Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5906 |
| ensemblid | ENSG00000116473.15 |
| hgncid | 9855 |
| symbol | RAP1A |
| name | RAP1A, member of RAS oncogene family |
| refseq_nuc | NM_002884.4 |
| refseq_prot | NP_002875.1 |
| ensembl_nuc | ENST00000369709.4 |
| ensembl_prot | ENSP00000358723.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 111619789 |
| end | 111716691 |
| strand | + |
| ver | v1.2 |
| region | chr1:111619789-111716691 |
| region5000 | chr1:111614789-111721691 |
| regionname0 | RAP1A_chr1_111619789_111716691 |
| regionname5000 | RAP1A_chr1_111614789_111721691 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 552 | 379 | 85 | 56 | 182 | 14 | 40 | RAP1A_chr1_111614789_111721691 | RAP1A | ATGCG others(547): Show |
chr1 | 111614789 | 111721691 | ||
| a0001c0002 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | ATGCG others(547): Show |
chr1 | 111614789 | 111721691 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5018 | 106 | 9 | 18 | 64 | 3 | 11 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0002 | 1/0 | 5018 | 86 | 29 | 10 | 32 | 6 | 8 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0003 | 0/0 | 5018 | 48 | 1 | 8 | 31 | 1 | 7 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0004 | 0/0 | 5019 | 41 | 0 | 9 | 26 | 0 | 6 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5014): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0005 | 0/0 | 5019 | 22 | 0 | 1 | 15 | 3 | 3 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5014): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0006 | 0/0 | 5019 | 11 | 10 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5014): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0007 | 0/0 | 5018 | 9 | 1 | 2 | 3 | 0 | 3 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0008 | 0/0 | 5018 | 8 | 8 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0009 | 0/0 | 5018 | 7 | 6 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0010 | 0/0 | 5018 | 6 | 0 | 0 | 6 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0011 | 0/0 | 5018 | 5 | 4 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0012 | 0/0 | 5018 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0013 | 0/0 | 5018 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0014 | 0/0 | 5018 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0015 | 0/0 | 5019 | 2 | 1 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5014): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0016 | 0/0 | 5018 | 2 | 2 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0017 | 0/0 | 5027 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5022): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0018 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5014): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0019 | 0/0 | 5018 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0020 | 0/0 | 5018 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0021 | 0/0 | 5018 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0022 | 0/0 | 5018 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0023 | 0/0 | 5018 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0024 | 0/0 | 5018 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0025 | 0/0 | 5019 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5014): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0026 | 0/0 | 5018 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0027 | 0/0 | 5018 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0028 | 0/0 | 5018 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0029 | 0/0 | 5018 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0030 | 0/0 | 5018 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0031 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5022): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0032 | 0/0 | 5027 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5022): Show |
chr1 | 111614789 | 111721691 |
| a0001c0001t0033 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5022): Show |
chr1 | 111614789 | 111721691 |
| a0001c0002t0008 | 0/0 | 5018 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | GCCGC others(5013): Show |
chr1 | 111614789 | 111721691 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0006g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0009g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0009g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0009g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0010g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0010g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0011g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0011g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0012g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0013g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0014g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0014g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0015g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0015g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0016g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0016g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0017g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0017g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0018g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0019g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0020g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0021g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0022g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0023g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0024g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0025g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0026g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0027g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0028g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0029g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0030g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0031g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0032g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0001t0033g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| a0001c0002t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0034 | EUR | GBR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0320 | EUR | GBR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00140 | hp1 | a0001 | c0001 | t0018 | g0039 | EUR | GBR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0303 | EUR | GBR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | FIN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0190 | EUR | FIN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0335 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0363 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0355 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | CHS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0343 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00735 | hp2 | a0001 | c0001 | t0030 | g0091 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01069 | hp1 | a0001 | c0001 | t0026 | g0049 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0339 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0342 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0346 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01106 | hp1 | a0001 | c0001 | t0022 | g0209 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0228 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0337 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0272 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0351 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0333 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0221 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0009 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01243 | hp1 | a0001 | c0001 | t0007 | g0271 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01256 | hp1 | a0001 | c0001 | t0015 | g0314 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01257 | hp1 | a0001 | c0001 | t0024 | g0315 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0033 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0215 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0361 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0027 | EUR | IBS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0321 | EUR | IBS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | IBS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0018 | EUR | IBS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0347 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0174 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0222 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | CDX | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02165 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | CDX | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0329 | EAS | CDX | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0289 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0309 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02258 | hp2 | a0001 | c0002 | t0008 | g0278 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0274 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0261 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0284 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0276 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02615 | hp2 | a0001 | c0001 | t0023 | g0294 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0285 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0331 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02723 | hp1 | a0001 | c0001 | t0020 | g0219 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02723 | hp2 | a0001 | c0001 | t0033 | g0035 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0281 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02886 | hp1 | a0001 | c0001 | t0027 | g0265 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0155 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0277 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0154 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0290 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0037 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0263 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0287 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0280 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0264 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03225 | hp2 | a0001 | c0001 | t0031 | g0153 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0311 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0341 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | ESN | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0259 | AFR | GWD | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0286 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0362 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0317 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0014 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03710 | hp1 | a0001 | c0001 | t0025 | g0023 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0330 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0356 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0269 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0364 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0270 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0262 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04204 | hp1 | a0001 | c0001 | t0028 | g0137 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0203 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0268 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | STU | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | YRI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18612 | hp1 | a0001 | c0001 | t0017 | g0048 | EAS | CHB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18747 | hp2 | a0001 | c0001 | t0017 | g0052 | EAS | CHB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0038 | AFR | YRI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0275 | AFR | YRI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0344 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18947 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0334 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0328 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18950 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0336 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0360 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18965 | hp2 | a0001 | c0001 | t0010 | g0195 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18970 | hp2 | a0001 | c0001 | t0010 | g0204 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18972 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18974 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0365 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18999 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0350 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0024 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19004 | hp1 | a0001 | c0001 | t0029 | g0245 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19010 | hp2 | a0001 | c0001 | t0032 | g0125 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0345 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | LWK | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | LWK | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0357 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19063 | hp1 | a0001 | c0001 | t0010 | g0210 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19078 | hp1 | a0001 | c0001 | t0021 | g0085 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0266 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0273 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0267 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | YRI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | YRI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ASW | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0305 | EUR | TSI | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | GIH | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0358 | SAS | GIH | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0291 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0009 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0016 | AFR | MSL | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG06807 | hp1 | a0001 | c0001 | t0019 | g0011 | AFR | USA | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0260 | AFR | USA | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | USA | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | USA | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0310 | AFR | LWK | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0075 | REF | REF | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0188 | REF | REF | RAP1A_chr1_111614789_111721691 | RAP1A | chr1 | 111614789 | 111721691 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:111703431 | A | G | 1 | a0001c0002 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.279A>G | p.Leu93Leu | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/8 | 452/5018 | 279/555 | 93/184 | chr1 | 111703431 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:111619884 | A | AGGAGGAG others(2): Show |
4 | a0001c0001t0017 a0001c0001t0031 a0001c0001t0032 others(1): Show |
5 | HG02723.hp2 HG03225.hp2 NA18612.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-51_-43dupTGGAGGAG others(1): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/8 | 71441 | INFO_REALIGN_3_PRIME | chr1 | 111619884 | |||||
| chr1:111712450 | G | C | 1 | a0001c0001t0018 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 3215 | chr1 | 111712450 | ||||||
| chr1:111712560 | A | T | 1 | a0001c0001t0030 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 3325 | chr1 | 111712560 | ||||||
| chr1:111712767 | C | A | 1 | a0001c0001t0004 | 41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 3532 | chr1 | 111712767 | ||||||
| chr1:111712848 | T | C | 1 | a0001c0001t0019 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 3613 | chr1 | 111712848 | ||||||
| chr1:111712953 | A | G | 1 | a0001c0001t0029 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 3718 | chr1 | 111712953 | ||||||
| chr1:111713985 | G | T | 1 | a0001c0001t0016 | 2 | HG03453.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1584G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 4750 | chr1 | 111713985 | ||||||
| chr1:111714356 | A | G | 1 | a0001c0001t0028 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1955A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5121 | chr1 | 111714356 | ||||||
| chr1:111714417 | C | A | 3 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0020 |
10 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2016C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5182 | chr1 | 111714417 | ||||||
| chr1:111714571 | T | C | 8 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(5): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2170T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5336 | chr1 | 111714571 | ||||||
| chr1:111714639 | A | G | 1 | a0001c0001t0027 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2238A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5404 | chr1 | 111714639 | ||||||
| chr1:111714670 | A | G | 1 | a0001c0001t0026 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5435 | chr1 | 111714670 | ||||||
| chr1:111715085 | C | CT | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(3): Show |
78 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2697dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5864 | INFO_REALIGN_3_PRIME | chr1 | 111715085 | |||||
| chr1:111715119 | C | T | 2 | a0001c0001t0010 a0001c0001t0027 |
7 | HG02886.hp1 NA18947.hp1 NA18965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2718C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5884 | chr1 | 111715119 | ||||||
| chr1:111715154 | C | G | 1 | a0001c0001t0024 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2753C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5919 | chr1 | 111715154 | ||||||
| chr1:111715162 | C | T | 5 | a0001c0001t0001 a0001c0001t0021 a0001c0001t0028 others(2): Show |
109 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2761C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5927 | chr1 | 111715162 | ||||||
| chr1:111715181 | A | G | 1 | a0001c0001t0013 | 3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2780A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5946 | chr1 | 111715181 | ||||||
| chr1:111715225 | C | T | 2 | a0001c0001t0008 a0001c0002t0008 |
9 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2824C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 5990 | chr1 | 111715225 | ||||||
| chr1:111715328 | T | C | 6 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0009 others(3): Show |
27 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2927T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 6093 | chr1 | 111715328 | ||||||
| chr1:111715367 | C | T | 7 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0009 others(4): Show |
28 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2966C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 6132 | chr1 | 111715367 | ||||||
| chr1:111715626 | C | G | 1 | a0001c0001t0011 | 5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3225C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 6391 | chr1 | 111715626 | ||||||
| chr1:111715630 | A | G | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(9): Show |
143 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*3229A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 6395 | chr1 | 111715630 | ||||||
| chr1:111715668 | T | G | 1 | a0001c0001t0021 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3267T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 6433 | chr1 | 111715668 | ||||||
| chr1:111715695 | A | C | 1 | a0001c0001t0023 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3294A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 6460 | chr1 | 111715695 | ||||||
| chr1:111715923 | G | T | 13 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(10): Show |
128 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*3522G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 6688 | chr1 | 111715923 | ||||||
| chr1:111716304 | G | C | 1 | a0001c0001t0025 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3903G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 7069 | chr1 | 111716304 | ||||||
| chr1:111716650 | T | C | 2 | a0001c0001t0004 a0001c0001t0015 |
43 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4249T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 7415 | chr1 | 111716650 | ||||||
| chr1:111716684 | A | T | 1 | a0001c0001t0022 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4283A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 8/8 | 7449 | chr1 | 111716684 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:111620084 | G | T | 1 | a0001c0001t0004g0365 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-28+150G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620084 | |||||||
| chr1:111620088 | G | T | 1 | a0001c0001t0002g0364 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-28+154G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620088 | |||||||
| chr1:111620153 | C | T | 44 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 others(41): Show |
45 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-28+219C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620153 | |||||||
| chr1:111620185 | T | C | 1 | a0001c0001t0019g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-28+251T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620185 | |||||||
| chr1:111620256 | A | G | 30 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+322A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620256 | |||||||
| chr1:111620303 | C | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+369C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620303 | |||||||
| chr1:111620311 | G | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0013 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-28+377G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620311 | |||||||
| chr1:111620543 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+609C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620543 | |||||||
| chr1:111620569 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-28+635C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620569 | |||||||
| chr1:111620584 | T | TC | 20 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28+655dupC | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111620584 | ||||||
| chr1:111620608 | C | G | 2 | a0001c0001t0005g0262 a0001c0001t0005g0263 |
2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-28+674C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620608 | |||||||
| chr1:111620675 | A | C | 4 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(1): Show |
5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+741A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620675 | |||||||
| chr1:111620688 | T | G | 1 | a0001c0001t0005g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-28+754T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620688 | |||||||
| chr1:111620785 | G | A | 46 | a0001c0001t0002g0322 a0001c0001t0002g0323 a0001c0001t0002g0324 others(43): Show |
47 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.-28+851G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620785 | |||||||
| chr1:111620883 | A | G | 35 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(32): Show |
35 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-28+949A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620883 | |||||||
| chr1:111620908 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-28+974C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620908 | |||||||
| chr1:111620924 | C | A | 201 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-28+990C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620924 | |||||||
| chr1:111620948 | T | G | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+1014T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111620948 | |||||||
| chr1:111621070 | A | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28+1136A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111621070 | |||||||
| chr1:111621204 | C | T | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-28+1270C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111621204 | |||||||
| chr1:111621615 | A | G | 3 | a0001c0001t0003g0224 a0001c0001t0014g0284 a0001c0001t0014g0285 |
3 | HG02572.hp2 HG02622.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.-28+1681A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111621615 | |||||||
| chr1:111621639 | C | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28+1705C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111621639 | |||||||
| chr1:111621899 | G | C | 1 | a0001c0001t0006g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-28+1965G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111621899 | |||||||
| chr1:111621933 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-28+1999G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111621933 | |||||||
| chr1:111621997 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+2063A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111621997 | |||||||
| chr1:111622027 | A | G | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+2093A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622027 | |||||||
| chr1:111622099 | A | G | 1 | a0001c0001t0018g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-28+2165A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622099 | |||||||
| chr1:111622211 | C | T | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+2277C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622211 | |||||||
| chr1:111622244 | A | G | 4 | a0001c0001t0001g0173 a0001c0001t0002g0319 a0001c0001t0002g0320 others(1): Show |
4 | HG00099.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+2310A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622244 | |||||||
| chr1:111622330 | T | G | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+2396T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622330 | |||||||
| chr1:111622383 | A | G | 26 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(23): Show |
28 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-28+2449A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622383 | |||||||
| chr1:111622387 | GCCT | G | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-28+2457_-28+2459d others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111622387 | ||||||
| chr1:111622549 | T | G | 173 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-28+2615T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622549 | |||||||
| chr1:111622613 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+2679A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622613 | |||||||
| chr1:111622622 | C | A | 38 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(35): Show |
38 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.-28+2688C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622622 | |||||||
| chr1:111622635 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-28+2701G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622635 | |||||||
| chr1:111622662 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-28+2728G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622662 | |||||||
| chr1:111622760 | T | C | 1 | a0001c0001t0004g0327 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-28+2826T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622760 | |||||||
| chr1:111622805 | C | G | 1 | a0001c0001t0003g0214 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-28+2871C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111622805 | |||||||
| chr1:111623014 | G | T | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+3080G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623014 | |||||||
| chr1:111623097 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-28+3163A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623097 | |||||||
| chr1:111623163 | A | G | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+3229A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623163 | |||||||
| chr1:111623184 | AT | A | 311 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(308): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-28+3264delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111623184 | ||||||
| chr1:111623209 | A | T | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+3275A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623209 | |||||||
| chr1:111623212 | G | A | 24 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+3278G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623212 | |||||||
| chr1:111623567 | C | T | 1 | a0001c0001t0004g0363 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-28+3633C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623567 | |||||||
| chr1:111623568 | G | A | 34 | a0001c0001t0001g0067 a0001c0001t0002g0040 a0001c0001t0002g0041 others(31): Show |
34 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.-28+3634G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623568 | |||||||
| chr1:111623587 | T | A | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-28+3653T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623587 | |||||||
| chr1:111623599 | G | C | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+3665G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623599 | |||||||
| chr1:111623661 | A | G | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+3727A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623661 | |||||||
| chr1:111623940 | C | T | 1 | a0001c0001t0003g0213 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-28+4006C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111623940 | |||||||
| chr1:111624052 | A | G | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+4118A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624052 | |||||||
| chr1:111624161 | C | T | 2 | a0001c0001t0011g0009 a0001c0001t0011g0261 |
3 | HG01192.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-28+4227C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624161 | |||||||
