Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23168 |
| ensemblid | ENSG00000137815.15 |
| hgncid | 28996 |
| symbol | RTF1 |
| name | RTF1 homolog, Paf1/RNA polymerase II complex component |
| refseq_nuc | NM_015138.5 |
| refseq_prot | NP_055953.3 |
| ensembl_nuc | ENST00000389629.9 |
| ensembl_prot | ENSP00000374280.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 41417095 |
| end | 41483563 |
| strand | + |
| ver | v1.2 |
| region | chr15:41417095-41483563 |
| region5000 | chr15:41412095-41488563 |
| regionname0 | RTF1_chr15_41417095_41483563 |
| regionname5000 | RTF1_chr15_41412095_41488563 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 710 | 225 | 54 | 48 | 73 | 14 | 34 | 55 | RTF1_chr15_41412095_41488563 | RTF1 | MRGRL others(705): Show |
chr15 | 41412095 | 41488563 |
| a0002 | 0/0 | 710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | MRGRL others(705): Show |
chr15 | 41412095 | 41488563 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2130 | 219 | 52 | 48 | 72 | 13 | 32 | RTF1_chr15_41412095_41488563 | RTF1 | ATGCG others(2125): Show |
chr15 | 41412095 | 41488563 | ||
| a0001c0002 | 0/0 | 2130 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | ATGCG others(2125): Show |
chr15 | 41412095 | 41488563 | ||
| a0001c0003 | 0/0 | 2130 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | ATGCG others(2125): Show |
chr15 | 41412095 | 41488563 | ||
| a0001c0004 | 0/0 | 2130 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | ATGCG others(2125): Show |
chr15 | 41412095 | 41488563 | ||
| a0001c0005 | 0/0 | 2130 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | ATGCG others(2125): Show |
chr15 | 41412095 | 41488563 | ||
| a0001c0006 | 0/0 | 2130 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | ATGCG others(2125): Show |
chr15 | 41412095 | 41488563 | ||
| a0002c0007 | 0/0 | 2130 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | ATGCG others(2125): Show |
chr15 | 41412095 | 41488563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5030 | 59 | 15 | 13 | 24 | 1 | 5 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0002 | 1/0 | 5030 | 32 | 1 | 6 | 16 | 4 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0003 | 0/0 | 5028 | 26 | 7 | 10 | 1 | 5 | 3 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0004 | 0/0 | 5028 | 22 | 1 | 6 | 14 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0005 | 0/0 | 5027 | 15 | 6 | 4 | 0 | 2 | 3 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5022): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0006 | 0/0 | 5029 | 11 | 0 | 3 | 4 | 0 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0007 | 0/0 | 5031 | 9 | 2 | 1 | 2 | 0 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5026): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0008 | 0/0 | 5031 | 5 | 0 | 0 | 2 | 1 | 2 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5026): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0009 | 0/0 | 5029 | 7 | 4 | 2 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0010 | 0/0 | 5030 | 4 | 4 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0011 | 0/0 | 5028 | 4 | 3 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0012 | 0/0 | 5028 | 3 | 3 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0013 | 0/0 | 5028 | 3 | 0 | 0 | 3 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0014 | 0/0 | 5028 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0016 | 0/0 | 5030 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0017 | 0/0 | 5029 | 2 | 0 | 1 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0018 | 0/0 | 5028 | 2 | 0 | 0 | 0 | 0 | 2 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0019 | 0/0 | 5030 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0020 | 0/0 | 5030 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0021 | 0/0 | 5029 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0022 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0023 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0024 | 0/0 | 5030 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0025 | 0/0 | 5028 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0026 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0027 | 0/0 | 5029 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0028 | 0/0 | 5029 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0001t0029 | 0/0 | 5029 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5024): Show |
chr15 | 41412095 | 41488563 |
| a0001c0002t0015 | 0/0 | 5030 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0003t0004 | 0/0 | 5028 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5023): Show |
chr15 | 41412095 | 41488563 |
| a0001c0004t0002 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5025): Show |
chr15 | 41412095 | 41488563 |
| a0001c0005t0007 | 0/0 | 5031 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5026): Show |
chr15 | 41412095 | 41488563 |
| a0001c0006t0008 | 0/0 | 5031 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5026): Show |
chr15 | 41412095 | 41488563 |
| a0002c0007t0008 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | GGGGG others(5026): Show |
chr15 | 41412095 | 41488563 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0107 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0013g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0013g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0014g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0014g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0016g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0016g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0017g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0017g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0018g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0018g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0019g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0020g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0021g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0022g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0023g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0024g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0025g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0026g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0027g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0028g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0029g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0002t0015g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0002t0015g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0003t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0005t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0006t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0002c0007t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0004 | g0188 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0153 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0152 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0141 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0140 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00423 | hp1 | a0001 | c0004 | t0002 | g0129 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0098 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0083 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00639 | hp1 | a0001 | c0001 | t0017 | g0155 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0128 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0213 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0219 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0011 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0137 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0217 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0215 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0160 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0197 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0020 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0214 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0216 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0006 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0089 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0184 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0037 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0024 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0182 | EAS | CDX | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0195 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02293 | hp2 | a0001 | c0001 | t0021 | g0134 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0154 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0198 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02572 | hp1 | a0001 | c0002 | t0015 | g0057 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0206 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02602 | hp1 | a0001 | c0001 | t0024 | g0070 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0196 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0054 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0190 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0204 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0067 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0010 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0146 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0028 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0132 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0208 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0169 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0066 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03139 | hp1 | a0001 | c0001 | t0016 | g0145 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0199 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0001 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03486 | hp1 | a0001 | c0001 | t0026 | g0147 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0170 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03491 | hp1 | a0001 | c0001 | t0018 | g0150 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03491 | hp2 | a0001 | c0006 | t0008 | g0143 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03492 | hp2 | a0001 | c0001 | t0018 | g0156 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0126 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03669 | hp1 | a0001 | c0001 | t0008 | g0017 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0119 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03834 | hp2 | a0001 | c0001 | t0025 | g0164 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0065 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0115 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0014 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0023 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04184 | hp1 | a0001 | c0001 | t0017 | g0149 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04184 | hp2 | a0001 | c0001 | t0020 | g0074 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0211 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0112 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04204 | hp1 | a0001 | c0005 | t0007 | g0082 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0218 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0121 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0007 | AFR | YRI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18943 | hp1 | a0001 | c0001 | t0023 | g0079 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0133 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0114 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18968 | hp2 | a0001 | c0001 | t0013 | g0202 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18971 | hp1 | a0002 | c0007 | t0008 | g0110 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18971 | hp2 | a0001 | c0001 | t0013 | g0201 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18975 | hp1 | a0001 | c0001 | t0027 | g0175 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0099 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19083 | hp1 | a0001 | c0001 | t0028 | g0200 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0086 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19085 | hp1 | a0001 | c0001 | t0029 | g0192 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19085 | hp2 | a0001 | c0001 | t0022 | g0044 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20129 | hp2 | a0001 | c0002 | t0015 | g0033 | AFR | ASW | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0101 | EUR | TSI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0159 | EUR | TSI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0212 | SAS | GIH | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18955 | hp2 | a0001 | c0001 | t0013 | g0027 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0078 | AFR | USA | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | USA | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0016 | REF | REF | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0107 | REF | REF | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41417147 | C | T | 1 | a0002 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.32C>T | p.Ala11Val | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/18 | 53/5030 | 32/2133 | 11/710 | chr15 | 41417147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41417289 | C | T | 1 | a0001c0006 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.174C>T | p.Ser58Ser | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/18 | 195/5030 | 174/2133 | 58/710 | chr15 | 41417289 | |||
| chr15:41438395 | C | T | 1 | a0001c0002 | 2 | HG02572.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.273C>T | p.Ala91Ala | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/18 | 294/5030 | 273/2133 | 91/710 | chr15 | 41438395 | |||
| chr15:41457718 | T | C | 1 | a0001c0003 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.504T>C | p.Asp168Asp | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/18 | 525/5030 | 504/2133 | 168/710 | chr15 | 41457718 | |||
| chr15:41470327 | G | A | 1 | a0001c0004 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.960G>A | p.Glu320Glu | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/18 | 981/5030 | 960/2133 | 320/710 | chr15 | 41470327 | |||
| chr15:41480216 | T | C | 1 | a0001c0005 | 1 | HG04204.hp1 | splice_region_variant&synonymous_variant | LOW | c.1917T>C | p.Gly639Gly | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/18 | 1938/5030 | 1917/2133 | 639/710 | chr15 | 41480216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41480750 | T | C | 1 | a0001c0001t0019 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 63 | chr15 | 41480750 | ||||||
| chr15:41480975 | G | A | 1 | a0001c0001t0020 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 288 | chr15 | 41480975 | ||||||
| chr15:41480977 | G | A | 1 | a0001c0001t0014 | 2 | HG02572.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 290 | chr15 | 41480977 | ||||||
| chr15:41481151 | G | A | 1 | a0001c0001t0021 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*464G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 464 | chr15 | 41481151 | ||||||
