| geneid | 116984 |
|---|---|
| ensemblid | ENSG00000047365.13 |
| hgncid | 16924 |
| symbol | ARAP2 |
| name | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 |
| refseq_nuc | NM_015230.4 |
| refseq_prot | NP_056045.2 |
| ensembl_nuc | ENST00000303965.9 |
| ensembl_prot | ENSP00000302895.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 36066004 |
| end | 36244514 |
| strand | - |
| ver | v1.2 |
| region | chr4:36066004-36244514 |
| region5000 | chr4:36061004-36249514 |
| regionname0 | ARAP2_chr4_36066004_36244514 |
| regionname5000 | ARAP2_chr4_36061004_36249514 |
| 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 | 0/1 | 1704 | 243 | 66 | 57 | 78 | 14 | 27 | 50 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0002 | 0/0 | 1704 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0003 | 0/0 | 1704 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0004 | 0/0 | 1704 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0005 | 0/0 | 1704 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0006 | 1/0 | 1704 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0007 | 0/0 | 1704 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0008 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0009 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0010 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0011 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0012 | 0/0 | 1704 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0013 | 0/0 | 1704 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0014 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0015 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0016 | 0/0 | 1704 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0017 | 0/0 | 1704 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0018 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0019 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| 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 | 0/1 | 5115 | 160 | 45 | 33 | 54 | 10 | 17 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0002 | 0/0 | 5115 | 28 | 2 | 9 | 9 | 2 | 6 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0003 | 0/0 | 5115 | 19 | 0 | 6 | 12 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0004 | 0/0 | 5115 | 14 | 13 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0005 | 0/0 | 5115 | 14 | 4 | 5 | 0 | 1 | 4 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0006 | 0/0 | 5115 | 8 | 8 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0007 | 0/0 | 5115 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0008 | 0/0 | 5115 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0009 | 0/0 | 5115 | 4 | 0 | 1 | 3 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0010 | 0/0 | 5115 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0011 | 1/0 | 5115 | 2 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0012 | 0/0 | 5115 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0013 | 0/0 | 5115 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0014 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0015 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0016 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0017 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0018 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0019 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0020 | 0/0 | 5115 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0021 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0022 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0023 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0024 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0025 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0026 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| c0027 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| 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 | 0/0 | 2399 | 85 | 22 | 16 | 26 | 6 | 15 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0002 | 0/1 | 2399 | 77 | 7 | 23 | 33 | 7 | 6 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0003 | 1/0 | 2399 | 76 | 24 | 18 | 26 | 1 | 6 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0004 | 0/0 | 2400 | 7 | 6 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0005 | 0/0 | 2399 | 7 | 5 | 2 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0006 | 0/0 | 2399 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0007 | 0/0 | 2399 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0008 | 0/0 | 2399 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0009 | 0/0 | 2399 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0010 | 0/0 | 2399 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0011 | 0/0 | 2399 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0012 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0013 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0014 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0015 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0016 | 0/0 | 2399 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0017 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0018 | 0/0 | 2399 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0019 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0020 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0021 | 0/0 | 2400 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0022 | 0/0 | 2399 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0023 | 0/0 | 2400 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0024 | 0/0 | 2399 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| t0025 | 0/0 | 2399 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| 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 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5115 | 160 | 45 | 33 | 54 | 10 | 17 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0002 | 0/0 | 5115 | 28 | 2 | 9 | 9 | 2 | 6 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0003 | 0/0 | 5115 | 19 | 0 | 6 | 12 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0004 | 0/0 | 5115 | 14 | 13 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0005 | 0/0 | 5115 | 14 | 4 | 5 | 0 | 1 | 4 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0009 | 0/0 | 5115 | 4 | 0 | 1 | 3 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0012 | 0/0 | 5115 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0016 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0023 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0002c0006 | 0/0 | 5115 | 8 | 8 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0003c0007 | 0/0 | 5115 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0004c0008 | 0/0 | 5115 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0005c0013 | 0/0 | 5115 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0006c0011 | 1/0 | 5115 | 2 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0007c0010 | 0/0 | 5115 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0008c0027 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0009c0014 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0010c0015 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0011c0022 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0012c0021 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0013c0024 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0014c0018 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0015c0017 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0016c0019 | 0/0 | 5115 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0017c0020 | 0/0 | 5115 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0018c0026 | 0/0 | 5115 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0019c0025 | 0/0 | 5115 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7513 | 26 | 9 | 3 | 6 | 3 | 5 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0002 | 0/1 | 7513 | 69 | 4 | 21 | 32 | 6 | 5 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0003 | 0/0 | 7513 | 41 | 13 | 7 | 15 | 1 | 5 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0004 | 0/0 | 7514 | 6 | 6 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0005 | 0/0 | 7513 | 7 | 5 | 2 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0007 | 0/0 | 7513 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0009 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0010 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0011 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0013 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0015 | 0/0 | 7514 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0019 | 0/0 | 7514 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0020 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0023 | 0/0 | 7514 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0001t0024 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0002t0001 | 0/0 | 7513 | 28 | 2 | 9 | 9 | 2 | 6 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0003t0001 | 0/0 | 7513 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0003t0002 | 0/0 | 7513 | 3 | 0 | 1 | 1 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0003t0003 | 0/0 | 7513 | 11 | 0 | 5 | 6 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0003t0016 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0004t0001 | 0/0 | 7513 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0004t0002 | 0/0 | 7513 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0004t0003 | 0/0 | 7513 | 7 | 7 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0004t0022 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0004t0025 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0005t0001 | 0/0 | 7513 | 8 | 0 | 3 | 0 | 1 | 4 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0005t0002 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0005t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0005t0006 | 0/0 | 7513 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0005t0012 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0009t0001 | 0/0 | 7513 | 4 | 0 | 1 | 3 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0012t0003 | 0/0 | 7513 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0016t0003 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0001c0023t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0002c0006t0001 | 0/0 | 7513 | 6 | 6 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0002c0006t0003 | 0/0 | 7513 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0003c0007t0003 | 0/0 | 7513 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0004c0008t0001 | 0/0 | 7513 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0004c0008t0021 | 0/0 | 7514 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0005c0013t0008 | 0/0 | 7513 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0006c0011t0003 | 1/0 | 7513 | 2 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0007c0010t0001 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0007c0010t0004 | 0/0 | 7514 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0008c0027t0003 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0009c0014t0017 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0010c0015t0010 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0011c0022t0001 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0012c0021t0009 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0013c0024t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0014c0018t0002 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0015c0017t0002 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0016c0019t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0017c0020t0001 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0018c0026t0014 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| a0019c0025t0018 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | copy fasta | chr4 | 36061004 | 36249514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0019g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0020g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0023g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0024g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0016g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0022g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0025g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0012t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0012t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0016t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0023t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0021g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0005c0013t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0005c0013t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0006c0011t0003g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0006c0011t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0007c0010t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0007c0010t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0008c0027t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0009c0014t0017g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0010c0015t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0011c0022t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0012c0021t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0013c0024t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0014c0018t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0015c0017t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0016c0019t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0017c0020t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0018c0026t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0019c0025t0018g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0029 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0255 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0070 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0214 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0239 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00558 | hp1 | a0003 | c0007 | t0003 | g0109 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00738 | hp2 | a0001 | c0005 | t0002 | g0023 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0083 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01099 | hp1 | a0007 | c0010 | t0004 | g0091 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01106 | hp2 | a0001 | c0009 | t0001 | g0025 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01168 | hp1 | a0001 | c0005 | t0001 | g0039 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01243 | hp1 | a0012 | c0021 | t0009 | g0117 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01243 | hp2 | a0001 | c0012 | t0003 | g0063 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01255 | hp1 | a0001 | c0004 | t0025 | g0247 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01257 | hp1 | a0001 | c0003 | t0003 | g0228 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01257 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0079 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01361 | hp2 | a0006 | c0011 | t0003 | g0185 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01433 | hp1 | a0001 | c0005 | t0003 | g0102 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01516 | hp2 | a0001 | c0005 | t0001 | g0143 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01943 | hp1 | a0001 | c0023 | t0003 | g0084 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01975 | hp2 | a0013 | c0024 | t0003 | g0059 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01978 | hp1 | a0001 | c0003 | t0003 | g0085 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0080 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02055 | hp2 | a0011 | c0022 | t0001 | g0111 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02071 | hp2 | a0001 | c0003 | t0003 | g0058 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02074 | hp2 | a0003 | c0007 | t0003 | g0081 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0074 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0076 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0010 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0075 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02257 | hp2 | a0001 | c0016 | t0003 | g0260 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02258 | hp1 | a0002 | c0006 | t0001 | g0124 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02258 | hp2 | a0007 | c0010 | t0001 | g0237 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02273 | hp1 | a0016 | c0019 | t0003 | g0150 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02280 | hp1 | a0002 | c0006 | t0001 | g0119 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02280 | hp2 | a0001 | c0004 | t0002 | g0265 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0107 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02723 | hp2 | a0001 | c0004 | t0003 | g0262 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02818 | hp1 | a0010 | c0015 | t0010 | g0275 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02818 | hp2 | a0001 | c0005 | t0006 | g0106 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02896 | hp1 | a0002 | c0006 | t0001 | g0125 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02896 | hp2 | a0001 | c0001 | t0023 | g0093 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02897 | hp2 | a0002 | c0006 | t0001 | g0126 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0269 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0090 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0261 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03017 | hp2 | a0014 | c0018 | t0002 | g0240 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03041 | hp1 | a0001 | c0004 | t0022 | g0264 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03041 | hp2 | a0002 | c0006 | t0003 | g0121 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03130 | hp1 | a0001 | c0005 | t0006 | g0105 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03139 | hp1 | a0002 | c0006 | t0001 | g0120 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03139 | hp2 | a0001 | c0005 | t0006 | g0104 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03209 | hp1 | a0001 | c0004 | t0003 | g0263 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03225 | hp1 | a0001 | c0004 | t0002 | g0267 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03225 | hp2 | a0001 | c0012 | t0003 | g0060 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03453 | hp1 | a0002 | c0006 | t0003 | g0123 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0266 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03490 | hp1 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0004 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03516 | hp1 | a0018 | c0026 | t0014 | g0009 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03654 | hp2 | a0008 | c0027 | t0003 | g0048 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03831 | hp1 | a0019 | c0025 | t0018 | g0209 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03834 | hp2 | a0001 | c0001 | t0024 | g0137 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0197 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04228 | hp2 | a0001 | c0005 | t0001 | g0041 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18612 | hp2 | a0001 | c0009 | t0001 | g0035 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18906 | hp1 | a0001 | c0005 | t0012 | g0008 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18944 | hp1 | a0004 | c0008 | t0001 | g0232 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18944 | hp2 | a0001 | c0009 | t0001 | g0037 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0100 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0057 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18954 | hp2 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18965 | hp2 | a0003 | c0007 | t0003 | g0108 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18968 | hp1 | a0003 | c0007 | t0003 | g0077 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18993 | hp1 | a0004 | c0008 | t0001 | g0204 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18993 | hp2 | a0001 | c0001 | t0019 | g0113 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18999 | hp1 | a0003 | c0007 | t0003 | g0072 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19007 | hp2 | a0001 | c0009 | t0001 | g0036 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19012 | hp2 | a0005 | c0013 | t0008 | g0112 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19030 | hp1 | a0015 | c0017 | t0002 | g0061 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19030 | hp2 | a0001 | c0004 | t0003 | g0268 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19060 | hp2 | a0004 | c0008 | t0001 | g0233 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19064 | hp2 | a0001 | c0003 | t0016 | g0073 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19078 | hp1 | a0005 | c0013 | t0008 | g0067 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19078 | hp2 | a0004 | c0008 | t0021 | g0231 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0274 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0044 | EUR | TSI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | TSI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0024 | SAS | GIH | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02486 | hp1 | a0001 | c0004 | t0003 | g0270 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02559 | hp1 | a0002 | c0006 | t0001 | g0122 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0005 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03471 | hp2 | a0001 | c0004 | t0003 | g0271 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18955 | hp1 | a0017 | c0020 | t0001 | g0034 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0198 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA21309 | hp2 | a0009 | c0014 | t0017 | g0088 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0135 | REF | REF | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| homoSapiens_grch38 | hp1 | a0006 | c0011 | t0003 | g0164 | REF | REF | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36073751
|
C | T | 1 | a0015 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.4681G>A | p.Gly1561Ser | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/33 | 5176/7513 | 4681/5115 | 1561/1704 | chr4 | 36073751 | ||
| chr4:36080256
|
C | T | 18 | a0001a0002a0003others(15): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
missense_variant | MODERATE | c.4568G>A | p.Arg1523Gln | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/33 | 5063/7513 | 4568/5115 | 1523/1704 | chr4 | 36080256 | ||
| chr4:36117081
|
C | T | 1 | a0003 | 5 | HG00558.hp1 HG02074.hp2 NA18965.hp2 others(2): Show |
missense_variant | MODERATE | c.4018G>A | p.Asp1340Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/33 | 4513/7513 | 4018/5115 | 1340/1704 | chr4 | 36117081 | ||
| chr4:36124964
|
G | A | 1 | a0014 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.3644C>T | p.Thr1215Met | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/33 | 4139/7513 | 3644/5115 | 1215/1704 | chr4 | 36124964 | ||
| chr4:36128635
|
G | A | 1 | a0016 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.3538C>T | p.His1180Tyr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/33 | 4033/7513 | 3538/5115 | 1180/1704 | chr4 | 36128635 | ||
| chr4:36147309
|
C | A | 1 | a0013 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.3250G>T | p.Val1084Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/33 | 3745/7513 | 3250/5115 | 1084/1704 | chr4 | 36147309 | ||
| chr4:36147731
|
A | G | 1 | a0007 | 2 | HG01099.hp1 HG02258.hp2 |
missense_variant | MODERATE | c.3016T>C | p.Phe1006Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 18/33 | 3511/7513 | 3016/5115 | 1006/1704 | chr4 | 36147731 | ||
| chr4:36148469
|
C | T | 1 | a0005 | 2 | NA19012.hp2 NA19078.hp1 |
missense_variant | MODERATE | c.2936G>A | p.Arg979His | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/33 | 3431/7513 | 2936/5115 | 979/1704 | chr4 | 36148469 | ||
| chr4:36150957
|
T | C | 1 | a0017 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.2840A>G | p.Asn947Ser | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3335/7513 | 2840/5115 | 947/1704 | chr4 | 36150957 | ||
| chr4:36150958
|
T | G | 1 | a0012 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2839A>C | p.Asn947His | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3334/7513 | 2839/5115 | 947/1704 | chr4 | 36150958 | ||
| chr4:36150970
|
T | G | 1 | a0011 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.2827A>C | p.Asn943His | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3322/7513 | 2827/5115 | 943/1704 | chr4 | 36150970 | ||
| chr4:36158819
|
T | A | 1 | a0018 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2663A>T | p.Glu888Val | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/33 | 3158/7513 | 2663/5115 | 888/1704 | chr4 | 36158819 | ||
| chr4:36187535
|
T | C | 1 | a0019 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1594A>G | p.Ile532Val | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/33 | 2089/7513 | 1594/5115 | 532/1704 | chr4 | 36187535 | ||
| chr4:36210427
|
C | A | 1 | a0004 | 4 | NA18944.hp1 NA18993.hp1 NA19060.hp2 others(1): Show |
missense_variant | MODERATE | c.1450G>T | p.Val484Phe | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1945/7513 | 1450/5115 | 484/1704 | chr4 | 36210427 | ||
| chr4:36210725
|
C | A | 1 | a0002 | 8 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.1152G>T | p.Lys384Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1647/7513 | 1152/5115 | 384/1704 | chr4 | 36210725 | ||
| chr4:36212438
|
C | T | 1 | a0010 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1091G>A | p.Gly364Glu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/33 | 1586/7513 | 1091/5115 | 364/1704 | chr4 | 36212438 | ||
| chr4:36229155
|
C | T | 1 | a0009 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.332G>A | p.Ser111Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | 827/7513 | 332/5115 | 111/1704 | chr4 | 36229155 | ||
| chr4:36229221
|
G | A | 1 | a0008 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.266C>T | p.Pro89Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | 761/7513 | 266/5115 | 89/1704 | chr4 | 36229221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36068183
|
G | A | 3 | a0001c0002a0001c0009a0017c0020 | 33 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(30): Show |
synonymous_variant | LOW | c.4839C>T | p.Ala1613Ala | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 5334/7513 | 4839/5115 | 1613/1704 | chr4 | 36068183 | ||
| chr4:36128615
|
C | G | 1 | a0016c0019 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.3558G>C | p.Thr1186Thr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/33 | 4053/7513 | 3558/5115 | 1186/1704 | chr4 | 36128615 | ||
| chr4:36133233
|
T | C | 1 | a0001c0023 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.3420A>G | p.Thr1140Thr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/33 | 3915/7513 | 3420/5115 | 1140/1704 | chr4 | 36133233 | ||
| chr4:36133257
|
C | A | 1 | a0001c0012 | 2 | HG01243.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.3396G>T | p.Val1132Val | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/33 | 3891/7513 | 3396/5115 | 1132/1704 | chr4 | 36133257 | ||
| chr4:36150962
|
G | T | 2 | a0001c0005a0009c0014 | 15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
synonymous_variant | LOW | c.2835C>A | p.Thr945Thr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3330/7513 | 2835/5115 | 945/1704 | chr4 | 36150962 | ||
| chr4:36158764
|
A | G | 2 | a0001c0004a0001c0016 | 15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
synonymous_variant | LOW | c.2718T>C | p.Ala906Ala | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/33 | 3213/7513 | 2718/5115 | 906/1704 | chr4 | 36158764 | ||
| chr4:36161506
|
G | A | 5 | a0001c0003a0001c0023a0003c0007others(2): Show | 28 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(25): Show |
synonymous_variant | LOW | c.2218C>T | p.Leu740Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/33 | 2713/7513 | 2218/5115 | 740/1704 | chr4 | 36161506 | ||
| chr4:36210455
|
G | C | 1 | a0018c0026 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1422C>G | p.Ala474Ala | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1917/7513 | 1422/5115 | 474/1704 | chr4 | 36210455 | ||
| chr4:36210536
|
A | G | 1 | a0001c0016 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1341T>C | p.Asn447Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1836/7513 | 1341/5115 | 447/1704 | chr4 | 36210536 | ||
| chr4:36228956
|
T | C | 1 | a0001c0009 | 4 | HG01106.hp2 NA18612.hp2 NA18944.hp2 others(1): Show |
synonymous_variant | LOW | c.531A>G | p.Lys177Lys | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | 1026/7513 | 531/5115 | 177/1704 | chr4 | 36228956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36066456
|
T | C | 1 | a0001c0004t0022 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1451A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1451 | chr4 | 36066456 | |||||
| chr4:36066458
|
C | T | 1 | a0001c0001t0023 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1449G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1449 | chr4 | 36066458 | |||||
| chr4:36066570
|
T | TA | 6 | a0001c0001t0004a0001c0001t0015a0001c0001t0019others(3): Show | 11 | HG01099.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1336dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1336 | chr4 | 36066570 | |||||
| chr4:36066664
|
A | G | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(14): Show | 99 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1243T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1243 | chr4 | 36066664 | |||||
| chr4:36066808
|
C | T | 1 | a0009c0014t0017 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1099G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1099 | chr4 | 36066808 | |||||
| chr4:36066824
|
C | T | 1 | a0005c0013t0008 | 2 | NA19012.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1083G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1083 | chr4 | 36066824 | |||||
| chr4:36066880
|
C | T | 1 | a0001c0001t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1027G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1027 | chr4 | 36066880 | |||||
| chr4:36066949
|
A | T | 12 | a0001c0001t0002a0001c0001t0011a0001c0001t0019others(9): Show | 83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*958T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 958 | chr4 | 36066949 | |||||
| chr4:36067408
|
T | A | 1 | a0001c0005t0006 | 3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*499A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 499 | chr4 | 36067408 | |||||
| chr4:36067425
|
C | G | 1 | a0001c0003t0016 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 482 | chr4 | 36067425 | |||||
| chr4:36067460
|
G | A | 1 | a0001c0001t0015 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 447 | chr4 | 36067460 | |||||
| chr4:36067471
|
G | A | 1 | a0001c0001t0024 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 436 | chr4 | 36067471 | |||||
| chr4:36067536
|
T | C | 2 | a0001c0001t0009a0012c0021t0009 | 2 | HG01243.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*371A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 371 | chr4 | 36067536 | |||||
| chr4:36229529
|
G | A | 4 | a0001c0001t0005a0001c0001t0007a0001c0001t0013others(1): Show | 11 | HG01109.hp2 HG01255.hp1 HG01361.hp1 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-43C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | chr4 | 36229529 | ||||||
| chr4:36244306
|
C | T | 1 | a0001c0001t0015 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 14820 | chr4 | 36244306 | |||||
| chr4:36244351
|
C | T | 1 | a0018c0026t0014 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-332G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 14865 | chr4 | 36244351 | |||||
| chr4:36244382
|
G | A | 2 | a0001c0001t0010a0010c0015t0010 | 2 | HG02818.hp1 NA19240.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-363C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | chr4 | 36244382 | ||||||
| chr4:36244406
|
G | T | 3 | a0001c0001t0007a0001c0001t0013a0001c0005t0012 | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-387C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 14920 | chr4 | 36244406 | |||||
| chr4:36244486
|
C | T | 1 | a0001c0001t0011 | 1 | HG03490.hp2 | 5_prime_UTR_variant | MODIFIER | c.-467G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 15000 | chr4 | 36244486 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36068330
|
G | C | 1 | a0001c0001t0002g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4744-52C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068330 | ||||||
| chr4:36068419
|
A | C | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4744-141T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068419 | ||||||
| chr4:36068501
|
G | A | 9 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4744-223C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068501 | ||||||
| chr4:36068555
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4744-277G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068555 | ||||||
| chr4:36068596
|
C | T | 5 | a0001c0001t0003g0154a0001c0001t0003g0162a0001c0001t0003g0226others(2): Show | 5 | HG01081.hp1 HG02040.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.4744-318G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068596 | ||||||
| chr4:36068608
|
C | A | 2 | a0001c0001t0005g0245a0001c0001t0005g0246 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.4744-330G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068608 | ||||||
| chr4:36068691
|
T | C | 17 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(14): Show | 17 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.4744-413A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068691 | ||||||
| chr4:36068971
|
C | T | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4744-693G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068971 | ||||||
| chr4:36069027
|
AT | A | 249 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4744-750delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069027 | ||||||
| chr4:36069822
|
T | A | 10 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(7): Show | 10 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.4744-1544A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069822 | ||||||
| chr4:36069930
|
T | C | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-1652A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069930 | ||||||
| chr4:36069937
|
C | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0114others(1): Show | 4 | HG02080.hp1 HG03942.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.4744-1659G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069937 | ||||||
| chr4:36070203
|
G | C | 30 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(27): Show | 32 | HG01099.hp1 HG01168.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.4744-1925C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070203 | ||||||
| chr4:36070204
|
A | C | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-1926T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070204 | ||||||
| chr4:36070286
|
C | T | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4744-2008G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070286 | ||||||
| chr4:36070350
|
C | T | 2 | a0001c0001t0011g0004a0001c0001t0024g0137 | 2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4744-2072G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070350 | ||||||
| chr4:36070488
|
G | A | 1 | a0001c0003t0003g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4744-2210C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070488 | ||||||
| chr4:36070599
|
A | T | 10 | a0001c0001t0001g0202a0001c0001t0003g0033a0001c0001t0003g0153others(7): Show | 10 | HG00544.hp1 HG02132.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.4744-2321T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070599 | ||||||
| chr4:36070779
|
C | T | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-2501G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070779 | ||||||
| chr4:36070807
|
A | G | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-2529T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070807 | ||||||
| chr4:36070882
|
T | C | 71 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(68): Show | 72 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.4744-2604A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070882 | ||||||
| chr4:36070912
|
T | G | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-2634A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070912 | ||||||
| chr4:36071115
|
T | C | 3 | a0001c0001t0002g0139a0001c0001t0002g0141a0001c0001t0002g0205 | 3 | HG00323.hp2 HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.4743+2574A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071115 | ||||||
| chr4:36071221
|
G | A | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4743+2468C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071221 | ||||||
| chr4:36071223
|
T | G | 1 | a0001c0001t0002g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4743+2466A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071223 | ||||||
| chr4:36071311
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4743+2378G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071311 | ||||||
| chr4:36071318
|
G | A | 1 | a0001c0001t0005g0246 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4743+2371C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071318 | ||||||
| chr4:36071670
|
AT | A | 7 | a0001c0001t0002g0133a0001c0001t0002g0210a0001c0001t0002g0211others(4): Show | 7 | HG01517.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4743+2018delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071670 | ||||||
| chr4:36071693
|
A | AT | 239 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(236): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.4743+1995dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071693 | ||||||
| chr4:36071702
|
C | T | 7 | a0001c0004t0003g0261a0001c0004t0003g0262a0001c0004t0003g0263others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4743+1987G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071702 | ||||||
| chr4:36071703
|
T | C | 7 | a0001c0004t0003g0261a0001c0004t0003g0262a0001c0004t0003g0263others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4743+1986A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071703 | ||||||
| chr4:36072099
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4743+1590T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072099 | ||||||
| chr4:36072104
|
T | C | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4743+1585A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072104 | ||||||
| chr4:36072110
|
T | A | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4743+1579A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072110 | ||||||
| chr4:36072110
|
TA | T | 2 | a0001c0005t0001g0001a0001c0005t0001g0002 | 4 | HG01257.hp2 HG01258.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.4743+1578delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072110 | ||||||
| chr4:36072122
|
T | A | 37 | a0001c0001t0001g0026a0001c0001t0003g0129a0001c0002t0001g0003others(34): Show | 38 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.4743+1567A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072122 | ||||||
| chr4:36072195
|
T | G | 6 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0118others(3): Show | 6 | HG02280.hp2 HG02895.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4743+1494A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072195 | ||||||
| chr4:36072319
|
T | C | 1 | a0001c0003t0002g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4743+1370A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072319 | ||||||
| chr4:36072667
|
C | CA | 128 | a0001c0001t0001g0015a0001c0001t0001g0082a0001c0001t0001g0149others(125): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.4743+1021dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072667 | ||||||
| chr4:36072678
|
C | A | 9 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0156others(6): Show | 9 | HG02015.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.4743+1011G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072678 | ||||||
| chr4:36072681
|
C | A | 2 | a0001c0009t0001g0036a0001c0009t0001g0037 | 2 | NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.4743+1008G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072681 | ||||||
| chr4:36072682
|
A | C | 47 | a0001c0001t0001g0050a0001c0001t0001g0179a0001c0001t0001g0193others(44): Show | 47 | HG00438.hp1 HG00741.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.4743+1007T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072682 | ||||||
| chr4:36072689
|
A | C | 124 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0082others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.4743+1000T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072689 | ||||||
| chr4:36072690
|
C | A | 124 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0082others(121): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.4743+999G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072690 | ||||||
| chr4:36073186
|
C | CAA | 4 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0212others(1): Show | 4 | HG02080.hp2 NA18945.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.4743+501_4743+502d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36073186 | ||||||
| chr4:36073295
|
A | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4743+394T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36073295 | ||||||
| chr4:36073353
|
G | A | 8 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0151others(5): Show | 8 | HG00741.hp2 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4743+336C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36073353 | ||||||
| chr4:36074006
|
C | T | 9 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4609-183G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074006 | ||||||
| chr4:36074072
|
T | C | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4609-249A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074072 | ||||||
| chr4:36074446
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4609-623T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074446 | ||||||
| chr4:36074592
|
G | T | 1 | a0001c0001t0002g0011 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4609-769C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074592 | ||||||
| chr4:36074602
|
T | C | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4609-779A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074602 | ||||||
| chr4:36074604
|
T | C | 50 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0149others(47): Show | 50 | HG00558.hp1 HG01074.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.4609-781A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074604 | ||||||
| chr4:36074630
|
G | T | 2 | a0001c0001t0003g0094a0001c0001t0003g0095 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4609-807C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074630 | ||||||
| chr4:36074705
|
T | C | 2 | a0001c0004t0003g0266a0001c0004t0003g0268 | 2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4609-882A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074705 | ||||||
| chr4:36074834
|
C | T | 10 | a0001c0001t0001g0202a0001c0001t0003g0033a0001c0001t0003g0153others(7): Show | 10 | HG00544.hp1 HG02132.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.4609-1011G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074834 | ||||||
| chr4:36074881
|
CT | C | 8 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0151others(5): Show | 8 | HG00741.hp2 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4609-1059delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074881 | ||||||
| chr4:36075035
|
T | C | 2 | a0001c0001t0003g0162a0001c0001t0003g0249 | 2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.4609-1212A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075035 | ||||||
| chr4:36075054
|
C | T | 115 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0045others(112): Show | 118 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.4609-1231G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075054 | ||||||
| chr4:36075150
|