| chr1:111624404 | C | T | 30 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+4470C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624404 | |||||||
| chr1:111624436 | G | A | 2 | a0001c0001t0007g0264 a0001c0001t0019g0011 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-28+4502G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624436 | |||||||
| chr1:111624553 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-28+4619A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624553 | |||||||
| chr1:111624633 | T | C | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+4699T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624633 | |||||||
| chr1:111624634 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG02083.hp2 NA19063.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-28+4700G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624634 | |||||||
| chr1:111624746 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-28+4812C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624746 | |||||||
| chr1:111624750 | C | T | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+4816C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624750 | |||||||
| chr1:111624809 | C | T | 5 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(2): Show |
7 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+4875C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624809 | |||||||
| chr1:111624984 | C | T | 12 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG02015.hp2 NA18944.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28+5050C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111624984 | |||||||
| chr1:111625070 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-28+5136C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111625070 | |||||||
| chr1:111625144 | A | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28+5210A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111625144 | |||||||
| chr1:111625447 | A | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+5513A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111625447 | |||||||
| chr1:111625685 | C | G | 1 | a0001c0001t0004g0362 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-28+5751C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111625685 | |||||||
| chr1:111626011 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-28+6077T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626011 | |||||||
| chr1:111626194 | T | G | 2 | a0001c0001t0004g0328 a0001c0001t0004g0329 |
2 | HG02165.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-28+6260T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626194 | |||||||
| chr1:111626238 | T | A | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-28+6304T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626238 | |||||||
| chr1:111626370 | T | TAC | 34 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(31): Show |
36 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.-28+6466_-28+6467d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111626370 | ||||||
| chr1:111626370 | TAC | T | 41 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0043 others(38): Show |
41 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+6466_-28+6467d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111626370 | ||||||
| chr1:111626370 | TACAC | T | 127 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0063 others(124): Show |
130 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-28+6464_-28+6467d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111626370 | ||||||
| chr1:111626370 | TACACACA others(1): Show |
T | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+6460_-28+6467d others(10): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111626370 | ||||||
| chr1:111626398 | CACAT | C | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG00733.hp2 HG01884.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+6466_-28+6469d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111626398 | ||||||
| chr1:111626400 | CAT | C | 5 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(2): Show |
6 | HG01192.hp1 HG02055.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+6469_-28+6470d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111626400 | ||||||
| chr1:111626402 | T | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(102): Show |
106 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.-28+6468T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626402 | |||||||
| chr1:111626523 | G | T | 146 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28+6589G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626523 | |||||||
| chr1:111626585 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-28+6651A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626585 | |||||||
| chr1:111626655 | C | T | 30 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+6721C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626655 | |||||||
| chr1:111626656 | G | A | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+6722G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626656 | |||||||
| chr1:111626799 | T | C | 2 | a0001c0001t0007g0264 a0001c0001t0019g0011 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-28+6865T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626799 | |||||||
| chr1:111626874 | C | T | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+6940C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111626874 | |||||||
| chr1:111627083 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-28+7149A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111627083 | |||||||
| chr1:111627190 | A | G | 146 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28+7256A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111627190 | |||||||
| chr1:111627261 | TTTTA | T | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+7335_-28+7338d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111627261 | ||||||
| chr1:111627433 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-28+7499C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111627433 | |||||||
| chr1:111627529 | A | G | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+7595A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111627529 | |||||||
| chr1:111627535 | C | G | 1 | a0001c0001t0004g0361 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-28+7601C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111627535 | |||||||
| chr1:111627576 | A | G | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+7642A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111627576 | |||||||
| chr1:111627602 | G | A | 8 | a0001c0001t0003g0007 a0001c0001t0003g0179 a0001c0001t0003g0180 others(5): Show |
9 | HG00733.hp1 HG01496.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+7668G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111627602 | |||||||
| chr1:111627777 | A | AT | 11 | a0001c0001t0002g0316 a0001c0001t0002g0317 a0001c0001t0002g0318 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG03239.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28+7854dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111627777 | ||||||
| chr1:111627937 | C | CA | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+8013dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111627937 | ||||||
| chr1:111627937 | CA | C | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-28+8013delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111627937 | ||||||
| chr1:111628036 | C | T | 1 | a0001c0001t0007g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28+8102C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111628036 | |||||||
| chr1:111628373 | C | T | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-28+8439C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111628373 | |||||||
| chr1:111628422 | T | C | 30 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+8488T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111628422 | |||||||
| chr1:111628496 | C | G | 361 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(358): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-28+8562C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111628496 | |||||||
| chr1:111628640 | G | C | 25 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0229 others(22): Show |
25 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+8706G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111628640 | |||||||
| chr1:111628724 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-28+8790C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111628724 | |||||||
| chr1:111628889 | A | G | 1 | a0001c0001t0003g0211 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-28+8955A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111628889 | |||||||
| chr1:111629165 | T | C | 2 | a0001c0001t0007g0266 a0001c0001t0007g0267 |
2 | NA19078.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-28+9231T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111629165 | |||||||
| chr1:111629249 | G | A | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+9315G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111629249 | |||||||
| chr1:111629643 | C | T | 38 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(35): Show |
38 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.-28+9709C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111629643 | |||||||
| chr1:111629704 | G | A | 4 | a0001c0001t0006g0288 a0001c0001t0006g0289 a0001c0001t0006g0290 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+9770G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111629704 | |||||||
| chr1:111629869 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-28+9935C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111629869 | |||||||
| chr1:111630011 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-28+10077A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111630011 | |||||||
| chr1:111630033 | C | T | 2 | a0001c0001t0007g0264 a0001c0001t0019g0011 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-28+10099C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111630033 | |||||||
| chr1:111630165 | T | A | 5 | a0001c0001t0003g0006 a0001c0001t0003g0175 a0001c0001t0003g0176 others(2): Show |
6 | HG02056.hp2 NA18943.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+10231T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111630165 | |||||||
| chr1:111630447 | G | A | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-28+10513G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111630447 | |||||||
| chr1:111630571 | A | G | 1 | a0001c0001t0004g0360 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-28+10637A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111630571 | |||||||
| chr1:111630683 | A | G | 5 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(2): Show |
7 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+10749A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111630683 | |||||||
| chr1:111630743 | G | C | 1 | a0001c0001t0004g0331 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-28+10809G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111630743 | |||||||
| chr1:111631011 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+11077A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631011 | |||||||
| chr1:111631061 | C | T | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+11127C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631061 | |||||||
| chr1:111631149 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+11215G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631149 | |||||||
| chr1:111631165 | A | G | 19 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(16): Show |
19 | HG02015.hp2 HG02040.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.-28+11231A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631165 | |||||||
| chr1:111631303 | G | A | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+11369G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631303 | |||||||
| chr1:111631414 | A | T | 23 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(20): Show |
23 | HG01109.hp2 HG01243.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-28+11480A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631414 | |||||||
| chr1:111631588 | A | G | 33 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(30): Show |
33 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-28+11654A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631588 | |||||||
| chr1:111631788 | T | C | 5 | a0001c0001t0002g0293 a0001c0001t0002g0295 a0001c0001t0002g0296 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+11854T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631788 | |||||||
| chr1:111631805 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(105): Show |
109 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-28+11871C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631805 | |||||||
| chr1:111631904 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-28+11970T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631904 | |||||||
| chr1:111631904 | T | TA | 65 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(62): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.-28+11981dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111631904 | ||||||
| chr1:111631939 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-28+12005A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111631939 | |||||||
| chr1:111632033 | G | A | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+12099G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632033 | |||||||
| chr1:111632041 | A | G | 1 | a0001c0001t0002g0326 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-28+12107A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632041 | |||||||
| chr1:111632057 | G | A | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+12123G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632057 | |||||||
| chr1:111632078 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+12144T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632078 | |||||||
| chr1:111632158 | G | A | 3 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG00280.hp2 HG01256.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-28+12224G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632158 | |||||||
| chr1:111632225 | CT | C | 288 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(285): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-28+12305delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111632225 | ||||||
| chr1:111632225 | CTT | C | 39 | a0001c0001t0003g0214 a0001c0001t0004g0010 a0001c0001t0004g0327 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+12304_-28+1230 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111632225 | ||||||
| chr1:111632393 | T | A | 1 | a0001c0001t0002g0364 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-28+12459T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632393 | |||||||
| chr1:111632465 | A | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+12531A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632465 | |||||||
| chr1:111632612 | A | G | 1 | a0001c0001t0002g0321 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-28+12678A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632612 | |||||||
| chr1:111632656 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+12722T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632656 | |||||||
| chr1:111632703 | G | A | 58 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(55): Show |
58 | HG00408.hp1 HG01106.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28+12769G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632703 | |||||||
| chr1:111632741 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-28+12807C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632741 | |||||||
| chr1:111632746 | T | C | 264 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-28+12812T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632746 | |||||||
| chr1:111632867 | GCCAGGAT others(13): Show |
G | 1 | a0001c0001t0002g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-28+12934_-28+1295 others(24): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632867 | |||||||
| chr1:111632916 | G | C | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+12982G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111632916 | |||||||
| chr1:111632921 | C | CA | 112 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(109): Show |
114 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-28+13010dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111632921 | ||||||
| chr1:111632921 | C | CAA | 65 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(62): Show |
66 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.-28+13009_-28+1301 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111632921 | ||||||
| chr1:111632921 | C | CAAA | 26 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0229 others(23): Show |
26 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-28+13008_-28+1301 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111632921 | ||||||
| chr1:111632921 | CA | C | 36 | a0001c0001t0002g0040 a0001c0001t0002g0042 a0001c0001t0002g0043 others(33): Show |
36 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-28+13010delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111632921 | ||||||
| chr1:111633003 | G | A | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+13069G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633003 | |||||||
| chr1:111633004 | C | A | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+13070C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633004 | |||||||
| chr1:111633049 | G | A | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-28+13115G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633049 | |||||||
| chr1:111633277 | C | T | 1 | a0001c0001t0002g0320 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-28+13343C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633277 | |||||||
| chr1:111633278 | A | G | 30 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+13344A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633278 | |||||||
| chr1:111633348 | ATTGT | A | 8 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(5): Show |
10 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28+13418_-28+1342 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111633348 | ||||||
| chr1:111633377 | A | G | 20 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28+13443A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633377 | |||||||
| chr1:111633400 | A | G | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+13466A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633400 | |||||||
| chr1:111633409 | A | G | 264 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(261): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-28+13475A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633409 | |||||||
| chr1:111633449 | C | T | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+13515C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633449 | |||||||
| chr1:111633742 | A | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+13808A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633742 | |||||||
| chr1:111633769 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+13835A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633769 | |||||||
| chr1:111633856 | C | A | 24 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+13922C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111633856 | |||||||
| chr1:111634070 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-28+14136C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634070 | |||||||
| chr1:111634131 | G | A | 146 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(143): Show |
148 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.-28+14197G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634131 | |||||||
| chr1:111634200 | A | G | 1 | a0001c0001t0028g0137 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-28+14266A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634200 | |||||||
| chr1:111634212 | A | T | 38 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(35): Show |
38 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.-28+14278A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634212 | |||||||
| chr1:111634214 | T | C | 38 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(35): Show |
38 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.-28+14280T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634214 | |||||||
| chr1:111634229 | G | A | 1 | a0001c0001t0002g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-28+14295G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634229 | |||||||
| chr1:111634283 | T | G | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-28+14349T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634283 | |||||||
| chr1:111634319 | A | G | 4 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(1): Show |
5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+14385A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634319 | |||||||
| chr1:111634359 | C | G | 2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-28+14425C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634359 | |||||||
| chr1:111634500 | G | A | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+14566G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634500 | |||||||
| chr1:111634517 | TTTA | T | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01106.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-28+14588_-28+1459 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111634517 | ||||||
| chr1:111634599 | T | TTA | 3 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 |
3 | HG00140.hp2 HG01123.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-28+14677_-28+1467 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111634599 | ||||||
| chr1:111634629 | T | G | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-28+14695T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634629 | |||||||
| chr1:111634700 | A | C | 9 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28+14766A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634700 | |||||||
| chr1:111634769 | T | C | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+14835T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634769 | |||||||
| chr1:111634857 | A | T | 33 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(30): Show |
33 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-28+14923A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111634857 | |||||||
| chr1:111635135 | A | G | 1 | a0001c0001t0008g0282 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-28+15201A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635135 | |||||||
| chr1:111635303 | A | G | 2 | a0001c0001t0002g0251 a0001c0001t0002g0252 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-28+15369A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635303 | |||||||
| chr1:111635343 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-28+15409A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635343 | |||||||
| chr1:111635458 | T | C | 28 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(25): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-28+15524T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635458 | |||||||
| chr1:111635565 | G | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+15631G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635565 | |||||||
| chr1:111635567 | G | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+15633G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635567 | |||||||
| chr1:111635572 | G | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+15638G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635572 | |||||||
| chr1:111635576 | T | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+15642T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635576 | |||||||
| chr1:111635577 | G | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+15643G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635577 | |||||||
| chr1:111635580 | TCTGAAAC others(895): Show |
T | 1 | a0001c0001t0014g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28+15647_-28+1654 others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635580 | |||||||
| chr1:111635581 | C | T | 1 | a0001c0001t0014g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28+15647C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635581 | |||||||
| chr1:111635582 | TGAAACAG others(894): Show |
T | 1 | a0001c0001t0014g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-28+15649_-28+1654 others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635582 | |||||||
| chr1:111635604 | G | A | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+15670G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635604 | |||||||
| chr1:111635638 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-28+15704T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111635638 | |||||||
| chr1:111636105 | A | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28+16171A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636105 | |||||||
| chr1:111636120 | T | G | 2 | a0001c0001t0002g0302 a0001c0001t0002g0306 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28+16186T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636120 | |||||||
| chr1:111636139 | A | G | 33 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(30): Show |
33 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-28+16205A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636139 | |||||||
| chr1:111636332 | A | G | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+16398A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636332 | |||||||
| chr1:111636483 | A | T | 1 | a0001c0001t0014g0285 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28+16549A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636483 | |||||||
| chr1:111636488 | T | G | 1 | a0001c0001t0006g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-28+16554T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636488 | |||||||
| chr1:111636500 | G | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16566G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636500 | |||||||
| chr1:111636506 | G | A | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-28+16572G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636506 | |||||||
| chr1:111636511 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16577T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636511 | |||||||
| chr1:111636513 | C | T | 3 | a0001c0001t0012g0154 a0001c0001t0012g0155 a0001c0001t0031g0153 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-28+16579C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636513 | |||||||
| chr1:111636515 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16581T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636515 | |||||||
| chr1:111636522 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16588T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636522 | |||||||
| chr1:111636523 | G | A | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16589G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636523 | |||||||
| chr1:111636535 | G | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16601G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636535 | |||||||
| chr1:111636540 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16606A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636540 | |||||||
| chr1:111636543 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16609A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636543 | |||||||
| chr1:111636544 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16610T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636544 | |||||||
| chr1:111636546 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16612T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636546 | |||||||
| chr1:111636547 | G | A | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16613G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636547 | |||||||
| chr1:111636565 | C | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16631C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636565 | |||||||
| chr1:111636570 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16636A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636570 | |||||||
| chr1:111636572 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16638C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636572 | |||||||
| chr1:111636577 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16643A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636577 | |||||||
| chr1:111636584 | A | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16650A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636584 | |||||||
| chr1:111636586 | G | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16652G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636586 | |||||||
| chr1:111636587 | G | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16653G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636587 | |||||||
| chr1:111636591 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16657T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636591 | |||||||
| chr1:111636606 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16672T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636606 | |||||||
| chr1:111636608 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16674T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636608 | |||||||
| chr1:111636621 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16687T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636621 | |||||||
| chr1:111636629 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16695A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636629 | |||||||
| chr1:111636630 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16696T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636630 | |||||||
| chr1:111636631 | G | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16697G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636631 | |||||||
| chr1:111636639 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16705A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636639 | |||||||
