Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 777 | 91 | 50 | 18 | 17 | 3 | 3 | 7 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002 | 1/0 | 777 | 61 | 6 | 16 | 27 | 3 | 8 | 17 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003 | 0/1 | 777 | 11 | 6 | 0 | 1 | 2 | 1 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0004 | 0/0 | 777 | 7 | 2 | 4 | 1 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005 | 0/0 | 777 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0006 | 0/0 | 777 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0007 | 0/0 | 673 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0008 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0009 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0010 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0011 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0012 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0013 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 2334 | 58 | 5 | 16 | 25 | 3 | 8 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0002 | 0/0 | 2334 | 55 | 27 | 8 | 16 | 1 | 3 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0003 | 0/0 | 2334 | 18 | 17 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0004 | 0/0 | 2334 | 8 | 0 | 8 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0005 | 0/1 | 2334 | 7 | 2 | 0 | 1 | 2 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0006 | 0/0 | 2334 | 5 | 0 | 4 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0007 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0008 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0009 | 0/0 | 2334 | 4 | 2 | 1 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0010 | 0/0 | 2334 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0011 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0012 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0013 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0014 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0015 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0016 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0017 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0018 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0019 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0020 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0021 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0022 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0023 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0024 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0025 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0026 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0027 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| c0028 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3124 | 72 | 13 | 19 | 32 | 2 | 5 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0002 | 0/0 | 3123 | 39 | 20 | 5 | 10 | 1 | 3 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0003 | 0/0 | 3119 | 23 | 19 | 3 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0004 | 0/1 | 3119 | 10 | 0 | 1 | 4 | 2 | 2 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0005 | 0/0 | 3124 | 8 | 0 | 8 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0006 | 0/0 | 3124 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0007 | 0/0 | 3119 | 4 | 3 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0008 | 0/0 | 3124 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0009 | 0/0 | 3116 | 4 | 2 | 2 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0010 | 0/0 | 3121 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0011 | 0/0 | 3124 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0012 | 0/0 | 3122 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0013 | 0/0 | 3123 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0014 | 0/0 | 3123 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0015 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0016 | 0/0 | 3124 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0017 | 0/0 | 3124 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0018 | 0/0 | 3124 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0019 | 0/0 | 3124 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0020 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0021 | 0/0 | 3124 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| t0022 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2334 | 55 | 27 | 8 | 16 | 1 | 3 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0003 | 0/0 | 2334 | 18 | 17 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0004 | 0/0 | 2334 | 8 | 0 | 8 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0009 | 0/0 | 2334 | 4 | 2 | 1 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0010 | 0/0 | 2334 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0018 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0024 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0025 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001 | 1/0 | 2334 | 58 | 5 | 16 | 25 | 3 | 8 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0017 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0023 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0027 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003c0005 | 0/1 | 2334 | 7 | 2 | 0 | 1 | 2 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003c0007 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0004c0006 | 0/0 | 2334 | 5 | 0 | 4 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0004c0012 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005c0008 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005c0020 | 0/0 | 2334 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005c0028 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0006c0011 | 0/0 | 2334 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0006c0026 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0007c0019 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0008c0022 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0009c0021 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0010c0016 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0011c0015 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0012c0013 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0013c0014 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 5457 | 8 | 2 | 2 | 4 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0002 | 0/0 | 5456 | 25 | 8 | 4 | 10 | 0 | 3 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0003 | 0/0 | 5452 | 14 | 11 | 2 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0004 | 0/0 | 5452 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0007 | 0/0 | 5452 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0011 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0012 | 0/0 | 5455 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0002t0014 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0003t0002 | 0/0 | 5456 | 6 | 5 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0003t0003 | 0/0 | 5452 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0003t0007 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0003t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0003t0009 | 0/0 | 5449 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0003t0011 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0004t0005 | 0/0 | 5457 | 6 | 0 | 6 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0004t0009 | 0/0 | 5449 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0009t0002 | 0/0 | 5456 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0009t0007 | 0/0 | 5452 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0009t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0009t0015 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0010t0006 | 0/0 | 5457 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0018t0006 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0024t0004 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0001c0025t0004 | 0/0 | 5452 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0001 | 1/0 | 5457 | 51 | 4 | 14 | 25 | 2 | 5 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0002 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0004 | 0/0 | 5452 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0005 | 0/0 | 5457 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0016 | 0/0 | 5457 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0017 | 0/0 | 5457 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0018 | 0/0 | 5457 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0001t0019 | 0/0 | 5457 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0017t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0023t0001 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0002c0027t0001 | 0/0 | 5457 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003c0005t0004 | 0/1 | 5452 | 5 | 0 | 0 | 1 | 2 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003c0005t0008 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003c0005t0012 | 0/0 | 5455 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003c0007t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0003c0007t0002 | 0/0 | 5456 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0004c0006t0001 | 0/0 | 5457 | 4 | 0 | 3 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0004c0006t0010 | 0/0 | 5454 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0004c0012t0006 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0004c0012t0010 | 0/0 | 5454 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005c0008t0001 | 0/0 | 5457 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005c0008t0003 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005c0020t0003 | 0/0 | 5452 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0005c0028t0020 | 0/0 | 5450 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0006c0011t0002 | 0/0 | 5456 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0006c0026t0002 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0007c0019t0005 | 0/0 | 5145 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0008c0022t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0009c0021t0001 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0010c0016t0022 | 0/0 | 5452 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0011c0015t0021 | 0/0 | 5457 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0012c0013t0013 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| a0013c0014t0013 | 0/0 | 5456 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | copy fasta | chr4 | 105547620 | 105685914 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0008g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0012g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0002t0014g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0003t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0004t0005g0039 | 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 |
| a0001c0004t0005g0085 | 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 |
| a0001c0009t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0009t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0009t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0009t0015g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0010t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0010t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0010t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0018t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0024t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0001c0025t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0120 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0016g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0017g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0018g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0001t0019g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0017t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0023t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0002c0027t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0005t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0005t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0005t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0005t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0005t0004g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0005t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0005t0012g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0007t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0007t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0007t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0003c0007t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0006t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0006t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0006t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0006t0010g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0012t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0004c0012t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0005c0008t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0005c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0005c0008t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0005c0008t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0005c0020t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0005c0028t0020g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0006c0011t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0006c0011t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0006c0026t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0007c0019t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0008c0022t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0009c0021t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0010c0016t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0011c0015t0021g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0012c0013t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| a0013c0014t0013g0008 | 0/0 | 1 | 1 | 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 | c0009 | t0007 | g0086 | EUR | FIN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0152 | EUR | FIN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0049 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00639 | hp1 | a0002 | c0001 | t0005 | g0081 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00639 | hp2 | a0004 | c0006 | t0001 | g0038 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00735 | hp1 | a0002 | 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 | a0002 | c0001 | t0001 | g0058 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG00741 | hp2 | a0001 | c0004 | t0005 | g0085 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0087 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0169 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01070 | hp1 | a0005 | c0020 | t0003 | g0021 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0185 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01074 | hp1 | a0004 | c0006 | t0001 | g0093 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01074 | hp2 | a0002 | c0001 | t0016 | g0165 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01106 | hp2 | a0002 | 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 | c0009 | t0002 | g0095 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01167 | hp1 | a0001 | c0004 | t0005 | g0036 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0125 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01175 | hp1 | a0001 | c0002 | 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 | a0004 | c0006 | t0010 | g0139 | AMR | PUR | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01256 | hp2 | a0002 | c0001 | t0001 | g0050 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0178 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0064 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01346 | hp2 | a0001 | c0004 | t0005 | g0039 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0084 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0079 | AMR | CLM | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01516 | hp1 | a0003 | c0005 | t0004 | g0136 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01516 | hp2 | a0002 | c0001 | t0001 | g0083 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01517 | hp1 | a0003 | c0005 | t0004 | g0137 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01517 | hp2 | a0002 | c0001 | t0018 | g0040 | EUR | IBS | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0175 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01884 | hp2 | a0001 | c0018 | t0006 | g0026 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0062 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01975 | hp2 | a0001 | c0002 | t0003 | g0088 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0060 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01981 | hp1 | a0001 | c0004 | t0005 | g0037 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG01981 | hp2 | a0004 | c0006 | t0001 | g0159 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02004 | hp1 | a0007 | c0019 | t0005 | g0005 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0126 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02015 | hp1 | a0001 | c0002 | t0004 | g0135 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02015 | hp2 | a0002 | c0001 | t0001 | g0119 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02027 | hp1 | a0002 | c0027 | t0001 | g0055 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0061 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02071 | hp1 | a0001 | c0025 | t0004 | g0065 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0054 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0162 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02145 | hp1 | a0008 | c0022 | t0001 | g0133 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02145 | hp2 | a0003 | c0007 | t0002 | g0029 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0116 | EAS | CDX | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02155 | hp2 | a0002 | c0001 | t0001 | g0073 | EAS | CDX | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0052 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02257 | hp2 | a0005 | c0028 | t0020 | g0114 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02300 | hp1 | a0002 | c0001 | t0001 | g0127 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02300 | hp2 | a0001 | c0024 | t0004 | g0041 | AMR | PEL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0014 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02451 | hp2 | a0003 | c0005 | t0012 | g0124 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02523 | hp1 | a0002 | c0023 | t0001 | g0161 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02523 | hp2 | a0001 | c0002 | t0004 | g0110 | EAS | KHV | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0016 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0156 