G | A | 3 | a0001c0001t0001g0078a0001c0001t0001g0236a0007c0010t0001g0237 | 3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4609-1327C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075150 | ||||||
| chr4:36075160
|
G | C | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4609-1337C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075160 | ||||||
| chr4:36075249
|
C | T | 1 | a0007c0010t0004g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4609-1426G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075249 | ||||||
| chr4:36075270
|
T | C | 83 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(80): Show | 84 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.4609-1447A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075270 | ||||||
| chr4:36075361
|
A | G | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4609-1538T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075361 | ||||||
| chr4:36075592
|
T | C | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4609-1769A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075592 | ||||||
| chr4:36075725
|
C | T | 13 | a0001c0001t0001g0050a0001c0001t0001g0179a0001c0001t0001g0193others(10): Show | 13 | HG00438.hp1 HG01361.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.4609-1902G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075725 | ||||||
| chr4:36075834
|
C | G | 249 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4609-2011G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075834 | ||||||
| chr4:36075877
|
T | C | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4609-2054A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075877 | ||||||
| chr4:36075925
|
C | G | 1 | a0001c0003t0002g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4609-2102G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075925 | ||||||
| chr4:36075982
|
C | T | 21 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(18): Show | 21 | HG01099.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4609-2159G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075982 | ||||||
| chr4:36076382
|
C | G | 113 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0045others(110): Show | 116 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.4609-2559G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076382 | ||||||
| chr4:36076449
|
A | G | 127 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0082others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.4609-2626T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076449 | ||||||
| chr4:36076470
|
G | C | 249 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4609-2647C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076470 | ||||||
| chr4:36076530
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4609-2707C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076530 | ||||||
| chr4:36076693
|
A | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056 | 3 | HG02257.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4609-2870T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076693 | ||||||
| chr4:36076694
|
G | C | 2 | a0001c0001t0003g0157a0001c0001t0003g0158 | 2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4609-2871C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076694 | ||||||
| chr4:36076799
|
T | A | 12 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(9): Show | 12 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4609-2976A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076799 | ||||||
| chr4:36076817
|
G | T | 1 | a0001c0001t0003g0161 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4609-2994C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076817 | ||||||
| chr4:36076999
|
G | C | 126 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0082others(123): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.4609-3176C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076999 | ||||||
| chr4:36077262
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4608+2954T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077262 | ||||||
| chr4:36077286
|
G | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0082others(124): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.4608+2930C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077286 | ||||||
| chr4:36077461
|
G | A | 10 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(7): Show | 10 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.4608+2755C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077461 | ||||||
| chr4:36077684
|
C | T | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG01099.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.4608+2532G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077684 | ||||||
| chr4:36077868
|
C | A | 1 | a0001c0001t0007g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4608+2348G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077868 | ||||||
| chr4:36077972
|
T | C | 136 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0236others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.4608+2244A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077972 | ||||||
| chr4:36078092
|
A | C | 2 | a0001c0004t0001g0090a0001c0004t0001g0269 | 2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4608+2124T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078092 | ||||||
| chr4:36078113
|
C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0127 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4608+2103G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078113 | ||||||
| chr4:36078116
|
A | G | 3 | a0001c0001t0007g0006a0001c0001t0007g0007a0002c0006t0003g0121 | 3 | HG02622.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4608+2100T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078116 | ||||||
| chr4:36078354
|
G | A | 136 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0236others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.4608+1862C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078354 | ||||||
| chr4:36078441
|
G | C | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4608+1775C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078441 | ||||||
| chr4:36078651
|
C | A | 2 | a0001c0001t0005g0245a0001c0001t0005g0246 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.4608+1565G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078651 | ||||||
| chr4:36078904
|
TG | T | 28 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(25): Show | 30 | HG01099.hp1 HG01168.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.4608+1311delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078904 | ||||||
| chr4:36078982
|
T | C | 130 | a0001c0001t0001g0078a0001c0001t0001g0082a0001c0001t0001g0149others(127): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.4608+1234A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078982 | ||||||
| chr4:36078983
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4608+1233C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078983 | ||||||
| chr4:36079036
|
C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4608+1180G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079036 | ||||||
| chr4:36079037
|
G | A | 69 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0064others(66): Show | 70 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.4608+1179C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079037 | ||||||
| chr4:36079100
|
G | A | 19 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(16): Show | 19 | HG01099.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.4608+1116C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079100 | ||||||
| chr4:36079173
|
C | CA | 129 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0082others(126): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.4608+1042dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | ||||||
| chr4:36079173
|
C | CAA | 14 | a0001c0001t0001g0050a0001c0001t0002g0151a0001c0001t0002g0176others(11): Show | 14 | HG00280.hp2 HG00741.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.4608+1041_4608+104 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | ||||||
| chr4:36079173
|
CA | C | 68 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0087others(65): Show | 71 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.4608+1042delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | ||||||
| chr4:36079173
|
CAA | C | 9 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(6): Show | 9 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4608+1041_4608+104 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | ||||||
| chr4:36079173
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0002g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4608+1031_4608+104 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | ||||||
| chr4:36079321
|
T | C | 7 | a0001c0001t0001g0202a0001c0001t0003g0033a0001c0001t0003g0153others(4): Show | 7 | HG00544.hp1 HG02132.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.4608+895A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079321 | ||||||
| chr4:36079475
|
C | T | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4608+741G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079475 | ||||||
| chr4:36079543
|
C | T | 7 | a0001c0004t0003g0261a0001c0004t0003g0262a0001c0004t0003g0263others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4608+673G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079543 | ||||||
| chr4:36079619
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4608+597G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079619 | ||||||
| chr4:36079621
|
G | A | 9 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4608+595C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079621 | ||||||
| chr4:36079850
|
C | T | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4608+366G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079850 | ||||||
| chr4:36080197
|
G | A | 5 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0005g0245others(2): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4608+19C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36080197 | ||||||
| chr4:36080533
|
G | C | 136 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0082others(133): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.4545-254C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36080533 | ||||||
| chr4:36080773
|
A | T | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4545-494T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36080773 | ||||||
| chr4:36080976
|
A | C | 1 | a0001c0001t0002g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4545-697T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36080976 | ||||||
| chr4:36081528
|
C | T | 1 | a0001c0004t0003g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4544+723G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081528 | ||||||
| chr4:36081623
|
T | G | 6 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0019others(3): Show | 6 | HG01074.hp2 HG01109.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.4544+628A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081623 | ||||||
| chr4:36081629
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4544+622C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081629 | ||||||
| chr4:36081692
|
A | G | 2 | a0001c0001t0002g0151a0015c0017t0002g0061 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4544+559T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081692 | ||||||
| chr4:36081770
|
A | G | 3 | a0001c0004t0003g0266a0001c0004t0003g0268a0001c0004t0003g0270 | 3 | HG02486.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4544+481T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081770 | ||||||
| chr4:36082029
|
G | A | 2 | a0001c0001t0002g0156a0001c0001t0010g0274 | 2 | NA19084.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4544+222C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36082029 | ||||||
| chr4:36082158
|
C | A | 18 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(15): Show | 18 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.4544+93G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36082158 | ||||||
| chr4:36082177
|
A | G | 1 | a0006c0011t0003g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4544+74T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36082177 | ||||||
| chr4:36082299
|
G | GA | 13 | a0001c0001t0001g0015a0001c0001t0001g0202a0001c0001t0003g0033others(10): Show | 13 | HG00280.hp1 HG00544.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.4509-14dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082299 | ||||||
| chr4:36082603
|
G | T | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4509-317C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082603 | ||||||
| chr4:36082667
|
C | T | 2 | a0001c0001t0003g0162a0001c0001t0003g0249 | 2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.4509-381G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082667 | ||||||
| chr4:36082750
|
G | A | 7 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0151others(4): Show | 7 | HG00741.hp2 HG02280.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4509-464C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082750 | ||||||
| chr4:36082899
|
T | C | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4508+469A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082899 | ||||||
| chr4:36083036
|
G | A | 76 | a0001c0001t0001g0015a0001c0001t0002g0011a0001c0001t0002g0018others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.4508+332C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36083036 | ||||||
| chr4:36083138
|
T | C | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4508+230A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36083138 | ||||||
| chr4:36083242
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4508+126G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36083242 | ||||||
| chr4:36083472
|
T | C | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4426-22A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083472 | ||||||
| chr4:36083761
|
G | A | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4426-311C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083761 | ||||||
| chr4:36083790
|
A | G | 146 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0001g0078others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.4426-340T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083790 | ||||||
| chr4:36083809
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4426-359A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083809 | ||||||
| chr4:36083811
|
G | T | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.4426-361C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083811 | ||||||
| chr4:36084226
|
C | T | 2 | a0001c0001t0009g0046a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4426-776G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084226 | ||||||
| chr4:36084319
|
T | C | 9 | a0001c0001t0001g0202a0001c0001t0003g0033a0001c0001t0003g0153others(6): Show | 9 | HG00544.hp1 HG02132.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.4426-869A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084319 | ||||||
| chr4:36084359
|
G | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4426-909C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084359 | ||||||
| chr4:36084579
|
T | C | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4426-1129A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084579 | ||||||
| chr4:36084672
|
C | T | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4426-1222G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084672 | ||||||
| chr4:36084921
|
C | T | 2 | a0001c0001t0002g0151a0015c0017t0002g0061 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4426-1471G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084921 | ||||||
| chr4:36084938
|
A | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0236a0007c0010t0001g0237 | 3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4426-1488T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084938 | ||||||
| chr4:36084968
|
C | T | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4426-1518G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084968 | ||||||
| chr4:36084987
|
T | C | 78 | a0001c0001t0002g0011a0001c0001t0002g0018a0001c0001t0002g0042others(75): Show | 78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.4426-1537A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084987 | ||||||
| chr4:36085341
|
G | C | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4426-1891C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085341 | ||||||
| chr4:36085379
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4426-1929A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085379 | ||||||
| chr4:36085411
|
A | T | 1 | a0007c0010t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4426-1961T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085411 | ||||||
| chr4:36085429
|
A | T | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4426-1979T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085429 | ||||||
| chr4:36085552
|
C | T | 7 | a0001c0001t0001g0202a0001c0001t0003g0033a0001c0001t0003g0153others(4): Show | 7 | HG00544.hp1 HG02132.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.4426-2102G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085552 | ||||||
| chr4:36085585
|
T | C | 2 | a0001c0001t0001g0199a0001c0001t0020g0198 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4426-2135A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085585 | ||||||
| chr4:36085668
|
ATTC | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0118others(2): Show | 5 | HG02280.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4426-2221_4426-221 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085668 | ||||||
| chr4:36085683
|
T | C | 8 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0118others(5): Show | 8 | HG02280.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4426-2233A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085683 | ||||||
| chr4:36086030
|
T | G | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056 | 3 | HG02257.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4426-2580A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086030 | ||||||
| chr4:36086050
|
A | G | 2 | a0001c0001t0002g0151a0015c0017t0002g0061 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4426-2600T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086050 | ||||||
| chr4:36086106
|
T | C | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4426-2656A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086106 | ||||||
| chr4:36086161
|
C | T | 1 | a0008c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4426-2711G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086161 | ||||||
| chr4:36086172
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4426-2722C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086172 | ||||||
| chr4:36086202
|
G | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0118others(2): Show | 5 | HG02280.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4426-2752C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086202 | ||||||
| chr4:36086260
|
C | A | 1 | a0001c0001t0002g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4426-2810G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086260 | ||||||
| chr4:36086488
|
G | C | 1 | a0001c0004t0003g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4426-3038C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086488 | ||||||
| chr4:36086794
|
C | T | 1 | a0016c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4426-3344G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086794 | ||||||
| chr4:36086977
|
T | C | 2 | a0001c0001t0002g0151a0015c0017t0002g0061 | 2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4426-3527A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086977 | ||||||
| chr4:36087369
|
T | A | 249 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4426-3919A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087369 | ||||||
| chr4:36087375
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4426-3925A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087375 | ||||||
| chr4:36087427
|
T | C | 3 | a0001c0001t0004g0152a0001c0012t0003g0060a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4426-3977A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087427 | ||||||
| chr4:36087606
|
CA | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01993.hp1 HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4426-4157delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087606 | ||||||
| chr4:36087701
|
C | A | 3 | a0001c0001t0004g0152a0001c0012t0003g0060a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+4180G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087701 | ||||||
| chr4:36087791
|
A | C | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4425+4090T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087791 | ||||||
| chr4:36087891
|
G | C | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4425+3990C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087891 | ||||||
| chr4:36087917
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4425+3964A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087917 | ||||||
| chr4:36087936
|
T | C | 78 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0089others(75): Show | 78 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.4425+3945A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087936 | ||||||
| chr4:36087938
|
T | G | 1 | a0001c0001t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4425+3943A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087938 | ||||||
| chr4:36087948
|
T | C | 57 | a0001c0001t0001g0089a0001c0001t0001g0149a0001c0001t0003g0094others(54): Show | 57 | HG00558.hp1 HG01074.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.4425+3933A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087948 | ||||||
| chr4:36088115
|
G | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4425+3766C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088115 | ||||||
| chr4:36088430
|
T | C | 21 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0127others(18): Show | 23 | HG01081.hp1 HG01168.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.4425+3451A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088430 | ||||||
| chr4:36088446
|
T | C | 256 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.4425+3435A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088446 | ||||||
| chr4:36088681
|
T | C | 256 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.4425+3200A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088681 | ||||||
| chr4:36088701
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4425+3180G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088701 | ||||||
| chr4:36088786
|
C | T | 11 | a0001c0001t0001g0082a0001c0001t0003g0235a0001c0001t0004g0054others(8): Show | 11 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4425+3095G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088786 | ||||||
| chr4:36088812
|
A | G | 4 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(1): Show | 4 | HG02818.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4425+3069T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088812 | ||||||
| chr4:36089047
|
C | T | 60 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0149others(57): Show | 60 | HG00558.hp1 HG01074.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.4425+2834G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089047 | ||||||
| chr4:36089077
|
G | T | 3 | a0001c0001t0004g0152a0001c0012t0003g0060a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+2804C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089077 | ||||||
| chr4:36089145
|
C | T | 17 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0193others(14): Show | 17 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.4425+2736G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089145 | ||||||
| chr4:36089381
|
A | T | 3 | a0001c0001t0004g0092a0001c0001t0004g0103a0001c0001t0023g0093 | 3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4425+2500T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089381 | ||||||
| chr4:36089455
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4425+2426C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089455 | ||||||
| chr4:36089465
|
A | C | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4425+2416T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089465 | ||||||
| chr4:36089505
|
G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4425+2376C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089505 | ||||||
| chr4:36089715
|
T | C | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4425+2166A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089715 | ||||||
| chr4:36089748
|
C | G | 81 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.4425+2133G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089748 | ||||||
| chr4:36089791
|
T | C | 3 | a0001c0001t0004g0152a0001c0012t0003g0060a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+2090A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089791 | ||||||
| chr4:36089794
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4425+2087A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089794 | ||||||
| chr4:36089868
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4425+2013A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089868 | ||||||
| chr4:36089873
|
G | T | 1 | a0001c0001t0002g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4425+2008C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089873 | ||||||
| chr4:36089927
|
T | C | 1 | a0001c0003t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4425+1954A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089927 | ||||||
| chr4:36089950
|
G | A | 3 | a0001c0001t0004g0152a0001c0012t0003g0060a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+1931C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089950 | ||||||
| chr4:36090222
|
C | T | 9 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4425+1659G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090222 | ||||||
| chr4:36090293
|
A | T | 9 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(6): Show | 11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4425+1588T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090293 | ||||||
| chr4:36090403
|
A | C | 1 | a0016c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4425+1478T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090403 | ||||||
| chr4:36090435
|
G | C | 1 | a0001c0001t0003g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4425+1446C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090435 | ||||||
| chr4:36090672
|
T | C | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4425+1209A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090672 | ||||||
| chr4:36090676
|
G | A | 6 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(3): Show | 8 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425+1205C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090676 | ||||||
| chr4:36090719
|
T | C | 257 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(254): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.4425+1162A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090719 | ||||||
| chr4:36091032
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0236a0007c0010t0001g0237 | 3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4425+849A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091032 | ||||||
| chr4:36091089
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0069a0001c0001t0002g0174others(2): Show | 5 | HG00280.hp1 HG02145.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425+792C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091089 | ||||||
| chr4:36091185
|
T | C | 2 | a0001c0001t0001g0082a0011c0022t0001g0111 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4425+696A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091185 | ||||||
| chr4:36091297
|
C | G | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425+584G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091297 | ||||||
| chr4:36091403
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0005g0052a0001c0004t0001g0062 | 3 | HG00741.hp2 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4425+478G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091403 | ||||||
| chr4:36091750
|
C | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4425+131G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091750 | ||||||
| chr4:36091778
|
A | G | 1 | a0011c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4425+103T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091778 | ||||||
| chr4:36092130
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4286-110T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092130 | ||||||
| chr4:36092155
|
C | T | 1 | a0001c0004t0025g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4286-135G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092155 | ||||||
| chr4:36092180
|
A | G | 6 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(3): Show | 6 | HG01243.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4286-160T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092180 | ||||||
| chr4:36092324
|
T | C | 91 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(88): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4286-304A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092324 | ||||||
| chr4:36092324
|
T | G | 89 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(86): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.4286-304A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092324 | ||||||
| chr4:36092404
|
G | GT | 27 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0064others(24): Show | 27 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.4286-385dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092404 | ||||||
| chr4:36092481
|
T | C | 6 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(3): Show | 6 | HG01243.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4286-461A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092481 | ||||||
| chr4:36092492
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4286-472G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092492 | ||||||
| chr4:36092509
|
T | C | 71 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(68): Show | 71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-489A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092509 | ||||||
| chr4:36092689
|
T | C | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4286-669A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092689 | ||||||
| chr4:36092756
|
T | C | 1 | a0001c0001t0002g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4286-736A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092756 | ||||||
| chr4:36092873
|
C | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-853G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092873 | ||||||
| chr4:36092923
|
A | G | 1 | a0001c0005t0002g0023 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4286-903T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092923 | ||||||
| chr4:36092970
|
G | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-950C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092970 | ||||||
| chr4:36092971
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-951T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092971 | ||||||
| chr4:36092992
|
C | T | 2 | a0001c0001t0004g0054a0001c0001t0004g0055 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4286-972G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092992 | ||||||
| chr4:36093006
|
C | A | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4286-986G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093006 | ||||||
| chr4:36093036
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-1016A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093036 | ||||||
| chr4:36093046
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4286-1026A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093046 | ||||||
| chr4:36093170
|
C | G | 3 | a0001c0001t0005g0066a0001c0004t0001g0090a0001c0004t0001g0269 | 3 | HG02922.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4286-1150G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093170 | ||||||
| chr4:36093209
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4286-1189G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093209 | ||||||
| chr4:36093217
|
G | T | 3 | a0001c0001t0005g0066a0001c0004t0001g0090a0001c0004t0001g0269 | 3 | HG02922.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4286-1197C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093217 | ||||||
| chr4:36093317
|
C | T | 182 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.4286-1297G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093317 | ||||||
| chr4:36093335
|
G | A | 179 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.4286-1315C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093335 | ||||||
| chr4:36093450
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4286-1430C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093450 | ||||||
| chr4:36093665
|
A | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4286-1645T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093665 | ||||||
| chr4:36093705
|
C | G | 71 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(68): Show | 71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-1685G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093705 | ||||||
| chr4:36093750
|
C | A | 72 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(69): Show | 72 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.4286-1730G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093750 | ||||||
| chr4:36093897
|
G | A | 39 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.4286-1877C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093897 | ||||||
| chr4:36094019
|
T | C | 179 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.4286-1999A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094019 | ||||||
| chr4:36094085
|
G | A | 70 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(67): Show | 70 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.4286-2065C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094085 | ||||||
| chr4:36094128
|
C | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4286-2108G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094128 | ||||||
| chr4:36094321
|
T | C | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-2301A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094321 | ||||||
| chr4:36094484
|
T | G | 5 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4286-2464A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094484 | ||||||
| chr4:36094561
|
T | G | 75 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(72): Show | 75 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(72): Show |
intron_variant | MODIFIER | c.4286-2541A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094561 | ||||||
| chr4:36095023
|
T | C | 1 | a0001c0001t0002g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4286-3003A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095023 | ||||||
| chr4:36095382
|
C | T | 1 | a0001c0001t0005g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4286-3362G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095382 | ||||||
| chr4:36095522
|
T | A | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-3502A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095522 | ||||||
| chr4:36095603
|
C | T | 76 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0149others(73): Show | 76 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(73): Show |
intron_variant | MODIFIER | c.4286-3583G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095603 | ||||||
| chr4:36095700
|
TTGTATTT others(11): Show |
T | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-3698_4286-368 others(22): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095700 | ||||||
| chr4:36095800
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4286-3780C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095800 | ||||||
| chr4:36096017
|
T | C | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.4286-3997A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096017 | ||||||
| chr4:36096095
|
G | A | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-4075C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096095 | ||||||
| chr4:36096191
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4286-4171G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096191 | ||||||
| chr4:36096217
|
T | C | 71 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(68): Show | 71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-4197A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096217 | ||||||
| chr4:36096283
|
T | G | 2 | a0001c0002t0001g0163a0001c0009t0001g0025 | 2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.4286-4263A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096283 | ||||||
| chr4:36096315
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-4295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096315 | ||||||
| chr4:36096357
|
T | C | 1 | a0001c0001t0003g0129 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4286-4337A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096357 | ||||||
| chr4:36096362
|
C | CA | 45 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(42): Show | 46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.4286-4343dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096362 | ||||||
| chr4:36096374
|
A | AAAAAAAA others(6): Show |
9 | a0001c0001t0001g0089a0001c0001t0005g0053a0001c0001t0005g0066others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4286-4355_4286-435 others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | ||||||
| chr4:36096374
|
A | AAAAAAAA others(5): Show |
3 | a0001c0001t0013g0005a0001c0003t0003g0074a0005c0013t0008g0067 | 3 | HG02083.hp1 HG02559.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.4286-4355_4286-435 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | ||||||
| chr4:36096374
|
A | AAAAAAAA others(4): Show |
58 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0149others(55): Show | 58 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.4286-4355_4286-435 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | ||||||
| chr4:36096374
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0094 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4286-4355_4286-435 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | ||||||
| chr4:36096375
|
A | G | 14 | a0001c0001t0002g0110a0001c0001t0003g0101a0001c0001t0003g0235others(11): Show | 16 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.4286-4355T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096375 | ||||||
| chr4:36096472
|
C | T | 73 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(70): Show | 73 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.4286-4452G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096472 | ||||||
| chr4:36096477
|
A | G | 71 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(68): Show | 71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-4457T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096477 | ||||||
| chr4:36096564
|
G | A | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4286-4544C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096564 | ||||||
| chr4:36096645
|
C | T | 70 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0149others(67): Show | 70 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.4286-4625G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096645 | ||||||
| chr4:36096666
|
T | C | 2 | a0001c0003t0002g0070a0001c0003t0002g0107 | 2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4286-4646A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096666 | ||||||
| chr4:36096794
|
T | C | 3 | a0001c0001t0001g0179a0001c0001t0002g0131a0001c0001t0002g0155 | 3 | HG02083.hp2 HG02132.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.4286-4774A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096794 | ||||||
| chr4:36096942
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0005g0051 | 2 | HG01361.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4286-4922C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096942 | ||||||
| chr4:36097058
|
T | C | 1 | a0001c0003t0003g0075 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4286-5038A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097058 | ||||||
| chr4:36097254
|
T | C | 1 | a0016c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4286-5234A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097254 | ||||||
| chr4:36097287
|
C | CA | 14 | a0001c0001t0001g0202a0001c0001t0003g0153a0001c0001t0003g0188others(11): Show | 14 | HG00544.hp1 HG02132.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.4286-5268dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097287 | ||||||
| chr4:36097545
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4286-5525T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097545 | ||||||
| chr4:36097652
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-5632C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097652 | ||||||
| chr4:36097691
|
T | A | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4286-5671A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097691 | ||||||
| chr4:36097722
|
C | A | 1 | a0017c0020t0001g0034 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4286-5702G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097722 | ||||||
| chr4:36097797
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4286-5777G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097797 | ||||||
| chr4:36097863
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-5843C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097863 | ||||||
| chr4:36097901
|
T | C | 1 | a0001c0004t0003g0266 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4286-5881A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097901 | ||||||
| chr4:36098048
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4286-6028C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098048 | ||||||
| chr4:36098055
|
CA | C | 248 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(245): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4286-6036delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098055 | ||||||
| chr4:36098106
|
C | T | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-6086G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098106 | ||||||
| chr4:36098112
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4286-6092A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098112 | ||||||
| chr4:36098163
|
G | T | 1 | a0001c0001t0003g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4286-6143C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098163 | ||||||
| chr4:36098204
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-6184G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098204 | ||||||
| chr4:36098232
|
T | C | 2 | a0001c0001t0001g0082a0011c0022t0001g0111 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4286-6212A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098232 | ||||||
| chr4:36098290
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-6270G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098290 | ||||||
| chr4:36098428
|
A | G | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4286-6408T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098428 | ||||||
| chr4:36098881
|
CTTTT | C | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-6865_4286-686 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098881 | ||||||
| chr4:36099053
|
C | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-7033G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099053 | ||||||
| chr4:36099092
|
C | G | 14 | a0001c0001t0002g0110a0001c0001t0003g0101a0001c0001t0003g0235others(11): Show | 16 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.4286-7072G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099092 | ||||||
| chr4:36099149
|
C | T | 2 | a0001c0002t0001g0165a0001c0002t0001g0234 | 2 | HG01071.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.4286-7129G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099149 | ||||||
| chr4:36099253
|