| chr1:111636641 | T | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16707T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636641 | |||||||
| chr1:111636645 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16711A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636645 | |||||||
| chr1:111636672 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16738A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636672 | |||||||
| chr1:111636680 | T | A | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16746T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636680 | |||||||
| chr1:111636683 | A | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16749A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636683 | |||||||
| chr1:111636684 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-28+16750T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636684 | |||||||
| chr1:111636688 | G | A | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16754G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636688 | |||||||
| chr1:111636690 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16756T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636690 | |||||||
| chr1:111636697 | G | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16763G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636697 | |||||||
| chr1:111636698 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16764A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636698 | |||||||
| chr1:111636699 | G | A | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16765G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636699 | |||||||
| chr1:111636705 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16771C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636705 | |||||||
| chr1:111636706 | C | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16772C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636706 | |||||||
| chr1:111636729 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16795T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636729 | |||||||
| chr1:111636735 | C | T | 26 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(23): Show |
28 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-28+16801C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636735 | |||||||
| chr1:111636736 | G | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+16802G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636736 | |||||||
| chr1:111636846 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-28+16912G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636846 | |||||||
| chr1:111636982 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28+17048T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111636982 | |||||||
| chr1:111637373 | T | C | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28+17439T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111637373 | |||||||
| chr1:111637424 | T | C | 1 | a0001c0001t0031g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-28+17490T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111637424 | |||||||
| chr1:111637460 | A | G | 24 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+17526A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111637460 | |||||||
| chr1:111637561 | A | G | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-28+17627A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111637561 | |||||||
| chr1:111637708 | A | G | 1 | a0001c0001t0007g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28+17774A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111637708 | |||||||
| chr1:111637984 | C | T | 1 | a0001c0001t0005g0032 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-28+18050C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111637984 | |||||||
| chr1:111638035 | C | T | 202 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-28+18101C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638035 | |||||||
| chr1:111638048 | A | C | 30 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(27): Show |
30 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+18114A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638048 | |||||||
| chr1:111638089 | A | G | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-28+18155A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638089 | |||||||
| chr1:111638226 | A | G | 3 | a0001c0001t0005g0004 a0001c0001t0005g0030 a0001c0001t0005g0031 |
4 | HG02027.hp1 NA18963.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+18292A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638226 | |||||||
| chr1:111638268 | T | C | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0013g0036 others(2): Show |
5 | HG02965.hp2 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+18334T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638268 | |||||||
| chr1:111638276 | C | T | 87 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0043 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.-28+18342C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638276 | |||||||
| chr1:111638425 | TTTTC | T | 105 | a0001c0001t0001g0065 a0001c0001t0001g0086 a0001c0001t0001g0134 others(102): Show |
106 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-28+18507_-28+1851 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111638425 | ||||||
| chr1:111638484 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG00621.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.-28+18550C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638484 | |||||||
| chr1:111638867 | CT | C | 52 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(49): Show |
55 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.-28+18945delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111638867 | ||||||
| chr1:111638883 | A | T | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-28+18949A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111638883 | |||||||
| chr1:111639092 | G | GACTTAT | 361 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(358): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-28+19161_-28+1916 others(10): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639092 | ||||||
| chr1:111639303 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-28+19369G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111639303 | |||||||
| chr1:111639341 | G | A | 289 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-28+19407G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111639341 | |||||||
| chr1:111639345 | G | A | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+19411G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111639345 | |||||||
| chr1:111639406 | T | TTACACTT others(2558): Show |
1 | a0001c0001t0006g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2569): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2558): Show |
1 | a0001c0001t0006g0015 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2569): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2582): Show |
1 | a0001c0001t0002g0324 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2593): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2595): Show |
1 | a0001c0001t0002g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2606): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2595): Show |
1 | a0001c0001t0002g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2606): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2600): Show |
1 | a0001c0001t0002g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2611): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2459): Show |
1 | a0001c0001t0002g0043 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2470): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2580): Show |
2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG02559.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2591): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2580): Show |
1 | a0001c0001t0002g0058 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2591): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2579): Show |
12 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0050 others(9): Show |
12 | HG00280.hp1 HG01069.hp1 HG03490.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2590): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2598): Show |
3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 |
3 | NA18953.hp2 NA18961.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2609): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2580): Show |
1 | a0001c0001t0002g0364 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2591): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2580): Show |
1 | a0001c0001t0002g0056 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2591): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2596): Show |
3 | a0001c0001t0002g0042 a0001c0001t0002g0060 a0001c0001t0002g0063 |
3 | HG01099.hp1 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2607): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2580): Show |
1 | a0001c0001t0002g0041 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2591): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2580): Show |
1 | a0001c0001t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2591): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639406 | T | TTACACTT others(2579): Show |
1 | a0001c0001t0002g0057 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-28+19487_-28+1948 others(2590): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639406 | ||||||
| chr1:111639566 | C | CT | 241 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(238): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.-28+19644dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639566 | ||||||
| chr1:111639566 | C | CTT | 9 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-28+19643_-28+1964 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111639566 | ||||||
| chr1:111639684 | G | A | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-28+19750G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111639684 | |||||||
| chr1:111639736 | G | A | 2 | a0001c0001t0002g0302 a0001c0001t0002g0306 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28+19802G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111639736 | |||||||
| chr1:111639848 | G | A | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-28+19914G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111639848 | |||||||
| chr1:111639948 | C | A | 1 | a0001c0001t0028g0137 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-28+20014C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111639948 | |||||||
| chr1:111640169 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0172 |
2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-28+20235G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640169 | |||||||
| chr1:111640311 | CTA | C | 38 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(35): Show |
38 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.-28+20379_-28+2038 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111640311 | ||||||
| chr1:111640366 | C | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+20432C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640366 | |||||||
| chr1:111640395 | A | T | 1 | a0001c0001t0017g0052 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-28+20461A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640395 | |||||||
| chr1:111640441 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-28+20507A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640441 | |||||||
| chr1:111640518 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-28+20584G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640518 | |||||||
| chr1:111640731 | A | G | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+20797A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640731 | |||||||
| chr1:111640737 | A | G | 1 | a0001c0001t0004g0356 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-28+20803A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640737 | |||||||
| chr1:111640940 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-28+21006G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111640940 | |||||||
| chr1:111641018 | A | G | 206 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-28+21084A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641018 | |||||||
| chr1:111641067 | A | G | 2 | a0001c0001t0005g0033 a0001c0001t0005g0034 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-28+21133A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641067 | |||||||
| chr1:111641170 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-28+21236C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641170 | |||||||
| chr1:111641499 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-28+21565C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641499 | |||||||
| chr1:111641601 | G | A | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-28+21667G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641601 | |||||||
| chr1:111641650 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+21716C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641650 | |||||||
| chr1:111641651 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-28+21717G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641651 | |||||||
| chr1:111641701 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-28+21767A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641701 | |||||||
| chr1:111641708 | C | CAGATTTC others(12): Show |
1 | a0001c0001t0001g0073 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-28+21775_-28+2179 others(23): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111641708 | ||||||
| chr1:111641877 | T | A | 263 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(260): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-28+21943T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111641877 | |||||||
| chr1:111642076 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28+22142C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642076 | |||||||
| chr1:111642153 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-28+22219G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642153 | |||||||
| chr1:111642298 | C | T | 361 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(358): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-28+22364C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642298 | |||||||
| chr1:111642371 | A | C | 1 | a0001c0001t0007g0272 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-28+22437A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642371 | |||||||
| chr1:111642463 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-28+22529G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642463 | |||||||
| chr1:111642492 | CTT | C | 39 | a0001c0001t0004g0010 a0001c0001t0004g0327 a0001c0001t0004g0328 others(36): Show |
40 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-28+22572_-28+2257 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111642492 | ||||||
| chr1:111642510 | G | T | 8 | a0001c0001t0003g0007 a0001c0001t0003g0179 a0001c0001t0003g0180 others(5): Show |
9 | HG00733.hp1 HG01496.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+22576G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642510 | |||||||
| chr1:111642576 | T | C | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+22642T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642576 | |||||||
| chr1:111642601 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+22667C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642601 | |||||||
| chr1:111642648 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-28+22714C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642648 | |||||||
| chr1:111642654 | G | A | 362 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(359): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-28+22720G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642654 | |||||||
| chr1:111642655 | T | A | 173 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-28+22721T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642655 | |||||||
| chr1:111642734 | G | A | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-28+22800G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642734 | |||||||
| chr1:111642751 | A | T | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+22817A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642751 | |||||||
| chr1:111642757 | G | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28+22823G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642757 | |||||||
| chr1:111642774 | G | A | 10 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+22840G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642774 | |||||||
| chr1:111642786 | C | CT | 202 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-28+22869dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111642786 | ||||||
| chr1:111642786 | C | CTT | 20 | a0001c0001t0001g0065 a0001c0001t0001g0070 a0001c0001t0001g0073 others(17): Show |
20 | HG00544.hp2 HG01123.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28+22868_-28+2286 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111642786 | ||||||
| chr1:111642817 | G | A | 4 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(1): Show |
5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+22883G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642817 | |||||||
| chr1:111642825 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0129 |
2 | HG02056.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-28+22891G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642825 | |||||||
| chr1:111642924 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+22990C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642924 | |||||||
| chr1:111642930 | C | T | 2 | a0001c0001t0002g0302 a0001c0001t0002g0306 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28+22996C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642930 | |||||||
| chr1:111642982 | G | C | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-28+23048G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111642982 | |||||||
| chr1:111643001 | A | T | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-28+23067A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643001 | |||||||
| chr1:111643054 | G | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+23120G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643054 | |||||||
| chr1:111643144 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+23210A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643144 | |||||||
| chr1:111643269 | G | A | 1 | a0001c0001t0018g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-28+23335G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643269 | |||||||
| chr1:111643276 | C | A | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-28+23342C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643276 | |||||||
| chr1:111643307 | A | C | 57 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(54): Show |
57 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-28+23373A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643307 | |||||||
| chr1:111643354 | A | G | 1 | a0001c0001t0004g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-28+23420A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643354 | |||||||
| chr1:111643389 | T | G | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+23455T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643389 | |||||||
| chr1:111643415 | A | T | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+23481A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643415 | |||||||
| chr1:111643508 | A | G | 5 | a0001c0001t0003g0193 a0001c0001t0003g0205 a0001c0001t0003g0206 others(2): Show |
5 | NA18945.hp2 NA18967.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+23574A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643508 | |||||||
| chr1:111643519 | T | C | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+23585T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643519 | |||||||
| chr1:111643695 | T | A | 1 | a0001c0001t0004g0336 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-28+23761T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643695 | |||||||
| chr1:111643715 | T | C | 318 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(315): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-28+23781T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643715 | |||||||
| chr1:111643925 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0150 |
2 | HG02040.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-28+23991C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111643925 | |||||||
| chr1:111644180 | G | A | 2 | a0001c0001t0005g0262 a0001c0001t0005g0263 |
2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-28+24246G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111644180 | |||||||
| chr1:111644185 | A | AAT | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+24258_-28+2425 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111644185 | ||||||
| chr1:111644211 | G | A | 1 | a0001c0001t0002g0292 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-28+24277G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111644211 | |||||||
| chr1:111644735 | T | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+24801T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111644735 | |||||||
| chr1:111644815 | T | A | 1 | a0001c0001t0001g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-28+24881T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111644815 | |||||||
| chr1:111645064 | A | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-28+25130A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645064 | |||||||
| chr1:111645115 | G | A | 2 | a0001c0001t0002g0258 a0001c0001t0010g0195 |
2 | HG02976.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-28+25181G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645115 | |||||||
| chr1:111645156 | C | CAA | 326 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(323): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-28+25223_-28+2522 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111645156 | ||||||
| chr1:111645162 | G | C | 1 | a0001c0001t0001g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-28+25228G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645162 | |||||||
| chr1:111645163 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-28+25229C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645163 | |||||||
| chr1:111645175 | G | A | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-28+25241G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645175 | |||||||
| chr1:111645365 | A | G | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-28+25431A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645365 | |||||||
| chr1:111645477 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-28+25543A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645477 | |||||||
| chr1:111645483 | T | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+25549T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645483 | |||||||
| chr1:111645622 | A | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+25688A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645622 | |||||||
| chr1:111645685 | A | G | 4 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(1): Show |
4 | HG00140.hp2 HG01123.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+25751A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645685 | |||||||
| chr1:111645757 | A | G | 1 | a0001c0001t0003g0182 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-28+25823A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645757 | |||||||
| chr1:111645781 | A | G | 23 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 others(20): Show |
23 | HG01109.hp2 HG01243.hp1 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-28+25847A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645781 | |||||||
| chr1:111645867 | G | A | 1 | a0001c0001t0004g0228 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-28+25933G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111645867 | |||||||
| chr1:111646031 | T | A | 1 | a0001c0001t0010g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-28+26097T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646031 | |||||||
| chr1:111646220 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-28+26286G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646220 | |||||||
| chr1:111646249 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-28+26315A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646249 | |||||||
| chr1:111646347 | T | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+26413T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646347 | |||||||
| chr1:111646420 | T | TA | 25 | a0001c0001t0001g0076 a0001c0001t0001g0087 a0001c0001t0001g0088 others(22): Show |
25 | HG00597.hp1 HG01109.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+26500dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111646420 | ||||||
| chr1:111646420 | T | TAA | 35 | a0001c0001t0002g0040 a0001c0001t0002g0042 a0001c0001t0002g0043 others(32): Show |
35 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-28+26499_-28+2650 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111646420 | ||||||
| chr1:111646421 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-28+26487A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646421 | |||||||
| chr1:111646430 | AAAAAC | A | 30 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0227 others(27): Show |
30 | HG00408.hp1 HG01243.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+26507_-28+2651 others(9): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111646430 | ||||||
| chr1:111646432 | A | AC | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+26498_-28+2649 others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646432 | |||||||
| chr1:111646433 | A | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0128 |
2 | HG02738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-28+26499A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646433 | |||||||
| chr1:111646434 | AC | A | 34 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(31): Show |
34 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.-28+26501delC | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646434 | |||||||
| chr1:111646435 | C | A | 250 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(247): Show |
256 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-28+26501C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646435 | |||||||
| chr1:111646440 | C | A | 56 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(53): Show |
57 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-28+26506C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646440 | |||||||
| chr1:111646563 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-28+26629C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646563 | |||||||
| chr1:111646576 | T | G | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+26642T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646576 | |||||||
| chr1:111646641 | C | T | 1 | a0001c0001t0004g0358 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-28+26707C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646641 | |||||||
| chr1:111646760 | C | T | 1 | a0001c0001t0005g0030 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-28+26826C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646760 | |||||||
| chr1:111646778 | A | G | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-28+26844A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646778 | |||||||
| chr1:111646786 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28+26852G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646786 | |||||||
| chr1:111646790 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-28+26856C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646790 | |||||||
| chr1:111646806 | C | G | 3 | a0001c0001t0005g0018 a0001c0001t0005g0027 a0001c0001t0018g0039 |
3 | HG00140.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-28+26872C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646806 | |||||||
| chr1:111646827 | C | A | 37 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(34): Show |
37 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.-28+26893C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646827 | |||||||
| chr1:111646829 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-28+26895G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646829 | |||||||
| chr1:111646875 | T | A | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-28+26941T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646875 | |||||||
| chr1:111646982 | G | A | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+27048G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111646982 | |||||||
| chr1:111647120 | C | T | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-28+27186C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647120 | |||||||
| chr1:111647175 | TTC | T | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+27244_-28+2724 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111647175 | ||||||
| chr1:111647496 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+27562C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647496 | |||||||
| chr1:111647519 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-28+27585G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647519 | |||||||
| chr1:111647531 | A | G | 1 | a0001c0001t0006g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-28+27597A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647531 | |||||||
| chr1:111647710 | CT | C | 26 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0286 others(23): Show |
27 | HG01192.hp1 HG02055.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.-28+27789delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111647710 | ||||||
| chr1:111647748 | G | T | 26 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(23): Show |
28 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-28+27814G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647748 | |||||||
| chr1:111647755 | C | A | 1 | a0001c0001t0006g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-28+27821C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647755 | |||||||