| chr15:41481244 | T | TG | 5 | a0001c0001t0007 a0001c0001t0008 a0001c0005t0007 others(2): Show |
17 | HG00280.hp2 HG00544.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*569dupG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 570 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | |||||
| chr15:41481244 | TG | T | 11 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0009 others(8): Show |
55 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*569delG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 569 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | |||||
| chr15:41481244 | TGG | T | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0013 others(2): Show |
32 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*568_*569delGG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 568 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | |||||
| chr15:41481244 | TGGG | T | 1 | a0001c0001t0005 | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*567_*569delGGG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 567 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | |||||
| chr15:41481245 | G | C | 1 | a0001c0001t0016 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 558 | chr15 | 41481245 | ||||||
| chr15:41481335 | C | A | 1 | a0001c0001t0018 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*648C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 648 | chr15 | 41481335 | ||||||
| chr15:41481543 | G | T | 6 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0027 others(3): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 856 | chr15 | 41481543 | ||||||
| chr15:41481625 | C | T | 1 | a0001c0001t0024 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 938 | chr15 | 41481625 | ||||||
| chr15:41481738 | G | C | 1 | a0001c0001t0025 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1051G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1051 | chr15 | 41481738 | ||||||
| chr15:41481860 | A | G | 1 | a0001c0001t0029 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1173A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1173 | chr15 | 41481860 | ||||||
| chr15:41482095 | G | A | 1 | a0001c0001t0012 | 3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1408G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1408 | chr15 | 41482095 | ||||||
| chr15:41482225 | A | G | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(22): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*1538A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1538 | chr15 | 41482225 | ||||||
| chr15:41482353 | G | C | 1 | a0001c0002t0015 | 2 | HG02572.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1666G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1666 | chr15 | 41482353 | ||||||
| chr15:41482892 | CA | C | 5 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0017 others(2): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2206delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2206 | chr15 | 41482892 | ||||||
| chr15:41483023 | C | T | 5 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0017 others(2): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2336C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2336 | chr15 | 41483023 | ||||||
| chr15:41483059 | G | A | 1 | a0001c0001t0022 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2372G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2372 | chr15 | 41483059 | ||||||
| chr15:41483192 | G | C | 2 | a0001c0001t0016 a0001c0001t0026 |
3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2505G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2505 | chr15 | 41483192 | ||||||
| chr15:41483247 | A | G | 1 | a0001c0001t0023 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2560A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2560 | chr15 | 41483247 | ||||||
| chr15:41483248 | T | G | 1 | a0001c0001t0010 | 4 | HG01891.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2561T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2561 | chr15 | 41483248 | ||||||
| chr15:41483350 | C | G | 2 | a0001c0001t0013 a0001c0001t0028 |
4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2663C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2663 | chr15 | 41483350 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41417394 | G | C | 1 | a0001c0001t0003g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198+81G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417394 | |||||||
| chr15:41417716 | C | G | 1 | a0001c0001t0004g0222 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.198+403C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417716 | |||||||
| chr15:41417818 | T | G | 1 | a0001c0001t0002g0006 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.198+505T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417818 | |||||||
| chr15:41417957 | A | G | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+644A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417957 | |||||||
| chr15:41418129 | T | G | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+816T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418129 | |||||||
| chr15:41418485 | T | C | 4 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1172T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418485 | |||||||
| chr15:41418572 | C | T | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+1259C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418572 | |||||||
| chr15:41418632 | G | T | 1 | a0001c0001t0007g0205 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.198+1319G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418632 | |||||||
| chr15:41418784 | C | CA | 14 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0002g0018 others(11): Show |
14 | HG01515.hp1 HG01975.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+1488dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41418784 | ||||||
| chr15:41418784 | C | CAA | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1487_198+1488d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41418784 | ||||||
| chr15:41418867 | T | A | 16 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(13): Show |
16 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.198+1554T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418867 | |||||||
| chr15:41419094 | A | G | 1 | a0001c0001t0019g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.198+1781A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419094 | |||||||
| chr15:41419132 | T | C | 1 | a0001c0001t0003g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198+1819T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419132 | |||||||
| chr15:41419186 | C | T | 1 | a0001c0001t0004g0203 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.198+1873C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419186 | |||||||
| chr15:41419216 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1903T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419216 | |||||||
| chr15:41419249 | C | T | 88 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.198+1936C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419249 | |||||||
| chr15:41419316 | T | G | 88 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.198+2003T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419316 | |||||||
| chr15:41419493 | T | A | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+2180T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419493 | |||||||
| chr15:41419544 | A | C | 4 | a0001c0001t0013g0027 a0001c0001t0013g0201 a0001c0001t0013g0202 others(1): Show |
4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+2231A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419544 | |||||||
| chr15:41419911 | C | T | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.198+2598C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419911 | |||||||
| chr15:41420307 | T | C | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.198+2994T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420307 | |||||||
| chr15:41420470 | C | T | 1 | a0001c0001t0014g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+3157C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420470 | |||||||
| chr15:41420494 | C | G | 3 | a0001c0001t0016g0145 a0001c0001t0016g0146 a0001c0001t0026g0147 |
3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.198+3181C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420494 | |||||||
| chr15:41420593 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.198+3280C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420593 | |||||||
| chr15:41420609 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.198+3296T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420609 | |||||||
| chr15:41420678 | T | TTTACCTC others(3): Show |
1 | a0001c0001t0002g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+3368_198+3377d others(12): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41420678 | ||||||
| chr15:41420738 | C | A | 3 | a0001c0001t0006g0126 a0001c0001t0006g0127 a0001c0001t0006g0128 |
3 | HG00639.hp2 HG00738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.198+3425C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420738 | |||||||
| chr15:41420810 | G | C | 1 | a0001c0001t0002g0097 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.198+3497G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420810 | |||||||
| chr15:41420909 | G | A | 1 | a0001c0001t0014g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+3596G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420909 | |||||||
| chr15:41421021 | A | G | 54 | a0001c0001t0001g0009 a0001c0001t0004g0004 a0001c0001t0004g0176 others(51): Show |
55 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.198+3708A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421021 | |||||||
| chr15:41421028 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.198+3715G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421028 | |||||||
| chr15:41421138 | A | C | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+3825A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421138 | |||||||
| chr15:41421246 | T | G | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+3933T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421246 | |||||||
| chr15:41421449 | T | A | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+4136T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421449 | |||||||
| chr15:41421456 | TA | T | 25 | a0001c0001t0004g0004 a0001c0001t0004g0178 a0001c0001t0004g0179 others(22): Show |
26 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.198+4159delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41421456 | ||||||
| chr15:41421590 | C | T | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+4277C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421590 | |||||||
| chr15:41421709 | C | CT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0095 a0001c0001t0002g0096 others(4): Show |
7 | HG01978.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+4413dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41421709 | ||||||
| chr15:41421852 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+4539A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421852 | |||||||
| chr15:41421862 | C | T | 3 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0025g0164 |
3 | HG02602.hp2 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.198+4549C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421862 | |||||||
| chr15:41421866 | A | G | 3 | a0001c0001t0005g0208 a0001c0001t0005g0209 a0001c0001t0005g0210 |
3 | HG01891.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.198+4553A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421866 | |||||||
| chr15:41421874 | C | T | 33 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+4561C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421874 | |||||||
| chr15:41422006 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.198+4693C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422006 | |||||||
| chr15:41422023 | A | G | 1 | a0001c0006t0008g0143 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.198+4710A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422023 | |||||||
| chr15:41422023 | ATTTG | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(16): Show |
19 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+4722_198+4725d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41422023 | ||||||
| chr15:41422077 | C | T | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+4764C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422077 | |||||||
| chr15:41422217 | G | GT | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+4905dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41422217 | ||||||
| chr15:41422223 | A | G | 4 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 others(1): Show |
4 | HG01496.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+4910A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422223 | |||||||
| chr15:41422305 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+4992T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422305 | |||||||
| chr15:41422306 | A | T | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+4993A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422306 | |||||||
| chr15:41422334 | A | C | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5021A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422334 | |||||||
| chr15:41422401 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5088C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422401 | |||||||
| chr15:41422402 | A | C | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5089A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422402 | |||||||
| chr15:41422403 | T | A | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5090T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422403 | |||||||
| chr15:41422498 | A | T | 1 | a0001c0001t0005g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198+5185A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422498 | |||||||
| chr15:41422600 | A | G | 1 | a0001c0001t0010g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198+5287A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422600 | |||||||
| chr15:41422860 | C | T | 3 | a0001c0001t0005g0208 a0001c0001t0005g0209 a0001c0001t0005g0210 |
3 | HG01891.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.198+5547C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422860 | |||||||
| chr15:41422923 | G | A | 33 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+5610G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422923 | |||||||
| chr15:41422935 | A | G | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.198+5622A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422935 | |||||||
| chr15:41423213 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5900G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423213 | |||||||
| chr15:41423260 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.198+5947G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423260 | |||||||
