |||||||
| chr4:105602552 | A | T | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.385-10832A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602552 | |||||||
| chr4:105602606 | C | T | 1 | a0001c0002t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.385-10778C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602606 | |||||||
| chr4:105602775 | C | A | 13 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 others(10): Show |
13 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.385-10609C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602775 | |||||||
| chr4:105602820 | T | C | 58 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(55): Show |
59 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.385-10564T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602820 | |||||||
| chr4:105602912 | C | G | 1 | a0001c0002t0007g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.385-10472C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602912 | |||||||
| chr4:105603005 | C | T | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-10379C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603005 | |||||||
| chr4:105603270 | C | T | 2 | a0001c0001t0003g0101 a0001c0001t0011g0091 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.385-10114C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603270 | |||||||
| chr4:105603287 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-10097G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603287 | |||||||
| chr4:105603298 | T | C | 58 | a0001c0001t0001g0083 a0001c0001t0001g0104 a0001c0001t0001g0135 others(55): Show |
59 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.385-10086T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603298 | |||||||
| chr4:105603322 | C | T | 1 | a0007c0014t0005g0005 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.385-10062C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603322 | |||||||
| chr4:105603526 | G | T | 4 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-9858G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603526 | |||||||
| chr4:105603573 | T | G | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-9811T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603573 | |||||||
| chr4:105603735 | A | G | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-9649A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603735 | |||||||
| chr4:105603797 | C | T | 11 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 others(8): Show |
11 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-9587C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603797 | |||||||
| chr4:105603907 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-9477C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603907 | |||||||
| chr4:105603908 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.385-9476G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105603908 | |||||||
| chr4:105604027 | C | G | 1 | a0001c0007t0008g0045 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.385-9357C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604027 | |||||||
| chr4:105604099 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.385-9285C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604099 | |||||||
| chr4:105604365 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0167 |
2 | HG00609.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.385-9019G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604365 | |||||||
| chr4:105604546 | A | G | 31 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(28): Show |
31 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.385-8838A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604546 | |||||||
| chr4:105604563 | T | C | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-8821T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604563 | |||||||
| chr4:105604707 | T | G | 26 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(23): Show |
26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.385-8677T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604707 | |||||||
| chr4:105604812 | C | T | 4 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-8572C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604812 | |||||||
| chr4:105604838 | C | G | 1 | a0006c0010t0021g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.385-8546C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105604838 | |||||||
| chr4:105605185 | C | A | 4 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 others(1): Show |
4 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-8199C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605185 | |||||||
| chr4:105605247 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.385-8137A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605247 | |||||||
| chr4:105605387 | T | C | 26 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(23): Show |
26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.385-7997T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605387 | |||||||
| chr4:105605388 | C | T | 2 | a0001c0001t0012g0092 a0001c0002t0002g0113 |
2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.385-7996C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605388 | |||||||
| chr4:105605537 | C | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-7847C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605537 | |||||||
| chr4:105605709 | C | A | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-7675C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605709 | |||||||
| chr4:105605830 | A | G | 26 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(23): Show |
26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.385-7554A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605830 | |||||||
| chr4:105605861 | T | C | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-7523T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605861 | |||||||
| chr4:105605909 | G | C | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-7475G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605909 | |||||||
| chr4:105605949 | C | T | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-7435C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605949 | |||||||
| chr4:105606008 | A | G | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-7376A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606008 | |||||||
| chr4:105606042 | T | G | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.385-7342T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606042 | |||||||
| chr4:105606224 | A | G | 26 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(23): Show |
26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.385-7160A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606224 | |||||||
| chr4:105606243 | A | C | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-7141A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606243 | |||||||
| chr4:105606252 | A | C | 2 | a0002c0003t0004g0136 a0002c0003t0004g0137 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.385-7132A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606252 | |||||||
| chr4:105606267 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.385-7117A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606267 | |||||||
| chr4:105606351 | T | G | 11 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 others(8): Show |
11 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-7033T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606351 | |||||||
| chr4:105606411 | C | T | 26 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(23): Show |
26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.385-6973C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606411 | |||||||
| chr4:105606456 | A | G | 26 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(23): Show |
26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.385-6928A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606456 | |||||||
| chr4:105606651 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.385-6733T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606651 | |||||||
| chr4:105606716 | T | A | 3 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 |
3 | HG00735.hp2 HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.385-6668T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606716 | |||||||
| chr4:105606739 | T | C | 53 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(50): Show |
53 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.385-6645T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606739 | |||||||
| chr4:105606787 | T | A | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-6597T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606787 | |||||||
| chr4:105607025 | C | T | 1 | a0001c0019t0004g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385-6359C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607025 | |||||||
| chr4:105607048 | G | C | 2 | a0001c0002t0001g0020 a0008c0017t0001g0131 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.385-6336G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607048 | |||||||
| chr4:105607066 | A | G | 4 | a0001c0001t0001g0079 a0001c0001t0001g0177 a0001c0001t0001g0183 others(1): Show |
4 | HG00639.hp1 HG01106.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-6318A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607066 | |||||||
| chr4:105607441 | A | C | 4 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-5943A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607441 | |||||||
| chr4:105607476 | C | A | 53 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(50): Show |
53 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.385-5908C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607476 | |||||||
| chr4:105607518 | A | AAT | 18 | a0001c0001t0003g0145 a0001c0001t0004g0110 a0001c0001t0004g0132 others(15): Show |
18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.385-5866_385-5865i others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607518 | |||||||
| chr4:105607519 | T | G | 18 | a0001c0001t0003g0145 a0001c0001t0004g0110 a0001c0001t0004g0132 others(15): Show |
18 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.385-5865T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607519 | |||||||
| chr4:105607784 | G | A | 1 | a0003c0006t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385-5600G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607784 | |||||||
| chr4:105607827 | AG | A | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-5555delG | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105607827 | ||||||
| chr4:105607968 | T | TA | 8 | a0001c0001t0001g0059 a0001c0001t0002g0100 a0001c0001t0003g0101 others(5): Show |
8 | HG00735.hp2 HG01243.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-5407dupA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105607968 | ||||||
| chr4:105607969 | A | T | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-5415A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607969 | |||||||
| chr4:105608553 | C | G | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-4831C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105608553 | |||||||
| chr4:105608851 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.385-4533A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105608851 | |||||||
| chr4:105608922 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.385-4462G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105608922 | |||||||
| chr4:105609147 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.385-4237C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609147 | |||||||
| chr4:105609270 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0128 |
2 | NA18939.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.385-4114T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609270 | |||||||
| chr4:105609292 | T | G | 4 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 others(1): Show |
4 | HG02630.hp2 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-4092T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609292 | |||||||
| chr4:105609544 | T | C | 1 | a0001c0001t0004g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.385-3840T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609544 | |||||||
| chr4:105609617 | T | C | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.385-3767T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609617 | |||||||
| chr4:105609705 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-3679C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609705 | |||||||
| chr4:105609756 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.385-3628G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609756 | |||||||
| chr4:105609793 | G | A | 22 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(19): Show |
22 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.385-3591G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609793 | |||||||
| chr4:105609980 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.385-3404G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105609980 | |||||||
| chr4:105610234 | T | C | 1 | a0001c0022t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.385-3150T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610234 | |||||||
| chr4:105610337 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.385-3047T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610337 | |||||||
| chr4:105610467 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.385-2917A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610467 | |||||||
| chr4:105610509 | T | C | 2 | a0001c0001t0003g0171 a0001c0001t0003g0172 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.385-2875T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610509 | |||||||
| chr4:105610551 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.385-2833A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610551 | |||||||
| chr4:105610587 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-2797T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610587 | |||||||
| chr4:105610592 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.385-2792G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610592 | |||||||
| chr4:105610601 | A | G | 111 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0071 others(108): Show |
111 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.385-2783A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610601 | |||||||
| chr4:105610604 | TTTGTTTG others(3): Show |
T | 1 | a0001c0001t0001g0169 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.385-2779_385-2770d others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610604 | |||||||
| chr4:105610678 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-2706A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610678 | |||||||
| chr4:105610689 | C | T | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-2695C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610689 | |||||||
| chr4:105610690 | G | T | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-2694G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610690 | |||||||
| chr4:105610764 | T | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.385-2620T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610764 | |||||||
| chr4:105610781 | G | T | 6 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-2603G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610781 | |||||||
| chr4:105610859 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-2525T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610859 | |||||||
| chr4:105610875 | C | T | 6 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-2509C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610875 | |||||||
| chr4:105610916 | A | C | 3 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 |
3 | HG00735.hp2 HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.385-2468A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610916 | |||||||
| chr4:105610925 | C | A | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-2459C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610925 | |||||||
| chr4:105610954 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.385-2430A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610954 | |||||||
| chr4:105610984 | C | T | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.385-2400C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105610984 | |||||||
| chr4:105611006 | C | T | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.385-2378C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611006 | |||||||
| chr4:105611043 | T | C | 3 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 |
3 | HG00735.hp2 HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.385-2341T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611043 | |||||||
| chr4:105611063 | T | C | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.385-2321T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611063 | |||||||
| chr4:105611172 | A | G | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.385-2212A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611172 | |||||||