| chr1:111647855 | T | A | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+27921T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647855 | |||||||
| chr1:111647922 | T | C | 317 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-28+27988T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111647922 | |||||||
| chr1:111647934 | C | CGTTTAGT others(18): Show |
1 | a0001c0001t0004g0352 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-28+28004_-28+2802 others(29): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111647934 | ||||||
| chr1:111648174 | A | AGT | 3 | a0001c0001t0002g0064 a0001c0001t0003g0181 a0001c0001t0010g0204 |
3 | HG00280.hp1 NA18970.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-28+28269_-28+2827 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111648174 | ||||||
| chr1:111648174 | A | AGTGT | 3 | a0001c0001t0001g0152 a0001c0001t0018g0039 a0001c0001t0022g0209 |
3 | HG00140.hp1 HG01106.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-28+28267_-28+2827 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111648174 | ||||||
| chr1:111648174 | A | AGTGTGT | 6 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0126 others(3): Show |
6 | HG01257.hp2 HG01346.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+28265_-28+2827 others(10): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111648174 | ||||||
| chr1:111648196 | TGTGTGTG others(2): Show |
T | 29 | a0001c0001t0002g0292 a0001c0001t0002g0293 a0001c0001t0002g0295 others(26): Show |
29 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-28+28263_-28+2827 others(13): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648196 | |||||||
| chr1:111648200 | TGTGTA | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0253 others(1): Show |
4 | HG02257.hp1 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+28267_-28+2827 others(9): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648200 | |||||||
| chr1:111648202 | TGTA | T | 32 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0229 others(29): Show |
32 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.-28+28269_-28+2827 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648202 | |||||||
| chr1:111648205 | A | G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0067 others(171): Show |
177 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.-28+28271A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648205 | |||||||
| chr1:111648205 | AT | A | 58 | a0001c0001t0002g0256 a0001c0001t0004g0010 a0001c0001t0004g0228 others(55): Show |
61 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-28+28284delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111648205 | ||||||
| chr1:111648205 | ATT | A | 8 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+28283_-28+2828 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111648205 | ||||||
| chr1:111648206 | T | A | 67 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(64): Show |
67 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.-28+28272T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648206 | |||||||
| chr1:111648206 | T | TA | 30 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(27): Show |
30 | HG00673.hp2 HG01069.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.-28+28272_-28+2827 others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648206 | |||||||
| chr1:111648206 | T | TGTA | 16 | a0001c0001t0001g0077 a0001c0001t0001g0092 a0001c0001t0001g0093 others(13): Show |
16 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-28+28272_-28+2827 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648206 | |||||||
| chr1:111648206 | T | TGTGTA | 110 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0068 others(107): Show |
112 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-28+28272_-28+2827 others(9): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648206 | |||||||
| chr1:111648206 | T | TGTGTGTA | 8 | a0001c0001t0001g0065 a0001c0001t0001g0071 a0001c0001t0001g0124 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+28272_-28+2827 others(11): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648206 | |||||||
| chr1:111648206 | T | TGTGTGTG others(2): Show |
6 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(3): Show |
7 | HG01192.hp1 HG02451.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+28272_-28+2827 others(13): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648206 | |||||||
| chr1:111648206 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0012g0174 a0001c0001t0031g0153 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-28+28272_-28+2827 others(15): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648206 | |||||||
| chr1:111648207 | T | A | 5 | a0001c0001t0001g0152 a0001c0001t0002g0250 a0001c0001t0002g0251 others(2): Show |
5 | HG00140.hp1 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+28273T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648207 | |||||||
| chr1:111648508 | G | A | 1 | a0001c0001t0004g0363 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-28+28574G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648508 | |||||||
| chr1:111648510 | C | T | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28+28576C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648510 | |||||||
| chr1:111648569 | T | A | 218 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(215): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-28+28635T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648569 | |||||||
| chr1:111648593 | G | C | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+28659G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648593 | |||||||
| chr1:111648629 | G | A | 1 | a0001c0001t0004g0329 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-28+28695G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648629 | |||||||
| chr1:111648663 | T | C | 1 | a0001c0001t0022g0209 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-28+28729T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648663 | |||||||
| chr1:111648786 | T | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+28852T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648786 | |||||||
| chr1:111648793 | G | T | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-28+28859G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648793 | |||||||
| chr1:111648958 | C | T | 12 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(9): Show |
15 | HG01175.hp2 HG01192.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28+29024C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111648958 | |||||||
| chr1:111649030 | C | T | 5 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(2): Show |
7 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28+29096C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649030 | |||||||
| chr1:111649175 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+29241G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649175 | |||||||
| chr1:111649287 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG03654.hp1 HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-28+29353C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649287 | |||||||
| chr1:111649358 | C | CCAGCCCC others(13): Show |
1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-28+29430_-28+2944 others(24): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111649358 | ||||||
| chr1:111649377 | T | C | 1 | a0001c0001t0002g0316 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-28+29443T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649377 | |||||||
| chr1:111649422 | C | T | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-28+29488C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649422 | |||||||
| chr1:111649461 | C | T | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-28+29527C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649461 | |||||||
| chr1:111649493 | C | G | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-28+29559C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649493 | |||||||
| chr1:111649500 | T | C | 158 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(155): Show |
169 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.-28+29566T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649500 | |||||||
| chr1:111649595 | G | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0172 |
2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-28+29661G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649595 | |||||||
| chr1:111649948 | A | G | 56 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(53): Show |
56 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.-28+30014A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111649948 | |||||||
| chr1:111650054 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-28+30120A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650054 | |||||||
| chr1:111650074 | T | C | 1 | a0001c0001t0009g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28+30140T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650074 | |||||||
| chr1:111650093 | C | CT | 7 | a0001c0001t0002g0063 a0001c0001t0002g0302 a0001c0001t0004g0333 others(4): Show |
7 | HG00673.hp2 HG01168.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+30184dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111650093 | ||||||
| chr1:111650093 | CT | C | 59 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(56): Show |
59 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.-28+30184delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111650093 | ||||||
| chr1:111650093 | CTT | C | 175 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(172): Show |
186 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-28+30183_-28+3018 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111650093 | ||||||
| chr1:111650093 | CTTT | C | 50 | a0001c0001t0001g0068 a0001c0001t0001g0078 a0001c0001t0001g0172 others(47): Show |
50 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.-28+30182_-28+3018 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111650093 | ||||||
| chr1:111650118 | T | A | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-28+30184T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650118 | |||||||
| chr1:111650239 | C | T | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-28+30305C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650239 | |||||||
| chr1:111650311 | T | A | 2 | a0001c0001t0005g0018 a0001c0001t0005g0027 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-28+30377T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650311 | |||||||
| chr1:111650753 | A | G | 1 | a0001c0001t0006g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-28+30819A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650753 | |||||||
| chr1:111650753 | A | T | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-28+30819A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650753 | |||||||
| chr1:111650808 | T | G | 5 | a0001c0001t0004g0228 a0001c0001t0004g0330 a0001c0001t0004g0339 others(2): Show |
5 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+30874T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650808 | |||||||
| chr1:111650856 | C | T | 1 | a0001c0001t0002g0321 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-28+30922C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650856 | |||||||
| chr1:111650962 | C | T | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-28+31028C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650962 | |||||||
| chr1:111650967 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-28+31033A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650967 | |||||||
| chr1:111650970 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-28+31036T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650970 | |||||||
| chr1:111650988 | C | G | 118 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(115): Show |
128 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.-28+31054C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111650988 | |||||||
| chr1:111651016 | A | G | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+31082A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651016 | |||||||
| chr1:111651048 | C | T | 4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(1): Show |
4 | HG01070.hp1 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+31114C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651048 | |||||||
| chr1:111651093 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+31159C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651093 | |||||||
| chr1:111651117 | A | G | 1 | a0001c0001t0005g0026 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-28+31183A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651117 | |||||||
| chr1:111651315 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-28+31381C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651315 | |||||||
| chr1:111651406 | T | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+31472T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651406 | |||||||
| chr1:111651473 | A | AT | 152 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0086 others(149): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.-28+31561dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111651473 | ||||||
| chr1:111651473 | A | ATT | 6 | a0001c0001t0002g0051 a0001c0001t0002g0238 a0001c0001t0003g0207 others(3): Show |
6 | HG02572.hp2 HG02622.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+31560_-28+3156 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111651473 | ||||||
| chr1:111651473 | AT | A | 28 | a0001c0001t0001g0094 a0001c0001t0001g0134 a0001c0001t0001g0160 others(25): Show |
28 | HG01109.hp2 HG01243.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.-28+31561delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111651473 | ||||||
| chr1:111651579 | T | C | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.-28+31645T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651579 | |||||||
| chr1:111651728 | C | T | 1 | a0001c0001t0005g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-28+31794C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651728 | |||||||
| chr1:111651769 | G | T | 2 | a0001c0001t0002g0302 a0001c0001t0002g0306 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-28+31835G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651769 | |||||||
| chr1:111651823 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-28+31889A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651823 | |||||||
| chr1:111651833 | C | T | 37 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(34): Show |
37 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.-28+31899C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651833 | |||||||
| chr1:111651903 | T | G | 1 | a0001c0001t0005g0019 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-28+31969T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111651903 | |||||||
| chr1:111651937 | C | CT | 47 | a0001c0001t0001g0139 a0001c0001t0002g0012 a0001c0001t0002g0013 others(44): Show |
47 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(44): Show |
intron_variant | MODIFIER | c.-28+32015dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111651937 | ||||||
| chr1:111651937 | CT | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+32015delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111651937 | ||||||
| chr1:111652132 | C | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+32198C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652132 | |||||||
| chr1:111652188 | C | T | 1 | a0001c0001t0015g0314 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-28+32254C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652188 | |||||||
| chr1:111652189 | G | A | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-28+32255G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652189 | |||||||
| chr1:111652193 | C | T | 10 | a0001c0001t0002g0293 a0001c0001t0002g0295 a0001c0001t0002g0296 others(7): Show |
10 | HG02572.hp1 HG02615.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+32259C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652193 | |||||||
| chr1:111652266 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-28+32332A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652266 | |||||||
| chr1:111652320 | G | A | 33 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(30): Show |
33 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.-28+32386G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652320 | |||||||
| chr1:111652469 | A | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-28+32535A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652469 | |||||||
| chr1:111652592 | G | A | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-28+32658G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652592 | |||||||
| chr1:111652771 | G | T | 3 | a0001c0001t0006g0215 a0001c0001t0006g0216 a0001c0001t0006g0217 |
3 | HG01433.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+32837G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652771 | |||||||
| chr1:111652847 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG00423.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-28+32913C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652847 | |||||||
| chr1:111652853 | A | G | 9 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0250 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-28+32919A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111652853 | |||||||
| chr1:111653100 | A | C | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-28+33166A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111653100 | |||||||
| chr1:111653191 | T | C | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-28+33257T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111653191 | |||||||
| chr1:111653230 | T | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0196 a0001c0001t0003g0197 others(4): Show |
10 | HG02129.hp2 NA18947.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.-28+33296T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111653230 | |||||||
| chr1:111653457 | G | A | 58 | a0001c0001t0001g0161 a0001c0001t0002g0012 a0001c0001t0002g0013 others(55): Show |
58 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.-28+33523G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111653457 | |||||||
| chr1:111653669 | G | A | 20 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-28+33735G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111653669 | |||||||
| chr1:111653683 | C | CA | 30 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0080 others(27): Show |
30 | HG00140.hp2 HG00408.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28+33775dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111653683 | ||||||
| chr1:111653683 | CA | C | 57 | a0001c0001t0001g0078 a0001c0001t0001g0112 a0001c0001t0001g0113 others(54): Show |
58 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-28+33775delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111653683 | ||||||
| chr1:111653683 | CAA | C | 19 | a0001c0001t0002g0013 a0001c0001t0002g0258 a0001c0001t0003g0175 others(16): Show |
21 | HG00423.hp2 HG01175.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28+33774_-28+3377 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111653683 | ||||||
| chr1:111653683 | CAAA | C | 44 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(41): Show |
52 | HG00280.hp2 HG00609.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.-28+33773_-28+3377 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111653683 | ||||||
| chr1:111653683 | CAAAAAAA others(1): Show |
C | 36 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(33): Show |
37 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-28+33768_-28+3377 others(12): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111653683 | ||||||
| chr1:111653915 | A | G | 1 | a0001c0001t0004g0349 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-28+33981A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111653915 | |||||||
| chr1:111654034 | A | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-28+34100A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654034 | |||||||
| chr1:111654077 | C | T | 5 | a0001c0001t0004g0228 a0001c0001t0004g0330 a0001c0001t0004g0339 others(2): Show |
5 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.-28+34143C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654077 | |||||||
| chr1:111654100 | C | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-28+34166C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654100 | |||||||
| chr1:111654117 | T | G | 362 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(359): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.-28+34183T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654117 | |||||||
| chr1:111654288 | C | T | 8 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+34354C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654288 | |||||||
| chr1:111654655 | CAGTA | C | 5 | a0001c0001t0005g0020 a0001c0001t0005g0024 a0001c0001t0005g0025 others(2): Show |
5 | NA18950.hp1 NA18968.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+34725_-28+3472 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111654655 | ||||||
| chr1:111654706 | G | A | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+34772G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654706 | |||||||
| chr1:111654734 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-28+34800A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654734 | |||||||
| chr1:111654908 | G | A | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-28+34974G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111654908 | |||||||
| chr1:111655007 | G | C | 24 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+35073G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655007 | |||||||
| chr1:111655008 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-28+35074C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655008 | |||||||
| chr1:111655204 | T | C | 106 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(103): Show |
107 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-28+35270T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655204 | |||||||
| chr1:111655240 | A | AAAG | 116 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(113): Show |
126 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-28+35309_-28+3531 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655240 | ||||||
| chr1:111655244 | A | AAG | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-28+35311_-28+3531 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655244 | ||||||
| chr1:111655266 | C | CA | 25 | a0001c0001t0002g0258 a0001c0001t0004g0340 a0001c0001t0004g0362 others(22): Show |
25 | HG01109.hp2 HG01243.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.-28+35343dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655266 | ||||||
| chr1:111655266 | C | CAA | 33 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(30): Show |
33 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.-28+35342_-28+3534 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655266 | ||||||
| chr1:111655266 | CA | C | 222 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(219): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-28+35343delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655266 | ||||||
| chr1:111655297 | C | T | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-28+35363C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655297 | |||||||
| chr1:111655357 | G | A | 1 | a0001c0001t0004g0340 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-28+35423G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655357 | |||||||
| chr1:111655371 | A | T | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-28+35437A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655371 | |||||||
| chr1:111655413 | A | G | 4 | a0001c0001t0004g0344 a0001c0001t0004g0345 a0001c0001t0004g0353 others(1): Show |
4 | NA18945.hp1 NA18946.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+35479A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655413 | |||||||
| chr1:111655428 | C | T | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-28+35494C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655428 | |||||||
| chr1:111655490 | C | T | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-28+35556C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655490 | |||||||
| chr1:111655576 | T | C | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+35642T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655576 | |||||||
| chr1:111655619 | AAACTAAT others(10): Show |
A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-28+35689_-27-3569 others(21): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655619 | ||||||
| chr1:111655658 | C | CT | 150 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(147): Show |
160 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-27-35649dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655658 | ||||||
| chr1:111655658 | C | CTT | 66 | a0001c0001t0001g0065 a0001c0001t0001g0082 a0001c0001t0001g0111 others(63): Show |
69 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-27-35650_-27-3564 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655658 | ||||||
| chr1:111655658 | C | CTTT | 18 | a0001c0001t0001g0152 a0001c0001t0002g0237 a0001c0001t0002g0246 others(15): Show |
18 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-27-35651_-27-3564 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655658 | ||||||
| chr1:111655658 | CTTTTTTT others(1): Show |
C | 37 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(34): Show |
38 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-27-35656_-27-3564 others(12): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655658 | ||||||
| chr1:111655728 | CGCAATCT others(15): Show |
C | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-27-35601_-27-3558 others(26): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111655728 | ||||||
| chr1:111655883 | C | T | 1 | a0001c0001t0031g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-27-35451C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655883 | |||||||
| chr1:111655976 | A | G | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-27-35358A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655976 | |||||||
| chr1:111655994 | A | G | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-27-35340A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111655994 | |||||||
| chr1:111656094 | A | G | 1 | a0001c0001t0002g0305 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-27-35240A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111656094 | |||||||
| chr1:111656383 | AAAAT | A | 4 | a0001c0001t0002g0232 a0001c0001t0002g0241 a0001c0001t0002g0246 others(1): Show |
4 | NA18940.hp2 NA18952.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-34944_-27-3494 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111656383 | ||||||
| chr1:111656498 | T | G | 1 | a0001c0001t0006g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-27-34836T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111656498 | |||||||
| chr1:111656639 | C | A | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-27-34695C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111656639 | |||||||
| chr1:111656663 | T | C | 351 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(348): Show |
365 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-27-34671T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111656663 | |||||||
| chr1:111656873 | T | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-34461T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111656873 | |||||||
| chr1:111656911 | CATT | C | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-34422_-27-3442 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111656911 | |||||||
| chr1:111657148 | C | T | 1 | a0001c0001t0017g0052 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-27-34186C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111657148 | |||||||
| chr1:111657172 | C | T | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27-34162C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111657172 | |||||||
| chr1:111657459 | A | G | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-33875A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111657459 | |||||||
| chr1:111657834 | G | A | 9 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-27-33500G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111657834 | |||||||
| chr1:111657996 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-27-33338A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111657996 | |||||||
| chr1:111658135 | C | T | 9 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0250 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-27-33199C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658135 | |||||||
| chr1:111658280 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-27-33054A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658280 | |||||||
| chr1:111658381 | A | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-32953A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658381 | |||||||
| chr1:111658548 | G | A | 162 | a0001c0001t0001g0116 a0001c0001t0002g0012 a0001c0001t0002g0013 others(159): Show |
173 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.-27-32786G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658548 | |||||||
| chr1:111658634 | T | C | 1 | a0001c0001t0004g0352 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-27-32700T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658634 | |||||||
| chr1:111658699 | G | A | 22 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(19): Show |
23 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.-27-32635G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658699 | |||||||
| chr1:111658706 | A | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-32628A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658706 | |||||||
| chr1:111658739 | A | G | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-32595A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658739 | |||||||
| chr1:111658812 | G | A | 1 | a0001c0001t0002g0316 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-27-32522G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658812 | |||||||