A | T | 1 | a0006c0011t0003g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4286-7233T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099253 | ||||||
| chr4:36099389
|
G | T | 1 | a0001c0005t0001g0024 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4286-7369C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099389 | ||||||
| chr4:36099516
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-7496A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099516 | ||||||
| chr4:36099676
|
C | T | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4286-7656G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099676 | ||||||
| chr4:36099815
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+7750C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099815 | ||||||
| chr4:36099895
|
A | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+7670T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099895 | ||||||
| chr4:36100116
|
C | A | 176 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(173): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.4285+7449G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100116 | ||||||
| chr4:36100117
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+7448C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100117 | ||||||
| chr4:36100140
|
C | T | 73 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0002g0151others(70): Show | 73 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.4285+7425G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100140 | ||||||
| chr4:36100173
|
A | C | 176 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(173): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.4285+7392T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100173 | ||||||
| chr4:36100259
|
T | C | 70 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0149others(67): Show | 70 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.4285+7306A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100259 | ||||||
| chr4:36100272
|
T | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4285+7293A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100272 | ||||||
| chr4:36100330
|
C | T | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4285+7235G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100330 | ||||||
| chr4:36100380
|
T | TCAGAGCT others(55): Show |
2 | a0001c0001t0003g0162a0001c0001t0003g0249 | 2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.4285+7123_4285+718 others(66): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100380 | ||||||
| chr4:36100392
|
C | T | 1 | a0001c0004t0003g0262 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4285+7173G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100392 | ||||||
| chr4:36100434
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+7131A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100434 | ||||||
| chr4:36100590
|
T | C | 1 | a0001c0001t0002g0253 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4285+6975A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100590 | ||||||
| chr4:36100606
|
AT | A | 7 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(4): Show | 7 | NA18747.hp2 NA18942.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.4285+6958delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100606 | ||||||
| chr4:36100743
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4285+6822G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100743 | ||||||
| chr4:36100743
|
CTTCT | C | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4285+6818_4285+682 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100743 | ||||||
| chr4:36100830
|
C | A | 6 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0139others(3): Show | 6 | HG00323.hp2 HG00642.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.4285+6735G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100830 | ||||||
| chr4:36100907
|
A | G | 3 | a0001c0002t0001g0165a0001c0002t0001g0234a0001c0002t0001g0243 | 3 | HG00735.hp2 HG01071.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.4285+6658T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100907 | ||||||
| chr4:36100978
|
C | G | 1 | a0001c0003t0003g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4285+6587G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100978 | ||||||
| chr4:36101098
|
G | A | 1 | a0001c0001t0002g0217 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4285+6467C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101098 | ||||||
| chr4:36101214
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+6351C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101214 | ||||||
| chr4:36101394
|
G | C | 5 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4285+6171C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101394 | ||||||
| chr4:36101396
|
G | GA | 87 | a0001c0001t0001g0069a0001c0001t0001g0194a0001c0001t0002g0021others(84): Show | 89 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(86): Show |
intron_variant | MODIFIER | c.4285+6168_4285+616 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101396 | ||||||
| chr4:36101396
|
G | GAT | 149 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.4285+6168_4285+616 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101396 | ||||||
| chr4:36101396
|
G | GATT | 6 | a0001c0001t0001g0202a0001c0001t0003g0153a0001c0001t0003g0188others(3): Show | 6 | HG00544.hp1 HG00544.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.4285+6168_4285+616 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101396 | ||||||
| chr4:36101397
|
T | A | 7 | a0001c0001t0005g0066a0001c0001t0009g0046a0001c0004t0001g0090others(4): Show | 7 | HG02486.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4285+6168A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101397 | ||||||
| chr4:36101398
|
T | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+6167A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101398 | ||||||
| chr4:36101729
|
T | C | 18 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0110others(15): Show | 20 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.4285+5836A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101729 | ||||||
| chr4:36101900
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4285+5665G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101900 | ||||||
| chr4:36101975
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+5590G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101975 | ||||||
| chr4:36101987
|
C | CTCTT | 251 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4285+5574_4285+557 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101987 | ||||||
| chr4:36102036
|
A | C | 175 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.4285+5529T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102036 | ||||||
| chr4:36102069
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4285+5496A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102069 | ||||||
| chr4:36102142
|
G | A | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4285+5423C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102142 | ||||||
| chr4:36102173
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0003g0118a0018c0026t0014g0009 | 3 | HG02895.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4285+5392G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102173 | ||||||
| chr4:36102196
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4285+5369G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102196 | ||||||
| chr4:36102220
|
G | A | 7 | a0001c0001t0003g0101a0001c0001t0003g0235a0001c0001t0004g0054others(4): Show | 7 | HG01081.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.4285+5345C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102220 | ||||||
| chr4:36102247
|
C | A | 1 | a0001c0001t0002g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4285+5318G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102247 | ||||||
| chr4:36102344
|
G | A | 16 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0078others(13): Show | 16 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4285+5221C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102344 | ||||||
| chr4:36102487
|
T | C | 251 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4285+5078A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102487 | ||||||
| chr4:36102807
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+4758G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102807 | ||||||
| chr4:36102841
|
A | G | 2 | a0001c0001t0002g0141a0001c0001t0002g0205 | 2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.4285+4724T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102841 | ||||||
| chr4:36102872
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4285+4693C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102872 | ||||||
| chr4:36102903
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+4662T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102903 | ||||||
| chr4:36102992
|
T | C | 1 | a0001c0002t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4285+4573A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102992 | ||||||
| chr4:36103079
|
G | T | 69 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0002g0151others(66): Show | 69 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.4285+4486C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103079 | ||||||
| chr4:36103557
|
G | C | 1 | a0001c0001t0002g0049 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4285+4008C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103557 | ||||||
| chr4:36103566
|
T | C | 1 | a0001c0001t0023g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4285+3999A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103566 | ||||||
| chr4:36103572
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+3993T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103572 | ||||||
| chr4:36103624
|
T | A | 251 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4285+3941A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103624 | ||||||
| chr4:36103798
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4285+3767A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103798 | ||||||
| chr4:36104202
|
C | CT | 72 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4285+3362dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104202 | ||||||
| chr4:36104219
|
A | G | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4285+3346T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104219 | ||||||
| chr4:36104256
|
C | T | 1 | a0001c0009t0001g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4285+3309G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104256 | ||||||
| chr4:36104383
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+3182C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104383 | ||||||
| chr4:36104431
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+3134T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104431 | ||||||
| chr4:36104468
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+3097A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104468 | ||||||
| chr4:36104609
|
G | A | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4285+2956C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104609 | ||||||
| chr4:36104620
|
T | C | 2 | a0005c0013t0008g0067a0005c0013t0008g0112 | 2 | NA19012.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.4285+2945A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104620 | ||||||
| chr4:36104622
|
G | C | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4285+2943C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104622 | ||||||
| chr4:36104646
|
C | T | 73 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0002g0151others(70): Show | 73 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.4285+2919G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104646 | ||||||
| chr4:36104663
|
T | A | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+2902A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104663 | ||||||
| chr4:36104702
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4285+2863T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104702 | ||||||
| chr4:36104704
|
T | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4285+2861A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104704 | ||||||
| chr4:36104945
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+2620A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104945 | ||||||
| chr4:36105011
|
T | C | 4 | a0001c0001t0009g0046a0001c0004t0003g0266a0001c0004t0003g0268others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4285+2554A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105011 | ||||||
| chr4:36105110
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+2455T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105110 | ||||||
| chr4:36105118
|
G | A | 3 | a0001c0005t0003g0102a0001c0005t0012g0008a0008c0027t0003g0048 | 3 | HG01433.hp1 HG03654.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4285+2447C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105118 | ||||||
| chr4:36105155
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4285+2410T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105155 | ||||||
| chr4:36105175
|
A | C | 251 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4285+2390T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105175 | ||||||
| chr4:36105205
|
AG | A | 4 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4285+2359delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105205 | ||||||
| chr4:36105292
|
C | G | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4285+2273G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105292 | ||||||
| chr4:36105364
|
A | T | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4285+2201T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105364 | ||||||
| chr4:36105490
|
T | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0114others(2): Show | 5 | HG02080.hp1 HG03942.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.4285+2075A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105490 | ||||||
| chr4:36105511
|
A | T | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4285+2054T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105511 | ||||||
| chr4:36105594
|
G | A | 4 | a0001c0001t0002g0151a0001c0001t0004g0152a0001c0001t0010g0274others(1): Show | 4 | HG00741.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.4285+1971C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105594 | ||||||
| chr4:36105635
|
A | G | 4 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4285+1930T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105635 | ||||||
| chr4:36105673
|
G | A | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4285+1892C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105673 | ||||||
| chr4:36105872
|
A | G | 6 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(3): Show | 8 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4285+1693T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105872 | ||||||
| chr4:36106159
|
G | T | 1 | a0017c0020t0001g0034 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4285+1406C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36106159 | ||||||
| chr4:36106478
|
TAA | T | 72 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4285+1085_4285+108 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36106478 | ||||||
| chr4:36106772
|
TA | T | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4285+792delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36106772 | ||||||
| chr4:36107161
|
T | A | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4285+404A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107161 | ||||||
| chr4:36107222
|
C | A | 3 | a0001c0005t0003g0102a0001c0005t0012g0008a0008c0027t0003g0048 | 3 | HG01433.hp1 HG03654.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4285+343G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107222 | ||||||
| chr4:36107300
|
G | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0193others(8): Show | 11 | HG00280.hp1 HG00438.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.4285+265C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107300 | ||||||
| chr4:36107364
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4285+201G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107364 | ||||||
| chr4:36107398
|
T | C | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4285+167A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107398 | ||||||
| chr4:36107486
|
T | C | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4285+79A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107486 | ||||||
| chr4:36107783
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4157-90T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107783 | ||||||
| chr4:36107787
|
C | G | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4157-94G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107787 | ||||||
| chr4:36107818
|
CTTATG | C | 172 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(169): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.4157-130_4157-126d others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107818 | ||||||
| chr4:36107854
|
T | C | 3 | a0001c0005t0003g0102a0001c0005t0012g0008a0008c0027t0003g0048 | 3 | HG01433.hp1 HG03654.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4157-161A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107854 | ||||||
| chr4:36107893
|
A | G | 5 | a0001c0001t0002g0011a0001c0001t0002g0068a0001c0001t0002g0207others(2): Show | 5 | HG00438.hp2 HG01106.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.4157-200T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107893 | ||||||
| chr4:36108112
|
A | G | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4157-419T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108112 | ||||||
| chr4:36108122
|
T | C | 72 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4157-429A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108122 | ||||||
| chr4:36108421
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-728G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108421 | ||||||
| chr4:36108559
|
G | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0236a0007c0010t0001g0237 | 3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4157-866C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108559 | ||||||
| chr4:36108724
|
G | T | 7 | a0001c0004t0002g0267a0001c0004t0003g0261a0001c0004t0003g0262others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4157-1031C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108724 | ||||||
| chr4:36108906
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-1213T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108906 | ||||||
| chr4:36108958
|
G | A | 9 | a0001c0001t0001g0202a0001c0001t0003g0153a0001c0001t0003g0188others(6): Show | 9 | HG00544.hp1 HG02132.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.4157-1265C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108958 | ||||||
| chr4:36109385
|
A | G | 10 | a0001c0001t0001g0082a0001c0001t0002g0151a0001c0001t0003g0118others(7): Show | 10 | HG00741.hp2 HG01243.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4157-1692T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109385 | ||||||
| chr4:36109399
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4157-1706G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109399 | ||||||
| chr4:36109456
|
A | G | 8 | a0001c0001t0001g0082a0001c0001t0002g0151a0001c0001t0003g0118others(5): Show | 8 | HG00741.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4157-1763T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109456 | ||||||
| chr4:36109520
|
G | A | 3 | a0001c0004t0003g0266a0001c0004t0003g0268a0001c0004t0003g0270 | 3 | HG02486.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4157-1827C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109520 | ||||||
| chr4:36109542
|
C | A | 1 | a0001c0001t0002g0147 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4157-1849G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109542 | ||||||
| chr4:36109594
|
T | G | 10 | a0001c0001t0001g0082a0001c0001t0002g0151a0001c0001t0003g0118others(7): Show | 10 | HG00741.hp2 HG01243.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4157-1901A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109594 | ||||||
| chr4:36109658
|
A | G | 8 | a0001c0001t0001g0082a0001c0001t0002g0151a0001c0001t0003g0118others(5): Show | 8 | HG00741.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4157-1965T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109658 | ||||||
| chr4:36109766
|
G | T | 7 | a0001c0004t0002g0267a0001c0004t0003g0261a0001c0004t0003g0262others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4157-2073C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109766 | ||||||
| chr4:36109841
|
A | T | 1 | a0001c0001t0002g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4157-2148T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109841 | ||||||
| chr4:36109856
|
T | TC | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4157-2164dupG | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109856 | ||||||
| chr4:36109923
|
C | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-2230G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109923 | ||||||
| chr4:36110097
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-2404C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110097 | ||||||
| chr4:36110133
|
T | C | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4157-2440A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110133 | ||||||
| chr4:36110170
|
T | C | 1 | a0001c0001t0003g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4157-2477A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110170 | ||||||
| chr4:36110183
|
G | C | 5 | a0001c0001t0005g0066a0001c0001t0005g0245a0001c0001t0005g0246others(2): Show | 5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4157-2490C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110183 | ||||||
| chr4:36110349
|
A | G | 3 | a0001c0001t0011g0004a0001c0001t0024g0137a0014c0018t0002g0240 | 3 | HG03017.hp2 HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4157-2656T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110349 | ||||||
| chr4:36110491
|
T | C | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4157-2798A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110491 | ||||||
| chr4:36110527
|
C | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4157-2834G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110527 | ||||||
| chr4:36110687
|
G | T | 7 | a0001c0004t0002g0267a0001c0004t0003g0261a0001c0004t0003g0262others(4): Show | 7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4157-2994C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110687 | ||||||
| chr4:36111257
|
T | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4156+2913A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111257 | ||||||
| chr4:36111408
|
T | C | 24 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0064others(21): Show | 24 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4156+2762A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111408 | ||||||
| chr4:36111781
|
G | A | 1 | a0001c0001t0002g0147 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4156+2389C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111781 | ||||||
| chr4:36111985
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4156+2185A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111985 | ||||||
| chr4:36112099
|
T | C | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4156+2071A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112099 | ||||||
| chr4:36112131
|
C | T | 1 | a0001c0001t0003g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4156+2039G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112131 | ||||||
| chr4:36112190
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4156+1980C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112190 | ||||||
| chr4:36112266
|
A | G | 5 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4156+1904T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112266 | ||||||
| chr4:36112312
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4156+1858T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112312 | ||||||
| chr4:36112337
|
T | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4156+1833A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112337 | ||||||
| chr4:36112401
|
G | T | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4156+1769C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112401 | ||||||
| chr4:36112488
|
T | A | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4156+1682A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112488 | ||||||
| chr4:36112642
|
T | C | 30 | a0001c0001t0001g0149a0001c0001t0002g0208a0001c0003t0001g0180others(27): Show | 30 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.4156+1528A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112642 | ||||||
| chr4:36112911
|
T | G | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4156+1259A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112911 | ||||||
| chr4:36113053
|
A | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4156+1117T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113053 | ||||||
| chr4:36113241
|
G | A | 2 | a0001c0002t0001g0047a0001c0002t0001g0197 | 2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.4156+929C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113241 | ||||||
| chr4:36113312
|
A | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4156+858T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113312 | ||||||
| chr4:36113469
|
T | C | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4156+701A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113469 | ||||||
| chr4:36113703
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4156+467G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113703 | ||||||
| chr4:36113790
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0003g0153a0001c0001t0010g0274others(1): Show | 4 | HG02132.hp2 NA18948.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.4156+380G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113790 | ||||||
| chr4:36113831
|
T | C | 1 | a0001c0002t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4156+339A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113831 | ||||||
| chr4:36113840
|
C | T | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4156+330G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113840 | ||||||
| chr4:36114044
|
A | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4156+126T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36114044 | ||||||
| chr4:36114070
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4156+100T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36114070 | ||||||
| chr4:36114421
|
C | T | 4 | a0001c0001t0005g0053a0001c0001t0005g0066a0001c0001t0005g0273others(1): Show | 4 | HG02109.hp1 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4039-134G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114421 | ||||||
| chr4:36114484
|
G | C | 1 | a0002c0006t0001g0120 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4039-197C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114484 | ||||||
| chr4:36114489
|
C | T | 271 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4039-202G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114489 | ||||||
| chr4:36114560
|
C | T | 1 | a0001c0009t0001g0037 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4039-273G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114560 | ||||||
| chr4:36114587
|
C | T | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4039-300G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114587 | ||||||
| chr4:36114600
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4039-313G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114600 | ||||||
| chr4:36114697
|
G | C | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4039-410C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114697 | ||||||
| chr4:36114705
|
C | T | 1 | a0002c0006t0003g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4039-418G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114705 | ||||||
| chr4:36114779
|
G | A | 3 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106 | 3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4039-492C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114779 | ||||||
| chr4:36114827
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4039-540A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114827 | ||||||
| chr4:36114844
|
G | C | 1 | a0014c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4039-557C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114844 | ||||||
| chr4:36114847
|
G | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4039-560C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114847 | ||||||
| chr4:36114850
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4039-563C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114850 | ||||||
| chr4:36114885
|
A | T | 24 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0064others(21): Show | 24 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4039-598T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114885 | ||||||
| chr4:36114992
|
T | C | 1 | a0001c0001t0007g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4039-705A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114992 | ||||||
| chr4:36115049
|
T | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4039-762A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115049 | ||||||
| chr4:36115098
|
G | A | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4039-811C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115098 | ||||||
| chr4:36115103
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4039-816C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115103 | ||||||
| chr4:36115125
|
A | C | 77 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.4039-838T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115125 | ||||||
| chr4:36115285
|
C | G | 61 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0089others(58): Show | 61 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.4039-998G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115285 | ||||||
| chr4:36115629
|
A | G | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4039-1342T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115629 | ||||||
| chr4:36115686
|
C | T | 1 | a0001c0002t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4038+1375G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115686 | ||||||
| chr4:36115807
|
T | G | 24 | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0064others(21): Show | 24 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4038+1254A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115807 | ||||||
| chr4:36115928
|
T | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4038+1133A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115928 | ||||||
| chr4:36116078
|
A | C | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4038+983T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116078 | ||||||
| chr4:36116099
|
T | C | 5 | a0001c0002t0001g0163a0001c0009t0001g0025a0001c0009t0001g0035others(2): Show | 5 | HG00741.hp1 HG01106.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.4038+962A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116099 | ||||||
| chr4:36116215
|
T | C | 2 | a0001c0001t0002g0136a0001c0001t0002g0140 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4038+846A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116215 | ||||||
| chr4:36116280
|
ATGT | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0004t0002g0265 | 3 | HG02280.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4038+778_4038+780d others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116280 | ||||||
| chr4:36116618
|
T | C | 75 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.4038+443A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116618 | ||||||
| chr4:36116710
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4038+351C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116710 | ||||||
| chr4:36116836
|
T | G | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.4038+225A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116836 | ||||||
| chr4:36116855
|
G | A | 37 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0002g0110others(34): Show | 37 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.4038+206C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116855 | ||||||
| chr4:36116934
|
T | A | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4038+127A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116934 | ||||||
| chr4:36116975
|
T | C | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4038+86A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116975 | ||||||
| chr4:36117008
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4038+53C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36117008 | ||||||
| chr4:36117025
|
C | A | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4038+36G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36117025 | ||||||
| chr4:36117141
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | splice_region_variant&intron_variant | LOW | c.3964-6T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117141 | ||||||
| chr4:36117285
|
T | G | 2 | a0001c0001t0002g0170a0001c0001t0003g0129 | 2 | NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.3964-150A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117285 | ||||||
| chr4:36117292
|
T | C | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3964-157A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117292 | ||||||
| chr4:36117347
|
A | C | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3964-212T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117347 | ||||||
| chr4:36117450
|
T | C | 37 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(34): Show | 38 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.3964-315A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117450 | ||||||
| chr4:36117484
|
C | A | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3964-349G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117484 | ||||||
| chr4:36117601
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0003g0118a0018c0026t0014g0009 | 3 | HG02895.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3964-466C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117601 | ||||||
| chr4:36117680
|
A | C | 4 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3964-545T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117680 | ||||||
| chr4:36117865
|
A | G | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3964-730T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117865 | ||||||
| chr4:36117969
|
G | A | 1 | a0001c0001t0002g0210 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3964-834C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117969 | ||||||
| chr4:36117976
|
T | C | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3964-841A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117976 | ||||||
| chr4:36118119
|
T | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0127 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3964-984A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118119 | ||||||
| chr4:36118159
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3964-1024G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118159 | ||||||
| chr4:36118166
|
T | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3964-1031A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118166 | ||||||
| chr4:36118290
|
T | TA | 55 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0050others(52): Show | 56 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.3964-1156dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118290 | ||||||
| chr4:36118290
|
T | TAA | 7 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0114others(4): Show | 7 | HG02055.hp1 HG02080.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.3964-1157_3964-115 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118290 | ||||||
| chr4:36118302
|
A | C | 12 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(9): Show | 12 | HG01099.hp1 HG01243.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.3964-1167T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118302 | ||||||
| chr4:36118897
|
T | C | 1 | a0001c0001t0002g0189 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3963+753A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118897 | ||||||
| chr4:36119106
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3963+544T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119106 | ||||||
| chr4:36119324
|
A | T | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3963+326T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119324 | ||||||
| chr4:36119392
|
T | C | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3963+258A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119392 | ||||||
| chr4:36119472
|
A | T | 3 | a0001c0004t0003g0266a0001c0004t0003g0268a0001c0004t0003g0270 | 3 | HG02486.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3963+178T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119472 | ||||||
| chr4:36119473
|
T | C | 5 | a0001c0004t0002g0267a0001c0004t0003g0261a0001c0004t0022g0264others(2): Show | 5 | HG01255.hp1 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3963+177A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119473 | ||||||
| chr4:36119518
|
G | GT | 71 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.3963+131dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119518 | ||||||
| chr4:36119518
|
GT | G | 11 | a0001c0004t0001g0090a0001c0004t0002g0267a0001c0004t0003g0261others(8): Show | 11 | HG01255.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3963+131delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119518 | ||||||
| chr4:36119761
|
C | T | 3 | a0001c0003t0001g0180a0001c0003t0001g0181a0001c0003t0001g0182 | 3 | NA18947.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3895-43G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36119761 | ||||||
| chr4:36119829
|
G | C | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3895-111C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36119829 | ||||||
| chr4:36119943
|
A | G | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3895-225T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36119943 | ||||||
| chr4:36120013
|
T | A | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3895-295A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120013 | ||||||
| chr4:36120402
|
G | T | 1 | a0001c0003t0003g0080 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3895-684C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120402 | ||||||
| chr4:36120479
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3894+700G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120479 | ||||||
| chr4:36120499
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3894+680A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120499 | ||||||
| chr4:36120588
|
T | C | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3894+591A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120588 | ||||||
| chr4:36120590
|
T | C | 6 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(3): Show | 8 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3894+589A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120590 | ||||||
| chr4:36120699
|
T | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3894+480A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120699 | ||||||
| chr4:36120814
|
C | T | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3894+365G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120814 | ||||||
| chr4:36120945
|
T | C | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3894+234A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120945 | ||||||
| chr4:36121060
|
T | C | 2 | a0001c0001t0005g0052a0001c0004t0001g0062 | 2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3894+119A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36121060 | ||||||
| chr4:36121115
|
A | T | 77 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3894+64T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36121115 | ||||||
| chr4:36121367
|
T | A | 1 | a0001c0001t0003g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3747-41A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121367 | ||||||
| chr4:36121379
|
T | C | 1 | a0001c0009t0001g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3747-53A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121379 | ||||||
| chr4:36121402
|
A | G | 60 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(57): Show | 63 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.3747-76T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121402 | ||||||
| chr4:36121496
|
A | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-170T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121496 | ||||||
| chr4:36121654
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-328G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121654 | ||||||
| chr4:36121837
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3747-511G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121837 | ||||||
| chr4:36121839
|
A | G | 136 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(133): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3747-513T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121839 | ||||||
| chr4:36121845
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-519G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121845 | ||||||
| chr4:36121923
|
C | G | 77 | a0001c0001t0001g0082a0001c0001t0001g0179a0001c0001t0001g0199others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.3747-597G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121923 | ||||||
| chr4:36121985
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0005g0051 | 2 | HG01361.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3747-659G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121985 | ||||||
| chr4:36122018
|
G | A | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3747-692C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122018 | ||||||
| chr4:36122063
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-737A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122063 | ||||||
| chr4:36122212
|
T | C | 8 | a0001c0001t0001g0149a0001c0001t0002g0208a0001c0003t0001g0180others(5): Show | 8 | HG01346.hp1 HG02004.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.3747-886A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122212 | ||||||
| chr4:36122239
|
T | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3747-913A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122239 | ||||||
| chr4:36122270
|
T | A | 51 | a0001c0001t0001g0089a0001c0001t0001g0149a0001c0001t0002g0110others(48): Show | 51 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.3747-944A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122270 | ||||||
| chr4:36122469
|
A | G | 1 | a0001c0001t0002g0222 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3747-1143T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122469 | ||||||
| chr4:36122509
|
C | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1183G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122509 | ||||||
| chr4:36122515
|
C | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1189G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122515 | ||||||
| chr4:36122529
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1203G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122529 | ||||||
| chr4:36122532
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1206A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122532 | ||||||
| chr4:36122557
|
T | C | 4 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106others(1): Show | 4 | HG02818.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3747-1231A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122557 | ||||||
| chr4:36122675
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1349T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122675 | ||||||
| chr4:36122716
|
C | G | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3747-1390G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122716 | ||||||
