Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 5909 |
|---|---|
| ensemblid | ENSG00000076864.21 |
| hgncid | 9858 |
| symbol | RAP1GAP |
| name | RAP1 GTPase activating protein |
| refseq_nuc | NM_002885.4 |
| refseq_prot | NP_002876.2 |
| ensembl_nuc | ENST00000374765.9 |
| ensembl_prot | ENSP00000363897.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 21596221 |
| end | 21669357 |
| strand | - |
| ver | v1.2 |
| region | chr1:21596221-21669357 |
| region5000 | chr1:21591221-21674357 |
| regionname0 | RAP1GAP_chr1_21596221_21669357 |
| regionname5000 | RAP1GAP_chr1_21591221_21674357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001 | 1/0 | 663 | 208 | 52 | 51 | 75 | 6 | 23 | 43 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002 | 0/1 | 663 | 154 | 34 | 25 | 71 | 8 | 15 | 61 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0003 | 0/0 | 663 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0004 | 0/0 | 663 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0005 | 0/0 | 663 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0006 | 0/0 | 663 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0007 | 0/0 | 663 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| 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 | 1992 | 123 | 21 | 21 | 61 | 7 | 12 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0002 | 0/0 | 1992 | 83 | 14 | 19 | 47 | 1 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0003 | 1/0 | 1992 | 63 | 28 | 14 | 7 | 3 | 10 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0004 | 0/0 | 1992 | 43 | 0 | 14 | 19 | 0 | 10 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0005 | 0/0 | 1992 | 12 | 0 | 0 | 10 | 0 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0006 | 0/0 | 1992 | 10 | 7 | 2 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0007 | 0/0 | 1992 | 5 | 5 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0008 | 0/0 | 1992 | 4 | 3 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0009 | 0/0 | 1992 | 3 | 2 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0010 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0011 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0012 | 0/0 | 1992 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0013 | 0/0 | 1992 | 2 | 0 | 1 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0014 | 0/0 | 1992 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0015 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0016 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0017 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0018 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0019 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0020 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0021 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0022 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0023 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0024 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0025 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0026 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0027 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| c0028 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1331 | 277 | 57 | 55 | 127 | 9 | 28 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0002 | 0/0 | 1330 | 47 | 10 | 11 | 15 | 4 | 7 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0003 | 0/0 | 1331 | 27 | 14 | 6 | 4 | 1 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0004 | 0/1 | 1331 | 11 | 6 | 4 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0005 | 0/0 | 1330 | 2 | 1 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0006 | 0/0 | 1331 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0007 | 0/0 | 1331 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0008 | 0/0 | 1331 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0009 | 0/0 | 1331 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0010 | 0/0 | 1330 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0011 | 0/0 | 1330 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0012 | 0/0 | 1331 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| t0013 | 0/0 | 1331 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| 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 | 0 | 0 | 0 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0351 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0014 | 0/0 | 1992 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0002 | 0/0 | 1992 | 83 | 14 | 19 | 47 | 1 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0003 | 1/0 | 1992 | 63 | 28 | 14 | 7 | 3 | 10 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0004 | 0/0 | 1992 | 43 | 0 | 14 | 19 | 0 | 10 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0007 | 0/0 | 1992 | 5 | 5 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0009 | 0/0 | 1992 | 3 | 2 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0011 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0012 | 0/0 | 1992 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0013 | 0/0 | 1992 | 2 | 0 | 1 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0017 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0024 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0025 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0026 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0027 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001 | 0/1 | 1992 | 123 | 21 | 21 | 61 | 7 | 12 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0005 | 0/0 | 1992 | 12 | 0 | 0 | 10 | 0 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0006 | 0/0 | 1992 | 10 | 7 | 2 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0008 | 0/0 | 1992 | 4 | 3 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0016 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0018 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0022 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0023 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0003c0010 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0003c0015 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0004c0028 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0005c0020 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0006c0021 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0007c0019 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0014t0001 | 0/0 | 3322 | 2 | 0 | 2 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0002t0001 | 0/0 | 3322 | 77 | 11 | 16 | 47 | 1 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0002t0002 | 0/0 | 3321 | 3 | 0 | 3 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0002t0003 | 0/0 | 3322 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0002t0008 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0003t0001 | 1/0 | 3322 | 41 | 11 | 10 | 7 | 3 | 9 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0003t0002 | 0/0 | 3321 | 9 | 8 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0003t0003 | 0/0 | 3322 | 9 | 6 | 3 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0003t0004 | 0/0 | 3322 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0003t0007 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0004t0001 | 0/0 | 3322 | 43 | 0 | 14 | 19 | 0 | 10 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0007t0001 | 0/0 | 3322 | 5 | 5 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0009t0001 | 0/0 | 3322 | 3 | 2 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0011t0001 | 0/0 | 3322 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0012t0001 | 0/0 | 3322 | 2 | 0 | 0 | 0 | 1 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0013t0003 | 0/0 | 3322 | 2 | 0 | 1 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0017t0001 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0024t0001 | 0/0 | 3322 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0025t0001 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0026t0001 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0001c0027t0001 | 0/0 | 3322 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0001 | 0/0 | 3322 | 69 | 12 | 8 | 41 | 2 | 6 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0002 | 0/0 | 3321 | 32 | 2 | 7 | 15 | 3 | 5 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0003 | 0/0 | 3322 | 9 | 4 | 1 | 4 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0004 | 0/1 | 3322 | 7 | 2 | 4 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0005 | 0/0 | 3321 | 2 | 1 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0009 | 0/0 | 3322 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0010 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0011 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0001t0013 | 0/0 | 3322 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0005t0001 | 0/0 | 3322 | 9 | 0 | 0 | 9 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0005t0003 | 0/0 | 3322 | 2 | 0 | 0 | 0 | 0 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0005t0006 | 0/0 | 3322 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0006t0001 | 0/0 | 3322 | 9 | 7 | 2 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0006t0002 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0008t0003 | 0/0 | 3322 | 3 | 2 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0008t0012 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0016t0001 | 0/0 | 3322 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0018t0002 | 0/0 | 3321 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0022t0002 | 0/0 | 3321 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0002c0023t0001 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0003c0010t0001 | 0/0 | 3322 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0003c0015t0001 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0003c0015t0004 | 0/0 | 3322 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0004c0028t0001 | 0/0 | 3322 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0005c0020t0001 | 0/0 | 3322 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0006c0021t0001 | 0/0 | 3322 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| a0007c0019t0001 | 0/0 | 3322 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | copy fasta | chr1 | 21591221 | 21674357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0014t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0000c0014t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0002t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0351 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0003g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0003t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0004t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0007t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0007t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0007t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0007t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0007t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0009t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0009t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0009t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0011t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0011t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0012t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0012t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0013t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0013t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0017t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0024t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0025t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0026t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0001c0027t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0004g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0004g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0009g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0010g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0001t0013g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0005t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0006t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0008t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0008t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0008t0003g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0008t0012g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0016t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0016t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0018t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0022t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0002c0023t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0003c0010t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0003c0010t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0003c0015t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0003c0015t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0004c0028t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0005c0020t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0006c0021t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| a0007c0019t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0007 | c0019 | t0001 | g0366 | EUR | GBR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00099 | hp2 | a0002 | c0001 | t0005 | g0130 | EUR | GBR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00140 | hp1 | a0002 | c0001 | t0001 | g0139 | EUR | GBR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00140 | hp2 | a0001 | c0013 | t0003 | g0143 | EUR | GBR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00280 | hp1 | a0005 | c0020 | t0001 | g0084 | EUR | FIN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00280 | hp2 | a0002 | c0001 | t0013 | g0247 | EUR | FIN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0131 | EUR | FIN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00323 | hp2 | a0001 | c0012 | t0001 | g0059 | EUR | FIN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0209 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0249 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00423 | hp2 | a0002 | c0001 | t0002 | g0338 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0041 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00558 | hp2 | a0001 | c0004 | t0001 | g0199 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00609 | hp1 | a0002 | c0001 | t0003 | g0334 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0197 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00639 | hp1 | a0002 | c0001 | t0004 | g0006 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0256 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00642 | hp2 | a0002 | c0001 | t0004 | g0122 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0044 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | CHS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0267 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00738 | hp2 | a0002 | c0001 | t0002 | g0067 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00741 | hp1 | a0002 | c0001 | t0002 | g0147 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01069 | hp1 | a0001 | c0003 | t0007 | g0161 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0154 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01070 | hp1 | a0002 | c0001 | t0004 | g0367 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01070 | hp2 | a0002 | c0006 | t0001 | g0119 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0155 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01071 | hp2 | a0002 | c0006 | t0001 | g0118 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0280 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01074 | hp2 | a0001 | c0003 | t0001 | g0288 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01081 | hp2 | a0002 | c0001 | t0003 | g0341 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01099 | hp1 | a0001 | c0009 | t0001 | g0308 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0276 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01106 | hp1 | a0002 | c0001 | t0001 | g0311 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01106 | hp2 | a0002 | c0001 | t0009 | g0309 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01109 | hp2 | a0002 | c0008 | t0003 | g0365 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01168 | hp1 | a0001 | c0026 | t0001 | g0224 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0136 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01169 | hp2 | a0002 | c0001 | t0001 | g0135 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01175 | hp1 | a0002 | c0001 | t0002 | g0072 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0363 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01192 | hp1 | a0001 | c0013 | t0003 | g0076 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0233 | AMR | PUR | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01256 | hp2 | a0002 | c0001 | t0002 | g0089 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01257 | hp2 | a0001 | c0003 | t0001 | g0370 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01258 | hp1 | a0001 | c0003 | t0001 | g0371 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01258 | hp2 | a0002 | c0001 | t0002 | g0090 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01261 | hp1 | a0000 | c0014 | t0001 | g0171 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0169 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0368 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0205 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0110 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01361 | hp1 | a0001 | c0003 | t0001 | g0030 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01361 | hp2 | a0002 | c0018 | t0002 | g0058 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0321 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01433 | hp2 | a0002 | c0001 | t0001 | g0150 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01496 | hp1 | a0001 | c0003 | t0003 | g0369 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0068 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01515 | hp1 | a0002 | c0001 | t0002 | g0108 | EUR | IBS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01515 | hp2 | a0001 | c0003 | t0001 | g0342 | EUR | IBS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0109 | EUR | IBS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0148 | EUR | IBS | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0346 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01891 | hp1 | a0002 | c0006 | t0001 | g0152 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0307 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01928 | hp1 | a0001 | c0004 | t0001 | g0215 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01934 | hp1 | a0001 | c0025 | t0001 | g0278 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01934 | hp2 | a0002 | c0001 | t0002 | g0107 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0221 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0071 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0279 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0083 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01975 | hp2 | a0002 | c0001 | t0001 | g0082 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01978 | hp1 | a0002 | c0001 | t0002 | g0073 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01978 | hp2 | a0001 | c0004 | t0001 | g0284 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01981 | hp1 | a0002 | c0001 | t0001 | g0184 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01981 | hp2 | a0000 | c0014 | t0001 | g0170 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0281 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02004 | hp1 | a0001 | c0004 | t0001 | g0232 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0265 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02015 | hp2 | a0002 | c0001 | t0002 | g0017 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02027 | hp1 | a0001 | c0024 | t0001 | g0146 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02040 | hp1 | a0001 | c0004 | t0001 | g0273 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0245 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0336 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02074 | hp2 | a0001 | c0004 | t0001 | g0271 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0050 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02080 | hp2 | a0001 | c0004 | t0001 | g0335 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0292 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02135 | hp2 | a0001 | c0004 | t0001 | g0269 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02145 | hp1 | a0001 | c0003 | t0003 | g0347 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02145 | hp2 | a0001 | c0009 | t0001 | g0317 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02155 | hp1 | a0002 | c0001 | t0003 | g0212 | EAS | CDX | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | CDX | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02165 | hp1 | a0002 | c0001 | t0002 | g0113 | EAS | CDX | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | CDX | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0328 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0057 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02258 | hp1 | a0002 | c0001 | t0003 | g0324 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02273 | hp1 | a0001 | c0004 | t0001 | g0253 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02273 | hp2 | a0001 | c0004 | t0001 | g0200 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02280 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02280 | hp2 | a0001 | c0003 | t0003 | g0349 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02293 | hp1 | a0001 | c0004 | t0001 | g0069 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0206 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02300 | hp1 | a0002 | c0001 | t0004 | g0007 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | PEL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02451 | hp1 | a0002 | c0001 | t0002 | g0260 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02523 | hp2 | a0002 | c0001 | t0002 | g0091 | EAS | KHV | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02572 | hp1 | a0001 | c0003 | t0003 | g0179 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0313 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02615 | hp1 | a0001 | c0003 | t0003 | g0329 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02615 | hp2 | a0003 | c0015 | t0004 | g0055 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02622 | hp2 | a0001 | c0011 | t0001 | g0350 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0202 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0312 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02683 | hp1 | a0001 | c0003 | t0001 | g0137 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02683 | hp2 | a0001 | c0004 | t0001 | g0286 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0144 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0244 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02717 | hp1 | a0002 | c0008 | t0003 | g0063 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02717 | hp2 | a0002 | c0001 | t0003 | g0323 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0358 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02723 | hp2 | a0002 | c0001 | t0001 | g0163 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0060 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0201 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02738 | hp1 | a0001 | c0004 | t0001 | g0114 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02738 | hp2 | a0002 | c0005 | t0003 | g0332 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02809 | hp2 | a0001 | c0003 | t0004 | g0354 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0066 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0322 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0316 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0164 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02895 | hp2 | a0002 | c0016 | t0001 | g0129 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0315 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02896 | hp2 | a0002 | c0006 | t0001 | g0151 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02897 | hp1 | a0002 | c0006 | t0001 | g0140 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02897 | hp2 | a0002 | c0016 | t0001 | g0128 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02922 | hp2 | a0002 | c0008 | t0012 | g0064 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0210 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02976 | hp2 | a0001 | c0003 | t0004 | g0362 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03017 | hp1 | a0001 | c0003 | t0002 | g0134 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03017 | hp2 | a0002 | c0005 | t0003 | g0185 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0231 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03041 | hp2 | a0001 | c0002 | t0008 | g0126 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0320 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0348 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0177 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0359 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0355 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03139 | hp2 | a0001 | c0017 | t0001 | g0319 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03195 | hp1 | a0002 | c0006 | t0001 | g0301 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0156 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0304 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03209 | hp2 | a0001 | c0007 | t0001 | g0188 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0056 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0303 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03239 | hp1 | a0001 | c0012 | t0001 | g0024 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03239 | hp2 | a0001 | c0004 | t0001 | g0364 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03453 | hp1 | a0003 | c0015 | t0001 | g0002 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0331 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03486 | hp1 | a0002 | c0006 | t0001 | g0306 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03486 | hp2 | a0003 | c0010 | t0001 | g0327 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03490 | hp1 | a0002 | c0001 | t0002 | g0132 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03490 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03492 | hp2 | a0001 | c0003 | t0001 | g0070 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03516 | hp1 | a0001 | c0003 | t0001 | g0314 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03516 | hp2 | a0002 | c0006 | t0001 | g0302 | AFR | ESN | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03540 | hp1 | a0002 | c0023 | t0001 | g0310 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | GWD | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03579 | hp1 | a0002 | c0006 | t0001 | g0357 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0360 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0123 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03654 | hp2 | a0002 | c0001 | t0010 | g0261 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03669 | hp1 | a0001 | c0004 | t0001 | g0217 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03669 | hp2 | a0002 | c0001 | t0002 | g0115 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03688 | hp1 | a0001 | c0003 | t0001 | g0061 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03688 | hp2 | a0001 | c0004 | t0001 | g0160 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0218 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0094 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0226 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03710 | hp2 | a0002 | c0001 | t0002 | g0080 | SAS | PJL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03831 | hp1 | a0001 | c0003 | t0001 | g0176 | SAS | BEB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03831 | hp2 | a0001 | c0004 | t0001 | g0290 | SAS | BEB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0289 | SAS | BEB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0175 | SAS | BEB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0165 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04115 | hp2 | a0002 | c0001 | t0002 | g0159 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0012 | SAS | BEB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0029 | SAS | BEB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04199 | hp2 | a0002 | c0022 | t0002 | g0145 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04228 | hp1 | a0002 | c0001 | t0002 | g0104 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG04228 | hp2 | a0002 | c0001 | t0001 | g0009 | SAS | STU | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | YRI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18522 | hp2 | a0003 | c0010 | t0001 | g0054 | AFR | YRI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | CHB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | CHB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18906 | hp1 | a0002 | c0008 | t0003 | g0065 | AFR | YRI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18906 | hp2 | a0001 | c0003 | t0002 | g0361 | AFR | YRI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0295 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18942 | hp1 | a0002 | c0005 | t0001 | g0020 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0036 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18944 | hp1 | a0002 | c0001 | t0002 | g0268 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18944 | hp2 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18945 | hp1 | a0002 | c0001 | t0002 | g0101 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18945 | hp2 | a0002 | c0001 | t0001 | g0039 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18946 | hp1 | a0002 | c0001 | t0002 | g0040 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18946 | hp2 | a0004 | c0028 | t0001 | g0277 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18949 | hp2 | a0002 | c0001 | t0002 | g0352 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18950 | hp1 | a0002 | c0005 | t0001 | g0032 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18950 | hp2 | a0006 | c0021 | t0001 | g0035 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18952 | hp2 | a0001 | c0004 | t0001 | g0243 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18953 | hp2 | a0002 | c0005 | t0001 | g0052 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18954 | hp1 | a0002 | c0001 | t0001 | g0043 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18957 | hp1 | a0002 | c0005 | t0001 | g0042 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18957 | hp2 | a0002 | c0001 | t0002 | g0079 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18960 | hp2 | a0002 | c0001 | t0002 | g0337 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18962 | hp2 | a0002 | c0005 | t0001 | g0053 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0098 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18963 | hp2 | a0002 | c0001 | t0003 | g0038 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18964 | hp1 | a0002 | c0001 | t0001 | g0031 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18966 | hp1 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0228 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0223 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18971 | hp1 | a0002 | c0005 | t0006 | g0078 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0014 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0049 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18980 | hp2 | a0002 | c0005 | t0001 | g0021 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18984 | hp1 | a0001 | c0027 | t0001 | g0095 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18984 | hp2 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18986 | hp1 | a0001 | c0004 | t0001 | g0254 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0028 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0106 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18994 | hp2 | a0002 | c0001 | t0001 | g0033 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18995 | hp1 | a0001 | c0004 | t0001 | g0189 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18995 | hp2 | a0002 | c0001 | t0002 | g0343 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18999 | hp1 | a0002 | c0001 | t0002 | g0252 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0018 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19000 | hp2 | a0002 | c0001 | t0001 | g0259 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19002 | hp2 | a0002 | c0001 | t0001 | g0282 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19003 | hp1 | a0002 | c0001 | t0011 | g0120 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19005 | hp2 | a0002 | c0001 | t0003 | g0037 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0345 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0181 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0330 | AFR | LWK | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19030 | hp2 | a0002 | c0001 | t0001 | g0158 | AFR | LWK | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19043 | hp1 | a0002 | c0001 | t0003 | g0297 | AFR | LWK | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19043 | hp2 | a0002 | c0001 | t0004 | g0121 | AFR | LWK | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0074 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0229 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19055 | hp2 | a0002 | c0001 | t0002 | g0344 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19056 | hp2 | a0002 | c0001 | t0002 | g0340 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19058 | hp1 | a0002 | c0005 | t0001 | g0333 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19058 | hp2 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0013 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19065 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0097 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19068 | hp2 | a0002 | c0005 | t0001 | g0027 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19070 | hp1 | a0002 | c0001 | t0001 | g0257 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19077 | hp1 | a0001 | c0004 | t0001 | g0195 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19077 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0100 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19080 | hp1 | a0001 | c0004 | t0001 | g0270 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19080 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19082 | hp2 | a0002 | c0001 | t0002 | g0048 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19084 | hp1 | a0002 | c0005 | t0001 | g0294 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19084 | hp2 | a0002 | c0001 | t0001 | g0045 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19085 | hp1 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19085 | hp2 | a0001 | c0004 | t0001 | g0198 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19088 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0296 | AFR | YRI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0305 | AFR | YRI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA20129 | hp1 | a0002 | c0001 | t0002 | g0142 | AFR | ASW | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0356 | AFR | ASW | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0264 | EUR | TSI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA20752 | hp2 | a0002 | c0001 | t0002 | g0133 | EUR | TSI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0124 | EUR | TSI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA20805 | hp2 | a0002 | c0006 | t0002 | g0125 | EUR | TSI | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0298 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0287 | AMR | CLM | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02109 | hp1 | a0001 | c0011 | t0001 | g0157 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02486 | hp1 | a0001 | c0007 | t0001 | g0186 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02486 | hp2 | a0001 | c0009 | t0001 | g0318 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02559 | hp1 | a0002 | c0001 | t0003 | g0325 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG02559 | hp2 | a0002 | c0001 | t0005 | g0092 | AFR | ACB | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03471 | hp1 | a0001 | c0007 | t0001 | g0326 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0353 | AFR | MSL | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG06807 | hp1 | a0001 | c0007 | t0001 | g0187 | AFR | USA | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| HG06807 | hp2 | a0002 | c0001 | t0001 | g0174 | AFR | USA | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA21309 | hp1 | a0001 | c0007 | t0001 | g0300 | AFR | LWK | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| NA21309 | hp2 | a0002 | c0001 | t0004 | g0180 | AFR | LWK | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0004 | g0005 | REF | REF | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0351 | REF | REF | RAP1GAP_chr1_21591221_21674357 | RAP1GAP | chr1 | 21591221 | 21674357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21597720