| chr4:105611343 | T | C | 30 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0003g0145 others(27): Show |
30 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.385-2041T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611343 | |||||||
| chr4:105611643 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.385-1741T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611643 | |||||||
| chr4:105611648 | A | T | 1 | a0007c0014t0005g0005 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.385-1736A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611648 | |||||||
| chr4:105611649 | T | A | 1 | a0007c0014t0005g0005 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.385-1735T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611649 | |||||||
| chr4:105611757 | T | C | 4 | a0001c0001t0003g0145 a0001c0002t0007g0023 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-1627T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611757 | |||||||
| chr4:105612039 | C | A | 22 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(19): Show |
22 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.385-1345C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612039 | |||||||
| chr4:105612145 | A | T | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-1239A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612145 | |||||||
| chr4:105612180 | C | G | 3 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 |
3 | HG00735.hp2 HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.385-1204C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612180 | |||||||
| chr4:105612189 | ACC | A | 3 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 |
3 | HG00735.hp2 HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.385-1192_385-1191d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105612189 | ||||||
| chr4:105612308 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.385-1076A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612308 | |||||||
| chr4:105612315 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0158 |
3 | HG00735.hp1 HG00741.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.385-1069C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612315 | |||||||
| chr4:105612534 | G | A | 1 | a0001c0001t0001g0049 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.385-850G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612534 | |||||||
| chr4:105612585 | A | G | 5 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 others(2): Show |
5 | HG02630.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.385-799A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612585 | |||||||
| chr4:105612761 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.385-623G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612761 | |||||||
| chr4:105612925 | A | T | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-459A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612925 | |||||||
| chr4:105612953 | A | G | 40 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0004g0110 others(37): Show |
40 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.385-431A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105612953 | |||||||
| chr4:105613000 | C | A | 111 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0080 others(108): Show |
111 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.385-384C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105613000 | |||||||
| chr4:105613128 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.385-256G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105613128 | |||||||
| chr4:105613268 | CAGAA | C | 22 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(19): Show |
22 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.385-114_385-111del others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr4 | 105613268 | ||||||
| chr4:105613270 | G | A | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-114G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105613270 | |||||||
| chr4:105613374 | G | C | 12 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0001c0007t0002g0093 others(9): Show |
12 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.385-10G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105613374 | |||||||
| chr4:105613534 | A | G | 25 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0004g0110 others(22): Show |
25 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.508+27A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613534 | |||||||
| chr4:105613565 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.508+58C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613565 | |||||||
| chr4:105613619 | T | C | 10 | a0001c0001t0003g0090 a0001c0001t0003g0142 a0001c0001t0014g0107 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.508+112T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613619 | |||||||
| chr4:105613650 | G | A | 9 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 others(6): Show |
9 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+143G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613650 | |||||||
| chr4:105613710 | A | C | 1 | a0001c0001t0002g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.508+203A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613710 | |||||||
| chr4:105613740 | AT | A | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.508+236delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105613740 | ||||||
| chr4:105613795 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.508+288G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613795 | |||||||
| chr4:105613851 | C | G | 1 | a0001c0001t0011g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508+344C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613851 | |||||||
| chr4:105613905 | A | G | 32 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(29): Show |
32 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.508+398A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105613905 | |||||||
| chr4:105614045 | A | C | 3 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 |
3 | HG00735.hp2 HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.508+538A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614045 | |||||||
| chr4:105614047 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508+540A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614047 | |||||||
| chr4:105614157 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.508+650G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614157 | |||||||
| chr4:105614193 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.508+686C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614193 | |||||||
| chr4:105614245 | C | G | 22 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(19): Show |
22 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.508+738C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614245 | |||||||
| chr4:105614324 | C | T | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508+817C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614324 | |||||||
| chr4:105614325 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.508+818G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614325 | |||||||
| chr4:105614381 | G | A | 1 | a0001c0001t0007g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.508+874G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614381 | |||||||
| chr4:105614509 | T | G | 7 | a0001c0001t0003g0171 a0001c0001t0003g0172 a0001c0002t0002g0002 others(4): Show |
7 | HG02572.hp1 HG03453.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.508+1002T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614509 | |||||||
| chr4:105614793 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.508+1286A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614793 | |||||||
| chr4:105614948 | T | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.508+1441T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614948 | |||||||
| chr4:105614964 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.508+1457C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105614964 | |||||||
| chr4:105615036 | A | T | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508+1529A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105615036 | |||||||
| chr4:105615280 | G | A | 1 | a0001c0007t0007g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.508+1773G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105615280 | |||||||
| chr4:105615647 | A | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.508+2140A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105615647 | |||||||
| chr4:105616556 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508+3049C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105616556 | |||||||
| chr4:105616643 | A | T | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.508+3136A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105616643 | |||||||
| chr4:105616810 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.508+3303C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105616810 | |||||||
| chr4:105617054 | A | G | 1 | a0001c0002t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.508+3547A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617054 | |||||||
| chr4:105617327 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0003c0023t0020g0114 |
3 | HG02257.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.508+3820C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617327 | |||||||
| chr4:105617380 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0016g0168 |
2 | HG01074.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.508+3873T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617380 | |||||||
| chr4:105617765 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.508+4258A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617765 | |||||||
| chr4:105617872 | A | T | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.508+4365A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617872 | |||||||
| chr4:105617924 | A | G | 1 | a0001c0002t0009g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.508+4417A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617924 | |||||||
| chr4:105617944 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.508+4437A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617944 | |||||||
| chr4:105617973 | A | G | 3 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0003c0023t0020g0114 |
3 | HG02257.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.508+4466A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105617973 | |||||||
| chr4:105618111 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.508+4604A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618111 | |||||||
| chr4:105618204 | T | C | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.508+4697T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618204 | |||||||
| chr4:105618244 | TA | T | 2 | a0001c0004t0009g0103 a0001c0004t0009g0105 |
2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.508+4738delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618244 | |||||||
| chr4:105618276 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.508+4769G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618276 | |||||||
| chr4:105618311 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.508+4804A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618311 | |||||||
| chr4:105618425 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.508+4918C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618425 | |||||||
| chr4:105618452 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508+4945C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618452 | |||||||
| chr4:105618477 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+4970C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618477 | |||||||
| chr4:105618482 | G | A | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.508+4975G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618482 | |||||||
| chr4:105618602 | C | G | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+5095C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618602 | |||||||
| chr4:105618645 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+5138A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618645 | |||||||
| chr4:105618925 | G | T | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.508+5418G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105618925 | |||||||
| chr4:105619386 | C | G | 1 | a0001c0001t0002g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.508+5879C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105619386 | |||||||
| chr4:105619871 | A | C | 9 | a0001c0007t0002g0093 a0001c0007t0007g0087 a0001c0007t0008g0045 others(6): Show |
9 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.508+6364A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105619871 | |||||||
| chr4:105620009 | T | G | 53 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(50): Show |
53 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.508+6502T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620009 | |||||||
| chr4:105620152 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508+6645G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620152 | |||||||
| chr4:105620194 | T | A | 1 | a0001c0001t0002g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.508+6687T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620194 | |||||||
| chr4:105620247 | G | C | 2 | a0001c0002t0008g0029 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.508+6740G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620247 | |||||||
| chr4:105620308 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.508+6801G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620308 | |||||||
| chr4:105620439 | T | A | 3 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0003c0023t0020g0114 |
3 | HG02257.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.508+6932T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620439 | |||||||
| chr4:105620445 | C | G | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.508+6938C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620445 | |||||||
| chr4:105620467 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.508+6960T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620467 | |||||||
| chr4:105620495 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508+6988A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620495 | |||||||
| chr4:105620499 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.508+6992C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620499 | |||||||
| chr4:105620603 | A | G | 2 | a0001c0001t0012g0092 a0001c0002t0002g0113 |
2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.508+7096A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620603 | |||||||
| chr4:105620825 | TG | T | 50 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.508+7319delG | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620825 | |||||||
| chr4:105621321 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.508+7814T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105621321 | |||||||
| chr4:105621375 | A | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.508+7868A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105621375 | |||||||
| chr4:105621669 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.508+8162A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105621669 | |||||||
| chr4:105621779 | T | C | 1 | a0001c0019t0004g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.508+8272T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105621779 | |||||||
| chr4:105622122 | A | G | 1 | a0003c0006t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.508+8615A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105622122 | |||||||
| chr4:105622126 | A | C | 1 | a0001c0001t0002g0047 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.508+8619A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105622126 | |||||||
| chr4:105622280 | G | A | 1 | a0001c0002t0007g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.509-8618G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105622280 | |||||||
| chr4:105622687 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-8211A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105622687 | |||||||
| chr4:105622844 | T | C | 11 | a0001c0001t0003g0090 a0001c0001t0003g0142 a0001c0001t0014g0107 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.509-8054T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105622844 | |||||||
| chr4:105622881 | TACAC | T | 5 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-8011_509-8008d others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105622881 | ||||||
| chr4:105623166 | G | A | 2 | a0001c0001t0012g0092 a0001c0002t0002g0113 |
2 | HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.509-7732G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623166 | |||||||
| chr4:105623292 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-7606G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623292 | |||||||