| chr1:111658857 | T | A | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-32477T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658857 | |||||||
| chr1:111658976 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-27-32358C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111658976 | |||||||
| chr1:111659080 | GCATGAT | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-32253_-27-3224 others(10): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111659080 | |||||||
| chr1:111659124 | A | C | 1 | a0001c0001t0004g0348 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-27-32210A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111659124 | |||||||
| chr1:111659157 | C | G | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-32177C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111659157 | |||||||
| chr1:111659490 | T | C | 1 | a0001c0001t0004g0352 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-27-31844T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111659490 | |||||||
| chr1:111659511 | C | CT | 40 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0139 others(37): Show |
41 | HG00280.hp1 HG00544.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.-27-31810dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111659511 | ||||||
| chr1:111659524 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-27-31810T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111659524 | |||||||
| chr1:111659617 | T | G | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-27-31717T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111659617 | |||||||
| chr1:111659645 | A | G | 1 | a0001c0001t0006g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-27-31689A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111659645 | |||||||
| chr1:111660031 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-27-31303A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660031 | |||||||
| chr1:111660287 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-27-31047T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660287 | |||||||
| chr1:111660369 | T | C | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-30965T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660369 | |||||||
| chr1:111660398 | C | G | 1 | a0001c0001t0011g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-27-30936C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660398 | |||||||
| chr1:111660549 | A | T | 4 | a0001c0001t0002g0042 a0001c0001t0002g0059 a0001c0001t0002g0060 others(1): Show |
4 | HG01099.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-30785A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660549 | |||||||
| chr1:111660563 | G | T | 106 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(103): Show |
107 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-27-30771G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660563 | |||||||
| chr1:111660830 | G | T | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-30504G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660830 | |||||||
| chr1:111660905 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-27-30429C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660905 | |||||||
| chr1:111660989 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-27-30345G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111660989 | |||||||
| chr1:111661007 | T | G | 1 | a0001c0001t0032g0125 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27-30327T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111661007 | |||||||
| chr1:111661137 | G | A | 4 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(1): Show |
5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-30197G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111661137 | |||||||
| chr1:111661139 | A | G | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-30195A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111661139 | |||||||
| chr1:111661720 | A | G | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-29614A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111661720 | |||||||
| chr1:111661778 | G | A | 4 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(1): Show |
5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-29556G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111661778 | |||||||
| chr1:111661800 | G | GA | 23 | a0001c0001t0001g0073 a0001c0001t0001g0087 a0001c0001t0001g0100 others(20): Show |
23 | HG00140.hp1 HG01109.hp2 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.-27-29517dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111661800 | ||||||
| chr1:111661800 | GA | G | 75 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(72): Show |
76 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.-27-29517delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111661800 | ||||||
| chr1:111661883 | G | A | 1 | a0001c0001t0004g0357 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-27-29451G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111661883 | |||||||
| chr1:111661941 | T | A | 5 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(2): Show |
7 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-29393T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111661941 | |||||||
| chr1:111662290 | G | A | 7 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(4): Show |
8 | HG01192.hp1 HG02451.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-29044G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111662290 | |||||||
| chr1:111662366 | G | T | 1 | a0001c0001t0003g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-27-28968G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111662366 | |||||||
| chr1:111662373 | C | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-28961C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111662373 | |||||||
| chr1:111662394 | CA | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(100): Show |
104 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-27-28916delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111662394 | ||||||
| chr1:111662394 | CAA | C | 76 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0086 others(73): Show |
79 | HG00408.hp1 HG00621.hp2 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.-27-28917_-27-2891 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111662394 | ||||||
| chr1:111662394 | CAAA | C | 13 | a0001c0001t0001g0081 a0001c0001t0001g0118 a0001c0001t0002g0230 others(10): Show |
13 | HG01081.hp1 HG01433.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-27-28918_-27-2891 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111662394 | ||||||
| chr1:111662394 | CAAAA | C | 42 | a0001c0001t0003g0187 a0001c0001t0003g0212 a0001c0001t0004g0010 others(39): Show |
43 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.-27-28919_-27-2891 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111662394 | ||||||
| chr1:111662394 | CAAAAA | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(42): Show |
53 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.-27-28920_-27-2891 others(9): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111662394 | ||||||
| chr1:111662550 | C | T | 2 | a0001c0001t0007g0264 a0001c0001t0019g0011 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-27-28784C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111662550 | |||||||
| chr1:111662686 | C | A | 3 | a0001c0001t0002g0322 a0001c0001t0002g0324 a0001c0001t0002g0325 |
3 | HG00544.hp1 NA18955.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-27-28648C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111662686 | |||||||
| chr1:111662729 | T | TA | 115 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(112): Show |
117 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.-27-28604dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111662729 | ||||||
| chr1:111662869 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-27-28465C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111662869 | |||||||
| chr1:111662910 | T | TTTG | 11 | a0001c0001t0005g0018 a0001c0001t0005g0027 a0001c0001t0007g0266 others(8): Show |
11 | HG00140.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-28407_-27-2840 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111662910 | ||||||
| chr1:111662913 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-27-28421G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111662913 | |||||||
| chr1:111663060 | C | T | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-28274C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111663060 | |||||||
| chr1:111663142 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0047 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-27-28192G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111663142 | |||||||
| chr1:111663276 | C | T | 1 | a0001c0001t0009g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-27-28058C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111663276 | |||||||
| chr1:111663769 | T | C | 192 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(189): Show |
203 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-27-27565T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111663769 | |||||||
| chr1:111663777 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-27-27557T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111663777 | |||||||
| chr1:111663807 | A | G | 101 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(98): Show |
112 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-27-27527A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111663807 | |||||||
| chr1:111663910 | TCTTC | T | 101 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(98): Show |
112 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-27-27419_-27-2741 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111663910 | ||||||
| chr1:111663974 | T | C | 2 | a0001c0001t0012g0154 a0001c0001t0012g0155 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-27-27360T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111663974 | |||||||
| chr1:111664098 | G | GCACGGTG others(3): Show |
1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-27-27231_-27-2722 others(14): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111664098 | ||||||
| chr1:111664142 | G | A | 3 | a0001c0001t0012g0154 a0001c0001t0012g0155 a0001c0001t0031g0153 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-27-27192G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664142 | |||||||
| chr1:111664144 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-27-27190A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664144 | |||||||
| chr1:111664220 | A | G | 3 | a0001c0001t0002g0295 a0001c0001t0002g0297 a0001c0001t0023g0294 |
3 | HG02615.hp2 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-27-27114A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664220 | |||||||
| chr1:111664313 | G | A | 52 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(49): Show |
52 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(49): Show |
intron_variant | MODIFIER | c.-27-27021G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664313 | |||||||
| chr1:111664368 | C | T | 363 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(360): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-27-26966C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664368 | |||||||
| chr1:111664373 | C | CA | 12 | a0001c0001t0001g0066 a0001c0001t0001g0078 a0001c0001t0002g0303 others(9): Show |
14 | HG00140.hp2 HG01123.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-27-26936dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111664373 | ||||||
| chr1:111664373 | CA | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0067 others(90): Show |
95 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-27-26936delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111664373 | ||||||
| chr1:111664373 | CAA | C | 43 | a0001c0001t0001g0167 a0001c0001t0002g0040 a0001c0001t0002g0041 others(40): Show |
43 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-27-26937_-27-2693 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111664373 | ||||||
| chr1:111664373 | CAAA | C | 118 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0227 others(115): Show |
120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-27-26938_-27-2693 others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111664373 | ||||||
| chr1:111664373 | CAAAA | C | 51 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(48): Show |
59 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-26939_-27-2693 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111664373 | ||||||
| chr1:111664387 | A | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-26947A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664387 | |||||||
| chr1:111664388 | A | C | 2 | a0001c0001t0001g0133 a0001c0001t0016g0310 |
2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-27-26946A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664388 | |||||||
| chr1:111664390 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-27-26944A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664390 | |||||||
| chr1:111664391 | A | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-26943A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664391 | |||||||
| chr1:111664392 | A | C | 52 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(49): Show |
53 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-27-26942A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664392 | |||||||
| chr1:111664395 | A | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-26939A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664395 | |||||||
| chr1:111664397 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-26937A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664397 | |||||||
| chr1:111664632 | C | T | 6 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0253 others(3): Show |
6 | HG02257.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-26702C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664632 | |||||||
| chr1:111664648 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-27-26686C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664648 | |||||||
| chr1:111664803 | T | C | 1 | a0001c0001t0007g0273 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-27-26531T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664803 | |||||||
| chr1:111664869 | A | G | 3 | a0001c0001t0002g0316 a0001c0001t0002g0317 a0001c0001t0002g0318 |
3 | HG03239.hp2 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-27-26465A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111664869 | |||||||
| chr1:111665179 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-27-26155A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665179 | |||||||
| chr1:111665241 | A | G | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27-26093A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665241 | |||||||
| chr1:111665246 | G | A | 3 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0321 |
3 | HG00099.hp2 HG01358.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-27-26088G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665246 | |||||||
| chr1:111665259 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-27-26075T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665259 | |||||||
| chr1:111665358 | G | A | 1 | a0001c0001t0003g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-27-25976G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665358 | |||||||
| chr1:111665561 | T | C | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27-25773T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665561 | |||||||
| chr1:111665693 | A | G | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-27-25641A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665693 | |||||||
| chr1:111665828 | A | G | 10 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-25506A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665828 | |||||||
| chr1:111665931 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0099 a0001c0001t0001g0130 |
3 | HG00544.hp2 NA18955.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-27-25403G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665931 | |||||||
| chr1:111665970 | T | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-25364T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111665970 | |||||||
| chr1:111666046 | G | T | 1 | a0001c0001t0006g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-27-25288G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666046 | |||||||
| chr1:111666069 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0108 others(2): Show |
6 | HG00733.hp2 HG00738.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-25265A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666069 | |||||||
| chr1:111666605 | T | C | 20 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27-24729T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666605 | |||||||
| chr1:111666609 | G | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-24725G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666609 | |||||||
| chr1:111666643 | T | TA | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.-27-24680dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111666643 | ||||||
| chr1:111666643 | TA | T | 27 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0229 others(24): Show |
27 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.-27-24680delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111666643 | ||||||
| chr1:111666666 | C | T | 3 | a0001c0001t0012g0154 a0001c0001t0012g0155 a0001c0001t0031g0153 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-27-24668C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666666 | |||||||
| chr1:111666697 | C | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-24637C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666697 | |||||||
| chr1:111666878 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-27-24456C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666878 | |||||||
| chr1:111666913 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-27-24421T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111666913 | |||||||
| chr1:111666931 | A | AATAGGGA others(11): Show |
160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-24400_-27-2438 others(22): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111666931 | ||||||
| chr1:111667085 | G | A | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-24249G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667085 | |||||||
| chr1:111667466 | C | G | 8 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(5): Show |
10 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27-23868C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667466 | |||||||
| chr1:111667583 | T | C | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-23751T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667583 | |||||||
| chr1:111667613 | C | T | 1 | a0001c0001t0006g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-27-23721C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667613 | |||||||
| chr1:111667637 | G | A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-23697G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667637 | |||||||
| chr1:111667682 | C | CA | 49 | a0001c0001t0002g0233 a0001c0001t0004g0010 a0001c0001t0004g0228 others(46): Show |
50 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-27-23637dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111667682 | ||||||
| chr1:111667831 | T | A | 1 | a0001c0001t0002g0326 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-27-23503T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667831 | |||||||
| chr1:111667943 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-23391G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667943 | |||||||
| chr1:111667951 | G | A | 5 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(2): Show |
7 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-23383G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667951 | |||||||
| chr1:111667975 | C | T | 7 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0240 others(4): Show |
7 | HG01243.hp2 NA18940.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-23359C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111667975 | |||||||
| chr1:111668100 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-23234C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668100 | |||||||
| chr1:111668106 | A | G | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27-23228A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668106 | |||||||
| chr1:111668147 | A | G | 20 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27-23187A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668147 | |||||||
| chr1:111668352 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-27-22982T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668352 | |||||||
| chr1:111668410 | A | G | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-22924A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668410 | |||||||
| chr1:111668427 | A | G | 1 | a0001c0001t0007g0273 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-27-22907A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668427 | |||||||
| chr1:111668784 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-27-22550T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668784 | |||||||
| chr1:111668889 | G | T | 1 | a0001c0001t0011g0261 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-27-22445G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111668889 | |||||||
| chr1:111669009 | A | G | 1 | a0001c0001t0004g0340 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-27-22325A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669009 | |||||||
| chr1:111669038 | A | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-22296A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669038 | |||||||
| chr1:111669040 | A | AAG | 32 | a0001c0001t0001g0136 a0001c0001t0002g0040 a0001c0001t0002g0041 others(29): Show |
32 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.-27-22293_-27-2229 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111669040 | ||||||
| chr1:111669040 | A | AG | 292 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(289): Show |
306 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.-27-22294_-27-2229 others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669040 | |||||||
| chr1:111669040 | A | G | 2 | a0001c0001t0002g0241 a0001c0001t0005g0022 |
2 | NA18959.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-27-22294A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669040 | |||||||
| chr1:111669043 | AAAAAAG | A | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-22287_-27-2228 others(10): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111669043 | ||||||
| chr1:111669088 | A | G | 1 | a0001c0001t0001g0080 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-27-22246A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669088 | |||||||
| chr1:111669155 | A | G | 121 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(118): Show |
132 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-27-22179A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669155 | |||||||
| chr1:111669254 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-27-22080A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669254 | |||||||
| chr1:111669329 | G | A | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-22005G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669329 | |||||||
| chr1:111669402 | G | T | 8 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(5): Show |
10 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27-21932G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669402 | |||||||
| chr1:111669679 | A | G | 75 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(72): Show |
85 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.-27-21655A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669679 | |||||||
| chr1:111669854 | A | T | 1 | a0001c0001t0022g0209 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-27-21480A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111669854 | |||||||
| chr1:111670080 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-27-21254G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670080 | |||||||
| chr1:111670244 | G | A | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-27-21090G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670244 | |||||||
| chr1:111670288 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-27-21046A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670288 | |||||||
| chr1:111670311 | A | G | 6 | a0001c0001t0003g0193 a0001c0001t0003g0205 a0001c0001t0003g0206 others(3): Show |
6 | NA18945.hp2 NA18948.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-21023A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670311 | |||||||
| chr1:111670351 | G | C | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-20983G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670351 | |||||||
| chr1:111670479 | T | A | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-20855T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670479 | |||||||
| chr1:111670647 | G | T | 5 | a0001c0001t0006g0286 a0001c0001t0006g0288 a0001c0001t0006g0289 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-20687G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670647 | |||||||
| chr1:111670764 | T | G | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-20570T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670764 | |||||||
| chr1:111670834 | T | C | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-20500T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111670834 | |||||||
| chr1:111671018 | T | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-20316T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671018 | |||||||
| chr1:111671054 | T | C | 5 | a0001c0001t0004g0332 a0001c0001t0004g0338 a0001c0001t0004g0348 others(2): Show |
5 | HG00673.hp2 HG02071.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-20280T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671054 | |||||||
| chr1:111671120 | G | A | 1 | a0001c0001t0008g0280 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-27-20214G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671120 | |||||||
| chr1:111671266 | A | G | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-20068A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671266 | |||||||
| chr1:111671467 | TTTTC | T | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-19855_-27-1985 others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111671467 | ||||||
| chr1:111671483 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-19851T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671483 | |||||||
| chr1:111671507 | T | C | 218 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(215): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.-27-19827T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671507 | |||||||
| chr1:111671530 | G | A | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.-27-19804G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671530 | |||||||
| chr1:111671589 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-27-19745C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671589 | |||||||
| chr1:111671623 | T | C | 5 | a0001c0001t0006g0286 a0001c0001t0006g0288 a0001c0001t0006g0289 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-19711T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671623 | |||||||
| chr1:111671634 | G | C | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-19700G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671634 | |||||||
| chr1:111671830 | A | T | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-19504A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111671830 | |||||||
| chr1:111672048 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-19286T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672048 | |||||||
| chr1:111672099 | C | CTTAAG | 57 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(54): Show |
57 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-27-19232_-27-1922 others(9): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111672099 | ||||||
| chr1:111672393 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-27-18941A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672393 | |||||||
| chr1:111672420 | T | G | 9 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-27-18914T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672420 | |||||||
| chr1:111672454 | A | G | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-18880A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672454 | |||||||
| chr1:111672486 | G | T | 1 | a0001c0001t0001g0072 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-27-18848G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672486 | |||||||
| chr1:111672590 | A | G | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-27-18744A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672590 | |||||||
| chr1:111672597 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-27-18737G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672597 | |||||||
| chr1:111672601 | G | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0024 a0001c0001t0005g0025 others(2): Show |
5 | NA18950.hp1 NA18968.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-18733G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672601 | |||||||
| chr1:111672831 | A | G | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-27-18503A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672831 | |||||||
| chr1:111672887 | A | C | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-27-18447A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672887 | |||||||
| chr1:111672911 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-18423C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111672911 | |||||||
| chr1:111673205 | C | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-18129C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111673205 | |||||||
| chr1:111673733 | A | G | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(2): Show |
5 | HG01433.hp2 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-17601A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111673733 | |||||||
| chr1:111673816 | G | A | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.-27-17518G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111673816 | |||||||