| chr4:36122813
|
T | A | 4 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061others(1): Show | 4 | HG00741.hp2 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3747-1487A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122813 | ||||||
| chr4:36122821
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3747-1495G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122821 | ||||||
| chr4:36122831
|
A | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3747-1505T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122831 | ||||||
| chr4:36122944
|
T | C | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3747-1618A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122944 | ||||||
| chr4:36122946
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1620C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122946 | ||||||
| chr4:36122958
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3747-1632C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122958 | ||||||
| chr4:36123080
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1754G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123080 | ||||||
| chr4:36123268
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1594G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123268 | ||||||
| chr4:36123293
|
G | A | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3746+1569C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123293 | ||||||
| chr4:36123305
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1557T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123305 | ||||||
| chr4:36123309
|
T | C | 63 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0149others(60): Show | 63 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.3746+1553A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123309 | ||||||
| chr4:36123517
|
T | C | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3746+1345A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123517 | ||||||
| chr4:36123525
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1337G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123525 | ||||||
| chr4:36123641
|
T | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1221A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123641 | ||||||
| chr4:36123663
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1199A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123663 | ||||||
| chr4:36123743
|
G | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3746+1119C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123743 | ||||||
| chr4:36123807
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1055A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123807 | ||||||
| chr4:36123859
|
T | TTTCTCCT others(4): Show |
2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1002_3746+100 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123859 | ||||||
| chr4:36123868
|
C | T | 38 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(35): Show | 39 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.3746+994G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123868 | ||||||
| chr4:36123874
|
A | G | 75 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3746+988T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123874 | ||||||
| chr4:36124079
|
A | G | 1 | a0001c0005t0012g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3746+783T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124079 | ||||||
| chr4:36124170
|
C | T | 2 | a0001c0001t0005g0245a0001c0001t0005g0246 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.3746+692G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124170 | ||||||
| chr4:36124313
|
A | T | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3746+549T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124313 | ||||||
| chr4:36124529
|
A | G | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3746+333T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124529 | ||||||
| chr4:36124616
|
C | T | 11 | a0001c0004t0001g0090a0001c0004t0002g0267a0001c0004t0003g0261others(8): Show | 11 | HG01255.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3746+246G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124616 | ||||||
| chr4:36124642
|
A | T | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3746+220T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124642 | ||||||
| chr4:36124671
|
A | G | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3746+191T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124671 | ||||||
| chr4:36124771
|
G | A | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3746+91C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124771 | ||||||
| chr4:36124775
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+87G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124775 | ||||||
| chr4:36124976
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-9C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36124976 | ||||||
| chr4:36125048
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-81G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125048 | ||||||
| chr4:36125074
|
G | A | 75 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3641-107C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125074 | ||||||
| chr4:36125126
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-159G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125126 | ||||||
| chr4:36125174
|
T | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-207A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125174 | ||||||
| chr4:36125188
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-221G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125188 | ||||||
| chr4:36125381
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-414A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125381 | ||||||
| chr4:36125490
|
A | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128 | 3 | HG01993.hp1 HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3641-523T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125490 | ||||||
| chr4:36125530
|
G | T | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3641-563C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125530 | ||||||
| chr4:36125554
|
T | C | 136 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0127others(133): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3641-587A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125554 | ||||||
| chr4:36125636
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-669T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125636 | ||||||
| chr4:36125883
|
T | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-916A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125883 | ||||||
| chr4:36126080
|
C | A | 75 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3641-1113G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126080 | ||||||
| chr4:36126137
|
C | T | 8 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(5): Show | 10 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3641-1170G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126137 | ||||||
| chr4:36126290
|
A | C | 73 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3641-1323T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126290 | ||||||
| chr4:36126298
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3641-1331C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126298 | ||||||
| chr4:36126333
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1366G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126333 | ||||||
| chr4:36126427
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1460T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126427 | ||||||
| chr4:36126476
|
A | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1509T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126476 | ||||||
| chr4:36126489
|
T | C | 1 | a0003c0007t0003g0109 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3641-1522A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126489 | ||||||
| chr4:36126570
|
T | C | 251 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3641-1603A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126570 | ||||||
| chr4:36126581
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1614T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126581 | ||||||
| chr4:36126805
|
T | G | 2 | a0001c0002t0001g0028a0001c0002t0001g0029 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.3640+1728A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126805 | ||||||
| chr4:36126855
|
C | G | 249 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3640+1678G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126855 | ||||||
| chr4:36126874
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+1659C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126874 | ||||||
| chr4:36126898
|
C | A | 1 | a0001c0004t0003g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3640+1635G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126898 | ||||||
| chr4:36126974
|
C | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+1559G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126974 | ||||||
| chr4:36127348
|
C | G | 2 | a0001c0001t0002g0136a0001c0001t0002g0140 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3640+1185G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127348 | ||||||
| chr4:36127706
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+827C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127706 | ||||||
| chr4:36127740
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+793A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127740 | ||||||
| chr4:36127763
|
A | G | 74 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3640+770T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127763 | ||||||
| chr4:36127780
|
A | G | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3640+753T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127780 | ||||||
| chr4:36127812
|
G | C | 1 | a0001c0002t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3640+721C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127812 | ||||||
| chr4:36127865
|
G | T | 222 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0065others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.3640+668C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127865 | ||||||
| chr4:36127899
|
G | A | 1 | a0001c0001t0020g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3640+634C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127899 | ||||||
| chr4:36127949
|
C | G | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3640+584G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127949 | ||||||
| chr4:36128078
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+455T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128078 | ||||||
| chr4:36128116
|
T | C | 2 | a0001c0001t0004g0054a0001c0001t0004g0055 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3640+417A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128116 | ||||||
| chr4:36128279
|
T | C | 2 | a0001c0001t0005g0053a0001c0001t0005g0273 | 2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3640+254A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128279 | ||||||
| chr4:36128374
|
A | C | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3640+159T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128374 | ||||||
| chr4:36128438
|
T | G | 1 | a0002c0006t0001g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3640+95A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128438 | ||||||
| chr4:36128477
|
T | TAC | 31 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(28): Show | 31 | HG00280.hp1 HG00438.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.3640+54_3640+55dup others(2): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACAC | 29 | a0001c0001t0001g0078a0001c0001t0004g0092a0001c0001t0004g0103others(26): Show | 31 | HG01168.hp1 HG01255.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.3640+52_3640+55dup others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACACAC | 91 | a0001c0001t0001g0045a0001c0001t0001g0069a0001c0001t0001g0082others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.3640+50_3640+55dup others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACACACA others(1): Show |
8 | a0001c0001t0001g0149a0001c0001t0002g0110a0001c0001t0002g0208others(5): Show | 8 | HG01069.hp2 HG01167.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3640+48_3640+55dup others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACACACA others(3): Show |
10 | a0001c0001t0003g0033a0001c0001t0003g0248a0001c0002t0001g0003others(7): Show | 11 | HG00544.hp2 HG02040.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.3640+46_3640+55dup others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACACACA others(5): Show |
18 | a0001c0001t0001g0179a0001c0001t0002g0011a0001c0001t0002g0068others(15): Show | 18 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.3640+44_3640+55dup others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACACACA others(7): Show |
45 | a0001c0001t0002g0018a0001c0001t0002g0049a0001c0001t0002g0130others(42): Show | 45 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.3640+42_3640+55dup others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACACACA others(9): Show |
8 | a0001c0001t0002g0136a0001c0001t0002g0140a0001c0001t0002g0147others(5): Show | 8 | HG00558.hp2 HG00642.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.3640+40_3640+55dup others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TACACACA others(11): Show |
3 | a0001c0001t0001g0199a0001c0001t0020g0198a0001c0002t0001g0142 | 3 | HG00642.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3640+38_3640+55dup others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128477
|
T | TATACACA others(7): Show |
2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+55_3640+56ins others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | ||||||
| chr4:36128503
|
C | CACAT | 3 | a0001c0001t0001g0202a0001c0001t0003g0153a0001c0003t0002g0076 | 3 | HG02132.hp2 NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.3640+29_3640+30ins others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128503 | ||||||
| chr4:36128505
|
T | C | 72 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3640+28A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128505 | ||||||
| chr4:36128507
|
T | C | 2 | a0001c0001t0002g0218a0001c0001t0002g0256 | 2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.3640+26A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128507 | ||||||
| chr4:36128753
|
TA | T | 246 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(243): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.3428-9delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128753 | ||||||
| chr4:36128771
|
C | T | 74 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3428-26G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128771 | ||||||
| chr4:36128837
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-92G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128837 | ||||||
| chr4:36128994
|
T | C | 1 | a0001c0001t0002g0210 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3428-249A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128994 | ||||||
| chr4:36129011
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-266G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129011 | ||||||
| chr4:36129256
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3428-511A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129256 | ||||||
| chr4:36129287
|
A | T | 18 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(15): Show | 18 | HG00280.hp1 HG00438.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.3428-542T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129287 | ||||||
| chr4:36129298
|
C | T | 59 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(56): Show | 62 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.3428-553G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129298 | ||||||
| chr4:36129351
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0004t0002g0265 | 3 | HG02280.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3428-606G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129351 | ||||||
| chr4:36129438
|
C | T | 72 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3428-693G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129438 | ||||||
| chr4:36129458
|
C | G | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3428-713G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129458 | ||||||
| chr4:36129491
|
T | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-746A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129491 | ||||||
| chr4:36129584
|
C | T | 74 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3428-839G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129584 | ||||||
| chr4:36129834
|
A | C | 63 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0149others(60): Show | 63 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.3428-1089T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129834 | ||||||
| chr4:36129844
|
T | TAC | 72 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3428-1101_3428-110 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129844 | ||||||
| chr4:36129968
|
T | A | 3 | a0001c0001t0004g0092a0001c0001t0004g0103a0001c0001t0023g0093 | 3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3428-1223A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129968 | ||||||
| chr4:36129975
|
T | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-1230A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129975 | ||||||
| chr4:36130023
|
T | G | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3428-1278A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130023 | ||||||
| chr4:36130319
|
T | C | 72 | a0001c0001t0001g0179a0001c0001t0001g0199a0001c0001t0002g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3428-1574A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130319 | ||||||
| chr4:36130431
|
T | C | 2 | a0001c0001t0001g0082a0011c0022t0001g0111 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3428-1686A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130431 | ||||||
| chr4:36130619
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3428-1874G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130619 | ||||||
| chr4:36130749
|
G | A | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(11): Show | 14 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3428-2004C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130749 | ||||||
| chr4:36130790
|
T | C | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3428-2045A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130790 | ||||||
| chr4:36130837
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-2092C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130837 | ||||||
| chr4:36131004
|
A | C | 4 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0019g0113others(1): Show | 4 | HG02165.hp1 NA18945.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.3427+2222T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131004 | ||||||
| chr4:36131036
|
T | G | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3427+2190A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131036 | ||||||
| chr4:36131394
|
C | A | 37 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0002g0110others(34): Show | 37 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.3427+1832G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131394 | ||||||
| chr4:36131459
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3427+1767A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131459 | ||||||
| chr4:36131551
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3427+1675A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131551 | ||||||
| chr4:36131720
|
T | C | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3427+1506A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131720 | ||||||
| chr4:36132440
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3427+786T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132440 | ||||||
| chr4:36132536
|
T | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3427+690A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132536 | ||||||
| chr4:36132604
|
C | A | 1 | a0001c0002t0001g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3427+622G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132604 | ||||||
| chr4:36132616
|
T | A | 1 | a0001c0002t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3427+610A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132616 | ||||||
| chr4:36132631
|
T | C | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3427+595A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132631 | ||||||
| chr4:36132805
|
T | C | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3427+421A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132805 | ||||||
| chr4:36132847
|
T | C | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3427+379A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132847 | ||||||
| chr4:36132912
|
T | G | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3427+314A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132912 | ||||||
| chr4:36132949
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3427+277G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132949 | ||||||
| chr4:36133180
|
G | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3427+46C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36133180 | ||||||
| chr4:36133680
|
G | A | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3264-291C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133680 | ||||||
| chr4:36133682
|
C | T | 2 | a0001c0001t0002g0201a0001c0001t0002g0216 | 2 | NA18973.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3264-293G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133682 | ||||||
| chr4:36133699
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-310C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133699 | ||||||
| chr4:36133722
|
C | A | 1 | a0008c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3264-333G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133722 | ||||||
| chr4:36133771
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3264-382A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133771 | ||||||
| chr4:36134220
|
T | C | 1 | a0011c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3264-831A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134220 | ||||||
| chr4:36134267
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3264-878T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134267 | ||||||
| chr4:36134327
|
C | A | 1 | a0001c0001t0002g0011 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3264-938G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134327 | ||||||
| chr4:36134399
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1010T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134399 | ||||||
| chr4:36134405
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1016G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134405 | ||||||
| chr4:36134521
|
C | A | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3264-1132G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134521 | ||||||
| chr4:36134582
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1193C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134582 | ||||||
| chr4:36134699
|
T | C | 1 | a0001c0001t0003g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3264-1310A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134699 | ||||||
| chr4:36134707
|
G | A | 225 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0065others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.3264-1318C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134707 | ||||||
| chr4:36134735
|
T | TAC | 72 | a0001c0001t0001g0045a0001c0001t0001g0050a0001c0001t0001g0127others(69): Show | 75 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.3264-1348_3264-134 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134735 | ||||||
| chr4:36134735
|
T | TACAC | 12 | a0001c0001t0001g0082a0001c0001t0002g0187a0001c0001t0003g0118others(9): Show | 12 | HG00280.hp2 HG00544.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.3264-1350_3264-134 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134735 | ||||||
| chr4:36134735
|
T | TACACACA others(5): Show |
1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3264-1358_3264-134 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134735 | ||||||
| chr4:36134760
|
A | ACACC | 69 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.3264-1372_3264-137 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134760 | ||||||
| chr4:36134760
|
A | ACC | 4 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0135others(1): Show | 4 | HG00735.hp1 HG01433.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.3264-1373_3264-137 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134760 | ||||||
| chr4:36134769
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1380C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134769 | ||||||
| chr4:36134973
|
A | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1584T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134973 | ||||||
| chr4:36134980
|
A | C | 25 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(22): Show | 25 | HG00280.hp1 HG00438.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.3264-1591T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134980 | ||||||
| chr4:36135126
|
T | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1737A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36135126 | ||||||
| chr4:36135220
|
G | A | 5 | a0001c0001t0001g0069a0001c0001t0003g0116a0001c0001t0003g0238others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-1831C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36135220 | ||||||
| chr4:36135336
|
CT | C | 3 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3264-1948delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36135336 | ||||||
| chr4:36136006
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-2617T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136006 | ||||||
| chr4:36136007
|
T | A | 2 | a0001c0001t0002g0133a0001c0005t0002g0023 | 2 | HG00738.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3264-2618A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136007 | ||||||
| chr4:36136022
|
T | C | 1 | a0001c0005t0001g0024 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3264-2633A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136022 | ||||||
| chr4:36136095
|
T | C | 1 | a0001c0001t0002g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3264-2706A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136095 | ||||||
| chr4:36136206
|
A | C | 1 | a0001c0003t0003g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3264-2817T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136206 | ||||||
| chr4:36136262
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3264-2873G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136262 | ||||||
| chr4:36136465
|
T | A | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3264-3076A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136465 | ||||||
| chr4:36136579
|
T | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3190A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136579 | ||||||
| chr4:36136617
|
G | A | 5 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-3228C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136617 | ||||||
| chr4:36136693
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3304A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136693 | ||||||
| chr4:36136781
|
ATATGTGT others(7): Show |
A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3406_3264-339 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136781 | ||||||
| chr4:36136783
|
A | ATG | 21 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0086others(18): Show | 21 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.3264-3396_3264-339 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | ||||||
| chr4:36136783
|
A | ATGTG | 24 | a0001c0001t0001g0114a0001c0001t0002g0021a0001c0001t0002g0022others(21): Show | 25 | HG01081.hp1 HG01255.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3264-3398_3264-339 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | ||||||
| chr4:36136783
|
A | ATGTGTG | 19 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(16): Show | 20 | HG00280.hp1 HG00438.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3264-3400_3264-339 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | ||||||
| chr4:36136783
|
A | ATGTGTGT others(1): Show |
9 | a0001c0001t0001g0078a0001c0001t0001g0194a0001c0001t0001g0236others(6): Show | 9 | HG02258.hp2 HG02723.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.3264-3402_3264-339 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | ||||||
| chr4:36136783
|
ATG | A | 5 | a0001c0001t0002g0169a0001c0001t0002g0171a0001c0001t0003g0101others(2): Show | 5 | HG02109.hp2 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-3396_3264-339 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | ||||||
| chr4:36136783
|
ATGTG | A | 5 | a0001c0001t0001g0179a0001c0001t0002g0131a0001c0001t0002g0155others(2): Show | 5 | HG01109.hp2 HG02083.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.3264-3398_3264-339 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | ||||||
| chr4:36136810
|
T | C | 2 | a0001c0001t0002g0136a0001c0001t0002g0140 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3264-3421A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136810 | ||||||
| chr4:36136814
|
T | C | 6 | a0001c0001t0002g0049a0001c0001t0002g0133a0001c0001t0002g0210others(3): Show | 6 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.3264-3425A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136814 | ||||||
| chr4:36136816
|
T | C | 59 | a0001c0001t0001g0149a0001c0001t0001g0199a0001c0001t0002g0011others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.3264-3427A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | ||||||
| chr4:36136816
|
T | TGTGC | 34 | a0001c0001t0001g0069a0001c0001t0003g0094a0001c0001t0003g0095others(31): Show | 34 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.3264-3431_3264-342 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | ||||||
| chr4:36136816
|
T | TGTGTGC | 3 | a0001c0001t0003g0257a0001c0001t0003g0258a0001c0001t0003g0272 | 3 | HG02647.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3264-3428_3264-342 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | ||||||
| chr4:36136816
|
T | TGTGTGTG others(1): Show |
13 | a0001c0001t0001g0089a0001c0001t0002g0110a0001c0001t0003g0097others(10): Show | 13 | HG01167.hp1 HG02165.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3264-3428_3264-342 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | ||||||
| chr4:36136816
|
T | TGTGTGTG others(3): Show |
5 | a0001c0001t0005g0245a0001c0001t0023g0093a0001c0004t0001g0269others(2): Show | 5 | HG01099.hp1 HG01884.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-3428_3264-342 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | ||||||
| chr4:36136816
|
TGTGC | T | 6 | a0001c0001t0002g0049a0001c0001t0002g0133a0001c0001t0002g0210others(3): Show | 6 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.3264-3431_3264-342 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | ||||||
| chr4:36136818
|
T | C | 7 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0218others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.3264-3429A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136818 | ||||||
| chr4:36136818
|
TGC | T | 58 | a0001c0001t0001g0149a0001c0001t0001g0199a0001c0001t0002g0011others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.3264-3431_3264-343 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136818 | ||||||
| chr4:36136820
|
C | T | 7 | a0001c0001t0002g0183a0001c0001t0002g0184a0001c0001t0002g0218others(4): Show | 7 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.3264-3431G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136820 | ||||||
| chr4:36136828
|
T | C | 74 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3264-3439A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136828 | ||||||
| chr4:36136885
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3264-3496A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136885 | ||||||
| chr4:36136921
|
C | A | 1 | a0001c0001t0003g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3264-3532G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136921 | ||||||
| chr4:36136921
|
C | T | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3264-3532G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136921 | ||||||
| chr4:36136925
|
C | T | 7 | a0001c0001t0005g0052a0001c0001t0005g0066a0001c0001t0005g0245others(4): Show | 7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3264-3536G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136925 | ||||||
| chr4:36136926
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3264-3537C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136926 | ||||||
| chr4:36136931
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3264-3542G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136931 | ||||||
| chr4:36136932
|
GCA | G | 105 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(102): Show | 107 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.3264-3545_3264-354 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136932 | ||||||
| chr4:36136932
|
GCACA | G | 139 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0149others(136): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.3264-3547_3264-354 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136932 | ||||||
| chr4:36136932
|
GCACACA | G | 3 | a0001c0001t0002g0220a0001c0003t0002g0107a0001c0012t0003g0060 | 3 | HG02300.hp2 HG03225.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3264-3549_3264-354 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136932 | ||||||
| chr4:36136934
|
A | G | 1 | a0001c0002t0001g0243 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3264-3545T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136934 | ||||||
| chr4:36136936
|
A | G | 65 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(62): Show | 67 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3264-3547T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136936 | ||||||
| chr4:36136938
|
A | G | 75 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(72): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3264-3549T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136938 | ||||||
| chr4:36136940
|
A | G | 74 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3264-3551T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136940 | ||||||
| chr4:36136942
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3264-3553T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136942 | ||||||
| chr4:36137008
|
A | G | 3 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0019 | 3 | HG01884.hp1 HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.3264-3619T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137008 | ||||||
| chr4:36137053
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0003g0118 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3264-3664T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137053 | ||||||
| chr4:36137127
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0003g0118 | 2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3264-3738C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137127 | ||||||
| chr4:36137278
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3889T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137278 | ||||||
| chr4:36137417
|
T | C | 1 | a0001c0005t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3264-4028A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137417 | ||||||
| chr4:36137547
|
T | C | 47 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0127others(44): Show | 48 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3264-4158A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137547 | ||||||
| chr4:36137631
|
T | C | 73 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3264-4242A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137631 | ||||||
| chr4:36137696
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-4307T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137696 | ||||||
| chr4:36138405
|
T | G | 13 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(10): Show | 13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3264-5016A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138405 | ||||||
| chr4:36138451
|
G | A | 73 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3264-5062C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138451 | ||||||
| chr4:36138748
|
T | G | 73 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(70): Show | 73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3264-5359A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138748 | ||||||
| chr4:36138957
|
T | G | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3264-5568A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138957 | ||||||
| chr4:36139035
|
T | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-5646A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139035 | ||||||
| chr4:36139104
|
CATTTT | C | 60 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0128others(57): Show | 63 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.3264-5720_3264-571 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139104 | ||||||
| chr4:36139111
|
T | C | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3264-5722A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139111 | ||||||
| chr4:36139287
|
C | T | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3264-5898G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139287 | ||||||
| chr4:36139300
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3264-5911A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139300 | ||||||
| chr4:36139455
|
T | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3264-6066A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139455 | ||||||
| chr4:36139520
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-6131C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139520 | ||||||
| chr4:36139551
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0002g0208 | 2 | NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.3264-6162A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139551 | ||||||
| chr4:36139565
|
C | T | 59 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0002g0110others(56): Show | 59 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.3264-6176G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139565 | ||||||
| chr4:36140101
|
A | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-6712T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140101 | ||||||
| chr4:36140134
|
A | ACAATACA others(7): Show |
2 | a0001c0001t0002g0136a0001c0001t0002g0140 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3264-6746_3264-674 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140134 | ||||||
| chr4:36140135
|
A | T | 3 | a0001c0005t0006g0104a0001c0005t0006g0105a0009c0014t0017g0088 | 3 | HG03130.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3264-6746T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140135 | ||||||
| chr4:36140136
|
C | A | 3 | a0001c0005t0006g0104a0001c0005t0006g0105a0009c0014t0017g0088 | 3 | HG03130.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3264-6747G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140136 | ||||||
| chr4:36140137
|
A | AC | 3 | a0001c0001t0002g0136a0001c0001t0002g0140a0001c0005t0006g0106 | 3 | HG01168.hp2 HG01169.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3264-6749_3264-674 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140137 | ||||||
| chr4:36140137
|
A | C | 3 | a0001c0005t0006g0104a0001c0005t0006g0105a0009c0014t0017g0088 | 3 | HG03130.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3264-6748T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140137 | ||||||
| chr4:36140139
|
T | C | 6 | a0001c0001t0002g0136a0001c0001t0002g0140a0001c0005t0006g0104others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3264-6750A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TAC | 72 | a0001c0001t0001g0045a0001c0001t0001g0069a0001c0001t0001g0082others(69): Show | 74 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.3264-6752_3264-675 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TACAC | 48 | a0001c0001t0001g0015a0001c0001t0001g0078a0001c0001t0001g0089others(45): Show | 49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.3264-6754_3264-675 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TACACAC | 15 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(12): Show | 15 | HG01167.hp1 HG01928.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.3264-6756_3264-675 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TACACACA others(1): Show |
7 | a0001c0001t0001g0199a0001c0001t0002g0176a0001c0001t0002g0218others(4): Show | 7 | HG01361.hp1 HG02074.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3264-6758_3264-675 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TACACACA others(3): Show |
18 | a0001c0001t0002g0011a0001c0001t0002g0138a0001c0001t0002g0172others(15): Show | 18 | HG00280.hp2 HG01081.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3264-6760_3264-675 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TACACACA others(5): Show |
30 | a0001c0001t0001g0179a0001c0001t0002g0049a0001c0001t0002g0131others(27): Show | 30 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.3264-6762_3264-675 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TACACACA others(7): Show |
8 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0135others(5): Show | 8 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.3264-6764_3264-675 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
T | TACACACA others(9): Show |
5 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0189others(2): Show | 5 | HG01952.hp2 HG02004.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-6766_3264-675 others(20): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140139
|
TAC | T | 8 | a0001c0001t0003g0235a0001c0001t0004g0092a0001c0001t0004g0103others(5): Show | 8 | HG01081.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3264-6752_3264-675 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | ||||||
| chr4:36140172
|
A | ACACACAC others(6): Show |
1 | a0001c0001t0002g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3264-6784_3264-678 others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140172 | ||||||
| chr4:36140261
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0236a0007c0010t0001g0237 | 3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3264-6872A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140261 | ||||||
| chr4:36140386
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3263+6910A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140386 | ||||||
| chr4:36140616
|
T | A | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3263+6680A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140616 | ||||||
| chr4:36140681
|
T | C | 92 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(89): Show | 92 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.3263+6615A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140681 | ||||||
| chr4:36140744
|
C | T | 1 | a0002c0006t0003g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3263+6552G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140744 | ||||||
| chr4:36141236
|
A | T | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3263+6060T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141236 | ||||||
| chr4:36141264
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3263+6032C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141264 | ||||||
| chr4:36141264
|
G | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+6032C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141264 | ||||||
| chr4:36141284
|
G | A | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3263+6012C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141284 | ||||||
| chr4:36141397
|