|
C | G | 1 | a0000 | 2 | HG01261.hp1 HG01981.hp2 |
stop_lost | HIGH | c.1992G>C | p.Ter664Tyrext*? | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 24/25 | 2244/3322 | 1992/1992 | 664/663 | chr1 | 21597720 | ||
| chr1:21598037
|
G | A | 1 | a0003 | 4 | HG02615.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
missense_variant | MODERATE | c.1907C>T | p.Ala636Val | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 23/25 | 2159/3322 | 1907/1992 | 636/663 | chr1 | 21598037 | ||
| chr1:21598453
|
T | C | 1 | a0007 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.1826A>G | p.Tyr609Cys | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 22/25 | 2078/3322 | 1826/1992 | 609/663 | chr1 | 21598453 | ||
| chr1:21599570
|
C | T | 1 | a0006 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.1700G>A | p.Arg567His | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/25 | 1952/3322 | 1700/1992 | 567/663 | chr1 | 21599570 | ||
| chr1:21602852
|
C | T | 1 | a0005 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.1490G>A | p.Arg497His | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/25 | 1742/3322 | 1490/1992 | 497/663 | chr1 | 21602852 | ||
| chr1:21613674
|
G | C | 1 | a0004 | 1 | NA18946.hp2 | missense_variant | MODERATE | c.428C>G | p.Pro143Arg | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 9/25 | 680/3322 | 428/1992 | 143/663 | chr1 | 21613674 | ||
| chr1:21614062
|
C | T | 4 | a0002a0005a0006others(1): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
missense_variant | MODERATE | c.319G>A | p.Ala107Thr | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 8/25 | 571/3322 | 319/1992 | 107/663 | chr1 | 21614062 | ||
| chr1:21649796
|
C | T | 1 | a0002 | 2 | HG00099.hp2 HG02559.hp2 |
splice_region_variant | LOW | c.-148G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/25 | chr1 | 21649796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21598039
|
G | A | 1 | a0002c0022 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1905C>T | p.Asp635Asp | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 23/25 | 2157/3322 | 1905/1992 | 635/663 | chr1 | 21598039 | ||
| chr1:21598419
|
A | G | 1 | a0001c0013 | 2 | HG00140.hp2 HG01192.hp1 |
synonymous_variant | LOW | c.1860T>C | p.Thr620Thr | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 22/25 | 2112/3322 | 1860/1992 | 620/663 | chr1 | 21598419 | ||
| chr1:21606117
|
G | A | 1 | a0001c0025 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1377C>T | p.His459His | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/25 | 1629/3322 | 1377/1992 | 459/663 | chr1 | 21606117 | ||
| chr1:21606132
|
G | A | 5 | a0001c0004a0001c0011a0001c0026others(2): Show | 59 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
synonymous_variant | LOW | c.1362C>T | p.Thr454Thr | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/25 | 1614/3322 | 1362/1992 | 454/663 | chr1 | 21606132 | ||
| chr1:21608865
|
C | T | 2 | a0002c0008a0007c0019 | 5 | HG00099.hp1 HG01109.hp2 HG02717.hp1 others(2): Show |
synonymous_variant | LOW | c.1143G>A | p.Lys381Lys | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 16/25 | 1395/3322 | 1143/1992 | 381/663 | chr1 | 21608865 | ||
| chr1:21610207
|
G | A | 2 | a0001c0007a0002c0023 | 6 | HG02486.hp1 HG03209.hp2 HG03471.hp1 others(3): Show |
synonymous_variant | LOW | c.912C>T | p.Phe304Phe | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 14/25 | 1164/3322 | 912/1992 | 304/663 | chr1 | 21610207 | ||
| chr1:21610243
|
G | A | 1 | a0001c0027 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.876C>T | p.Ile292Ile | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 14/25 | 1128/3322 | 876/1992 | 292/663 | chr1 | 21610243 | ||
| chr1:21611530
|
C | T | 1 | a0001c0024 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.765G>A | p.Val255Val | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/25 | 1017/3322 | 765/1992 | 255/663 | chr1 | 21611530 | ||
| chr1:21614057
|
G | A | 1 | a0001c0009 | 3 | HG01099.hp1 HG02145.hp2 HG02486.hp2 |
synonymous_variant | LOW | c.324C>T | p.Ala108Ala | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 8/25 | 576/3322 | 324/1992 | 108/663 | chr1 | 21614057 | ||
| chr1:21617327
|
G | A | 6 | a0001c0002a0001c0004a0001c0007others(3): Show | 135 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(132): Show |
synonymous_variant | LOW | c.270C>T | p.Tyr90Tyr | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/25 | 522/3322 | 270/1992 | 90/663 | chr1 | 21617327 | ||
| chr1:21617372
|
G | C | 1 | a0002c0016 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.225C>G | p.Pro75Pro | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/25 | 477/3322 | 225/1992 | 75/663 | chr1 | 21617372 | ||
| chr1:21617946
|
C | T | 1 | a0002c0018 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.93G>A | p.Pro31Pro | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/25 | 345/3322 | 93/1992 | 31/663 | chr1 | 21617946 | ||
| chr1:21619037
|
C | T | 6 | a0001c0009a0001c0011a0001c0012others(3): Show | 20 | HG00323.hp2 HG01070.hp2 HG01071.hp2 others(17): Show |
synonymous_variant | LOW | c.54G>A | p.Pro18Pro | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/25 | 306/3322 | 54/1992 | 18/663 | chr1 | 21619037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21596238
|
G | T | 1 | a0002c0001t0009 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 1482 | chr1 | 21596238 | |||||
| chr1:21596365
|
C | T | 1 | a0002c0001t0010 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*934G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 1355 | chr1 | 21596365 | |||||
| chr1:21596400
|
CG | C | 9 | a0001c0002t0002a0001c0003t0002a0002c0001t0002others(6): Show | 51 | HG00099.hp2 HG00423.hp2 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*898delC | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 1319 | chr1 | 21596400 | |||||
| chr1:21596616
|
C | T | 1 | a0001c0002t0008 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*683G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 1104 | chr1 | 21596616 | |||||
| chr1:21596629
|
C | T | 1 | a0001c0003t0007 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*670G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 1091 | chr1 | 21596629 | |||||
| chr1:21597051
|
C | G | 7 | a0001c0002t0003a0001c0003t0003a0001c0013t0003others(4): Show | 28 | HG00140.hp2 HG00609.hp1 HG01081.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*248G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 669 | chr1 | 21597051 | |||||
| chr1:21597108
|
G | A | 1 | a0002c0001t0011 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 612 | chr1 | 21597108 | |||||
| chr1:21597158
|
G | A | 1 | a0002c0001t0013 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*141C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 25/25 | 562 | chr1 | 21597158 | |||||
| chr1:21597719
|
G | A | 1 | a0002c0008t0012 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 24/25 | 1 | chr1 | 21597719 | |||||
| chr1:21626391
|
G | A | 4 | a0001c0003t0004a0002c0001t0004a0002c0001t0013others(1): Show | 12 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-106C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/25 | 6359 | chr1 | 21626391 | |||||
| chr1:21649786
|
A | T | 1 | a0002c0005t0006 | 1 | NA18971.hp1 | 5_prime_UTR_variant | MODIFIER | c.-138T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/25 | 29754 | chr1 | 21649786 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:21597306
|
T | G | 2 | a0002c0001t0003g0212a0002c0001t0003g0334 | 2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.*35-42A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 24/24 | chr1 | 21597306 | ||||||
| chr1:21597778
|
C | G | 1 | a0002c0001t0001g0177 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1984-50G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 23/24 | chr1 | 21597778 | ||||||
| chr1:21597778
|
C | T | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1984-50G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 23/24 | chr1 | 21597778 | ||||||
| chr1:21598584
|
C | T | 19 | a0001c0002t0003g0303a0001c0002t0003g0307a0001c0003t0003g0156others(16): Show | 19 | HG00140.hp2 HG00609.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1777-82G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598584 | ||||||
| chr1:21598615
|
T | C | 346 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1777-113A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598615 | ||||||
| chr1:21598690
|
C | A | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1777-188G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598690 | ||||||
| chr1:21598818
|
A | G | 2 | a0001c0002t0001g0287a0001c0002t0001g0299 | 2 | HG00741.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1777-316T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598818 | ||||||
| chr1:21598850
|
CTG | C | 4 | a0003c0010t0001g0054a0003c0010t0001g0327a0003c0015t0001g0002others(1): Show | 4 | HG02615.hp2 HG03453.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-350_1777-349d others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598850 | ||||||
| chr1:21598881
|
ACT | A | 4 | a0001c0002t0001g0266a0001c0002t0001g0280a0001c0002t0001g0287others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-381_1777-380d others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598881 | ||||||
| chr1:21598895
|
T | C | 346 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1777-393A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598895 | ||||||
| chr1:21598917
|
G | A | 5 | a0003c0010t0001g0054a0003c0010t0001g0327a0003c0015t0001g0002others(2): Show | 5 | HG00280.hp1 HG02615.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1777-415C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21598917 | ||||||
| chr1:21599013
|
G | A | 8 | a0001c0003t0001g0141a0001c0003t0001g0313a0001c0003t0001g0328others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1776+481C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21599013 | ||||||
| chr1:21599110
|
A | G | 21 | a0001c0002t0003g0303a0001c0002t0003g0307a0001c0003t0003g0156others(18): Show | 21 | HG00140.hp2 HG00609.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1776+384T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21599110 | ||||||
| chr1:21599164
|
C | T | 346 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1776+330G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21599164 | ||||||
| chr1:21599214
|
G | A | 1 | a0001c0003t0004g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1776+280C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21599214 | ||||||
| chr1:21599450
|
C | T | 1 | a0002c0001t0002g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1776+44G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 21/24 | chr1 | 21599450 | ||||||
| chr1:21599655
|
C | T | 2 | a0002c0001t0002g0067a0002c0001t0002g0133 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1653-38G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21599655 | ||||||
| chr1:21599674
|
G | C | 1 | a0002c0001t0001g0031 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1653-57C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21599674 | ||||||
| chr1:21599675
|
C | T | 1 | a0006c0021t0001g0035 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1653-58G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21599675 | ||||||
| chr1:21599694
|
C | T | 203 | a0001c0002t0001g0046a0001c0002t0001g0190a0001c0002t0001g0191others(200): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1653-77G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21599694 | ||||||
| chr1:21599695
|
C | T | 10 | a0001c0002t0001g0330a0001c0003t0001g0173a0001c0003t0001g0353others(7): Show | 10 | HG00642.hp2 HG02109.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1653-78G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21599695 | ||||||
| chr1:21600005
|
G | A | 122 | a0001c0002t0001g0046a0001c0002t0001g0191a0001c0002t0001g0196others(119): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1653-388C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600005 | ||||||
| chr1:21600107
|
G | A | 112 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(109): Show | 112 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1653-490C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600107 | ||||||
| chr1:21600172
|
T | C | 3 | a0001c0003t0001g0008a0001c0003t0001g0061a0001c0003t0001g0233 | 3 | HG01081.hp1 HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1653-555A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600172 | ||||||
| chr1:21600223
|
C | T | 4 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0234others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1653-606G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600223 | ||||||
| chr1:21600249
|
G | A | 1 | a0002c0001t0003g0334 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1653-632C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600249 | ||||||
| chr1:21600438
|
G | A | 1 | a0002c0001t0010g0261 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1653-821C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600438 | ||||||
| chr1:21600624
|
C | T | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1653-1007G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600624 | ||||||
| chr1:21600675
|
G | A | 3 | a0001c0002t0001g0190a0001c0009t0001g0317a0001c0009t0001g0318 | 3 | HG02145.hp2 HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1652+1009C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600675 | ||||||
| chr1:21600713
|
C | T | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1652+971G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600713 | ||||||
| chr1:21600714
|
G | A | 2 | a0001c0009t0001g0317a0001c0009t0001g0318 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1652+970C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600714 | ||||||
| chr1:21600863
|
A | T | 6 | a0002c0001t0001g0184a0002c0001t0004g0005a0002c0001t0004g0006others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1652+821T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600863 | ||||||
| chr1:21600872
|
A | G | 5 | a0001c0003t0001g0210a0001c0003t0001g0231a0001c0003t0001g0314others(2): Show | 5 | HG02896.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1652+812T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600872 | ||||||
| chr1:21600884
|
C | CA | 53 | a0001c0002t0001g0235a0001c0002t0001g0241a0001c0004t0001g0041others(50): Show | 53 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1652+799dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA | 14 | a0001c0002t0001g0339a0001c0003t0001g0070a0001c0003t0001g0138others(11): Show | 14 | HG00733.hp2 HG01106.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1652+793_1652+799d others(9): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(2): Show |
73 | a0001c0002t0001g0015a0001c0002t0001g0025a0001c0002t0001g0026others(70): Show | 73 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1652+791_1652+799d others(11): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(3): Show |
12 | a0001c0002t0001g0016a0001c0002t0001g0127a0001c0002t0001g0149others(9): Show | 12 | HG00099.hp1 HG00621.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1652+790_1652+799d others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(4): Show |
6 | a0001c0003t0001g0231a0001c0003t0001g0233a0001c0003t0004g0316others(3): Show | 6 | HG01081.hp2 HG01192.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1652+789_1652+799d others(13): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(5): Show |
50 | a0001c0002t0001g0248a0001c0002t0001g0330a0001c0002t0003g0303others(47): Show | 50 | HG00140.hp2 HG00609.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.1652+788_1652+799d others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(6): Show |
102 | a0001c0002t0001g0046a0001c0002t0001g0220a0001c0002t0001g0255others(99): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1652+787_1652+799d others(15): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(7): Show |
26 | a0001c0002t0001g0196a0001c0002t0001g0293a0001c0003t0001g0353others(23): Show | 26 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1652+786_1652+799d others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0191 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1652+785_1652+799d others(17): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600884
|
C | CAAAAAAA others(9): Show |
1 | a0001c0003t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1652+799_1652+800i others(18): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600884 | ||||||
| chr1:21600926
|
G | A | 2 | a0002c0001t0001g0355a0002c0001t0001g0356 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1652+758C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21600926 | ||||||
| chr1:21601022
|
C | CT | 342 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1652+661dupA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601022 | ||||||
| chr1:21601286
|
C | G | 1 | a0001c0012t0001g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1652+398G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601286 | ||||||
| chr1:21601314
|
T | C | 151 | a0001c0002t0001g0015a0001c0002t0001g0019a0001c0002t0001g0025others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1652+370A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601314 | ||||||
| chr1:21601316
|
TC | T | 32 | a0001c0002t0001g0190a0001c0002t0001g0330a0001c0003t0001g0314others(29): Show | 32 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1652+367delG | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601316 | ||||||
| chr1:21601325
|
A | T | 1 | a0002c0001t0001g0031 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1652+359T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601325 | ||||||
| chr1:21601327
|
C | G | 173 | a0001c0002t0001g0015a0001c0002t0001g0019a0001c0002t0001g0025others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.1652+357G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601327 | ||||||
| chr1:21601355
|
C | T | 66 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0190others(63): Show | 66 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.1652+329G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601355 | ||||||
| chr1:21601363
|
C | T | 64 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0190others(61): Show | 64 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1652+321G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601363 | ||||||
| chr1:21601367
|
C | T | 2 | a0001c0003t0001g0008a0001c0003t0001g0061 | 2 | HG01081.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1652+317G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601367 | ||||||
| chr1:21601422
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1652+262G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601422 | ||||||
| chr1:21601440
|
C | A | 1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1652+244G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601440 | ||||||
| chr1:21601526
|
G | T | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1652+158C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601526 | ||||||
| chr1:21601629
|
G | A | 1 | a0002c0001t0001g0031 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1652+55C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601629 | ||||||
| chr1:21601631
|
A | G | 1 | a0002c0001t0001g0031 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1652+53T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601631 | ||||||
| chr1:21601674
|
G | A | 1 | a0001c0002t0001g0292 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1652+10C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 20/24 | chr1 | 21601674 | ||||||
| chr1:21601817
|
A | G | 1 | a0002c0001t0002g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1539-20T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21601817 | ||||||
| chr1:21601851
|
C | G | 174 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(171): Show | 174 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1539-54G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21601851 | ||||||
| chr1:21601896
|
C | T | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1539-99G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21601896 | ||||||
| chr1:21602081
|
C | T | 1 | a0001c0004t0001g0195 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1539-284G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602081 | ||||||
| chr1:21602215
|
G | A | 2 | a0002c0001t0001g0057a0002c0001t0001g0321 | 2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1539-418C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602215 | ||||||
| chr1:21602303
|
G | A | 1 | a0001c0003t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1538+501C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602303 | ||||||
| chr1:21602310
|
G | A | 3 | a0001c0002t0001g0190a0001c0009t0001g0317a0001c0009t0001g0318 | 3 | HG02145.hp2 HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1538+494C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602310 | ||||||
| chr1:21602335
|
C | T | 4 | a0002c0001t0001g0164a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1538+469G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602335 | ||||||
| chr1:21602368
|
C | T | 2 | a0002c0001t0001g0057a0002c0001t0001g0321 | 2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1538+436G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602368 | ||||||
| chr1:21602497
|
A | T | 1 | a0002c0001t0001g0031 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1538+307T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602497 | ||||||
| chr1:21602599
|
C | T | 5 | a0001c0003t0001g0210a0001c0003t0001g0231a0001c0003t0001g0313others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1538+205G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602599 | ||||||
| chr1:21602682
|
T | C | 2 | a0001c0011t0001g0157a0001c0011t0001g0350 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1538+122A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602682 | ||||||
| chr1:21602694
|
A | T | 1 | a0002c0001t0001g0031 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1538+110T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602694 | ||||||
| chr1:21602724
|
C | A | 4 | a0002c0001t0001g0164a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1538+80G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602724 | ||||||
| chr1:21602767
|
A | G | 345 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1538+37T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 19/24 | chr1 | 21602767 | ||||||
| chr1:21602963
|
GC | G | 261 | a0001c0002t0001g0046a0001c0002t0001g0190a0001c0002t0001g0220others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1429-51delG | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21602963 | ||||||
| chr1:21603016
|
T | C | 2 | a0001c0003t0001g0137a0001c0003t0001g0176 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1429-103A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603016 | ||||||
| chr1:21603105
|
G | C | 1 | a0001c0004t0001g0336 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1429-192C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603105 | ||||||
| chr1:21603162
|
C | T | 2 | a0001c0003t0003g0368a0001c0003t0003g0369 | 2 | HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1429-249G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603162 | ||||||
| chr1:21603192
|
G | A | 1 | a0001c0003t0003g0329 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429-279C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603192 | ||||||
| chr1:21603195
|
C | T | 1 | a0001c0003t0004g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1429-282G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603195 | ||||||
| chr1:21603299
|
G | A | 5 | a0001c0003t0001g0328a0002c0001t0001g0056a0002c0006t0001g0301others(2): Show | 5 | HG02257.hp1 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1429-386C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603299 | ||||||
| chr1:21603364
|
G | C | 1 | a0001c0026t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1429-451C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603364 | ||||||
| chr1:21603713
|
C | T | 1 | a0001c0003t0002g0361 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1429-800G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603713 | ||||||
| chr1:21603873
|
G | A | 1 | a0002c0001t0001g0295 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1429-960C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21603873 | ||||||
| chr1:21604012
|
A | G | 8 | a0002c0001t0004g0121a0002c0001t0004g0122a0002c0006t0001g0118others(5): Show | 8 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1429-1099T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604012 | ||||||
| chr1:21604041
|
G | C | 3 | a0001c0002t0001g0190a0001c0009t0001g0317a0001c0009t0001g0318 | 3 | HG02145.hp2 HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1429-1128C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604041 | ||||||
| chr1:21604049
|
C | T | 97 | a0001c0002t0001g0190a0001c0002t0003g0307a0001c0003t0001g0342others(94): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1429-1136G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604049 | ||||||
| chr1:21604062
|
A | G | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1429-1149T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604062 | ||||||
| chr1:21604093
|
C | T | 9 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0192others(6): Show | 9 | HG02071.hp2 HG02132.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1429-1180G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604093 | ||||||
| chr1:21604156
|
G | A | 1 | a0001c0003t0004g0354 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1429-1243C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604156 | ||||||
| chr1:21604229
|
G | A | 2 | a0001c0002t0001g0162a0001c0002t0001g0172 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1429-1316C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604229 | ||||||
| chr1:21604343
|
C | CA | 122 | a0001c0002t0001g0046a0001c0002t0001g0220a0001c0002t0001g0292others(119): Show | 122 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1429-1431dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604343 | ||||||
| chr1:21604384
|
A | C | 3 | a0001c0003t0001g0008a0001c0003t0001g0061a0001c0003t0001g0233 | 3 | HG01081.hp1 HG01192.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1429-1471T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604384 | ||||||
| chr1:21604717
|
G | A | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1428+1349C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604717 | ||||||
| chr1:21604774
|
AGGAT | A | 339 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(336): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1428+1288_1428+129 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604774 | ||||||
| chr1:21604803
|
G | A | 5 | a0001c0002t0003g0303a0002c0001t0001g0163a0002c0001t0003g0323others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428+1263C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604803 | ||||||
| chr1:21604828
|
T | G | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1428+1238A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604828 | ||||||
| chr1:21604843
|
A | AGATG | 21 | a0001c0002t0001g0182a0001c0002t0001g0211a0001c0002t0001g0339others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1428+1219_1428+122 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604843 | ||||||
| chr1:21604843
|
AGATG | A | 96 | a0001c0002t0001g0046a0001c0002t0001g0178a0001c0002t0001g0220others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1428+1219_1428+122 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604843 | ||||||
| chr1:21604843
|
AGATGGAT others(1): Show |
A | 4 | a0002c0001t0001g0164a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428+1215_1428+122 others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604843 | ||||||
| chr1:21604843
|
AGATGGAT others(5): Show |
A | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1428+1211_1428+122 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604843 | ||||||
| chr1:21604873
|
A | G | 1 | a0001c0003t0001g0077 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1428+1193T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604873 | ||||||
| chr1:21604917
|
ATGGGTGG others(5): Show |
A | 84 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(81): Show | 84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.1428+1137_1428+114 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604917 | ||||||
| chr1:21604937
|
A | ATGGGTGG others(17): Show |
1 | a0002c0001t0002g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1428+1105_1428+112 others(28): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21604937 | ||||||
| chr1:21605041
|
ATGGATGG others(9): Show |
A | 3 | a0001c0004t0001g0071a0001c0004t0001g0110a0001c0026t0001g0224 | 3 | HG01168.hp1 HG01358.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1428+1009_1428+102 others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21605041 | ||||||
| chr1:21605057
|
G | C | 1 | a0001c0004t0001g0245 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1428+1009C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21605057 | ||||||
| chr1:21605286
|
C | T | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1428+780G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21605286 | ||||||
| chr1:21605535
|
A | G | 1 | a0002c0001t0011g0120 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1428+531T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21605535 | ||||||
| chr1:21605603
|
G | C | 6 | a0001c0003t0001g0328a0002c0001t0001g0056a0002c0001t0001g0311others(3): Show | 6 | HG01106.hp1 HG02257.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428+463C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21605603 | ||||||
| chr1:21605976
|
G | A | 2 | a0002c0001t0001g0124a0002c0001t0001g0139 | 2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1428+90C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21605976 | ||||||
| chr1:21606037
|
C | A | 312 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(309): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1428+29G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 18/24 | chr1 | 21606037 | ||||||
| chr1:21606412
|
C | T | 5 | a0001c0017t0001g0319a0002c0001t0001g0164a0002c0001t0001g0312others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297-215G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606412 | ||||||
| chr1:21606660
|