| chr1:111673971 | C | T | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27-17363C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111673971 | |||||||
| chr1:111674066 | T | C | 4 | a0001c0001t0002g0050 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | NA18953.hp2 NA18961.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-17268T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674066 | |||||||
| chr1:111674207 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-27-17127G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674207 | |||||||
| chr1:111674221 | G | A | 1 | a0001c0001t0004g0329 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-27-17113G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674221 | |||||||
| chr1:111674289 | C | CT | 144 | a0001c0001t0001g0166 a0001c0001t0002g0012 a0001c0001t0002g0013 others(141): Show |
155 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.-27-17033dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111674289 | ||||||
| chr1:111674289 | C | CTT | 10 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-17034_-27-1703 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111674289 | ||||||
| chr1:111674300 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-27-17034T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674300 | |||||||
| chr1:111674339 | C | T | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-16995C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674339 | |||||||
| chr1:111674356 | A | C | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-16978A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674356 | |||||||
| chr1:111674368 | C | T | 1 | a0001c0001t0024g0315 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-27-16966C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674368 | |||||||
| chr1:111674452 | C | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-16882C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674452 | |||||||
| chr1:111674477 | A | G | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-16857A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674477 | |||||||
| chr1:111674684 | A | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-16650A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674684 | |||||||
| chr1:111674704 | A | G | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-27-16630A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111674704 | |||||||
| chr1:111675022 | T | A | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-16312T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675022 | |||||||
| chr1:111675211 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-27-16123G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675211 | |||||||
| chr1:111675247 | C | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-16087C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675247 | |||||||
| chr1:111675252 | C | T | 1 | a0001c0001t0022g0209 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-27-16082C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675252 | |||||||
| chr1:111675253 | G | A | 1 | a0001c0001t0015g0314 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-27-16081G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675253 | |||||||
| chr1:111675337 | T | C | 1 | a0001c0001t0004g0330 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-27-15997T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675337 | |||||||
| chr1:111675418 | G | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-15916G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675418 | |||||||
| chr1:111675450 | C | T | 1 | a0001c0001t0003g0175 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-27-15884C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675450 | |||||||
| chr1:111675470 | TAAAAAAA others(7): Show |
T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-15853_-27-1584 others(18): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111675470 | ||||||
| chr1:111675479 | CAA | C | 5 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(2): Show |
7 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-15852_-27-1585 others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111675479 | ||||||
| chr1:111675534 | A | G | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-15800A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675534 | |||||||
| chr1:111675642 | T | A | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-27-15692T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675642 | |||||||
| chr1:111675665 | G | A | 2 | a0001c0001t0011g0259 a0001c0001t0011g0260 |
2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-27-15669G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675665 | |||||||
| chr1:111675839 | G | A | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-27-15495G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675839 | |||||||
| chr1:111675850 | C | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-15484C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675850 | |||||||
| chr1:111675952 | T | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-15382T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111675952 | |||||||
| chr1:111676049 | C | T | 3 | a0001c0001t0003g0218 a0001c0001t0014g0284 a0001c0001t0014g0285 |
3 | HG02572.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-27-15285C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111676049 | |||||||
| chr1:111676145 | C | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-15189C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111676145 | |||||||
| chr1:111676210 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0104 |
2 | HG00408.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-27-15124G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111676210 | |||||||
| chr1:111676498 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-14836T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111676498 | |||||||
| chr1:111676600 | A | C | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-14734A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111676600 | |||||||
| chr1:111676716 | C | T | 75 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(72): Show |
85 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.-27-14618C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111676716 | |||||||
| chr1:111676796 | A | AT | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-14525dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111676796 | ||||||
| chr1:111677046 | G | A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-14288G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677046 | |||||||
| chr1:111677090 | G | A | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-14244G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677090 | |||||||
| chr1:111677357 | A | C | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-27-13977A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677357 | |||||||
| chr1:111677370 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-13964A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677370 | |||||||
| chr1:111677379 | C | CTTGTG | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-13952_-27-1394 others(9): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111677379 | ||||||
| chr1:111677390 | G | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-13944G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677390 | |||||||
| chr1:111677494 | A | G | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-13840A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677494 | |||||||
| chr1:111677628 | C | G | 2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-27-13706C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677628 | |||||||
| chr1:111677670 | C | T | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-27-13664C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677670 | |||||||
| chr1:111677721 | A | G | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27-13613A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111677721 | |||||||
| chr1:111678016 | G | A | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-13318G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678016 | |||||||
| chr1:111678094 | T | A | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-13240T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678094 | |||||||
| chr1:111678180 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-27-13154T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678180 | |||||||
| chr1:111678186 | T | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-13148T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678186 | |||||||
| chr1:111678323 | A | G | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-13011A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678323 | |||||||
| chr1:111678387 | T | A | 1 | a0001c0001t0002g0046 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-27-12947T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678387 | |||||||
| chr1:111678388 | A | T | 8 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(5): Show |
8 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-12946A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678388 | |||||||
| chr1:111678701 | G | A | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01070.hp1 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-12633G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678701 | |||||||
| chr1:111678762 | G | GT | 64 | a0001c0001t0001g0101 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
64 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(61): Show |
intron_variant | MODIFIER | c.-27-12561dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111678762 | ||||||
| chr1:111678799 | C | T | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-12535C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678799 | |||||||
| chr1:111678892 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-27-12442C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678892 | |||||||
| chr1:111678918 | C | T | 5 | a0001c0001t0006g0286 a0001c0001t0006g0288 a0001c0001t0006g0289 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-12416C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678918 | |||||||
| chr1:111678994 | C | T | 12 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG02015.hp2 NA18944.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27-12340C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111678994 | |||||||
| chr1:111679028 | A | G | 12 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG02015.hp2 NA18944.hp1 NA18953.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27-12306A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679028 | |||||||
| chr1:111679089 | G | A | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-12245G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679089 | |||||||
| chr1:111679123 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-27-12211G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679123 | |||||||
| chr1:111679257 | G | A | 33 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(30): Show |
33 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.-27-12077G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679257 | |||||||
| chr1:111679264 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0151 |
2 | NA18942.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-27-12070G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679264 | |||||||
| chr1:111679292 | C | T | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-12042C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679292 | |||||||
| chr1:111679320 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-27-12014C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679320 | |||||||
| chr1:111679405 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-27-11929G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679405 | |||||||
| chr1:111679412 | T | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-11922T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679412 | |||||||
| chr1:111679497 | T | C | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-11837T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679497 | |||||||
| chr1:111679497 | T | TTTTTC | 37 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(34): Show |
38 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-27-11817_-27-1181 others(9): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111679497 | ||||||
| chr1:111679497 | T | TTTTTCTT others(3): Show |
3 | a0001c0001t0004g0329 a0001c0001t0004g0337 a0001c0001t0004g0341 |
3 | HG01109.hp1 HG02165.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-27-11822_-27-1181 others(14): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111679497 | ||||||
| chr1:111679522 | T | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-11812T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679522 | |||||||
| chr1:111679556 | C | G | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-11778C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679556 | |||||||
| chr1:111679633 | A | T | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-27-11701A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679633 | |||||||
| chr1:111679657 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-11677C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679657 | |||||||
| chr1:111679777 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-27-11557C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679777 | |||||||
| chr1:111679997 | T | C | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-11337T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111679997 | |||||||
| chr1:111680080 | T | C | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-27-11254T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680080 | |||||||
| chr1:111680181 | A | G | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.-27-11153A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680181 | |||||||
| chr1:111680214 | G | A | 2 | a0001c0001t0004g0327 a0001c0001t0004g0335 |
2 | HG00558.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-27-11120G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680214 | |||||||
| chr1:111680237 | A | C | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-27-11097A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680237 | |||||||
| chr1:111680285 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-27-11049G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680285 | |||||||
| chr1:111680302 | C | T | 9 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(6): Show |
9 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-27-11032C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680302 | |||||||
| chr1:111680333 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-11001C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680333 | |||||||
| chr1:111680521 | C | T | 2 | a0001c0001t0002g0322 a0001c0001t0002g0325 |
2 | NA18955.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-27-10813C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680521 | |||||||
| chr1:111680532 | C | T | 121 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(118): Show |
132 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-27-10802C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680532 | |||||||
| chr1:111680604 | G | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-10730G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680604 | |||||||
| chr1:111680798 | TAGAAGGA others(8): Show |
T | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-27-10519_-27-1050 others(19): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111680798 | ||||||
| chr1:111680839 | C | G | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-10495C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680839 | |||||||
| chr1:111680984 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-10350C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111680984 | |||||||
| chr1:111681021 | C | T | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-10313C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681021 | |||||||
| chr1:111681064 | G | T | 2 | a0001c0001t0007g0264 a0001c0001t0019g0011 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-27-10270G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681064 | |||||||
| chr1:111681216 | C | G | 2 | a0001c0001t0007g0268 a0001c0001t0007g0270 |
2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-27-10118C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681216 | |||||||
| chr1:111681232 | A | C | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-10102A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681232 | |||||||
| chr1:111681243 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-27-10091G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681243 | |||||||
| chr1:111681334 | T | C | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-10000T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681334 | |||||||
| chr1:111681389 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-27-9945A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681389 | |||||||
| chr1:111681592 | A | G | 1 | a0001c0001t0002g0292 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-27-9742A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681592 | |||||||
| chr1:111681696 | C | T | 101 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(98): Show |
112 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-27-9638C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681696 | |||||||
| chr1:111681715 | C | T | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27-9619C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681715 | |||||||
| chr1:111681734 | C | T | 1 | a0001c0001t0004g0352 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-27-9600C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681734 | |||||||
| chr1:111681859 | C | T | 2 | a0001c0001t0011g0009 a0001c0001t0011g0261 |
3 | HG01192.hp1 HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-27-9475C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681859 | |||||||
| chr1:111681915 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-9419C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681915 | |||||||
| chr1:111681927 | C | T | 8 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-9407C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111681927 | |||||||
| chr1:111682034 | T | C | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-9300T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682034 | |||||||
| chr1:111682096 | G | A | 1 | a0001c0001t0005g0032 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-27-9238G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682096 | |||||||
| chr1:111682137 | C | G | 1 | a0001c0001t0002g0307 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-27-9197C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682137 | |||||||
| chr1:111682219 | G | A | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-9115G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682219 | |||||||
| chr1:111682290 | A | T | 1 | a0001c0001t0004g0362 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-27-9044A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682290 | |||||||
| chr1:111682293 | T | G | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(2): Show |
5 | HG01433.hp2 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-9041T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682293 | |||||||
| chr1:111682504 | C | CA | 70 | a0001c0001t0001g0083 a0001c0001t0001g0144 a0001c0001t0001g0159 others(67): Show |
72 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-27-8816dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111682504 | ||||||
| chr1:111682504 | CA | C | 33 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(30): Show |
33 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.-27-8816delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111682504 | ||||||
| chr1:111682521 | G | A | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-8813G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682521 | |||||||
| chr1:111682524 | G | A | 11 | a0001c0001t0001g0078 a0001c0001t0001g0111 a0001c0001t0001g0112 others(8): Show |
11 | HG00673.hp1 HG02027.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-8810G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682524 | |||||||
| chr1:111682529 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-8805C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682529 | |||||||
| chr1:111682617 | A | G | 1 | a0001c0001t0002g0246 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-27-8717A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682617 | |||||||
| chr1:111682627 | A | C | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-8707A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682627 | |||||||
| chr1:111682931 | A | G | 8 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG00423.hp1 HG01081.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-8403A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682931 | |||||||
| chr1:111682955 | G | A | 1 | a0001c0001t0022g0209 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-27-8379G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682955 | |||||||
| chr1:111682961 | A | C | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-8373A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682961 | |||||||
| chr1:111682986 | G | A | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-8348G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111682986 | |||||||
| chr1:111683034 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-27-8300A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683034 | |||||||
| chr1:111683065 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-27-8269A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683065 | |||||||
| chr1:111683249 | A | G | 1 | a0001c0001t0006g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-27-8085A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683249 | |||||||
| chr1:111683316 | A | G | 106 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(103): Show |
107 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-27-8018A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683316 | |||||||
| chr1:111683342 | GAC | G | 10 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-7988_-27-7987d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111683342 | ||||||
| chr1:111683385 | G | T | 1 | a0001c0001t0002g0230 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-27-7949G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683385 | |||||||
| chr1:111683426 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-27-7908A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683426 | |||||||
| chr1:111683478 | G | A | 8 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(5): Show |
10 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27-7856G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683478 | |||||||
| chr1:111683615 | A | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-7719A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683615 | |||||||
| chr1:111683816 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-7518C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683816 | |||||||
| chr1:111683959 | C | T | 20 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.-27-7375C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111683959 | |||||||
| chr1:111684056 | A | G | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-27-7278A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684056 | |||||||
| chr1:111684209 | T | G | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-7125T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684209 | |||||||
| chr1:111684296 | A | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-7038A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684296 | |||||||
| chr1:111684399 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-6935C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684399 | |||||||
| chr1:111684441 | C | T | 63 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(60): Show |
65 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27-6893C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684441 | |||||||
| chr1:111684501 | C | T | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.-27-6833C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684501 | |||||||
| chr1:111684525 | A | C | 1 | a0001c0001t0003g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-27-6809A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684525 | |||||||
| chr1:111684687 | C | T | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-27-6647C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684687 | |||||||
| chr1:111684710 | A | G | 4 | a0001c0001t0006g0288 a0001c0001t0006g0289 a0001c0001t0006g0290 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-6624A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684710 | |||||||
| chr1:111684730 | G | GCT | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-6602_-27-6601d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111684730 | ||||||
| chr1:111684749 | T | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-6585T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684749 | |||||||
| chr1:111684778 | G | A | 191 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-27-6556G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684778 | |||||||
| chr1:111684980 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-27-6354A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111684980 | |||||||
| chr1:111685095 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-27-6239A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685095 | |||||||
| chr1:111685319 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-27-6015A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685319 | |||||||
| chr1:111685374 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-5960C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685374 | |||||||
| chr1:111685433 | AAG | A | 113 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(110): Show |
123 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.-27-5899_-27-5898d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111685433 | ||||||
| chr1:111685434 | AG | A | 220 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(217): Show |
224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.-27-5899delG | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685434 | |||||||
| chr1:111685435 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-27-5899G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685435 | |||||||
| chr1:111685438 | A | C | 1 | a0001c0001t0001g0109 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-27-5896A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685438 | |||||||
| chr1:111685443 | C | G | 8 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-5891C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685443 | |||||||
| chr1:111685459 | C | T | 2 | a0001c0001t0008g0274 a0001c0001t0008g0275 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-27-5875C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685459 | |||||||
| chr1:111685481 | C | G | 24 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-27-5853C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685481 | |||||||
| chr1:111685682 | T | C | 6 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0253 others(3): Show |
6 | HG02257.hp1 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-5652T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685682 | |||||||
| chr1:111685852 | T | C | 28 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(25): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-27-5482T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685852 | |||||||
| chr1:111685855 | CAGAGACT others(14): Show |
C | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-27-5477_-27-5457d others(23): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111685855 | ||||||
| chr1:111685871 | A | T | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-5463A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685871 | |||||||
| chr1:111685946 | G | T | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(2): Show |
5 | HG01433.hp2 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-5388G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685946 | |||||||
| chr1:111685952 | G | A | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-5382G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111685952 | |||||||
| chr1:111686038 | A | G | 3 | a0001c0001t0004g0328 a0001c0001t0004g0329 a0001c0001t0004g0347 |
3 | HG02040.hp1 HG02165.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.-27-5296A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686038 | |||||||
| chr1:111686194 | A | G | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-27-5140A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686194 | |||||||
| chr1:111686202 | A | C | 4 | a0001c0001t0003g0008 a0001c0001t0003g0194 a0001c0001t0003g0200 others(1): Show |
5 | HG02132.hp1 NA18966.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-5132A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686202 | |||||||
| chr1:111686233 | C | G | 10 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-5101C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686233 | |||||||
| chr1:111686235 | C | T | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(2): Show |
5 | HG01433.hp2 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-5099C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686235 | |||||||
| chr1:111686257 | A | T | 10 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-5077A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686257 | |||||||
| chr1:111686372 | C | T | 9 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0250 others(6): Show |
9 | HG02145.hp1 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-27-4962C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686372 | |||||||
| chr1:111686390 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-27-4944G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686390 | |||||||