| chr15:41423301 | T | G | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5988T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423301 | |||||||
| chr15:41423302 | G | C | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5989G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423302 | |||||||
| chr15:41423303 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5990C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423303 | |||||||
| chr15:41423387 | A | G | 88 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.198+6074A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423387 | |||||||
| chr15:41423426 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.198+6113G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423426 | |||||||
| chr15:41423434 | A | G | 54 | a0001c0001t0001g0009 a0001c0001t0004g0004 a0001c0001t0004g0176 others(51): Show |
55 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.198+6121A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423434 | |||||||
| chr15:41423458 | C | T | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+6145C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423458 | |||||||
| chr15:41423495 | G | A | 1 | a0001c0001t0006g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.198+6182G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423495 | |||||||
| chr15:41423595 | C | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.198+6282C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423595 | |||||||
| chr15:41423596 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.198+6283C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423596 | |||||||
| chr15:41423610 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG00741.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.198+6297C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423610 | |||||||
| chr15:41423657 | C | T | 1 | a0001c0001t0007g0086 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.198+6344C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423657 | |||||||
| chr15:41423832 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.198+6519C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423832 | |||||||
| chr15:41423838 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.198+6525C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423838 | |||||||
| chr15:41423953 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198+6640A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423953 | |||||||
| chr15:41424056 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+6743A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424056 | |||||||
| chr15:41424077 | G | T | 2 | a0001c0001t0014g0196 a0001c0001t0014g0206 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.198+6764G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424077 | |||||||
| chr15:41424836 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.198+7523C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424836 | |||||||
| chr15:41424948 | G | T | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+7635G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424948 | |||||||
| chr15:41425061 | C | T | 1 | a0001c0001t0009g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.198+7748C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425061 | |||||||
| chr15:41425115 | A | T | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+7802A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425115 | |||||||
| chr15:41425126 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.198+7813G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425126 | |||||||
| chr15:41425611 | C | T | 1 | a0001c0001t0005g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198+8298C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425611 | |||||||
| chr15:41425940 | G | A | 2 | a0001c0001t0005g0211 a0001c0001t0005g0212 |
2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.198+8627G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425940 | |||||||
| chr15:41425972 | C | G | 1 | a0001c0001t0002g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.198+8659C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425972 | |||||||
| chr15:41426134 | A | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0140 a0001c0001t0008g0141 |
3 | HG00280.hp2 HG00323.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.198+8821A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426134 | |||||||
| chr15:41426135 | T | A | 2 | a0001c0001t0008g0099 a0001c0002t0015g0033 |
2 | NA19011.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.198+8822T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426135 | |||||||
| chr15:41426144 | G | A | 1 | a0001c0001t0017g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.198+8831G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426144 | |||||||
| chr15:41426312 | A | AT | 33 | a0001c0001t0001g0009 a0001c0001t0004g0004 a0001c0001t0004g0176 others(30): Show |
34 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.198+9010dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426312 | ||||||
| chr15:41426323 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.198+9010T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426323 | |||||||
| chr15:41426394 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+9081C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426394 | |||||||
| chr15:41426395 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+9082T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426395 | |||||||
| chr15:41426606 | T | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.198+9293T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426606 | |||||||
| chr15:41426689 | G | A | 1 | a0001c0001t0009g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.198+9376G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426689 | |||||||
| chr15:41426690 | CCCCCCCC others(8): Show |
C | 1 | a0001c0001t0001g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198+9390_198+9404d others(17): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426690 | ||||||
| chr15:41426691 | CCCCCCCC others(7): Show |
C | 3 | a0001c0001t0005g0216 a0001c0001t0005g0220 a0001c0001t0005g0221 |
3 | HG01517.hp1 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.198+9391_198+9404d others(16): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426691 | ||||||
| chr15:41426692 | CCCCCCCC others(6): Show |
C | 14 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(11): Show |
14 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+9395_198+9407d others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426692 | ||||||
| chr15:41426693 | CCCCCCCC others(5): Show |
C | 1 | a0001c0001t0005g0219 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198+9392_198+9403d others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426693 | ||||||
| chr15:41426694 | CCCCCCCC others(4): Show |
C | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+9392_198+9402d others(13): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426694 | ||||||
| chr15:41426699 | C | A | 18 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(15): Show |
18 | HG00323.hp2 HG00639.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.198+9386C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426699 | |||||||
| chr15:41426700 | C | A | 14 | a0001c0001t0003g0025 a0001c0001t0003g0148 a0001c0001t0003g0152 others(11): Show |
14 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+9387C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426700 | |||||||
| chr15:41426700 | C | G | 1 | a0001c0001t0001g0002 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.198+9387C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426700 | |||||||
| chr15:41426701 | C | CG | 2 | a0001c0001t0001g0039 a0001c0001t0009g0083 |
2 | HG00609.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.198+9388_198+9389i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426701 | |||||||
| chr15:41426701 | C | G | 5 | a0001c0001t0001g0073 a0001c0001t0001g0094 a0001c0001t0014g0196 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+9388C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426701 | |||||||
| chr15:41426702 | C | CG | 6 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0093 others(3): Show |
6 | HG01978.hp2 HG02896.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+9389_198+9390i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426702 | |||||||
| chr15:41426702 | C | G | 18 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0032 others(15): Show |
18 | HG01981.hp2 HG02027.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.198+9389C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426702 | |||||||
| chr15:41426703 | C | CG | 15 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0072 others(12): Show |
15 | HG01517.hp2 HG01884.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+9390_198+9391i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426703 | |||||||
| chr15:41426703 | C | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0034 others(20): Show |
24 | HG00423.hp2 HG00544.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.198+9390C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426703 | |||||||
| chr15:41426703 | CCG | C | 12 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0073 others(9): Show |
12 | HG00642.hp2 HG01975.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+9392_198+9393d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426703 | ||||||
| chr15:41426704 | C | G | 13 | a0001c0001t0001g0046 a0001c0001t0001g0052 a0001c0001t0001g0068 others(10): Show |
13 | HG00558.hp1 HG00558.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+9391C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426704 | |||||||
| chr15:41426704 | CG | C | 23 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
23 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+9392delG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426704 | |||||||
| chr15:41426705 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.198+9392G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426705 | |||||||
| chr15:41426705 | G | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0013 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.198+9392G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426705 | |||||||
| chr15:41426705 | G | GCCCCCCC others(4): Show |
1 | a0001c0001t0013g0027 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.198+9394_198+9404d others(13): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426705 | ||||||
| chr15:41426707 | C | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+9394C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426707 | |||||||
| chr15:41426708 | C | A | 2 | a0001c0001t0014g0196 a0001c0001t0014g0206 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.198+9395C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426708 | |||||||
| chr15:41426708 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0023g0079 |
2 | HG02148.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.198+9395C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426708 | |||||||
| chr15:41426711 | C | G | 1 | a0001c0001t0002g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198+9398C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426711 | |||||||
| chr15:41426712 | C | G | 1 | a0001c0001t0014g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+9399C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426712 | |||||||
| chr15:41426713 | C | A | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+9400C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426713 | |||||||
| chr15:41426715 | C | G | 1 | a0001c0001t0002g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.198+9402C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426715 | |||||||
| chr15:41426774 | CAT | C | 11 | a0001c0001t0003g0005 a0001c0001t0003g0172 a0001c0001t0003g0173 others(8): Show |
11 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.198+9468_198+9469d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426774 | ||||||
| chr15:41426778 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.198+9465T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426778 | |||||||
| chr15:41426779 | A | ATG | 2 | a0001c0001t0003g0162 a0001c0001t0003g0166 |
2 | HG01081.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.198+9467_198+9468i others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | ||||||
| chr15:41426779 | A | ATGTG | 2 | a0001c0001t0001g0030 a0001c0001t0006g0137 |
2 | HG01168.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.198+9467_198+9468i others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | ||||||
| chr15:41426779 | ATATG | A | 22 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.198+9468_198+9471d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | ||||||
| chr15:41426779 | ATATGTG | A | 8 | a0001c0001t0003g0020 a0001c0001t0003g0163 a0001c0001t0003g0168 others(5): Show |
8 | HG00323.hp2 HG01515.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+9468_198+9473d others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | ||||||
| chr15:41426779 | ATATGTGT others(11): Show |
A | 2 | a0001c0001t0005g0211 a0001c0001t0005g0212 |
2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.198+9468_198+9485d others(20): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | ||||||
| chr15:41426779 | ATATGTGT others(13): Show |
A | 1 | a0001c0001t0005g0208 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.198+9468_198+9487d others(22): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | ||||||
| chr15:41426781 | A | ATG | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(55): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.198+9512_198+9513d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | A | ATGTG | 33 | a0001c0001t0001g0041 a0001c0001t0001g0050 a0001c0001t0001g0056 others(30): Show |
33 | HG00099.hp1 HG00544.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+9510_198+9513d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | A | ATGTGTG | 9 | a0001c0001t0001g0029 a0001c0001t0002g0019 a0001c0001t0002g0103 others(6): Show |
9 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+9508_198+9513d others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | A | ATGTGTGT others(1): Show |
6 | a0001c0001t0001g0013 a0001c0001t0002g0096 a0001c0001t0002g0113 others(3): Show |
6 | HG01978.hp1 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+9506_198+9513d others(10): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | A | ATGTGTGT others(3): Show |
4 | a0001c0001t0001g0032 a0001c0001t0002g0144 a0001c0001t0004g0182 others(1): Show |
4 | HG02027.hp2 HG02165.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+9504_198+9513d others(12): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | A | ATGTGTGT others(9): Show |
1 | a0001c0001t0004g0203 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.198+9498_198+9513d others(18): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | A | G | 7 | a0001c0001t0001g0030 a0001c0001t0003g0162 a0001c0001t0003g0166 others(4): Show |