C | G | 3 | a0001c0003t0007g0161a0001c0009t0001g0308a0002c0001t0001g0066 | 3 | HG01069.hp1 HG01099.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1297-463G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606660 | ||||||
| chr1:21606671
|
T | C | 2 | a0001c0011t0001g0157a0001c0011t0001g0350 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1297-474A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606671 | ||||||
| chr1:21606692
|
C | T | 2 | a0001c0002t0001g0249a0001c0002t0001g0263 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.1297-495G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606692 | ||||||
| chr1:21606700
|
C | T | 347 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1297-503G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606700 | ||||||
| chr1:21606716
|
T | C | 4 | a0002c0001t0001g0164a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-519A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606716 | ||||||
| chr1:21606769
|
A | T | 1 | a0001c0004t0001g0271 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1297-572T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606769 | ||||||
| chr1:21606834
|
C | T | 1 | a0001c0003t0004g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1297-637G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606834 | ||||||
| chr1:21606852
|
G | A | 61 | a0001c0002t0001g0046a0001c0002t0001g0220a0001c0002t0001g0248others(58): Show | 62 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1297-655C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606852 | ||||||
| chr1:21606922
|
G | C | 1 | a0002c0005t0003g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1297-725C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606922 | ||||||
| chr1:21606974
|
T | C | 7 | a0002c0001t0001g0057a0002c0001t0001g0321a0002c0008t0003g0063others(4): Show | 7 | HG00099.hp1 HG01109.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.1297-777A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21606974 | ||||||
| chr1:21607015
|
C | T | 1 | a0001c0004t0001g0197 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1297-818G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607015 | ||||||
| chr1:21607065
|
C | A | 1 | a0002c0022t0002g0145 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1297-868G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607065 | ||||||
| chr1:21607075
|
C | T | 35 | a0001c0002t0003g0307a0001c0003t0001g0328a0001c0003t0003g0156others(32): Show | 35 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.1297-878G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607075 | ||||||
| chr1:21607092
|
C | G | 1 | a0001c0002t0001g0026 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1297-895G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607092 | ||||||
| chr1:21607095
|
G | A | 6 | a0002c0001t0001g0184a0002c0001t0004g0005a0002c0001t0004g0006others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297-898C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607095 | ||||||
| chr1:21607551
|
ACTCTATT others(1): Show |
A | 162 | a0001c0002t0001g0046a0001c0002t0001g0220a0001c0002t0001g0248others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.1296+654_1296+661d others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607551 | ||||||
| chr1:21607574
|
A | C | 7 | a0001c0003t0001g0210a0001c0003t0001g0231a0001c0003t0001g0313others(4): Show | 7 | HG02572.hp2 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1296+639T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607574 | ||||||
| chr1:21607599
|
T | C | 1 | a0002c0001t0001g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1296+614A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607599 | ||||||
| chr1:21607833
|
A | C | 6 | a0002c0001t0001g0184a0002c0001t0004g0005a0002c0001t0004g0006others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1296+380T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607833 | ||||||
| chr1:21607999
|
C | T | 4 | a0002c0001t0001g0164a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+214G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21607999 | ||||||
| chr1:21608001
|
G | C | 4 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0234others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+212C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21608001 | ||||||
| chr1:21608174
|
G | A | 163 | a0001c0002t0001g0046a0001c0002t0001g0220a0001c0002t0001g0248others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1296+39C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21608174 | ||||||
| chr1:21608185
|
C | G | 15 | a0001c0004t0001g0110a0001c0004t0001g0206a0001c0004t0001g0269others(12): Show | 15 | HG01358.hp2 HG02135.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.1296+28G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21608185 | ||||||
| chr1:21608200
|
T | C | 27 | a0001c0002t0001g0339a0001c0003t0001g0070a0001c0003t0001g0138others(24): Show | 27 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1296+13A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 17/24 | chr1 | 21608200 | ||||||
| chr1:21608560
|
C | T | 3 | a0001c0003t0003g0363a0001c0003t0003g0368a0001c0003t0003g0369 | 3 | HG01175.hp2 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1159-210G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 16/24 | chr1 | 21608560 | ||||||
| chr1:21608611
|
C | G | 4 | a0002c0001t0001g0164a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1158+239G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 16/24 | chr1 | 21608611 | ||||||
| chr1:21608729
|
C | T | 1 | a0001c0002t0001g0345 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1158+121G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 16/24 | chr1 | 21608729 | ||||||
| chr1:21608747
|
A | C | 1 | a0001c0003t0001g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1158+103T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 16/24 | chr1 | 21608747 | ||||||
| chr1:21608810
|
G | A | 1 | a0001c0002t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1158+40C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 16/24 | chr1 | 21608810 | ||||||
| chr1:21608940
|
G | T | 179 | a0001c0002t0001g0046a0001c0002t0001g0220a0001c0002t0001g0248others(176): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
splice_region_variant&intron_variant | LOW | c.1072-4C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 15/24 | chr1 | 21608940 | ||||||
| chr1:21608945
|
T | C | 3 | a0001c0017t0001g0319a0003c0015t0001g0002a0003c0015t0004g0055 | 3 | HG02615.hp2 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1072-9A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 15/24 | chr1 | 21608945 | ||||||
| chr1:21608974
|
G | A | 29 | a0001c0002t0001g0190a0001c0002t0001g0339a0001c0003t0001g0070others(26): Show | 29 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.1072-38C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 15/24 | chr1 | 21608974 | ||||||
| chr1:21608999
|
C | T | 17 | a0001c0002t0001g0192a0001c0002t0003g0307a0001c0003t0003g0156others(14): Show | 17 | HG00140.hp2 HG00609.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1072-63G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 15/24 | chr1 | 21608999 | ||||||
| chr1:21609212
|
T | G | 143 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(140): Show | 143 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1072-276A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 15/24 | chr1 | 21609212 | ||||||
| chr1:21609391
|
GA | G | 184 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(181): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.1071+183delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 15/24 | chr1 | 21609391 | ||||||
| chr1:21609721
|
T | C | 1 | a0002c0005t0003g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1000-75A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 14/24 | chr1 | 21609721 | ||||||
| chr1:21610342
|
C | A | 4 | a0001c0003t0003g0363a0001c0003t0003g0368a0001c0003t0003g0369others(1): Show | 4 | HG01175.hp2 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.844-67G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610342 | ||||||
| chr1:21610342
|
C | T | 1 | a0001c0003t0001g0087 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.844-67G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610342 | ||||||
| chr1:21610416
|
A | G | 7 | a0002c0001t0001g0135a0002c0001t0001g0136a0002c0001t0001g0169others(4): Show | 7 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-141T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610416 | ||||||
| chr1:21610496
|
A | G | 1 | a0001c0026t0001g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.844-221T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610496 | ||||||
| chr1:21610558
|
T | C | 1 | a0002c0006t0002g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.844-283A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610558 | ||||||
| chr1:21610621
|
A | C | 8 | a0002c0001t0004g0121a0002c0001t0004g0122a0002c0006t0001g0118others(5): Show | 8 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.844-346T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610621 | ||||||
| chr1:21610682
|
C | T | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.844-407G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610682 | ||||||
| chr1:21610824
|
C | T | 31 | a0002c0001t0001g0056a0002c0001t0001g0066a0002c0001t0001g0163others(28): Show | 31 | HG00099.hp1 HG00423.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.844-549G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610824 | ||||||
| chr1:21610955
|
G | A | 1 | a0001c0002t0001g0203 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.843+497C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21610955 | ||||||
| chr1:21611066
|
G | A | 20 | a0002c0001t0001g0066a0002c0001t0001g0164a0002c0001t0001g0184others(17): Show | 20 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.843+386C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21611066 | ||||||
| chr1:21611125
|
A | C | 1 | a0002c0001t0001g0028 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.843+327T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21611125 | ||||||
| chr1:21611314
|
C | G | 365 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(362): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.843+138G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 13/24 | chr1 | 21611314 | ||||||
| chr1:21611641
|
G | A | 1 | a0001c0003t0004g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.714-60C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 12/24 | chr1 | 21611641 | ||||||
| chr1:21611882
|
T | G | 84 | a0001c0003t0001g0210a0001c0003t0001g0231a0001c0003t0001g0313others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.613-66A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 11/24 | chr1 | 21611882 | ||||||
| chr1:21612017
|
T | G | 1 | a0002c0006t0001g0301 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.612+9A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 11/24 | chr1 | 21612017 | ||||||
| chr1:21612127
|
G | A | 1 | a0001c0003t0001g0077 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.529-18C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612127 | ||||||
| chr1:21612178
|
G | A | 1 | a0002c0001t0002g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.529-69C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612178 | ||||||
| chr1:21612335
|
G | A | 15 | a0001c0003t0001g0328a0001c0003t0002g0304a0001c0003t0002g0305others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.529-226C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612335 | ||||||
| chr1:21612404
|
A | G | 344 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.529-295T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612404 | ||||||
| chr1:21612430
|
A | C | 33 | a0001c0003t0002g0134a0002c0001t0001g0057a0002c0001t0001g0075others(30): Show | 33 | HG00099.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.529-321T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612430 | ||||||
| chr1:21612517
|
G | A | 1 | a0002c0001t0003g0341 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.529-408C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612517 | ||||||
| chr1:21612543
|
C | T | 3 | a0001c0003t0003g0363a0001c0003t0003g0368a0001c0003t0003g0369 | 3 | HG01175.hp2 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.529-434G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612543 | ||||||
| chr1:21612739
|
C | T | 1 | a0002c0001t0002g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.528+437G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612739 | ||||||
| chr1:21612777
|
C | T | 1 | a0001c0003t0001g0342 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.528+399G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612777 | ||||||
| chr1:21612798
|
A | G | 1 | a0002c0001t0002g0067 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.528+378T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612798 | ||||||
| chr1:21612854
|
C | T | 1 | a0002c0006t0001g0306 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.528+322G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612854 | ||||||
| chr1:21612904
|
A | C | 1 | a0001c0004t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.528+272T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21612904 | ||||||
| chr1:21613000
|
G | C | 71 | a0002c0001t0001g0056a0002c0001t0001g0057a0002c0001t0001g0066others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.528+176C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21613000 | ||||||
| chr1:21613106
|
T | C | 1 | a0001c0002t0001g0272 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.528+70A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 10/24 | chr1 | 21613106 | ||||||
| chr1:21613248
|
G | C | 171 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(168): Show | 171 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.475-19C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 9/24 | chr1 | 21613248 | ||||||
| chr1:21613275
|
G | A | 1 | a0002c0018t0002g0058 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.475-46C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 9/24 | chr1 | 21613275 | ||||||
| chr1:21613324
|
C | A | 3 | a0001c0009t0001g0308a0001c0009t0001g0317a0001c0009t0001g0318 | 3 | HG01099.hp1 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.475-95G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 9/24 | chr1 | 21613324 | ||||||
| chr1:21613611
|
C | G | 3 | a0003c0010t0001g0054a0003c0015t0001g0002a0003c0015t0004g0055 | 3 | HG02615.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.474+17G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 9/24 | chr1 | 21613611 | ||||||
| chr1:21613616
|
C | T | 2 | a0001c0011t0001g0157a0001c0011t0001g0350 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.474+12G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 9/24 | chr1 | 21613616 | ||||||
| chr1:21613617
|
G | A | 1 | a0002c0001t0001g0093 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.474+11C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 9/24 | chr1 | 21613617 | ||||||
| chr1:21613726
|
C | T | 1 | a0003c0015t0001g0002 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.396-20G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 8/24 | chr1 | 21613726 | ||||||
| chr1:21613769
|
C | A | 1 | a0001c0002t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.396-63G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 8/24 | chr1 | 21613769 | ||||||
| chr1:21613792
|
G | C | 2 | a0001c0004t0001g0232a0001c0004t0001g0244 | 2 | HG02004.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.396-86C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 8/24 | chr1 | 21613792 | ||||||
| chr1:21613792
|
G | T | 5 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0234others(2): Show | 5 | HG01891.hp2 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-86C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 8/24 | chr1 | 21613792 | ||||||
| chr1:21614274
|
G | C | 1 | a0002c0006t0002g0125 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.292-185C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614274 | ||||||
| chr1:21614299
|
G | T | 80 | a0002c0001t0001g0056a0002c0001t0001g0057a0002c0001t0001g0066others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.292-210C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614299 | ||||||
| chr1:21614329
|
A | G | 3 | a0003c0010t0001g0054a0003c0015t0001g0002a0003c0015t0004g0055 | 3 | HG02615.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292-240T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614329 | ||||||
| chr1:21614492
|
G | A | 3 | a0002c0001t0001g0057a0002c0001t0001g0321a0002c0001t0002g0142 | 3 | HG01433.hp1 HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.292-403C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614492 | ||||||
| chr1:21614530
|
T | C | 337 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(334): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.292-441A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614530 | ||||||
| chr1:21614747
|
C | T | 1 | a0003c0015t0001g0002 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.292-658G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614747 | ||||||
| chr1:21614748
|
G | A | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.292-659C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614748 | ||||||
| chr1:21614769
|
G | T | 2 | a0001c0002t0001g0249a0001c0002t0001g0263 | 2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.292-680C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614769 | ||||||
| chr1:21614809
|
C | T | 1 | a0002c0005t0003g0332 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.292-720G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614809 | ||||||
| chr1:21614810
|
G | A | 6 | a0001c0003t0001g0210a0001c0003t0001g0231a0001c0003t0001g0313others(3): Show | 6 | HG02572.hp2 HG02896.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-721C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614810 | ||||||
| chr1:21614817
|
T | C | 344 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.292-728A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614817 | ||||||
| chr1:21614870
|
G | GC | 6 | a0001c0003t0001g0077a0001c0003t0001g0085a0001c0003t0001g0086others(3): Show | 6 | NA18970.hp1 NA18975.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-782dupG | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21614870 | ||||||
| chr1:21615151
|
G | T | 344 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.292-1062C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615151 | ||||||
| chr1:21615233
|
A | G | 1 | a0003c0010t0001g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.292-1144T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615233 | ||||||
| chr1:21615306
|
C | G | 6 | a0002c0001t0001g0066a0002c0008t0003g0063a0002c0008t0003g0065others(3): Show | 6 | HG00099.hp1 HG01109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-1217G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615306 | ||||||
| chr1:21615359
|
C | T | 3 | a0003c0010t0001g0054a0003c0015t0001g0002a0003c0015t0004g0055 | 3 | HG02615.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292-1270G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615359 | ||||||
| chr1:21615399
|
C | CT | 159 | a0001c0002t0001g0220a0001c0002t0001g0292a0001c0003t0001g0201others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.292-1311dupA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615399 | ||||||
| chr1:21615420
|
C | T | 9 | a0001c0003t0001g0008a0001c0003t0001g0061a0001c0003t0001g0077others(6): Show | 9 | HG01081.hp1 HG01192.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.292-1331G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615420 | ||||||
| chr1:21615455
|
C | T | 1 | a0001c0004t0001g0199 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.292-1366G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615455 | ||||||
| chr1:21615495
|
G | A | 4 | a0001c0009t0001g0308a0001c0009t0001g0317a0001c0009t0001g0318others(1): Show | 4 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1406C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615495 | ||||||
| chr1:21615643
|
C | T | 11 | a0002c0001t0001g0003a0002c0001t0001g0004a0002c0001t0001g0028others(8): Show | 11 | NA18968.hp1 NA18970.hp2 NA18971.hp2 others(8): Show |
intron_variant | MODIFIER | c.292-1554G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615643 | ||||||
| chr1:21615680
|
G | C | 338 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.292-1591C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615680 | ||||||
| chr1:21615748
|
C | G | 3 | a0002c0008t0003g0063a0002c0008t0003g0065a0002c0008t0012g0064 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.291+1558G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615748 | ||||||
| chr1:21615841
|
C | T | 1 | a0001c0002t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.291+1465G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615841 | ||||||
| chr1:21615886
|
G | C | 157 | a0001c0002t0001g0220a0001c0002t0001g0292a0001c0003t0001g0210others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.291+1420C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615886 | ||||||
| chr1:21615894
|
C | G | 3 | a0002c0001t0002g0040a0002c0001t0002g0048a0002c0001t0002g0101 | 3 | NA18945.hp1 NA18946.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.291+1412G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21615894 | ||||||
| chr1:21616039
|
T | C | 1 | a0002c0001t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.291+1267A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616039 | ||||||
| chr1:21616107
|
G | C | 178 | a0001c0003t0001g0070a0001c0003t0001g0138a0001c0003t0001g0144others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.291+1199C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616107 | ||||||
| chr1:21616134
|
CCAACACA others(8): Show |
C | 1 | a0002c0001t0001g0257 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.291+1157_291+1171d others(17): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616134 | ||||||
| chr1:21616134
|
CCAACACA others(10): Show |
C | 2 | a0001c0002t0001g0182a0001c0002t0001g0196 | 2 | NA18747.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.291+1155_291+1171d others(19): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616134 | ||||||
| chr1:21616136
|
A | AAC | 4 | a0001c0003t0001g0210a0001c0003t0001g0231a0001c0003t0004g0362others(1): Show | 4 | HG02976.hp1 HG02976.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1168_291+1169d others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
A | AACACACA others(5): Show |
1 | a0001c0003t0001g0314 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.291+1158_291+1169d others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AAC | A | 10 | a0002c0001t0001g0057a0002c0001t0001g0158a0002c0001t0001g0177others(7): Show | 10 | HG00099.hp1 HG01106.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.291+1168_291+1169d others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACAC | A | 21 | a0001c0003t0001g0131a0001c0003t0001g0173a0001c0003t0001g0315others(18): Show | 21 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.291+1166_291+1169d others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACAC | A | 27 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0003t0001g0030others(24): Show | 27 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.291+1164_291+1169d others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(1): Show |
A | 28 | a0001c0003t0001g0008a0001c0003t0001g0061a0001c0003t0001g0086others(25): Show | 28 | HG00423.hp2 HG00609.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.291+1162_291+1169d others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(3): Show |
A | 2 | a0001c0009t0001g0317a0001c0009t0001g0318 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.291+1160_291+1169d others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(5): Show |
A | 3 | a0002c0001t0001g0013a0002c0001t0001g0031a0006c0021t0001g0035 | 3 | NA18950.hp2 NA18964.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.291+1158_291+1169d others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(7): Show |
A | 15 | a0002c0001t0001g0004a0002c0001t0001g0012a0002c0001t0001g0018others(12): Show | 15 | HG00408.hp2 HG00673.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.291+1156_291+1169d others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(9): Show |
A | 52 | a0001c0004t0001g0290a0002c0001t0001g0001a0002c0001t0001g0003others(49): Show | 53 | HG00140.hp1 HG00280.hp1 HG01168.hp2 others(50): Show |
intron_variant | MODIFIER | c.291+1154_291+1169d others(18): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(11): Show |
A | 15 | a0001c0002t0001g0015a0001c0002t0001g0183a0001c0002t0001g0208others(12): Show | 15 | HG00639.hp2 HG01993.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.291+1152_291+1169d others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(13): Show |
A | 151 | a0001c0002t0001g0016a0001c0002t0001g0019a0001c0002t0001g0025others(148): Show | 151 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.291+1150_291+1169d others(22): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(15): Show |
A | 6 | a0001c0002t0001g0081a0001c0003t0003g0179a0001c0003t0003g0346others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+1148_291+1169d others(24): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616136
|
AACACACA others(17): Show |
A | 1 | a0001c0012t0001g0024 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.291+1146_291+1169d others(26): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616136 | ||||||
| chr1:21616190
|
C | CACACACA others(5): Show |
6 | a0002c0001t0001g0075a0002c0001t0001g0106a0002c0001t0002g0072others(3): Show | 6 | HG00673.hp2 HG01175.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.291+1115_291+1116i others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616190 | ||||||
| chr1:21616190
|
C | CACACACA others(3): Show |
2 | a0002c0001t0002g0067a0002c0001t0002g0073 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.291+1115_291+1116i others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616190 | ||||||
| chr1:21616190
|
C | CACACACA others(1): Show |
4 | a0002c0001t0001g0082a0002c0001t0002g0091a0002c0001t0002g0113others(1): Show | 4 | HG01975.hp2 HG02165.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.291+1115_291+1116i others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616190 | ||||||
| chr1:21616190
|
C | CACACAT | 7 | a0001c0003t0002g0134a0002c0001t0002g0017a0002c0001t0002g0108others(4): Show | 7 | HG01515.hp1 HG01517.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.291+1115_291+1116i others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616190 | ||||||
| chr1:21616190
|
C | CACAT | 7 | a0002c0001t0001g0296a0002c0001t0002g0089a0002c0001t0002g0090others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.291+1115_291+1116i others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616190 | ||||||
| chr1:21616190
|
C | CAT | 4 | a0002c0001t0001g0174a0002c0001t0002g0104a0002c0001t0002g0268others(1): Show | 4 | HG02559.hp2 HG04228.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+1114_291+1115d others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616190 | ||||||
| chr1:21616190
|
C | T | 305 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(302): Show | 306 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.291+1116G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616190 | ||||||
| chr1:21616432
|
C | T | 1 | a0003c0015t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.291+874G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616432 | ||||||
| chr1:21616464
|
G | A | 20 | a0002c0001t0001g0163a0002c0001t0001g0169a0002c0001t0002g0079others(17): Show | 20 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.291+842C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616464 | ||||||
| chr1:21616478
|
A | G | 21 | a0001c0003t0001g0070a0001c0003t0001g0138a0001c0003t0001g0144others(18): Show | 21 | HG00140.hp2 HG00733.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.291+828T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616478 | ||||||
| chr1:21616643
|
C | T | 90 | a0001c0002t0001g0203a0001c0002t0001g0330a0001c0002t0001g0339others(87): Show | 90 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.291+663G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616643 | ||||||
| chr1:21616818
|
G | T | 2 | a0003c0010t0001g0054a0003c0015t0004g0055 | 2 | HG02615.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.291+488C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616818 | ||||||
| chr1:21616985
|
T | C | 2 | a0001c0003t0001g0008a0001c0003t0001g0061 | 2 | HG01081.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.291+321A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21616985 | ||||||
| chr1:21617011
|
A | G | 343 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.291+295T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21617011 | ||||||
| chr1:21617014
|
C | T | 1 | a0003c0015t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.291+292G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21617014 | ||||||
| chr1:21617156
|
G | C | 1 | a0001c0003t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.291+150C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21617156 | ||||||
| chr1:21617201
|
C | T | 3 | a0002c0006t0001g0301a0002c0006t0001g0302a0002c0006t0001g0357 | 3 | HG03195.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.291+105G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21617201 | ||||||
| chr1:21617288
|
C | A | 70 | a0002c0001t0001g0001a0002c0001t0001g0003a0002c0001t0001g0004others(67): Show | 71 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.291+18G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | 21617288 | ||||||
| chr1:21617552
|
C | G | 29 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0234others(26): Show | 29 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.106-61G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617552 | ||||||
| chr1:21617629
|
C | T | 4 | a0001c0003t0004g0362a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-138G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617629 | ||||||
| chr1:21617670
|
C | G | 19 | a0001c0003t0004g0362a0001c0009t0001g0308a0001c0009t0001g0317others(16): Show | 19 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.106-179G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617670 | ||||||
| chr1:21617672
|
G | A | 3 | a0001c0009t0001g0308a0001c0009t0001g0317a0001c0009t0001g0318 | 3 | HG01099.hp1 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.106-181C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617672 | ||||||
| chr1:21617676
|
C | T | 74 | a0001c0003t0003g0179a0001c0003t0003g0346a0001c0003t0003g0347others(71): Show | 75 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.106-185G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617676 | ||||||
| chr1:21617803
|
C | T | 3 | a0001c0003t0003g0363a0001c0003t0003g0368a0001c0003t0003g0369 | 3 | HG01175.hp2 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.105+131G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617803 | ||||||
| chr1:21617859
|
A | G | 61 | a0001c0002t0001g0330a0001c0003t0001g0008a0001c0003t0001g0061others(58): Show | 61 | HG00099.hp2 HG00673.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.105+75T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617859 | ||||||
| chr1:21617904
|
A | G | 25 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(22): Show | 25 | HG01106.hp1 HG01175.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.105+30T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617904 | ||||||
| chr1:21617908
|
G | A | 14 | a0001c0003t0001g0328a0001c0003t0002g0320a0001c0003t0002g0358others(11): Show | 14 | HG01106.hp1 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.105+26C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617908 | ||||||
| chr1:21617920
|
T | G | 6 | a0001c0003t0002g0358a0001c0003t0002g0360a0001c0003t0002g0361others(3): Show | 6 | HG00280.hp2 HG01981.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+14A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 6/24 | chr1 | 21617920 | ||||||
| chr1:21618129
|
G | A | 1 | a0001c0002t0008g0126 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67-157C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618129 | ||||||
| chr1:21618265
|
C | A | 69 | a0001c0009t0001g0308a0001c0009t0001g0317a0001c0009t0001g0318others(66): Show | 70 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.67-293G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618265 | ||||||
| chr1:21618443
|
T | C | 7 | a0001c0003t0001g0328a0001c0003t0003g0156a0001c0003t0003g0179others(4): Show | 7 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-471A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618443 | ||||||
| chr1:21618597
|
T | TC | 54 | a0001c0002t0001g0203a0001c0002t0001g0330a0001c0002t0001g0339others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.66+427_66+428insG | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618597 | ||||||
| chr1:21618610
|
C | T | 1 | a0002c0001t0001g0259 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.66+415G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618610 | ||||||
| chr1:21618658
|
T | C | 3 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311 | 3 | HG01106.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.66+367A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618658 | ||||||
| chr1:21618734
|
G | A | 1 | a0001c0002t0001g0248 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.66+291C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618734 | ||||||
| chr1:21618887
|
C | T | 3 | a0001c0003t0001g0201a0001c0025t0001g0278a0001c0026t0001g0224 | 3 | HG01168.hp1 HG01934.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.66+138G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618887 | ||||||
| chr1:21618888
|