| chr1:111686408 | C | T | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-4926C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686408 | |||||||
| chr1:111686492 | T | C | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-4842T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686492 | |||||||
| chr1:111686558 | G | T | 2 | a0001c0001t0007g0264 a0001c0001t0019g0011 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-27-4776G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686558 | |||||||
| chr1:111686580 | A | G | 6 | a0001c0001t0002g0227 a0001c0001t0002g0229 a0001c0001t0002g0230 others(3): Show |
6 | HG00408.hp1 HG02135.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-4754A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686580 | |||||||
| chr1:111686597 | G | A | 1 | a0001c0001t0003g0208 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-27-4737G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686597 | |||||||
| chr1:111686638 | T | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(105): Show |
109 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.-27-4696T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686638 | |||||||
| chr1:111686690 | C | CA | 107 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0112 others(104): Show |
108 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.-27-4621dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111686690 | ||||||
| chr1:111686690 | C | CAA | 190 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(187): Show |
202 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.-27-4622_-27-4621d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111686690 | ||||||
| chr1:111686690 | C | CAAA | 23 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0077 others(20): Show |
23 | HG00423.hp1 HG00544.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-27-4623_-27-4621d others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111686690 | ||||||
| chr1:111686963 | G | A | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-4371G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111686963 | |||||||
| chr1:111687184 | ATACT | A | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-4148_-27-4145d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111687184 | ||||||
| chr1:111687208 | A | AT | 29 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(26): Show |
29 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.-27-4109dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111687208 | ||||||
| chr1:111687208 | A | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-4126A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687208 | |||||||
| chr1:111687208 | AT | A | 193 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(190): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.-27-4109delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111687208 | ||||||
| chr1:111687208 | ATT | A | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-4110_-27-4109d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111687208 | ||||||
| chr1:111687212 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-27-4122T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687212 | |||||||
| chr1:111687213 | T | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(42): Show |
53 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.-27-4121T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687213 | |||||||
| chr1:111687239 | G | A | 33 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(30): Show |
33 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.-27-4095G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687239 | |||||||
| chr1:111687487 | C | T | 2 | a0001c0001t0008g0274 a0001c0001t0008g0275 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-27-3847C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687487 | |||||||
| chr1:111687588 | A | G | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-3746A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687588 | |||||||
| chr1:111687597 | A | G | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-3737A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687597 | |||||||
| chr1:111687646 | CTT | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-3687_-27-3686d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687646 | |||||||
| chr1:111687728 | T | C | 1 | a0001c0001t0005g0004 | 2 | NA18983.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-27-3606T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687728 | |||||||
| chr1:111687774 | G | A | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-3560G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687774 | |||||||
| chr1:111687861 | A | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-3473A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111687861 | |||||||
| chr1:111688009 | A | G | 1 | a0001c0001t0008g0280 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-27-3325A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688009 | |||||||
| chr1:111688026 | C | CA | 136 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0067 others(133): Show |
137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.-27-3285dupA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688026 | ||||||
| chr1:111688026 | C | CAA | 94 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0084 others(91): Show |
98 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-27-3286_-27-3285d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688026 | ||||||
| chr1:111688026 | C | CAAA | 28 | a0001c0001t0002g0044 a0001c0001t0002g0056 a0001c0001t0002g0250 others(25): Show |
28 | HG00597.hp1 HG00621.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-3287_-27-3285d others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688026 | ||||||
| chr1:111688026 | CA | C | 6 | a0001c0001t0002g0303 a0001c0001t0002g0304 a0001c0001t0002g0305 others(3): Show |
6 | HG00140.hp2 HG01123.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-3285delA | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688026 | ||||||
| chr1:111688026 | CAAAA | C | 5 | a0001c0001t0003g0006 a0001c0001t0003g0175 a0001c0001t0003g0176 others(2): Show |
6 | NA18943.hp1 NA18954.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27-3288_-27-3285d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688026 | ||||||
| chr1:111688026 | CAAAAA | C | 39 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0007 others(36): Show |
46 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.-27-3289_-27-3285d others(7): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688026 | ||||||
| chr1:111688096 | G | A | 24 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-27-3238G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688096 | |||||||
| chr1:111688097 | C | CT | 182 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(179): Show |
194 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.-27-3222dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688097 | ||||||
| chr1:111688097 | C | CTT | 79 | a0001c0001t0001g0101 a0001c0001t0001g0132 a0001c0001t0002g0012 others(76): Show |
80 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.-27-3223_-27-3222d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688097 | ||||||
| chr1:111688190 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-3144C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688190 | |||||||
| chr1:111688206 | G | A | 34 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(31): Show |
34 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(31): Show |
intron_variant | MODIFIER | c.-27-3128G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688206 | |||||||
| chr1:111688265 | C | CTG | 3 | a0001c0001t0002g0293 a0001c0001t0015g0309 a0001c0001t0015g0314 |
3 | HG01256.hp1 HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-27-3035_-27-3034d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688265 | ||||||
| chr1:111688265 | CTGTG | C | 42 | a0001c0001t0002g0295 a0001c0001t0002g0297 a0001c0001t0004g0010 others(39): Show |
43 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.-27-3037_-27-3034d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688265 | ||||||
| chr1:111688265 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-27-3043_-27-3034d others(12): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688265 | ||||||
| chr1:111688293 | G | A | 215 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(212): Show |
218 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-27-3041G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688293 | |||||||
| chr1:111688293 | G | GTA | 56 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0138 others(53): Show |
65 | HG00280.hp2 HG00609.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.-27-3040_-27-3039i others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688293 | ||||||
| chr1:111688293 | G | GTGTA | 5 | a0001c0001t0003g0196 a0001c0001t0003g0199 a0001c0001t0003g0202 others(2): Show |
5 | HG00423.hp2 HG02572.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-3038_-27-3037i others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688293 | ||||||
| chr1:111688293 | G | GTGTGTA | 6 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(3): Show |
6 | HG03927.hp1 HG03942.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-3036_-27-3035i others(8): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688293 | ||||||
| chr1:111688297 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-27-3037G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688297 | |||||||
| chr1:111688299 | G | A | 283 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(280): Show |
295 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.-27-3035G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688299 | |||||||
| chr1:111688299 | G | GTATGTGT others(1): Show |
12 | a0001c0001t0007g0264 a0001c0001t0007g0272 a0001c0001t0008g0274 others(9): Show |
12 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27-3032_-27-3031i others(10): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688299 | ||||||
| chr1:111688299 | G | GTGTATGT others(3): Show |
8 | a0001c0001t0007g0271 a0001c0001t0008g0276 a0001c0001t0009g0003 others(5): Show |
10 | HG01175.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-3034_-27-3033i others(12): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688299 | ||||||
| chr1:111688299 | G | GTGTGTAT others(5): Show |
24 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0043 others(21): Show |
24 | HG00280.hp1 HG01069.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.-27-3034_-27-3033i others(14): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688299 | ||||||
| chr1:111688299 | G | GTGTGTGT others(7): Show |
3 | a0001c0001t0002g0042 a0001c0001t0002g0063 a0001c0001t0002g0323 |
3 | HG01099.hp1 HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-27-3034_-27-3033i others(16): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688299 | ||||||
| chr1:111688299 | G | GTGTGTGT others(11): Show |
3 | a0001c0001t0002g0322 a0001c0001t0002g0324 a0001c0001t0002g0325 |
3 | HG00544.hp1 NA18955.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-27-3034_-27-3033i others(20): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688299 | ||||||
| chr1:111688299 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0002g0326 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-27-3034_-27-3033i others(22): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688299 | ||||||
| chr1:111688307 | A | T | 2 | a0001c0001t0002g0297 a0001c0001t0004g0362 |
2 | HG02647.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-27-3027A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688307 | |||||||
| chr1:111688320 | TTTC | T | 26 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(23): Show |
28 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-27-3011_-27-3009d others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688320 | ||||||
| chr1:111688323 | C | CT | 93 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(90): Show |
102 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.-27-2997dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688323 | ||||||
| chr1:111688338 | G | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-2996G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688338 | |||||||
| chr1:111688345 | A | T | 3 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG00280.hp2 HG01256.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-27-2989A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688345 | |||||||
| chr1:111688388 | C | T | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-27-2946C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688388 | |||||||
| chr1:111688437 | C | T | 27 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(24): Show |
27 | HG00423.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-27-2897C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688437 | |||||||
| chr1:111688482 | G | T | 4 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(1): Show |
5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27-2852G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688482 | |||||||
| chr1:111688540 | G | A | 8 | a0001c0001t0001g0087 a0001c0001t0001g0094 a0001c0001t0001g0101 others(5): Show |
8 | HG00597.hp2 NA18942.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27-2794G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688540 | |||||||
| chr1:111688609 | C | T | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-27-2725C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688609 | |||||||
| chr1:111688802 | G | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0172 |
2 | HG02922.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-27-2532G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688802 | |||||||
| chr1:111688808 | G | GT | 67 | a0001c0001t0001g0107 a0001c0001t0002g0012 a0001c0001t0002g0013 others(64): Show |
67 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-27-2513dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688808 | ||||||
| chr1:111688810 | TTTTTTTT others(5): Show |
T | 99 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(96): Show |
110 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.-27-2504_-27-2493d others(14): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688810 | ||||||
| chr1:111688811 | TTTTTTTT others(4): Show |
T | 3 | a0001c0001t0003g0183 a0001c0001t0003g0205 a0001c0001t0005g0024 |
3 | HG03831.hp1 NA19001.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-27-2512_-27-2502d others(13): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688811 | ||||||
| chr1:111688814 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-27-2520T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688814 | |||||||
| chr1:111688822 | G | GT | 45 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0108 others(42): Show |
47 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-27-2501dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111688822 | ||||||
| chr1:111688822 | G | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0051 |
2 | NA18973.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.-27-2512G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688822 | |||||||
| chr1:111688830 | T | G | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.-27-2504T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688830 | |||||||
| chr1:111688846 | T | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-2488T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688846 | |||||||
| chr1:111688903 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-27-2431C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111688903 | |||||||
| chr1:111689044 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-27-2290C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689044 | |||||||
| chr1:111689524 | G | A | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-27-1810G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689524 | |||||||
| chr1:111689595 | G | A | 1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-27-1739G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689595 | |||||||
| chr1:111689664 | C | G | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-27-1670C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689664 | |||||||
| chr1:111689732 | C | T | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.-27-1602C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689732 | |||||||
| chr1:111689755 | C | T | 1 | a0001c0001t0004g0347 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-27-1579C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689755 | |||||||
| chr1:111689797 | G | C | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-27-1537G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689797 | |||||||
| chr1:111689897 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-27-1437C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689897 | |||||||
| chr1:111689922 | C | T | 28 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(25): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-27-1412C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689922 | |||||||
| chr1:111689967 | C | T | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-27-1367C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689967 | |||||||
| chr1:111689978 | A | G | 1 | a0001c0001t0002g0300 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-27-1356A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111689978 | |||||||
| chr1:111690428 | T | A | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-27-906T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111690428 | |||||||
| chr1:111690431 | A | G | 4 | a0001c0001t0006g0288 a0001c0001t0006g0289 a0001c0001t0006g0290 others(1): Show |
4 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-903A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111690431 | |||||||
| chr1:111690722 | C | T | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.-27-612C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111690722 | |||||||
| chr1:111690779 | A | G | 28 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(25): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-27-555A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111690779 | |||||||
| chr1:111690838 | T | C | 1 | a0001c0001t0012g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-27-496T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111690838 | |||||||
| chr1:111690926 | A | G | 363 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(360): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-27-408A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111690926 | |||||||
| chr1:111690930 | A | G | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-27-404A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111690930 | |||||||
| chr1:111691119 | T | C | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.-27-215T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111691119 | |||||||
| chr1:111691176 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-27-158G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | chr1 | 111691176 | |||||||
| chr1:111691240 | AAAAC | A | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(2): Show |
5 | HG01433.hp2 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-90_-27-87delCA others(2): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 111691240 | ||||||
| chr1:111691446 | T | A | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.57+29T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691446 | |||||||
| chr1:111691462 | G | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.57+45G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691462 | |||||||
| chr1:111691490 | T | A | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.57+73T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691490 | |||||||
| chr1:111691556 | A | T | 1 | a0001c0001t0002g0231 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.57+139A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691556 | |||||||
| chr1:111691593 | C | T | 28 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(25): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.57+176C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691593 | |||||||
| chr1:111691838 | G | A | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.57+421G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691838 | |||||||
| chr1:111691844 | A | G | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+427A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691844 | |||||||
| chr1:111691954 | C | A | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.57+537C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111691954 | |||||||
| chr1:111692076 | G | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+659G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692076 | |||||||
| chr1:111692136 | G | A | 2 | a0001c0001t0004g0337 a0001c0001t0004g0341 |
2 | HG01109.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.57+719G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692136 | |||||||
| chr1:111692166 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.57+749T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692166 | |||||||
| chr1:111692183 | G | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(48): Show |
52 | HG00423.hp1 HG00597.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.57+766G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692183 | |||||||
| chr1:111692355 | T | C | 1 | a0001c0001t0008g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.57+938T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692355 | |||||||
| chr1:111692483 | T | C | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1066T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692483 | |||||||
| chr1:111692675 | G | T | 31 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(28): Show |
31 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.57+1258G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692675 | |||||||
| chr1:111692786 | T | G | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.57+1369T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692786 | |||||||
| chr1:111692840 | A | T | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1423A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692840 | |||||||
| chr1:111692853 | A | G | 1 | a0001c0001t0005g0014 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.57+1436A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692853 | |||||||
| chr1:111692957 | A | G | 1 | a0001c0001t0002g0320 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.57+1540A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111692957 | |||||||
| chr1:111693208 | A | G | 1 | a0001c0001t0003g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.57+1791A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111693208 | |||||||
| chr1:111693365 | A | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG02083.hp2 NA19063.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.57+1948A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111693365 | |||||||
| chr1:111693483 | G | T | 1 | a0001c0001t0002g0046 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.58-1858G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111693483 | |||||||
| chr1:111693680 | T | A | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.58-1661T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111693680 | |||||||
| chr1:111693716 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.58-1625A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111693716 | |||||||
| chr1:111693885 | G | A | 1 | a0001c0001t0004g0355 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.58-1456G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111693885 | |||||||
| chr1:111693897 | C | CT | 61 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(58): Show |
71 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.58-1430dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 111693897 | ||||||
| chr1:111693897 | C | CTT | 87 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(84): Show |
88 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.58-1431_58-1430dup others(2): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 111693897 | ||||||
| chr1:111693897 | C | CTTT | 10 | a0001c0001t0008g0274 a0001c0001t0008g0275 a0001c0001t0008g0276 others(7): Show |
10 | HG02258.hp2 HG02280.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-1432_58-1430dup others(3): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 111693897 | ||||||
| chr1:111693927 | A | G | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58-1414A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111693927 | |||||||
| chr1:111694064 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-1277A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111694064 | |||||||
| chr1:111694185 | C | T | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG02083.hp2 NA19063.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.58-1156C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111694185 | |||||||
| chr1:111694416 | C | A | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.58-925C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111694416 | |||||||
| chr1:111694459 | C | T | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-882C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111694459 | |||||||
| chr1:111694682 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0129 |
2 | HG02056.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.58-659A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111694682 | |||||||
| chr1:111694783 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.58-558T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111694783 | |||||||
| chr1:111695001 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.58-340A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111695001 | |||||||
| chr1:111695209 | A | ATAATAT | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.58-130_58-129insAT others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 111695209 | ||||||
| chr1:111695293 | A | T | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.58-48A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 2/7 | chr1 | 111695293 | |||||||
| chr1:111695594 | A | G | 8 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+185A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111695594 | |||||||
| chr1:111695791 | T | A | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.126+382T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111695791 | |||||||
| chr1:111695876 | T | C | 1 | a0001c0001t0004g0331 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.126+467T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111695876 | |||||||
| chr1:111695880 | A | C | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+471A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111695880 | |||||||
| chr1:111695935 | A | G | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+526A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111695935 | |||||||
| chr1:111696428 | A | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(105): Show |
109 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.127-1013A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111696428 | |||||||
| chr1:111696505 | G | T | 1 | a0001c0001t0015g0314 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.127-936G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111696505 | |||||||
| chr1:111696515 | G | A | 1 | a0001c0001t0024g0315 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.127-926G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111696515 | |||||||
| chr1:111696699 | G | A | 218 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(215): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.127-742G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111696699 | |||||||
| chr1:111696826 | A | G | 5 | a0001c0001t0002g0293 a0001c0001t0002g0295 a0001c0001t0002g0296 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-615A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111696826 | |||||||
| chr1:111696863 | C | T | 1 | a0001c0001t0003g0187 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.127-578C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111696863 | |||||||
| chr1:111697038 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127-403C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111697038 | |||||||
| chr1:111697100 | T | C | 61 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(58): Show |
61 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.127-341T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111697100 | |||||||
| chr1:111697229 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(105): Show |
109 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.127-212C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | chr1 | 111697229 | |||||||
| chr1:111697416 | C | CT | 97 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0108 others(94): Show |
98 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.127-11dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr1 | 111697416 | ||||||
| chr1:111697503 | G | A | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.183+6G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111697503 | |||||||
| chr1:111697672 | T | C | 1 | a0001c0001t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.183+175T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111697672 | |||||||
| chr1:111697894 | C | G | 1 | a0001c0001t0004g0358 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.183+397C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111697894 | |||||||
| chr1:111698035 | T | A | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.183+538T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698035 | |||||||
| chr1:111698072 | A | G | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.183+575A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698072 | |||||||
| chr1:111698181 | A | G | 5 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(2): Show |
7 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+684A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698181 | |||||||
| chr1:111698275 | G | A | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.183+778G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698275 | |||||||