| chr4:105623369 | A | G | 50 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.509-7529A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623369 | |||||||
| chr4:105623415 | G | A | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-7483G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623415 | |||||||
| chr4:105623534 | C | CA | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-7360dupA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105623534 | ||||||
| chr4:105623545 | C | T | 22 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(19): Show |
22 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.509-7353C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623545 | |||||||
| chr4:105623678 | A | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-7220A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623678 | |||||||
| chr4:105623763 | T | C | 1 | a0002c0005t0001g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.509-7135T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623763 | |||||||
| chr4:105623868 | C | T | 3 | a0001c0001t0003g0145 a0001c0004t0009g0103 a0001c0004t0009g0105 |
3 | HG00735.hp2 HG01243.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.509-7030C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623868 | |||||||
| chr4:105623914 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-6984A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105623914 | |||||||
| chr4:105624126 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0181 |
2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.509-6772C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105624126 | |||||||
| chr4:105624146 | T | C | 5 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(2): Show |
5 | HG02630.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.509-6752T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105624146 | |||||||
| chr4:105624350 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.509-6548G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105624350 | |||||||
| chr4:105624466 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.509-6432A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105624466 | |||||||
| chr4:105624550 | C | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.509-6348C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105624550 | |||||||
| chr4:105624985 | C | T | 10 | a0001c0007t0002g0093 a0001c0007t0007g0087 a0001c0007t0008g0045 others(7): Show |
10 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.509-5913C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105624985 | |||||||
| chr4:105625174 | A | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.509-5724A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625174 | |||||||
| chr4:105625203 | C | T | 4 | a0001c0002t0002g0009 a0001c0008t0006g0076 a0001c0008t0006g0077 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-5695C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625203 | |||||||
| chr4:105625233 | T | C | 1 | a0006c0010t0021g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.509-5665T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625233 | |||||||
| chr4:105625456 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.509-5442G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625456 | |||||||
| chr4:105625651 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.509-5247C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625651 | |||||||
| chr4:105625731 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.509-5167G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625731 | |||||||
| chr4:105625754 | G | C | 2 | a0002c0005t0002g0007 a0002c0005t0002g0013 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.509-5144G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625754 | |||||||
| chr4:105625755 | G | A | 10 | a0001c0007t0002g0093 a0001c0007t0007g0087 a0001c0007t0008g0045 others(7): Show |
10 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.509-5143G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625755 | |||||||
| chr4:105625924 | T | A | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.509-4974T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625924 | |||||||
| chr4:105625950 | C | A | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509-4948C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625950 | |||||||
| chr4:105625959 | A | G | 3 | a0001c0001t0002g0100 a0001c0001t0003g0101 a0001c0001t0011g0091 |
3 | HG02630.hp2 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.509-4939A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625959 | |||||||
| chr4:105626126 | C | T | 2 | a0001c0001t0008g0017 a0002c0003t0008g0102 |
2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.509-4772C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105626126 | |||||||
| chr4:105626586 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.509-4312C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105626586 | |||||||
| chr4:105626602 | C | T | 1 | a0001c0002t0007g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.509-4296C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105626602 | |||||||
| chr4:105626634 | A | C | 50 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.509-4264A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105626634 | |||||||
| chr4:105626743 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509-4155C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105626743 | |||||||
| chr4:105626803 | T | G | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.509-4095T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105626803 | |||||||
| chr4:105627256 | G | A | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.509-3642G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105627256 | |||||||
| chr4:105627476 | C | T | 15 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0001g0020 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.509-3422C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105627476 | |||||||
| chr4:105627516 | A | G | 2 | a0001c0001t0003g0101 a0001c0001t0011g0091 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.509-3382A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105627516 | |||||||
| chr4:105627626 | A | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0156 |
2 | HG01175.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.509-3272A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105627626 | |||||||
| chr4:105627649 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.509-3249G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105627649 | |||||||
| chr4:105627939 | G | T | 100 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(97): Show |
100 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.509-2959G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105627939 | |||||||
| chr4:105628030 | TA | T | 86 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(83): Show |
86 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.509-2856delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105628030 | ||||||
| chr4:105628051 | T | C | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.509-2847T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628051 | |||||||
| chr4:105628113 | G | T | 1 | a0001c0001t0002g0149 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509-2785G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628113 | |||||||
| chr4:105628127 | T | C | 87 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(84): Show |
87 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.509-2771T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628127 | |||||||
| chr4:105628371 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509-2527C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628371 | |||||||
| chr4:105628410 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.509-2488T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628410 | |||||||
| chr4:105628542 | C | T | 1 | a0001c0002t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509-2356C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628542 | |||||||
| chr4:105628590 | C | A | 107 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(104): Show |
107 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.509-2308C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628590 | |||||||
| chr4:105628637 | T | C | 2 | a0003c0006t0001g0175 a0006c0010t0022g0006 |
2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.509-2261T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628637 | |||||||
| chr4:105628986 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.509-1912G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105628986 | |||||||
| chr4:105629057 | T | A | 4 | a0001c0001t0002g0108 a0001c0001t0007g0147 a0001c0001t0007g0148 others(1): Show |
4 | HG02622.hp2 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.509-1841T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629057 | |||||||
| chr4:105629115 | C | A | 13 | a0001c0002t0001g0020 a0001c0004t0005g0034 a0001c0004t0005g0035 others(10): Show |
13 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.509-1783C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629115 | |||||||
| chr4:105629262 | G | C | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.509-1636G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629262 | |||||||
| chr4:105629336 | G | A | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.509-1562G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629336 | |||||||
| chr4:105629414 | T | C | 19 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(16): Show |
19 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.509-1484T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629414 | |||||||
| chr4:105629448 | G | A | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.509-1450G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629448 | |||||||
| chr4:105629589 | T | TCAAATCT others(312): Show |
2 | a0001c0001t0002g0100 a0001c0001t0002g0108 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.509-1292_509-1291i others(321): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629589 | T | TCAAATCT others(313): Show |
1 | a0001c0001t0002g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.509-1292_509-1291i others(322): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629589 | T | TCAAATCT others(313): Show |
1 | a0001c0001t0002g0116 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.509-1292_509-1291i others(322): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629589 | T | TCAAATCT others(311): Show |
3 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 |
3 | HG02559.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.509-1292_509-1291i others(320): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629589 | T | TCAAATCT others(313): Show |
42 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0164 others(39): Show |
42 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.509-1292_509-1291i others(322): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629589 | T | TCAAATCT others(314): Show |
1 | a0001c0001t0001g0070 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.509-1292_509-1291i others(323): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629589 | T | TCAAATCT others(314): Show |
1 | a0001c0001t0002g0074 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.509-1292_509-1291i others(323): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629589 | T | TCAAATCT others(314): Show |
9 | a0001c0001t0001g0163 a0001c0001t0002g0055 a0001c0001t0002g0081 others(6): Show |
9 | HG00438.hp2 HG01361.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.509-1292_509-1291i others(323): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105629589 | ||||||
| chr4:105629620 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.509-1278G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629620 | |||||||
| chr4:105629682 | A | C | 104 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(101): Show |
104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.509-1216A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629682 | |||||||
| chr4:105629728 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.509-1170C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629728 | |||||||
| chr4:105629779 | C | T | 106 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.509-1119C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629779 | |||||||
| chr4:105630095 | A | G | 20 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(17): Show |
20 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.509-803A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105630095 | |||||||
| chr4:105630249 | C | CT | 71 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(68): Show |
71 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.509-633dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105630249 | ||||||
| chr4:105630249 | C | CTT | 9 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0004t0005g0034 others(6): Show |
9 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.509-634_509-633dup others(2): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105630249 | ||||||
| chr4:105630249 | CT | C | 5 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0001c0002t0002g0009 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.509-633delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr4 | 105630249 | ||||||
| chr4:105630392 | T | G | 106 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.509-506T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105630392 | |||||||
| chr4:105630419 | T | C | 1 | a0003c0006t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509-479T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105630419 | |||||||
| chr4:105630865 | G | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.509-33G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105630865 | |||||||
| chr4:105631077 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.656+32C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105631077 | |||||||
| chr4:105631257 | A | G | 106 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.656+212A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105631257 | |||||||
| chr4:105631305 | T | C | 4 | a0001c0001t0003g0088 a0001c0001t0003g0112 a0001c0001t0003g0153 others(1): Show |
4 | HG01975.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+260T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105631305 | |||||||
| chr4:105631331 | T | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.656+286T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105631331 | |||||||
| chr4:105631397 | T | G | 20 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(17): Show |
20 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656+352T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105631397 | |||||||
| chr4:105631576 | A | T | 104 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(101): Show |
104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.656+531A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105631576 | |||||||
| chr4:105631822 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.656+777G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105631822 | |||||||
| chr4:105632076 | G | A | 1 | a0001c0007t0008g0045 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.656+1031G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105632076 | |||||||
| chr4:105632090 | A | G | 20 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(17): Show |
20 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656+1045A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105632090 | |||||||
| chr4:105632207 | G | C | 104 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(101): Show |
104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.656+1162G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105632207 | |||||||
| chr4:105632638 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.656+1593A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105632638 | |||||||
| chr4:105632737 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.656+1692A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105632737 | |||||||
| chr4:105632869 | T | C | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656+1824T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105632869 | |||||||
| chr4:105633001 | G | T | 19 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(16): Show |
19 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.656+1956G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105633001 | |||||||
| chr4:105633272 | T | C | 6 | a0001c0002t0001g0020 a0002c0003t0001g0036 a0002c0003t0001g0159 others(3): Show |
6 | HG00639.hp2 HG01243.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.656+2227T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105633272 | |||||||
| chr4:105633300 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.656+2255G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105633300 | |||||||
| chr4:105633477 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.656+2432C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105633477 | |||||||