C | A | 2 | a0002c0001t0003g0037a0002c0001t0003g0038 | 2 | NA18963.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.66+137G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618888 | ||||||
| chr1:21618889
|
CT | C | 5 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311others(2): Show | 5 | HG01106.hp1 HG01106.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+135delA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618889 | ||||||
| chr1:21618890
|
T | G | 4 | a0002c0001t0001g0097a0002c0001t0001g0098a0002c0001t0001g0099others(1): Show | 4 | NA18963.hp1 NA18984.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+135A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618890 | ||||||
| chr1:21618896
|
C | T | 22 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0234others(19): Show | 22 | HG00140.hp2 HG00733.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.66+129G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618896 | ||||||
| chr1:21618912
|
T | C | 1 | a0001c0003t0001g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.66+113A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 5/24 | chr1 | 21618912 | ||||||
| chr1:21619111
|
T | G | 1 | a0001c0002t0001g0102 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.19-39A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619111 | ||||||
| chr1:21619121
|
C | T | 3 | a0001c0002t0001g0178a0001c0002t0001g0250a0001c0002t0001g0264 | 3 | HG01109.hp1 HG01358.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.19-49G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619121 | ||||||
| chr1:21619220
|
C | G | 1 | a0001c0003t0003g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19-148G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619220 | ||||||
| chr1:21619309
|
G | A | 2 | a0001c0011t0001g0157a0001c0011t0001g0350 | 2 | HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.19-237C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619309 | ||||||
| chr1:21619351
|
G | A | 2 | a0002c0006t0001g0301a0002c0006t0001g0357 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.19-279C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619351 | ||||||
| chr1:21619376
|
A | G | 334 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(331): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.19-304T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619376 | ||||||
| chr1:21619440
|
AAGAC | A | 24 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0234others(21): Show | 24 | HG00140.hp2 HG00733.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.19-372_19-369delGT others(2): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619440 | ||||||
| chr1:21619497
|
A | G | 369 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(366): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.19-425T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619497 | ||||||
| chr1:21619514
|
C | T | 298 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(295): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.19-442G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619514 | ||||||
| chr1:21619649
|
C | G | 1 | a0001c0004t0001g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.18+366G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619649 | ||||||
| chr1:21619794
|
T | G | 2 | a0002c0001t0009g0309a0003c0015t0001g0002 | 2 | HG01106.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.18+221A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619794 | ||||||
| chr1:21619851
|
C | T | 1 | a0001c0002t0001g0279 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.18+164G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619851 | ||||||
| chr1:21619903
|
T | C | 124 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(121): Show | 124 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.18+112A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619903 | ||||||
| chr1:21619922
|
G | A | 302 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(299): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.18+93C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 4/24 | chr1 | 21619922 | ||||||
| chr1:21620338
|
C | T | 3 | a0001c0003t0001g0342a0001c0003t0001g0370a0001c0003t0001g0371 | 3 | HG01257.hp2 HG01258.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-18-288G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620338 | ||||||
| chr1:21620369
|
G | A | 11 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-319C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620369 | ||||||
| chr1:21620388
|
A | T | 2 | a0001c0012t0001g0024a0001c0012t0001g0059 | 2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-18-338T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620388 | ||||||
| chr1:21620539
|
G | A | 1 | a0001c0003t0007g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-18-489C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620539 | ||||||
| chr1:21620542
|
G | T | 92 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(89): Show | 92 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-18-492C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620542 | ||||||
| chr1:21620552
|
T | TG | 364 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(361): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.-18-503_-18-502ins others(1): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620552 | ||||||
| chr1:21620574
|
C | T | 1 | a0001c0002t0001g0330 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18-524G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620574 | ||||||
| chr1:21620657
|
C | T | 302 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(299): Show | 303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.-18-607G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620657 | ||||||
| chr1:21620668
|
G | C | 2 | a0001c0012t0001g0024a0001c0012t0001g0059 | 2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-18-618C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620668 | ||||||
| chr1:21620723
|
C | T | 3 | a0001c0003t0003g0363a0001c0003t0003g0368a0001c0003t0003g0369 | 3 | HG01175.hp2 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-18-673G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620723 | ||||||
| chr1:21620725
|
C | G | 347 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.-18-675G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620725 | ||||||
| chr1:21620744
|
C | T | 2 | a0002c0001t0001g0174a0002c0001t0001g0177 | 2 | HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-18-694G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620744 | ||||||
| chr1:21620852
|
A | ACT | 7 | a0001c0002t0001g0330a0002c0001t0001g0184a0002c0001t0004g0005others(4): Show | 7 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-804_-18-803dup others(2): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620852 | ||||||
| chr1:21620852
|
ACTCT | A | 178 | a0001c0002t0001g0203a0001c0002t0001g0339a0001c0002t0002g0256others(175): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.-18-806_-18-803del others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620852 | ||||||
| chr1:21620890
|
C | T | 3 | a0002c0001t0001g0135a0002c0001t0001g0136a0002c0001t0001g0150 | 3 | HG01168.hp2 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-18-840G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21620890 | ||||||
| chr1:21621148
|
C | T | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-18-1098G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621148 | ||||||
| chr1:21621227
|
G | A | 62 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(59): Show | 63 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.-18-1177C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621227 | ||||||
| chr1:21621231
|
C | A | 1 | a0002c0001t0001g0259 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-18-1181G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621231 | ||||||
| chr1:21621358
|
A | C | 317 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(314): Show | 318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.-18-1308T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621358 | ||||||
| chr1:21621387
|
C | A | 11 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-1337G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621387 | ||||||
| chr1:21621402
|
A | G | 6 | a0002c0001t0001g0184a0002c0001t0004g0005a0002c0001t0004g0006others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-1352T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621402 | ||||||
| chr1:21621811
|
AG | A | 15 | a0001c0002t0001g0330a0002c0001t0001g0056a0002c0001t0001g0158others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-1762delC | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621811 | ||||||
| chr1:21621996
|
C | T | 11 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-18-1946G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21621996 | ||||||
| chr1:21622047
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-18-1997C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622047 | ||||||
| chr1:21622162
|
G | C | 1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-2112C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622162 | ||||||
| chr1:21622272
|
C | A | 3 | a0002c0001t0001g0174a0002c0001t0001g0177a0002c0001t0001g0296 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-18-2222G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622272 | ||||||
| chr1:21622374
|
G | T | 1 | a0001c0004t0001g0271 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-18-2324C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622374 | ||||||
| chr1:21622443
|
G | C | 303 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(300): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.-18-2393C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622443 | ||||||
| chr1:21622445
|
G | A | 6 | a0002c0001t0001g0184a0002c0001t0004g0005a0002c0001t0004g0006others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-2395C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622445 | ||||||
| chr1:21622513
|
A | T | 1 | a0002c0001t0001g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18-2463T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622513 | ||||||
| chr1:21622654
|
G | A | 3 | a0002c0001t0001g0312a0002c0001t0001g0355a0002c0001t0001g0356 | 3 | HG02630.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-18-2604C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622654 | ||||||
| chr1:21622698
|
C | G | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-18-2648G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622698 | ||||||
| chr1:21622707
|
C | A | 3 | a0001c0004t0001g0199a0001c0004t0001g0245a0001c0004t0001g0273 | 3 | HG00558.hp2 HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-18-2657G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622707 | ||||||
| chr1:21622859
|
C | A | 1 | a0001c0004t0001g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-18-2809G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622859 | ||||||
| chr1:21622969
|
A | G | 103 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(100): Show | 103 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-18-2919T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21622969 | ||||||
| chr1:21623044
|
A | G | 103 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(100): Show | 103 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-18-2994T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21623044 | ||||||
| chr1:21623231
|
A | G | 92 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(89): Show | 92 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-19+3073T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21623231 | ||||||
| chr1:21623326
|
T | C | 4 | a0001c0002t0001g0330a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+2978A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21623326 | ||||||
| chr1:21623829
|
G | C | 11 | a0001c0003t0001g0328a0001c0003t0002g0320a0001c0003t0003g0156others(8): Show | 11 | HG01433.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+2475C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21623829 | ||||||
| chr1:21623904
|
G | A | 3 | a0001c0003t0004g0316a0001c0003t0004g0362a0003c0015t0004g0055 | 3 | HG02615.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-19+2400C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21623904 | ||||||
| chr1:21624294
|
G | A | 1 | a0001c0002t0001g0192 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19+2010C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624294 | ||||||
| chr1:21624335
|
A | T | 6 | a0002c0001t0001g0184a0002c0001t0004g0005a0002c0001t0004g0006others(3): Show | 6 | HG00280.hp2 HG00639.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+1969T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624335 | ||||||
| chr1:21624366
|
G | C | 1 | a0002c0001t0002g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-19+1938C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624366 | ||||||
| chr1:21624515
|
G | C | 1 | a0004c0028t0001g0277 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-19+1789C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624515 | ||||||
| chr1:21624649
|
C | T | 3 | a0002c0006t0001g0140a0002c0006t0001g0151a0002c0006t0001g0152 | 3 | HG01891.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-19+1655G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624649 | ||||||
| chr1:21624672
|
G | C | 1 | a0002c0001t0001g0012 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19+1632C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624672 | ||||||
| chr1:21624722
|
C | G | 1 | a0002c0001t0003g0334 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-19+1582G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624722 | ||||||
| chr1:21624766
|
G | A | 4 | a0001c0002t0001g0330a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1538C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624766 | ||||||
| chr1:21624843
|
GCT | G | 307 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(304): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.-19+1459_-19+1460d others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624843 | ||||||
| chr1:21624843
|
GCTCT | G | 4 | a0001c0002t0001g0330a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1457_-19+1460d others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624843 | ||||||
| chr1:21624866
|
G | T | 1 | a0002c0001t0001g0259 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-19+1438C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624866 | ||||||
| chr1:21624871
|
G | C | 11 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+1433C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624871 | ||||||
| chr1:21624907
|
A | G | 1 | a0002c0001t0001g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-19+1397T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21624907 | ||||||
| chr1:21625057
|
G | A | 22 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0234others(19): Show | 22 | HG00140.hp2 HG00733.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+1247C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625057 | ||||||
| chr1:21625125
|
C | A | 1 | a0002c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-19+1179G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625125 | ||||||
| chr1:21625138
|
C | G | 323 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(320): Show | 324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.-19+1166G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625138 | ||||||
| chr1:21625154
|
G | C | 4 | a0001c0002t0001g0330a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1150C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625154 | ||||||
| chr1:21625457
|
G | A | 2 | a0002c0001t0002g0108a0002c0001t0002g0109 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-19+847C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625457 | ||||||
| chr1:21625496
|
G | A | 3 | a0001c0003t0004g0316a0001c0003t0004g0362a0003c0015t0004g0055 | 3 | HG02615.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-19+808C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625496 | ||||||
| chr1:21625531
|
C | T | 173 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0203others(170): Show | 174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-19+773G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625531 | ||||||
| chr1:21625664
|
A | G | 1 | a0002c0001t0001g0009 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-19+640T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625664 | ||||||
| chr1:21625771
|
TG | T | 4 | a0001c0002t0001g0330a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+532delC | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625771 | ||||||
| chr1:21625859
|
T | G | 3 | a0002c0001t0002g0040a0002c0001t0002g0048a0002c0001t0002g0101 | 3 | NA18945.hp1 NA18946.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-19+445A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625859 | ||||||
| chr1:21625896
|
G | A | 3 | a0001c0003t0004g0316a0001c0003t0004g0362a0003c0015t0004g0055 | 3 | HG02615.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-19+408C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625896 | ||||||
| chr1:21625913
|
C | T | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-19+391G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21625913 | ||||||
| chr1:21626097
|
G | A | 116 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(113): Show | 117 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-19+207C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21626097 | ||||||
| chr1:21626117
|
C | T | 1 | a0001c0002t0003g0303 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-19+187G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21626117 | ||||||
| chr1:21626211
|
C | T | 7 | a0001c0002t0001g0019a0001c0002t0001g0220a0001c0002t0001g0249others(4): Show | 7 | HG00423.hp1 HG00544.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+93G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21626211 | ||||||
| chr1:21626286
|
A | G | 3 | a0001c0003t0004g0316a0001c0003t0004g0362a0003c0015t0004g0055 | 3 | HG02615.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-19+18T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 3/24 | chr1 | 21626286 | ||||||
| chr1:21626456
|
T | C | 1 | a0001c0003t0007g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-112-59A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626456 | ||||||
| chr1:21626496
|
T | C | 1 | a0002c0022t0002g0145 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-112-99A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626496 | ||||||
| chr1:21626533
|
A | C | 56 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(53): Show | 56 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-112-136T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626533 | ||||||
| chr1:21626547
|
G | A | 53 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0162others(50): Show | 53 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.-112-150C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626547 | ||||||
| chr1:21626555
|
T | C | 3 | a0001c0003t0004g0354a0002c0001t0004g0005a0002c0001t0004g0367 | 3 | HG01070.hp1 HG02809.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-112-158A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626555 | ||||||
| chr1:21626558
|
G | A | 1 | a0001c0003t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-112-161C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626558 | ||||||
| chr1:21626566
|
A | G | 46 | a0001c0002t0001g0162a0001c0002t0001g0330a0001c0003t0001g0210others(43): Show | 46 | HG00423.hp2 HG00609.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.-112-169T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626566 | ||||||
| chr1:21626645
|
A | G | 273 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(270): Show | 273 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.-112-248T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626645 | ||||||
| chr1:21626653
|
A | G | 10 | a0001c0003t0004g0316a0001c0003t0004g0362a0002c0001t0001g0056others(7): Show | 10 | HG01070.hp1 HG01106.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-112-256T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626653 | ||||||
| chr1:21626794
|
G | A | 62 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(59): Show | 62 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-112-397C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626794 | ||||||
| chr1:21626811
|
G | A | 160 | a0001c0002t0001g0019a0001c0002t0001g0203a0001c0002t0001g0230others(157): Show | 161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.-112-414C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626811 | ||||||
| chr1:21626943
|
A | G | 321 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(318): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.-112-546T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626943 | ||||||
| chr1:21626952
|
C | G | 2 | a0001c0003t0001g0138a0001c0024t0001g0146 | 2 | HG02027.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-112-555G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21626952 | ||||||
| chr1:21627074
|
G | C | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-112-677C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627074 | ||||||
| chr1:21627233
|
C | T | 3 | a0001c0003t0004g0316a0001c0003t0004g0362a0003c0015t0004g0055 | 3 | HG02615.hp2 HG02886.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-112-836G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627233 | ||||||
| chr1:21627402
|
C | CCTT | 23 | a0002c0001t0001g0011a0002c0001t0001g0033a0002c0001t0001g0034others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.-112-1008_-112-100 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627402 | ||||||
| chr1:21627406
|
C | G | 1 | a0002c0001t0002g0344 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-112-1009G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627406 | ||||||
| chr1:21627408
|
T | C | 1 | a0002c0001t0002g0344 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-112-1011A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627408 | ||||||
| chr1:21627409
|
C | CT | 57 | a0000c0014t0001g0171a0001c0002t0001g0116a0001c0002t0001g0117others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.-112-1013dupA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627409 | ||||||
| chr1:21627409
|
C | CTT | 15 | a0001c0003t0001g0144a0001c0003t0001g0313a0001c0003t0001g0314others(12): Show | 15 | HG01071.hp2 HG01175.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.-112-1014_-112-101 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627409 | ||||||
| chr1:21627409
|
C | T | 1 | a0002c0001t0002g0344 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-112-1012G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627409 | ||||||
| chr1:21627409
|
CT | C | 9 | a0001c0002t0001g0051a0001c0003t0001g0153a0001c0003t0001g0154others(6): Show | 9 | HG00323.hp2 HG01069.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-112-1013delA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627409 | ||||||
| chr1:21627410
|
T | TTC | 60 | a0001c0002t0001g0208a0001c0002t0001g0249a0001c0002t0001g0250others(57): Show | 61 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-112-1014_-112-101 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627410 | ||||||
| chr1:21627411
|
T | TC | 151 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(148): Show | 151 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.-112-1015_-112-101 others(5): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627411 | ||||||
| chr1:21627412
|
T | C | 2 | a0001c0002t0001g0235a0001c0003t0003g0179 | 2 | HG01993.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-112-1015A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627412 | ||||||
| chr1:21627642
|
C | T | 3 | a0002c0005t0001g0020a0002c0005t0001g0021a0002c0005t0001g0032 | 3 | NA18942.hp1 NA18950.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-112-1245G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627642 | ||||||
| chr1:21627771
|
G | A | 2 | a0001c0003t0001g0138a0001c0024t0001g0146 | 2 | HG02027.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-112-1374C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627771 | ||||||
| chr1:21627801
|
T | C | 66 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-112-1404A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627801 | ||||||
| chr1:21627826
|
T | G | 2 | a0002c0001t0002g0089a0002c0001t0002g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-112-1429A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627826 | ||||||
| chr1:21627997
|
C | G | 1 | a0001c0003t0001g0353 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-112-1600G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21627997 | ||||||
| chr1:21628032
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-112-1635C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628032 | ||||||
| chr1:21628173
|
G | A | 79 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(76): Show | 79 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-112-1776C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628173 | ||||||
| chr1:21628400
|
T | TA | 33 | a0000c0014t0001g0170a0001c0002t0001g0102a0001c0002t0001g0207others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.-112-2004dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
T | TAA | 19 | a0001c0002t0001g0029a0001c0002t0001g0211a0001c0002t0001g0248others(16): Show | 19 | HG00621.hp1 HG01346.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-112-2005_-112-200 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
T | TAAAA | 6 | a0001c0003t0001g0165a0001c0003t0001g0313a0001c0003t0004g0354others(3): Show | 6 | HG01099.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-2007_-112-200 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TA | T | 19 | a0001c0002t0001g0019a0001c0002t0001g0167a0001c0002t0001g0193others(16): Show | 19 | HG00639.hp2 HG01069.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.-112-2004delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TAAAA | T | 14 | a0001c0002t0001g0203a0001c0003t0001g0070a0001c0003t0001g0138others(11): Show | 14 | HG00621.hp2 HG01928.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.-112-2007_-112-200 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TAAAAA | T | 71 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0230others(68): Show | 71 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-112-2008_-112-200 others(9): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TAAAAAA | T | 33 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0001g0172others(30): Show | 33 | HG00099.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-112-2009_-112-200 others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TAAAAAAA others(4): Show |
T | 1 | a0001c0003t0007g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-112-2014_-112-200 others(15): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TAAAAAAA others(6): Show |
T | 3 | a0002c0001t0001g0060a0002c0005t0001g0032a0002c0022t0002g0145 | 3 | HG02735.hp1 HG04199.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-112-2016_-112-200 others(17): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TAAAAAAA others(7): Show |
T | 75 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(72): Show | 76 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.-112-2017_-112-200 others(18): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628400
|
TAAAAAAA others(8): Show |
T | 3 | a0002c0001t0001g0094a0002c0001t0001g0169a0002c0016t0001g0128 | 3 | HG01261.hp2 HG02897.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-112-2018_-112-200 others(19): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628400 | ||||||
| chr1:21628459
|
C | T | 3 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311 | 3 | HG01106.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-112-2062G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628459 | ||||||
| chr1:21628472
|
C | T | 107 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(104): Show | 107 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.-112-2075G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628472 | ||||||
| chr1:21628676
|
C | T | 1 | a0002c0001t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-112-2279G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628676 | ||||||
| chr1:21628775
|
C | T | 2 | a0001c0002t0001g0204a0001c0002t0001g0239 | 2 | HG02132.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.-112-2378G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628775 | ||||||
| chr1:21628889
|
G | GA | 97 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(94): Show | 97 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-112-2493dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628889 | ||||||
| chr1:21628901
|
G | A | 1 | a0001c0002t0001g0255 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-112-2504C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628901 | ||||||
| chr1:21628903
|
A | G | 1 | a0001c0002t0001g0255 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-112-2506T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628903 | ||||||
| chr1:21628904
|
G | A | 1 | a0001c0002t0001g0255 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-112-2507C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21628904 | ||||||
| chr1:21629234
|
G | C | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-112-2837C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629234 | ||||||
| chr1:21629251
|
G | C | 57 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-112-2854C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629251 | ||||||
| chr1:21629254
|
C | T | 1 | a0001c0003t0001g0353 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-112-2857G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629254 | ||||||
| chr1:21629329
|
T | C | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-112-2932A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629329 | ||||||
| chr1:21629375
|
T | C | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-112-2978A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629375 | ||||||
| chr1:21629420
|
A | T | 2 | a0001c0003t0001g0173a0001c0003t0001g0353 | 2 | HG02109.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-112-3023T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629420 | ||||||
| chr1:21629526
|
C | A | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-112-3129G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629526 | ||||||
| chr1:21629557
|
C | G | 96 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(93): Show | 96 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-112-3160G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629557 | ||||||
| chr1:21629706
|
C | A | 79 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(76): Show | 79 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-112-3309G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629706 | ||||||
| chr1:21629716
|
G | C | 1 | a0001c0003t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-112-3319C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21629716 | ||||||
| chr1:21630170
|
T | C | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | NA18966.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-112-3773A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630170 | ||||||
| chr1:21630172
|
G | T | 5 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311others(2): Show | 5 | HG01106.hp1 HG01106.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-3775C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630172 | ||||||
| chr1:21630179
|
C | A | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | NA18966.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-112-3782G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630179 | ||||||
| chr1:21630233
|
G | A | 1 | a0002c0001t0001g0106 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-112-3836C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630233 | ||||||
| chr1:21630266
|
C | CT | 141 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(138): Show | 142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-112-3870dupA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630266 | ||||||
| chr1:21630483
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-112-4086G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630483 | ||||||
| chr1:21630737
|
G | T | 3 | a0002c0006t0001g0301a0002c0006t0001g0302a0002c0006t0001g0357 | 3 | HG03195.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-112-4340C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630737 | ||||||
| chr1:21630746
|
G | C | 57 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-112-4349C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630746 | ||||||
| chr1:21630974
|
C | T | 18 | a0002c0001t0001g0169a0002c0001t0002g0079a0002c0001t0002g0080others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-112-4577G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21630974 | ||||||
| chr1:21631011
|
C | T | 1 | a0001c0002t0003g0303 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-112-4614G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631011 | ||||||
| chr1:21631173
|
C | T | 6 | a0001c0003t0001g0165a0001c0003t0004g0354a0002c0001t0002g0115others(3): Show | 6 | HG00280.hp2 HG01070.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-112-4776G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631173 | ||||||
| chr1:21631177
|
G | A | 4 | a0001c0003t0003g0346a0001c0003t0004g0362a0001c0011t0001g0157others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-112-4780C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631177 | ||||||
| chr1:21631198
|
C | T | 1 | a0002c0001t0001g0096 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-112-4801G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631198 | ||||||
| chr1:21631254
|