| chr1:111698287 | G | T | 363 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(360): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.183+790G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698287 | |||||||
| chr1:111698366 | T | G | 1 | a0001c0001t0002g0062 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.183+869T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698366 | |||||||
| chr1:111698415 | C | T | 8 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0081 others(5): Show |
8 | HG00423.hp1 HG01081.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.183+918C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698415 | |||||||
| chr1:111698505 | G | T | 1 | a0001c0001t0033g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.183+1008G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698505 | |||||||
| chr1:111698614 | T | TTCCACTA others(322): Show |
1 | a0001c0001t0002g0258 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.183+1132_183+1133i others(331): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111698614 | ||||||
| chr1:111698727 | C | A | 3 | a0001c0001t0012g0154 a0001c0001t0012g0155 a0001c0001t0031g0153 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.183+1230C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698727 | |||||||
| chr1:111698780 | A | G | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.183+1283A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698780 | |||||||
| chr1:111698848 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.183+1351C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698848 | |||||||
| chr1:111698942 | C | CT | 146 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(143): Show |
148 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.183+1458dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111698942 | ||||||
| chr1:111698955 | T | A | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.183+1458T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111698955 | |||||||
| chr1:111699148 | A | G | 2 | a0001c0001t0008g0274 a0001c0001t0008g0275 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.183+1651A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699148 | |||||||
| chr1:111699173 | A | G | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.183+1676A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699173 | |||||||
| chr1:111699184 | T | G | 2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG03516.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.183+1687T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699184 | |||||||
| chr1:111699256 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.183+1759A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699256 | |||||||
| chr1:111699276 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0167 |
2 | NA18944.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.183+1779A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699276 | |||||||
| chr1:111699330 | C | A | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.183+1833C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699330 | |||||||
| chr1:111699366 | A | G | 23 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(20): Show |
24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.183+1869A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699366 | |||||||
| chr1:111699411 | G | A | 1 | a0001c0001t0004g0338 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.183+1914G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699411 | |||||||
| chr1:111699414 | T | A | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.183+1917T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699414 | |||||||
| chr1:111699463 | C | CT | 106 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0067 others(103): Show |
108 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.183+1982dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111699463 | ||||||
| chr1:111699463 | C | CTTT | 7 | a0001c0001t0008g0274 a0001c0001t0009g0003 a0001c0001t0009g0220 others(4): Show |
9 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.183+1980_183+1982d others(5): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111699463 | ||||||
| chr1:111699463 | C | CTTTT | 26 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(23): Show |
26 | HG01109.hp2 HG01243.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.183+1979_183+1982d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111699463 | ||||||
| chr1:111699463 | C | CTTTTTTT others(2): Show |
28 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(25): Show |
28 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.183+1974_183+1982d others(11): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111699463 | ||||||
| chr1:111699463 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0255 a0001c0001t0002g0256 a0001c0001t0002g0258 others(1): Show |
4 | HG02976.hp2 HG03516.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1973_183+1982d others(12): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111699463 | ||||||
| chr1:111699463 | CT | C | 10 | a0001c0001t0002g0042 a0001c0001t0002g0046 a0001c0001t0005g0027 others(7): Show |
10 | HG01069.hp1 HG01099.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+1982delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111699463 | ||||||
| chr1:111699463 | CTTTT | C | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.183+1979_183+1982d others(6): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111699463 | ||||||
| chr1:111699479 | T | TTTTTTTT others(1): Show |
38 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(35): Show |
39 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.183+1982_183+1983i others(10): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699479 | |||||||
| chr1:111699641 | T | A | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.183+2144T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699641 | |||||||
| chr1:111699642 | T | A | 158 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(155): Show |
169 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.183+2145T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699642 | |||||||
| chr1:111699697 | A | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0123 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.183+2200A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111699697 | |||||||
| chr1:111700070 | T | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.183+2573T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111700070 | |||||||
| chr1:111700413 | T | A | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.183+2916T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111700413 | |||||||
| chr1:111700448 | A | G | 24 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0229 others(21): Show |
24 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.184-2888A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111700448 | |||||||
| chr1:111700629 | G | A | 1 | a0001c0001t0004g0327 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.184-2707G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111700629 | |||||||
| chr1:111700849 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0115 a0001c0001t0001g0152 |
3 | NA18971.hp2 NA18999.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.184-2487T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111700849 | |||||||
| chr1:111700887 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.184-2449C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111700887 | |||||||
| chr1:111700991 | G | C | 1 | a0001c0001t0002g0298 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.184-2345G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111700991 | |||||||
| chr1:111701154 | CCT | C | 8 | a0001c0001t0003g0007 a0001c0001t0003g0179 a0001c0001t0003g0180 others(5): Show |
9 | HG00733.hp1 HG01496.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-2175_184-2174d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111701154 | ||||||
| chr1:111701196 | C | T | 1 | a0001c0001t0004g0357 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.184-2140C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701196 | |||||||
| chr1:111701201 | T | A | 1 | a0001c0001t0002g0246 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.184-2135T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701201 | |||||||
| chr1:111701258 | A | G | 1 | a0001c0001t0004g0349 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.184-2078A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701258 | |||||||
| chr1:111701325 | A | G | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.184-2011A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701325 | |||||||
| chr1:111701396 | T | C | 1 | a0001c0001t0006g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.184-1940T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701396 | |||||||
| chr1:111701478 | T | C | 1 | a0001c0001t0004g0352 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.184-1858T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701478 | |||||||
| chr1:111701482 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.184-1854T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701482 | |||||||
| chr1:111701558 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.184-1778A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701558 | |||||||
| chr1:111701594 | A | T | 3 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0191 |
3 | HG00280.hp2 HG01256.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.184-1742A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701594 | |||||||
| chr1:111701909 | A | G | 1 | a0001c0001t0004g0333 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.184-1427A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701909 | |||||||
| chr1:111701920 | A | G | 1 | a0001c0001t0003g0199 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.184-1416A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701920 | |||||||
| chr1:111701992 | T | C | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.184-1344T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111701992 | |||||||
| chr1:111702008 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.184-1328C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702008 | |||||||
| chr1:111702176 | A | T | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.184-1160A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702176 | |||||||
| chr1:111702304 | A | AAT | 6 | a0001c0001t0006g0286 a0001c0001t0006g0287 a0001c0001t0006g0288 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-1020_184-1019d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111702304 | ||||||
| chr1:111702309 | A | G | 1 | a0001c0001t0027g0265 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.184-1027A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702309 | |||||||
| chr1:111702437 | G | A | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.184-899G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702437 | |||||||
| chr1:111702466 | A | G | 1 | a0001c0001t0004g0361 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.184-870A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702466 | |||||||
| chr1:111702498 | C | T | 27 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(24): Show |
28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.184-838C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702498 | |||||||
| chr1:111702515 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.184-821A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702515 | |||||||
| chr1:111702585 | G | A | 2 | a0001c0001t0004g0010 a0001c0001t0004g0334 |
3 | NA18942.hp1 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.184-751G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702585 | |||||||
| chr1:111702727 | ATGT | A | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.184-605_184-603del others(3): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 111702727 | ||||||
| chr1:111702927 | T | C | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.184-409T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702927 | |||||||
| chr1:111702965 | T | C | 28 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(25): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.184-371T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111702965 | |||||||
| chr1:111703005 | A | G | 1 | a0001c0001t0002g0321 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.184-331A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111703005 | |||||||
| chr1:111703133 | G | A | 1 | a0001c0001t0005g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.184-203G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111703133 | |||||||
| chr1:111703172 | T | C | 1 | a0001c0001t0003g0006 | 2 | NA18954.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.184-164T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111703172 | |||||||
| chr1:111703245 | G | A | 2 | a0001c0001t0002g0226 a0001c0001t0002g0234 |
2 | HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.184-91G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 4/7 | chr1 | 111703245 | |||||||
| chr1:111703647 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.324+171G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111703647 | |||||||
| chr1:111703655 | A | T | 1 | a0001c0001t0005g0004 | 2 | NA18983.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.324+179A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111703655 | |||||||
| chr1:111703683 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.324+207A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111703683 | |||||||
| chr1:111703715 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.324+239C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111703715 | |||||||
| chr1:111703919 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.325-424C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111703919 | |||||||
| chr1:111703967 | T | A | 65 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(62): Show |
65 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(62): Show |
intron_variant | MODIFIER | c.325-376T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111703967 | |||||||
| chr1:111704137 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.325-206G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111704137 | |||||||
| chr1:111704148 | A | AT | 44 | a0001c0001t0001g0113 a0001c0001t0003g0001 a0001c0001t0003g0006 others(41): Show |
50 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.325-179dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 111704148 | ||||||
| chr1:111704148 | A | ATTT | 10 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-181_325-179dup others(3): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 111704148 | ||||||
| chr1:111704148 | AT | A | 135 | a0001c0001t0001g0084 a0001c0001t0001g0143 a0001c0001t0001g0172 others(132): Show |
138 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.325-179delT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 111704148 | ||||||
| chr1:111704239 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.325-104A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 5/7 | chr1 | 111704239 | |||||||
| chr1:111704685 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.468+199A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111704685 | |||||||
| chr1:111704770 | G | A | 4 | a0001c0001t0011g0009 a0001c0001t0011g0259 a0001c0001t0011g0260 others(1): Show |
5 | HG01192.hp1 HG02451.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+284G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111704770 | |||||||
| chr1:111704824 | A | G | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.468+338A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111704824 | |||||||
| chr1:111705037 | G | A | 1 | a0001c0001t0006g0216 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.468+551G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705037 | |||||||
| chr1:111705267 | G | A | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.468+781G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705267 | |||||||
| chr1:111705316 | C | T | 3 | a0001c0001t0012g0154 a0001c0001t0012g0155 a0001c0001t0031g0153 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.468+830C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705316 | |||||||
| chr1:111705343 | G | T | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.468+857G>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705343 | |||||||
| chr1:111705561 | C | T | 1 | a0001c0001t0019g0011 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.468+1075C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705561 | |||||||
| chr1:111705607 | T | C | 1 | a0001c0001t0004g0363 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.468+1121T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705607 | |||||||
| chr1:111705741 | A | C | 1 | a0001c0001t0007g0264 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.468+1255A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705741 | |||||||
| chr1:111705924 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.468+1438G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111705924 | |||||||
| chr1:111706040 | T | C | 2 | a0001c0001t0012g0154 a0001c0001t0012g0155 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.468+1554T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111706040 | |||||||
| chr1:111706046 | A | G | 2 | a0001c0001t0014g0284 a0001c0001t0014g0285 |
2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.468+1560A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111706046 | |||||||
| chr1:111706121 | A | G | 1 | a0001c0001t0004g0340 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.468+1635A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111706121 | |||||||
| chr1:111706455 | C | CAT | 9 | a0001c0001t0001g0099 a0001c0001t0001g0114 a0001c0001t0005g0014 others(6): Show |
11 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+1985_468+1986d others(4): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 111706455 | ||||||
| chr1:111706900 | A | G | 8 | a0001c0001t0007g0266 a0001c0001t0007g0267 a0001c0001t0007g0268 others(5): Show |
8 | HG01109.hp2 HG01243.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-2249A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111706900 | |||||||
| chr1:111707072 | A | G | 1 | a0001c0001t0020g0219 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.469-2077A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707072 | |||||||
| chr1:111707251 | G | A | 3 | a0001c0001t0002g0241 a0001c0001t0002g0246 a0001c0001t0002g0247 |
3 | NA18940.hp2 NA18978.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.469-1898G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707251 | |||||||
| chr1:111707261 | C | T | 55 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(52): Show |
65 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.469-1888C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707261 | |||||||
| chr1:111707306 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.469-1843A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707306 | |||||||
| chr1:111707540 | A | G | 4 | a0001c0001t0008g0277 a0001c0001t0008g0279 a0001c0001t0008g0281 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1609A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707540 | |||||||
| chr1:111707558 | A | G | 1 | a0001c0001t0008g0275 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.469-1591A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707558 | |||||||
| chr1:111707598 | A | G | 2 | a0001c0001t0002g0045 a0001c0001t0002g0058 |
2 | HG01516.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.469-1551A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707598 | |||||||
| chr1:111707696 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.469-1453A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707696 | |||||||
| chr1:111707779 | C | A | 6 | a0001c0001t0009g0003 a0001c0001t0009g0220 a0001c0001t0009g0221 others(3): Show |
8 | HG01175.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.469-1370C>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707779 | |||||||
| chr1:111707790 | T | C | 25 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(22): Show |
25 | HG01109.hp2 HG01243.hp1 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.469-1359T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707790 | |||||||
| chr1:111707805 | A | C | 1 | a0001c0001t0002g0257 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.469-1344A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111707805 | |||||||
| chr1:111708003 | T | C | 2 | a0001c0001t0007g0264 a0001c0001t0019g0011 |
2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.469-1146T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708003 | |||||||
| chr1:111708068 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.469-1081C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708068 | |||||||
| chr1:111708182 | A | C | 1 | a0001c0001t0004g0338 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.469-967A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708182 | |||||||
| chr1:111708252 | CG | C | 363 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(360): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.469-896delG | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708252 | |||||||
| chr1:111708306 | A | C | 1 | a0001c0001t0004g0348 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.469-843A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708306 | |||||||
| chr1:111708383 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.469-766C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708383 | |||||||
| chr1:111708490 | AAAACTAA others(8): Show |
A | 1 | a0001c0001t0006g0215 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.469-658_469-644del others(15): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708490 | |||||||
| chr1:111708519 | A | G | 2 | a0001c0001t0012g0154 a0001c0001t0012g0155 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.469-630A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708519 | |||||||
| chr1:111708604 | G | C | 1 | a0001c0001t0006g0215 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.469-545G>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708604 | |||||||
| chr1:111708605 | C | T | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.469-544C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708605 | |||||||
| chr1:111708703 | A | G | 24 | a0001c0001t0005g0004 a0001c0001t0005g0014 a0001c0001t0005g0017 others(21): Show |
25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.469-446A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708703 | |||||||
| chr1:111708772 | C | T | 3 | a0001c0001t0013g0036 a0001c0001t0013g0037 a0001c0001t0013g0038 |
3 | HG02965.hp2 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.469-377C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708772 | |||||||
| chr1:111708845 | A | AT | 59 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(56): Show |
59 | HG00408.hp1 HG01109.hp2 HG01243.hp1 others(56): Show |
intron_variant | MODIFIER | c.469-304_469-303ins others(1): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708845 | |||||||
| chr1:111708875 | C | T | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.469-274C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | 111708875 | |||||||
| chr1:111709280 | C | T | 46 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(43): Show |
54 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.*29+16C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111709280 | |||||||
| chr1:111709361 | C | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.*29+97C>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111709361 | |||||||
| chr1:111709489 | T | TG | 6 | a0001c0001t0001g0066 a0001c0001t0001g0090 a0001c0001t0001g0126 others(3): Show |
6 | HG01257.hp2 HG01346.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.*29+226dupG | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 111709489 | ||||||
| chr1:111709573 | T | G | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(2): Show |
5 | HG01433.hp2 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.*29+309T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111709573 | |||||||
| chr1:111709616 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*29+352T>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111709616 | |||||||
| chr1:111709728 | A | G | 33 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(30): Show |
33 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.*29+464A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111709728 | |||||||
| chr1:111709757 | A | G | 1 | a0001c0001t0002g0296 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*29+493A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111709757 | |||||||
| chr1:111709839 | G | A | 160 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(157): Show |
171 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.*29+575G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111709839 | |||||||
| chr1:111709884 | ATTC | A | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.*29+625_*29+627del others(3): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 111709884 | ||||||
| chr1:111710146 | GTCT | G | 39 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(36): Show |
39 | HG00408.hp1 HG01243.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.*29+887_*29+889del others(3): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 111710146 | ||||||
| chr1:111710154 | A | T | 1 | a0001c0001t0006g0215 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.*29+890A>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111710154 | |||||||
| chr1:111710213 | C | T | 5 | a0001c0001t0006g0015 a0001c0001t0006g0016 a0001c0001t0006g0215 others(2): Show |
5 | HG01433.hp2 HG02809.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.*29+949C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111710213 | |||||||
| chr1:111710492 | G | A | 163 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(160): Show |
174 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.*29+1228G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111710492 | |||||||
| chr1:111710590 | T | C | 218 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(215): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.*29+1326T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111710590 | |||||||
| chr1:111710711 | A | G | 28 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(25): Show |
30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.*29+1447A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111710711 | |||||||
| chr1:111710775 | G | A | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.*29+1511G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111710775 | |||||||
| chr1:111710842 | C | CT | 36 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(33): Show |
36 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(33): Show |
intron_variant | MODIFIER | c.*30-1581dupT | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr1 | 111710842 | ||||||
| chr1:111710864 | G | A | 1 | a0001c0001t0008g0282 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.*30-1567G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111710864 | |||||||
| chr1:111711069 | T | C | 32 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(29): Show |
32 | HG00280.hp1 HG00544.hp1 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.*30-1362T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711069 | |||||||
| chr1:111711117 | G | A | 3 | a0001c0001t0012g0154 a0001c0001t0012g0155 a0001c0001t0031g0153 |
3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.*30-1314G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711117 | |||||||
| chr1:111711144 | T | A | 334 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(331): Show |
348 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.*30-1287T>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711144 | |||||||
| chr1:111711353 | T | C | 1 | a0001c0001t0003g0212 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.*30-1078T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711353 | |||||||
| chr1:111711618 | A | G | 20 | a0001c0001t0007g0264 a0001c0001t0007g0266 a0001c0001t0007g0267 others(17): Show |
20 | HG01109.hp2 HG01243.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.*30-813A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711618 | |||||||
| chr1:111711790 | G | A | 33 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0226 others(30): Show |
33 | HG00408.hp1 HG01243.hp2 HG01928.hp1 others(30): Show |
intron_variant | MODIFIER | c.*30-641G>A | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711790 | |||||||
| chr1:111711813 | TTTTATAT others(6): Show |
T | 1 | a0001c0001t0006g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.*30-617_*30-605del others(13): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711813 | |||||||
| chr1:111711882 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.*30-549T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711882 | |||||||
| chr1:111711890 | C | T | 105 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(102): Show |
106 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.*30-541C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711890 | |||||||
| chr1:111711988 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0065 a0001c0001t0001g0066 others(113): Show |
118 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.*30-443T>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111711988 | |||||||
| chr1:111712028 | A | C | 40 | a0001c0001t0004g0010 a0001c0001t0004g0228 a0001c0001t0004g0327 others(37): Show |
41 | HG00558.hp1 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.*30-403A>C | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111712028 | |||||||
| chr1:111712052 | C | T | 47 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0006 others(44): Show |
55 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.*30-379C>T | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111712052 | |||||||
| chr1:111712177 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.*30-254A>G | RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 7/7 | chr1 | 111712177 |