7 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+9468A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426781 | |||||||
| chr15:41426781 | ATG | A | 10 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0090 others(7): Show |
10 | HG01496.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+9512_198+9513d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | ATGTG | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0087 a0001c0001t0001g0088 others(7): Show |
10 | HG00741.hp1 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+9510_198+9513d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | ATGTGTGT others(3): Show |
A | 4 | a0001c0001t0001g0093 a0001c0001t0006g0112 a0001c0001t0014g0196 others(1): Show |
4 | HG02293.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+9504_198+9513d others(12): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+9498_198+9513d others(18): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426781 | ATGTGTGT others(15): Show |
A | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+9492_198+9513d others(24): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | ||||||
| chr15:41426815 | G | T | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+9502G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426815 | |||||||
| chr15:41426830 | TTTTGTTT others(5): Show |
T | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+9533_198+9544d others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426830 | ||||||
| chr15:41426873 | A | G | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+9560A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426873 | |||||||
| chr15:41427145 | A | AT | 8 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0002g0135 others(5): Show |
8 | HG00544.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+9856dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | ||||||
| chr15:41427145 | AT | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0029 others(56): Show |
60 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.198+9856delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | ||||||
| chr15:41427145 | ATT | A | 37 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.198+9855_198+9856d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | ||||||
| chr15:41427145 | ATTT | A | 51 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0004g0004 others(48): Show |
52 | HG00099.hp1 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.198+9854_198+9856d others(5): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | ||||||
| chr15:41427183 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.198+9870G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427183 | |||||||
| chr15:41427301 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+9988G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427301 | |||||||
| chr15:41427446 | C | T | 2 | a0001c0001t0004g0177 a0001c0001t0004g0193 |
2 | HG02027.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.198+10133C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427446 | |||||||
| chr15:41427508 | A | G | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+10195A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427508 | |||||||
| chr15:41427669 | C | A | 1 | a0001c0001t0004g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+10356C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427669 | |||||||
| chr15:41427749 | T | C | 1 | a0001c0001t0007g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.198+10436T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427749 | |||||||
| chr15:41427880 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.199-10441G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427880 | |||||||
| chr15:41428092 | C | CTTTTTTT others(322): Show |
1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-10219_199-1021 others(333): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428092 | ||||||
| chr15:41428257 | C | CT | 24 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0058 others(21): Show |
24 | HG00609.hp2 HG00741.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.199-10036dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | ||||||
| chr15:41428257 | C | CTT | 11 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0210 others(8): Show |
11 | HG01106.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-10037_199-1003 others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | ||||||
| chr15:41428257 | CT | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0102 a0001c0001t0002g0006 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-10036delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | ||||||
| chr15:41428257 | CTT | C | 24 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(21): Show |
25 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.199-10037_199-1003 others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | ||||||
| chr15:41428257 | CTTTTTTT others(3): Show |
C | 30 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.199-10045_199-1003 others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | ||||||
| chr15:41428257 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0018g0150 a0001c0001t0025g0164 |
2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.199-10046_199-1003 others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | ||||||
| chr15:41428345 | G | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-9976G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428345 | |||||||
| chr15:41428376 | T | TC | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-9942dupC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428376 | ||||||
| chr15:41428390 | C | T | 1 | a0001c0001t0013g0202 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.199-9931C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428390 | |||||||
| chr15:41428546 | G | C | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-9775G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428546 | |||||||
| chr15:41428557 | C | G | 1 | a0001c0001t0004g0190 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.199-9764C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428557 | |||||||
| chr15:41428844 | G | A | 88 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.199-9477G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428844 | |||||||
| chr15:41429217 | A | G | 1 | a0001c0001t0016g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.199-9104A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429217 | |||||||
| chr15:41429518 | A | G | 1 | a0001c0001t0002g0019 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.199-8803A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429518 | |||||||
| chr15:41429590 | T | G | 54 | a0001c0001t0001g0009 a0001c0001t0004g0004 a0001c0001t0004g0176 others(51): Show |
55 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.199-8731T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429590 | |||||||
| chr15:41429613 | C | T | 2 | a0001c0002t0015g0033 a0001c0002t0015g0057 |
2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.199-8708C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429613 | |||||||
| chr15:41429637 | G | C | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-8684G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429637 | |||||||
| chr15:41429672 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.199-8649T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429672 | |||||||
| chr15:41429743 | T | G | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-8578T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429743 | |||||||
| chr15:41429786 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-8535G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429786 | |||||||
| chr15:41429827 | C | G | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-8494C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429827 | |||||||
| chr15:41430009 | T | TTTTCTTT others(306): Show |
1 | a0001c0001t0004g0178 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.199-8311_199-8310i others(315): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430009 | ||||||
| chr15:41430009 | T | TTTTTTTT others(306): Show |
1 | a0001c0001t0013g0202 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.199-8311_199-8310i others(315): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430009 | ||||||
| chr15:41430010 | T | TTTTTTTT others(298): Show |
1 | a0001c0001t0004g0179 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.199-8311_199-8310i others(307): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | |||||||
| chr15:41430010 | T | TTTTTTTT others(302): Show |
1 | a0001c0001t0004g0180 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.199-8311_199-8310i others(311): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | |||||||
| chr15:41430010 | T | TTTTTTTT others(303): Show |
15 | a0001c0001t0004g0004 a0001c0001t0004g0177 a0001c0001t0004g0181 others(12): Show |
16 | HG00609.hp1 HG01928.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-8311_199-8310i others(312): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | |||||||
| chr15:41430010 | T | TTTTTTTT others(304): Show |
6 | a0001c0001t0004g0189 a0001c0001t0004g0190 a0001c0001t0004g0191 others(3): Show |
6 | HG00099.hp1 HG01981.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-8311_199-8310i others(313): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | |||||||
| chr15:41430010 | T | TTTTTTTT others(304): Show |
1 | a0001c0001t0004g0193 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.199-8311_199-8310i others(313): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | |||||||
| chr15:41430010 | T | TTTTTTTT others(305): Show |
1 | a0001c0001t0004g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.199-8311_199-8310i others(314): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | |||||||
| chr15:41430011 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-8310C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430011 | |||||||
| chr15:41430011 | CT | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0002g0103 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-8296delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430011 | ||||||
| chr15:41430044 | A | G | 18 | a0001c0001t0003g0020 a0001c0001t0003g0022 a0001c0001t0003g0023 others(15): Show |
18 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.199-8277A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430044 | |||||||
| chr15:41430106 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-8215C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430106 | |||||||
| chr15:41430117 | C | T | 1 | a0001c0001t0007g0076 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.199-8204C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430117 | |||||||
| chr15:41430174 | A | AT | 29 | a0001c0001t0001g0056 a0001c0001t0001g0080 a0001c0001t0001g0088 others(26): Show |
29 | HG00609.hp2 HG00741.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.199-8125dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430174 | ||||||
| chr15:41430226 | G | A | 14 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(11): Show |
14 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-8095G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430226 | |||||||
| chr15:41430286 | C | T | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-8035C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430286 | |||||||
| chr15:41430296 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199-8025C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430296 | |||||||
| chr15:41430297 | G | A | 5 | a0001c0001t0004g0004 a0001c0001t0004g0181 a0001c0001t0004g0182 others(2): Show |
6 | HG00609.hp1 HG02165.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-8024G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430297 | |||||||
| chr15:41430405 | T | C | 1 | a0001c0002t0015g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.199-7916T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430405 | |||||||
| chr15:41430585 | C | T | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-7736C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430585 | |||||||
| chr15:41430655 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-7666C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430655 | |||||||
| chr15:41430680 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199-7641G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430680 | |||||||
| chr15:41430969 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-7352C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430969 | |||||||
| chr15:41431218 | C | CT | 30 | a0001c0001t0001g0032 a0001c0001t0002g0096 a0001c0001t0004g0004 others(27): Show |
31 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.199-7090dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41431218 | ||||||
| chr15:41431371 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0002g0130 a0001c0001t0002g0136 others(1): Show |
4 | HG00423.hp1 HG02040.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-6950C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431371 | |||||||
| chr15:41431634 | A | G | 1 | a0001c0001t0003g0161 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.199-6687A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431634 | |||||||
| chr15:41431638 | T | G | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-6683T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431638 | |||||||
| chr15:41431687 | C | T | 1 | a0001c0001t0009g0011 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.199-6634C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431687 | |||||||
| chr15:41431803 | C | CT | 7 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0009g0007 others(4): Show |
7 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-6503dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41431803 | ||||||
| chr15:41431926 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.199-6395G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431926 | |||||||
| chr15:41431948 | C | T | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.199-6373C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431948 | |||||||
| chr15:41431990 | G | A | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.199-6331G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431990 | |||||||
| chr15:41432185 | T | C | 1 | a0001c0001t0007g0076 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.199-6136T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432185 | |||||||
| chr15:41432196 | C | CT | 10 | a0001c0001t0003g0025 a0001c0001t0004g0178 a0001c0001t0005g0211 others(7): Show |
10 | HG00639.hp2 HG00738.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-6110dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41432196 | ||||||
| chr15:41432321 | C | T | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-6000C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432321 | |||||||
| chr15:41432355 | G | A | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-5966G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432355 | |||||||