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02615 | hp1 | a0003 | c0005 | t0008 | g0102 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0090 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02622 | hp1 | a0005 | c0008 | t0001 | g0144 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02622 | hp2 | a0001 | c0002 | t0007 | g0147 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02630 | hp1 | a0001 | c0002 | t0014 | g0107 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02630 | hp2 | a0001 | c0002 | t0003 | g0101 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02717 | hp2 | a0003 | c0007 | t0001 | g0010 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0142 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02723 | hp2 | a0001 | c0010 | t0006 | g0157 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02809 | hp2 | a0001 | c0002 | t0007 | g0148 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02818 | hp1 | a0001 | c0009 | t0008 | g0045 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02818 | hp2 | a0005 | c0008 | t0003 | g0143 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02886 | hp2 | a0001 | c0002 | t0011 | g0091 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02896 | hp1 | a0006 | c0011 | t0002 | g0004 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02896 | hp2 | a0001 | c0003 | t0003 | g0035 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02897 | hp1 | a0006 | c0011 | t0002 | g0003 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0034 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0153 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02922 | hp2 | a0013 | c0014 | t0013 | g0008 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02965 | hp1 | a0009 | c0021 | t0001 | g0023 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02965 | hp2 | a0003 | c0007 | t0002 | g0015 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03041 | hp1 | a0002 | c0001 | t0002 | g0155 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03041 | hp2 | a0002 | c0017 | t0001 | g0022 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0108 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03130 | hp2 | a0011 | c0015 | t0021 | g0013 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03139 | hp1 | a0006 | c0026 | t0002 | g0089 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0032 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03195 | hp1 | a0001 | c0002 | t0012 | g0092 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0024 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0096 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03209 | hp2 | a0001 | c0003 | t0008 | g0031 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0033 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03225 | hp2 | a0001 | c0002 | t0008 | g0019 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03453 | hp2 | a0001 | c0003 | t0009 | g0184 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03486 | hp1 | a0005 | c0008 | t0001 | g0177 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0150 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0082 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0141 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0140 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03492 | hp2 | a0002 | c0001 | t0001 | g0176 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03516 | hp1 | a0005 | c0008 | t0001 | g0151 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0174 | AFR | ESN | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0154 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03540 | hp2 | a0001 | c0003 | t0007 | g0027 | AFR | GWD | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03579 | hp1 | a0010 | c0016 | t0022 | g0007 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0011 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03710 | hp1 | a0002 | c0001 | t0017 | g0128 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0072 | SAS | PJL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03834 | hp1 | a0003 | c0005 | t0004 | g0056 | SAS | BEB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03834 | hp2 | a0002 | c0001 | t0019 | g0068 | SAS | BEB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG04115 | hp1 | a0002 | c0001 | t0001 | g0053 | SAS | STU | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG04115 | hp2 | a0002 | c0001 | t0004 | g0109 | SAS | STU | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18522 | hp1 | a0001 | c0010 | t0006 | g0077 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0020 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18939 | hp1 | a0002 | c0001 | t0001 | g0071 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0134 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18952 | hp2 | a0004 | c0006 | t0001 | g0164 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18959 | hp2 | a0002 | c0001 | t0001 | g0170 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18962 | hp2 | a0002 | c0001 | t0001 | g0063 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0059 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0051 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA18990 | hp2 | a0003 | c0005 | t0004 | g0098 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19003 | hp2 | a0002 | c0001 | t0001 | g0182 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0117 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0066 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0181 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0123 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0070 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19030 | hp1 | a0001 | c0003 | t0009 | g0018 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19030 | hp2 | a0012 | c0013 | t0013 | g0006 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19043 | hp1 | a0003 | c0007 | t0002 | g0009 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0145 | AFR | LWK | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19072 | hp1 | a0002 | c0001 | t0001 | g0180 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19081 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | JPT | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0044 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0173 | AFR | YRI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20129 | hp1 | a0004 | c0012 | t0006 | g0017 | AFR | ASW | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0113 | AFR | ASW | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0002 | EUR | TSI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0099 | EUR | TSI | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20905 | hp1 | a0002 | c0001 | t0001 | g0094 | SAS | GIH | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0048 | SAS | GIH | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02109 | hp1 | a0002 | c0001 | t0001 | g0046 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0025 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02559 | hp1 | a0001 | c0010 | t0006 | g0076 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG02559 | hp2 | a0004 | c0012 | t0010 | g0028 | AFR | ACB | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG03471 | hp2 | a0001 | c0009 | t0015 | g0106 | AFR | MSL | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG06807 | hp1 | a0001 | c0003 | t0011 | g0030 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0111 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20300 | hp1 | a0002 | c0001 | t0001 | g0097 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0112 | AFR | USA | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0005 | t0004 | g0160 | REF | REF | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| homoSapiens_grch38 | hp1 | a0002 | c0001 | t0001 | g0120 | REF | REF | ARHGEF38_chr4_105547620_105685914 | ARHGEF38 | chr4 | 105547620 | 105685914 |
| 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 | 4 | a0010a0011a0012others(1): Show | 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 | 2 | a0003a0004 | 18 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(15): 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 | a0006 | 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 | 5 | a0005a0008a0009others(2): 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 | a0012 | 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 | 8 | a0001a0003a0005others(5): Show | 113 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(110): 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 |
| 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 | 13 | a0001c0003a0001c0018a0002c0017others(10): 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 | a0009c0021 | 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 | a0001c0009a0003c0007a0005c0020others(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 | a0002c0027 | 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 | a0001c0025 | 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 | a0001c0024 | 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 | a0001c0004a0007c0019 | 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 | a0001c0010a0001c0018 | 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 | a0002c0023 | 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 |
| 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 | 4 | a0010c0016t0022a0011c0015t0021a0012c0013t0013others(1): Show | 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 | a0004c0006t0010a0004c0012t0010 | 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 | a0001c0002t0012a0003c0005t0012a0005c0028t0020 | 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 | a0001c0003t0009a0001c0004t0005a0001c0004t0009others(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 | 10 | a0001c0002t0002a0001c0002t0014a0001c0003t0002others(7): 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 | a0002c0001t0019 | 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 | a0001c0009t0015 | 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 | a0001c0003t0009a0001c0004t0005a0001c0004t0009others(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 | a0001c0002t0007a0001c0003t0007a0001c0009t0007others(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 | 11 | a0001c0002t0002a0001c0002t0011a0001c0003t0002others(8): 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 | a0001c0010t0006a0001c0018t0006a0004c0012t0006 | 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 | a0002c0001t0016 | 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 | a0001c0002t0008a0001c0003t0008a0001c0009t0008others(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 | a0001c0003t0009a0001c0004t0009 | 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 | 5 | a0001c0002t0004a0001c0024t0004a0001c0025t0004others(2): Show | 10 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(7): 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 | a0001c0003t0009a0001c0004t0009 | 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 | 15 | a0001c0002t0003a0001c0002t0004a0001c0002t0007others(12): Show | 40 | HG00280.hp1 HG01069.hp1 HG01070.hp1 others(37): 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 | a0002c0001t0018 | 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 | 12 | a0001c0002t0002a0001c0002t0011a0001c0003t0002others(9): 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 | 5 | a0001c0002t0004a0001c0024t0004a0001c0025t0004others(2): Show | 10 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2966T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 14/14 | 2966 | chr4 | 105680903 |
| 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 | a0002c0001t0001g0185 | 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 | a0001c0003t0009g0184 | 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 | a0002c0001t0001g0183 | 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 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(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 | a0002c0001t0001g0162a0002c0023t0001g0161 | 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 | 17 | a0001c0003t0002g0002a0001c0003t0002g0011a0001c0003t0002g0012others(14): 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 | 38 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(35): Show | 38 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.196+726C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553687 | ||||||
| chr4:105553818
|
C | A | 156 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(153): Show | 157 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.196+857C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105553818 | ||||||
| chr4:105553886
|
G | A | 156 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(153): Show | 157 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(154): 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 | a0005c0028t0020g0114 | 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 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(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 | a0005c0008t0001g0144 | 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 | 3 | a0001c0003t0002g0113a0003c0005t0004g0160a0004c0006t0001g0159 | 3 | HG01981.hp2 NA20129.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.196+1159A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554120 | ||||||
| chr4:105554378
|
T | C | 156 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(153): Show | 157 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.196+1417T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554378 | ||||||
| chr4:105554465
|
G | T | 156 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(153): Show | 157 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(154): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(117): Show | 121 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.196+1530A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554491 | ||||||
| chr4:105554756
|
C | CAT | 156 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(153): Show | 157 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(154): 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 | a0001c0003t0003g0032a0001c0003t0003g0033a0001c0003t0003g0034others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(117): Show | 121 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(118): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(117): Show | 121 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.196+1981A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105554942 | ||||||
| chr4:105554944
|
G | GT | 40 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(37): Show | 40 | HG00280.hp2 HG00408.hp2 HG00609.hp2 others(37): 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 | a0001c0002t0008g0019 | 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 | a0002c0001t0001g0185 | 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 | 158 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(155): Show | 159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): 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 | a0002c0001t0001g0117a0002c0001t0001g0118 | 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 | a0001c0002t0003g0145 | 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 | a0001c0002t0003g0112 | 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 | a0002c0001t0001g0158 | 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 | a0001c0002t0008g0019 | 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 | a0001c0002t0008g0019 | 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 | a0001c0002t0004g0110 | 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 | a0002c0001t0004g0109 | 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 | 17 | a0001c0003t0002g0002a0001c0003t0002g0011a0001c0003t0002g0012others(14): 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 | a0002c0001t0001g0119 | 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 | a0001c0003t0002g0113a0001c0003t0003g0020a0005c0020t0003g0021 | 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 | a0001c0002t0002g0146a0001c0002t0007g0147a0001c0002t0007g0148 | 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 | a0001c0003t0009g0018 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(117): Show | 121 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(118): 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 | a0001c0002t0002g0108a0001c0002t0014g0107a0001c0003t0003g0032others(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 | a0001c0003t0009g0184 | 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 | a0001c0002t0002g0108a0001c0002t0014g0107a0001c0003t0003g0032others(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 | a0001c0002t0002g0156a0001c0003t0003g0024a0001c0003t0003g0025others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(93): Show | 97 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(94): 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 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(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 | a0001c0003t0002g0002 | 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 | 155 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(152): Show | 156 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(153): 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 | a0002c0001t0001g0181 | 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 | a0001c0009t0015g0106 | 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 | 23 | a0001c0002t0001g0104a0001c0002t0002g0100a0001c0002t0002g0146others(20): Show | 23 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(20): 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 | a0001c0002t0008g0019 | 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 | 10 | a0001c0002t0002g0001a0001c0004t0005g0036a0001c0004t0005g0039others(7): 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 | a0001c0002t0003g0145 | 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 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(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 | a0002c0001t0001g0115 | 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 | 80 | a0001c0002t0001g0067a0001c0002t0001g0104a0001c0002t0001g0163others(77): Show | 80 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(77): 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 | a0001c0003t0002g0113a0001c0003t0003g0020a0005c0020t0003g0021 | 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 | a0001c0002t0003g0099 | 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 | a0001c0002t0002g0156a0001c0003t0011g0030a0001c0010t0006g0157 | 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 | a0001c0002t0002g0156a0001c0003t0011g0030a0001c0010t0006g0157 | 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 | a0001c0002t0002g0156a0001c0003t0011g0030a0001c0010t0006g0157 | 