C | T | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3263+5899G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141397 | ||||||
| chr4:36141708
|
T | G | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3263+5588A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141708 | ||||||
| chr4:36141898
|
T | C | 1 | a0001c0004t0001g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3263+5398A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141898 | ||||||
| chr4:36142126
|
A | G | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3263+5170T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142126 | ||||||
| chr4:36142347
|
G | A | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3263+4949C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142347 | ||||||
| chr4:36142402
|
C | G | 1 | a0014c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3263+4894G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142402 | ||||||
| chr4:36142546
|
G | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4750C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142546 | ||||||
| chr4:36142567
|
T | C | 251 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3263+4729A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142567 | ||||||
| chr4:36142588
|
A | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4708T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142588 | ||||||
| chr4:36142593
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4703A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142593 | ||||||
| chr4:36142795
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4501A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142795 | ||||||
| chr4:36142797
|
A | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4499T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142797 | ||||||
| chr4:36142862
|
T | C | 1 | a0001c0001t0003g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3263+4434A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142862 | ||||||
| chr4:36142941
|
T | G | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4355A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142941 | ||||||
| chr4:36143080
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4216A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143080 | ||||||
| chr4:36143194
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3263+4102A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143194 | ||||||
| chr4:36143227
|
G | T | 197 | a0001c0001t0001g0045a0001c0001t0001g0069a0001c0001t0001g0089others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.3263+4069C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143227 | ||||||
| chr4:36143346
|
C | G | 74 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3263+3950G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143346 | ||||||
| chr4:36143547
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3263+3749C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143547 | ||||||
| chr4:36143718
|
A | G | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3263+3578T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143718 | ||||||
| chr4:36143758
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3263+3538G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143758 | ||||||
| chr4:36143776
|
C | T | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3520G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143776 | ||||||
| chr4:36143811
|
G | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3485C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143811 | ||||||
| chr4:36143840
|
C | T | 26 | a0001c0003t0001g0180a0001c0003t0001g0181a0001c0003t0001g0182others(23): Show | 26 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.3263+3456G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143840 | ||||||
| chr4:36143863
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3433A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143863 | ||||||
| chr4:36143989
|
T | C | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3307A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143989 | ||||||
| chr4:36144015
|
C | G | 5 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3263+3281G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144015 | ||||||
| chr4:36144084
|
T | C | 137 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0127others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.3263+3212A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144084 | ||||||
| chr4:36144085
|
A | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3263+3211T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144085 | ||||||
| chr4:36144140
|
T | C | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3263+3156A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144140 | ||||||
| chr4:36144202
|
A | AC | 19 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(16): Show | 19 | HG00280.hp1 HG00438.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.3263+3093_3263+309 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144202 | ||||||
| chr4:36144226
|
T | G | 1 | a0001c0002t0001g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3263+3070A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144226 | ||||||
| chr4:36144239
|
A | G | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3263+3057T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144239 | ||||||
| chr4:36144414
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3263+2882G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144414 | ||||||
| chr4:36144760
|
T | C | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3263+2536A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144760 | ||||||
| chr4:36145121
|
A | C | 57 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0002g0110others(54): Show | 57 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.3263+2175T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145121 | ||||||
| chr4:36145273
|
C | G | 73 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0202others(70): Show | 73 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.3263+2023G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145273 | ||||||
| chr4:36145286
|
G | A | 2 | a0001c0012t0003g0060a0001c0012t0003g0063 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+2010C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145286 | ||||||
| chr4:36145459
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3263+1837A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145459 | ||||||
| chr4:36145585
|
T | C | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3263+1711A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145585 | ||||||
| chr4:36145703
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3263+1593A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145703 | ||||||
| chr4:36145757
|
T | C | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3263+1539A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145757 | ||||||
| chr4:36145766
|
T | C | 137 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0127others(134): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.3263+1530A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145766 | ||||||
| chr4:36145817
|
C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3263+1479G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145817 | ||||||
| chr4:36146415
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3263+881C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146415 | ||||||
| chr4:36146669
|
T | C | 1 | a0001c0005t0006g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3263+627A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146669 | ||||||
| chr4:36146884
|
A | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3263+412T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146884 | ||||||
| chr4:36146930
|
C | T | 3 | a0001c0001t0004g0092a0001c0001t0004g0103a0001c0001t0023g0093 | 3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3263+366G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146930 | ||||||
| chr4:36147094
|
T | C | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3263+202A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36147094 | ||||||
| chr4:36147126
|
T | C | 1 | a0001c0002t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3263+170A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36147126 | ||||||
| chr4:36147215
|
T | C | 76 | a0001c0001t0001g0026a0001c0001t0001g0149a0001c0001t0001g0179others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3263+81A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36147215 | ||||||
| chr4:36147403
|
G | A | 251 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3200-44C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 18/32 | chr4 | 36147403 | ||||||
| chr4:36147491
|
C | T | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.3199+57G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 18/32 | chr4 | 36147491 | ||||||
| chr4:36147756
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3001-10G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36147756 | ||||||
| chr4:36147826
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3001-80A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36147826 | ||||||
| chr4:36148093
|
C | A | 1 | a0001c0001t0002g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3000+312G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148093 | ||||||
| chr4:36148183
|
A | T | 13 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(10): Show | 15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3000+222T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148183 | ||||||
| chr4:36148229
|
T | G | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3000+176A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148229 | ||||||
| chr4:36148388
|
A | T | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3000+17T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148388 | ||||||
| chr4:36148718
|
A | G | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2898-211T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36148718 | ||||||
| chr4:36148952
|
A | T | 186 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2898-445T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36148952 | ||||||
| chr4:36149092
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2898-585G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149092 | ||||||
| chr4:36149101
|
T | A | 2 | a0001c0001t0001g0149a0001c0001t0002g0208 | 2 | NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2898-594A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149101 | ||||||
| chr4:36149144
|
A | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2898-637T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149144 | ||||||
| chr4:36149185
|
CTT | C | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2898-680_2898-679d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149185 | ||||||
| chr4:36149226
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2898-719A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149226 | ||||||
| chr4:36149247
|
C | G | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2898-740G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149247 | ||||||
| chr4:36149311
|
CCAGT | C | 74 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.2898-808_2898-805d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149311 | ||||||
| chr4:36149333
|
C | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2898-826G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149333 | ||||||
| chr4:36149354
|
T | C | 3 | a0004c0008t0001g0232a0004c0008t0001g0233a0004c0008t0021g0231 | 3 | NA18944.hp1 NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2898-847A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149354 | ||||||
| chr4:36149481
|
T | C | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2898-974A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149481 | ||||||
| chr4:36149557
|
C | A | 9 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0078others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.2898-1050G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149557 | ||||||
| chr4:36149775
|
A | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2897+1125T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149775 | ||||||
| chr4:36149830
|
T | C | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0002c0006t0001g0119 | 3 | HG01167.hp2 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2897+1070A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149830 | ||||||
| chr4:36149998
|
T | C | 13 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(10): Show | 15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2897+902A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149998 | ||||||
| chr4:36150019
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2897+881C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150019 | ||||||
| chr4:36150021
|
C | T | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2897+879G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150021 | ||||||
| chr4:36150164
|
T | C | 6 | a0001c0001t0001g0082a0001c0001t0002g0021a0001c0001t0002g0022others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2897+736A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150164 | ||||||
| chr4:36150215
|
A | G | 183 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2897+685T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150215 | ||||||
| chr4:36150316
|
A | G | 183 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2897+584T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150316 | ||||||
| chr4:36150343
|
C | T | 186 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2897+557G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150343 | ||||||
| chr4:36150693
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2897+207A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150693 | ||||||
| chr4:36150713
|
A | G | 1 | a0001c0001t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2897+187T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150713 | ||||||
| chr4:36150744
|
G | C | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2897+156C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150744 | ||||||
| chr4:36150805
|
C | T | 3 | a0002c0006t0001g0125a0002c0006t0001g0126a0010c0015t0010g0275 | 3 | HG02818.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2897+95G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150805 | ||||||
| chr4:36151506
|
C | T | 183 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2753-462G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151506 | ||||||
| chr4:36151587
|
G | T | 2 | a0001c0002t0001g0028a0001c0002t0001g0029 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2753-543C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151587 | ||||||
| chr4:36151588
|
A | C | 74 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(71): Show | 74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.2753-544T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151588 | ||||||
| chr4:36151686
|
G | A | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2753-642C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151686 | ||||||
| chr4:36151729
|
G | T | 186 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(183): Show | 186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.2753-685C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151729 | ||||||
| chr4:36151997
|
C | T | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2753-953G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151997 | ||||||
| chr4:36152010
|
T | C | 45 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0127others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2753-966A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152010 | ||||||
| chr4:36152032
|
G | A | 1 | a0001c0005t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2753-988C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152032 | ||||||
| chr4:36152182
|
T | C | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2753-1138A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152182 | ||||||
| chr4:36152459
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2753-1415C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152459 | ||||||
| chr4:36152514
|
T | C | 5 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2753-1470A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152514 | ||||||
| chr4:36152673
|
T | TA | 177 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(174): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2753-1630dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152673 | ||||||
| chr4:36152673
|
T | TAA | 22 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(19): Show | 22 | HG00438.hp1 HG01109.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.2753-1631_2753-163 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152673 | ||||||
| chr4:36152933
|
T | C | 199 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(196): Show | 201 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.2753-1889A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152933 | ||||||
| chr4:36153093
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2753-2049C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153093 | ||||||
| chr4:36153179
|
C | A | 1 | a0001c0001t0002g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2753-2135G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153179 | ||||||
| chr4:36153472
|
G | T | 13 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(10): Show | 15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2753-2428C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153472 | ||||||
| chr4:36153499
|
T | C | 252 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2753-2455A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153499 | ||||||
| chr4:36153812
|
C | T | 198 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.2753-2768G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153812 | ||||||
| chr4:36153907
|
T | G | 274 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.2753-2863A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153907 | ||||||
| chr4:36153968
|
C | T | 1 | a0002c0006t0001g0120 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2753-2924G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153968 | ||||||
| chr4:36153971
|
A | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2753-2927T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153971 | ||||||
| chr4:36154121
|
T | C | 8 | a0002c0006t0001g0120a0002c0006t0001g0122a0002c0006t0001g0124others(5): Show | 8 | HG02258.hp1 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2753-3077A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154121 | ||||||
| chr4:36154253
|
G | T | 16 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0005t0001g0001others(13): Show | 18 | HG00738.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2753-3209C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154253 | ||||||
| chr4:36154287
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2753-3243G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154287 | ||||||
| chr4:36154339
|
A | G | 4 | a0001c0001t0002g0011a0001c0001t0002g0068a0001c0001t0002g0207others(1): Show | 4 | HG01106.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2753-3295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154339 | ||||||
| chr4:36154446
|
C | T | 7 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(4): Show | 9 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2753-3402G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154446 | ||||||
| chr4:36154501
|
A | G | 3 | a0001c0001t0001g0179a0001c0001t0002g0131a0001c0001t0002g0155 | 3 | HG02083.hp2 HG02132.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.2753-3457T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154501 | ||||||
| chr4:36154893
|
T | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(48): Show | 52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.2752+3837A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154893 | ||||||
| chr4:36154934
|
A | G | 13 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(10): Show | 15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2752+3796T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154934 | ||||||
| chr4:36155041
|
G | T | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2752+3689C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155041 | ||||||
| chr4:36155173
|
G | A | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2752+3557C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155173 | ||||||
| chr4:36155288
|
T | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(48): Show | 52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.2752+3442A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155288 | ||||||
| chr4:36155329
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2752+3401A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155329 | ||||||
| chr4:36155425
|
G | T | 3 | a0001c0001t0001g0069a0001c0001t0003g0116a0001c0001t0003g0238 | 3 | HG02145.hp2 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2752+3305C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155425 | ||||||
| chr4:36155651
|
AT | A | 27 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0202others(24): Show | 29 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.2752+3078delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155651 | ||||||
| chr4:36155655
|
T | A | 20 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(17): Show | 20 | HG00438.hp1 HG01255.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2752+3075A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155655 | ||||||
| chr4:36155693
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+3037C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155693 | ||||||
| chr4:36155772
|
C | T | 72 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2752+2958G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155772 | ||||||
| chr4:36155777
|
A | T | 72 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.2752+2953T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155777 | ||||||
| chr4:36156148
|
G | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2752+2582C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156148 | ||||||
| chr4:36156198
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+2532G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156198 | ||||||
| chr4:36156265
|
G | A | 1 | a0001c0001t0023g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2752+2465C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156265 | ||||||
| chr4:36156334
|
A | AGG | 19 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(16): Show | 19 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.2752+2394_2752+239 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156334 | ||||||
| chr4:36156343
|
G | T | 1 | a0001c0002t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2752+2387C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156343 | ||||||
| chr4:36156351
|
GAGAGAGG others(67): Show |
G | 16 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(13): Show | 16 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.2752+2305_2752+237 others(78): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156351 | ||||||
| chr4:36156351
|
GAGAGAGG others(71): Show |
G | 3 | a0004c0008t0001g0232a0004c0008t0001g0233a0004c0008t0021g0231 | 3 | NA18944.hp1 NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2752+2301_2752+237 others(82): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156351 | ||||||
| chr4:36156354
|
A | AGAGG | 19 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0202others(16): Show | 19 | HG01074.hp1 HG01109.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2752+2372_2752+237 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156354 | ||||||
| chr4:36156354
|
A | AGAGGGAG others(1): Show |
131 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0086others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2752+2368_2752+237 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156354 | ||||||
| chr4:36156354
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2752+2376T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156354 | ||||||
| chr4:36156358
|
G | A | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2372C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156358 | ||||||
| chr4:36156374
|
GGGGAAA | G | 64 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(61): Show | 65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2752+2350_2752+235 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156374 | ||||||
| chr4:36156376
|
G | A | 3 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0002g0023 | 5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2354C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156376 | ||||||
| chr4:36156378
|
A | G | 4 | a0001c0001t0010g0274a0001c0005t0001g0001a0001c0005t0001g0002others(1): Show | 6 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2752+2352T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156378 | ||||||
| chr4:36156379
|
A | G | 3 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0002g0023 | 5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2351T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156379 | ||||||
| chr4:36156382
|
A | G | 6 | a0001c0002t0001g0017a0001c0005t0001g0001a0001c0005t0001g0002others(3): Show | 8 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2752+2348T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156382 | ||||||
| chr4:36156384
|
A | G | 67 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(64): Show | 70 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2752+2346T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156384 | ||||||
| chr4:36156386
|
A | G | 3 | a0001c0002t0001g0017a0001c0012t0003g0060a0019c0025t0018g0209 | 3 | HG02015.hp2 HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2752+2344T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156386 | ||||||
| chr4:36156387
|
G | A | 3 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0002g0023 | 5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2343C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156387 | ||||||
| chr4:36156388
|
A | G | 64 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(61): Show | 65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2752+2342T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156388 | ||||||
| chr4:36156389
|
G | GAGAA | 7 | a0001c0001t0002g0168a0001c0001t0002g0171a0001c0001t0002g0186others(4): Show | 7 | HG01928.hp2 HG01952.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.2752+2337_2752+234 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156389 | ||||||
| chr4:36156389
|
G | GAGAAAGA others(21): Show |
1 | a0001c0001t0003g0227 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2752+2313_2752+234 others(32): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156389 | ||||||
| chr4:36156389
|
GAGAA | G | 5 | a0001c0001t0003g0162a0001c0001t0003g0239a0001c0001t0003g0242others(2): Show | 5 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2337_2752+234 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156389 | ||||||
| chr4:36156390
|
A | G | 67 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(64): Show | 68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.2752+2340T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156390 | ||||||
| chr4:36156391
|
GAA | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0002t0001g0044 | 3 | HG02683.hp1 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2752+2337_2752+233 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | ||||||
| chr4:36156391
|
GAAAGAAA others(7): Show |
G | 2 | a0001c0002t0001g0017a0001c0012t0003g0060 | 2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2325_2752+233 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | ||||||
| chr4:36156391
|
GAAAGAAA others(11): Show |
G | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2321_2752+233 others(22): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | ||||||
| chr4:36156391
|
GAAAGAAA others(27): Show |
G | 151 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0086others(148): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.2752+2305_2752+233 others(38): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | ||||||
| chr4:36156391
|
GAAAGAAA others(35): Show |
G | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2752+2297_2752+233 others(46): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | ||||||
| chr4:36156393
|
A | G | 9 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0002g0023others(6): Show | 11 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2752+2337T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156393 | ||||||
| chr4:36156397
|
A | G | 64 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(61): Show | 67 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2752+2333T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156397 | ||||||
| chr4:36156401
|
A | G | 66 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(63): Show | 69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2752+2329T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156401 | ||||||
| chr4:36156405
|
A | G | 64 | a0001c0001t0001g0015a0001c0001t0001g0064a0001c0001t0001g0065others(61): Show | 65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2752+2325T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156405 | ||||||
| chr4:36156406
|
A | G | 2 | a0001c0002t0001g0017a0001c0012t0003g0060 | 2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2324T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156406 | ||||||
| chr4:36156409
|
A | G | 3 | a0001c0005t0001g0024a0001c0005t0001g0039a0001c0005t0001g0143 | 3 | HG01168.hp1 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2752+2321T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156409 | ||||||
| chr4:36156410
|
A | G | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2320T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156410 | ||||||
| chr4:36156411
|
GAA | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0002t0001g0044 | 3 | HG02683.hp1 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2752+2317_2752+231 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156411 | ||||||
| chr4:36156413
|
A | G | 3 | a0001c0002t0001g0017a0001c0005t0001g0024a0001c0012t0003g0060 | 3 | HG02015.hp2 HG03225.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2752+2317T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156413 | ||||||
| chr4:36156417
|
A | G | 3 | a0001c0002t0001g0017a0001c0012t0003g0060a0019c0025t0018g0209 | 3 | HG02015.hp2 HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2752+2313T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156417 | ||||||
| chr4:36156419
|
GAAAGAAA others(21): Show |
G | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+2283_2752+231 others(32): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156419 | ||||||
| chr4:36156421
|
A | G | 3 | a0001c0002t0001g0017a0001c0012t0003g0060a0019c0025t0018g0209 | 3 | HG02015.hp2 HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2752+2309T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156421 | ||||||
| chr4:36156423
|
GAAAGAAA others(7): Show |
G | 53 | a0001c0001t0001g0015a0001c0001t0001g0128a0001c0001t0002g0018others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2752+2293_2752+230 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156423 | ||||||
| chr4:36156423
|
GAAAGAAA others(17): Show |
G | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0003g0272others(1): Show | 4 | HG01243.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2752+2283_2752+230 others(28): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156423 | ||||||
| chr4:36156425
|
A | G | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2305T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156425 | ||||||
| chr4:36156429
|
A | G | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2752+2301T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156429 | ||||||
| chr4:36156435
|
GAAAGAAA others(5): Show |
G | 3 | a0001c0005t0003g0102a0001c0005t0012g0008a0009c0014t0017g0088 | 3 | HG01433.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2752+2283_2752+229 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156435 | ||||||
| chr4:36156435
|
GAAAGAAA others(20): Show |
G | 3 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0002t0001g0044 | 3 | HG02683.hp1 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2752+2268_2752+229 others(31): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156435 | ||||||
| chr4:36156439
|
GAAAGAGA others(1): Show |
G | 4 | a0001c0005t0001g0001a0001c0005t0002g0023a0001c0005t0006g0104others(1): Show | 5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2283_2752+229 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156439 | ||||||
| chr4:36156441
|
A | G | 2 | a0001c0002t0001g0017a0001c0012t0003g0060 | 2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2289T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156441 | ||||||
| chr4:36156441
|
AAG | A | 53 | a0001c0001t0001g0015a0001c0001t0001g0128a0001c0001t0002g0018others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2752+2287_2752+228 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156441 | ||||||
| chr4:36156443
|
G | A | 2 | a0001c0002t0001g0017a0001c0012t0003g0060 | 2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2287C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156443 | ||||||
| chr4:36156443
|
GAGAA | G | 4 | a0001c0005t0001g0024a0001c0005t0001g0039a0001c0005t0001g0041others(1): Show | 4 | HG01168.hp1 HG01516.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2752+2283_2752+228 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156443 | ||||||
| chr4:36156445
|
G | A | 2 | a0001c0005t0001g0002a0001c0005t0006g0106 | 3 | HG02818.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2752+2285C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156445 | ||||||
| chr4:36156447
|
A | G | 2 | a0001c0005t0001g0002a0001c0005t0006g0106 | 3 | HG02818.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2752+2283T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156447 | ||||||
| chr4:36156461
|
GA | G | 235 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2752+2268delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156461 | ||||||
| chr4:36156510
|
G | GAGGA | 183 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2752+2216_2752+221 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156510 | ||||||
| chr4:36157111
|
A | C | 238 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2752+1619T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157111 | ||||||
| chr4:36157290
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2752+1440A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157290 | ||||||
| chr4:36157381
|
CA | C | 15 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(12): Show | 17 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2752+1348delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157381 | ||||||
| chr4:36157381
|
CAA | C | 225 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2752+1347_2752+134 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157381 | ||||||
| chr4:36157381
|
CAAA | C | 11 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0004t0002g0265others(8): Show | 11 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2752+1346_2752+134 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157381 | ||||||
| chr4:36157453
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2752+1277A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157453 | ||||||
| chr4:36157471
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2752+1259T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157471 | ||||||
| chr4:36157496
|
C | T | 238 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2752+1234G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157496 | ||||||
| chr4:36157797
|
T | TTA | 21 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0001t0001g0087others(18): Show | 21 | HG00438.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2752+931_2752+932d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157797 | ||||||
| chr4:36157833
|
T | C | 1 | a0011c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2752+897A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157833 | ||||||
| chr4:36157866
|
A | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0002t0001g0013 | 3 | HG01884.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2752+864T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157866 | ||||||
| chr4:36157928
|
TATACCAC others(7): Show |
T | 3 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2752+788_2752+801d others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157928 | ||||||
| chr4:36158000
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+730G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158000 | ||||||
| chr4:36158420
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2752+310C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158420 | ||||||
| chr4:36158620
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2752+110T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158620 | ||||||
| chr4:36158718
|
G | T | 237 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2752+12C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158718 | ||||||
| chr4:36158981
|
G | A | 48 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0127others(45): Show | 49 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.2618-117C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36158981 | ||||||
| chr4:36159066
|
C | T | 2 | a0001c0002t0001g0003a0001c0002t0001g0166 | 3 | HG02040.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2618-202G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159066 | ||||||
| chr4:36159087
|
T | C | 11 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(8): Show | 11 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2618-223A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159087 | ||||||
| chr4:36159090
|
T | C | 2 | a0001c0001t0001g0202a0001c0001t0003g0153 | 2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2618-226A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159090 | ||||||
| chr4:36159138
|
C | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2617+193G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159138 | ||||||
| chr4:36159552
|
T | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2443-47A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36159552 | ||||||
| chr4:36159731
|
G | C | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2443-226C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36159731 | ||||||
| chr4:36160016
|
C | T | 2 | a0001c0002t0001g0047a0001c0002t0001g0197 | 2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2442+443G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160016 | ||||||
| chr4:36160066
|
C | A | 6 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(3): Show | 6 | HG02165.hp1 HG03927.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.2442+393G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160066 | ||||||
| chr4:36160330
|
C | T | 1 | a0001c0003t0002g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2442+129G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160330 | ||||||
| chr4:36160433
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2442+26C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160433 | ||||||
| chr4:36160651
|
C | CA | 237 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2260-11dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36160651 | ||||||
| chr4:36160743
|
T | C | 19 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(16): Show | 19 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.2260-102A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36160743 | ||||||
| chr4:36161146
|
AAC | A | 14 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0151others(11): Show | 16 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.2259+317_2259+318d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | ||||||
| chr4:36161146
|
AACAC | A | 7 | a0001c0001t0003g0157a0001c0001t0003g0158a0001c0005t0006g0104others(4): Show | 7 | HG02818.hp2 HG03130.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259+315_2259+318d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | ||||||
| chr4:36161146
|
AACACACA others(1): Show |
A | 183 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2259+311_2259+318d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | ||||||
| chr4:36161146
|
AACACACA others(3): Show |
A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2259+309_2259+318d others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | ||||||
| chr4:36161172
|
C | T | 233 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(230): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2259+293G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161172 | ||||||
| chr4:36161174
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2259+291G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161174 | ||||||
| chr4:36161211
|
A | C | 237 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2259+254T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161211 | ||||||
| chr4:36161301
|
G | A | 237 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2259+164C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161301 | ||||||
| chr4:36161367
|
G | T | 1 | a0001c0002t0001g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2259+98C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161367 | ||||||
| chr4:36161386
|
C | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2259+79G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161386 | ||||||
| chr4:36161408
|
C | T | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0002c0006t0001g0119others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2259+57G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161408 | ||||||
| chr4:36161432
|
A | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2259+33T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161432 | ||||||
| chr4:36161579
|
T | C | 1 | a0001c0001t0003g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2174-29A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161579 | ||||||
| chr4:36161793
|
CA | C | 20 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(17): Show | 20 | HG00323.hp1 HG01361.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2174-244delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | ||||||
| chr4:36161793
|
CAAAA | C | 12 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(9): Show | 14 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2174-247_2174-244d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | ||||||
| chr4:36161793
|
CAAAAAA | C | 17 | a0001c0001t0001g0045a0001c0001t0005g0066a0001c0002t0001g0243others(14): Show | 17 | HG00735.hp2 HG01346.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.2174-249_2174-244d others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | ||||||
| chr4:36161793
|
CAAAAAAA | C | 138 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0050others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2174-250_2174-244d others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | ||||||
| chr4:36161793
|
CAAAAAAA others(1): Show |
C | 77 | a0001c0001t0001g0026a0001c0001t0001g0089a0001c0001t0001g0149others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.2174-251_2174-244d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | ||||||
| chr4:36161793
|
CAAAAAAA others(7): Show |
C | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2174-257_2174-244d others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | ||||||
| chr4:36161831
|
T | G | 237 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2174-281A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161831 | ||||||
| chr4:36161905
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2174-355C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161905 | ||||||
| chr4:36162006
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2174-456C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162006 | ||||||
| chr4:36162013