| chr15:41432420 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-5901A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432420 | |||||||
| chr15:41432444 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-5877A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432444 | |||||||
| chr15:41432492 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-5829C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432492 | |||||||
| chr15:41432583 | A | T | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-5738A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432583 | |||||||
| chr15:41432707 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-5614G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432707 | |||||||
| chr15:41432825 | G | A | 33 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.199-5496G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432825 | |||||||
| chr15:41432863 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.199-5458A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432863 | |||||||
| chr15:41432876 | T | G | 1 | a0001c0001t0003g0021 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.199-5445T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432876 | |||||||
| chr15:41432885 | C | G | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-5436C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432885 | |||||||
| chr15:41432969 | G | A | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-5352G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432969 | |||||||
| chr15:41432980 | C | T | 2 | a0001c0001t0014g0196 a0001c0001t0014g0206 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.199-5341C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432980 | |||||||
| chr15:41433169 | A | G | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-5152A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433169 | |||||||
| chr15:41433196 | C | T | 2 | a0001c0001t0012g0170 a0001c0001t0014g0206 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-5125C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433196 | |||||||
| chr15:41433221 | C | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG01884.hp1 HG02055.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-5100C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433221 | |||||||
| chr15:41433256 | T | A | 1 | a0001c0001t0005g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-5065T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433256 | |||||||
| chr15:41433323 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.199-4998T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433323 | |||||||
| chr15:41433369 | C | G | 5 | a0001c0001t0003g0021 a0001c0001t0003g0165 a0001c0001t0003g0166 others(2): Show |
5 | HG02602.hp2 HG03834.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-4952C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433369 | |||||||
| chr15:41433407 | T | A | 1 | a0001c0001t0007g0205 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.199-4914T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433407 | |||||||
| chr15:41433459 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-4862T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433459 | |||||||
| chr15:41433479 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-4842C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433479 | |||||||
| chr15:41433598 | A | G | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-4723A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433598 | |||||||
| chr15:41433843 | C | CT | 11 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0055 others(8): Show |
11 | HG01928.hp1 HG02145.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-4457dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41433843 | ||||||
| chr15:41433843 | CT | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0002g0101 others(18): Show |
21 | HG00099.hp1 HG01081.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.199-4457delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41433843 | ||||||
| chr15:41433843 | CTT | C | 14 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(11): Show |
14 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-4458_199-4457d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41433843 | ||||||
| chr15:41433912 | T | C | 1 | a0001c0001t0016g0145 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.199-4409T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433912 | |||||||
| chr15:41434135 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-4186A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434135 | |||||||
| chr15:41434144 | C | CT | 18 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0002g0125 others(15): Show |
18 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.199-4159dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434144 | ||||||
| chr15:41434144 | CT | C | 45 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0094 others(42): Show |
45 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.199-4159delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434144 | ||||||
| chr15:41434144 | CTT | C | 30 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(27): Show |
31 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.199-4160_199-4159d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434144 | ||||||
| chr15:41434262 | C | T | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.199-4059C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434262 | |||||||
| chr15:41434620 | A | C | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-3701A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434620 | |||||||
| chr15:41434624 | CT | C | 27 | a0001c0001t0001g0055 a0001c0001t0001g0084 a0001c0001t0003g0020 others(24): Show |
27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.199-3682delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434624 | ||||||
| chr15:41434662 | C | A | 1 | a0001c0001t0004g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.199-3659C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434662 | |||||||
| chr15:41434849 | G | A | 1 | a0001c0001t0011g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.199-3472G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434849 | |||||||
| chr15:41434874 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-3447G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434874 | |||||||
| chr15:41434918 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.199-3403C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434918 | |||||||
| chr15:41434962 | C | CT | 5 | a0001c0001t0003g0167 a0001c0001t0003g0171 a0001c0001t0003g0174 others(2): Show |
5 | HG02027.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-3343dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434962 | ||||||
| chr15:41434962 | CT | C | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0022 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.199-3343delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434962 | ||||||
| chr15:41435000 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.199-3321G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435000 | |||||||
| chr15:41435201 | G | T | 1 | a0001c0001t0006g0123 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.199-3120G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435201 | |||||||
| chr15:41435378 | G | T | 1 | a0001c0001t0003g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.199-2943G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435378 | |||||||
| chr15:41435416 | C | G | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-2905C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435416 | |||||||
| chr15:41435458 | G | A | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-2863G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435458 | |||||||
| chr15:41435764 | T | C | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.199-2557T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435764 | |||||||
| chr15:41435908 | CAGTT | C | 2 | a0001c0001t0003g0167 a0001c0001t0003g0174 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.199-2410_199-2407d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41435908 | ||||||
| chr15:41436060 | A | T | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-2261A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436060 | |||||||
| chr15:41436078 | G | A | 34 | a0001c0001t0001g0034 a0001c0001t0003g0005 a0001c0001t0003g0020 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.199-2243G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436078 | |||||||
| chr15:41436287 | T | TA | 20 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0042 others(17): Show |
20 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.199-2011dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436287 | ||||||
| chr15:41436287 | TA | T | 44 | a0001c0001t0001g0073 a0001c0001t0001g0092 a0001c0001t0002g0104 others(41): Show |
45 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.199-2011delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436287 | ||||||
| chr15:41436456 | C | CA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0002g0018 others(12): Show |
15 | HG00609.hp2 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-1846dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436456 | ||||||
| chr15:41436457 | A | C | 1 | a0001c0001t0007g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.199-1864A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436457 | |||||||
| chr15:41436623 | C | CA | 14 | a0001c0001t0001g0043 a0001c0001t0002g0109 a0001c0001t0002g0111 others(11): Show |
14 | HG00544.hp2 HG00558.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-1677dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436623 | ||||||
| chr15:41436623 | CA | C | 7 | a0001c0001t0002g0019 a0001c0001t0002g0135 a0001c0001t0003g0022 others(4): Show |
7 | HG01496.hp1 HG01975.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-1677delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436623 | ||||||
| chr15:41436667 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.199-1654T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436667 | |||||||
| chr15:41436783 | GTC | G | 2 | a0001c0001t0001g0013 a0001c0001t0002g0018 |
2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.199-1534_199-1533d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436783 | ||||||
| chr15:41437001 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0007g0065 |
3 | HG00741.hp1 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.199-1320C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437001 | |||||||
| chr15:41437036 | G | A | 35 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.199-1285G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437036 | |||||||
| chr15:41437125 | AT | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-1195delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437125 | |||||||
| chr15:41437278 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0055 |
2 | HG02004.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.199-1043G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437278 | |||||||
| chr15:41437373 | C | T | 1 | a0001c0001t0014g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-948C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437373 | |||||||
| chr15:41437528 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199-793C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437528 | |||||||
| chr15:41437633 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0007g0086 |
2 | NA18946.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.199-688C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437633 | |||||||
| chr15:41437640 | G | A | 2 | a0001c0001t0007g0205 a0001c0001t0022g0044 |
2 | HG00544.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.199-681G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437640 | |||||||
| chr15:41437813 | G | A | 2 | a0001c0001t0004g0179 a0001c0001t0004g0189 |
2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.199-508G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437813 | |||||||
| chr15:41437860 | G | A | 5 | a0001c0001t0010g0066 a0001c0001t0010g0067 a0001c0001t0010g0078 others(2): Show |
5 | HG01891.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-461G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437860 | |||||||
| chr15:41437914 | C | T | 7 | a0001c0001t0003g0023 a0001c0001t0003g0148 a0001c0001t0003g0157 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-407C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437914 | |||||||
| chr15:41437915 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.199-406T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437915 | |||||||
| chr15:41437928 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-393C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437928 | |||||||
| chr15:41438048 | G | A | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-273G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41438048 | |||||||
| chr15:41438050 | T | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-271T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41438050 | |||||||
| chr15:41438967 | C | CT | 14 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0036 others(11): Show |
14 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.309+551dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41438967 | ||||||
| chr15:41438967 | C | CTT | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+550_309+551dup others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41438967 | ||||||
| chr15:41439085 | G | T | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.309+654G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439085 | |||||||
| chr15:41439162 | G | C | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.309+731G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439162 | |||||||
| chr15:41439176 | C | T | 1 | a0001c0001t0004g0178 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.309+745C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439176 | |||||||
| chr15:41439224 | C | T | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+793C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439224 | |||||||
| chr15:41439352 | G | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+921G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439352 | |||||||
| chr15:41439410 | T | A | 1 | a0001c0001t0001g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.309+979T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439410 | |||||||
| chr15:41439506 | A | T | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+1075A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439506 | |||||||
| chr15:41439709 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.309+1278C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439709 | |||||||
| chr15:41439729 | G | A | 3 | a0001c0001t0006g0126 a0001c0001t0006g0127 a0001c0001t0006g0128 |
3 | HG00639.hp2 HG00738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.309+1298G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439729 | |||||||