| chr4:105633572 | G | T | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656+2527G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105633572 | |||||||
| chr4:105633781 | GA | G | 2 | a0001c0004t0009g0103 a0001c0004t0009g0105 |
2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.657-2620delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 105633781 | ||||||
| chr4:105633796 | T | C | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.657-2607T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105633796 | |||||||
| chr4:105633912 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.657-2491A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105633912 | |||||||
| chr4:105634182 | C | T | 2 | a0001c0001t0003g0145 a0001c0001t0012g0092 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.657-2221C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105634182 | |||||||
| chr4:105634382 | G | A | 19 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(16): Show |
19 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.657-2021G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105634382 | |||||||
| chr4:105634708 | T | C | 1 | a0003c0006t0003g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.657-1695T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105634708 | |||||||
| chr4:105634725 | G | GT | 118 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(115): Show |
119 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.657-1673dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 105634725 | ||||||
| chr4:105634866 | C | T | 1 | a0002c0003t0008g0102 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.657-1537C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105634866 | |||||||
| chr4:105635241 | CAA | C | 4 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.657-1160_657-1159d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | 105635241 | ||||||
| chr4:105635361 | C | G | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.657-1042C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105635361 | |||||||
| chr4:105635367 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0128 |
2 | NA18939.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.657-1036T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105635367 | |||||||
| chr4:105635457 | C | A | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.657-946C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105635457 | |||||||
| chr4:105635567 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.657-836T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105635567 | |||||||
| chr4:105635616 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.657-787C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105635616 | |||||||
| chr4:105635673 | T | A | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.657-730T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105635673 | |||||||
| chr4:105635804 | A | T | 107 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(104): Show |
108 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.657-599A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105635804 | |||||||
| chr4:105636114 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.657-289C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105636114 | |||||||
| chr4:105636243 | A | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.657-160A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105636243 | |||||||
| chr4:105636265 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.657-138G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105636265 | |||||||
| chr4:105636272 | C | T | 17 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(14): Show |
17 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.657-131C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 4/13 | chr4 | 105636272 | |||||||
| chr4:105636575 | C | T | 6 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0001c0002t0002g0009 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.674+155C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105636575 | |||||||
| chr4:105636762 | C | G | 1 | a0001c0002t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.674+342C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105636762 | |||||||
| chr4:105636948 | A | T | 20 | a0001c0001t0002g0100 a0001c0001t0002g0108 a0001c0001t0003g0075 others(17): Show |
20 | HG01069.hp1 HG01975.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.674+528A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105636948 | |||||||
| chr4:105637152 | T | C | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.674+732T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637152 | |||||||
| chr4:105637171 | A | T | 1 | a0001c0001t0002g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.674+751A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637171 | |||||||
| chr4:105637449 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.674+1029C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637449 | |||||||
| chr4:105637451 | A | G | 2 | a0003c0006t0001g0144 a0005c0009t0013g0001 |
3 | HG02622.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.674+1031A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637451 | |||||||
| chr4:105637720 | A | C | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.674+1300A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637720 | |||||||
| chr4:105637728 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.674+1308A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637728 | |||||||
| chr4:105637736 | G | A | 97 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(94): Show |
97 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.674+1316G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637736 | |||||||
| chr4:105637812 | A | T | 1 | a0003c0006t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.674+1392A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637812 | |||||||
| chr4:105637832 | T | C | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.674+1412T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637832 | |||||||
| chr4:105637964 | T | C | 3 | a0003c0006t0001g0144 a0005c0009t0013g0001 a0008c0017t0001g0131 |
4 | HG02145.hp1 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.674+1544T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105637964 | |||||||
| chr4:105638027 | A | G | 6 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0001c0002t0002g0009 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.674+1607A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638027 | |||||||
| chr4:105638193 | T | C | 6 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0001c0002t0002g0009 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.674+1773T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638193 | |||||||
| chr4:105638221 | G | T | 108 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(105): Show |
109 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.674+1801G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638221 | |||||||
| chr4:105638222 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.674+1802T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638222 | |||||||
| chr4:105638342 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.674+1922T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638342 | |||||||
| chr4:105638442 | T | A | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.674+2022T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638442 | |||||||
| chr4:105638722 | G | A | 2 | a0001c0004t0009g0103 a0001c0004t0009g0105 |
2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.674+2302G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638722 | |||||||
| chr4:105638732 | CTCATTCA | C | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.674+2317_674+2323d others(9): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105638732 | ||||||
| chr4:105638827 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.674+2407T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105638827 | |||||||
| chr4:105639042 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.674+2622T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639042 | |||||||
| chr4:105639161 | G | C | 1 | a0003c0006t0001g0150 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.674+2741G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639161 | |||||||
| chr4:105639190 | C | T | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.674+2770C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639190 | |||||||
| chr4:105639347 | T | C | 4 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.674+2927T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639347 | |||||||
| chr4:105639400 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.674+2980G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639400 | |||||||
| chr4:105639539 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.674+3119G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639539 | |||||||
| chr4:105639641 | C | T | 1 | a0001c0002t0003g0030 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.674+3221C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639641 | |||||||
| chr4:105639901 | C | T | 108 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(105): Show |
109 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.674+3481C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105639901 | |||||||
| chr4:105640364 | C | T | 1 | a0003c0006t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.674+3944C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105640364 | |||||||
| chr4:105640485 | T | C | 16 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(13): Show |
16 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.674+4065T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105640485 | |||||||
| chr4:105640588 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.674+4168C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105640588 | |||||||
| chr4:105640664 | G | T | 1 | a0001c0001t0002g0063 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.674+4244G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105640664 | |||||||
| chr4:105640726 | G | A | 1 | a0001c0002t0002g0002 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.674+4306G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105640726 | |||||||
| chr4:105640961 | C | A | 1 | a0007c0014t0005g0005 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.675-4227C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105640961 | |||||||
| chr4:105641002 | C | A | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-4186C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641002 | |||||||
| chr4:105641118 | A | G | 4 | a0001c0001t0003g0088 a0001c0001t0003g0112 a0001c0001t0003g0153 others(1): Show |
4 | HG01975.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-4070A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641118 | |||||||
| chr4:105641380 | G | A | 44 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(41): Show |
44 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.675-3808G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641380 | |||||||
| chr4:105641405 | T | C | 2 | a0002c0005t0002g0007 a0002c0005t0002g0013 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.675-3783T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641405 | |||||||
| chr4:105641450 | T | C | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-3738T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641450 | |||||||
| chr4:105641474 | G | A | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.675-3714G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641474 | |||||||
| chr4:105641478 | A | T | 6 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0001c0002t0002g0009 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-3710A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641478 | |||||||
| chr4:105641496 | A | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0047 others(8): Show |
11 | HG00408.hp2 HG00438.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.675-3692A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641496 | |||||||
| chr4:105641518 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.675-3670G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641518 | |||||||
| chr4:105641521 | A | G | 181 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(178): Show |
182 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.675-3667A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641521 | |||||||
| chr4:105641566 | T | A | 3 | a0003c0006t0001g0144 a0005c0009t0013g0001 a0008c0017t0001g0131 |
4 | HG02145.hp1 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.675-3622T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641566 | |||||||
| chr4:105641661 | CT | C | 4 | a0001c0002t0002g0014 a0003c0006t0001g0144 a0005c0009t0013g0001 others(1): Show |
5 | HG02145.hp1 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.675-3519delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105641661 | ||||||
| chr4:105641671 | T | C | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-3517T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641671 | |||||||
| chr4:105641672 | G | A | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-3516G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641672 | |||||||
| chr4:105641705 | C | T | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-3483C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641705 | |||||||
| chr4:105641725 | A | AT | 82 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(79): Show |
82 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.675-3454dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105641725 | ||||||
| chr4:105642009 | A | G | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-3179A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642009 | |||||||
| chr4:105642116 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.675-3072T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642116 | |||||||
| chr4:105642127 | A | G | 17 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0007t0002g0093 others(14): Show |
17 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.675-3061A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642127 | |||||||
| chr4:105642154 | G | A | 6 | a0001c0001t0002g0146 a0001c0001t0003g0111 a0001c0002t0002g0009 others(3): Show |
6 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-3034G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642154 | |||||||
| chr4:105642185 | G | T | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-3003G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642185 | |||||||
| chr4:105642195 | C | A | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-2993C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642195 | |||||||
| chr4:105642222 | C | T | 6 | a0001c0004t0005g0035 a0001c0004t0005g0038 a0001c0004t0005g0042 others(3): Show |
6 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.675-2966C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642222 | |||||||
| chr4:105642250 | T | A | 108 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(105): Show |
109 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.675-2938T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642250 | |||||||
| chr4:105642278 | C | A | 1 | a0003c0006t0003g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.675-2910C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642278 | |||||||
| chr4:105642407 | T | A | 2 | a0001c0001t0001g0046 a0001c0001t0016g0168 |
2 | HG01074.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.675-2781T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642407 | |||||||
| chr4:105642443 | A | G | 103 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(100): Show |
103 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.675-2745A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642443 | |||||||
| chr4:105642449 | A | G | 1 | a0006c0010t0021g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.675-2739A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642449 | |||||||
| chr4:105642708 | C | T | 2 | a0001c0001t0001g0119 a0008c0017t0001g0131 |
2 | HG02015.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.675-2480C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642708 | |||||||
| chr4:105642750 | G | A | 19 | a0001c0001t0002g0100 a0001c0001t0003g0075 a0001c0001t0003g0084 others(16): Show |
19 | HG01069.hp1 HG01975.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.675-2438G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105642750 | |||||||
| chr4:105643037 | C | T | 115 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(112): Show |
116 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.675-2151C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643037 | |||||||
| chr4:105643065 | C | T | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.675-2123C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643065 | |||||||
| chr4:105643093 | T | C | 109 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(106): Show |