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 | a0002c0001t0001g0180 | 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 | 96 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0002g0047others(93): 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 | a0001c0002t0008g0019 | 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 | a0002c0001t0001g0185 | 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 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(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 | a0001c0002t0002g0140a0001c0002t0002g0141a0004c0006t0010g0139 | 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 | a0006c0011t0002g0003a0006c0011t0002g0004 | 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 | a0001c0003t0008g0031a0005c0028t0020g0114 | 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 | a0001c0002t0008g0019 | 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 | a0006c0011t0002g0003a0006c0011t0002g0004 | 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 | a0001c0002t0002g0116 | 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 | a0001c0003t0008g0031a0005c0028t0020g0114 | 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 | a0001c0003t0003g0020 | 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 | a0002c0001t0001g0183a0002c0001t0001g0185a0007c0019t0005g0005 | 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 | 26 | a0001c0002t0001g0080a0001c0002t0002g0001a0001c0002t0002g0078others(23): 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 | a0002c0001t0001g0183a0002c0001t0001g0185a0007c0019t0005g0005 | 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 | a0001c0002t0001g0163 | 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 | 62 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(59): 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 | a0001c0002t0002g0074 | 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 | a0001c0002t0003g0096a0005c0028t0020g0114 | 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 | a0002c0001t0001g0115 | 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 | a0001c0002t0002g0001a0001c0003t0002g0016a0001c0003t0009g0018others(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 | a0001c0002t0002g0072a0001c0003t0002g0002a0001c0004t0005g0039others(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 | a0004c0006t0001g0164 | 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 | a0002c0001t0001g0185 | 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 | a0001c0002t0001g0080a0001c0002t0003g0099a0001c0003t0002g0011others(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 | a0002c0001t0001g0183 | 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 | a0001c0002t0001g0104a0001c0002t0001g0167a0001c0002t0001g0172others(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 | a0001c0002t0002g0078 | 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 | a0001c0002t0002g0149 | 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 | a0001c0010t0006g0076a0010c0016t0022g0007a0013c0014t0013g0008 | 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 | a0001c0002t0003g0075 | 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 | a0012c0013t0013g0006 | 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 | a0001c0002t0002g0078a0001c0002t0002g0149a0001c0010t0006g0077 | 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 | a0001c0003t0007g0027a0004c0012t0010g0028 | 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 | 26 | a0001c0002t0001g0171a0001c0002t0002g0129a0001c0002t0002g0138others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(23): 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0008g0031 | 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 | a0001c0002t0008g0019 | 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 | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0002g0146others(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 | a0004c0006t0001g0159 | 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 | a0002c0001t0001g0162a0002c0001t0001g0181 | 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 | a0001c0002t0002g0116 | 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 | a0005c0008t0001g0151 | 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 | a0002c0001t0001g0158 | 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 | a0002c0001t0001g0130 | 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 | a0001c0002t0002g0001 | 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 | a0001c0002t0002g0154 | 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 | a0001c0002t0003g0112 | 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 | a0001c0002t0002g0153 | 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 | a0001c0002t0002g0140a0001c0002t0002g0141a0001c0002t0004g0135others(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 | a0001c0002t0002g0084 | 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 | a0001c0002t0003g0088 | 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 | a0001c0003t0003g0025 | 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 | a0001c0003t0003g0024 | 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 | a0001c0002t0003g0096 | 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 | a0001c0002t0001g0166a0002c0001t0016g0165a0003c0005t0012g0124 | 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 | a0001c0003t0008g0031a0002c0001t0001g0162a0002c0001t0001g0181 | 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 | a0001c0002t0002g0138a0001c0002t0003g0087a0001c0002t0003g0142others(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 | a0001c0002t0002g0140a0001c0002t0002g0141a0001c0009t0002g0095 | 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 | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0002g0108others(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 | a0002c0001t0018g0040 | 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 | a0001c0002t0003g0087 | 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 | a0001c0002t0004g0135 | 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 | a0003c0007t0002g0029 | 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 | 15 | a0001c0002t0001g0171a0001c0002t0002g0084a0001c0002t0002g0129others(12): Show | 15 | HG00280.hp2 HG00609.hp2 HG01109.hp2 others(12): 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 | a0001c0018t0006g0026 | 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 | 55 | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0001g0171others(52): Show | 55 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(52): 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 | a0002c0001t0001g0051 | 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 | a0001c0002t0004g0110 | 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 | a0002c0001t0001g0073 | 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 | a0001c0003t0002g0016 | 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 | a0001c0009t0015g0106 | 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 | a0001c0003t0002g0113 | 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 | a0003c0005t0004g0136a0008c0022t0001g0133 | 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 | a0001c0002t0003g0150a0002c0001t0001g0125 | 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 | a0001c0002t0001g0167a0002c0001t0001g0119a0002c0001t0001g0180 | 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 | a0002c0001t0001g0079a0002c0001t0001g0097 | 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 | a0001c0002t0002g0084a0001c0002t0002g0140a0001c0002t0002g0141others(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 | a0001c0002t0002g0108a0001c0003t0003g0032a0003c0007t0002g0015 | 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 | a0001c0003t0003g0033a0001c0003t0003g0034a0003c0007t0002g0009 | 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 | a0001c0002t0001g0104a0003c0007t0001g0010 | 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 | a0001c0003t0003g0035 | 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 | a0002c0001t0001g0123 | 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 | a0001c0002t0002g0084a0001c0002t0002g0140a0001c0002t0002g0141others(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 | a0001c0002t0001g0172 | 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 | a0001c0002t0003g0173 | 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 | a0001c0002t0003g0174 | 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 | a0001c0009t0007g0086 | 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 | a0002c0001t0001g0115 | 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 | a0001c0002t0003g0090a0006c0026t0002g0089 | 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 | a0001c0002t0002g0138a0001c0002t0002g0175a0001c0002t0003g0142others(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 | a0002c0001t0001g0176 | 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 | a0002c0001t0001g0134 | 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 | a0002c0001t0001g0178 | 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 | a0001c0002t0001g0104a0001c0002t0002g0084a0001c0002t0002g0108others(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 | a0001c0002t0002g0168 | 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 | a0002c0001t0005g0081 | 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 | a0001c0002t0002g0001 | 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 | a0003c0005t0004g0056 | 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 | a0002c0001t0001g0083 | 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 | a0004c0012t0006g0017 | 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 | a0004c0006t0001g0093 | 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 | a0001c0002t0001g0171 | 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 | a0005c0008t0003g0143 | 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 | a0001c0002t0002g0072a0001c0002t0007g0147a0002c0001t0004g0109 | 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 | a0001c0004t0005g0036a0001c0004t0005g0039 | 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 | a0001c0002t0007g0148 | 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 | a0001c0004t0005g0085a0004c0006t0001g0038 | 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 | a0002c0001t0001g0094 | 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 | a0001c0002t0002g0156 | 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 | a0001c0010t0006g0157 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0001others(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 | a0001c0002t0002g0069a0002c0001t0001g0070a0002c0001t0001g0127others(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 | 79 | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0002g0047others(76): Show | 79 | HG00280.hp2 HG00438.hp2 HG00735.hp1 others(76): 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 | a0001c0002t0002g0149a0001c0002t0008g0019a0001c0003t0003g0020others(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 | a0001c0002t0003g0112a0002c0001t0001g0044a0002c0001t0001g0117 | 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 | a0001c0003t0002g0011a0001c0003t0002g0012a0002c0001t0001g0049others(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 | a0001c0002t0001g0080a0002c0001t0001g0048 | 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 | a0002c0027t0001g0055 | 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 | a0002c0001t0001g0062 | 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 | a0002c0001t0001g0071 | 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 | 57 | a0001c0002t0001g0104a0001c0002t0001g0171a0001c0002t0001g0172others(54): 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 | a0002c0001t0001g0054a0002c0023t0001g0161 | 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 | a0002c0001t0001g0060a0002c0001t0001g0061 | 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 | a0001c0004t0005g0037 | 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 | a0001c0002t0003g0111 | 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 | a0002c0001t0001g0169 | 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 | a0005c0028t0020g0114 | 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 | a0004c0006t0010g0139 | 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 | a0001c0002t0001g0067a0001c0002t0001g0104a0001c0002t0001g0163others(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 | a0002c0001t0001g0046 | 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 | a0001c0004t0005g0042a0001c0004t0005g0043 | 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 | a0001c0002t0002g0121a0002c0001t0001g0058a0002c0001t0001g0122 | 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 | a0001c0025t0004g0065a0002c0001t0001g0064 | 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 | a0002c0001t0019g0068 | 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 | a0002c0001t0001g0182 | 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 | 65 | a0001c0002t0001g0104a0001c0002t0001g0171a0001c0002t0001g0172others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(62): 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 | a0002c0001t0001g0132 | 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 | a0001c0003t0009g0184 | 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 | a0001c0002t0002g0047a0002c0001t0001g0053 | 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 | a0001c0024t0004g0041 | 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 | a0002c0001t0001g0082 | 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 | a0001c0002t0014g0107 | 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 | a0001c0003t0002g0002 | 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 | a0001c0002t0001g0104a0001c0002t0001g0166a0001c0002t0001g0172others(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 | a0001c0003t0002g0014 | 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 | a0002c0001t0017g0128 | 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 | a0006c0011t0002g0003a0006c0011t0002g0004 | 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 | a0001c0002t0002g0179 | 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 | a0001c0003t0009g0018 | 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 | a0001c0002t0001g0172a0001c0002t0002g0057a0001c0002t0002g0069others(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 | a0002c0001t0001g0132 | 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 | a0002c0017t0001g0022 | 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 | a0001c0002t0002g0100 | 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 | a0002c0001t0001g0170a0005c0008t0001g0144 | 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 | a0001c0002t0001g0172a0001c0002t0002g0074a0001c0002t0002g0156others(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 | a0001c0002t0001g0172a0001c0002t0002g0156a0001c0002t0002g0168others(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 | a0001c0003t0011g0030 | 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 | a0001c0004t0005g0036a0002c0001t0001g0169a0003c0007t0001g0010others(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 | a0005c0020t0003g0021 | 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 | a0001c0003t0011g0030a0001c0004t0005g0036a0002c0001t0001g0169others(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 | a0001c0003t0011g0030a0003c0007t0002g0029 | 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 | a0002c0001t0001g0183a0002c0001t0001g0185a0004c0006t0001g0038 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0087others(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 | a0001c0002t0001g0171a0001c0002t0002g0047a0001c0002t0002g0057others(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 | a0001c0002t0003g0090a0001c0002t0011g0091a0001c0002t0012g0092 | 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 | a0001c0002t0003g0145a0009c0021t0001g0023 | 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 | a0002c0001t0001g0180 | 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 | 62 | a0001c0002t0001g0080a0001c0002t0001g0166a0001c0002t0001g0171others(59): 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 | a0001c0003t0003g0020 | 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 | a0001c0002t0001g0163a0001c0002t0002g0047a0001c0002t0002g0057others(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 | a0001c0002t0008g0019a0001c0003t0008g0031a0001c0018t0006g0026others(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 | 153 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(150): Show | 154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): 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 | a0001c0002t0002g0146a0001c0002t0003g0075a0001c0002t0003g0087others(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 | a0001c0002t0001g0163a0002c0001t0001g0059a0002c0001t0001g0066 | 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 | a0001c0002t0003g0096 | 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 | 178 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(175): Show | 179 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(176): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0004c0006t0001g0159 | 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 | a0002c0001t0001g0059a0002c0001t0001g0066 | 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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0003t0002g0016 | 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 | a0001c0002t0003g0090a0001c0002t0003g0101a0001c0002t0011g0091others(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 | 3 | a0010c0016t0022g0007a0012c0013t0013g0006a0013c0014t0013g0008 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0004t0005g0037 | 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 | a0001c0002t0003g0142 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | 160 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(157): 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0002c0001t0001g0050 | 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 | a0001c0002t0004g0135 | 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 | a0001c0002t0003g0096 | 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0002t0001g0080a0001c0002t0001g0163a0001c0002t0001g0166others(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 | a0001c0002t0001g0167 | 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 | 159 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(156): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(157): 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 | a0002c0001t0001g0185 | 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 | a0001c0003t0009g0018 | 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 | a0001c0002t0003g0096 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0004c0006t0010g0139 | 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 | a0004c0006t0010g0139 | 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 | 146 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(143): Show | 147 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(144): 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 | a0002c0001t0001g0046 | 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 | a0001c0003t0002g0113 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0018t0006g0026a0004c0012t0010g0028 | 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | 159 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(156): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(157): 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 | a0001c0003t0003g0024a0001c0003t0003g0025a0001c0003t0007g0027others(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 | a0001c0002t0002g0138a0002c0001t0001g0082a0002c0001t0001g0094others(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 | 159 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(156): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(157): 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 | a0001c0002t0003g0173a0001c0002t0003g0174 | 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 | a0002c0001t0001g0082a0002c0001t0001g0094 | 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 | a0002c0001t0001g0082a0002c0001t0001g0094 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0002t0003g0142 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | 3 | a0010c0016t0022g0007a0012c0013t0013g0006a0013c0014t0013g0008 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(142): Show | 146 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(143): 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 | 12 | a0001c0002t0002g0146a0001c0002t0003g0075a0001c0002t0003g0087others(9): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0002t0001g0067a0002c0001t0001g0062a0002c0001t0001g0064others(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 | a0001c0002t0012g0092 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157 | 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 | a0001c0004t0005g0085a0002c0001t0018g0040 | 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 | a0001c0002t0002g0074 | 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 | a0002c0001t0001g0060 | 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 | a0001c0002t0012g0092 | 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 | 145 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(142): Show | 146 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.196+14441G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105567402 | ||||||