| chr15:41439870 | T | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1439T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439870 | |||||||
| chr15:41439990 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.309+1559T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439990 | |||||||
| chr15:41440053 | A | AAAAAATG others(6): Show |
6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1622_309+1623i others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440053 | |||||||
| chr15:41440054 | T | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1623T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440054 | |||||||
| chr15:41440057 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1626G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440057 | |||||||
| chr15:41440184 | C | CT | 3 | a0001c0001t0003g0148 a0001c0001t0003g0163 a0001c0001t0003g0173 |
3 | HG00323.hp2 HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.309+1756dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440184 | ||||||
| chr15:41440186 | TTC | T | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.309+1757_309+1758d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440186 | ||||||
| chr15:41440187 | TC | T | 24 | a0001c0001t0001g0009 a0001c0001t0003g0025 a0001c0001t0004g0181 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.309+1757delC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440187 | |||||||
| chr15:41440188 | C | T | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+1757C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440188 | |||||||
| chr15:41440217 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01074.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.309+1786G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440217 | |||||||
| chr15:41440405 | G | C | 1 | a0001c0001t0010g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.309+1974G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440405 | |||||||
| chr15:41440468 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.309+2037C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440468 | |||||||
| chr15:41440490 | C | CT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0003g0167 others(9): Show |
12 | HG00609.hp2 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.309+2077dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440490 | ||||||
| chr15:41440490 | C | CTTT | 23 | a0001c0001t0004g0176 a0001c0001t0004g0177 a0001c0001t0004g0179 others(20): Show |
23 | HG00099.hp1 HG01106.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.309+2075_309+2077d others(5): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440490 | ||||||
| chr15:41440490 | C | CTTTT | 4 | a0001c0001t0004g0004 a0001c0001t0004g0178 a0001c0001t0004g0191 others(1): Show |
5 | HG00609.hp1 HG01981.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+2074_309+2077d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440490 | ||||||
| chr15:41440594 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+2163A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440594 | |||||||
| chr15:41440680 | G | A | 2 | a0001c0001t0011g0198 a0001c0001t0011g0199 |
2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+2249G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440680 | |||||||
| chr15:41440856 | T | TG | 7 | a0001c0001t0001g0009 a0001c0001t0003g0173 a0001c0001t0009g0007 others(4): Show |
7 | HG00642.hp2 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+2431dupG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440856 | ||||||
| chr15:41440968 | C | CT | 52 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0002g0122 others(49): Show |
52 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.309+2558dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440968 | ||||||
| chr15:41440968 | CT | C | 11 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0041 others(8): Show |
11 | HG00558.hp2 HG02004.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.309+2558delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440968 | ||||||
| chr15:41441051 | A | G | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+2620A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441051 | |||||||
| chr15:41441130 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.309+2699C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441130 | |||||||
| chr15:41441134 | G | A | 2 | a0001c0001t0011g0198 a0001c0001t0011g0199 |
2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+2703G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441134 | |||||||
| chr15:41441206 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0059 others(1): Show |
4 | HG00423.hp2 HG02040.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+2775T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441206 | |||||||
| chr15:41441390 | C | T | 1 | a0001c0001t0007g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.309+2959C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441390 | |||||||
| chr15:41441606 | T | G | 1 | a0001c0001t0002g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.309+3175T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441606 | |||||||
| chr15:41441743 | T | A | 1 | a0001c0001t0004g0190 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.309+3312T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441743 | |||||||
| chr15:41441760 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.309+3329C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441760 | |||||||
| chr15:41442170 | A | AT | 7 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0002g0096 others(4): Show |
7 | HG01358.hp2 HG01928.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+3754dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41442170 | ||||||
| chr15:41442241 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.309+3810C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442241 | |||||||
| chr15:41442281 | C | T | 1 | a0001c0001t0017g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.309+3850C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442281 | |||||||
| chr15:41442343 | A | G | 1 | a0001c0001t0002g0006 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.309+3912A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442343 | |||||||
| chr15:41442484 | G | A | 1 | a0001c0002t0015g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.309+4053G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442484 | |||||||
| chr15:41442603 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.309+4172G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442603 | |||||||
| chr15:41442617 | G | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+4186G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442617 | |||||||
| chr15:41442673 | G | A | 1 | a0001c0005t0007g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.309+4242G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442673 | |||||||
| chr15:41442692 | A | G | 1 | a0001c0001t0006g0121 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.309+4261A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442692 | |||||||
| chr15:41442747 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.309+4316G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442747 | |||||||
| chr15:41442857 | G | A | 2 | a0001c0001t0009g0007 a0001c0001t0009g0008 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.309+4426G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442857 | |||||||
| chr15:41443245 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0061 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.309+4814A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443245 | |||||||
| chr15:41443363 | A | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.309+4932A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443363 | |||||||
| chr15:41443510 | C | A | 89 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0003g0005 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.309+5079C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443510 | |||||||
| chr15:41443512 | T | G | 89 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0003g0005 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.309+5081T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443512 | |||||||
| chr15:41443587 | A | G | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.309+5156A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443587 | |||||||
| chr15:41443597 | G | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+5166G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443597 | |||||||
| chr15:41443602 | TA | T | 88 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0003g0005 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.309+5182delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41443602 | ||||||
| chr15:41443784 | T | C | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+5353T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443784 | |||||||
| chr15:41443846 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.309+5415T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443846 | |||||||
| chr15:41443961 | T | G | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+5530T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443961 | |||||||
| chr15:41444067 | C | CA | 7 | a0001c0001t0004g0176 a0001c0001t0004g0191 a0001c0001t0005g0207 others(4): Show |
7 | HG01981.hp1 NA18955.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.309+5645dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41444067 | ||||||
| chr15:41444076 | AC | A | 7 | a0001c0001t0001g0009 a0001c0001t0003g0152 a0001c0001t0009g0007 others(4): Show |
7 | HG00140.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+5646delC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444076 | |||||||
| chr15:41444077 | C | A | 82 | a0001c0001t0001g0060 a0001c0001t0003g0005 a0001c0001t0003g0020 others(79): Show |
83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.309+5646C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444077 | |||||||
| chr15:41444092 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5661A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444092 | |||||||
| chr15:41444104 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5673T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444104 | |||||||
| chr15:41444142 | G | A | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+5711G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444142 | |||||||
| chr15:41444243 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5812C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444243 | |||||||
| chr15:41444298 | A | AT | 6 | a0001c0001t0002g0120 a0001c0001t0002g0136 a0001c0001t0005g0214 others(3): Show |
6 | HG01496.hp1 HG01515.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+5880dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41444298 | ||||||
| chr15:41444433 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.309+6002A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444433 | |||||||
| chr15:41444448 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.309+6017C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444448 | |||||||
| chr15:41444454 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.309+6023C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444454 | |||||||
| chr15:41444494 | C | T | 5 | a0001c0001t0010g0066 a0001c0001t0010g0067 a0001c0001t0010g0078 others(2): Show |
5 | HG01891.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+6063C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444494 | |||||||
| chr15:41444503 | C | G | 1 | a0001c0001t0007g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.309+6072C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444503 | |||||||
| chr15:41444781 | A | G | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+6350A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444781 | |||||||
| chr15:41444804 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+6373A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444804 | |||||||
| chr15:41444861 | T | C | 89 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0003g0005 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.309+6430T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444861 | |||||||
| chr15:41444864 | G | A | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+6433G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444864 | |||||||
| chr15:41444942 | A | T | 1 | a0001c0001t0007g0076 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+6511A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444942 | |||||||
| chr15:41445077 | G | A | 1 | a0001c0001t0009g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.309+6646G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445077 | |||||||
| chr15:41445081 | A | G | 1 | a0001c0001t0003g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.309+6650A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445081 | |||||||
| chr15:41445171 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+6740G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445171 | |||||||
| chr15:41445449 | G | A | 1 | a0001c0001t0005g0211 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.309+7018G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445449 | |||||||
| chr15:41445583 | T | G | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+7152T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445583 | |||||||
| chr15:41445636 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+7205C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445636 | |||||||
| chr15:41445734 | A | AT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0060 a0001c0001t0004g0176 others(4): Show |
7 | HG01496.hp1 HG02027.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-7149dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41445734 | ||||||
| chr15:41445759 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.310-7142A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445759 | |||||||
| chr15:41445964 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.310-6937C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445964 | |||||||
| chr15:41446090 | C | T | 1 | a0001c0001t0014g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.310-6811C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446090 | |||||||
| chr15:41446318 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG01074.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.310-6583C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446318 | |||||||
| chr15:41446364 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.310-6537A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446364 | |||||||
| chr15:41446439 | G | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.310-6462G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446439 | |||||||
| chr15:41446525 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0071 |
3 | HG02129.hp2 HG02165.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.310-6376C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446525 | |||||||