109 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.675-2095T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643093 | |||||||
| chr4:105643133 | G | GT | 10 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0003g0088 others(7): Show |
11 | HG01069.hp1 HG01975.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.675-2044dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105643133 | ||||||
| chr4:105643133 | G | GTT | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.675-2045_675-2044d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105643133 | ||||||
| chr4:105643140 | T | TTTTTCAG others(18): Show |
1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.675-2037_675-2013d others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105643140 | ||||||
| chr4:105643376 | C | T | 1 | a0004c0021t0002g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.675-1812C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643376 | |||||||
| chr4:105643447 | T | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.675-1741T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643447 | |||||||
| chr4:105643780 | C | G | 11 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0008g0017 others(8): Show |
12 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.675-1408C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643780 | |||||||
| chr4:105643793 | A | G | 11 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0008g0017 others(8): Show |
12 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.675-1395A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643793 | |||||||
| chr4:105643872 | C | CT | 15 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0060 others(12): Show |
16 | HG00735.hp2 HG01243.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.675-1293dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105643872 | ||||||
| chr4:105643872 | CT | C | 92 | a0001c0001t0001g0048 a0001c0001t0001g0068 a0001c0001t0001g0070 others(89): Show |
92 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.675-1293delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105643872 | ||||||
| chr4:105643872 | CTT | C | 9 | a0001c0001t0012g0092 a0001c0004t0005g0035 a0001c0004t0005g0038 others(6): Show |
9 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.675-1294_675-1293d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr4 | 105643872 | ||||||
| chr4:105643997 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.675-1191T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643997 | |||||||
| chr4:105644009 | G | C | 3 | a0001c0001t0008g0017 a0001c0002t0002g0113 a0002c0003t0008g0102 |
3 | HG02615.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.675-1179G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644009 | |||||||
| chr4:105644056 | C | T | 2 | a0001c0001t0003g0099 a0001c0001t0005g0085 |
2 | HG00639.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.675-1132C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644056 | |||||||
| chr4:105644150 | A | G | 18 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0146 others(15): Show |
19 | HG00735.hp2 HG01243.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.675-1038A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644150 | |||||||
| chr4:105644215 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.675-973T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644215 | |||||||
| chr4:105644324 | T | A | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.675-864T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644324 | |||||||
| chr4:105644396 | G | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.675-792G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644396 | |||||||
| chr4:105644557 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.675-631A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644557 | |||||||
| chr4:105644760 | C | T | 1 | a0001c0001t0005g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.675-428C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644760 | |||||||
| chr4:105644774 | T | C | 52 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0080 others(49): Show |
52 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.675-414T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644774 | |||||||
| chr4:105644858 | T | C | 9 | a0001c0001t0008g0017 a0001c0002t0002g0113 a0002c0003t0008g0102 others(6): Show |
10 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.675-330T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644858 | |||||||
| chr4:105644906 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.675-282A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105644906 | |||||||
| chr4:105645151 | A | G | 9 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0003c0006t0001g0144 others(6): Show |
10 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.675-37A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105645151 | |||||||
| chr4:105645470 | G | C | 1 | a0001c0022t0001g0053 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.874+83G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105645470 | |||||||
| chr4:105645628 | G | T | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.874+241G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105645628 | |||||||
| chr4:105645684 | C | T | 1 | a0001c0020t0004g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.874+297C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105645684 | |||||||
| chr4:105645799 | A | T | 6 | a0003c0006t0001g0144 a0003c0006t0001g0150 a0003c0006t0001g0175 others(3): Show |
7 | HG02145.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.874+412A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105645799 | |||||||
| chr4:105646060 | A | G | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.874+673A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105646060 | |||||||
| chr4:105646122 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.874+735C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105646122 | |||||||
| chr4:105646364 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0122 |
2 | HG01346.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.874+977T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105646364 | |||||||
| chr4:105646832 | GT | G | 18 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0003g0145 others(15): Show |
19 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.874+1455delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 105646832 | ||||||
| chr4:105646842 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.874+1455T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105646842 | |||||||
| chr4:105646842 | TA | T | 52 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0121 others(49): Show |
52 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.874+1458delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 105646842 | ||||||
| chr4:105647028 | G | A | 2 | a0001c0001t0002g0100 a0001c0002t0007g0023 |
2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.875-1521G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647028 | |||||||
| chr4:105647029 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875-1520G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647029 | |||||||
| chr4:105647115 | T | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875-1434T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647115 | |||||||
| chr4:105647155 | A | G | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.875-1394A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647155 | |||||||
| chr4:105647164 | A | G | 52 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0121 others(49): Show |
52 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.875-1385A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647164 | |||||||
| chr4:105647280 | C | G | 8 | a0001c0001t0008g0017 a0001c0002t0002g0113 a0001c0007t0008g0045 others(5): Show |
9 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.875-1269C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647280 | |||||||
| chr4:105647340 | G | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875-1209G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647340 | |||||||
| chr4:105647359 | T | A | 1 | a0001c0002t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.875-1190T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647359 | |||||||
| chr4:105647444 | T | C | 2 | a0001c0004t0009g0103 a0001c0004t0009g0105 |
2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.875-1105T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647444 | |||||||
| chr4:105647489 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0002g0146 a0001c0001t0003g0111 |
3 | HG01167.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.875-1060G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647489 | |||||||
| chr4:105647888 | A | AT | 16 | a0001c0001t0001g0051 a0001c0001t0001g0121 a0001c0001t0002g0146 others(13): Show |
16 | HG00735.hp2 HG01167.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.875-642dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 105647888 | ||||||
| chr4:105647888 | A | ATT | 15 | a0001c0001t0001g0170 a0001c0001t0008g0017 a0001c0002t0002g0113 others(12): Show |
16 | HG01884.hp2 HG02145.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.875-643_875-642dup others(2): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 105647888 | ||||||
| chr4:105647888 | AT | A | 10 | a0001c0001t0001g0068 a0001c0001t0002g0149 a0001c0004t0005g0034 others(7): Show |
10 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.875-642delT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr4 | 105647888 | ||||||
| chr4:105647960 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875-589G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105647960 | |||||||
| chr4:105648031 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.875-518A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105648031 | |||||||
| chr4:105648064 | A | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.875-485A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105648064 | |||||||
| chr4:105648131 | G | A | 1 | a0001c0002t0003g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.875-418G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105648131 | |||||||
| chr4:105648377 | A | C | 2 | a0004c0011t0002g0003 a0004c0011t0002g0004 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.875-172A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105648377 | |||||||
| chr4:105648471 | G | A | 51 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0121 others(48): Show |
51 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.875-78G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 6/13 | chr4 | 105648471 | |||||||
| chr4:105648767 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1008+85T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105648767 | |||||||
| chr4:105648819 | C | CCT | 65 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0080 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1008+164_1008+165d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 105648819 | ||||||
| chr4:105648819 | C | CCTCT | 13 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0003g0088 others(10): Show |
13 | HG01069.hp1 HG01975.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1008+162_1008+165d others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 105648819 | ||||||
| chr4:105648832 | CTCTCTCT others(9): Show |
C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1008+166_1008+181d others(18): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 105648832 | ||||||
| chr4:105648848 | T | C | 1 | a0001c0002t0002g0011 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1008+166T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105648848 | |||||||
| chr4:105648858 | C | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1008+176C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105648858 | |||||||
| chr4:105648905 | C | T | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1008+223C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105648905 | |||||||
| chr4:105649224 | G | C | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1008+542G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649224 | |||||||
| chr4:105649227 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1008+545A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649227 | |||||||
| chr4:105649341 | A | G | 8 | a0001c0001t0008g0017 a0001c0002t0002g0113 a0001c0007t0008g0045 others(5): Show |
9 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+659A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649341 | |||||||
| chr4:105649411 | T | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1008+729T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649411 | |||||||
| chr4:105649512 | T | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1008+830T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649512 | |||||||
| chr4:105649936 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1008+1254G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649936 | |||||||
| chr4:105649983 | G | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1008+1301G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649983 | |||||||
| chr4:105649990 | A | G | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1008+1308A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105649990 | |||||||
| chr4:105650037 | G | T | 8 | a0001c0001t0008g0017 a0001c0002t0002g0113 a0001c0007t0008g0045 others(5): Show |
9 | HG02145.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+1355G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650037 | |||||||
| chr4:105650204 | T | A | 1 | a0001c0001t0011g0091 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1008+1522T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650204 | |||||||
| chr4:105650205 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1008+1523C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650205 | |||||||
| chr4:105650290 | C | G | 1 | a0001c0020t0004g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1008+1608C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650290 | |||||||
| chr4:105650508 | T | A | 1 | a0001c0001t0002g0047 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1008+1826T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650508 | |||||||
| chr4:105650628 | T | C | 2 | a0001c0001t0003g0145 a0001c0002t0008g0029 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1008+1946T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650628 | |||||||
| chr4:105650667 | A | T | 1 | a0001c0001t0019g0062 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1008+1985A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650667 | |||||||
| chr4:105650719 | C | T | 2 | a0001c0004t0009g0103 a0001c0004t0009g0105 |
2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1008+2037C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650719 | |||||||
| chr4:105650739 | A | T | 4 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+2057A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650739 | |||||||
| chr4:105650852 | T | A | 14 | a0001c0001t0002g0100 a0001c0001t0003g0075 a0001c0001t0003g0084 others(11): Show |
14 | HG01069.hp1 HG01975.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+2170T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105650852 | |||||||
| chr4:105651159 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1008+2477A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651159 | |||||||
| chr4:105651267 | T | C | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1008+2585T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651267 | |||||||
| chr4:105651299 | C | T | 9 | a0001c0001t0001g0044 a0001c0001t0001g0082 a0001c0001t0001g0154 others(6): Show |
9 | HG00280.hp2 HG01517.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1008+2617C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651299 | |||||||
| chr4:105651348 | C | G | 3 | a0001c0001t0008g0017 a0001c0007t0008g0045 a0002c0003t0008g0102 |
3 | HG02615.hp1 HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1008+2666C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651348 | |||||||
| chr4:105651394 | G | C | 4 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-2671G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651394 | |||||||
| chr4:105651522 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0002g0116 |
2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1009-2543G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651522 | |||||||
| chr4:105651536 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1009-2529G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651536 | |||||||
| chr4:105651583 | A | G | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1009-2482A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651583 | |||||||
| chr4:105651925 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1009-2140T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651925 | |||||||
| chr4:105651972 | T | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1009-2093T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105651972 | |||||||