| chr4:105567506
|
A | G | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0004c0006t0001g0093 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0004c0006t0001g0164 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0002c0001t0001g0117a0002c0001t0001g0118a0002c0001t0001g0119 | 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 | a0001c0002t0002g0078a0001c0002t0002g0156a0001c0002t0003g0075others(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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0002t0012g0092 | 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 | a0001c0002t0002g0149a0001c0002t0002g0153a0001c0002t0002g0154others(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 | a0002c0001t0001g0083 | 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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0001c0009t0002g0095 | 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 | a0001c0002t0001g0166 | 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 | 159 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(156): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(157): 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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0003t0002g0016 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | a0001c0002t0004g0110 | 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 | 159 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(156): Show | 160 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(157): 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 | a0001c0002t0002g0078a0001c0002t0002g0156a0001c0003t0002g0113others(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 | a0007c0019t0005g0005 | 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 | a0001c0002t0001g0172a0001c0002t0003g0090a0001c0002t0003g0101others(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 | a0001c0002t0002g0069a0002c0001t0001g0122 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | 9 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0008g0019others(6): 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0002c0001t0001g0127 | 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 | a0001c0002t0012g0092 | 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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0001c0002t0002g0078a0001c0002t0002g0156a0001c0010t0006g0076others(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 | 145 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(142): Show | 146 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(143): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0011c0015t0021g0013 | 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 | a0003c0005t0004g0056 | 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 | a0002c0001t0001g0176a0002c0001t0005g0081 | 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 | a0005c0020t0003g0021 | 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 | a0001c0002t0002g0078a0001c0002t0002g0156a0001c0002t0003g0145others(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 | 147 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(144): Show | 148 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(145): 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157 | 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 | a0002c0001t0001g0063 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | a0002c0017t0001g0022 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | a0001c0002t0002g0078a0001c0002t0002g0156 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0004c0006t0001g0093 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | 133 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(130): Show | 134 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(131): 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 | a0001c0002t0003g0099 | 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 | a0002c0001t0001g0048a0002c0001t0001g0178 | 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 | a0002c0017t0001g0022 | 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 | a0001c0004t0005g0042a0001c0004t0005g0043 | 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 | a0001c0002t0001g0172a0001c0002t0003g0173a0001c0002t0003g0174 | 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 | 168 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(165): Show | 169 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(166): 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 | a0002c0001t0001g0050 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0003t0002g0016 | 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 | a0005c0028t0020g0114 | 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 | a0001c0002t0001g0172a0001c0002t0002g0078a0001c0002t0002g0156others(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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | 13 | a0001c0002t0002g0146a0001c0002t0003g0075a0001c0002t0003g0087others(10): 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0001c0002t0003g0145 | 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 | 20 | a0001c0002t0001g0172a0001c0002t0002g0146a0001c0002t0002g0153others(17): 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 | a0001c0002t0002g0001a0001c0002t0002g0149a0001c0002t0002g0154others(13): Show | 17 | HG00280.hp2 HG00639.hp1 HG01109.hp1 others(14): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0001c0025t0004g0065 | 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 | a0001c0002t0003g0145 | 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 | a0001c0002t0001g0172a0001c0002t0003g0090a0001c0002t0003g0101others(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 | a0001c0002t0001g0172a0001c0002t0003g0090a0001c0002t0003g0101others(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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0002c0001t0001g0059a0002c0001t0001g0066 | 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 | a0001c0002t0002g0175 | 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 | a0001c0002t0003g0145 | 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 | 154 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(151): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(152): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0002t0002g0129a0001c0002t0003g0142 | 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 | a0001c0002t0003g0145a0001c0003t0002g0113a0004c0006t0010g0139 | 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 | 119 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(116): Show | 120 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(117): 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157others(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 | a0001c0002t0002g0129a0001c0002t0003g0142 | 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 | a0001c0002t0008g0019a0001c0003t0008g0031 | 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 | a0001c0003t0003g0020 | 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 | a0002c0001t0001g0083 | 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 | a0001c0003t0002g0113a0005c0028t0020g0114 | 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 | a0001c0003t0002g0113a0005c0028t0020g0114 | 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 | a0001c0002t0008g0019a0001c0003t0008g0031a0009c0021t0001g0023 | 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0003t0002g0113 | 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0005c0020t0003g0021 | 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 | a0001c0003t0009g0018a0001c0010t0006g0076a0001c0010t0006g0077others(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 | 116 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(113): 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0001c0004t0005g0042a0001c0004t0005g0043 | 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 | 6 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0003t0002g0016others(3): 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | 173 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(170): Show | 174 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(171): 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 | a0001c0002t0012g0092 | 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 | a0001c0002t0002g0149a0001c0002t0002g0153a0001c0002t0002g0154others(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 | a0001c0002t0003g0090a0001c0002t0003g0101a0001c0002t0011g0091others(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 | a0001c0002t0002g0149a0001c0002t0002g0153a0001c0002t0002g0154others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0001c0003t0003g0020 | 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 | a0001c0003t0003g0020 | 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 | a0004c0006t0001g0159 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0002g0138others(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 | a0005c0008t0001g0177 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0002t0002g0129 | 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0002t0003g0145 | 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 | a0001c0002t0003g0145 | 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 | 175 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(172): Show | 176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | 175 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(172): Show | 176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.197-9980A>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105579268 | ||||||
| chr4:105579386
|
T | C | 139 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(136): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): 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 | a0001c0003t0003g0020 | 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 | 141 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(138): Show | 142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): 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 | a0001c0002t0002g0069a0002c0001t0001g0054a0002c0001t0001g0071others(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 | 175 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(172): Show | 176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): 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 | a0003c0005t0012g0124 | 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 | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.197-9234T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580014 | ||||||
| chr4:105580015
|
G | A | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.197-9233G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580015 | ||||||
| chr4:105580019
|
T | A | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0002t0001g0067a0001c0002t0001g0167a0001c0002t0002g0069others(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 | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0002t0002g0149a0001c0002t0002g0153a0001c0002t0002g0154 | 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 | a0001c0002t0002g0001a0001c0002t0002g0149a0001c0002t0002g0153others(13): Show | 17 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(14): 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 | a0005c0028t0020g0114 | 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 | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.197-8442T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105580806 | ||||||
| chr4:105580816
|
A | G | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0002c0001t0017g0128 | 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 | a0005c0028t0020g0114 | 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 | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0002c0001t0001g0131 | 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 | a0001c0002t0002g0001a0001c0002t0002g0149a0001c0002t0002g0153others(13): Show | 17 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(14): 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 | a0001c0002t0002g0149a0001c0002t0002g0153a0001c0002t0002g0154others(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 | 175 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(172): Show | 176 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(173): 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 | a0001c0002t0003g0150 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0003t0002g0113 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | a0001c0024t0004g0041 | 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 | a0002c0001t0019g0068 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0002c0001t0001g0162a0002c0023t0001g0161 | 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 | a0001c0002t0001g0080a0001c0002t0001g0163a0001c0002t0001g0166others(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 | a0002c0001t0001g0170 | 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 | a0005c0028t0020g0114 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0014g0107others(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 | a0001c0002t0002g0001a0001c0002t0002g0149a0001c0002t0002g0153others(13): Show | 17 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(14): 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 | a0005c0028t0020g0114 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0002g0138others(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 | 54 | a0001c0002t0001g0167a0001c0002t0001g0172a0001c0002t0002g0069others(51): 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 | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0001g0166others(74): Show | 78 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(75): 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 | a0001c0002t0001g0080a0001c0002t0001g0171a0001c0002t0003g0112others(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 | a0001c0002t0002g0001a0001c0002t0008g0019a0001c0003t0008g0031others(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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0002g0138others(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 | a0003c0005t0008g0102 | 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 | a0001c0002t0001g0172a0001c0002t0003g0173a0001c0002t0003g0174 | 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 | a0005c0020t0003g0021 | 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 | 152 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(149): Show | 153 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(150): 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157 | 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 | a0001c0002t0001g0104a0001c0002t0002g0108a0001c0002t0003g0096others(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 | a0001c0002t0002g0138a0001c0003t0003g0024a0001c0003t0003g0025others(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 | a0002c0001t0001g0050 | 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 | a0001c0003t0002g0113a0005c0028t0020g0114 | 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 | 151 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(148): Show | 152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): 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 | a0001c0003t0002g0113 | 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157 | 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | a0001c0003t0002g0113 | 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 | 138 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(135): Show | 139 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.197-5803C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | chr4 | 105583445 | ||||||
| chr4:105583473
|