| chr15:41446568 | A | G | 1 | a0001c0001t0004g0178 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.310-6333A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446568 | |||||||
| chr15:41446569 | A | ATTACT | 88 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0003g0005 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.310-6329_310-6328i others(7): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41446569 | ||||||
| chr15:41446645 | C | A | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.310-6256C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446645 | |||||||
| chr15:41446803 | A | AT | 7 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0001g0095 others(4): Show |
7 | HG01106.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-6081dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41446803 | ||||||
| chr15:41446807 | T | A | 24 | a0001c0001t0001g0045 a0001c0001t0003g0020 a0001c0001t0003g0021 others(21): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.310-6094T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446807 | |||||||
| chr15:41446811 | T | A | 1 | a0001c0001t0003g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.310-6090T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446811 | |||||||
| chr15:41447158 | T | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(3): Show |
6 | HG02145.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-5743T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447158 | |||||||
| chr15:41447278 | T | G | 1 | a0001c0001t0009g0083 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.310-5623T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447278 | |||||||
| chr15:41447346 | G | A | 2 | a0001c0001t0001g0015 a0001c0001t0007g0076 |
2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.310-5555G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447346 | |||||||
| chr15:41447440 | C | T | 1 | a0001c0006t0008g0143 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.310-5461C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447440 | |||||||
| chr15:41447774 | G | A | 4 | a0001c0001t0013g0027 a0001c0001t0013g0201 a0001c0001t0013g0202 others(1): Show |
4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-5127G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447774 | |||||||
| chr15:41447811 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.310-5090G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447811 | |||||||
| chr15:41447811 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.310-5090G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447811 | |||||||
| chr15:41448275 | A | G | 1 | a0001c0001t0003g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.310-4626A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448275 | |||||||
| chr15:41448281 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-4620A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448281 | |||||||
| chr15:41448366 | T | A | 1 | a0001c0001t0008g0141 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.310-4535T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448366 | |||||||
| chr15:41448946 | G | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.310-3955G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448946 | |||||||
| chr15:41449227 | A | AT | 16 | a0001c0001t0001g0013 a0001c0001t0001g0035 a0001c0001t0001g0053 others(13): Show |
16 | HG00741.hp1 HG01496.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.310-3653dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATT | 31 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.310-3654_310-3653d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTT | 17 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(14): Show |
18 | HG00609.hp1 HG01106.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.310-3657_310-3653d others(7): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTT | 10 | a0001c0001t0004g0181 a0001c0001t0004g0182 a0001c0001t0004g0184 others(7): Show |
10 | HG00099.hp1 HG01928.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.310-3658_310-3653d others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(1): Show |
4 | HG01243.hp1 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-3664_310-3653d others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0009g0011 a0001c0001t0009g0012 |
2 | HG01109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.310-3665_310-3653d others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTTT others(7): Show |
9 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(6): Show |
9 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-3666_310-3653d others(16): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTTT others(8): Show |
3 | a0001c0001t0005g0210 a0001c0001t0005g0211 a0001c0001t0005g0219 |
3 | HG01106.hp2 HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.310-3667_310-3653d others(17): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0005g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.310-3668_310-3653d others(18): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0005g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.310-3669_310-3653d others(19): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449227 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0005g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.310-3670_310-3653d others(20): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | ||||||
| chr15:41449284 | G | A | 34 | a0001c0001t0002g0006 a0001c0001t0003g0005 a0001c0001t0003g0020 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.310-3617G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449284 | |||||||
| chr15:41449481 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.310-3420C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449481 | |||||||
| chr15:41449543 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-3358A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449543 | |||||||
| chr15:41449659 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.310-3242T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449659 | |||||||
| chr15:41449799 | T | C | 1 | a0001c0001t0006g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.310-3102T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449799 | |||||||
| chr15:41450013 | T | A | 1 | a0001c0001t0024g0070 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.310-2888T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450013 | |||||||
| chr15:41450036 | A | C | 1 | a0001c0001t0005g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.310-2865A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450036 | |||||||
| chr15:41450414 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.310-2487C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450414 | |||||||
| chr15:41450445 | C | T | 27 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(24): Show |
28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.310-2456C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450445 | |||||||
| chr15:41450454 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.310-2447A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450454 | |||||||
| chr15:41450519 | A | C | 2 | a0001c0001t0005g0211 a0001c0001t0005g0212 |
2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-2382A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450519 | |||||||
| chr15:41450564 | G | A | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.310-2337G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450564 | |||||||
| chr15:41450584 | C | CA | 7 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0001t0001g0068 others(4): Show |
7 | HG00558.hp1 HG01928.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-2300dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41450584 | ||||||
| chr15:41450837 | G | T | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.310-2064G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450837 | |||||||
| chr15:41451228 | C | T | 88 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.310-1673C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451228 | |||||||
| chr15:41451244 | A | T | 1 | a0001c0001t0003g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.310-1657A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451244 | |||||||
| chr15:41451302 | T | C | 1 | a0001c0001t0004g0222 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.310-1599T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451302 | |||||||
| chr15:41451376 | T | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.310-1525T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451376 | |||||||
| chr15:41451408 | G | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.310-1493G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451408 | |||||||
| chr15:41451499 | A | G | 1 | a0001c0001t0011g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.310-1402A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451499 | |||||||
| chr15:41451630 | T | A | 88 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.310-1271T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451630 | |||||||
| chr15:41451760 | C | A | 1 | a0001c0001t0004g0178 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.310-1141C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451760 | |||||||
| chr15:41451964 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.310-937C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451964 | |||||||
| chr15:41452136 | T | C | 1 | a0001c0001t0019g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.310-765T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452136 | |||||||
| chr15:41452270 | T | C | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.310-631T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452270 | |||||||
| chr15:41452321 | A | G | 1 | a0001c0001t0029g0192 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.310-580A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452321 | |||||||
| chr15:41452410 | C | T | 30 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(27): Show |
31 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.310-491C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452410 | |||||||
| chr15:41452517 | T | A | 2 | a0001c0001t0001g0102 a0001c0001t0002g0038 |
2 | NA19089.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.310-384T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452517 | |||||||
| chr15:41452891 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.310-10C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452891 | |||||||
| chr15:41453130 | G | C | 3 | a0001c0001t0006g0098 a0001c0001t0006g0123 a0001c0001t0006g0133 |
3 | HG00544.hp2 NA18961.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.457+82G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453130 | |||||||
| chr15:41453499 | G | A | 1 | a0001c0001t0014g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.457+451G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453499 | |||||||
| chr15:41453632 | C | T | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.457+584C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453632 | |||||||
| chr15:41453993 | A | G | 3 | a0001c0001t0012g0024 a0001c0001t0012g0169 a0001c0001t0012g0170 |
3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457+945A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453993 | |||||||
| chr15:41454078 | G | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.457+1030G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454078 | |||||||
| chr15:41454126 | C | T | 1 | a0001c0001t0004g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.457+1078C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454126 | |||||||
| chr15:41454127 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.457+1079G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454127 | |||||||
| chr15:41454170 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.457+1122C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454170 | |||||||
| chr15:41454281 | G | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1233G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454281 | |||||||
| chr15:41454337 | T | C | 89 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.457+1289T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454337 | |||||||
| chr15:41454400 | T | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1352T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454400 | |||||||
| chr15:41454427 | A | G | 89 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.457+1379A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454427 | |||||||
| chr15:41454812 | T | C | 1 | a0001c0001t0005g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.457+1764T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454812 | |||||||
| chr15:41454863 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.457+1815T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454863 | |||||||
| chr15:41454890 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.457+1842A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454890 | |||||||
| chr15:41455069 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.457+2021A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455069 | |||||||
| chr15:41455185 | C | A | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.457+2137C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455185 | |||||||
| chr15:41455400 | G | A | 89 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.458-2272G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455400 | |||||||
| chr15:41455443 | G | A | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.458-2229G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455443 | |||||||
| chr15:41455458 | G | GT | 4 | a0001c0001t0013g0027 a0001c0001t0013g0201 a0001c0001t0013g0202 others(1): Show |
4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-2213dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41455458 | ||||||
| chr15:41455498 | G | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0144 a0001c0001t0008g0099 others(2): Show |
5 | NA18962.hp2 NA18971.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-2174G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455498 | |||||||
| chr15:41455603 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.458-2069G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455603 | |||||||
| chr15:41455675 | C | T | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.458-1997C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455675 | |||||||
| chr15:41455745 | C | T | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.458-1927C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455745 | |||||||
| chr15:41455847 | A | G | 1 | a0001c0001t0004g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.458-1825A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455847 | |||||||
| chr15:41456130 | C | G | 3 | a0001c0001t0003g0167 a0001c0001t0003g0171 a0001c0001t0003g0174 |
3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.458-1542C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456130 | |||||||
| chr15:41456190 | C | CA | 36 | a0001c0001t0001g0009 a0001c0001t0001g0080 a0001c0001t0003g0151 others(33): Show |