| chr4:105652104 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1009-1961C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652104 | |||||||
| chr4:105652137 | A | C | 4 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1928A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652137 | |||||||
| chr4:105652172 | A | G | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1009-1893A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652172 | |||||||
| chr4:105652320 | T | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1009-1745T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652320 | |||||||
| chr4:105652381 | T | C | 4 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009-1684T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652381 | |||||||
| chr4:105652458 | G | A | 1 | a0001c0001t0004g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1009-1607G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652458 | |||||||
| chr4:105652543 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0002g0146 a0001c0001t0003g0111 |
3 | HG01167.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1009-1522G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652543 | |||||||
| chr4:105652578 | G | A | 1 | a0001c0004t0005g0035 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1009-1487G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652578 | |||||||
| chr4:105652720 | A | G | 1 | a0001c0002t0002g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1009-1345A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652720 | |||||||
| chr4:105652723 | TA | T | 97 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0104 others(94): Show |
98 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1009-1333delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 105652723 | ||||||
| chr4:105652758 | A | G | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1009-1307A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652758 | |||||||
| chr4:105652831 | C | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1009-1234C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652831 | |||||||
| chr4:105652932 | C | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1009-1133C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652932 | |||||||
| chr4:105652944 | A | G | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1009-1121A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105652944 | |||||||
| chr4:105653324 | C | CT | 5 | a0003c0006t0001g0144 a0003c0006t0001g0175 a0005c0009t0013g0001 others(2): Show |
6 | HG02145.hp1 HG02622.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1009-725dupT | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr4 | 105653324 | ||||||
| chr4:105653353 | C | T | 1 | a0001c0001t0008g0017 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1009-712C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653353 | |||||||
| chr4:105653379 | A | G | 83 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0104 others(80): Show |
84 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1009-686A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653379 | |||||||
| chr4:105653415 | C | T | 4 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-650C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653415 | |||||||
| chr4:105653546 | C | A | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1009-519C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653546 | |||||||
| chr4:105653557 | G | A | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1009-508G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653557 | |||||||
| chr4:105653631 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1009-434T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653631 | |||||||
| chr4:105653674 | G | A | 1 | a0001c0001t0003g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1009-391G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653674 | |||||||
| chr4:105653753 | T | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1009-312T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105653753 | |||||||
| chr4:105654024 | G | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1009-41G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 7/13 | chr4 | 105654024 | |||||||
| chr4:105654507 | T | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113+338T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105654507 | |||||||
| chr4:105654652 | A | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113+483A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105654652 | |||||||
| chr4:105654769 | C | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113+600C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105654769 | |||||||
| chr4:105654874 | G | T | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1113+705G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105654874 | |||||||
| chr4:105654922 | C | T | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1114-681C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105654922 | |||||||
| chr4:105655125 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1114-478G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105655125 | |||||||
| chr4:105655302 | A | G | 4 | a0001c0001t0003g0088 a0001c0001t0003g0112 a0001c0001t0003g0153 others(1): Show |
4 | HG01975.hp2 HG03486.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114-301A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105655302 | |||||||
| chr4:105655381 | G | A | 5 | a0001c0001t0002g0055 a0001c0001t0002g0127 a0001c0001t0002g0165 others(2): Show |
5 | HG00408.hp2 HG00438.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.1114-222G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105655381 | |||||||
| chr4:105655526 | G | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1114-77G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105655526 | |||||||
| chr4:105655568 | C | G | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1114-35C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 8/13 | chr4 | 105655568 | |||||||
| chr4:105655872 | T | A | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+150T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105655872 | |||||||
| chr4:105656086 | G | T | 4 | a0003c0006t0001g0144 a0003c0006t0001g0175 a0005c0009t0013g0001 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+364G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656086 | |||||||
| chr4:105656302 | C | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1233+580C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656302 | |||||||
| chr4:105656472 | A | G | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1233+750A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656472 | |||||||
| chr4:105656676 | C | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1233+954C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656676 | |||||||
| chr4:105656681 | T | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0180 |
2 | NA19007.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1233+959T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656681 | |||||||
| chr4:105656887 | C | A | 12 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0003g0088 others(9): Show |
12 | HG01069.hp1 HG01975.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1233+1165C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656887 | |||||||
| chr4:105656982 | G | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0158 |
3 | HG00735.hp1 HG00741.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1233+1260G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656982 | |||||||
| chr4:105656994 | G | A | 86 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0104 others(83): Show |
87 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.1233+1272G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105656994 | |||||||
| chr4:105657028 | T | TGATA | 2 | a0001c0001t0001g0070 a0001c0002t0002g0014 |
2 | HG02572.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1233+1326_1233+132 others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr4 | 105657028 | ||||||
| chr4:105657028 | TGATA | T | 14 | a0001c0001t0002g0074 a0001c0001t0002g0116 a0001c0001t0004g0110 others(11): Show |
14 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1233+1326_1233+132 others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr4 | 105657028 | ||||||
| chr4:105657592 | G | GAT | 11 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(8): Show |
11 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234-1446_1234-144 others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr4 | 105657592 | ||||||
| chr4:105657597 | A | G | 13 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0007g0023 others(10): Show |
13 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1234-1457A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105657597 | |||||||
| chr4:105657608 | T | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1234-1446T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105657608 | |||||||
| chr4:105657907 | C | G | 1 | a0001c0002t0002g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1234-1147C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105657907 | |||||||
| chr4:105657997 | G | A | 6 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(3): Show |
6 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-1057G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105657997 | |||||||
| chr4:105658027 | A | T | 3 | a0004c0011t0002g0003 a0004c0011t0002g0004 a0004c0021t0002g0089 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1234-1027A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105658027 | |||||||
| chr4:105658102 | T | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1234-952T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105658102 | |||||||
| chr4:105658135 | C | T | 5 | a0001c0001t0002g0100 a0001c0008t0006g0076 a0001c0008t0006g0077 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1234-919C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105658135 | |||||||
| chr4:105658414 | A | G | 1 | a0002c0003t0004g0054 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1234-640A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105658414 | |||||||
| chr4:105658676 | T | C | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-378T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105658676 | |||||||
| chr4:105658986 | G | C | 1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1234-68G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105658986 | |||||||
| chr4:105659044 | C | A | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1234-10C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 9/13 | chr4 | 105659044 | |||||||
| chr4:105659432 | A | G | 1 | a0001c0008t0006g0077 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1545+67A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105659432 | |||||||
| chr4:105659775 | T | C | 1 | a0001c0007t0007g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1545+410T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105659775 | |||||||
| chr4:105659842 | C | T | 1 | a0001c0001t0004g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1545+477C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105659842 | |||||||
| chr4:105659849 | T | TTG | 25 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0073 others(22): Show |
26 | HG00280.hp1 HG00408.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1545+522_1545+523d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | T | TTGTG | 14 | a0001c0001t0001g0120 a0001c0001t0001g0161 a0001c0001t0001g0167 others(11): Show |
14 | HG00609.hp1 HG01167.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.1545+520_1545+523d others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | T | TTGTGTG | 7 | a0001c0001t0003g0145 a0001c0001t0007g0147 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1545+518_1545+523d others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | T | TTGTGTGT others(1): Show |
10 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0007g0148 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1545+516_1545+523d others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0008g0017 a0001c0007t0008g0045 |
2 | HG02818.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1545+514_1545+523d others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | T | TTGTGTGT others(5): Show |
2 | a0001c0001t0002g0100 a0001c0002t0009g0016 |
2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1545+512_1545+523d others(14): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | T | TTGTGTGT others(7): Show |
2 | a0001c0002t0009g0184 a0002c0003t0008g0102 |
2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1545+510_1545+523d others(16): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | T | TTGTGTGT others(11): Show |
1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1545+506_1545+523d others(20): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | TTG | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0002c0003t0010g0139 |
3 | HG00438.hp1 HG01243.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1545+522_1545+523d others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | TTGTGTGT others(3): Show |
T | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1545+514_1545+523d others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659849 | TTGTGTGT others(5): Show |
T | 1 | a0003c0023t0020g0114 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1545+512_1545+523d others(14): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659849 | ||||||
| chr4:105659886 | T | TGC | 14 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0173 others(11): Show |
14 | HG01256.hp1 HG01258.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1545+522_1545+523i others(4): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659886 | ||||||
| chr4:105659886 | T | TGTGTGC | 22 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0163 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.1545+523_1545+524i others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659886 | ||||||
| chr4:105659886 | T | TGTGTGTG others(1): Show |
7 | a0001c0001t0002g0078 a0001c0001t0002g0146 a0001c0001t0002g0156 others(4): Show |
7 | HG01175.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+523_1545+524i others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659886 | ||||||
| chr4:105659886 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0002g0149 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02922.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1545+523_1545+524i others(14): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105659886 | ||||||
| chr4:105659937 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1545+572G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105659937 | |||||||
| chr4:105660215 | C | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+850C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660215 | |||||||
| chr4:105660225 | T | C | 1 | a0001c0007t0007g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1545+860T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660225 | |||||||
| chr4:105660374 | G | T | 1 | a0001c0001t0005g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1545+1009G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660374 | |||||||
| chr4:105660407 | T | A | 2 | a0001c0004t0005g0042 a0001c0004t0005g0043 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1545+1042T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660407 | |||||||
| chr4:105660409 | A | G | 8 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0003g0088 others(5): Show |
8 | HG01069.hp1 HG01975.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+1044A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660409 | |||||||
| chr4:105660452 | G | T | 1 | a0001c0007t0007g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1545+1087G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660452 | |||||||
| chr4:105660454 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+1089G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660454 | |||||||
| chr4:105660454 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1545+1089G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660454 | |||||||
| chr4:105660454 | G | T | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1545+1089G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660454 | |||||||
| chr4:105660455 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1545+1090G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660455 | |||||||
| chr4:105660483 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1545+1118A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660483 | |||||||
| chr4:105660504 | A | C | 3 | a0001c0002t0002g0002 a0001c0002t0002g0010 a0001c0002t0002g0014 |
3 | HG02572.hp1 HG03579.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1545+1139A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660504 | |||||||
| chr4:105660508 | C | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+1143C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660508 | |||||||