G | A | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157 | 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 | a0001c0002t0002g0179 | 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 | 176 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(174): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0001c0002t0001g0067a0001c0002t0001g0167a0001c0002t0002g0069others(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 | a0001c0003t0003g0020 | 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 | a0001c0002t0003g0145 | 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 | a0001c0002t0003g0145 | 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 | a0001c0002t0002g0001a0001c0002t0002g0149a0001c0002t0002g0153others(14): Show | 18 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(15): 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 | a0001c0002t0002g0138a0001c0002t0003g0150a0001c0002t0007g0147others(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 | 47 | a0001c0002t0001g0172a0001c0002t0002g0001a0001c0002t0002g0078others(44): Show | 48 | HG00280.hp2 HG01069.hp1 HG01070.hp1 others(45): 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 | a0001c0002t0003g0145 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0001c0003t0002g0113 | 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 | a0001c0002t0001g0172a0001c0002t0003g0090a0001c0002t0003g0101others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0001c0002t0003g0142 | 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 | a0001c0002t0001g0172a0001c0002t0003g0090a0001c0002t0003g0101others(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 | a0001c0002t0003g0090a0001c0002t0011g0091a0001c0009t0002g0095others(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 | a0001c0002t0003g0101a0001c0002t0003g0150a0001c0002t0007g0147others(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 | 32 | a0001c0002t0001g0172a0001c0002t0002g0074a0001c0002t0002g0078others(29): 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 | a0001c0002t0001g0166a0001c0002t0002g0072a0001c0002t0002g0084others(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 | 61 | a0001c0002t0001g0104a0001c0002t0001g0171a0001c0002t0002g0001others(58): 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 | 38 | a0001c0002t0001g0080a0001c0002t0001g0163a0001c0002t0001g0167others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(35): 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 | a0001c0002t0001g0067a0001c0002t0002g0057a0002c0001t0001g0051others(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 | a0002c0001t0001g0062 | 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 | a0001c0002t0002g0078a0001c0002t0002g0156 | 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 | a0001c0002t0002g0001a0001c0002t0002g0149a0001c0002t0002g0153others(12): Show | 16 | HG01109.hp1 HG01175.hp2 HG01256.hp1 others(13): 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 | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0001g0166others(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 | a0002c0001t0004g0109a0003c0005t0004g0136a0003c0005t0004g0137 | 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 | a0001c0003t0002g0113 | 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 | a0001c0002t0002g0100 | 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 | a0001c0003t0009g0018 | 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 | a0001c0002t0003g0111a0001c0002t0003g0145 | 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 | a0001c0002t0002g0072a0001c0002t0002g0140a0001c0002t0002g0141others(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 | a0001c0002t0002g0084a0001c0002t0012g0092a0001c0003t0002g0011others(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 | a0005c0020t0003g0021 | 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 | a0009c0021t0001g0023 | 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 |
3 | a0001c0004t0005g0037a0002c0001t0001g0046a0003c0005t0004g0160 | 3 | HG01981.hp1 HG02109.hp1 homoSapiens_chm13v2.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 | a0001c0002t0003g0096 | 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 | a0001c0002t0007g0147 | 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 | a0001c0003t0003g0020 | 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 | a0001c0002t0002g0146a0001c0002t0002g0149a0001c0002t0002g0153others(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 | a0005c0020t0003g0021 | 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 | a0005c0020t0003g0021 | 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 | a0001c0002t0011g0091a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0002c0001t0001g0049 | 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 | a0002c0001t0001g0176 | 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 | a0002c0001t0019g0068 | 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 | a0001c0003t0009g0018 | 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 | a0001c0002t0002g0175 | 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 | a0001c0002t0002g0001a0001c0002t0002g0146a0001c0002t0003g0090others(51): Show | 55 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(52): 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 | a0002c0001t0001g0051 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0002c0001t0001g0079a0002c0001t0001g0178a0002c0001t0001g0183others(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 | a0002c0001t0001g0061 | 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 | a0009c0021t0001g0023 | 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 | a0002c0001t0001g0048 | 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 | a0001c0002t0012g0092a0001c0003t0003g0034a0001c0004t0009g0103others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0146others(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 | a0003c0005t0008g0102 | 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 | a0002c0017t0001g0022a0005c0008t0003g0143a0006c0011t0002g0003others(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 | 11 | a0003c0005t0004g0056a0003c0005t0004g0136a0003c0005t0004g0137others(8): Show | 11 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(8): 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 | a0006c0011t0002g0003a0006c0011t0002g0004 | 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 | a0001c0003t0008g0031 | 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 | a0002c0017t0001g0022a0005c0008t0003g0143a0006c0011t0002g0003others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | 11 | a0003c0005t0004g0056a0003c0005t0004g0136a0003c0005t0004g0137others(8): Show | 11 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(8): 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 | a0004c0006t0010g0139 | 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 | a0003c0007t0002g0009a0003c0007t0002g0015 | 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 | a0001c0003t0002g0113 | 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 | a0003c0007t0001g0010 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0003c0007t0002g0009a0003c0007t0002g0015 | 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 | a0001c0002t0002g0175 | 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 | a0011c0015t0021g0013 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0009c0021t0001g0023 | 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 | a0002c0001t0002g0155 | 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 | a0001c0002t0001g0067a0001c0002t0002g0047a0001c0002t0002g0057others(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 | a0001c0002t0002g0149 | 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 | a0001c0002t0012g0092a0001c0003t0003g0034a0001c0004t0009g0103others(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 | a0002c0017t0001g0022a0005c0008t0003g0143a0006c0011t0002g0003others(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 | a0002c0001t0001g0185 | 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 | a0001c0002t0012g0092 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0002g0153a0001c0002t0002g0156a0001c0002t0002g0179others(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 | a0001c0002t0002g0146a0001c0002t0002g0149a0001c0002t0003g0111others(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 | a0001c0002t0002g0154a0001c0002t0003g0075a0001c0002t0003g0087others(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 | a0001c0002t0003g0096 | 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 | a0001c0002t0001g0067a0001c0002t0001g0163a0001c0002t0001g0171others(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 | a0001c0002t0001g0080a0001c0002t0001g0104a0001c0002t0001g0172others(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 | a0001c0002t0003g0173a0001c0002t0003g0174a0002c0001t0018g0040others(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 | a0002c0001t0001g0052a0002c0001t0001g0058a0002c0001t0001g0158others(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 | a0001c0002t0012g0092a0002c0017t0001g0022a0005c0008t0003g0143others(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 | a0001c0004t0009g0103a0001c0004t0009g0105a0006c0011t0002g0003others(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 | a0001c0002t0001g0104a0001c0002t0001g0166a0001c0002t0001g0172others(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 | a0001c0002t0003g0150a0001c0003t0003g0020 | 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 | a0001c0002t0003g0150 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0002t0002g0146a0001c0002t0003g0090a0001c0002t0003g0101others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0003t0008g0031a0009c0021t0001g0023 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0003g0088others(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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0005c0008t0003g0143 | 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 | 11 | a0003c0005t0004g0136a0003c0005t0004g0137a0003c0005t0004g0160others(8): Show | 11 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(8): 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 | a0001c0002t0002g0100a0001c0002t0011g0091 | 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 | a0002c0001t0001g0062 | 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 | 8 | a0002c0017t0001g0022a0003c0005t0004g0056a0003c0005t0004g0160others(5): Show | 8 | HG00639.hp2 HG01074.hp1 HG01243.hp2 others(5): 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 | a0005c0008t0001g0151 | 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 | a0002c0001t0001g0044 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0003g0090a0001c0002t0003g0142a0001c0002t0014g0107others(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 | a0001c0003t0007g0027 | 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 | a0003c0005t0008g0102 | 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 | a0001c0002t0003g0090a0001c0002t0003g0142a0001c0002t0014g0107others(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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0005c0028t0020g0114 | 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 | a0002c0001t0001g0049a0002c0001t0001g0051a0002c0001t0001g0130others(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 | 143 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(140): Show | 144 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(141): 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 | a0007c0019t0005g0005 | 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 | a0002c0001t0018g0040 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | 14 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(11): Show | 14 | HG00639.hp2 HG00735.hp2 HG01070.hp1 others(11): 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 | a0003c0005t0008g0102 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0009t0002g0095a0001c0009t0007g0086a0001c0009t0008g0045others(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 | a0002c0001t0001g0162 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(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 | 31 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0003t0007g0027others(28): Show | 31 | HG00280.hp1 HG00639.hp2 HG01109.hp2 others(28): 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0002c0027t0001g0055 | 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 | 61 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(58): Show | 61 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(58): 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 | a0001c0002t0003g0099 | 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 | 2 | a0012c0013t0013g0006a0013c0014t0013g0008 | 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 | 53 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(50): Show | 53 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(50): 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | 4 | a0001c0002t0002g0146a0001c0002t0003g0111a0012c0013t0013g0006others(1): Show | 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 | 2 | a0012c0013t0013g0006a0013c0014t0013g0008 | 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 | a0001c0003t0002g0113 | 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 | a0001c0009t0002g0095a0001c0009t0007g0086a0001c0009t0008g0045others(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 | 4 | a0001c0002t0002g0146a0001c0002t0003g0111a0012c0013t0013g0006others(1): Show | 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 | a0001c0002t0003g0145a0005c0020t0003g0021 | 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 | a0001c0003t0007g0027 | 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 | a0002c0001t0001g0071a0002c0001t0001g0122 | 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 | 48 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(45): Show | 48 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(45): 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 | a0006c0011t0002g0003a0006c0011t0002g0004a0006c0026t0002g0089 | 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 | a0001c0003t0007g0027 | 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 | a0001c0002t0008g0019 | 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 | 56 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(53): Show | 56 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(53): 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 | a0001c0003t0002g0002 | 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 | a0006c0011t0002g0003a0006c0011t0002g0004a0006c0026t0002g0089 | 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0009t0002g0095a0001c0009t0007g0086a0001c0009t0008g0045others(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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0003t0009g0018 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0002t0012g0092a0003c0005t0012g0124 | 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 | 27 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0146others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(24): 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0003t0002g0113a0011c0015t0021g0013 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0003t0002g0014 | 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 | 59 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(56): Show | 59 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(56): 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(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 | a0006c0011t0002g0003a0006c0011t0002g0004a0006c0026t0002g0089 | 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 | 32 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(29): Show | 32 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.384+8324G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105597759 | ||||||
| chr4:105597813
|
A | T | 32 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(29): Show | 32 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(29): 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 | a0001c0002t0002g0072 | 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 | a0002c0001t0001g0126a0002c0001t0001g0169 | 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 | a0002c0001t0019g0068 | 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 | a0001c0003t0007g0027a0001c0004t0005g0036a0001c0004t0005g0037others(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 | 15 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(12): Show | 15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0003g0174a0001c0003t0002g0002a0001c0003t0002g0011others(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 | 43 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(40): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0002c0001t0001g0082a0002c0001t0018g0040 | 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 | 30 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(27): Show | 30 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.384+9843T>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105599278 | ||||||
| chr4:105599523
|
AT | A | 4 | a0001c0002t0002g0146a0001c0002t0003g0111a0012c0013t0013g0006others(1): Show | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(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 | 26 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): 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 | a0001c0002t0012g0092a0003c0005t0012g0124 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | 26 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.384+11254A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600689 | ||||||
| chr4:105600702
|
C | G | 26 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.384+11267C>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600702 | ||||||
| chr4:105600709
|
C | T | 26 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.384+11274C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105600709 | ||||||
| chr4:105600713
|
T | A | 26 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): 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 | a0001c0002t0003g0142 | 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0003t0002g0113 | 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 | 15 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(12): Show | 15 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(12): 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 | a0002c0001t0001g0119 | 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0003t0002g0113a0011c0015t0021g0013 | 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 | a0009c0021t0001g0023 | 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 | a0005c0028t0020g0114 | 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 | 29 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(26): Show | 29 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.385-11252T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105602132 | ||||||
| chr4:105602162
|