G | A | 1 | a0002c0005t0001g0294 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-112-4857C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631254 | ||||||
| chr1:21631254
|
G | C | 99 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(96): Show | 99 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112-4857C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631254 | ||||||
| chr1:21631290
|
C | T | 1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112-4893G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631290 | ||||||
| chr1:21631440
|
C | G | 3 | a0001c0004t0001g0069a0001c0004t0001g0071a0001c0004t0001g0110 | 3 | HG01358.hp2 HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-112-5043G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631440 | ||||||
| chr1:21631457
|
G | A | 2 | a0002c0016t0001g0128a0002c0016t0001g0129 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-112-5060C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631457 | ||||||
| chr1:21631461
|
G | A | 3 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311 | 3 | HG01106.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-112-5064C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631461 | ||||||
| chr1:21631465
|
C | G | 1 | a0001c0002t0001g0236 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-112-5068G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631465 | ||||||
| chr1:21631503
|
T | G | 1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112-5106A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631503 | ||||||
| chr1:21631579
|
G | A | 3 | a0002c0001t0001g0097a0002c0001t0001g0099a0002c0001t0001g0100 | 3 | NA18984.hp2 NA19068.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-112-5182C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631579 | ||||||
| chr1:21631601
|
G | A | 2 | a0001c0003t0001g0210a0001c0003t0001g0231 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-112-5204C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631601 | ||||||
| chr1:21631611
|
A | G | 1 | a0001c0003t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-112-5214T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631611 | ||||||
| chr1:21631617
|
C | T | 6 | a0002c0001t0001g0012a0002c0001t0001g0013a0002c0001t0001g0031others(3): Show | 6 | HG00673.hp1 HG04184.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-5220G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631617 | ||||||
| chr1:21631633
|
C | T | 1 | a0002c0001t0001g0033 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-112-5236G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631633 | ||||||
| chr1:21631848
|
T | C | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-112-5451A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631848 | ||||||
| chr1:21631950
|
G | A | 1 | a0001c0004t0001g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-112-5553C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631950 | ||||||
| chr1:21631996
|
C | T | 3 | a0001c0003t0004g0362a0001c0011t0001g0157a0001c0011t0001g0350 | 3 | HG02109.hp1 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-112-5599G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21631996 | ||||||
| chr1:21632043
|
C | T | 62 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(59): Show | 63 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.-112-5646G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632043 | ||||||
| chr1:21632047
|
G | A | 1 | a0001c0004t0001g0123 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-112-5650C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632047 | ||||||
| chr1:21632094
|
G | A | 309 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(306): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.-112-5697C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632094 | ||||||
| chr1:21632246
|
G | T | 69 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(66): Show | 69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.-112-5849C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632246 | ||||||
| chr1:21632249
|
C | T | 1 | a0001c0002t0001g0285 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-112-5852G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632249 | ||||||
| chr1:21632257
|
G | A | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-112-5860C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632257 | ||||||
| chr1:21632394
|
G | A | 2 | a0001c0003t0001g0165a0001c0003t0004g0354 | 2 | HG02809.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-112-5997C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632394 | ||||||
| chr1:21632416
|
G | A | 79 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(76): Show | 79 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-112-6019C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632416 | ||||||
| chr1:21632425
|
A | G | 106 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(103): Show | 106 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-112-6028T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632425 | ||||||
| chr1:21632464
|
A | G | 2 | a0001c0012t0001g0024a0001c0012t0001g0059 | 2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-112-6067T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632464 | ||||||
| chr1:21632517
|
A | G | 1 | a0001c0007t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-112-6120T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632517 | ||||||
| chr1:21632522
|
G | T | 309 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(306): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.-112-6125C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632522 | ||||||
| chr1:21632639
|
T | C | 323 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(320): Show | 324 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.-112-6242A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632639 | ||||||
| chr1:21632697
|
C | T | 1 | a0002c0005t0001g0027 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-112-6300G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632697 | ||||||
| chr1:21632772
|
A | AGTG | 122 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-112-6376_-112-637 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632772 | ||||||
| chr1:21632773
|
C | A | 122 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-112-6376G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21632773 | ||||||
| chr1:21633020
|
G | A | 1 | a0001c0003t0004g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-112-6623C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633020 | ||||||
| chr1:21633090
|
G | C | 2 | a0002c0001t0001g0057a0002c0001t0001g0321 | 2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-112-6693C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633090 | ||||||
| chr1:21633091
|
A | T | 2 | a0001c0002t0001g0025a0001c0002t0001g0026 | 2 | NA18966.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-112-6694T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633091 | ||||||
| chr1:21633097
|
T | C | 122 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-112-6700A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633097 | ||||||
| chr1:21633177
|
C | T | 1 | a0002c0001t0001g0094 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-112-6780G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633177 | ||||||
| chr1:21633313
|
C | T | 1 | a0002c0001t0009g0309 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-112-6916G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633313 | ||||||
| chr1:21633389
|
C | T | 3 | a0002c0001t0001g0174a0002c0001t0001g0177a0002c0001t0001g0296 | 3 | HG03130.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-112-6992G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633389 | ||||||
| chr1:21633464
|
G | A | 63 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(60): Show | 64 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-112-7067C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633464 | ||||||
| chr1:21633539
|
G | A | 54 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-112-7142C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633539 | ||||||
| chr1:21633551
|
A | C | 54 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-112-7154T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633551 | ||||||
| chr1:21633627
|
C | A | 57 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.-112-7230G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633627 | ||||||
| chr1:21633633
|
C | T | 1 | a0001c0002t0001g0248 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-112-7236G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633633 | ||||||
| chr1:21633679
|
C | T | 60 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-112-7282G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633679 | ||||||
| chr1:21633691
|
G | A | 5 | a0001c0003t0004g0316a0001c0003t0004g0362a0001c0011t0001g0157others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-112-7294C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633691 | ||||||
| chr1:21633701
|
G | T | 101 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(98): Show | 101 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-112-7304C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633701 | ||||||
| chr1:21633769
|
A | G | 1 | a0001c0004t0001g0068 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-112-7372T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633769 | ||||||
| chr1:21633811
|
T | C | 1 | a0001c0003t0001g0153 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-112-7414A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21633811 | ||||||
| chr1:21634058
|
CGG | C | 44 | a0001c0002t0001g0029a0001c0002t0001g0062a0001c0002t0001g0162others(41): Show | 44 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.-112-7663_-112-766 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634058 | ||||||
| chr1:21634058
|
CGGG | C | 91 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(88): Show | 91 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-112-7664_-112-766 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634058 | ||||||
| chr1:21634058
|
CGGGG | C | 136 | a0001c0002t0001g0190a0001c0002t0001g0203a0001c0002t0001g0230others(133): Show | 137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-112-7665_-112-766 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634058 | ||||||
| chr1:21634058
|
CGGGGGG | C | 60 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.-112-7667_-112-766 others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634058 | ||||||
| chr1:21634068
|
G | C | 1 | a0001c0003t0001g0137 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-112-7671C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634068 | ||||||
| chr1:21634074
|
C | G | 1 | a0001c0009t0001g0317 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-112-7677G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634074 | ||||||
| chr1:21634240
|
A | C | 2 | a0002c0001t0009g0309a0003c0015t0001g0002 | 2 | HG01106.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-112-7843T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634240 | ||||||
| chr1:21634270
|
G | C | 2 | a0001c0003t0001g0165a0001c0003t0004g0354 | 2 | HG02809.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-112-7873C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634270 | ||||||
| chr1:21634317
|
C | A | 18 | a0002c0001t0001g0169a0002c0001t0002g0079a0002c0001t0002g0080others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-112-7920G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634317 | ||||||
| chr1:21634326
|
G | A | 18 | a0002c0001t0001g0169a0002c0001t0002g0079a0002c0001t0002g0080others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.-112-7929C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634326 | ||||||
| chr1:21634399
|
T | C | 1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-112-8002A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634399 | ||||||
| chr1:21634598
|
C | T | 81 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(78): Show | 82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.-112-8201G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634598 | ||||||
| chr1:21634645
|
G | A | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-112-8248C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634645 | ||||||
| chr1:21634737
|
T | A | 1 | a0001c0003t0004g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-112-8340A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634737 | ||||||
| chr1:21634766
|
T | G | 1 | a0002c0001t0001g0047 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-112-8369A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634766 | ||||||
| chr1:21634844
|
C | T | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-112-8447G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634844 | ||||||
| chr1:21634845
|
G | A | 54 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(51): Show | 54 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-112-8448C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634845 | ||||||
| chr1:21634846
|
A | T | 366 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(363): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.-112-8449T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634846 | ||||||
| chr1:21634964
|
C | T | 1 | a0001c0003t0004g0316 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-112-8567G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21634964 | ||||||
| chr1:21635088
|
G | A | 81 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(78): Show | 82 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.-112-8691C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635088 | ||||||
| chr1:21635097
|
C | T | 1 | a0002c0001t0002g0142 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-112-8700G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635097 | ||||||
| chr1:21635304
|
A | G | 63 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(60): Show | 64 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-112-8907T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635304 | ||||||
| chr1:21635376
|
C | G | 1 | a0001c0012t0001g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-112-8979G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635376 | ||||||
| chr1:21635395
|
T | C | 1 | a0002c0001t0001g0184 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-112-8998A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635395 | ||||||
| chr1:21635502
|
A | G | 112 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(109): Show | 112 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-112-9105T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635502 | ||||||
| chr1:21635729
|
C | T | 1 | a0001c0004t0001g0217 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-112-9332G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635729 | ||||||
| chr1:21635741
|
G | A | 2 | a0002c0001t0002g0089a0002c0001t0002g0090 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-112-9344C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635741 | ||||||
| chr1:21635774
|
G | C | 1 | a0001c0003t0001g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-112-9377C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635774 | ||||||
| chr1:21635834
|
C | T | 1 | a0002c0005t0001g0020 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-112-9437G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21635834 | ||||||
| chr1:21636058
|
G | A | 101 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(98): Show | 101 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-112-9661C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636058 | ||||||
| chr1:21636738
|
T | C | 121 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(118): Show | 121 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-112-10341A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636738 | ||||||
| chr1:21636849
|
A | G | 20 | a0001c0004t0001g0050a0001c0004t0001g0194a0001c0004t0001g0254others(17): Show | 20 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-112-10452T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636849 | ||||||
| chr1:21636849
|
AAGG | A | 3 | a0001c0002t0001g0178a0001c0003t0001g0314a0002c0023t0001g0310 | 3 | HG01358.hp1 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-112-10455_-112-10 others(9): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636849 | ||||||
| chr1:21636903
|
GGGAA | G | 8 | a0002c0001t0001g0166a0002c0005t0001g0020a0002c0005t0001g0021others(5): Show | 8 | NA18942.hp1 NA18953.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-10510_-112-10 others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636903 | ||||||
| chr1:21636910
|
AAGGAAGG others(5): Show |
A | 5 | a0001c0002t0001g0162a0001c0003t0001g0210a0001c0003t0001g0231others(2): Show | 5 | HG02451.hp2 HG02723.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-10525_-112-10 others(18): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636910 | ||||||
| chr1:21636914
|
A | AAGGG | 7 | a0001c0002t0001g0214a0001c0002t0001g0248a0001c0004t0001g0200others(4): Show | 7 | HG01346.hp2 HG01433.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112-10521_-112-10 others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636914 | ||||||
| chr1:21636914
|
AAGGG | A | 38 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0116others(35): Show | 38 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-112-10521_-112-10 others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636914 | ||||||
| chr1:21636914
|
AAGGGAGG others(5): Show |
A | 2 | a0001c0002t0001g0221a0001c0012t0001g0059 | 2 | HG00323.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-112-10529_-112-10 others(18): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636914 | ||||||
| chr1:21636926
|
GAGGGAGG others(13): Show |
G | 12 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-112-10549_-112-10 others(26): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636926 | ||||||
| chr1:21636930
|
GAGGGAGG others(9): Show |
G | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112-10549_-112-10 others(22): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636930 | ||||||
| chr1:21636932
|
G | C | 2 | a0002c0001t0001g0010a0002c0001t0001g0181 | 2 | NA19007.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-112-10535C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21636932 | ||||||
| chr1:21637004
|
C | T | 60 | a0001c0003t0001g0008a0001c0003t0001g0061a0002c0001t0001g0001others(57): Show | 61 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-112-10607G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637004 | ||||||
| chr1:21637086
|
G | A | 32 | a0001c0003t0001g0233a0001c0003t0002g0134a0001c0004t0001g0160others(29): Show | 32 | HG00099.hp2 HG00673.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-112-10689C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637086 | ||||||
| chr1:21637145
|
C | CT | 24 | a0001c0002t0001g0242a0001c0003t0001g0165a0001c0003t0001g0176others(21): Show | 24 | HG00280.hp2 HG00642.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-112-10749dupA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637145 | ||||||
| chr1:21637145
|
CT | C | 17 | a0001c0002t0001g0230a0001c0003t0001g0313a0001c0003t0001g0314others(14): Show | 17 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-112-10749delA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637145 | ||||||
| chr1:21637156
|
T | C | 96 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(93): Show | 96 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-112-10759A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637156 | ||||||
| chr1:21637221
|
A | C | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112-10824T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637221 | ||||||
| chr1:21637247
|
C | T | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-112-10850G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637247 | ||||||
| chr1:21637323
|
AT | A | 322 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(319): Show | 323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.-112-10927delA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637323 | ||||||
| chr1:21637361
|
C | T | 96 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(93): Show | 96 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.-112-10964G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637361 | ||||||
| chr1:21637641
|
C | T | 110 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(107): Show | 110 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-112-11244G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637641 | ||||||
| chr1:21637670
|
C | G | 1 | a0001c0002t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-112-11273G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637670 | ||||||
| chr1:21637762
|
G | C | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-112-11365C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637762 | ||||||
| chr1:21637972
|
C | CA | 49 | a0001c0002t0001g0105a0001c0002t0001g0162a0001c0002t0001g0190others(46): Show | 49 | HG00280.hp2 HG00323.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.-112-11576dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637972 | ||||||
| chr1:21637972
|
C | CAA | 165 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(162): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-112-11577_-112-11 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637972 | ||||||
| chr1:21637972
|
C | CAAA | 28 | a0001c0002t0001g0029a0001c0002t0001g0207a0001c0002t0001g0219others(25): Show | 28 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.-112-11578_-112-11 others(9): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637972 | ||||||
| chr1:21637972
|
CA | C | 7 | a0001c0003t0001g0315a0002c0001t0001g0164a0002c0001t0002g0091others(4): Show | 7 | HG01361.hp2 HG01891.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.-112-11576delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637972 | ||||||
| chr1:21637993
|
C | A | 1 | a0002c0001t0002g0142 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-112-11596G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21637993 | ||||||
| chr1:21638055
|
G | A | 1 | a0001c0003t0003g0363 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-112-11658C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638055 | ||||||
| chr1:21638104
|
T | C | 5 | a0001c0003t0004g0316a0001c0003t0004g0362a0001c0011t0001g0157others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+11657A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638104 | ||||||
| chr1:21638148
|
TA | T | 63 | a0001c0002t0001g0105a0001c0002t0001g0116a0001c0002t0001g0117others(60): Show | 63 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.-113+11612delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638148 | ||||||
| chr1:21638150
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0003t0001g0314 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-113+11598_-113+11 others(19): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638150 | ||||||
| chr1:21638158
|
A | G | 1 | a0001c0004t0001g0197 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-113+11603T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638158 | ||||||
| chr1:21638294
|
T | A | 1 | a0001c0002t0001g0019 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-113+11467A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638294 | ||||||
| chr1:21638309
|
C | T | 342 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(339): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-113+11452G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638309 | ||||||
| chr1:21638456
|
C | CA | 141 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0025others(138): Show | 141 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.-113+11304dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638456 | ||||||
| chr1:21638456
|
C | CAA | 21 | a0001c0002t0001g0183a0001c0002t0001g0330a0001c0003t0002g0358others(18): Show | 21 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.-113+11303_-113+11 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638456 | ||||||
| chr1:21638456
|
CA | C | 80 | a0001c0002t0001g0019a0001c0002t0001g0116a0001c0002t0001g0117others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.-113+11304delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638456 | ||||||
| chr1:21638573
|
C | T | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-113+11188G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638573 | ||||||
| chr1:21638664
|
C | T | 5 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0192others(2): Show | 5 | HG02071.hp2 HG02135.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+11097G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638664 | ||||||
| chr1:21638670
|
C | T | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-113+11091G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638670 | ||||||
| chr1:21638718
|
T | G | 4 | a0001c0002t0001g0330a0002c0001t0001g0312a0002c0001t0001g0355others(1): Show | 4 | HG02630.hp2 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+11043A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638718 | ||||||
| chr1:21638775
|
G | T | 1 | a0001c0002t0001g0019 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-113+10986C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638775 | ||||||
| chr1:21638821
|
G | T | 1 | a0001c0002t0001g0298 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-113+10940C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638821 | ||||||
| chr1:21638993
|
C | T | 97 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(94): Show | 97 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-113+10768G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21638993 | ||||||
| chr1:21639076
|
C | A | 3 | a0001c0009t0001g0308a0001c0009t0001g0317a0001c0009t0001g0318 | 3 | HG01099.hp1 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-113+10685G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21639076 | ||||||
| chr1:21639757
|
A | C | 1 | a0002c0006t0001g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-113+10004T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21639757 | ||||||
| chr1:21639774
|
G | A | 6 | a0001c0003t0001g0165a0001c0003t0004g0354a0002c0001t0002g0115others(3): Show | 6 | HG00280.hp2 HG01070.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+9987C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21639774 | ||||||
| chr1:21639843
|
G | A | 1 | a0002c0001t0001g0028 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-113+9918C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21639843 | ||||||
| chr1:21640014
|
C | T | 1 | a0002c0001t0001g0282 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-113+9747G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640014 | ||||||
| chr1:21640023
|
C | T | 1 | a0002c0005t0006g0078 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-113+9738G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640023 | ||||||
| chr1:21640197
|
C | T | 1 | a0001c0002t0001g0345 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-113+9564G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640197 | ||||||
| chr1:21640340
|
G | T | 79 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-113+9421C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640340 | ||||||
| chr1:21640342
|
G | A | 3 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0311 | 3 | HG01106.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-113+9419C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640342 | ||||||
| chr1:21640357
|
G | A | 56 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.-113+9404C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640357 | ||||||
| chr1:21640418
|
C | A | 1 | a0001c0002t0001g0046 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-113+9343G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640418 | ||||||
| chr1:21640549
|
G | A | 1 | a0001c0004t0001g0286 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-113+9212C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640549 | ||||||
| chr1:21640553
|
T | C | 1 | a0002c0001t0001g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-113+9208A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640553 | ||||||
| chr1:21640626
|
G | A | 1 | a0002c0006t0001g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-113+9135C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640626 | ||||||
| chr1:21640693
|
CAG | C | 4 | a0002c0001t0002g0115a0002c0001t0004g0005a0002c0001t0004g0367others(1): Show | 4 | HG00280.hp2 HG01070.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113+9066_-113+906 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640693 | ||||||
| chr1:21640705
|
G | GCCAGGTA others(3): Show |
97 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(94): Show | 97 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-113+9046_-113+905 others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640705 | ||||||
| chr1:21640884
|
C | T | 6 | a0001c0003t0001g0233a0002c0001t0001g0014a0002c0001t0002g0067others(3): Show | 6 | HG00738.hp2 HG01192.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-113+8877G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21640884 | ||||||
| chr1:21641044
|
A | G | 3 | a0002c0001t0001g0097a0002c0001t0001g0099a0002c0001t0001g0100 | 3 | NA18984.hp2 NA19068.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-113+8717T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641044 | ||||||
| chr1:21641074
|
A | AT | 57 | a0000c0014t0001g0171a0001c0002t0001g0116a0001c0002t0001g0127others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.-113+8686dupA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641074 | ||||||
| chr1:21641074
|
A | ATT | 104 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(101): Show | 105 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.-113+8685_-113+868 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641074 | ||||||
| chr1:21641074
|
A | ATTT | 51 | a0001c0002t0001g0019a0001c0002t0001g0331a0001c0003t0001g0008others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-113+8684_-113+868 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641074 | ||||||
| chr1:21641074
|
A | ATTTT | 112 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0025others(109): Show | 112 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-113+8683_-113+868 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641074 | ||||||
| chr1:21641452
|
G | A | 79 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-113+8309C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641452 | ||||||
| chr1:21641517
|
G | C | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-113+8244C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641517 | ||||||
| chr1:21641798
|
C | T | 2 | a0001c0002t0001g0178a0001c0002t0001g0250 | 2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-113+7963G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641798 | ||||||
| chr1:21641880
|
G | A | 3 | a0001c0003t0004g0362a0001c0011t0001g0157a0001c0011t0001g0350 | 3 | HG02109.hp1 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-113+7881C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641880 | ||||||
| chr1:21641970
|
C | T | 2 | a0002c0001t0004g0121a0002c0001t0004g0122 | 2 | HG00642.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-113+7791G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21641970 | ||||||
| chr1:21642073
|
C | T | 1 | a0001c0002t0001g0183 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-113+7688G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642073 | ||||||
| chr1:21642093
|
G | A | 2 | a0001c0003t0001g0210a0001c0003t0001g0231 | 2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-113+7668C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642093 | ||||||
| chr1:21642167
|
C | T | 82 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(79): Show | 82 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113+7594G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642167 | ||||||
| chr1:21642187
|
G | A | 1 | a0001c0003t0001g0070 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-113+7574C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642187 | ||||||
| chr1:21642248
|
C | T | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-113+7513G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642248 | ||||||
| chr1:21642272
|
C | T | 2 | a0001c0003t0001g0008a0001c0003t0001g0061 | 2 | HG01081.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-113+7489G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642272 | ||||||
| chr1:21642273
|
A | G | 279 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-113+7488T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642273 | ||||||
| chr1:21642314
|
G | A | 5 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(2): Show | 5 | HG02572.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+7447C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642314 | ||||||
| chr1:21642554
|
C | T | 1 | a0002c0001t0001g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-113+7207G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642554 | ||||||
| chr1:21642714
|
A | G | 279 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-113+7047T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642714 | ||||||
| chr1:21642875
|
T | TAC | 61 | a0001c0002t0001g0016a0001c0002t0001g0081a0001c0002t0001g0116others(58): Show | 61 | HG00738.hp2 HG00741.hp2 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.-113+6884_-113+688 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
T | TACAC | 33 | a0001c0003t0001g0070a0001c0003t0001g0141a0001c0003t0002g0134others(30): Show | 33 | HG00408.hp1 HG00673.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.-113+6882_-113+688 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
T | TACACAC | 53 | a0001c0003t0001g0370a0001c0003t0001g0371a0001c0003t0002g0322others(50): Show | 54 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-113+6880_-113+688 others(10): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