|
C | T | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0002c0006t0001g0119others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2174-463G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162013 | ||||||
| chr4:36162094
|
C | T | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0151others(3): Show | 6 | HG00741.hp2 HG01243.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2174-544G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162094 | ||||||
| chr4:36162103
|
G | A | 189 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(186): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.2174-553C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162103 | ||||||
| chr4:36162107
|
CA | C | 230 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(227): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2174-558delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162107 | ||||||
| chr4:36162132
|
TTACTTAA others(1): Show |
T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2174-590_2174-583d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162132 | ||||||
| chr4:36162139
|
AAT | A | 232 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(229): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2174-591_2174-590d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162139 | ||||||
| chr4:36162139
|
AATAT | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2174-593_2174-590d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162139 | ||||||
| chr4:36162143
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2174-593A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162143 | ||||||
| chr4:36162252
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2174-702G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162252 | ||||||
| chr4:36162451
|
T | C | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2174-901A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162451 | ||||||
| chr4:36162452
|
C | A | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2174-902G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162452 | ||||||
| chr4:36162522
|
A | G | 5 | a0001c0003t0003g0083a0001c0003t0003g0085a0001c0003t0003g0228others(2): Show | 5 | HG01074.hp1 HG01257.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2174-972T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162522 | ||||||
| chr4:36162604
|
C | CT | 13 | a0001c0001t0001g0127a0001c0005t0001g0001a0001c0005t0001g0002others(10): Show | 15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2174-1055dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | ||||||
| chr4:36162604
|
C | CTT | 36 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0087others(33): Show | 37 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2174-1056_2174-105 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | ||||||
| chr4:36162604
|
C | CTTT | 20 | a0001c0001t0001g0050a0001c0001t0001g0086a0001c0001t0002g0255others(17): Show | 20 | HG00099.hp2 HG01081.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2174-1057_2174-105 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | ||||||
| chr4:36162604
|
C | CTTTT | 174 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0064others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.2174-1058_2174-105 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | ||||||
| chr4:36162604
|
C | CTTTTT | 5 | a0001c0001t0002g0156a0001c0001t0002g0222a0001c0001t0002g0251others(2): Show | 5 | HG02015.hp1 HG02647.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2174-1059_2174-105 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | ||||||
| chr4:36162878
|
G | A | 234 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2174-1328C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162878 | ||||||
| chr4:36162917
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2174-1367G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162917 | ||||||
| chr4:36163006
|
C | T | 183 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(180): Show | 183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2174-1456G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163006 | ||||||
| chr4:36163244
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2173+1670C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163244 | ||||||
| chr4:36163295
|
C | T | 238 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(235): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2173+1619G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163295 | ||||||
| chr4:36163442
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0236a0007c0010t0001g0237 | 3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2173+1472A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163442 | ||||||
| chr4:36163538
|
A | G | 235 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2173+1376T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163538 | ||||||
| chr4:36163590
|
G | A | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2173+1324C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163590 | ||||||
| chr4:36163635
|
C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2173+1279G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163635 | ||||||
| chr4:36163729
|
C | T | 18 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0086others(15): Show | 18 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2173+1185G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163729 | ||||||
| chr4:36163730
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2173+1184C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163730 | ||||||
| chr4:36163779
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2173+1135T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163779 | ||||||
| chr4:36164262
|
A | C | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2173+652T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164262 | ||||||
| chr4:36164551
|
T | A | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2173+363A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164551 | ||||||
| chr4:36164823
|
C | A | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0002c0006t0001g0119others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2173+91G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164823 | ||||||
| chr4:36164856
|
G | A | 3 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2173+58C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164856 | ||||||
| chr4:36165142
|
G | C | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1974-29C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165142 | ||||||
| chr4:36165155
|
A | G | 3 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096 | 3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1974-42T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165155 | ||||||
| chr4:36165179
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1974-66C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165179 | ||||||
| chr4:36165498
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1974-385G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165498 | ||||||
| chr4:36166135
|
G | A | 22 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0151others(19): Show | 24 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1973+797C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166135 | ||||||
| chr4:36166171
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1973+761T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166171 | ||||||
| chr4:36166358
|
T | C | 16 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096others(13): Show | 18 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1973+574A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166358 | ||||||
| chr4:36166659
|
C | CA | 9 | a0001c0001t0001g0050a0001c0001t0001g0149a0001c0001t0001g0193others(6): Show | 9 | HG00438.hp1 HG00741.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1973+272dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166659 | ||||||
| chr4:36166914
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1973+18A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166914 | ||||||
| chr4:36167084
|
C | CA | 22 | a0001c0001t0001g0114a0001c0001t0002g0211a0001c0001t0003g0098others(19): Show | 22 | HG01099.hp1 HG01109.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1858-38dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167084 | ||||||
| chr4:36167084
|
CAAAA | C | 81 | a0001c0001t0001g0089a0001c0001t0001g0179a0001c0001t0001g0199others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.1858-41_1858-38del others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167084 | ||||||
| chr4:36167207
|
C | T | 1 | a0001c0002t0001g0243 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1858-160G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167207 | ||||||
| chr4:36167212
|
G | A | 1 | a0001c0005t0001g0024 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1858-165C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167212 | ||||||
| chr4:36167453
|
C | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-406G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167453 | ||||||
| chr4:36167598
|
T | A | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1858-551A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167598 | ||||||
| chr4:36167813
|
C | A | 1 | a0001c0001t0002g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1858-766G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167813 | ||||||
| chr4:36167902
|
C | G | 1 | a0001c0001t0003g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1858-855G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167902 | ||||||
| chr4:36168012
|
CA | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0078others(8): Show | 11 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-966delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168012 | ||||||
| chr4:36168309
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1858-1262A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168309 | ||||||
| chr4:36168532
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1858-1485C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168532 | ||||||
| chr4:36168685
|
G | A | 2 | a0001c0001t0005g0245a0001c0001t0005g0246 | 2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1858-1638C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168685 | ||||||
| chr4:36168824
|
T | C | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1858-1777A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168824 | ||||||
| chr4:36168834
|
T | C | 1 | a0001c0002t0001g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1858-1787A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168834 | ||||||
| chr4:36169076
|
G | GA | 19 | a0001c0001t0002g0151a0001c0001t0003g0094a0001c0001t0003g0095others(16): Show | 21 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1858-2030dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169076 | ||||||
| chr4:36169459
|
T | C | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1858-2412A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169459 | ||||||
| chr4:36169532
|
CT | C | 90 | a0001c0001t0001g0089a0001c0001t0001g0149a0001c0001t0001g0179others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1858-2486delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169532 | ||||||
| chr4:36169578
|
T | C | 19 | a0001c0001t0002g0151a0001c0001t0003g0094a0001c0001t0003g0095others(16): Show | 21 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1858-2531A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169578 | ||||||
| chr4:36169834
|
T | G | 8 | a0001c0001t0002g0011a0001c0001t0002g0068a0001c0001t0002g0207others(5): Show | 8 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1858-2787A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169834 | ||||||
| chr4:36170081
|
A | T | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0002c0006t0001g0119others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-3034T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170081 | ||||||
| chr4:36170366
|
T | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1858-3319A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170366 | ||||||
| chr4:36170392
|
A | G | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1858-3345T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170392 | ||||||
| chr4:36170602
|
A | G | 22 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0002g0151others(19): Show | 24 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1858-3555T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170602 | ||||||
| chr4:36170867
|
A | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1858-3820T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170867 | ||||||
| chr4:36171277
|
CCAA | C | 3 | a0001c0001t0004g0092a0001c0001t0004g0103a0001c0001t0023g0093 | 3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1858-4233_1858-423 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171277 | ||||||
| chr4:36171351
|
A | T | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1858-4304T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171351 | ||||||
| chr4:36171357
|
C | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-4310G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171357 | ||||||
| chr4:36171513
|
A | C | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1858-4466T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171513 | ||||||
| chr4:36171534
|
T | G | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1858-4487A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171534 | ||||||
| chr4:36171592
|
G | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-4545C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171592 | ||||||
| chr4:36171784
|
TG | T | 11 | a0001c0001t0001g0086a0001c0001t0001g0087a0002c0006t0001g0119others(8): Show | 11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-4738delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171784 | ||||||
| chr4:36171793
|
T | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1858-4746A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171793 | ||||||
| chr4:36171865
|
T | G | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1858-4818A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171865 | ||||||
| chr4:36171931
|
G | C | 15 | a0001c0004t0001g0062a0001c0004t0001g0090a0001c0004t0001g0269others(12): Show | 15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1858-4884C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171931 | ||||||
| chr4:36172243
|
T | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-5196A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172243 | ||||||
| chr4:36172329
|
T | A | 1 | a0001c0001t0019g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1858-5282A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172329 | ||||||
| chr4:36172386
|
A | T | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1858-5339T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172386 | ||||||
| chr4:36172539
|
T | A | 1 | a0001c0002t0001g0234 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1857+5288A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172539 | ||||||
| chr4:36172714
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1857+5113T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172714 | ||||||
| chr4:36172918
|
C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1857+4909G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172918 | ||||||
| chr4:36172928
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1857+4899G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172928 | ||||||
| chr4:36172940
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1857+4887A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172940 | ||||||
| chr4:36173385
|
A | C | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1857+4442T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173385 | ||||||
| chr4:36173590
|
ATAAAG | A | 20 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(17): Show | 20 | HG01243.hp1 HG01255.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1857+4232_1857+423 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173590 | ||||||
| chr4:36173696
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1857+4131T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173696 | ||||||
| chr4:36173963
|
C | A | 3 | a0001c0001t0001g0050a0001c0001t0002g0214a0001c0002t0001g0166 | 3 | HG00140.hp2 HG02165.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1857+3864G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173963 | ||||||
| chr4:36173995
|
C | T | 39 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(36): Show | 40 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1857+3832G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173995 | ||||||
| chr4:36174315
|
T | A | 1 | a0001c0004t0003g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1857+3512A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174315 | ||||||
| chr4:36174540
|
A | C | 12 | a0001c0001t0001g0114a0001c0001t0003g0097a0001c0001t0003g0098others(9): Show | 12 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1857+3287T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174540 | ||||||
| chr4:36174606
|
G | T | 1 | a0001c0001t0004g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1857+3221C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174606 | ||||||
| chr4:36174824
|
C | T | 1 | a0001c0002t0001g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1857+3003G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174824 | ||||||
| chr4:36174834
|
C | T | 1 | a0001c0001t0003g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1857+2993G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174834 | ||||||
| chr4:36175250
|
C | T | 1 | a0001c0005t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1857+2577G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175250 | ||||||
| chr4:36175388
|
C | T | 2 | a0001c0001t0001g0015a0001c0002t0001g0016 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1857+2439G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175388 | ||||||
| chr4:36175495
|
C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1857+2332G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175495 | ||||||
| chr4:36175866
|
A | G | 5 | a0001c0001t0002g0186a0001c0001t0003g0159a0001c0001t0003g0239others(2): Show | 5 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857+1961T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175866 | ||||||
| chr4:36175885
|
C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1857+1942G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175885 | ||||||
| chr4:36175956
|
C | T | 5 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0135others(2): Show | 5 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857+1871G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175956 | ||||||
| chr4:36176024
|
C | T | 1 | a0001c0001t0007g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1857+1803G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176024 | ||||||
| chr4:36176240
|
TA | T | 250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1857+1586delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176240 | ||||||
| chr4:36176289
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1857+1538A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176289 | ||||||
| chr4:36176579
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1857+1248G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176579 | ||||||
| chr4:36176613
|
T | C | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1857+1214A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176613 | ||||||
| chr4:36176643
|
G | A | 5 | a0001c0001t0002g0011a0001c0001t0002g0068a0001c0001t0002g0207others(2): Show | 5 | HG00438.hp2 HG01106.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857+1184C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176643 | ||||||
| chr4:36176868
|
T | C | 2 | a0001c0001t0002g0156a0001c0001t0002g0251 | 2 | HG02015.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1857+959A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176868 | ||||||
| chr4:36177093
|
TA | T | 3 | a0001c0001t0004g0092a0001c0001t0004g0103a0001c0001t0023g0093 | 3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1857+733delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177093 | ||||||
| chr4:36177535
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1857+292G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177535 | ||||||
| chr4:36177721
|
T | C | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1857+106A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177721 | ||||||
| chr4:36177814
|
T | C | 1 | a0001c0001t0003g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1857+13A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177814 | ||||||
| chr4:36178166
|
C | A | 1 | a0001c0001t0011g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1679-161G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178166 | ||||||
| chr4:36178237
|
T | C | 1 | a0001c0001t0002g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1679-232A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178237 | ||||||
| chr4:36178402
|
C | T | 76 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1679-397G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178402 | ||||||
| chr4:36178417
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1679-412A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178417 | ||||||
| chr4:36178558
|
C | A | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1679-553G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178558 | ||||||
| chr4:36178814
|
G | A | 254 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1679-809C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178814 | ||||||
| chr4:36179264
|
G | T | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-1259C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179264 | ||||||
| chr4:36179267
|
G | A | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-1262C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179267 | ||||||
| chr4:36179307
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1679-1302T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179307 | ||||||
| chr4:36179314
|
A | G | 2 | a0002c0006t0001g0122a0002c0006t0001g0124 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1679-1309T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179314 | ||||||
| chr4:36179433
|
G | A | 27 | a0001c0003t0001g0180a0001c0003t0001g0181a0001c0003t0001g0182others(24): Show | 27 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1679-1428C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179433 | ||||||
| chr4:36179489
|
G | A | 271 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(268): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1679-1484C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179489 | ||||||
| chr4:36179544
|
C | A | 1 | a0001c0001t0003g0239 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1679-1539G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179544 | ||||||
| chr4:36179774
|
G | A | 1 | a0001c0002t0001g0003 | 2 | HG02040.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1679-1769C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179774 | ||||||
| chr4:36179863
|
C | T | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1679-1858G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179863 | ||||||
| chr4:36179938
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0002g0208 | 2 | NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1679-1933G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179938 | ||||||
| chr4:36180088
|
C | T | 2 | a0001c0001t0003g0099a0001c0001t0003g0115 | 2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1679-2083G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180088 | ||||||
| chr4:36180158
|
G | A | 3 | a0001c0002t0001g0003a0001c0004t0001g0062a0001c0004t0001g0090 | 4 | HG02040.hp2 HG02155.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-2153C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180158 | ||||||
| chr4:36180267
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1679-2262G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180267 | ||||||
| chr4:36180276
|
G | A | 6 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(3): Show | 6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-2271C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180276 | ||||||
| chr4:36180560
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1679-2555G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180560 | ||||||
| chr4:36180577
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1679-2572T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180577 | ||||||
| chr4:36180686
|
A | C | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1679-2681T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180686 | ||||||
| chr4:36180688
|
T | C | 15 | a0001c0004t0001g0062a0001c0004t0001g0090a0001c0004t0001g0269others(12): Show | 15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1679-2683A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180688 | ||||||
| chr4:36180720
|
C | A | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1679-2715G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180720 | ||||||
| chr4:36181092
|
C | T | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1679-3087G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181092 | ||||||
| chr4:36181196
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1679-3191G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181196 | ||||||
| chr4:36181254
|
G | A | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-3249C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181254 | ||||||
| chr4:36181367
|
G | C | 1 | a0001c0004t0003g0266 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1679-3362C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181367 | ||||||
| chr4:36181401
|
AT | A | 21 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(18): Show | 21 | HG01243.hp1 HG01255.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1679-3397delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181401 | ||||||
| chr4:36181403
|
T | A | 234 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1679-3398A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181403 | ||||||
| chr4:36181439
|
A | G | 1 | a0001c0002t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1679-3434T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181439 | ||||||
| chr4:36181687
|
C | T | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1679-3682G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181687 | ||||||
| chr4:36181826
|
A | G | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1679-3821T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181826 | ||||||
| chr4:36181889
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1679-3884T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181889 | ||||||
| chr4:36181985
|
G | A | 1 | a0001c0001t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1679-3980C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181985 | ||||||
| chr4:36182257
|
C | G | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1679-4252G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182257 | ||||||
| chr4:36182364
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1679-4359G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182364 | ||||||
| chr4:36182385
|
C | T | 51 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(48): Show | 52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1679-4380G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182385 | ||||||
| chr4:36182495
|
C | CTAAA | 176 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.1679-4494_1679-449 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | ||||||
| chr4:36182495
|
C | CTAAATAA others(1): Show |
23 | a0001c0001t0001g0045a0001c0001t0001g0082a0001c0001t0001g0127others(20): Show | 23 | HG00280.hp2 HG00544.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.1679-4498_1679-449 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | ||||||
| chr4:36182495
|
C | CTAAATAA others(5): Show |
11 | a0001c0001t0001g0114a0001c0001t0003g0097a0001c0001t0003g0098others(8): Show | 11 | HG01109.hp2 HG01884.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1679-4502_1679-449 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | ||||||
| chr4:36182495
|
CTAAA | C | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0089others(2): Show | 5 | HG01243.hp2 HG03209.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1679-4494_1679-449 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | ||||||
| chr4:36182495
|
CTAAATAA others(1): Show |
C | 4 | a0001c0001t0005g0052a0001c0001t0005g0066a0001c0001t0007g0006others(1): Show | 4 | HG02622.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-4498_1679-449 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | ||||||
| chr4:36182529
|
A | AAATAAAT others(4): Show |
1 | a0011c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1679-4525_1679-452 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182529 | ||||||
| chr4:36182600
|
T | C | 254 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1679-4595A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182600 | ||||||
| chr4:36182626
|
C | G | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1679-4621G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182626 | ||||||
| chr4:36182785
|
C | T | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1678+4666G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182785 | ||||||
| chr4:36182930
|
T | C | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1678+4521A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182930 | ||||||
| chr4:36182998
|
C | T | 1 | a0008c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1678+4453G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182998 | ||||||
| chr4:36183151
|
C | T | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1678+4300G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183151 | ||||||
| chr4:36183297
|
T | TA | 243 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1678+4153dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183297 | ||||||
| chr4:36183320
|
C | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0196 | 3 | HG02080.hp1 HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1678+4131G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183320 | ||||||
| chr4:36183406
|
G | A | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1678+4045C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183406 | ||||||
| chr4:36183486
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1678+3965C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183486 | ||||||
| chr4:36184176
|
T | TACTTTAT others(7): Show |
1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1678+3261_1678+327 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184176 | ||||||
| chr4:36184276
|
C | CAT | 3 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0002g0023 | 5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+3173_1678+317 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | ||||||
| chr4:36184276
|
CAT | C | 241 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1678+3173_1678+317 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | ||||||
| chr4:36184276
|
CATAT | C | 3 | a0001c0001t0010g0274a0002c0006t0001g0119a0008c0027t0003g0048 | 3 | HG02280.hp1 HG03654.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1678+3171_1678+317 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | ||||||
| chr4:36184276
|
CATATAT | C | 8 | a0002c0006t0001g0120a0002c0006t0001g0122a0002c0006t0001g0124others(5): Show | 8 | HG02258.hp1 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+3169_1678+317 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | ||||||
| chr4:36184294
|
TAC | T | 9 | a0001c0001t0002g0011a0001c0001t0002g0068a0001c0001t0002g0206others(6): Show | 9 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+3155_1678+315 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184294 | ||||||
| chr4:36184719
|
A | G | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1678+2732T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184719 | ||||||
| chr4:36184986
|
G | C | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1678+2465C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184986 | ||||||
| chr4:36185085
|
C | A | 6 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0032others(3): Show | 6 | HG00544.hp2 NA18955.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+2366G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185085 | ||||||
| chr4:36185157
|
C | T | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1678+2294G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185157 | ||||||
| chr4:36185399
|
G | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1678+2052C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185399 | ||||||
| chr4:36185477
|
G | T | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1678+1974C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185477 | ||||||
| chr4:36185700
|
G | T | 1 | a0019c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1678+1751C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185700 | ||||||
| chr4:36185788
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1678+1663G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185788 | ||||||
| chr4:36185920
|
G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1678+1531C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185920 | ||||||
| chr4:36185947
|
A | C | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1504T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185947 | ||||||
| chr4:36185951
|
T | C | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1500A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185951 | ||||||
| chr4:36185957
|
A | G | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1494T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185957 | ||||||
| chr4:36185965
|
T | C | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1486A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185965 | ||||||
| chr4:36185968
|
A | G | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1483T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185968 | ||||||
| chr4:36185973
|
T | C | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1478A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185973 | ||||||
| chr4:36185978
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1678+1472_1678+147 others(37): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185978 | ||||||
| chr4:36185991
|
G | A | 2 | a0001c0002t0001g0003a0001c0002t0001g0166 | 3 | HG02040.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1678+1460C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185991 | ||||||
| chr4:36186161
|
C | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(47): Show | 51 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1678+1290G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186161 | ||||||
| chr4:36186208
|
C | T | 8 | a0002c0006t0001g0120a0002c0006t0001g0122a0002c0006t0001g0124others(5): Show | 8 | HG02258.hp1 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+1243G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186208 | ||||||
| chr4:36186345
|
T | G | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1678+1106A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186345 | ||||||
| chr4:36186515
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1678+936G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186515 | ||||||
| chr4:36186530
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1678+921G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186530 | ||||||
| chr4:36186556
|
A | G | 1 | a0002c0006t0001g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1678+895T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186556 | ||||||
| chr4:36186743
|
A | G | 1 | a0001c0001t0003g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1678+708T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186743 | ||||||
| chr4:36186950
|
T | C | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1678+501A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186950 | ||||||
| chr4:36186964
|
G | A | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1678+487C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186964 | ||||||
| chr4:36186992
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1678+459C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186992 | ||||||
| chr4:36187007
|
T | C | 1 | a0001c0002t0001g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1678+444A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187007 | ||||||
| chr4:36187223
|
T | C | 1 | a0001c0003t0001g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1678+228A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187223 | ||||||
| chr4:36187230
|
A | G | 1 | a0001c0002t0001g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1678+221T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187230 | ||||||
| chr4:36187268
|
G | A | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1678+183C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187268 | ||||||
| chr4:36187272
|
C | T | 22 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0114others(19): Show | 22 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1678+179G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187272 | ||||||
| chr4:36187828
|
A | G | 1 | a0001c0009t0001g0036 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1558-257T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187828 | ||||||
| chr4:36187867
|
C | G | 1 | a0001c0002t0001g0032 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1558-296G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187867 | ||||||
| chr4:36187925
|
T | C | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1558-354A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187925 | ||||||
| chr4:36187943
|
T | C | 1 | a0001c0003t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1558-372A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187943 | ||||||
| chr4:36188476
|
T | C | 267 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1558-905A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188476 | ||||||
| chr4:36188543
|
G | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1558-972C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188543 | ||||||
| chr4:36188709
|
G | A | 2 | a0001c0001t0003g0157a0001c0001t0003g0158 | 2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1558-1138C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188709 | ||||||
| chr4:36188770
|
C | A | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1558-1199G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188770 | ||||||
| chr4:36188968
|
A | G | 50 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(47): Show | 51 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1558-1397T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188968 | ||||||
| chr4:36189027
|
T | C | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1558-1456A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189027 | ||||||
| chr4:36189142
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1558-1571A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189142 | ||||||
| chr4:36189213
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1558-1642T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189213 | ||||||
| chr4:36189246
|
T | A | 239 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0064others(236): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1558-1675A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189246 | ||||||
| chr4:36189247
|
T | A | 1 | a0001c0001t0002g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1558-1676A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189247 | ||||||
| chr4:36189280
|
C | T | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1558-1709G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189280 | ||||||
| chr4:36189446
|
T | G | 9 | a0001c0001t0005g0052a0001c0001t0005g0053a0001c0001t0005g0066others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-1875A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189446 | ||||||
| chr4:36189519
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1558-1948A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189519 | ||||||
| chr4:36189812
|
T | C | 204 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0050others(201): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1558-2241A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189812 | ||||||
| chr4:36189949
|
T | C | 3 | a0001c0001t0004g0092a0001c0001t0004g0103a0001c0001t0023g0093 | 3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1558-2378A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189949 | ||||||
| chr4:36190171
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1558-2600T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190171 | ||||||
| chr4:36190542
|
C | T | 9 | a0001c0001t0003g0101a0001c0001t0003g0235a0001c0001t0004g0054others(6): Show | 9 | HG01081.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-2971G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190542 | ||||||
| chr4:36190684
|
T | A | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1557+2894A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190684 | ||||||
| chr4:36190820
|
A | G | 1 | a0001c0001t0002g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1557+2758T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190820 | ||||||
| chr4:36190955
|
A | G | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1557+2623T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190955 | ||||||
| chr4:36191126
|
AGTTTATC others(6): Show |
A | 2 | a0002c0006t0001g0122a0002c0006t0001g0124 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1557+2439_1557+245 others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191126 | ||||||
| chr4:36191137
|
T | C | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1557+2441A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191137 | ||||||
| chr4:36191329
|
T | C | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1557+2249A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191329 | ||||||
| chr4:36191535
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1557+2043G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191535 | ||||||
| chr4:36191706
|
T | A | 2 | a0001c0001t0001g0202a0001c0001t0003g0153 | 2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1557+1872A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191706 | ||||||
| chr4:36191743
|
C | T | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1557+1835G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191743 | ||||||
| chr4:36191789
|
A | G | 1 | a0001c0003t0001g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1557+1789T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191789 | ||||||
| chr4:36191866
|
T | C | 41 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1557+1712A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191866 | ||||||
| chr4:36192168
|
G | GT | 4 | a0001c0005t0001g0001a0001c0005t0006g0104a0001c0005t0006g0105others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+1409dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | ||||||
| chr4:36192168
|
GT | G | 40 | a0001c0001t0001g0089a0001c0001t0001g0114a0001c0001t0001g0177others(37): Show | 40 | HG00438.hp1 HG00741.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1557+1409delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | ||||||
| chr4:36192168
|
GTT | G | 91 | a0001c0001t0001g0026a0001c0001t0001g0040a0001c0001t0001g0069others(88): Show | 91 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1557+1408_1557+140 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | ||||||
| chr4:36192168
|
GTTT | G | 71 | a0001c0001t0001g0064a0001c0001t0001g0149a0001c0001t0001g0179others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1557+1407_1557+140 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | ||||||
| chr4:36192168
|
GTTTT | G | 49 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0065others(46): Show | 50 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1557+1406_1557+140 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | ||||||