G | A | 26 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): 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 | a0001c0002t0002g0121 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0002c0001t0001g0134 | 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 | a0001c0003t0002g0014 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091others(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 | 60 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(57): Show | 60 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(57): 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 | a0001c0003t0007g0027 | 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 | a0003c0005t0012g0124 | 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 | a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | 60 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(57): Show | 60 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(57): 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 | a0007c0019t0005g0005 | 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0003g0145 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091others(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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0002c0001t0001g0158 | 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 | a0001c0009t0008g0045 | 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 | a0002c0001t0001g0048 | 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 | a0002c0001t0001g0130a0002c0001t0001g0170 | 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 | 32 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(29): Show | 32 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(29): 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 | a0003c0005t0012g0124 | 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 | 27 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(24): 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(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 | a0011c0015t0021g0013 | 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105others(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 | a0009c0021t0001g0023 | 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 | 27 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(24): 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 | a0001c0002t0012g0092a0001c0003t0002g0113 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.385-7675C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605709 | ||||||
| chr4:105605830
|
A | G | 27 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.385-7554A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605830 | ||||||
| chr4:105605861
|
T | C | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.385-7523T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605861 | ||||||
| chr4:105605909
|
G | C | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.385-7475G>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605909 | ||||||
| chr4:105605949
|
C | T | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.385-7435C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105605949 | ||||||
| chr4:105606008
|
A | G | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): 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 | a0001c0002t0003g0099 | 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 | 27 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.385-7160A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606224 | ||||||
| chr4:105606243
|
A | C | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): 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 | a0003c0005t0004g0136a0003c0005t0004g0137 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091others(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 | 27 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.385-6973C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105606411 | ||||||
| chr4:105606456
|
A | G | 27 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(24): Show | 27 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(24): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | 54 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(51): Show | 54 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(51): 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0024t0004g0041 | 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 | a0002c0017t0001g0022a0008c0022t0001g0133 | 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 | a0002c0001t0001g0079a0002c0001t0001g0178a0002c0001t0001g0183others(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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091others(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 | 54 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(51): Show | 54 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.385-5908C>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105607476 | ||||||
| chr4:105607518
|
A | AAT | 19 | a0001c0002t0003g0145a0001c0002t0004g0110a0001c0002t0004g0135others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(16): 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 | 19 | a0001c0002t0003g0145a0001c0002t0004g0110a0001c0002t0004g0135others(16): Show | 19 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(16): 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 | a0005c0008t0001g0144 | 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 | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(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 | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): 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 | a0003c0005t0012g0124 | 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 | a0002c0001t0001g0073 | 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 | a0001c0002t0003g0099 | 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 | a0002c0001t0001g0073 | 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 | a0002c0001t0001g0071a0002c0001t0001g0122 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091others(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 | a0002c0001t0004g0109 | 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 | a0001c0002t0012g0092 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0002c0001t0001g0131 | 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 | 23 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(20): Show | 23 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(20): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0002c0027t0001g0055 | 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 | a0002c0001t0001g0082 | 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 | a0002c0001t0001g0170 | 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 | a0001c0002t0003g0173a0001c0002t0003g0174 | 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 | a0001c0002t0001g0163 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0004g0135 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(108): Show | 112 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(109): 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 | a0001c0002t0001g0166 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0002c0001t0001g0176 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0003t0008g0031 | 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.385-2212A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 2/13 | chr4 | 105611172 | ||||||
| chr4:105611343
|
T | C | 31 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0003g0145others(28): Show | 31 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(28): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0007c0019t0005g0005 | 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 | a0007c0019t0005g0005 | 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 | a0001c0002t0003g0145a0001c0003t0007g0027a0001c0004t0009g0103others(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 | 23 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0004t0005g0036others(20): Show | 23 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(20): 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0002c0001t0001g0083 | 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 | a0002c0001t0001g0052a0002c0001t0001g0058a0002c0001t0001g0158 | 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 | a0002c0001t0001g0051 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091others(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 | a0002c0001t0001g0064 | 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | 41 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0004g0110others(38): Show | 41 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(38): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(108): Show | 112 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(109): 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 | a0002c0001t0001g0117a0002c0001t0001g0118 | 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 | 23 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0004t0005g0036others(20): Show | 23 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(20): 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 | a0003c0005t0012g0124 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0009t0002g0095others(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 | 26 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0004g0110others(23): Show | 26 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(23): 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 | a0002c0001t0001g0061 | 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 | a0001c0002t0003g0090a0001c0002t0003g0142a0001c0002t0014g0107others(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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091others(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 | a0001c0002t0002g0175 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0002t0011g0091 | 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 | 33 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0004t0005g0036others(30): Show | 33 | HG00280.hp1 HG00639.hp2 HG00741.hp2 others(30): 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0002c0001t0001g0178 | 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 | a0001c0002t0004g0135 | 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 | 23 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0004t0005g0036others(20): Show | 23 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(20): 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 | a0003c0005t0012g0124 | 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 | a0002c0001t0001g0049 | 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 | a0001c0002t0007g0147 | 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 | a0001c0002t0003g0173a0001c0002t0003g0174a0001c0003t0002g0002others(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 | a0002c0001t0001g0073 | 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 | a0005c0028t0020g0114 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0003c0005t0012g0124 | 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 | a0001c0009t0007g0086 | 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 | a0009c0021t0001g0023 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0005c0028t0020g0114 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0003t0002g0014 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0005c0028t0020g0114 | 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 | a0002c0001t0001g0046a0002c0001t0016g0165 | 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 | a0002c0001t0001g0083 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0003t0009g0184 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0005c0028t0020g0114 | 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 | a0009c0021t0001g0023 | 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 | a0003c0005t0012g0124 | 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 | a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0002c0001t0001g0097 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0002t0003g0099 | 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 | a0001c0002t0002g0100 | 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 | a0001c0009t0002g0095a0001c0009t0007g0086a0001c0009t0008g0045others(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 | 54 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(51): Show | 54 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(51): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0002g0074 | 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 | a0001c0003t0008g0031a0005c0008t0003g0143 | 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 | a0009c0021t0001g0023 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0005c0028t0020g0114 | 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0002t0002g0072 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0001g0080 | 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 | a0001c0002t0012g0092a0001c0003t0002g0113 | 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 | 51 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(48): Show | 51 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.508+7319delG | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105620825 | ||||||
| chr4:105621321
|
T | C | 2 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0002c0001t0001g0185 | 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 | a0001c0024t0004g0041 | 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 | a0005c0008t0001g0177 | 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 | a0001c0002t0002g0047 | 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 | a0001c0003t0007g0027 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0002t0003g0090a0001c0002t0003g0142a0001c0002t0014g0107others(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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0002t0012g0092a0001c0003t0002g0113 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | 51 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(48): Show | 51 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(48): 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | 23 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0004t0005g0036others(20): Show | 23 | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(20): 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0003c0007t0001g0010 | 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 | a0001c0002t0003g0145a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0002c0001t0001g0123a0002c0001t0001g0181 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0009c0021t0001g0023 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0009c0021t0001g0023 | 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 | a0001c0009t0002g0095a0001c0009t0007g0086a0001c0009t0008g0045others(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 | a0005c0028t0020g0114 | 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 | a0001c0003t0002g0014a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0011c0015t0021g0013 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.509-5665T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625233 | ||||||
| chr4:105625323
|
G | A | 184 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(181): Show | 185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.509-5575G>A | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105625323 | ||||||
| chr4:105625456
|
G | A | 2 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0002g0153 | 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 | a0002c0001t0001g0134 | 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 | a0003c0007t0002g0009a0003c0007t0002g0015 | 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 | a0001c0009t0002g0095a0001c0009t0007g0086a0001c0009t0008g0045others(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 | a0001c0002t0012g0092 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0002t0002g0100a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0008g0019a0003c0005t0008g0102 | 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 | a0002c0001t0001g0059 | 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 | a0001c0003t0007g0027 | 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 | 51 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(48): Show | 51 | HG00280.hp1 HG00639.hp2 HG00735.hp2 others(48): 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 | a0001c0002t0002g0108 | 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 | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): 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 | a0005c0028t0020g0114 | 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 | 16 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0025t0004g0065others(13): Show | 16 | HG00639.hp2 HG01243.hp2 HG01516.hp1 others(13): 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 | a0001c0002t0003g0101a0001c0002t0011g0091 | 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 | a0001c0002t0002g0078a0001c0002t0002g0156 | 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 | a0001c0002t0003g0099 | 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 | 99 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(96): 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 | 85 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(82): 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 | a0001c0003t0008g0031 | 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 | a0001c0002t0002g0149 | 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 | 86 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(83): 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0002c0001t0001g0062 | 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 | a0001c0003t0002g0014 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(104): Show | 108 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(105): 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 | a0005c0008t0001g0177a0010c0016t0022g0007 | 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 | a0001c0002t0002g0156 | 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 | a0001c0002t0002g0108a0001c0002t0007g0147a0001c0002t0007g0148others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0012g0092 | 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 | a0005c0028t0020g0114 | 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 | 20 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(17): Show | 20 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(17): 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 | a0005c0020t0003g0021 | 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 | a0001c0002t0002g0100a0001c0002t0002g0108 | 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 | a0001c0002t0002g0129 | 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 | a0001c0002t0002g0116 | 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157 | 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 |
41 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0166others(38): 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 | a0002c0001t0001g0066 | 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 | a0001c0002t0002g0074 | 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 | a0001c0002t0001g0163a0001c0002t0002g0057a0001c0002t0002g0084others(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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(101): Show | 105 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(102): 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 | a0002c0001t0001g0117a0002c0001t0001g0118 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(103): Show | 107 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.509-1119C>T | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 3/13 | chr4 | 105629779 | ||||||