T | TACACACA others(1): Show |
21 | a0001c0003t0001g0008a0001c0003t0001g0061a0001c0003t0001g0165others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(18): Show |
intron_variant | MODIFIER | c.-113+6878_-113+688 others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
T | TACACACA others(3): Show |
8 | a0001c0003t0001g0342a0002c0001t0001g0009a0002c0001t0001g0111others(5): Show | 8 | HG01433.hp2 HG01515.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.-113+6876_-113+688 others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
T | TACACACA others(5): Show |
5 | a0001c0003t0002g0360a0001c0003t0002g0361a0002c0001t0001g0098others(2): Show | 5 | HG02300.hp1 HG03579.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+6874_-113+688 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
T | TACACACA others(7): Show |
1 | a0002c0001t0003g0037 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-113+6872_-113+688 others(18): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
T | TACACACA others(9): Show |
1 | a0001c0003t0002g0359 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-113+6870_-113+688 others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
TAC | T | 17 | a0001c0002t0001g0029a0001c0002t0001g0149a0001c0002t0001g0214others(14): Show | 17 | HG00323.hp1 HG00733.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-113+6884_-113+688 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
TACAC | T | 22 | a0001c0002t0001g0046a0001c0002t0001g0191a0001c0011t0001g0157others(19): Show | 22 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-113+6882_-113+688 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21642875
|
TACACACA others(3): Show |
T | 4 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(1): Show | 4 | HG02572.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113+6876_-113+688 others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21642875 | ||||||
| chr1:21643119
|
T | TCCA | 279 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-113+6639_-113+664 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643119 | ||||||
| chr1:21643126
|
A | C | 53 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(50): Show | 53 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-113+6635T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643126 | ||||||
| chr1:21643126
|
A | T | 279 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-113+6635T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643126 | ||||||
| chr1:21643154
|
C | T | 5 | a0001c0003t0004g0354a0002c0001t0002g0115a0002c0001t0004g0005others(2): Show | 5 | HG00280.hp2 HG01070.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-113+6607G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643154 | ||||||
| chr1:21643335
|
G | A | 3 | a0001c0003t0004g0362a0001c0011t0001g0157a0001c0011t0001g0350 | 3 | HG02109.hp1 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-113+6426C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643335 | ||||||
| chr1:21643429
|
A | G | 332 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-113+6332T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643429 | ||||||
| chr1:21643433
|
C | T | 1 | a0007c0019t0001g0366 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-113+6328G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643433 | ||||||
| chr1:21643449
|
T | G | 13 | a0001c0003t0002g0358a0001c0003t0002g0359a0001c0003t0002g0360others(10): Show | 13 | HG00099.hp1 HG01109.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.-113+6312A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643449 | ||||||
| chr1:21643511
|
C | T | 168 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.-113+6250G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643511 | ||||||
| chr1:21643556
|
C | CA | 26 | a0000c0014t0001g0170a0001c0002t0001g0190a0001c0002t0001g0214others(23): Show | 26 | HG00099.hp1 HG01109.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.-113+6204dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643556 | ||||||
| chr1:21643556
|
CA | C | 56 | a0001c0002t0001g0240a0001c0002t0001g0251a0001c0002t0001g0258others(53): Show | 56 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-113+6204delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643556 | ||||||
| chr1:21643561
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0003t0003g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-113+6185_-113+619 others(19): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643561 | ||||||
| chr1:21643567
|
AAAAAAAA others(2): Show |
A | 30 | a0001c0003t0004g0354a0002c0001t0001g0056a0002c0001t0001g0158others(27): Show | 30 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.-113+6185_-113+619 others(13): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643567 | ||||||
| chr1:21643796
|
G | A | 279 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(276): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.-113+5965C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643796 | ||||||
| chr1:21643845
|
G | A | 4 | a0001c0003t0002g0358a0001c0003t0002g0359a0001c0003t0002g0360others(1): Show | 4 | HG02723.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-113+5916C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21643845 | ||||||
| chr1:21644089
|
G | A | 3 | a0001c0003t0004g0362a0001c0011t0001g0157a0001c0011t0001g0350 | 3 | HG02109.hp1 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-113+5672C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644089 | ||||||
| chr1:21644183
|
C | T | 2 | a0001c0004t0001g0226a0001c0004t0001g0364 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-113+5578G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644183 | ||||||
| chr1:21644273
|
T | A | 7 | a0001c0002t0001g0051a0001c0003t0001g0077a0001c0003t0001g0085others(4): Show | 7 | NA18970.hp1 NA18975.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+5488A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644273 | ||||||
| chr1:21644307
|
G | A | 2 | a0002c0001t0001g0096a0002c0001t0002g0101 | 2 | NA18945.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-113+5454C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644307 | ||||||
| chr1:21644472
|
A | G | 56 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(53): Show | 56 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-113+5289T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644472 | ||||||
| chr1:21644672
|
G | A | 3 | a0002c0001t0001g0312a0002c0001t0001g0355a0002c0001t0001g0356 | 3 | HG02630.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-113+5089C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644672 | ||||||
| chr1:21644900
|
C | CA | 62 | a0001c0002t0001g0331a0001c0003t0001g0008a0001c0003t0001g0061others(59): Show | 63 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.-113+4860dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644900 | ||||||
| chr1:21644900
|
C | CAA | 7 | a0001c0003t0004g0316a0001c0009t0001g0308a0001c0009t0001g0317others(4): Show | 7 | HG01099.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-113+4859_-113+486 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644900 | ||||||
| chr1:21644900
|
C | CAAA | 12 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-113+4858_-113+486 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644900 | ||||||
| chr1:21644900
|
CA | C | 87 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0116others(84): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-113+4860delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644900 | ||||||
| chr1:21644900
|
CAA | C | 82 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113+4859_-113+486 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644900 | ||||||
| chr1:21644900
|
CAAA | C | 8 | a0001c0002t0001g0183a0001c0002t0001g0251a0001c0002t0001g0264others(5): Show | 8 | HG01070.hp1 HG01975.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-113+4858_-113+486 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644900 | ||||||
| chr1:21644919
|
A | G | 153 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(150): Show | 153 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.-113+4842T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644919 | ||||||
| chr1:21644920
|
AG | A | 21 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0169others(18): Show | 21 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-113+4840delC | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644920 | ||||||
| chr1:21644921
|
G | A | 1 | a0002c0006t0001g0140 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-113+4840C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644921 | ||||||
| chr1:21644924
|
A | AAAAGAAA others(1): Show |
12 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-113+4829_-113+483 others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644924 | ||||||
| chr1:21644924
|
A | AGAAAAGA others(3): Show |
1 | a0002c0006t0001g0140 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-113+4836_-113+483 others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644924 | ||||||
| chr1:21644925
|
A | G | 21 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0169others(18): Show | 21 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-113+4836T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644925 | ||||||
| chr1:21644926
|
AAG | A | 21 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0169others(18): Show | 21 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-113+4833_-113+483 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21644926 | ||||||
| chr1:21645078
|
C | G | 2 | a0002c0001t0001g0355a0002c0001t0001g0356 | 2 | HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-113+4683G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645078 | ||||||
| chr1:21645079
|
G | A | 1 | a0003c0015t0001g0002 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-113+4682C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645079 | ||||||
| chr1:21645280
|
A | G | 85 | a0001c0002t0001g0331a0001c0003t0001g0008a0001c0003t0001g0061others(82): Show | 86 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-113+4481T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645280 | ||||||
| chr1:21645281
|
A | T | 108 | a0001c0002t0001g0331a0001c0003t0001g0008a0001c0003t0001g0061others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.-113+4480T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645281 | ||||||
| chr1:21645357
|
G | A | 1 | a0001c0003t0007g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-113+4404C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645357 | ||||||
| chr1:21645556
|
G | A | 1 | a0001c0004t0001g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-113+4205C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645556 | ||||||
| chr1:21645643
|
T | C | 23 | a0002c0001t0001g0056a0002c0001t0001g0158a0002c0001t0001g0169others(20): Show | 23 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.-113+4118A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645643 | ||||||
| chr1:21645778
|
G | A | 1 | a0002c0001t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-113+3983C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645778 | ||||||
| chr1:21645987
|
G | A | 163 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-113+3774C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21645987 | ||||||
| chr1:21646009
|
C | T | 2 | a0001c0003t0004g0316a0003c0015t0004g0055 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+3752G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646009 | ||||||
| chr1:21646046
|
G | A | 2 | a0002c0006t0001g0118a0002c0006t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-113+3715C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646046 | ||||||
| chr1:21646182
|
A | C | 1 | a0001c0004t0001g0284 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-113+3579T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646182 | ||||||
| chr1:21646200
|
T | C | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-113+3561A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646200 | ||||||
| chr1:21646211
|
T | C | 5 | a0001c0004t0001g0041a0001c0004t0001g0197a0002c0001t0001g0043others(2): Show | 5 | HG00544.hp2 HG00621.hp2 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113+3550A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646211 | ||||||
| chr1:21646401
|
G | A | 10 | a0001c0003t0002g0358a0001c0003t0002g0359a0001c0003t0002g0360others(7): Show | 10 | HG00099.hp1 HG01109.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-113+3360C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646401 | ||||||
| chr1:21646694
|
T | G | 1 | a0001c0002t0001g0183 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-113+3067A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646694 | ||||||
| chr1:21646726
|
A | C | 1 | a0003c0010t0001g0054 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-113+3035T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646726 | ||||||
| chr1:21646842
|
C | T | 9 | a0001c0002t0001g0062a0001c0002t0001g0221a0001c0002t0001g0222others(6): Show | 9 | HG00738.hp1 HG01123.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-113+2919G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21646842 | ||||||
| chr1:21647342
|
T | C | 90 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(87): Show | 90 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-113+2419A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647342 | ||||||
| chr1:21647397
|
A | G | 332 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-113+2364T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647397 | ||||||
| chr1:21647421
|
A | C | 87 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(84): Show | 87 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-113+2340T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647421 | ||||||
| chr1:21647446
|
A | G | 1 | a0002c0001t0001g0049 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-113+2315T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647446 | ||||||
| chr1:21647604
|
G | C | 6 | a0001c0003t0001g0165a0001c0003t0004g0354a0002c0001t0002g0115others(3): Show | 6 | HG00280.hp2 HG01070.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113+2157C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647604 | ||||||
| chr1:21647715
|
C | T | 237 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.-113+2046G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647715 | ||||||
| chr1:21647839
|
GCTGGAGG others(12): Show |
G | 1 | a0002c0018t0002g0058 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-113+1903_-113+192 others(23): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647839 | ||||||
| chr1:21647906
|
G | T | 1 | a0002c0001t0005g0130 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-113+1855C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21647906 | ||||||
| chr1:21648033
|
G | C | 2 | a0002c0001t0001g0111a0002c0001t0001g0112 | 2 | NA19010.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-113+1728C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648033 | ||||||
| chr1:21648052
|
G | A | 8 | a0001c0003t0001g0201a0001c0004t0001g0160a0001c0004t0001g0232others(5): Show | 8 | HG01168.hp1 HG01934.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.-113+1709C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648052 | ||||||
| chr1:21648116
|
G | A | 2 | a0001c0003t0004g0316a0003c0015t0004g0055 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-113+1645C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648116 | ||||||
| chr1:21648133
|
C | A | 2 | a0002c0001t0001g0057a0002c0001t0001g0321 | 2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-113+1628G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648133 | ||||||
| chr1:21648142
|
T | G | 1 | a0002c0001t0009g0309 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-113+1619A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648142 | ||||||
| chr1:21648341
|
C | T | 236 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.-113+1420G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648341 | ||||||
| chr1:21648350
|
C | T | 1 | a0001c0002t0003g0307 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-113+1411G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648350 | ||||||
| chr1:21648362
|
C | T | 1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-113+1399G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648362 | ||||||
| chr1:21648442
|
C | A | 1 | a0007c0019t0001g0366 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-113+1319G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648442 | ||||||
| chr1:21648483
|
C | G | 1 | a0002c0001t0001g0163 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-113+1278G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648483 | ||||||
| chr1:21648506
|
A | G | 1 | a0001c0003t0001g0148 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-113+1255T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648506 | ||||||
| chr1:21648562
|
C | CAT | 332 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-113+1198_-113+119 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648562 | ||||||
| chr1:21648627
|
G | A | 2 | a0001c0004t0001g0069a0001c0004t0001g0071 | 2 | HG01943.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-113+1134C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648627 | ||||||
| chr1:21648687
|
C | G | 18 | a0001c0003t0001g0233a0002c0001t0002g0067a0002c0001t0002g0089others(15): Show | 18 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-113+1074G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648687 | ||||||
| chr1:21648696
|
A | G | 9 | a0001c0002t0001g0062a0001c0002t0001g0221a0001c0002t0001g0222others(6): Show | 9 | HG00738.hp1 HG01123.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-113+1065T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648696 | ||||||
| chr1:21648721
|
A | G | 59 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0240others(56): Show | 59 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-113+1040T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21648721 | ||||||
| chr1:21649138
|
C | T | 1 | a0002c0001t0001g0047 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-113+623G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21649138 | ||||||
| chr1:21649163
|
T | C | 1 | a0002c0001t0002g0104 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-113+598A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21649163 | ||||||
| chr1:21649186
|
G | A | 1 | a0001c0004t0001g0215 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-113+575C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21649186 | ||||||
| chr1:21649203
|
G | A | 13 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(10): Show | 13 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-113+558C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21649203 | ||||||
| chr1:21649276
|
G | A | 2 | a0001c0009t0001g0317a0001c0009t0001g0318 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-113+485C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21649276 | ||||||
| chr1:21649430
|
G | T | 274 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-113+331C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21649430 | ||||||
| chr1:21649461
|
T | C | 1 | a0002c0001t0001g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-113+300A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | 21649461 | ||||||
| chr1:21650074
|
G | T | 1 | a0001c0004t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-148-278C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650074 | ||||||
| chr1:21650445
|
C | T | 61 | a0001c0002t0001g0331a0001c0003t0001g0008a0001c0003t0001g0061others(58): Show | 62 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-148-649G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650445 | ||||||
| chr1:21650448
|
G | A | 1 | a0001c0002t0001g0262 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-148-652C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650448 | ||||||
| chr1:21650452
|
A | G | 331 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(328): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-148-656T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650452 | ||||||
| chr1:21650472
|
G | C | 1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-148-676C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650472 | ||||||
| chr1:21650586
|
C | A | 5 | a0001c0002t0001g0182a0001c0002t0001g0183a0001c0002t0001g0208others(2): Show | 5 | HG01993.hp2 HG02027.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.-148-790G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650586 | ||||||
| chr1:21650663
|
C | G | 1 | a0001c0002t0001g0219 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-148-867G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650663 | ||||||
| chr1:21650762
|
C | T | 215 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-148-966G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650762 | ||||||
| chr1:21650839
|
C | T | 12 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-148-1043G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650839 | ||||||
| chr1:21650933
|
C | A | 2 | a0002c0001t0001g0124a0002c0001t0001g0139 | 2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-148-1137G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21650933 | ||||||
| chr1:21651072
|
C | T | 1 | a0004c0028t0001g0277 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-148-1276G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21651072 | ||||||
| chr1:21651587
|
A | G | 1 | a0001c0003t0001g0348 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-148-1791T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21651587 | ||||||
| chr1:21651721
|
C | A | 1 | a0002c0001t0002g0268 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-148-1925G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21651721 | ||||||
| chr1:21651763
|
C | G | 1 | a0002c0001t0001g0033 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-148-1967G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21651763 | ||||||
| chr1:21651972
|
G | A | 61 | a0001c0002t0001g0162a0001c0002t0001g0203a0001c0002t0001g0220others(58): Show | 61 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-148-2176C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21651972 | ||||||
| chr1:21652073
|
C | T | 1 | a0001c0003t0004g0354 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-148-2277G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652073 | ||||||
| chr1:21652100
|
C | A | 1 | a0001c0004t0001g0281 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-148-2304G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652100 | ||||||
| chr1:21652106
|
C | A | 2 | a0002c0001t0001g0018a0002c0001t0001g0103 | 2 | HG00408.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-148-2310G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652106 | ||||||
| chr1:21652129
|
C | A | 1 | a0001c0003t0001g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-148-2333G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652129 | ||||||
| chr1:21652155
|
A | G | 180 | a0001c0002t0001g0025a0001c0002t0001g0026a0001c0002t0001g0029others(177): Show | 181 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.-148-2359T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652155 | ||||||
| chr1:21652156
|
G | A | 3 | a0002c0001t0003g0323a0002c0001t0003g0324a0002c0001t0003g0325 | 3 | HG02258.hp1 HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-148-2360C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652156 | ||||||
| chr1:21652175
|
C | T | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-148-2379G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652175 | ||||||
| chr1:21652183
|
C | G | 1 | a0002c0001t0002g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-148-2387G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652183 | ||||||
| chr1:21652284
|
C | A | 1 | a0001c0024t0001g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-148-2488G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652284 | ||||||
| chr1:21652340
|
G | A | 2 | a0001c0004t0001g0335a0001c0004t0001g0336 | 2 | HG02056.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-148-2544C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652340 | ||||||
| chr1:21652737
|
C | T | 274 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(271): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-148-2941G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652737 | ||||||
| chr1:21652953
|
G | T | 3 | a0002c0006t0001g0301a0002c0006t0001g0302a0002c0006t0001g0357 | 3 | HG03195.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-148-3157C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652953 | ||||||
| chr1:21652989
|
C | T | 2 | a0001c0003t0002g0304a0001c0003t0002g0305 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-148-3193G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21652989 | ||||||
| chr1:21653057
|
C | T | 6 | a0001c0003t0001g0141a0002c0001t0001g0321a0002c0001t0003g0323others(3): Show | 6 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-148-3261G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653057 | ||||||
| chr1:21653087
|
C | T | 1 | a0001c0003t0001g0131 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-148-3291G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653087 | ||||||
| chr1:21653235
|
C | T | 1 | a0001c0002t0001g0051 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-148-3439G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653235 | ||||||
| chr1:21653303
|
C | G | 1 | a0002c0001t0001g0012 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-148-3507G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653303 | ||||||
| chr1:21653391
|
G | C | 2 | a0001c0002t0001g0208a0001c0002t0001g0235 | 2 | HG01993.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.-148-3595C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653391 | ||||||
| chr1:21653456
|
G | A | 51 | a0001c0002t0001g0019a0001c0002t0001g0102a0001c0002t0001g0182others(48): Show | 51 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-148-3660C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653456 | ||||||
| chr1:21653467
|
G | C | 2 | a0001c0007t0001g0300a0001c0012t0001g0059 | 2 | HG00323.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-148-3671C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653467 | ||||||
| chr1:21653491
|
G | A | 59 | a0001c0002t0001g0029a0001c0002t0001g0191a0001c0002t0001g0203others(56): Show | 59 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-148-3695C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653491 | ||||||
| chr1:21653543
|
A | ACTTC | 61 | a0001c0002t0001g0029a0001c0002t0001g0046a0001c0002t0001g0105others(58): Show | 62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.-148-3751_-148-374 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653543
|
A | ACTTCCTT others(1): Show |
27 | a0001c0002t0001g0015a0001c0002t0001g0203a0001c0002t0001g0220others(24): Show | 27 | HG00408.hp1 HG00558.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.-148-3755_-148-374 others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653543
|
A | ACTTCCTT others(5): Show |
2 | a0001c0004t0001g0123a0001c0004t0001g0189 | 2 | HG03654.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-148-3759_-148-374 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653543
|
A | ACTTCCTT others(9): Show |
1 | a0001c0004t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-148-3763_-148-374 others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653543
|
ACTTC | A | 23 | a0001c0002t0001g0127a0001c0002t0001g0162a0001c0002t0001g0193others(20): Show | 23 | HG00673.hp2 HG01257.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.-148-3751_-148-374 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653543
|
ACTTCCTT others(1): Show |
A | 5 | a0001c0002t0001g0190a0001c0003t0001g0210a0001c0003t0001g0231others(2): Show | 5 | HG02809.hp1 HG02895.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-148-3755_-148-374 others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653543
|
ACTTCCTT others(5): Show |
A | 8 | a0001c0003t0002g0358a0001c0003t0002g0359a0001c0003t0002g0360others(5): Show | 8 | HG02630.hp2 HG02723.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-148-3759_-148-374 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653543
|
ACTTCCTT others(13): Show |
A | 3 | a0001c0017t0001g0319a0002c0001t0001g0311a0003c0015t0001g0002 | 3 | HG01106.hp1 HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-148-3767_-148-374 others(24): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653543 | ||||||
| chr1:21653551
|
C | A | 1 | a0002c0001t0001g0014 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-148-3755G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653551 | ||||||
| chr1:21653570
|
TCCTTCCT others(17): Show |
T | 6 | a0001c0003t0001g0061a0001c0003t0001g0154a0001c0003t0001g0155others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.-148-3798_-148-377 others(28): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653570 | ||||||
| chr1:21653576
|
C | T | 14 | a0001c0002t0001g0216a0001c0002t0001g0225a0001c0002t0001g0250others(11): Show | 14 | HG00639.hp2 HG01109.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.-148-3780G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653576 | ||||||
| chr1:21653578
|
TCCTTCCT others(9): Show |
T | 1 | a0002c0001t0002g0337 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-148-3798_-148-378 others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653578 | ||||||
| chr1:21653580
|
C | CTTCCTTC others(17): Show |
2 | a0002c0008t0003g0365a0007c0019t0001g0366 | 2 | HG00099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-148-3785_-148-378 others(28): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653580 | ||||||
| chr1:21653580
|
C | CTTCCTTC others(13): Show |
1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-148-3785_-148-378 others(24): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653580 | ||||||
| chr1:21653580
|
C | CTTCCTTC others(9): Show |
1 | a0001c0003t0003g0363 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-148-3785_-148-378 others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653580 | ||||||
| chr1:21653580
|
C | CTTCCTTC others(5): Show |
1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-148-3785_-148-378 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653580 | ||||||
| chr1:21653580
|
C | CTTCT | 5 | a0001c0002t0001g0178a0001c0002t0001g0255a0001c0002t0001g0291others(2): Show | 5 | HG01358.hp1 HG03831.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-148-3785_-148-378 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653580 | ||||||
| chr1:21653580
|
C | T | 45 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0019others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-148-3784G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653580 | ||||||
| chr1:21653582
|
TCCTTCCT others(5): Show |
T | 5 | a0001c0003t0002g0320a0001c0012t0001g0059a0002c0001t0002g0104others(2): Show | 5 | HG00099.hp2 HG00323.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-148-3798_-148-378 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653582 | ||||||
| chr1:21653586
|
T | TCCTTCCT others(45): Show |
1 | a0001c0002t0001g0208 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-148-3791_-148-379 others(56): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653586 | ||||||
| chr1:21653586
|
TCCTTCCT others(1): Show |
T | 27 | a0001c0002t0001g0062a0001c0002t0001g0298a0001c0002t0001g0331others(24): Show | 27 | HG00280.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.-148-3798_-148-379 others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653586 | ||||||
| chr1:21653586
|
TCCTTCCT others(5): Show |
T | 3 | a0002c0006t0001g0118a0002c0006t0001g0119a0003c0010t0001g0327 | 3 | HG01070.hp2 HG01071.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-148-3802_-148-379 others(16): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653586 | ||||||
| chr1:21653590
|
T | C | 4 | a0001c0002t0001g0016a0001c0002t0003g0307a0001c0003t0003g0179others(1): Show | 4 | HG01891.hp2 HG02083.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-3794A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653590 | ||||||
| chr1:21653590
|
T | TCCTC | 3 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315 | 3 | HG02572.hp2 HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-148-3798_-148-379 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653590 | ||||||
| chr1:21653590
|
T | TCCTTCCT others(53): Show |
1 | a0002c0001t0001g0023 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-148-3795_-148-379 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653590 | ||||||
| chr1:21653590
|
T | TCCTTCCT others(9): Show |
1 | a0001c0003t0007g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-148-3795_-148-379 others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653590 | ||||||
| chr1:21653590
|
TCCTC | T | 34 | a0001c0002t0001g0051a0001c0002t0001g0081a0001c0002t0001g0216others(31): Show | 34 | HG00639.hp2 HG01109.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.-148-3798_-148-379 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653590 | ||||||
| chr1:21653594
|
C | T | 97 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0019others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.-148-3798G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653594 | ||||||
| chr1:21653598
|
C | T | 1 | a0002c0001t0001g0023 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-148-3802G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653598 | ||||||
| chr1:21653602
|
C | T | 1 | a0001c0002t0001g0208 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-148-3806G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653602 | ||||||
| chr1:21653701
|
AGAGAGGT others(280): Show |
A | 1 | a0001c0024t0001g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-148-4192_-148-390 others(4): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653701 | ||||||
| chr1:21653832
|