| chr4:36192175
|
T | C | 2 | a0001c0001t0003g0099a0001c0001t0003g0115 | 2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1557+1403A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192175 | ||||||
| chr4:36192362
|
C | T | 9 | a0002c0006t0001g0119a0002c0006t0001g0120a0002c0006t0001g0122others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+1216G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192362 | ||||||
| chr4:36192769
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1557+809C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192769 | ||||||
| chr4:36192775
|
T | A | 1 | a0001c0003t0003g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1557+803A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192775 | ||||||
| chr4:36192864
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1557+714A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192864 | ||||||
| chr4:36192878
|
C | A | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1557+700G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192878 | ||||||
| chr4:36193002
|
A | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(48): Show | 52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1557+576T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193002 | ||||||
| chr4:36193017
|
T | C | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1557+561A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193017 | ||||||
| chr4:36193252
|
G | C | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1557+326C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193252 | ||||||
| chr4:36193346
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1557+232T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193346 | ||||||
| chr4:36193404
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1557+174T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193404 | ||||||
| chr4:36193725
|
G | A | 2 | a0001c0001t0003g0012a0008c0027t0003g0048 | 2 | HG02451.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1488-78C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36193725 | ||||||
| chr4:36193826
|
T | C | 1 | a0002c0006t0003g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1488-179A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36193826 | ||||||
| chr4:36193975
|
G | A | 28 | a0001c0003t0001g0180a0001c0003t0001g0181a0001c0003t0001g0182others(25): Show | 28 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1488-328C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36193975 | ||||||
| chr4:36194107
|
T | C | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0167others(3): Show | 6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1488-460A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194107 | ||||||
| chr4:36194235
|
C | T | 1 | a0001c0004t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1488-588G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194235 | ||||||
| chr4:36194431
|
T | C | 135 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0089others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1488-784A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194431 | ||||||
| chr4:36194598
|
A | AAGTGTAG others(8): Show |
1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1488-966_1488-952d others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194598 | ||||||
| chr4:36194709
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1488-1062T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194709 | ||||||
| chr4:36194778
|
T | C | 51 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(48): Show | 52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1488-1131A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194778 | ||||||
| chr4:36194954
|
T | C | 1 | a0007c0010t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1488-1307A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194954 | ||||||
| chr4:36195018
|
T | A | 1 | a0001c0005t0006g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1488-1371A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195018 | ||||||
| chr4:36195143
|
G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1488-1496C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195143 | ||||||
| chr4:36195167
|
C | CA | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1488-1521dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195167 | ||||||
| chr4:36195308
|
G | C | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1488-1661C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195308 | ||||||
| chr4:36195489
|
C | T | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1488-1842G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195489 | ||||||
| chr4:36196346
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1488-2699G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36196346 | ||||||
| chr4:36196401
|
G | A | 75 | a0001c0001t0001g0149a0001c0001t0001g0179a0001c0001t0001g0199others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1488-2754C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36196401 | ||||||
| chr4:36196668
|
C | A | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1488-3021G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36196668 | ||||||
| chr4:36197134
|
T | C | 23 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0114others(20): Show | 23 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1488-3487A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197134 | ||||||
| chr4:36197156
|
T | C | 80 | a0001c0001t0001g0026a0001c0001t0001g0149a0001c0001t0001g0179others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1488-3509A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197156 | ||||||
| chr4:36197157
|
G | A | 34 | a0001c0001t0002g0132a0001c0001t0002g0134a0001c0001t0002g0135others(31): Show | 34 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(31): Show |
intron_variant | MODIFIER | c.1488-3510C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197157 | ||||||
| chr4:36197188
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1488-3541G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197188 | ||||||
| chr4:36197189
|
A | G | 254 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1488-3542T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197189 | ||||||
| chr4:36197275
|
T | C | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1488-3628A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197275 | ||||||
| chr4:36197625
|
C | G | 14 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0177others(11): Show | 14 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1488-3978G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197625 | ||||||
| chr4:36197739
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1488-4092C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197739 | ||||||
| chr4:36197810
|
G | A | 2 | a0001c0001t0002g0218a0001c0001t0002g0256 | 2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1488-4163C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197810 | ||||||
| chr4:36197952
|
T | TTC | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1488-4307_1488-430 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197952 | ||||||
| chr4:36197958
|
T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1488-4311A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197958 | ||||||
| chr4:36198101
|
G | A | 9 | a0001c0001t0002g0011a0001c0001t0002g0068a0001c0001t0002g0206others(6): Show | 9 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-4454C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198101 | ||||||
| chr4:36198240
|
T | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1488-4593A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198240 | ||||||
| chr4:36198264
|
C | T | 2 | a0001c0001t0001g0082a0011c0022t0001g0111 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1488-4617G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198264 | ||||||
| chr4:36198265
|
G | A | 22 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0114others(19): Show | 22 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1488-4618C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198265 | ||||||
| chr4:36198283
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1488-4636C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198283 | ||||||
| chr4:36198314
|
T | C | 255 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(252): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1488-4667A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198314 | ||||||
| chr4:36198376
|
G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1488-4729C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198376 | ||||||
| chr4:36198388
|
A | G | 2 | a0001c0005t0003g0102a0001c0005t0012g0008 | 2 | HG01433.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1488-4741T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198388 | ||||||
| chr4:36198556
|
C | T | 4 | a0001c0001t0002g0011a0001c0001t0002g0068a0001c0001t0002g0207others(1): Show | 4 | HG01106.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1488-4909G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198556 | ||||||
| chr4:36198689
|
C | T | 15 | a0001c0004t0001g0062a0001c0004t0001g0090a0001c0004t0001g0269others(12): Show | 15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1488-5042G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198689 | ||||||
| chr4:36198690
|
G | A | 4 | a0001c0001t0002g0186a0001c0001t0003g0239a0001c0001t0003g0242others(1): Show | 4 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1488-5043C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198690 | ||||||
| chr4:36198928
|
A | G | 254 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1488-5281T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198928 | ||||||
| chr4:36199067
|
C | T | 2 | a0001c0004t0001g0269a0001c0004t0003g0271 | 2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1488-5420G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199067 | ||||||
| chr4:36199102
|
C | T | 1 | a0001c0003t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1488-5455G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199102 | ||||||
| chr4:36199213
|
A | G | 9 | a0002c0006t0001g0119a0002c0006t0001g0120a0002c0006t0001g0122others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-5566T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199213 | ||||||
| chr4:36199323
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1488-5676T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199323 | ||||||
| chr4:36199368
|
T | G | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1488-5721A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199368 | ||||||
| chr4:36199424
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1488-5777A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199424 | ||||||
| chr4:36199537
|
G | A | 2 | a0001c0001t0010g0274a0001c0002t0001g0144 | 2 | HG03834.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1488-5890C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199537 | ||||||
| chr4:36199889
|
C | A | 59 | a0001c0001t0001g0040a0001c0001t0001g0086a0001c0001t0001g0087others(56): Show | 59 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1488-6242G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199889 | ||||||
| chr4:36199906
|
C | T | 19 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(16): Show | 19 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1488-6259G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199906 | ||||||
| chr4:36199936
|
C | T | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1488-6289G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199936 | ||||||
| chr4:36199940
|
A | G | 1 | a0001c0002t0001g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1488-6293T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199940 | ||||||
| chr4:36199969
|
T | A | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1488-6322A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199969 | ||||||
| chr4:36200031
|
C | CA | 245 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1488-6385dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200031 | ||||||
| chr4:36200038
|
T | C | 5 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488-6391A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200038 | ||||||
| chr4:36200217
|
T | C | 9 | a0002c0006t0001g0119a0002c0006t0001g0120a0002c0006t0001g0122others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-6570A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200217 | ||||||
| chr4:36200235
|
CT | C | 248 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1488-6589delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200235 | ||||||
| chr4:36200261
|
A | T | 1 | a0012c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1488-6614T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200261 | ||||||
| chr4:36200261
|
AT | A | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488-6615delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200261 | ||||||
| chr4:36200396
|
C | T | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1488-6749G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200396 | ||||||
| chr4:36200454
|
C | T | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1488-6807G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200454 | ||||||
| chr4:36200537
|
G | T | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1488-6890C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200537 | ||||||
| chr4:36200849
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1488-7202G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200849 | ||||||
| chr4:36200894
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1488-7247G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200894 | ||||||
| chr4:36200953
|
T | A | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1488-7306A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200953 | ||||||
| chr4:36200970
|
G | A | 9 | a0002c0006t0001g0119a0002c0006t0001g0120a0002c0006t0001g0122others(6): Show | 9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-7323C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200970 | ||||||
| chr4:36201010
|
G | A | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488-7363C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201010 | ||||||
| chr4:36201043
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1488-7396A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201043 | ||||||
| chr4:36201054
|
G | C | 1 | a0001c0001t0004g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1488-7407C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201054 | ||||||
| chr4:36201429
|
A | G | 1 | a0001c0001t0003g0160 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1488-7782T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201429 | ||||||
| chr4:36201438
|
G | C | 2 | a0001c0001t0001g0202a0001c0001t0003g0153 | 2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1488-7791C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201438 | ||||||
| chr4:36201628
|
T | A | 57 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0089others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1488-7981A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201628 | ||||||
| chr4:36201666
|
T | C | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1488-8019A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201666 | ||||||
| chr4:36201704
|
A | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1488-8057T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201704 | ||||||
| chr4:36201790
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1488-8143T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201790 | ||||||
| chr4:36201840
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1488-8193T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201840 | ||||||
| chr4:36202049
|
T | C | 16 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(13): Show | 16 | HG00438.hp1 HG01361.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1487+8341A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202049 | ||||||
| chr4:36202234
|
T | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1487+8156A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202234 | ||||||
| chr4:36202366
|
C | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1487+8024G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202366 | ||||||
| chr4:36202495
|
GA | G | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+7894delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202495 | ||||||
| chr4:36202562
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1487+7828C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202562 | ||||||
| chr4:36202633
|
G | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0003g0116 | 3 | HG02145.hp2 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1487+7757C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202633 | ||||||
| chr4:36202915
|
C | A | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+7475G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202915 | ||||||
| chr4:36203175
|
G | T | 1 | a0001c0002t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1487+7215C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203175 | ||||||
| chr4:36203265
|
T | C | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+7125A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203265 | ||||||
| chr4:36203413
|
C | A | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1487+6977G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203413 | ||||||
| chr4:36203497
|
T | C | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6893A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203497 | ||||||
| chr4:36203503
|
G | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1487+6887C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203503 | ||||||
| chr4:36203578
|
T | C | 1 | a0001c0003t0001g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1487+6812A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203578 | ||||||
| chr4:36203618
|
G | A | 1 | a0001c0004t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1487+6772C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203618 | ||||||
| chr4:36203682
|
C | T | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6708G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203682 | ||||||
| chr4:36203772
|
G | A | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6618C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203772 | ||||||
| chr4:36203896
|
C | G | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6494G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203896 | ||||||
| chr4:36203989
|
C | T | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6401G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203989 | ||||||
| chr4:36204293
|
A | T | 1 | a0001c0009t0001g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1487+6097T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204293 | ||||||
| chr4:36204323
|
G | A | 1 | a0001c0001t0002g0225 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1487+6067C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204323 | ||||||
| chr4:36204450
|
C | G | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1487+5940G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204450 | ||||||
| chr4:36204620
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1487+5770C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204620 | ||||||
| chr4:36204668
|
T | G | 51 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(48): Show | 52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1487+5722A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204668 | ||||||
| chr4:36204798
|
G | T | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1487+5592C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204798 | ||||||
| chr4:36204899
|
A | G | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1487+5491T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204899 | ||||||
| chr4:36204987
|
C | CA | 8 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0005g0051others(5): Show | 8 | HG00438.hp1 HG01361.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1487+5402dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36204987
|
C | CAA | 9 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096others(6): Show | 9 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1487+5401_1487+540 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36204987
|
CAAAAAAA | C | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0078others(3): Show | 6 | HG03195.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1487+5396_1487+540 others(11): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36204987
|
CAAAAAAA others(1): Show |
C | 25 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0178others(22): Show | 25 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1487+5395_1487+540 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36204987
|
CAAAAAAA others(2): Show |
C | 160 | a0001c0001t0001g0026a0001c0001t0001g0082a0001c0001t0001g0086others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1487+5394_1487+540 others(13): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36204987
|
CAAAAAAA others(3): Show |
C | 44 | a0001c0001t0001g0045a0001c0001t0001g0069a0001c0001t0001g0089others(41): Show | 44 | HG00140.hp1 HG00544.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1487+5393_1487+540 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36204987
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0002g0169a0001c0001t0002g0186a0001c0001t0002g0241others(1): Show | 4 | HG02886.hp1 NA18747.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487+5392_1487+540 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36204987
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0003g0239a0001c0001t0003g0242a0006c0011t0003g0185 | 3 | HG00323.hp1 HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1487+5391_1487+540 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | ||||||
| chr4:36205081
|
T | C | 3 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0256 | 3 | HG00558.hp2 HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1487+5309A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205081 | ||||||
| chr4:36205117
|
A | C | 242 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1487+5273T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205117 | ||||||
| chr4:36205121
|
G | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+5269C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205121 | ||||||
| chr4:36205133
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+5257A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205133 | ||||||
| chr4:36205161
|
C | T | 242 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1487+5229G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205161 | ||||||
| chr4:36205285
|
C | G | 242 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1487+5105G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205285 | ||||||
| chr4:36205290
|
A | G | 78 | a0001c0001t0001g0026a0001c0001t0001g0149a0001c0001t0001g0179others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.1487+5100T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205290 | ||||||
| chr4:36205324
|
G | A | 242 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1487+5066C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205324 | ||||||
| chr4:36205334
|
T | C | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1487+5056A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205334 | ||||||
| chr4:36205400
|
T | G | 242 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(239): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1487+4990A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205400 | ||||||
| chr4:36205601
|
GAA | G | 225 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1487+4787_1487+478 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205601 | ||||||
| chr4:36205601
|
GAAA | G | 15 | a0001c0001t0002g0021a0001c0004t0001g0062a0001c0004t0001g0090others(12): Show | 15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1487+4786_1487+478 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205601 | ||||||
| chr4:36205641
|
A | G | 1 | a0001c0002t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1487+4749T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205641 | ||||||
| chr4:36205873
|
A | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1487+4517T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205873 | ||||||
| chr4:36205874
|
ATATTAAA others(10): Show |
A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1487+4499_1487+451 others(21): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205874 | ||||||
| chr4:36205985
|
C | T | 1 | a0001c0001t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1487+4405G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205985 | ||||||
| chr4:36206124
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0002g0131a0001c0001t0002g0155 | 3 | HG02083.hp2 HG02132.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1487+4266G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206124 | ||||||
| chr4:36206137
|
A | G | 248 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1487+4253T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206137 | ||||||
| chr4:36206667
|
T | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1487+3723A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206667 | ||||||
| chr4:36206675
|
G | C | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1487+3715C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206675 | ||||||
| chr4:36206816
|
T | A | 2 | a0001c0001t0001g0202a0001c0001t0003g0153 | 2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1487+3574A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206816 | ||||||
| chr4:36206820
|
G | A | 2 | a0001c0001t0003g0257a0001c0001t0003g0258 | 2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1487+3570C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206820 | ||||||
| chr4:36207004
|
T | G | 3 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0003g0129 | 3 | NA18747.hp2 NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1487+3386A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207004 | ||||||
| chr4:36207025
|
A | G | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1487+3365T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207025 | ||||||
| chr4:36207047
|
C | A | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1487+3343G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207047 | ||||||
| chr4:36207075
|
C | T | 1 | a0008c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1487+3315G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207075 | ||||||
| chr4:36207569
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+2821A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207569 | ||||||
| chr4:36207745
|
A | C | 20 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(17): Show | 20 | HG01243.hp1 HG01255.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1487+2645T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207745 | ||||||
| chr4:36207773
|
C | T | 248 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1487+2617G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207773 | ||||||
| chr4:36207778
|
G | A | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+2612C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207778 | ||||||
| chr4:36207808
|
C | G | 1 | a0001c0001t0002g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1487+2582G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207808 | ||||||
| chr4:36208010
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1487+2380A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208010 | ||||||
| chr4:36208201
|
T | A | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+2189A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208201 | ||||||
| chr4:36208239
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+2151A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208239 | ||||||
| chr4:36208355
|
G | A | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+2035C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208355 | ||||||
| chr4:36208524
|
C | G | 16 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(13): Show | 16 | HG00438.hp1 HG01361.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1487+1866G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208524 | ||||||
| chr4:36208872
|
TC | T | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+1517delG | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208872 | ||||||
| chr4:36208878
|
A | T | 10 | a0001c0001t0010g0274a0002c0006t0001g0119a0002c0006t0001g0120others(7): Show | 10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+1512T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208878 | ||||||
| chr4:36208879
|
A | G | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1487+1511T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208879 | ||||||
| chr4:36209084
|
G | A | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056 | 3 | HG02257.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1487+1306C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209084 | ||||||
| chr4:36209101
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1487+1289G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209101 | ||||||
| chr4:36209229
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1487+1161A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209229 | ||||||
| chr4:36209293
|
T | A | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1487+1097A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209293 | ||||||
| chr4:36209485
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1487+905A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209485 | ||||||
| chr4:36209653
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1487+737G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209653 | ||||||
| chr4:36209684
|
G | T | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1487+706C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209684 | ||||||
| chr4:36209858
|
G | T | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1487+532C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209858 | ||||||
| chr4:36209876
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1487+514C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209876 | ||||||
| chr4:36209954
|
T | C | 2 | a0001c0001t0005g0053a0001c0001t0005g0273 | 2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1487+436A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209954 | ||||||
| chr4:36210292
|
C | A | 258 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(255): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1487+98G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36210292 | ||||||
| chr4:36210891
|
A | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1134-148T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36210891 | ||||||
| chr4:36210918
|
T | G | 3 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106 | 3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1134-175A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36210918 | ||||||
| chr4:36211296
|
C | A | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1134-553G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211296 | ||||||
| chr4:36211358
|
T | G | 1 | a0001c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1134-615A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211358 | ||||||
| chr4:36211409
|
G | A | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1134-666C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211409 | ||||||
| chr4:36211754
|
G | A | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1133+642C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211754 | ||||||
| chr4:36211786
|
T | C | 2 | a0001c0001t0002g0171a0001c0001t0002g0241 | 2 | NA18977.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1133+610A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211786 | ||||||
| chr4:36211890
|
C | T | 10 | a0001c0001t0010g0274a0001c0005t0003g0102a0002c0006t0001g0119others(7): Show | 10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1133+506G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211890 | ||||||
| chr4:36211955
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1133+441T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211955 | ||||||
| chr4:36212087
|
T | TAACCTCC others(30): Show |
250 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(247): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1133+308_1133+309i others(39): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36212087 | ||||||
| chr4:36212139
|
C | T | 245 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1133+257G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36212139 | ||||||
| chr4:36212507
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1042-20T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36212507 | ||||||
| chr4:36212646
|
T | A | 260 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1042-159A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36212646 | ||||||
| chr4:36212671
|
A | AT | 240 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1042-185dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36212671 | ||||||
| chr4:36213021
|
A | C | 8 | a0001c0001t0001g0114a0001c0001t0003g0097a0001c0001t0003g0098others(5): Show | 8 | HG02165.hp1 HG03927.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041+222T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213021 | ||||||
| chr4:36213122
|
G | A | 1 | a0001c0005t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1041+121C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213122 | ||||||
| chr4:36213150
|
T | C | 1 | a0001c0001t0002g0225 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1041+93A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213150 | ||||||
| chr4:36213167
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1041+76C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213167 | ||||||
| chr4:36213424
|
G | A | 2 | a0001c0001t0010g0274a0001c0005t0003g0102 | 2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.965-105C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213424 | ||||||
| chr4:36213510
|
T | C | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.965-191A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213510 | ||||||
| chr4:36213627
|
T | C | 2 | a0001c0001t0010g0274a0001c0005t0003g0102 | 2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.965-308A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213627 | ||||||
| chr4:36213849
|
A | C | 241 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.965-530T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213849 | ||||||
| chr4:36214017
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.964+405C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36214017 | ||||||
| chr4:36214094
|
C | T | 15 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(12): Show | 15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.964+328G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36214094 | ||||||
| chr4:36214346
|
C | T | 2 | a0001c0001t0010g0274a0001c0005t0003g0102 | 2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.964+76G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36214346 | ||||||
| chr4:36214492
|
A | T | 24 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(21): Show | 24 | HG00323.hp1 HG00741.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.906-12T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36214492 | ||||||
| chr4:36214825
|
T | G | 1 | a0001c0001t0003g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.906-345A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36214825 | ||||||
| chr4:36214968
|
A | T | 2 | a0001c0001t0011g0004a0001c0001t0024g0137 | 2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.906-488T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36214968 | ||||||
| chr4:36215011
|
G | T | 1 | a0016c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.906-531C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215011 | ||||||
| chr4:36215113
|
C | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-633G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215113 | ||||||
| chr4:36215236
|
T | C | 260 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.906-756A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215236 | ||||||
| chr4:36215252
|
T | C | 245 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.906-772A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215252 | ||||||
| chr4:36215303
|
C | T | 245 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.906-823G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215303 | ||||||
| chr4:36215335
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.906-855A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215335 | ||||||
| chr4:36215345
|
G | A | 245 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.906-865C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215345 | ||||||
| chr4:36215380
|
T | G | 245 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.906-900A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215380 | ||||||
| chr4:36215730
|
T | C | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.906-1250A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215730 | ||||||
| chr4:36215781
|
G | A | 2 | a0001c0001t0010g0274a0001c0005t0003g0102 | 2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.906-1301C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215781 | ||||||
| chr4:36215804
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.906-1324G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215804 | ||||||
| chr4:36215849
|
CA | C | 15 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(12): Show | 15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.906-1370delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215849 | ||||||
| chr4:36215849
|
CAA | C | 245 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(242): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.906-1371_906-1370d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215849 | ||||||
| chr4:36216082
|
C | CA | 8 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0002g0151others(5): Show | 8 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.906-1603dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216082 | ||||||
| chr4:36216082
|
CA | C | 16 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0002g0169others(13): Show | 16 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.906-1603delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216082 | ||||||
| chr4:36216098
|
C | A | 2 | a0001c0001t0001g0082a0011c0022t0001g0111 | 2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.906-1618G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216098 | ||||||
| chr4:36216190
|
A | C | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.906-1710T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216190 | ||||||
| chr4:36216248
|
C | T | 91 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(88): Show | 92 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.906-1768G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216248 | ||||||
| chr4:36216282
|
G | A | 1 | a0008c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.906-1802C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216282 | ||||||
| chr4:36216460
|
G | A | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906-1980C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216460 | ||||||
| chr4:36216775
|
A | G | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-2295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216775 | ||||||
| chr4:36216782
|
T | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0177a0001c0001t0001g0178others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-2302A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216782 | ||||||
| chr4:36216782
|
T | G | 1 | a0001c0001t0002g0222 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.906-2302A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216782 | ||||||
| chr4:36216951
|
G | A | 10 | a0001c0001t0010g0274a0001c0005t0003g0102a0002c0006t0001g0119others(7): Show | 10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.906-2471C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216951 | ||||||
| chr4:36217006
|
G | A | 9 | a0001c0001t0001g0040a0001c0001t0001g0177a0001c0001t0001g0178others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-2526C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217006 | ||||||
| chr4:36217007
|
C | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0177a0001c0001t0001g0178others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-2527G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217007 | ||||||
| chr4:36217180
|
A | T | 260 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(257): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.906-2700T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217180 | ||||||
| chr4:36217223
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.906-2743T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217223 | ||||||
| chr4:36217322
|
G | A | 2 | a0001c0001t0010g0274a0001c0005t0003g0102 | 2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.906-2842C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217322 | ||||||
| chr4:36217329
|
T | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.906-2849A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217329 | ||||||
| chr4:36217373
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.906-2893C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217373 | ||||||
| chr4:36217452
|
C | T | 4 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-2972G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217452 | ||||||
| chr4:36217492
|
G | A | 2 | a0001c0001t0001g0015a0001c0002t0001g0016 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.906-3012C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217492 | ||||||
| chr4:36217873
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.906-3393G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217873 | ||||||
| chr4:36217956
|
G | A | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906-3476C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217956 | ||||||
| chr4:36218066
|
C | T | 1 | a0001c0001t0020g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.906-3586G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218066 | ||||||
| chr4:36218197
|
C | T | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906-3717G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218197 | ||||||
| chr4:36218289
|
A | G | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.906-3809T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218289 | ||||||
| chr4:36218310
|
C | T | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-3830G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218310 | ||||||
| chr4:36218450
|
A | C | 77 | a0001c0001t0001g0026a0001c0001t0001g0149a0001c0001t0001g0179others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.906-3970T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218450 | ||||||
| chr4:36218493
|
C | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.906-4013G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218493 | ||||||
| chr4:36218499
|
G | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.906-4019C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218499 | ||||||
| chr4:36218533
|
G | A | 1 | a0001c0002t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.906-4053C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218533 | ||||||
| chr4:36218582
|
C | CCAATTCA others(2): Show |
3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-4103_906-4102i others(11): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218582 | ||||||
| chr4:36218623
|
T | C | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.906-4143A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218623 | ||||||
| chr4:36218667
|
T | C | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.906-4187A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218667 | ||||||
| chr4:36218717
|
T | C | 1 | a0001c0001t0002g0225 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.906-4237A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218717 | ||||||