| chr4:105660532 | C | A | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1545+1167C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660532 | |||||||
| chr4:105660620 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1545+1255A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660620 | |||||||
| chr4:105660687 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+1322G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660687 | |||||||
| chr4:105660715 | T | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+1350T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660715 | |||||||
| chr4:105660731 | C | T | 1 | a0001c0002t0002g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1545+1366C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660731 | |||||||
| chr4:105660805 | C | T | 1 | a0001c0019t0004g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1545+1440C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660805 | |||||||
| chr4:105660880 | A | T | 2 | a0001c0001t0003g0145 a0001c0002t0008g0029 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1545+1515A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105660880 | |||||||
| chr4:105661048 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1545+1683A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661048 | |||||||
| chr4:105661091 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1545+1726A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661091 | |||||||
| chr4:105661123 | A | G | 49 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0163 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1545+1758A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661123 | |||||||
| chr4:105661174 | C | T | 11 | a0001c0001t0002g0173 a0001c0001t0003g0090 a0001c0001t0003g0142 others(8): Show |
11 | HG01884.hp1 HG02109.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1545+1809C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661174 | |||||||
| chr4:105661224 | C | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+1859C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661224 | |||||||
| chr4:105661316 | C | T | 182 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(179): Show |
183 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1545+1951C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661316 | |||||||
| chr4:105661393 | A | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+2028A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661393 | |||||||
| chr4:105661394 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1545+2029A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661394 | |||||||
| chr4:105661474 | T | TTTA | 16 | a0001c0001t0001g0059 a0001c0001t0002g0072 a0001c0001t0002g0100 others(13): Show |
16 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1545+2151_1545+215 others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105661474 | ||||||
| chr4:105661474 | T | TTTATTA | 2 | a0001c0001t0002g0155 a0001c0002t0008g0029 |
2 | HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1545+2148_1545+215 others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105661474 | ||||||
| chr4:105661474 | TTTA | T | 66 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(63): Show |
66 | HG00438.hp1 HG00735.hp1 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.1545+2151_1545+215 others(7): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105661474 | ||||||
| chr4:105661474 | TTTATTA | T | 35 | a0001c0001t0001g0070 a0001c0001t0001g0104 a0001c0001t0001g0115 others(32): Show |
35 | HG00280.hp2 HG00408.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1545+2148_1545+215 others(10): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105661474 | ||||||
| chr4:105661474 | TTTATTAT others(2): Show |
T | 7 | a0001c0001t0001g0064 a0001c0004t0005g0034 a0001c0004t0005g0035 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+2145_1545+215 others(13): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105661474 | ||||||
| chr4:105661474 | TTTATTAT others(5): Show |
T | 10 | a0001c0001t0001g0120 a0001c0001t0004g0110 a0001c0001t0004g0132 others(7): Show |
10 | HG00609.hp1 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1545+2142_1545+215 others(16): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105661474 | ||||||
| chr4:105661474 | TTTATTAT others(11): Show |
T | 1 | a0001c0007t0007g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1545+2136_1545+215 others(22): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105661474 | ||||||
| chr4:105661519 | G | T | 5 | a0001c0001t0002g0100 a0001c0008t0006g0076 a0001c0008t0006g0077 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1545+2154G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661519 | |||||||
| chr4:105661542 | G | A | 8 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0019t0004g0041 others(5): Show |
8 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+2177G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661542 | |||||||
| chr4:105661660 | T | A | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1545+2295T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661660 | |||||||
| chr4:105661686 | T | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1545+2321T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661686 | |||||||
| chr4:105661769 | G | T | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1545+2404G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661769 | |||||||
| chr4:105661808 | G | A | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1545+2443G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661808 | |||||||
| chr4:105661885 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1545+2520T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661885 | |||||||
| chr4:105661940 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1545+2575G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661940 | |||||||
| chr4:105661987 | G | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+2622G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105661987 | |||||||
| chr4:105662273 | T | C | 11 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0100 others(8): Show |
11 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1545+2908T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662273 | |||||||
| chr4:105662327 | T | C | 3 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0003g0096 |
3 | HG01069.hp1 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1545+2962T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662327 | |||||||
| chr4:105662455 | A | G | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1545+3090A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662455 | |||||||
| chr4:105662669 | G | A | 99 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0104 others(96): Show |
100 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1545+3304G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662669 | |||||||
| chr4:105662710 | T | C | 2 | a0001c0001t0003g0145 a0001c0002t0008g0029 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1545+3345T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662710 | |||||||
| chr4:105662759 | A | C | 2 | a0001c0004t0009g0103 a0001c0004t0009g0105 |
2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1545+3394A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662759 | |||||||
| chr4:105662826 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1546-3351A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662826 | |||||||
| chr4:105662909 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1546-3268A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105662909 | |||||||
| chr4:105663021 | T | A | 118 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0104 others(115): Show |
119 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1546-3156T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663021 | |||||||
| chr4:105663087 | G | A | 2 | a0001c0007t0002g0093 a0001c0007t0015g0106 |
2 | HG01109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1546-3090G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663087 | |||||||
| chr4:105663359 | T | C | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1546-2818T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663359 | |||||||
| chr4:105663421 | C | T | 4 | a0001c0004t0005g0038 a0001c0004t0005g0042 a0001c0004t0005g0043 others(1): Show |
4 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546-2756C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663421 | |||||||
| chr4:105663475 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1546-2702C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663475 | |||||||
| chr4:105663491 | A | T | 2 | a0001c0007t0008g0045 a0002c0003t0008g0102 |
2 | HG02615.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1546-2686A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663491 | |||||||
| chr4:105663614 | G | A | 47 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0163 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1546-2563G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663614 | |||||||
| chr4:105663647 | TTAACTGT others(9): Show |
T | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1546-2529_1546-251 others(20): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663647 | |||||||
| chr4:105663874 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1546-2303G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663874 | |||||||
| chr4:105663904 | A | G | 5 | a0001c0002t0007g0023 a0001c0007t0002g0093 a0001c0007t0007g0087 others(2): Show |
5 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-2273A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663904 | |||||||
| chr4:105663931 | T | C | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1546-2246T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663931 | |||||||
| chr4:105663966 | G | A | 2 | a0001c0001t0003g0145 a0001c0002t0008g0029 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1546-2211G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663966 | |||||||
| chr4:105663970 | C | CA | 14 | a0001c0001t0001g0183 a0001c0001t0004g0110 a0001c0001t0004g0132 others(11): Show |
14 | HG00280.hp1 HG01070.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1546-2193dupA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105663970 | ||||||
| chr4:105663970 | CA | C | 52 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0002g0039 others(49): Show |
53 | HG00408.hp2 HG00438.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.1546-2193delA | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105663970 | ||||||
| chr4:105663970 | CAA | C | 28 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0169 others(25): Show |
28 | HG00609.hp2 HG01175.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1546-2194_1546-219 others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr4 | 105663970 | ||||||
| chr4:105663981 | A | C | 1 | a0001c0001t0018g0037 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1546-2196A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663981 | |||||||
| chr4:105663990 | A | C | 2 | a0001c0001t0002g0146 a0001c0001t0003g0111 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1546-2187A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663990 | |||||||
| chr4:105663999 | C | A | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546-2178C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105663999 | |||||||
| chr4:105664046 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1546-2131T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664046 | |||||||
| chr4:105664099 | C | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546-2078C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664099 | |||||||
| chr4:105664238 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1546-1939A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664238 | |||||||
| chr4:105664401 | A | T | 47 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0163 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1546-1776A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664401 | |||||||
| chr4:105664444 | T | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1546-1733T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664444 | |||||||
| chr4:105664446 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0124 |
2 | NA18939.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1546-1731C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664446 | |||||||
| chr4:105664561 | G | T | 1 | a0001c0002t0009g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1546-1616G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664561 | |||||||
| chr4:105664826 | G | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1546-1351G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664826 | |||||||
| chr4:105664860 | T | A | 49 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0163 others(46): Show |
49 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1546-1317T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664860 | |||||||
| chr4:105664943 | G | C | 1 | a0003c0006t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1546-1234G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105664943 | |||||||
| chr4:105665005 | G | T | 5 | a0001c0002t0007g0023 a0001c0007t0002g0093 a0001c0007t0007g0087 others(2): Show |
5 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-1172G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105665005 | |||||||
| chr4:105665223 | G | A | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1546-954G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105665223 | |||||||
| chr4:105665260 | C | T | 12 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0003g0088 others(9): Show |
12 | HG01069.hp1 HG01975.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1546-917C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105665260 | |||||||
| chr4:105665302 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1546-875G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105665302 | |||||||
| chr4:105665598 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1546-579G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105665598 | |||||||
| chr4:105665661 | C | A | 1 | a0003c0015t0003g0019 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1546-516C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105665661 | |||||||
| chr4:105665855 | C | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1546-322C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105665855 | |||||||
| chr4:105666159 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1546-18T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 10/13 | chr4 | 105666159 | |||||||
| chr4:105666435 | A | G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1689+115A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 11/13 | chr4 | 105666435 | |||||||
| chr4:105666490 | T | A | 2 | a0001c0001t0001g0044 a0001c0001t0002g0149 |
2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1689+170T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 11/13 | chr4 | 105666490 | |||||||
| chr4:105666673 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0002g0151 |
2 | HG02922.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1689+353G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 11/13 | chr4 | 105666673 | |||||||
| chr4:105666736 | G | A | 1 | a0001c0001t0012g0092 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1690-393G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 11/13 | chr4 | 105666736 | |||||||
| chr4:105667107 | A | C | 3 | a0001c0001t0002g0173 a0001c0001t0014g0107 a0001c0002t0003g0026 |
3 | HG01884.hp1 HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1690-22A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 11/13 | chr4 | 105667107 | |||||||
| chr4:105667352 | C | T | 84 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0104 others(81): Show |
85 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.1888+25C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 12/13 | chr4 | 105667352 | |||||||
| chr4:105667939 | G | A | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2148+236G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105667939 | |||||||
| chr4:105668130 | G | C | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2148+427G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668130 | |||||||
| chr4:105668251 | G | A | 1 | a0001c0004t0005g0034 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2148+548G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668251 | |||||||
| chr4:105668550 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2148+847T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668550 | |||||||
| chr4:105668551 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2148+848C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668551 | |||||||
| chr4:105668593 | T | C | 11 | a0001c0001t0008g0017 a0001c0007t0008g0045 a0002c0003t0008g0102 others(8): Show |
12 | HG02145.hp1 HG02145.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.2148+890T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668593 | |||||||