A | G | 151 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0046others(148): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.-148-4036T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653832 | ||||||
| chr1:21653892
|
C | T | 1 | a0002c0001t0001g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-148-4096G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653892 | ||||||
| chr1:21653988
|
G | A | 5 | a0001c0002t0001g0345a0002c0001t0002g0338a0002c0001t0002g0340others(2): Show | 5 | HG00423.hp2 NA18949.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-148-4192C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21653988 | ||||||
| chr1:21654188
|
C | T | 42 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(39): Show | 42 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.-148-4392G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654188 | ||||||
| chr1:21654257
|
A | C | 145 | a0001c0002t0001g0029a0001c0002t0001g0051a0001c0002t0001g0062others(142): Show | 145 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-148-4461T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654257 | ||||||
| chr1:21654303
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-148-4507C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654303 | ||||||
| chr1:21654320
|
G | A | 4 | a0002c0001t0001g0014a0002c0001t0001g0034a0002c0001t0001g0036others(1): Show | 4 | NA18942.hp2 NA18961.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-4524C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654320 | ||||||
| chr1:21654360
|
G | T | 4 | a0001c0003t0003g0368a0001c0003t0003g0369a0001c0003t0004g0354others(1): Show | 4 | HG01070.hp1 HG01346.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-4564C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654360 | ||||||
| chr1:21654747
|
G | A | 4 | a0001c0003t0002g0304a0001c0003t0002g0305a0001c0009t0001g0317others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-4951C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654747 | ||||||
| chr1:21654829
|
C | T | 1 | a0001c0003t0002g0320 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-148-5033G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654829 | ||||||
| chr1:21654868
|
C | T | 61 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(58): Show | 61 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.-148-5072G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654868 | ||||||
| chr1:21654985
|
CA | C | 7 | a0001c0003t0002g0358a0001c0003t0002g0359a0001c0003t0002g0360others(4): Show | 7 | HG02630.hp2 HG02723.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-148-5190delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654985 | ||||||
| chr1:21654996
|
C | T | 5 | a0001c0002t0001g0190a0001c0007t0001g0186a0001c0007t0001g0187others(2): Show | 5 | HG02486.hp1 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-148-5200G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21654996 | ||||||
| chr1:21655105
|
A | G | 56 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(53): Show | 57 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.-148-5309T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21655105 | ||||||
| chr1:21655330
|
A | G | 1 | a0002c0006t0001g0306 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-148-5534T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21655330 | ||||||
| chr1:21655393
|
C | T | 2 | a0002c0001t0001g0056a0003c0015t0004g0055 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-148-5597G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21655393 | ||||||
| chr1:21655451
|
G | A | 2 | a0002c0006t0001g0118a0002c0006t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-148-5655C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21655451 | ||||||
| chr1:21655621
|
TTAC | T | 54 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(51): Show | 55 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-148-5828_-148-582 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21655621 | ||||||
| chr1:21656168
|
C | T | 5 | a0001c0002t0001g0249a0001c0002t0001g0263a0001c0002t0001g0272others(2): Show | 5 | HG00423.hp1 HG00544.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.-148-6372G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656168 | ||||||
| chr1:21656209
|
A | G | 203 | a0001c0002t0001g0029a0001c0002t0001g0051a0001c0002t0001g0062others(200): Show | 203 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-148-6413T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656209 | ||||||
| chr1:21656292
|
G | T | 1 | a0002c0006t0001g0301 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-148-6496C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656292 | ||||||
| chr1:21656417
|
TA | T | 122 | a0001c0002t0001g0029a0001c0002t0001g0167a0001c0002t0001g0168others(119): Show | 122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-148-6622delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656417 | ||||||
| chr1:21656417
|
TAAA | T | 12 | a0001c0002t0001g0019a0001c0002t0001g0026a0001c0004t0001g0041others(9): Show | 12 | HG00544.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-148-6624_-148-662 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656417 | ||||||
| chr1:21656417
|
TAAAA | T | 74 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0025others(71): Show | 75 | HG00099.hp1 HG00639.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.-148-6625_-148-662 others(8): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656417 | ||||||
| chr1:21656417
|
TAAAAA | T | 15 | a0001c0002t0001g0339a0001c0002t0001g0345a0001c0003t0001g0342others(12): Show | 15 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(12): Show |
intron_variant | MODIFIER | c.-148-6626_-148-662 others(9): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656417 | ||||||
| chr1:21656417
|
TAAAAAAA others(1): Show |
T | 13 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0172others(10): Show | 13 | HG01261.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-148-6629_-148-662 others(12): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656417 | ||||||
| chr1:21656417
|
TAAAAAAA others(9): Show |
T | 1 | a0003c0010t0001g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-148-6637_-148-662 others(20): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656417 | ||||||
| chr1:21656417
|
TAAAAAAA others(11): Show |
T | 1 | a0001c0013t0003g0076 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-148-6639_-148-662 others(22): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656417 | ||||||
| chr1:21656424
|
A | C | 3 | a0002c0008t0003g0063a0002c0008t0003g0065a0002c0008t0012g0064 | 3 | HG02717.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-148-6628T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656424 | ||||||
| chr1:21656425
|
A | C | 3 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0242 | 3 | NA19000.hp1 NA19054.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-148-6629T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656425 | ||||||
| chr1:21656426
|
A | C | 63 | a0001c0002t0001g0029a0001c0002t0001g0167a0001c0002t0001g0168others(60): Show | 63 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-148-6630T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656426 | ||||||
| chr1:21656427
|
A | C | 1 | a0001c0002t0001g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-148-6631T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656427 | ||||||
| chr1:21656428
|
A | C | 3 | a0001c0002t0001g0127a0001c0002t0001g0149a0001c0002t0008g0126 | 3 | HG02886.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-148-6632T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656428 | ||||||
| chr1:21656429
|
A | C | 72 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.-148-6633T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656429 | ||||||
| chr1:21656430
|
A | C | 4 | a0001c0002t0001g0203a0001c0002t0001g0230a0001c0002t0001g0242others(1): Show | 4 | HG00741.hp2 NA19000.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-6634T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656430 | ||||||
| chr1:21656431
|
A | C | 124 | a0001c0002t0001g0029a0001c0002t0001g0127a0001c0002t0001g0149others(121): Show | 124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-148-6635T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656431 | ||||||
| chr1:21656432
|
A | C | 3 | a0001c0002t0001g0240a0002c0001t0001g0057a0002c0001t0001g0229 | 3 | HG02257.hp2 NA18964.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-148-6636T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656432 | ||||||
| chr1:21656433
|
A | C | 2 | a0001c0002t0008g0126a0002c0023t0001g0310 | 2 | HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-148-6637T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656433 | ||||||
| chr1:21656434
|
A | C | 73 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-148-6638T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656434 | ||||||
| chr1:21656435
|
A | C | 43 | a0001c0002t0001g0248a0001c0002t0001g0330a0001c0002t0001g0331others(40): Show | 43 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.-148-6639T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656435 | ||||||
| chr1:21656436
|
A | C | 11 | a0001c0002t0002g0256a0001c0002t0002g0275a0001c0002t0002g0276others(8): Show | 11 | HG00621.hp2 HG00642.hp1 HG00733.hp1 others(8): Show |
intron_variant | MODIFIER | c.-148-6640T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656436 | ||||||
| chr1:21656439
|
A | C | 5 | a0002c0001t0001g0066a0002c0001t0001g0158a0002c0008t0003g0063others(2): Show | 5 | HG02717.hp1 HG02818.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-148-6643T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656439 | ||||||
| chr1:21656441
|
A | C | 29 | a0001c0002t0001g0339a0001c0002t0001g0345a0001c0003t0001g0165others(26): Show | 29 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.-148-6645T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656441 | ||||||
| chr1:21656442
|
A | C | 57 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(54): Show | 58 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.-148-6646T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656442 | ||||||
| chr1:21656447
|
A | AC | 4 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0003t0001g0148others(1): Show | 4 | HG00741.hp1 HG01517.hp2 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.-148-6652_-148-665 others(5): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656447 | ||||||
| chr1:21656447
|
A | C | 347 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(344): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.-148-6651T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656447 | ||||||
| chr1:21656448
|
A | C | 1 | a0003c0015t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-148-6652T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656448 | ||||||
| chr1:21656761
|
C | T | 202 | a0001c0002t0001g0029a0001c0002t0001g0051a0001c0002t0001g0062others(199): Show | 202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-148-6965G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21656761 | ||||||
| chr1:21657066
|
C | T | 1 | a0002c0006t0001g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-148-7270G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657066 | ||||||
| chr1:21657074
|
A | T | 130 | a0001c0002t0001g0029a0001c0002t0001g0167a0001c0002t0001g0168others(127): Show | 130 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-148-7278T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657074 | ||||||
| chr1:21657107
|
G | C | 1 | a0002c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-148-7311C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657107 | ||||||
| chr1:21657118
|
C | T | 203 | a0001c0002t0001g0029a0001c0002t0001g0051a0001c0002t0001g0062others(200): Show | 203 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-148-7322G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657118 | ||||||
| chr1:21657147
|
C | T | 1 | a0001c0003t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-148-7351G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657147 | ||||||
| chr1:21657207
|
C | G | 1 | a0002c0001t0002g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-148-7411G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657207 | ||||||
| chr1:21657300
|
C | T | 129 | a0001c0002t0001g0029a0001c0002t0001g0167a0001c0002t0001g0168others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-148-7504G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657300 | ||||||
| chr1:21657338
|
A | T | 11 | a0001c0002t0001g0025a0001c0002t0001g0026a0002c0001t0001g0039others(8): Show | 11 | NA18942.hp1 NA18945.hp2 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.-148-7542T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657338 | ||||||
| chr1:21657400
|
G | T | 1 | a0002c0001t0001g0311 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-148-7604C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657400 | ||||||
| chr1:21657446
|
G | A | 3 | a0001c0002t0001g0330a0001c0003t0001g0328a0001c0003t0003g0329 | 3 | HG02257.hp1 HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-148-7650C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657446 | ||||||
| chr1:21657720
|
C | T | 54 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(51): Show | 55 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-148-7924G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657720 | ||||||
| chr1:21657800
|
A | C | 1 | a0002c0001t0001g0001 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-148-8004T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21657800 | ||||||
| chr1:21658096
|
T | G | 1 | a0001c0002t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-148-8300A>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658096 | ||||||
| chr1:21658311
|
T | C | 1 | a0001c0002t0001g0062 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-148-8515A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658311 | ||||||
| chr1:21658366
|
G | A | 2 | a0002c0006t0001g0118a0002c0006t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-148-8570C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658366 | ||||||
| chr1:21658440
|
C | T | 1 | a0002c0001t0001g0075 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-148-8644G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658440 | ||||||
| chr1:21658476
|
G | A | 55 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(52): Show | 56 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-148-8680C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658476 | ||||||
| chr1:21658724
|
A | G | 3 | a0001c0002t0001g0330a0001c0003t0001g0328a0001c0003t0003g0329 | 3 | HG02257.hp1 HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-148-8928T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658724 | ||||||
| chr1:21658779
|
T | C | 4 | a0001c0003t0002g0304a0001c0003t0002g0305a0001c0009t0001g0317others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-8983A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658779 | ||||||
| chr1:21658869
|
A | G | 2 | a0002c0006t0001g0118a0002c0006t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-148-9073T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658869 | ||||||
| chr1:21658941
|
C | CT | 242 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0029others(239): Show | 242 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.-148-9146dupA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658941 | ||||||
| chr1:21658941
|
C | CTT | 25 | a0001c0002t0001g0225a0001c0002t0001g0238a0001c0002t0001g0283others(22): Show | 25 | HG00280.hp2 HG01106.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.-148-9147_-148-914 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658941 | ||||||
| chr1:21658941
|
C | CTTT | 54 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(51): Show | 55 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-148-9148_-148-914 others(7): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21658941 | ||||||
| chr1:21659022
|
C | G | 1 | a0001c0004t0001g0197 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-148-9226G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659022 | ||||||
| chr1:21659070
|
A | AC | 4 | a0002c0001t0001g0043a0002c0001t0001g0044a0002c0001t0001g0045others(1): Show | 4 | HG00673.hp1 NA18954.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-9275_-148-927 others(5): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659070 | ||||||
| chr1:21659071
|
A | T | 4 | a0002c0001t0001g0043a0002c0001t0001g0044a0002c0001t0001g0045others(1): Show | 4 | HG00673.hp1 NA18954.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-148-9275T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659071 | ||||||
| chr1:21659189
|
A | G | 307 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(304): Show | 308 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.-148-9393T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659189 | ||||||
| chr1:21659194
|
A | C | 74 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(71): Show | 74 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.-148-9398T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659194 | ||||||
| chr1:21659406
|
G | C | 1 | a0002c0001t0001g0012 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-148-9610C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659406 | ||||||
| chr1:21659502
|
C | T | 67 | a0001c0002t0001g0029a0001c0002t0001g0167a0001c0002t0001g0168others(64): Show | 67 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.-148-9706G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659502 | ||||||
| chr1:21659931
|
A | C | 1 | a0002c0001t0001g0296 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-149+9323T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659931 | ||||||
| chr1:21659978
|
T | A | 1 | a0002c0001t0001g0229 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-149+9276A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21659978 | ||||||
| chr1:21660339
|
C | CCATATAT others(43): Show |
1 | a0001c0003t0003g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CCATATAT others(47): Show |
1 | a0001c0002t0001g0178 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(58): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CCATATAT others(49): Show |
2 | a0001c0003t0001g0176a0002c0001t0001g0177 | 2 | HG03130.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(60): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CCATATAT others(51): Show |
1 | a0001c0003t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(62): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CCATATAT others(53): Show |
2 | a0001c0003t0001g0353a0002c0001t0001g0174 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CCATATAT others(55): Show |
1 | a0001c0003t0001g0173 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(66): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATATAT others(11): Show |
1 | a0001c0003t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(22): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATATAT others(43): Show |
1 | a0001c0003t0004g0354 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATATAT others(51): Show |
2 | a0002c0001t0001g0057a0002c0001t0004g0367 | 2 | HG01070.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(62): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATATAT others(53): Show |
2 | a0001c0003t0003g0368a0001c0003t0003g0369 | 2 | HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(13): Show |
7 | a0001c0002t0001g0162a0001c0003t0002g0320a0002c0001t0001g0163others(4): Show | 7 | HG01433.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(24): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(15): Show |
38 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(35): Show | 38 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(26): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(17): Show |
6 | a0001c0002t0001g0105a0002c0001t0001g0106a0002c0001t0002g0067others(3): Show | 6 | HG00738.hp2 HG01934.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(28): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(19): Show |
8 | a0001c0004t0001g0068a0001c0004t0001g0069a0001c0004t0001g0110others(5): Show | 8 | HG01358.hp2 HG01496.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(30): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(21): Show |
2 | a0001c0003t0002g0358a0002c0001t0002g0113 | 2 | HG02165.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(32): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(23): Show |
2 | a0001c0003t0001g0070a0001c0004t0001g0071 | 2 | HG01943.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(34): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(35): Show |
1 | a0002c0001t0001g0355 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(43): Show |
1 | a0002c0001t0001g0356 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(47): Show |
2 | a0002c0001t0001g0312a0002c0023t0001g0310 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(58): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(49): Show |
1 | a0001c0003t0002g0359 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(60): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(53): Show |
1 | a0001c0003t0002g0360 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(59): Show |
1 | a0001c0003t0002g0361 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-149+8914_-149+891 others(70): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660339
|
C | CTATTTAT others(13): Show |
4 | a0002c0001t0001g0066a0002c0008t0003g0063a0002c0008t0003g0065others(1): Show | 4 | HG02717.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149+8914_-149+891 others(24): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660339 | ||||||
| chr1:21660340
|
T | C | 5 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0172others(2): Show | 5 | HG01261.hp1 HG01261.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149+8914A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660340 | ||||||
| chr1:21660345
|
A | ATATATAT others(71): Show |
1 | a0002c0001t0002g0340 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(82): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(63): Show |
1 | a0002c0001t0002g0344 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(74): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(59): Show |
1 | a0003c0010t0001g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(70): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(57): Show |
4 | a0001c0002t0001g0345a0002c0001t0002g0343a0002c0001t0003g0334others(1): Show | 4 | HG00099.hp1 HG00609.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(68): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(55): Show |
2 | a0001c0017t0001g0319a0002c0006t0001g0357 | 2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(66): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(53): Show |
1 | a0001c0003t0001g0342 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(57): Show |
1 | a0002c0001t0001g0169 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(68): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(55): Show |
5 | a0000c0014t0001g0170a0001c0002t0001g0339a0002c0001t0002g0040others(2): Show | 5 | HG01981.hp2 NA18946.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(66): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(49): Show |
1 | a0002c0001t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(60): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(53): Show |
1 | a0002c0001t0001g0039 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(51): Show |
3 | a0000c0014t0001g0171a0001c0003t0003g0363a0002c0001t0003g0038 | 3 | HG01175.hp2 HG01261.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(62): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(45): Show |
1 | a0002c0008t0003g0365 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(56): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(49): Show |
1 | a0002c0001t0003g0037 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(60): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(53): Show |
2 | a0001c0003t0001g0314a0002c0001t0004g0005 | 2 | HG03516.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(43): Show |
1 | a0001c0004t0001g0364 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(47): Show |
2 | a0001c0007t0001g0300a0002c0001t0002g0338 | 2 | HG00423.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(58): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(55): Show |
1 | a0001c0004t0001g0335 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(66): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(41): Show |
1 | a0002c0006t0001g0301 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(52): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(45): Show |
2 | a0001c0003t0001g0008a0002c0001t0001g0009 | 2 | HG01081.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(56): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(39): Show |
1 | a0002c0001t0001g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(50): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(43): Show |
2 | a0001c0002t0001g0172a0002c0001t0001g0036 | 2 | NA18522.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(47): Show |
1 | a0001c0004t0001g0336 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(58): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(41): Show |
5 | a0002c0001t0001g0033a0002c0001t0001g0034a0002c0001t0001g0047others(2): Show | 5 | NA18950.hp1 NA18950.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(52): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(35): Show |
1 | a0002c0001t0003g0341 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(39): Show |
5 | a0002c0001t0001g0031a0002c0001t0004g0006a0002c0001t0004g0007others(2): Show | 5 | HG00639.hp1 HG02300.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(50): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(33): Show |
1 | a0002c0006t0001g0302 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(44): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(37): Show |
1 | a0001c0003t0001g0030 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(48): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(31): Show |
1 | a0002c0001t0001g0049 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(42): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(35): Show |
4 | a0001c0002t0001g0029a0001c0002t0001g0046a0002c0001t0001g0044others(1): Show | 4 | HG00673.hp1 HG04184.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(39): Show |
1 | a0002c0001t0001g0013 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(50): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(29): Show |
2 | a0001c0002t0001g0330a0001c0002t0001g0331 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(40): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(33): Show |
7 | a0001c0002t0001g0025a0001c0002t0001g0026a0002c0001t0001g0028others(4): Show | 7 | NA18954.hp1 NA18957.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(44): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(37): Show |
1 | a0001c0003t0001g0313 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(48): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(27): Show |
3 | a0001c0003t0001g0328a0001c0003t0003g0329a0003c0015t0001g0002 | 3 | HG02257.hp1 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(38): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(31): Show |
5 | a0001c0012t0001g0024a0002c0001t0001g0022a0002c0001t0001g0023others(2): Show | 5 | HG03239.hp1 NA18942.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(42): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(35): Show |
2 | a0001c0003t0001g0315a0002c0001t0001g0001 | 3 | HG02896.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(25): Show |
2 | a0001c0009t0001g0317a0001c0009t0001g0318 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(36): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(29): Show |
3 | a0001c0002t0001g0019a0002c0001t0001g0018a0002c0001t0002g0017 | 3 | HG02015.hp2 NA18999.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(40): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(23): Show |
2 | a0001c0003t0002g0304a0001c0003t0002g0305 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(34): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(27): Show |
4 | a0001c0002t0001g0015a0001c0002t0001g0016a0002c0001t0001g0003others(1): Show | 4 | HG02071.hp1 HG02083.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(38): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(31): Show |
2 | a0002c0005t0001g0052a0002c0005t0001g0053 | 2 | NA18953.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(42): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(21): Show |
1 | a0001c0003t0004g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(32): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(25): Show |
4 | a0001c0002t0003g0307a0001c0009t0001g0308a0002c0001t0001g0014others(1): Show | 4 | HG01099.hp1 HG01891.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(36): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(29): Show |
1 | a0002c0001t0001g0012 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(40): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(23): Show |
1 | a0002c0001t0009g0309 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(34): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(27): Show |
2 | a0001c0004t0001g0041a0002c0001t0001g0011 | 2 | HG00544.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(38): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(71): Show |
1 | a0002c0001t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(82): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(11): Show |
1 | a0001c0002t0003g0303 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(22): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(17): Show |
1 | a0001c0012t0001g0059 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-149+8908_-149+890 others(28): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(15): Show |
2 | a0002c0006t0001g0118a0002c0006t0001g0119 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(26): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | ATATATAT others(3): Show |
2 | a0002c0001t0001g0056a0003c0015t0004g0055 | 2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-149+8908_-149+890 others(14): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660345
|
A | T | 8 | a0001c0002t0001g0178a0001c0003t0001g0173a0001c0003t0001g0175others(5): Show | 8 | HG01358.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149+8909T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660345 | ||||||
| chr1:21660349
|
T | A | 203 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(200): Show | 203 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-149+8905A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660349 | ||||||
| chr1:21660352
|
T | TATATATA others(39): Show |
1 | a0001c0003t0001g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(50): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(35): Show |
1 | a0001c0002t0001g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(43): Show |
2 | a0001c0002t0001g0203a0002c0001t0001g0295 | 2 | NA18941.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(41): Show |
1 | a0001c0004t0001g0195 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(52): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(43): Show |
3 | a0001c0002t0001g0168a0001c0004t0001g0197a0001c0004t0001g0198 | 3 | HG00621.hp2 HG02135.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(35): Show |
2 | a0001c0007t0001g0188a0001c0007t0001g0326 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(43): Show |
1 | a0001c0002t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(53): Show |
1 | a0001c0004t0001g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(64): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(35): Show |
1 | a0001c0007t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(47): Show |
1 | a0001c0004t0001g0199 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(58): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(35): Show |
1 | a0001c0007t0001g0186 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(46): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(41): Show |
1 | a0001c0004t0001g0189 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(52): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(43): Show |
3 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193 | 3 | HG02015.hp1 HG02071.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(57): Show |
1 | a0001c0004t0001g0215 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(68): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(65): Show |
1 | a0001c0004t0001g0265 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(76): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(77): Show |
1 | a0001c0002t0001g0291 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(88): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(67): Show |
2 | a0001c0002t0001g0266a0001c0003t0001g0267 | 2 | HG00733.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(78): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(61): Show |
1 | a0001c0002t0001g0216 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(72): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(65): Show |
1 | a0002c0001t0001g0184 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(76): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(51): Show |
1 | a0001c0004t0001g0194 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(62): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(71): Show |
1 | a0002c0001t0002g0268 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(82): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(57): Show |
1 | a0001c0004t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(68): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(63): Show |
1 | a0002c0018t0002g0058 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(74): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(67): Show |