| chr4:36218722
|
T | G | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-4242A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218722 | ||||||
| chr4:36219010
|
A | G | 1 | a0008c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.906-4530T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219010 | ||||||
| chr4:36219024
|
C | T | 1 | a0001c0002t0001g0165 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.906-4544G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219024 | ||||||
| chr4:36219029
|
C | T | 217 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(214): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.906-4549G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219029 | ||||||
| chr4:36219037
|
C | A | 3 | a0001c0001t0002g0151a0001c0001t0004g0152a0015c0017t0002g0061 | 3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-4557G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219037 | ||||||
| chr4:36219089
|
T | C | 4 | a0001c0003t0001g0180a0001c0003t0001g0181a0001c0003t0001g0182others(1): Show | 4 | NA18947.hp1 NA18973.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-4609A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219089 | ||||||
| chr4:36219117
|
T | A | 2 | a0001c0001t0002g0141a0001c0002t0001g0142 | 2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.906-4637A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219117 | ||||||
| chr4:36219268
|
C | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.906-4788G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219268 | ||||||
| chr4:36219333
|
A | G | 15 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(12): Show | 15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.906-4853T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219333 | ||||||
| chr4:36219420
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.906-4940A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219420 | ||||||
| chr4:36219454
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.906-4974A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219454 | ||||||
| chr4:36219479
|
T | C | 24 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0114others(21): Show | 24 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.906-4999A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219479 | ||||||
| chr4:36219540
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.906-5060C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219540 | ||||||
| chr4:36219588
|
A | G | 14 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096others(11): Show | 16 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.906-5108T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219588 | ||||||
| chr4:36219755
|
A | G | 4 | a0004c0008t0001g0204a0004c0008t0001g0232a0004c0008t0001g0233others(1): Show | 4 | NA18944.hp1 NA18993.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-5275T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219755 | ||||||
| chr4:36219857
|
T | A | 1 | a0001c0001t0002g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.906-5377A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219857 | ||||||
| chr4:36219875
|
A | C | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906-5395T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219875 | ||||||
| chr4:36219956
|
T | C | 5 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0003g0012others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-5476A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219956 | ||||||
| chr4:36220228
|
C | CGT | 16 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(13): Show | 16 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.906-5750_906-5749d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220228 | ||||||
| chr4:36220342
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.906-5862G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220342 | ||||||
| chr4:36220557
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.906-6077G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220557 | ||||||
| chr4:36220560
|
A | AT | 18 | a0001c0001t0002g0151a0001c0001t0003g0094a0001c0001t0003g0095others(15): Show | 20 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.906-6081dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220560 | ||||||
| chr4:36220641
|
G | T | 1 | a0001c0001t0019g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.906-6161C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220641 | ||||||
| chr4:36220757
|
T | A | 15 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(12): Show | 15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.906-6277A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220757 | ||||||
| chr4:36220757
|
T | C | 14 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0003g0096others(11): Show | 16 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.906-6277A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220757 | ||||||
| chr4:36220915
|
T | C | 3 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0106 | 3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906-6435A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220915 | ||||||
| chr4:36220965
|
C | T | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.906-6485G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220965 | ||||||
| chr4:36221063
|
C | T | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.906-6583G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221063 | ||||||
| chr4:36221489
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.906-7009G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221489 | ||||||
| chr4:36221557
|
C | T | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.905+7025G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221557 | ||||||
| chr4:36221732
|
T | A | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.905+6850A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221732 | ||||||
| chr4:36222002
|
T | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.905+6580A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222002 | ||||||
| chr4:36222249
|
C | A | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+6333G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222249 | ||||||
| chr4:36222529
|
G | T | 44 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(41): Show | 45 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.905+6053C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222529 | ||||||
| chr4:36222653
|
G | A | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.905+5929C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222653 | ||||||
| chr4:36222694
|
T | C | 1 | a0001c0001t0003g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.905+5888A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222694 | ||||||
| chr4:36222724
|
AT | A | 13 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0267others(10): Show | 13 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+5857delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222724 | ||||||
| chr4:36222751
|
T | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.905+5831A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222751 | ||||||
| chr4:36222782
|
G | A | 15 | a0001c0004t0001g0062a0001c0004t0001g0090a0001c0004t0001g0269others(12): Show | 15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+5800C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222782 | ||||||
| chr4:36222999
|
C | T | 3 | a0001c0001t0001g0202a0001c0001t0002g0130a0001c0001t0003g0153 | 3 | NA18948.hp1 NA18975.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.905+5583G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222999 | ||||||
| chr4:36223083
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0002g0224 | 2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.905+5499C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223083 | ||||||
| chr4:36223576
|
C | T | 10 | a0001c0001t0010g0274a0001c0005t0003g0102a0002c0006t0001g0119others(7): Show | 10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.905+5006G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223576 | ||||||
| chr4:36223614
|
G | C | 2 | a0001c0001t0001g0114a0001c0001t0019g0113 | 2 | NA18939.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.905+4968C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223614 | ||||||
| chr4:36223718
|
GCT | G | 72 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(69): Show | 75 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.905+4862_905+4863d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223718 | ||||||
| chr4:36223753
|
A | G | 1 | a0001c0002t0001g0234 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+4829T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223753 | ||||||
| chr4:36224176
|
G | A | 75 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(72): Show | 78 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.905+4406C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224176 | ||||||
| chr4:36224216
|
AAAAT | A | 79 | a0001c0001t0001g0026a0001c0001t0001g0149a0001c0001t0001g0179others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.905+4362_905+4365d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224216 | ||||||
| chr4:36224249
|
A | G | 14 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0177others(11): Show | 14 | HG00438.hp1 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.905+4333T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224249 | ||||||
| chr4:36224301
|
T | TA | 110 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(107): Show | 113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.905+4280dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224301 | ||||||
| chr4:36224345
|
T | C | 137 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(134): Show | 140 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.905+4237A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224345 | ||||||
| chr4:36224377
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.905+4205G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224377 | ||||||
| chr4:36224442
|
T | C | 7 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0171others(4): Show | 7 | NA18747.hp2 NA18942.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+4140A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224442 | ||||||
| chr4:36224892
|
T | C | 14 | a0001c0001t0001g0040a0001c0001t0001g0050a0001c0001t0001g0177others(11): Show | 14 | HG00438.hp1 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.905+3690A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224892 | ||||||
| chr4:36225052
|
A | C | 1 | a0001c0001t0003g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.905+3530T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225052 | ||||||
| chr4:36225316
|
G | A | 11 | a0001c0005t0001g0001a0001c0005t0001g0002a0001c0005t0001g0024others(8): Show | 13 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+3266C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225316 | ||||||
| chr4:36225418
|
TG | T | 72 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(69): Show | 75 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.905+3163delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225418 | ||||||
| chr4:36225616
|
A | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.905+2966T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225616 | ||||||
| chr4:36225664
|
T | C | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.905+2918A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225664 | ||||||
| chr4:36225941
|
G | C | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+2641C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225941 | ||||||
| chr4:36225955
|
GTTATA | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.905+2622_905+2626d others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225955 | ||||||
| chr4:36225972
|
T | C | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.905+2610A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225972 | ||||||
| chr4:36226085
|
A | G | 1 | a0005c0013t0008g0112 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.905+2497T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226085 | ||||||
| chr4:36226087
|
G | A | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+2495C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226087 | ||||||
| chr4:36226091
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.905+2491G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226091 | ||||||
| chr4:36226155
|
G | GA | 13 | a0001c0004t0001g0269a0001c0004t0002g0265a0001c0004t0002g0267others(10): Show | 13 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+2426dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226155 | ||||||
| chr4:36226324
|
T | G | 1 | a0001c0001t0005g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.905+2258A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226324 | ||||||
| chr4:36226497
|
C | T | 1 | a0010c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+2085G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226497 | ||||||
| chr4:36226509
|
G | GC | 18 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(15): Show | 18 | HG00438.hp1 HG01928.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.905+2072dupG | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226509 | ||||||
| chr4:36226663
|
A | G | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.905+1919T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226663 | ||||||
| chr4:36226852
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0019g0113 | 2 | NA18939.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.905+1730G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226852 | ||||||
| chr4:36226945
|
A | T | 2 | a0001c0005t0001g0039a0001c0005t0001g0041 | 2 | HG01168.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.905+1637T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226945 | ||||||
| chr4:36227011
|
G | A | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.905+1571C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227011 | ||||||
| chr4:36227239
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.905+1343G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227239 | ||||||
| chr4:36227539
|
C | A | 73 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0050others(70): Show | 76 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.905+1043G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227539 | ||||||
| chr4:36227878
|
A | G | 2 | a0001c0001t0001g0199a0001c0001t0020g0198 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.905+704T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227878 | ||||||
| chr4:36227917
|
G | T | 211 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(208): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.905+665C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227917 | ||||||
| chr4:36228027
|
C | A | 3 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0003g0188 | 3 | HG00544.hp1 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.905+555G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228027 | ||||||
| chr4:36228064
|
G | A | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.905+518C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228064 | ||||||
| chr4:36228169
|
T | C | 1 | a0002c0006t0001g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.905+413A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228169 | ||||||
| chr4:36228178
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.905+404C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228178 | ||||||
| chr4:36228194
|
C | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0177a0001c0001t0001g0178others(6): Show | 9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.905+388G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228194 | ||||||
| chr4:36228233
|
T | C | 1 | a0001c0002t0001g0243 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.905+349A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228233 | ||||||
| chr4:36228287
|
A | G | 1 | a0018c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.905+295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228287 | ||||||
| chr4:36228364
|
A | T | 1 | a0001c0001t0003g0249 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.905+218T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228364 | ||||||
| chr4:36228519
|
G | C | 12 | a0001c0001t0001g0050a0001c0001t0001g0193a0001c0001t0001g0194others(9): Show | 12 | HG00438.hp1 HG02258.hp1 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.905+63C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228519 | ||||||
| chr4:36228566
|
T | C | 2 | a0001c0001t0003g0101a0001c0001t0003g0235 | 2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.905+16A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228566 | ||||||
| chr4:36229675
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0012t0003g0063 | 3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-159-30C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36229675 | ||||||
| chr4:36229706
|
T | C | 18 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0114others(15): Show | 18 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-159-61A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36229706 | ||||||
| chr4:36230136
|
T | C | 1 | a0014c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-159-491A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230136 | ||||||
| chr4:36230569
|
A | C | 96 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0050others(93): Show | 99 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-159-924T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230569 | ||||||
| chr4:36230593
|
G | T | 6 | a0001c0001t0002g0018a0001c0002t0001g0013a0001c0002t0001g0014others(3): Show | 6 | HG01074.hp2 HG01109.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-159-948C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230593 | ||||||
| chr4:36230665
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-159-1020T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230665 | ||||||
| chr4:36230886
|
C | T | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-159-1241G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230886 | ||||||
| chr4:36230942
|
G | C | 4 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159-1297C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230942 | ||||||
| chr4:36230968
|
T | C | 1 | a0009c0014t0017g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-159-1323A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230968 | ||||||
| chr4:36230983
|
G | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-159-1338C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230983 | ||||||
| chr4:36231059
|
A | T | 28 | a0001c0001t0003g0012a0001c0001t0003g0118a0001c0001t0005g0051others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-159-1414T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231059 | ||||||
| chr4:36231078
|
T | G | 1 | a0009c0014t0017g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-159-1433A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231078 | ||||||
| chr4:36231101
|
C | G | 45 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-159-1456G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231101 | ||||||
| chr4:36231230
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-159-1585C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231230 | ||||||
| chr4:36231310
|
T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-159-1665A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231310 | ||||||
| chr4:36231336
|
AAAAT | A | 46 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0127others(43): Show | 47 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.-159-1695_-159-169 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231336 | ||||||
| chr4:36231527
|
T | C | 4 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159-1882A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231527 | ||||||
| chr4:36231710
|
C | T | 28 | a0001c0001t0003g0012a0001c0001t0003g0118a0001c0001t0005g0051others(25): Show | 28 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-159-2065G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231710 | ||||||
| chr4:36231814
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-159-2169G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231814 | ||||||
| chr4:36231815
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-159-2170G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231815 | ||||||
| chr4:36232089
|
T | C | 45 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0082others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-159-2444A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232089 | ||||||
| chr4:36232240
|
T | C | 4 | a0001c0001t0005g0051a0001c0001t0005g0245a0001c0001t0005g0246others(1): Show | 4 | HG01109.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159-2595A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232240 | ||||||
| chr4:36232254
|
C | A | 3 | a0001c0001t0001g0236a0001c0001t0003g0238a0007c0010t0001g0237 | 3 | HG02258.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-159-2609G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232254 | ||||||
| chr4:36232280
|
G | A | 1 | a0011c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-159-2635C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232280 | ||||||
| chr4:36232312
|
C | T | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-159-2667G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232312 | ||||||
| chr4:36232334
|
A | C | 1 | a0005c0013t0008g0067 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159-2689T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232334 | ||||||
| chr4:36232661
|
T | C | 2 | a0001c0001t0003g0239a0001c0001t0003g0242 | 2 | HG00323.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-159-3016A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232661 | ||||||
| chr4:36232883
|
C | T | 1 | a0001c0005t0006g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-159-3238G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232883 | ||||||
| chr4:36233099
|
A | C | 3 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0003g0188 | 3 | HG00544.hp1 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-159-3454T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233099 | ||||||
| chr4:36233122
|
T | C | 1 | a0001c0002t0001g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-159-3477A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233122 | ||||||
| chr4:36233152
|
A | G | 1 | a0001c0009t0001g0025 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-159-3507T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233152 | ||||||
| chr4:36233164
|
T | A | 2 | a0001c0001t0003g0118a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-159-3519A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233164 | ||||||
| chr4:36233352
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-159-3707C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233352 | ||||||
| chr4:36233391
|
G | A | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-159-3746C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233391 | ||||||
| chr4:36233609
|
A | G | 28 | a0001c0001t0001g0015a0001c0001t0002g0021a0001c0001t0002g0022others(25): Show | 30 | HG00280.hp1 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-159-3964T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233609 | ||||||
| chr4:36233732
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-159-4087C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233732 | ||||||
| chr4:36233753
|
C | T | 3 | a0001c0001t0002g0186a0001c0002t0001g0019a0001c0002t0001g0020 | 3 | HG01346.hp2 HG02886.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-159-4108G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233753 | ||||||
| chr4:36233761
|
T | C | 1 | a0014c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-159-4116A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233761 | ||||||
| chr4:36233932
|
G | A | 5 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | NA18747.hp2 NA18942.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-4287C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233932 | ||||||
| chr4:36234176
|
A | G | 140 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(137): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-159-4531T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234176 | ||||||
| chr4:36234263
|
C | T | 2 | a0001c0001t0003g0118a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-159-4618G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234263 | ||||||
| chr4:36234264
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0005g0273 | 3 | HG02109.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-159-4619C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234264 | ||||||
| chr4:36234431
|
A | C | 119 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-159-4786T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234431 | ||||||
| chr4:36234449
|
G | C | 2 | a0001c0001t0003g0118a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-159-4804C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234449 | ||||||
| chr4:36234474
|
G | C | 2 | a0002c0006t0001g0125a0002c0006t0001g0126 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-159-4829C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234474 | ||||||
| chr4:36234475
|
G | A | 18 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0003g0272others(15): Show | 18 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-159-4830C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234475 | ||||||
| chr4:36234495
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-159-4850A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234495 | ||||||
| chr4:36234503
|
T | C | 33 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0082others(30): Show | 33 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-159-4858A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234503 | ||||||
| chr4:36234744
|
A | G | 1 | a0001c0001t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-159-5099T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234744 | ||||||
| chr4:36234929
|
A | G | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159-5284T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234929 | ||||||
| chr4:36234943
|
A | C | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-159-5298T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234943 | ||||||
| chr4:36234997
|
T | C | 1 | a0009c0014t0017g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-159-5352A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234997 | ||||||
| chr4:36235287
|
C | T | 33 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0082others(30): Show | 33 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-159-5642G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235287 | ||||||
| chr4:36235474
|
C | T | 3 | a0001c0003t0001g0180a0001c0003t0001g0181a0001c0003t0001g0182 | 3 | NA18947.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-159-5829G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235474 | ||||||
| chr4:36235567
|
C | T | 33 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0082others(30): Show | 33 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-159-5922G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235567 | ||||||
| chr4:36235617
|
C | G | 1 | a0016c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-159-5972G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235617 | ||||||
| chr4:36235747
|
T | C | 2 | a0001c0001t0010g0274a0010c0015t0010g0275 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159-6102A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235747 | ||||||
| chr4:36235945
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-159-6300C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235945 | ||||||
| chr4:36236035
|
C | T | 2 | a0001c0001t0010g0274a0010c0015t0010g0275 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159-6390G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236035 | ||||||
| chr4:36236178
|
C | CA | 24 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0114others(21): Show | 24 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.-159-6534dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236178 | ||||||
| chr4:36236178
|
CA | C | 89 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0045others(86): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-159-6534delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236178 | ||||||
| chr4:36236232
|
G | A | 14 | a0001c0001t0003g0272a0001c0004t0001g0269a0001c0004t0002g0265others(11): Show | 14 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-159-6587C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236232 | ||||||
| chr4:36236268
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-159-6623G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236268 | ||||||
| chr4:36236287
|
T | C | 1 | a0001c0005t0001g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-159-6642A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236287 | ||||||
| chr4:36236799
|
G | A | 2 | a0001c0001t0010g0274a0010c0015t0010g0275 | 2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159-7154C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236799 | ||||||
| chr4:36236851
|
A | G | 119 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-159-7206T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236851 | ||||||
| chr4:36236857
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-159-7212T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236857 | ||||||
| chr4:36236921
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0176 | 2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-160+7258T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236921 | ||||||
| chr4:36236928
|
G | A | 18 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0114others(15): Show | 18 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160+7251C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236928 | ||||||
| chr4:36237206
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-160+6973G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237206 | ||||||
| chr4:36237524
|
G | C | 1 | a0001c0001t0002g0042 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-160+6655C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237524 | ||||||
| chr4:36237565
|
C | G | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-160+6614G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237565 | ||||||
| chr4:36237816
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+6363C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237816 | ||||||
| chr4:36237823
|
T | C | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-160+6356A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237823 | ||||||
| chr4:36238046
|
T | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+6133A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238046 | ||||||
| chr4:36238079
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-160+6100C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238079 | ||||||
| chr4:36238145
|
G | T | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-160+6034C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238145 | ||||||
| chr4:36238173
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-160+6006A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238173 | ||||||
| chr4:36238322
|
T | C | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-160+5857A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238322 | ||||||
| chr4:36238561
|
G | C | 76 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(73): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-160+5618C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238561 | ||||||
| chr4:36238561
|
G | T | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-160+5618C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238561 | ||||||
| chr4:36238695
|
T | C | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-160+5484A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238695 | ||||||
| chr4:36238863
|
T | C | 5 | a0001c0001t0001g0050a0001c0001t0002g0049a0001c0001t0002g0174others(2): Show | 5 | HG01255.hp2 HG01361.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160+5316A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238863 | ||||||
| chr4:36238935
|
T | TA | 106 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0149others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-160+5243dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238935 | ||||||
| chr4:36238973
|
C | T | 1 | a0001c0001t0002g0130 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-160+5206G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238973 | ||||||
| chr4:36239137
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-160+5042T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239137 | ||||||
| chr4:36239210
|
AG | A | 3 | a0001c0001t0005g0052a0001c0001t0005g0053a0001c0001t0005g0066 | 3 | HG02886.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-160+4968delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239210 | ||||||
| chr4:36239380
|
T | TATGAATG others(1): Show |
23 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(20): Show | 23 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-160+4791_-160+479 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239380 | ||||||
| chr4:36239515
|
T | G | 2 | a0001c0002t0001g0043a0001c0002t0001g0044 | 2 | HG01074.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-160+4664A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239515 | ||||||
| chr4:36239601
|
T | C | 1 | a0001c0001t0004g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-160+4578A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239601 | ||||||
| chr4:36239642
|
A | G | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+4537T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239642 | ||||||
| chr4:36239748
|
C | T | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+4431G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239748 | ||||||
| chr4:36239938
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0148 | 2 | NA18939.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-160+4241G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239938 | ||||||
| chr4:36240066
|
C | T | 32 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0082others(29): Show | 32 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-160+4113G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240066 | ||||||
| chr4:36240150
|
A | AT | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+4028_-160+402 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240150 | ||||||
| chr4:36240171
|
C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-160+4008G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240171 | ||||||
| chr4:36240270
|
CTTGGT | C | 3 | a0001c0001t0005g0052a0001c0001t0005g0053a0001c0001t0005g0066 | 3 | HG02886.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-160+3904_-160+390 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240270 | ||||||
| chr4:36240308
|
T | C | 8 | a0002c0006t0001g0119a0002c0006t0001g0120a0002c0006t0001g0122others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160+3871A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240308 | ||||||
| chr4:36240402
|
C | A | 4 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056others(1): Show | 4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160+3777G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240402 | ||||||
| chr4:36240420
|
G | A | 4 | a0001c0003t0003g0083a0001c0003t0003g0085a0001c0023t0003g0084others(1): Show | 4 | HG01074.hp1 HG01943.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+3759C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240420 | ||||||
| chr4:36240436
|
T | C | 5 | a0001c0001t0005g0273a0001c0001t0007g0006a0001c0001t0007g0007others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-160+3743A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240436 | ||||||
| chr4:36240787
|
T | G | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+3392A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240787 | ||||||
| chr4:36240922
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+3257C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240922 | ||||||
| chr4:36241170
|
G | A | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+3009C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241170 | ||||||
| chr4:36241684
|
A | C | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+2495T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241684 | ||||||
| chr4:36241697
|
G | T | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+2482C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241697 | ||||||
| chr4:36241858
|
T | C | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+2321A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241858 | ||||||
| chr4:36241892
|
A | G | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+2287T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241892 | ||||||
| chr4:36242004
|
A | T | 2 | a0001c0001t0001g0015a0001c0002t0001g0016 | 2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-160+2175T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242004 | ||||||
| chr4:36242077
|
A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-160+2102T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242077 | ||||||
| chr4:36242192
|
T | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0004t0001g0062others(1): Show | 4 | HG01243.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+1987A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242192 | ||||||
| chr4:36242247
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-160+1932T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242247 | ||||||
| chr4:36242248
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-160+1931T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242248 | ||||||
| chr4:36242345
|
G | T | 9 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0139others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-160+1834C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242345 | ||||||
| chr4:36242477
|
C | A | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+1702G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242477 | ||||||
| chr4:36242522
|
C | T | 13 | a0001c0001t0003g0272a0001c0004t0001g0269a0001c0004t0002g0265others(10): Show | 13 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-160+1657G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242522 | ||||||
| chr4:36242593
|
G | A | 32 | a0001c0001t0001g0069a0001c0001t0001g0078a0001c0001t0001g0082others(29): Show | 32 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-160+1586C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242593 | ||||||
| chr4:36242745
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-160+1434G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242745 | ||||||
| chr4:36242766
|
A | G | 10 | a0001c0001t0004g0103a0001c0005t0003g0102a0002c0006t0001g0119others(7): Show | 10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-160+1413T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242766 | ||||||
| chr4:36242882
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-160+1297A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242882 | ||||||
| chr4:36243094
|
T | TA | 9 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0089others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.-160+1084dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | ||||||
| chr4:36243094
|
T | TAA | 16 | a0001c0001t0001g0114a0001c0001t0003g0094a0001c0001t0003g0095others(13): Show | 16 | HG01099.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-160+1083_-160+108 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | ||||||
| chr4:36243094
|
T | TAAA | 13 | a0001c0001t0003g0272a0001c0004t0001g0269a0001c0004t0002g0265others(10): Show | 13 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-160+1082_-160+108 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | ||||||
| chr4:36243094
|
TA | T | 6 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0002t0001g0013others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-160+1084delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | ||||||
| chr4:36243110
|
T | C | 4 | a0001c0001t0007g0006a0001c0001t0007g0007a0001c0001t0013g0005others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+1069A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243110 | ||||||
| chr4:36243222
|
T | G | 139 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(136): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-160+957A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243222 | ||||||
| chr4:36243231
|
A | T | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-160+948T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243231 | ||||||
| chr4:36243325
|
A | AT | 6 | a0001c0001t0002g0132a0001c0001t0002g0133a0001c0001t0002g0134others(3): Show | 6 | HG00735.hp1 HG01433.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.-160+853dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243325 | ||||||
| chr4:36243383
|
C | CA | 60 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(57): Show | 60 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.-160+795dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | ||||||
| chr4:36243383
|
C | CAA | 24 | a0001c0001t0001g0114a0001c0001t0002g0110a0001c0001t0003g0115others(21): Show | 24 | HG00558.hp1 HG01167.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-160+794_-160+795d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | ||||||
| chr4:36243383
|
CA | C | 10 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0003g0272others(7): Show | 10 | HG02083.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-160+795delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | ||||||
| chr4:36243383
|
CAA | C | 9 | a0001c0004t0002g0265a0001c0004t0002g0267a0001c0004t0003g0261others(6): Show | 9 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-160+794_-160+795d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | ||||||
| chr4:36243383
|
CAAAAAAA others(1): Show |
C | 36 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(33): Show | 38 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-160+788_-160+795d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | ||||||
| chr4:36243520
|
C | T | 14 | a0001c0001t0003g0272a0001c0001t0005g0273a0001c0004t0001g0269others(11): Show | 14 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-160+659G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243520 | ||||||
| chr4:36243611
|
T | C | 2 | a0001c0001t0003g0118a0012c0021t0009g0117 | 2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-160+568A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243611 | ||||||
| chr4:36243651
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG01993.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-160+528G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243651 | ||||||
| chr4:36243676
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-160+503T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243676 | ||||||
| chr4:36243735
|
A | G | 18 | a0001c0001t0003g0272a0001c0001t0005g0273a0001c0001t0007g0006others(15): Show | 18 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160+444T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243735 | ||||||
| chr4:36243747
|
G | A | 8 | a0002c0006t0001g0119a0002c0006t0001g0120a0002c0006t0001g0122others(5): Show | 8 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160+432C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243747 | ||||||
| chr4:36243921
|
C | T | 138 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-160+258G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243921 | ||||||
| chr4:36244061
|
T | C | 14 | a0001c0001t0003g0272a0001c0001t0005g0273a0001c0004t0001g0269others(11): Show | 14 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-160+118A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36244061 | ||||||
| chr4:36244174
|
C | T | 1 | a0001c0001t0002g0011 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.-160+5G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36244174 |