| chr4:105630095
|
A | G | 21 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(18): Show | 21 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(18): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | 8 | a0001c0002t0002g0001a0001c0004t0005g0036a0001c0004t0005g0037others(5): 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0003t0002g0014others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(103): Show | 107 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(104): 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 | a0005c0008t0001g0177 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0002c0001t0001g0053 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(103): Show | 107 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(104): 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 | a0001c0002t0003g0088a0001c0002t0003g0112a0001c0002t0003g0150others(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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | 21 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(18): Show | 21 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(18): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(101): Show | 105 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(102): 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 | a0002c0001t0001g0070 | 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 | a0001c0009t0008g0045 | 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 | 21 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(18): Show | 21 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(18): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(101): Show | 105 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(102): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0002c0001t0001g0071 | 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 | a0001c0002t0003g0145 | 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 | 20 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(17): Show | 20 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(17): 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 | a0002c0017t0001g0022a0004c0006t0001g0038a0004c0006t0001g0159others(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 | a0002c0001t0001g0117a0002c0001t0001g0118 | 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 | a0001c0002t0001g0104 | 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 | a0001c0002t0003g0145 | 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 | a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0002t0002g0084 | 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 | a0001c0002t0003g0145a0001c0002t0012g0092 | 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 | 20 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(17): Show | 20 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(17): 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 | a0005c0008t0003g0143 | 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 | 119 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(116): Show | 120 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(117): 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 | a0003c0005t0008g0102 | 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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0002c0001t0001g0071a0002c0001t0001g0122 | 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 | a0001c0003t0008g0031 | 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 | a0002c0001t0001g0122 | 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 | a0001c0002t0002g0057 | 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 | a0001c0002t0012g0092 | 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 | 108 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(105): Show | 109 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(106): 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 | a0002c0001t0001g0083 | 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 | a0009c0021t0001g0023 | 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 | a0001c0002t0003g0145 | 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 | 18 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(15): Show | 18 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(15): 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0003t0002g0014others(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 | a0001c0003t0002g0014 | 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 | a0001c0002t0002g0100a0001c0002t0002g0108a0001c0002t0003g0075others(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 | a0001c0002t0003g0145 | 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 | a0001c0002t0002g0129 | 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 | a0002c0001t0001g0044 | 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 | 3 | a0005c0008t0001g0144a0012c0013t0013g0006a0013c0014t0013g0008 | 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 | a0003c0005t0012g0124 | 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 | a0001c0002t0001g0166 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(94): Show | 98 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(95): 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 | a0005c0008t0001g0177 | 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 | a0001c0002t0012g0092 | 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 | 4 | a0005c0008t0001g0144a0008c0022t0001g0133a0012c0013t0013g0006others(1): Show | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0003t0002g0014others(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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0003t0002g0014others(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 | 109 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(106): Show | 110 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(107): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0002c0001t0001g0152 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0002g0108 | 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 | a0002c0001t0001g0182 | 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 | a0005c0008t0001g0151 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0001g0171 | 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 | a0001c0003t0003g0032 | 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 | 109 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(106): Show | 110 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(107): 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 | a0005c0008t0001g0177 | 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 | 17 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(14): Show | 17 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(14): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0002g0069 | 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 | a0001c0003t0002g0002 | 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 | a0007c0019t0005g0005 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0003g0088a0001c0002t0003g0112a0001c0002t0003g0150others(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 | 43 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(40): 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 | a0003c0007t0002g0009a0003c0007t0002g0015 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0003t0008g0031 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0003t0002g0014others(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 | a0001c0002t0001g0067a0001c0002t0002g0047a0001c0002t0002g0057others(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 | a0002c0001t0001g0064 | 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 | 182 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(179): Show | 183 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.675-3667A>G | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105641521 | ||||||
| chr4:105641566
|
T | A | 4 | a0005c0008t0001g0144a0008c0022t0001g0133a0012c0013t0013g0006others(1): Show | 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 | 5 | a0001c0003t0002g0016a0005c0008t0001g0144a0008c0022t0001g0133others(2): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0166others(79): Show | 83 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(80): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | 18 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0009t0002g0095others(15): Show | 18 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(15): 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0003t0002g0014others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0001c0004t0005g0037a0001c0004t0005g0039a0001c0004t0005g0042others(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 | 109 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(106): Show | 110 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(107): 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 | a0005c0008t0003g0143 | 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 | a0002c0001t0001g0046a0002c0001t0016g0165 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(100): Show | 104 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(101): 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 | a0011c0015t0021g0013 | 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 | a0002c0001t0001g0119a0008c0022t0001g0133 | 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 | a0001c0002t0002g0100a0001c0002t0003g0075a0001c0002t0003g0087others(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 | 116 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(113): Show | 117 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(114): 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 | a0005c0028t0020g0114 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(106): Show | 110 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.675-2095T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 5/13 | chr4 | 105643093 | ||||||
| chr4:105643133
|
G | GT | 11 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0003g0088others(8): 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0009c0021t0001g0023 | 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 | a0006c0026t0002g0089 | 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 | a0005c0028t0020g0114 | 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 | 12 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0008g0019others(9): 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 | 12 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0008g0019others(9): 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 | 16 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0121others(13): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(89): Show | 93 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(90): 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 | a0001c0002t0012g0092a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0001g0104 | 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 | a0001c0002t0008g0019a0001c0003t0002g0113a0003c0005t0008g0102 | 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 | a0001c0002t0003g0099a0002c0001t0005g0081 | 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 | 19 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0146others(16): 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 | a0002c0001t0002g0155 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0002c0001t0005g0081 | 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 | 51 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(48): 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 | 10 | a0001c0002t0008g0019a0001c0003t0002g0113a0003c0005t0008g0102others(7): 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 | a0002c0001t0001g0132 | 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 | 10 | a0001c0002t0001g0104a0001c0002t0001g0172a0005c0008t0001g0144others(7): 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 | a0002c0027t0001g0055 | 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 | a0005c0020t0003g0021 | 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 | a0001c0025t0004g0065 | 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 | 7 | a0005c0008t0001g0144a0005c0008t0001g0151a0005c0008t0001g0177others(4): 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0002g0108 | 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 | a0002c0001t0001g0064a0002c0001t0001g0127 | 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 | 19 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0003g0145others(16): 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 | a0002c0001t0001g0123 | 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 | 51 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(48): 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 | a0001c0002t0002g0100a0001c0003t0007g0027 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | 51 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(48): 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 | 9 | a0001c0002t0008g0019a0001c0003t0002g0113a0001c0009t0008g0045others(6): 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0002g0014 | 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 | a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0002c0001t0001g0125 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0001c0002t0012g0092others(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 | 16 | a0001c0002t0001g0172a0001c0002t0008g0019a0001c0003t0002g0113others(13): 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 | a0001c0002t0002g0149a0001c0004t0005g0036a0001c0004t0005g0037others(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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0005c0028t0020g0114 | 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 | a0001c0003t0003g0033 | 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 | a0006c0011t0002g0003a0006c0011t0002g0004 | 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 | 50 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(47): 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 | a0001c0002t0001g0080 | 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 | 66 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(63): Show | 67 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(64): 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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0003g0088others(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 | a0009c0021t0001g0023 | 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 | a0001c0003t0002g0012 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | 9 | a0001c0002t0008g0019a0001c0003t0002g0113a0001c0009t0008g0045others(6): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0009c0021t0001g0023 | 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 | a0001c0002t0003g0099 | 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0008g0031 | 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 | 9 | a0001c0002t0008g0019a0001c0003t0002g0113a0001c0009t0008g0045others(6): 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 | a0001c0002t0011g0091 | 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 | a0002c0001t0001g0131 | 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 | a0001c0025t0004g0065 | 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 | a0001c0002t0002g0047 | 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 | a0001c0002t0003g0145a0001c0003t0008g0031 | 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 | a0002c0001t0019g0068 | 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 | a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0001c0002t0002g0100a0001c0002t0003g0075a0001c0002t0003g0087others(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 | a0009c0021t0001g0023 | 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 | a0001c0002t0003g0145 | 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 | a0002c0001t0001g0044a0002c0001t0001g0082a0002c0001t0001g0152others(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 | a0001c0002t0008g0019a0001c0009t0008g0045a0003c0005t0008g0102 | 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157others(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 | a0001c0002t0002g0074a0001c0002t0002g0116 | 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 | a0002c0001t0001g0059 | 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 | a0001c0002t0012g0092 | 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 | a0002c0001t0001g0061 | 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 | a0009c0021t0001g0023 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157others(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 | a0005c0020t0003g0021 | 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 | a0009c0021t0001g0023 | 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157others(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 | a0001c0002t0004g0110 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111a0002c0001t0001g0125 | 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 | a0001c0004t0005g0037 | 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 | a0001c0003t0002g0016 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0005c0028t0020g0114 | 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 | 6 | a0005c0008t0001g0144a0005c0008t0001g0177a0008c0022t0001g0133others(3): 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 | a0001c0002t0008g0019 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0001c0003t0008g0031 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0002c0001t0001g0125 | 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 | a0001c0002t0003g0145 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0008g0031 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0002c0001t0001g0131 | 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 | a0001c0002t0003g0088a0001c0002t0003g0112a0001c0002t0003g0150others(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 | a0001c0002t0002g0057a0001c0002t0002g0121a0001c0002t0002g0168others(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 | a0009c0021t0001g0023 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | 5 | a0005c0008t0001g0144a0005c0008t0001g0177a0008c0022t0001g0133others(2): 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0008g0031 | 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 | a0009c0021t0001g0023 | 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 | a0002c0001t0001g0066a0002c0001t0001g0180 | 