3 | a0001c0004t0001g0227a0002c0001t0001g0228a0002c0001t0001g0229 | 3 | NA18944.hp2 NA18968.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(78): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(65): Show |
1 | a0001c0002t0001g0208 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(76): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(71): Show |
3 | a0001c0002t0001g0240a0001c0002t0001g0241a0001c0002t0001g0242 | 3 | HG02523.hp1 NA18964.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(82): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(75): Show |
1 | a0001c0004t0001g0269 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(86): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(79): Show |
1 | a0001c0004t0001g0281 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(90): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(85): Show |
2 | a0001c0003t0001g0288a0001c0004t0001g0289 | 2 | HG01074.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(96): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(69): Show |
1 | a0001c0004t0001g0217 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(80): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(71): Show |
1 | a0001c0002t0001g0230 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(82): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(75): Show |
1 | a0002c0001t0002g0252 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(86): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(81): Show |
1 | a0002c0001t0001g0282 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(92): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(91): Show |
1 | a0001c0002t0001g0292 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(102): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(93): Show |
1 | a0001c0002t0001g0293 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(104): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(73): Show |
1 | a0001c0003t0001g0231 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(84): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(77): Show |
1 | a0001c0004t0001g0253 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(88): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(79): Show |
2 | a0001c0004t0001g0270a0001c0004t0001g0271 | 2 | HG02074.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(90): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(81): Show |
1 | a0001c0025t0001g0278 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(92): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(89): Show |
1 | a0001c0002t0001g0183 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(100): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(77): Show |
1 | a0001c0002t0001g0239 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(88): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(67): Show |
1 | a0001c0004t0001g0200 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(78): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(75): Show |
3 | a0001c0002t0001g0234a0001c0003t0001g0233a0001c0004t0001g0232 | 3 | HG01192.hp2 HG02004.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(86): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(81): Show |
4 | a0001c0002t0001g0272a0001c0002t0001g0274a0001c0002t0001g0299others(1): Show | 4 | HG00741.hp2 HG01928.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(92): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
1 | a0001c0004t0001g0286 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(73): Show |
1 | a0001c0004t0001g0209 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(84): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(75): Show |
1 | a0001c0003t0001g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(86): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(77): Show |
2 | a0001c0002t0001g0235a0001c0002t0001g0298 | 2 | HG01123.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(88): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(81): Show |
1 | a0001c0004t0001g0254 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(92): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(85): Show |
1 | a0002c0001t0001g0166 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(96): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
1 | a0001c0002t0001g0283 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(93): Show |
1 | a0001c0004t0001g0290 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(104): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(71): Show |
1 | a0001c0003t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(82): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(75): Show |
1 | a0001c0003t0001g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(86): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(77): Show |
2 | a0001c0002t0001g0219a0001c0002t0001g0220 | 2 | HG00558.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(88): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(79): Show |
2 | a0001c0002t0001g0236a0001c0002t0001g0237 | 2 | HG00609.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(90): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(81): Show |
1 | a0001c0004t0001g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(92): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(83): Show |
1 | a0001c0002t0001g0255 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(94): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
2 | a0001c0002t0001g0279a0002c0001t0002g0159 | 2 | HG01952.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(93): Show |
1 | a0001c0002t0001g0287 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(104): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(77): Show |
1 | a0001c0002t0001g0211 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(88): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(83): Show |
1 | a0001c0004t0001g0244 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(94): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(85): Show |
1 | a0001c0002t0002g0256 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(96): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
2 | a0001c0002t0002g0275a0001c0002t0002g0276 | 2 | HG00733.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(89): Show |
2 | a0001c0002t0001g0280a0001c0004t0001g0160 | 2 | HG01074.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(100): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(93): Show |
1 | a0002c0005t0001g0294 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(104): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(65): Show |
1 | a0001c0003t0001g0061 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(76): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(77): Show |
2 | a0001c0002t0001g0204a0001c0004t0001g0205 | 2 | HG01346.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(88): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(81): Show |
1 | a0001c0002t0001g0221 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(92): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
2 | a0001c0002t0001g0258a0002c0001t0001g0257 | 2 | HG01256.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(93): Show |
2 | a0001c0002t0001g0285a0001c0004t0001g0284 | 2 | HG01978.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(104): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(93): Show |
1 | a0001c0002t0001g0250 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(104): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(79): Show |
1 | a0001c0004t0001g0050 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(90): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(83): Show |
1 | a0001c0002t0001g0222 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(94): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(85): Show |
1 | a0001c0002t0001g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(96): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
2 | a0001c0004t0001g0245a0002c0001t0001g0246 | 2 | HG02056.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(89): Show |
1 | a0002c0001t0001g0259 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(100): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(81): Show |
1 | a0002c0001t0001g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(92): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(83): Show |
2 | a0002c0001t0003g0212a0002c0005t0003g0185 | 2 | HG02155.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(94): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(89): Show |
2 | a0001c0002t0001g0248a0002c0001t0013g0247 | 2 | HG00280.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(100): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(91): Show |
1 | a0002c0001t0002g0260 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(102): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(95): Show |
1 | a0001c0002t0001g0182 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(106): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(83): Show |
1 | a0001c0004t0001g0206 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(94): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
2 | a0001c0003t0001g0223a0001c0026t0001g0224 | 2 | HG01168.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(85): Show |
1 | a0001c0002t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(96): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(87): Show |
1 | a0001c0002t0001g0213 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(98): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(93): Show |
1 | a0001c0002t0001g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(104): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(95): Show |
2 | a0001c0002t0001g0262a0002c0001t0010g0261 | 2 | HG02300.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.-149+8901_-149+890 others(106): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(97): Show |
1 | a0001c0002t0001g0263 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(108): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(85): Show |
1 | a0001c0002t0001g0196 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(96): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(97): Show |
1 | a0001c0002t0001g0225 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(108): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(105): Show |
1 | a0004c0028t0001g0277 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(116): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(119): Show |
1 | a0001c0002t0001g0264 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(130): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(165): Show |
1 | a0002c0001t0001g0181 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(176): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(89): Show |
1 | a0001c0002t0001g0251 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(100): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660352
|
T | TATATATA others(83): Show |
1 | a0001c0002t0001g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-149+8901_-149+890 others(94): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660352 | ||||||
| chr1:21660353
|
T | A | 129 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0182others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-149+8901A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660353 | ||||||
| chr1:21660365
|
G | T | 1 | a0003c0010t0001g0327 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-149+8889C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660365 | ||||||
| chr1:21660572
|
G | T | 1 | a0002c0001t0001g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-149+8682C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660572 | ||||||
| chr1:21660601
|
C | T | 65 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.-149+8653G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660601 | ||||||
| chr1:21660625
|
C | T | 130 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0182others(127): Show | 130 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-149+8629G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660625 | ||||||
| chr1:21660658
|
G | A | 1 | a0001c0002t0001g0299 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-149+8596C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660658 | ||||||
| chr1:21660701
|
T | TCTTAGCT others(43): Show |
1 | a0002c0005t0001g0294 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-149+8503_-149+855 others(54): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660701 | ||||||
| chr1:21660779
|
C | T | 1 | a0002c0001t0002g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-149+8475G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21660779 | ||||||
| chr1:21661063
|
C | T | 4 | a0002c0001t0001g0066a0002c0008t0003g0063a0002c0008t0003g0065others(1): Show | 4 | HG02717.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149+8191G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661063 | ||||||
| chr1:21661082
|
T | C | 3 | a0002c0001t0003g0323a0002c0001t0003g0324a0002c0001t0003g0325 | 3 | HG02258.hp1 HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-149+8172A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661082 | ||||||
| chr1:21661159
|
C | A | 1 | a0002c0001t0001g0295 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-149+8095G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661159 | ||||||
| chr1:21661184
|
C | T | 1 | a0002c0001t0002g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-149+8070G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661184 | ||||||
| chr1:21661252
|
C | CA | 60 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(57): Show | 61 | HG00639.hp1 HG01081.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.-149+8001dupT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661252 | ||||||
| chr1:21661252
|
C | CAA | 11 | a0001c0002t0001g0046a0001c0004t0001g0041a0002c0001t0001g0003others(8): Show | 11 | HG00544.hp2 HG00673.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-149+8000_-149+800 others(6): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661252 | ||||||
| chr1:21661252
|
CA | C | 35 | a0001c0002t0001g0162a0001c0003t0001g0070a0001c0003t0001g0165others(32): Show | 35 | HG00738.hp2 HG01070.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.-149+8001delT | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661252 | ||||||
| chr1:21661568
|
G | C | 1 | a0002c0001t0001g0049 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-149+7686C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661568 | ||||||
| chr1:21661610
|
G | A | 4 | a0001c0003t0002g0304a0001c0003t0002g0305a0001c0009t0001g0317others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149+7644C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661610 | ||||||
| chr1:21661634
|
A | G | 1 | a0001c0002t0001g0062 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-149+7620T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661634 | ||||||
| chr1:21661837
|
G | C | 1 | a0001c0003t0001g0153 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-149+7417C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661837 | ||||||
| chr1:21661955
|
C | T | 1 | a0002c0005t0003g0185 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-149+7299G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661955 | ||||||
| chr1:21661969
|
C | G | 4 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149+7285G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21661969 | ||||||
| chr1:21662013
|
G | A | 1 | a0001c0002t0001g0345 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-149+7241C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662013 | ||||||
| chr1:21662070
|
C | T | 65 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.-149+7184G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662070 | ||||||
| chr1:21662123
|
G | A | 1 | a0001c0003t0001g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-149+7131C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662123 | ||||||
| chr1:21662129
|
C | T | 307 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(304): Show | 308 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.-149+7125G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662129 | ||||||
| chr1:21662292
|
A | C | 5 | a0001c0003t0001g0165a0001c0003t0003g0368a0001c0003t0003g0369others(2): Show | 5 | HG01070.hp1 HG01346.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149+6962T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662292 | ||||||
| chr1:21662349
|
C | T | 1 | a0002c0001t0001g0184 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-149+6905G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662349 | ||||||
| chr1:21662350
|
G | A | 65 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.-149+6904C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662350 | ||||||
| chr1:21662483
|
C | T | 42 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0002t0001g0339others(39): Show | 42 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.-149+6771G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662483 | ||||||
| chr1:21662550
|
C | T | 3 | a0000c0014t0001g0170a0000c0014t0001g0171a0002c0001t0001g0169 | 3 | HG01261.hp1 HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-149+6704G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662550 | ||||||
| chr1:21662559
|
G | A | 2 | a0002c0001t0004g0121a0002c0001t0004g0122 | 2 | HG00642.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-149+6695C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662559 | ||||||
| chr1:21662846
|
G | A | 63 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(60): Show | 64 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.-149+6408C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662846 | ||||||
| chr1:21662861
|
T | C | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+6393A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662861 | ||||||
| chr1:21662862
|
A | T | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+6392T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662862 | ||||||
| chr1:21662882
|
A | G | 13 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0172others(10): Show | 13 | HG01261.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-149+6372T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662882 | ||||||
| chr1:21662904
|
G | T | 2 | a0002c0001t0004g0121a0002c0001t0004g0122 | 2 | HG00642.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-149+6350C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662904 | ||||||
| chr1:21662908
|
C | G | 3 | a0001c0002t0001g0182a0001c0002t0001g0183a0002c0001t0001g0181 | 3 | NA18747.hp2 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-149+6346G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662908 | ||||||
| chr1:21662909
|
C | A | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+6345G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662909 | ||||||
| chr1:21662910
|
A | G | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+6344T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662910 | ||||||
| chr1:21662911
|
G | C | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+6343C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662911 | ||||||
| chr1:21662936
|
C | G | 136 | a0001c0002t0001g0167a0001c0002t0001g0168a0001c0002t0001g0182others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-149+6318G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662936 | ||||||
| chr1:21662939
|
C | G | 8 | a0001c0003t0002g0320a0001c0003t0002g0322a0001c0003t0004g0362others(5): Show | 8 | HG01433.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149+6315G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662939 | ||||||
| chr1:21662952
|
A | G | 63 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(60): Show | 64 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.-149+6302T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21662952 | ||||||
| chr1:21663037
|
A | G | 13 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0172others(10): Show | 13 | HG01261.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-149+6217T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663037 | ||||||
| chr1:21663064
|
T | A | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+6190A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663064 | ||||||
| chr1:21663162
|
G | T | 5 | a0001c0003t0001g0008a0002c0001t0001g0009a0002c0001t0004g0005others(2): Show | 5 | HG00639.hp1 HG01081.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149+6092C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663162 | ||||||
| chr1:21663337
|
C | T | 1 | a0001c0003t0007g0161 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-149+5917G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663337 | ||||||
| chr1:21663370
|
C | G | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+5884G>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663370 | ||||||
| chr1:21663402
|
C | T | 7 | a0001c0003t0002g0358a0001c0003t0002g0359a0001c0003t0002g0360others(4): Show | 7 | HG02723.hp1 HG03130.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-149+5852G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663402 | ||||||
| chr1:21663415
|
A | G | 1 | a0002c0001t0003g0334 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-149+5839T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663415 | ||||||
| chr1:21663480
|
C | T | 41 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0002t0001g0339others(38): Show | 41 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.-149+5774G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663480 | ||||||
| chr1:21663486
|
A | G | 67 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(64): Show | 67 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-149+5768T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663486 | ||||||
| chr1:21663581
|
T | A | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+5673A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663581 | ||||||
| chr1:21663696
|
C | A | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+5558G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663696 | ||||||
| chr1:21663698
|
A | G | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+5556T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663698 | ||||||
| chr1:21663699
|
G | C | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+5555C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663699 | ||||||
| chr1:21663821
|
A | G | 2 | a0001c0002t0001g0167a0001c0002t0001g0168 | 2 | HG02135.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-149+5433T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663821 | ||||||
| chr1:21663908
|
T | A | 1 | a0002c0001t0002g0352 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-149+5346A>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21663908 | ||||||
| chr1:21664057
|
C | T | 1 | a0002c0006t0001g0301 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-149+5197G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664057 | ||||||
| chr1:21664082
|
G | A | 3 | a0001c0003t0003g0368a0001c0003t0003g0369a0002c0001t0004g0367 | 3 | HG01070.hp1 HG01346.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-149+5172C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664082 | ||||||
| chr1:21664179
|
G | C | 1 | a0002c0001t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-149+5075C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664179 | ||||||
| chr1:21664280
|
C | T | 1 | a0002c0001t0001g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-149+4974G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664280 | ||||||
| chr1:21664439
|
T | C | 1 | a0002c0001t0002g0115 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-149+4815A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664439 | ||||||
| chr1:21664742
|
G | C | 58 | a0001c0002t0001g0051a0001c0002t0001g0062a0001c0002t0001g0081others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.-149+4512C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664742 | ||||||
| chr1:21664749
|
AT | A | 319 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(316): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-149+4504delA | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664749 | ||||||
| chr1:21664779
|
G | T | 319 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(316): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.-149+4475C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664779 | ||||||
| chr1:21664834
|
G | C | 3 | a0001c0002t0001g0162a0002c0001t0001g0163a0002c0001t0001g0164 | 3 | HG02451.hp2 HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-149+4420C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664834 | ||||||
| chr1:21664903
|
C | T | 1 | a0002c0023t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-149+4351G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664903 | ||||||
| chr1:21664981
|
G | A | 53 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(50): Show | 54 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.-149+4273C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21664981 | ||||||
| chr1:21665085
|
C | T | 1 | a0002c0001t0001g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-149+4169G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21665085 | ||||||
| chr1:21665143
|
A | T | 1 | a0002c0001t0001g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-149+4111T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21665143 | ||||||
| chr1:21665158
|
T | C | 2 | a0002c0005t0001g0052a0002c0005t0001g0053 | 2 | NA18953.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-149+4096A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21665158 | ||||||
| chr1:21665267
|
C | T | 53 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(50): Show | 54 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.-149+3987G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21665267 | ||||||
| chr1:21665479
|
T | C | 7 | a0001c0003t0001g0313a0001c0003t0001g0314a0001c0003t0001g0315others(4): Show | 7 | HG01106.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149+3775A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21665479 | ||||||
| chr1:21665537
|
T | C | 5 | a0001c0003t0001g0154a0001c0003t0001g0155a0001c0003t0003g0156others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-149+3717A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21665537 | ||||||
| chr1:21665997
|
G | T | 1 | a0001c0017t0001g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-149+3257C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21665997 | ||||||
| chr1:21666023
|
G | A | 2 | a0001c0002t0001g0298a0001c0002t0001g0299 | 2 | HG00741.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-149+3231C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666023 | ||||||
| chr1:21666054
|
G | A | 2 | a0001c0009t0001g0317a0001c0009t0001g0318 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-149+3200C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666054 | ||||||
| chr1:21666075
|
T | C | 144 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0167others(141): Show | 144 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-149+3179A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666075 | ||||||
| chr1:21666107
|
A | G | 350 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(347): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-149+3147T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666107 | ||||||
| chr1:21666142
|
T | C | 53 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(50): Show | 54 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.-149+3112A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666142 | ||||||
| chr1:21666213
|
T | C | 1 | a0001c0003t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-149+3041A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666213 | ||||||
| chr1:21666385
|
G | A | 8 | a0001c0003t0002g0320a0001c0003t0002g0322a0001c0007t0001g0326others(5): Show | 8 | HG01433.hp1 HG02258.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-149+2869C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666385 | ||||||
| chr1:21666399
|
C | T | 2 | a0001c0002t0001g0116a0001c0002t0001g0117 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-149+2855G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666399 | ||||||
| chr1:21666456
|
A | T | 45 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.-149+2798T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666456 | ||||||
| chr1:21666548
|
C | T | 147 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0167others(144): Show | 147 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.-149+2706G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666548 | ||||||
| chr1:21666666
|
G | A | 1 | a0002c0001t0001g0166 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-149+2588C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666666 | ||||||
| chr1:21666677
|
A | C | 342 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(339): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.-149+2577T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666677 | ||||||
| chr1:21666682
|
C | T | 2 | a0002c0001t0001g0003a0002c0001t0001g0004 | 2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-149+2572G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666682 | ||||||
| chr1:21666728
|
A | T | 1 | a0002c0001t0001g0166 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-149+2526T>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666728 | ||||||
| chr1:21666757
|
G | A | 5 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0003t0001g0328others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-149+2497C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666757 | ||||||
| chr1:21666813
|
C | T | 62 | a0001c0002t0001g0062a0001c0002t0001g0081a0001c0002t0001g0102others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.-149+2441G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666813 | ||||||
| chr1:21666891
|
T | C | 53 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(50): Show | 54 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.-149+2363A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21666891 | ||||||
| chr1:21667107
|
A | G | 342 | a0000c0014t0001g0170a0000c0014t0001g0171a0001c0002t0001g0015others(339): Show | 343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.-149+2147T>C | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667107 | ||||||
| chr1:21667123
|
GC | G | 53 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(50): Show | 54 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.-149+2130delG | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667123 | ||||||
| chr1:21667172
|
G | C | 1 | a0002c0001t0001g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-149+2082C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667172 | ||||||
| chr1:21667499
|
G | T | 45 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0001g0127others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(42): Show |
intron_variant | MODIFIER | c.-149+1755C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667499 | ||||||
| chr1:21667670
|
G | A | 1 | a0001c0003t0001g0353 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-149+1584C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667670 | ||||||
| chr1:21667709
|
G | A | 1 | a0001c0003t0004g0354 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-149+1545C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667709 | ||||||
| chr1:21667941
|
A | C | 54 | a0001c0002t0001g0062a0001c0002t0001g0081a0001c0002t0001g0102others(51): Show | 54 | HG00280.hp1 HG00408.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.-149+1313T>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667941 | ||||||
| chr1:21667977
|
G | A | 3 | a0002c0001t0001g0355a0002c0001t0001g0356a0002c0006t0001g0357 | 3 | HG03139.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-149+1277C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21667977 | ||||||
| chr1:21668062
|
G | C | 4 | a0001c0003t0002g0358a0001c0003t0002g0359a0001c0003t0002g0360others(1): Show | 4 | HG02723.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149+1192C>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21668062 | ||||||
| chr1:21668277
|
T | C | 1 | a0001c0003t0004g0362 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-149+977A>G | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21668277 | ||||||
| chr1:21668325
|
C | T | 1 | a0003c0015t0001g0002 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-149+929G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21668325 | ||||||
| chr1:21668366
|
G | A | 7 | a0001c0003t0003g0363a0001c0003t0003g0368a0001c0003t0003g0369others(4): Show | 7 | HG00099.hp1 HG01070.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-149+888C>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21668366 | ||||||
| chr1:21668551
|
G | T | 4 | a0001c0003t0001g0061a0001c0012t0001g0059a0002c0001t0001g0060others(1): Show | 4 | HG00323.hp2 HG01361.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-149+703C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21668551 | ||||||
| chr1:21668610
|
C | A | 2 | a0001c0003t0001g0370a0001c0003t0001g0371 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-149+644G>T | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21668610 | ||||||
| chr1:21668890
|
C | T | 1 | a0002c0001t0001g0057 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-149+364G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21668890 | ||||||
| chr1:21669081
|
C | T | 56 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(53): Show | 57 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.-149+173G>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21669081 | ||||||
| chr1:21669241
|
G | T | 56 | a0001c0002t0001g0015a0001c0002t0001g0016a0001c0002t0001g0019others(53): Show | 57 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.-149+13C>A | RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 1/24 | chr1 | 21669241 |