| chr4:105668625 | A | C | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2148+922A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668625 | |||||||
| chr4:105668662 | G | GTAGA | 3 | a0001c0001t0001g0080 a0001c0001t0001g0135 a0001c0001t0001g0182 |
3 | HG01106.hp1 NA18952.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2148+1001_2148+100 others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668662 | ||||||
| chr4:105668662 | GTAGA | G | 55 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0052 others(52): Show |
56 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2148+1001_2148+100 others(8): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668662 | ||||||
| chr4:105668662 | GTAGATAG others(1): Show |
G | 16 | a0001c0001t0001g0065 a0001c0001t0001g0117 a0001c0001t0001g0122 others(13): Show |
16 | HG02300.hp1 HG02451.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2148+997_2148+1004 others(11): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668662 | ||||||
| chr4:105668662 | GTAGATAG others(5): Show |
G | 2 | a0001c0013t0006g0022 a0003c0006t0003g0143 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2148+993_2148+1004 others(15): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668662 | ||||||
| chr4:105668662 | GTAGATAG others(17): Show |
G | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2148+981_2148+1004 others(27): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668662 | ||||||
| chr4:105668668 | A | AGAT | 6 | a0001c0004t0005g0035 a0001c0004t0005g0038 a0001c0004t0005g0042 others(3): Show |
6 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.2148+966_2148+968d others(5): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668668 | ||||||
| chr4:105668698 | A | ATAGATAG others(1): Show |
2 | a0001c0002t0009g0184 a0001c0004t0009g0105 |
2 | HG00735.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2148+1002_2148+100 others(12): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668698 | ||||||
| chr4:105668698 | A | ATAGG | 2 | a0001c0002t0009g0016 a0001c0004t0009g0103 |
2 | HG01243.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2148+998_2148+999i others(6): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105668698 | ||||||
| chr4:105668745 | A | C | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2148+1042A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668745 | |||||||
| chr4:105668751 | C | T | 1 | a0003c0006t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2148+1048C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668751 | |||||||
| chr4:105668970 | G | A | 47 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0163 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2148+1267G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668970 | |||||||
| chr4:105668995 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2148+1292G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105668995 | |||||||
| chr4:105669048 | G | T | 12 | a0001c0001t0003g0075 a0001c0001t0003g0084 a0001c0001t0003g0088 others(9): Show |
12 | HG01069.hp1 HG01975.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2148+1345G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669048 | |||||||
| chr4:105669121 | G | A | 1 | a0002c0003t0012g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2148+1418G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669121 | |||||||
| chr4:105669131 | A | T | 11 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0005g0034 others(8): Show |
11 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2148+1428A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669131 | |||||||
| chr4:105669137 | T | G | 11 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0005g0034 others(8): Show |
11 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2148+1434T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669137 | |||||||
| chr4:105669187 | A | G | 1 | a0001c0007t0007g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2148+1484A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669187 | |||||||
| chr4:105669340 | C | T | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2148+1637C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669340 | |||||||
| chr4:105669553 | C | T | 13 | a0001c0001t0004g0110 a0001c0001t0004g0132 a0001c0002t0007g0023 others(10): Show |
13 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2148+1850C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669553 | |||||||
| chr4:105669673 | A | C | 4 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2148+1970A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105669673 | |||||||
| chr4:105670048 | T | C | 2 | a0003c0006t0001g0150 a0003c0006t0003g0143 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2148+2345T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105670048 | |||||||
| chr4:105670270 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2148+2567T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105670270 | |||||||
| chr4:105670451 | A | T | 1 | a0001c0004t0005g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2148+2748A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105670451 | |||||||
| chr4:105670936 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2148+3233T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105670936 | |||||||
| chr4:105670977 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2148+3274A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105670977 | |||||||
| chr4:105671159 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2148+3456A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105671159 | |||||||
| chr4:105671187 | A | G | 1 | a0001c0019t0004g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2148+3484A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105671187 | |||||||
| chr4:105671238 | T | A | 1 | a0001c0001t0003g0088 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2148+3535T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105671238 | |||||||
| chr4:105671304 | C | A | 2 | a0004c0011t0002g0003 a0004c0011t0002g0004 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2148+3601C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105671304 | |||||||
| chr4:105671400 | C | G | 1 | a0001c0002t0008g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2148+3697C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105671400 | |||||||
| chr4:105671401 | G | A | 1 | a0001c0018t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2148+3698G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105671401 | |||||||
| chr4:105671460 | G | C | 84 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(81): Show |
84 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.2148+3757G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105671460 | |||||||
| chr4:105672126 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0009c0016t0001g0021 |
3 | HG02809.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2148+4423G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672126 | |||||||
| chr4:105672158 | G | C | 3 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0009c0016t0001g0021 |
3 | HG02809.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2148+4455G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672158 | |||||||
| chr4:105672205 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA19007.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2148+4502T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672205 | |||||||
| chr4:105672337 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2148+4634A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672337 | |||||||
| chr4:105672417 | T | C | 11 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0005g0034 others(8): Show |
11 | HG00735.hp2 HG00741.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2148+4714T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672417 | |||||||
| chr4:105672693 | A | G | 98 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0104 others(95): Show |
99 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.2148+4990A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672693 | |||||||
| chr4:105672729 | C | G | 182 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0048 others(179): Show |
183 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.2149-5023C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672729 | |||||||
| chr4:105672815 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0009c0016t0001g0021 |
3 | HG02809.hp1 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2149-4937G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105672815 | |||||||
| chr4:105673011 | A | G | 56 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0163 others(53): Show |
56 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.2149-4741A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673011 | |||||||
| chr4:105673057 | T | A | 2 | a0001c0001t0003g0145 a0001c0002t0008g0029 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2149-4695T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673057 | |||||||
| chr4:105673060 | A | G | 2 | a0001c0001t0003g0145 a0001c0002t0008g0029 |
2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2149-4692A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673060 | |||||||
| chr4:105673232 | C | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2149-4520C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673232 | |||||||
| chr4:105673359 | G | A | 7 | a0001c0004t0005g0034 a0001c0004t0005g0035 a0001c0004t0005g0038 others(4): Show |
7 | HG00741.hp2 HG01109.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.2149-4393G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673359 | |||||||
| chr4:105673448 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2149-4304C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673448 | |||||||
| chr4:105673468 | G | A | 46 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0002g0039 others(43): Show |
46 | HG00408.hp2 HG00438.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2149-4284G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673468 | |||||||
| chr4:105673486 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2149-4266C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673486 | |||||||
| chr4:105673633 | T | C | 4 | a0001c0008t0006g0076 a0001c0008t0006g0077 a0001c0008t0006g0157 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-4119T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673633 | |||||||
| chr4:105673638 | T | A | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-4114T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673638 | |||||||
| chr4:105673720 | G | A | 1 | a0009c0016t0001g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2149-4032G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673720 | |||||||
| chr4:105673764 | GGTTTT | G | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-3966_2149-396 others(9): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr4 | 105673764 | ||||||
| chr4:105673830 | T | C | 1 | a0006c0010t0021g0012 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2149-3922T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673830 | |||||||
| chr4:105673898 | A | C | 56 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0047 others(53): Show |
57 | HG00408.hp2 HG00438.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2149-3854A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105673898 | |||||||
| chr4:105674000 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2149-3752T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105674000 | |||||||
| chr4:105674089 | C | T | 1 | a0002c0003t0010g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2149-3663C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105674089 | |||||||
| chr4:105674260 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2149-3492C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105674260 | |||||||
| chr4:105674372 | C | A | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-3380C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105674372 | |||||||
| chr4:105674496 | G | T | 1 | a0001c0002t0002g0010 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2149-3256G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105674496 | |||||||
| chr4:105674630 | T | C | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-3122T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105674630 | |||||||
| chr4:105674913 | A | T | 1 | a0001c0001t0002g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149-2839A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105674913 | |||||||
| chr4:105675142 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2149-2610G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105675142 | |||||||
| chr4:105675149 | T | A | 1 | a0001c0001t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2149-2603T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105675149 | |||||||
| chr4:105675150 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2149-2602C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105675150 | |||||||
| chr4:105675447 | T | C | 1 | a0001c0002t0002g0113 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2149-2305T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105675447 | |||||||
| chr4:105675527 | C | G | 1 | a0001c0001t0001g0064 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2149-2225C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105675527 | |||||||
| chr4:105675528 | T | C | 14 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0132 others(11): Show |
14 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.2149-2224T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105675528 | |||||||
| chr4:105676057 | A | C | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-1695A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676057 | |||||||
| chr4:105676114 | G | T | 42 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0047 others(39): Show |
43 | HG00408.hp2 HG00438.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.2149-1638G>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676114 | |||||||
| chr4:105676138 | G | C | 71 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0039 others(68): Show |
72 | HG00408.hp2 HG00438.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2149-1614G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676138 | |||||||
| chr4:105676181 | T | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0170 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2149-1571T>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676181 | |||||||
| chr4:105676288 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2149-1464A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676288 | |||||||
| chr4:105676295 | T | C | 114 | a0001c0001t0001g0104 a0001c0001t0001g0170 a0001c0001t0002g0039 others(111): Show |
115 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.2149-1457T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676295 | |||||||
| chr4:105676363 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2149-1389G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676363 | |||||||
| chr4:105676424 | TC | T | 2 | a0001c0001t0001g0079 a0001c0001t0005g0085 |
2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2149-1327delC | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676424 | |||||||
| chr4:105676497 | A | T | 5 | a0001c0001t0002g0078 a0001c0001t0002g0156 a0002c0005t0002g0007 others(2): Show |
5 | HG01175.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2149-1255A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676497 | |||||||
| chr4:105676562 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0124 |
2 | NA18939.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2149-1190C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676562 | |||||||
| chr4:105676601 | C | G | 4 | a0001c0002t0009g0016 a0001c0002t0009g0184 a0001c0004t0009g0103 others(1): Show |
4 | HG00735.hp2 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149-1151C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676601 | |||||||
| chr4:105676654 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2149-1098A>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676654 | |||||||
| chr4:105676782 | T | C | 1 | a0001c0001t0005g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2149-970T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105676782 | |||||||
| chr4:105677092 | T | C | 4 | a0001c0001t0002g0072 a0001c0001t0002g0081 a0001c0001t0002g0140 others(1): Show |
4 | HG01361.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149-660T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105677092 | |||||||
| chr4:105677525 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2149-227A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105677525 | |||||||
| chr4:105677526 | T | C | 1 | a0001c0002t0011g0028 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2149-226T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105677526 | |||||||
| chr4:105677665 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2149-87T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105677665 |