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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0003g0088others(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 | a0002c0001t0001g0052a0002c0001t0001g0058a0002c0001t0001g0158 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(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 | a0001c0003t0002g0016a0002c0001t0001g0066 | 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 | a0001c0002t0002g0074a0001c0002t0002g0116a0001c0002t0004g0110others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | 14 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0003t0007g0027others(11): Show | 14 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(11): 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0002g0016 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0006c0011t0002g0003a0006c0011t0002g0004a0006c0026t0002g0089 | 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 | a0009c0021t0001g0023 | 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 | a0001c0002t0002g0100a0001c0010t0006g0076a0001c0010t0006g0077others(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 | a0003c0005t0004g0056 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0003t0009g0018 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0010t0006g0076 | 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 | a0001c0009t0007g0086 | 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 | a0001c0002t0004g0110 | 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 | 26 | a0001c0002t0003g0096a0001c0003t0002g0113a0001c0003t0007g0027others(23): 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 | a0001c0002t0012g0092a0001c0004t0005g0036a0001c0004t0005g0037others(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 | a0001c0002t0003g0145a0001c0002t0007g0147a0001c0004t0005g0039others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0007g0148others(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 | a0001c0002t0008g0019a0001c0009t0008g0045 | 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 | a0001c0002t0002g0100a0001c0003t0009g0018 | 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 | a0001c0003t0009g0184a0003c0005t0008g0102 | 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 | a0001c0003t0008g0031 | 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 | a0002c0001t0001g0044a0002c0001t0001g0049a0004c0006t0010g0139 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0005c0028t0020g0114 | 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 | 13 | a0001c0002t0002g0001a0001c0002t0002g0175a0001c0002t0003g0090others(10): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(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 | a0001c0002t0002g0078a0001c0002t0002g0146a0001c0002t0002g0156others(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 | a0001c0002t0002g0149a0001c0002t0002g0153a0001c0002t0002g0154 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0009c0021t0001g0023 | 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 | a0001c0009t0007g0086 | 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 | a0002c0001t0005g0081 | 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 | a0001c0004t0005g0042a0001c0004t0005g0043 | 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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0003g0088others(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 | a0001c0009t0007g0086 | 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 | a0009c0021t0001g0023 | 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 | a0002c0001t0001g0134 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0002c0001t0001g0049 | 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 | a0002c0001t0001g0123 | 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 | a0001c0003t0002g0002a0001c0003t0002g0011a0001c0003t0002g0016 | 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0008g0031 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0002g0016 | 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 | a0001c0024t0004g0041 | 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 | a0001c0002t0003g0145a0001c0003t0008g0031 | 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 | a0002c0001t0001g0123 | 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 | a0002c0001t0001g0181 | 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 | 48 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(45): 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 | a0001c0002t0002g0175a0001c0002t0003g0090a0001c0002t0003g0142others(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 | a0009c0021t0001g0023 | 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 | 183 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(180): Show | 184 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(181): 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 | a0009c0021t0001g0023 | 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 | a0002c0001t0001g0053 | 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 | a0001c0002t0002g0072a0001c0002t0002g0100a0001c0002t0007g0147others(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 | a0001c0003t0008g0031a0002c0001t0002g0155 | 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 | a0001c0002t0001g0080a0001c0002t0001g0163a0001c0002t0001g0166others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0175others(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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | 11 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0024t0004g0041others(8): Show | 11 | HG00609.hp1 HG01516.hp1 HG01517.hp1 others(8): 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 | a0001c0009t0007g0086 | 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 | a0001c0002t0002g0100a0001c0010t0006g0076a0001c0010t0006g0077others(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 | 9 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0024t0004g0041others(6): Show | 9 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(6): 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0009c0021t0001g0023 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0002t0012g0092 | 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 | a0002c0001t0001g0183 | 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 | a0002c0001t0001g0131 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0100others(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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0003g0096 | 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 | a0001c0003t0008g0031 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(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 | a0001c0002t0003g0145a0001c0003t0008g0031 | 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 | a0001c0004t0009g0103a0001c0004t0009g0105 | 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 | a0009c0021t0001g0023 | 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 | a0009c0021t0001g0023 | 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 | 119 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(116): Show | 120 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(117): 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 | a0001c0009t0002g0095a0001c0009t0015g0106 | 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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0001c0004t0005g0039a0001c0004t0005g0042a0001c0004t0005g0043others(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 | a0002c0001t0001g0097 | 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 | a0001c0009t0008g0045a0003c0005t0008g0102 | 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 | 46 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(43): 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 | a0002c0001t0001g0050 | 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 | a0002c0001t0001g0050 | 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 | a0001c0003t0007g0027a0001c0009t0002g0095a0001c0009t0007g0086others(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 | a0001c0002t0012g0092 | 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 | a0001c0002t0003g0145a0001c0003t0008g0031 | 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 | 15 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0003t0007g0027others(12): Show | 15 | HG00280.hp1 HG01070.hp1 HG01106.hp2 others(12): 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0002g0001others(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 | a0001c0002t0001g0163a0001c0002t0001g0166a0001c0002t0001g0167others(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 | a0002c0001t0018g0040 | 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 | a0001c0002t0002g0146a0001c0002t0003g0111 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0002t0002g0179 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0009c0021t0001g0023 | 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 | 46 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(43): 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 | a0009c0021t0001g0023 | 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 | a0002c0001t0001g0063a0002c0001t0001g0132 | 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 | a0001c0003t0009g0018 | 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 | a0009c0021t0001g0023 | 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 | 48 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(45): 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 | a0005c0008t0001g0144 | 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 | a0001c0003t0007g0027a0001c0009t0002g0095a0001c0009t0007g0086others(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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0003g0088others(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 | a0002c0001t0001g0094 | 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 | a0009c0021t0001g0023 | 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 | a0005c0020t0003g0021 | 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 | a0009c0021t0001g0023 | 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 | a0002c0001t0001g0083 | 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 | a0009c0021t0001g0023 | 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 | a0001c0002t0002g0149a0002c0001t0001g0044 | 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 | a0001c0002t0002g0149a0001c0002t0002g0153 | 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 | a0001c0002t0012g0092 | 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 | a0001c0002t0002g0175a0001c0002t0014g0107a0001c0003t0003g0025 | 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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(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 | a0001c0003t0002g0113 | 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 | a0001c0003t0008g0031 | 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 | a0001c0004t0005g0036 | 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 | a0002c0001t0001g0050 | 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 | a0002c0001t0001g0050 | 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 | 12 | a0001c0002t0008g0019a0001c0009t0008g0045a0003c0005t0008g0102others(9): 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0001c0002t0001g0080a0002c0001t0001g0134a0002c0001t0001g0182 | 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 | 56 | a0001c0002t0001g0067a0001c0002t0001g0172a0001c0002t0002g0047others(53): 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 | a0001c0002t0002g0069a0001c0002t0002g0072a0001c0002t0002g0100others(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 | a0001c0018t0006g0026a0005c0008t0003g0143 | 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 | a0009c0021t0001g0023 | 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 | a0001c0004t0005g0037a0001c0004t0005g0039a0001c0004t0005g0042others(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 | a0001c0003t0009g0184a0001c0004t0009g0105 | 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 | a0001c0003t0009g0018a0001c0004t0009g0103 | 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 | a0009c0021t0001g0023 | 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 | a0005c0008t0001g0144 | 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 | 46 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(43): 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 | a0002c0001t0001g0049 | 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 | a0001c0002t0003g0075a0001c0002t0003g0087a0001c0002t0003g0088others(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 | a0003c0005t0012g0124 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0005g0036others(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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0005g0036others(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 | a0001c0009t0007g0086 | 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 | a0009c0021t0001g0023 | 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 | 14 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0003t0007g0027others(11): Show | 14 | HG00280.hp1 HG01070.hp1 HG01109.hp2 others(11): 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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0005c0008t0001g0151a0005c0008t0003g0143 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0004t0005g0085 | 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 | a0002c0001t0001g0094 | 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 | a0001c0002t0002g0100 | 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 | a0001c0002t0002g0057 | 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 | a0001c0024t0004g0041 | 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 | a0001c0002t0003g0088 | 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 | a0006c0011t0002g0003a0006c0011t0002g0004 | 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 | a0001c0003t0008g0031 | 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 | a0002c0023t0001g0161 | 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 | 85 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0003t0007g0027others(82): Show | 85 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(82): 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0009c0021t0001g0023 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0009c0021t0001g0023 | 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 | a0002c0001t0001g0117a0002c0001t0001g0118 | 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 | a0002c0001t0001g0182 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0005g0036others(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 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(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 | 183 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0104others(180): Show | 184 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(181): 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 | a0001c0002t0001g0104a0001c0002t0001g0172a0009c0021t0001g0023 | 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 | 55 | a0001c0002t0001g0067a0001c0002t0001g0080a0001c0002t0001g0163others(52): 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 | a0001c0002t0003g0145a0001c0003t0008g0031 | 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 | a0001c0002t0003g0145a0001c0003t0008g0031 | 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0004t0005g0036a0001c0004t0005g0037a0001c0004t0005g0039others(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 | a0002c0001t0001g0062 | 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 | 45 | a0001c0002t0001g0163a0001c0002t0001g0167a0001c0002t0002g0001others(42): 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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0010t0006g0076a0001c0010t0006g0077a0001c0010t0006g0157others(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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0009c0021t0001g0023 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0011c0015t0021g0013 | 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 | a0001c0002t0002g0001a0001c0002t0002g0047a0001c0002t0002g0057others(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 | a0002c0001t0001g0134 | 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 | a0004c0006t0010g0139 | 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 | a0001c0002t0002g0108 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0003t0002g0011 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0002t0002g0146 | 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 | a0002c0001t0001g0178 | 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 | a0002c0001t0001g0178 | 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 | a0002c0001t0001g0178 | 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 | a0001c0003t0002g0113 | 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 | a0002c0001t0001g0070 | 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 | 15 | a0001c0002t0004g0110a0001c0002t0004g0135a0001c0002t0007g0147others(12): Show | 15 | HG00280.hp1 HG01516.hp1 HG01517.hp1 others(12): 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0002t0002g0001a0001c0002t0002g0047a0001c0002t0002g0057others(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 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0001others(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 | a0001c0002t0001g0104a0001c0002t0001g0172 | 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 | a0001c0002t0002g0146 | 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 | 115 | a0001c0002t0001g0104a0001c0002t0001g0172a0001c0002t0002g0001others(112): Show | 116 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(113): 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 | a0002c0001t0001g0127 | 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 | a0002c0001t0001g0079a0002c0001t0005g0081 | 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 | a0001c0002t0002g0078a0001c0002t0002g0156a0003c0007t0002g0009others(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 | a0002c0001t0001g0063a0002c0001t0001g0132 | 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 | a0001c0003t0009g0018a0001c0003t0009g0184a0001c0004t0009g0103others(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 | a0001c0002t0001g0080 | 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 | a0002c0001t0005g0081 | 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 | a0001c0002t0002g0072a0001c0002t0002g0084a0001c0002t0002g0140others(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 | a0002c0001t0001g0131 | 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 | a0001c0003t0011g0030 | 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 | a0002c0001t0001g0059 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2149-87T>C | ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 13/13 | chr4 | 105677665 |