37 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.458-1468dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41456190 | ||||||
| chr15:41456330 | T | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-1342T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456330 | |||||||
| chr15:41456350 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0095 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.458-1322G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456350 | |||||||
| chr15:41456414 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0034 others(43): Show |
47 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.458-1258G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456414 | |||||||
| chr15:41456488 | C | CA | 50 | a0001c0001t0001g0034 a0001c0001t0001g0055 a0001c0001t0003g0005 others(47): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.458-1169dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41456488 | ||||||
| chr15:41456586 | C | T | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.458-1086C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456586 | |||||||
| chr15:41456635 | G | A | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.458-1037G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456635 | |||||||
| chr15:41456713 | C | T | 1 | a0001c0001t0007g0028 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.458-959C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456713 | |||||||
| chr15:41456950 | G | C | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-722G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456950 | |||||||
| chr15:41456952 | C | T | 1 | a0001c0001t0009g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.458-720C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456952 | |||||||
| chr15:41457012 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-660G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457012 | |||||||
| chr15:41457136 | G | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.458-536G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457136 | |||||||
| chr15:41457174 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-498G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457174 | |||||||
| chr15:41457193 | A | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0108 a0001c0001t0002g0109 others(2): Show |
5 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-479A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457193 | |||||||
| chr15:41457232 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.458-440A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457232 | |||||||
| chr15:41457294 | G | C | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-378G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457294 | |||||||
| chr15:41457295 | AG | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-375delG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41457295 | ||||||
| chr15:41457387 | G | T | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-285G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457387 | |||||||
| chr15:41457457 | C | T | 1 | a0001c0001t0006g0123 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.458-215C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457457 | |||||||
| chr15:41457478 | T | C | 1 | a0001c0001t0003g0151 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.458-194T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457478 | |||||||
| chr15:41457898 | T | TC | 12 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0088 others(9): Show |
12 | HG00738.hp1 HG00741.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.662+31dupC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41457898 | ||||||
| chr15:41457898 | TC | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(81): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.662+31delC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41457898 | ||||||
| chr15:41458250 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+374C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41458250 | |||||||
| chr15:41458616 | T | G | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.662+740T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41458616 | |||||||
| chr15:41458750 | AAAAAAT | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.662+890_662+895del others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41458750 | ||||||
| chr15:41459107 | G | A | 1 | a0001c0001t0003g0161 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.662+1231G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459107 | |||||||
| chr15:41459160 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.662+1284C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459160 | |||||||
| chr15:41459480 | C | T | 22 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.662+1604C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459480 | |||||||
| chr15:41459829 | G | C | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.662+1953G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459829 | |||||||
| chr15:41459861 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.662+1985C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459861 | |||||||
| chr15:41459957 | G | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.662+2081G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459957 | |||||||
| chr15:41460052 | T | G | 1 | a0001c0001t0010g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.662+2176T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460052 | |||||||
| chr15:41460117 | TTTTG | T | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.662+2245_662+2248d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41460117 | ||||||
| chr15:41460126 | T | G | 34 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.662+2250T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460126 | |||||||
| chr15:41460126 | T | TG | 17 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0030 others(14): Show |
17 | HG00140.hp2 HG02027.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.662+2250_662+2251i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460126 | |||||||
| chr15:41460126 | T | TTG | 25 | a0001c0001t0001g0080 a0001c0001t0004g0004 a0001c0001t0004g0176 others(22): Show |
26 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.662+2251_662+2252i others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41460126 | ||||||
| chr15:41460127 | T | TG | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(91): Show |
95 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.662+2251_662+2252i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460127 | |||||||
| chr15:41460577 | C | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.662+2701C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460577 | |||||||
| chr15:41460654 | C | T | 89 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.662+2778C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460654 | |||||||
| chr15:41460962 | C | T | 3 | a0001c0001t0012g0024 a0001c0001t0012g0169 a0001c0001t0012g0170 |
3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.662+3086C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460962 | |||||||
| chr15:41461042 | A | AT | 5 | a0001c0001t0002g0109 a0001c0001t0005g0221 a0001c0001t0007g0037 others(2): Show |
5 | HG01981.hp2 HG02300.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.662+3183dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41461042 | ||||||
| chr15:41461354 | G | A | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.663-3417G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461354 | |||||||
| chr15:41461527 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.663-3244C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461527 | |||||||
| chr15:41461586 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.663-3185G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461586 | |||||||
| chr15:41461621 | C | G | 1 | a0001c0001t0003g0020 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.663-3150C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461621 | |||||||
| chr15:41461704 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.663-3067C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461704 | |||||||
| chr15:41461785 | G | A | 3 | a0001c0001t0012g0024 a0001c0001t0012g0169 a0001c0001t0012g0170 |
3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.663-2986G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461785 | |||||||
| chr15:41461913 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.663-2858T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461913 | |||||||
| chr15:41461935 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.663-2836T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461935 | |||||||
| chr15:41461936 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.663-2835T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461936 | |||||||
| chr15:41462268 | G | C | 1 | a0001c0001t0006g0137 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.663-2503G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462268 | |||||||
| chr15:41462451 | C | G | 14 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(11): Show |
14 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.663-2320C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462451 | |||||||
| chr15:41462459 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0002g0103 |
2 | NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.663-2312C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462459 | |||||||
| chr15:41462581 | A | G | 1 | a0001c0001t0003g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.663-2190A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462581 | |||||||
| chr15:41462890 | G | T | 1 | a0001c0001t0007g0076 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.663-1881G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462890 | |||||||
| chr15:41462910 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.663-1861C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462910 | |||||||
| chr15:41463349 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.663-1422A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463349 | |||||||
| chr15:41463632 | C | T | 1 | a0001c0001t0011g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.663-1139C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463632 | |||||||
| chr15:41463749 | T | C | 4 | a0001c0001t0013g0027 a0001c0001t0013g0201 a0001c0001t0013g0202 others(1): Show |
4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-1022T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463749 | |||||||
| chr15:41463813 | G | A | 1 | a0001c0006t0008g0143 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.663-958G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463813 | |||||||
| chr15:41463999 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.663-772A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463999 | |||||||
| chr15:41464167 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0009g0001 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.663-604A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464167 | |||||||
| chr15:41464331 | A | G | 10 | a0001c0001t0003g0005 a0001c0001t0003g0167 a0001c0001t0003g0168 others(7): Show |
10 | HG00642.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.663-440A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464331 | |||||||
| chr15:41464438 | G | A | 1 | a0001c0001t0005g0212 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.663-333G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464438 | |||||||
| chr15:41464637 | G | C | 1 | a0001c0001t0017g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.663-134G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464637 | |||||||
| chr15:41464714 | A | G | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.663-57A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464714 | |||||||
| chr15:41464933 | A | AGT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(89): Show |
92 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.777+81_777+82dupGT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | ||||||
| chr15:41464933 | A | AGTGT | 19 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0039 others(16): Show |
20 | HG01074.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+79_777+82dupGT others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | ||||||
| chr15:41464933 | A | AGTGTGT | 4 | a0001c0001t0001g0060 a0001c0001t0001g0095 a0001c0001t0005g0220 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+77_777+82dupGT others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | ||||||
| chr15:41464933 | A | AGTGTGTG others(1): Show |
12 | a0001c0001t0001g0015 a0001c0001t0005g0207 a0001c0001t0005g0208 others(9): Show |
12 | HG01081.hp2 HG01106.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.777+75_777+82dupGT others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | ||||||
| chr15:41464933 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0005g0215 a0001c0001t0005g0217 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.777+73_777+82dupGT others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | ||||||
| chr15:41464933 | AGT | A | 33 | a0001c0001t0002g0069 a0001c0001t0002g0106 a0001c0001t0002g0116 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.777+81_777+82delGT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | ||||||
| chr15:41464933 | AGTGT | A | 36 | a0001c0001t0001g0073 a0001c0001t0003g0023 a0001c0001t0003g0025 others(33): Show |
37 | HG00099.hp1 HG00609.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.777+79_777+82delGT others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | ||||||
| chr15:41465069 | G | C | 1 | a0001c0001t0003g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.777+184G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465069 | |||||||
| chr15:41465325 | C | T | 1 | a0001c0001t0003g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.777+440C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465325 | |||||||
| chr15:41465389 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.777+504C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465389 | |||||||
| chr15:41465406 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.777+521C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465406 | |||||||
| chr15:41465469 | T | C | 90 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0003g0005 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.777+584T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465469 | |||||||
| chr15:41465641 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.778-500A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465641 | |||||||
| chr15:41465936 | C | T | 1 | a0001c0001t0003g0163 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.778-205C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465936 | |||||||
| chr15:41465955 | A | G | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.778-186A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465955 | |||||||
| chr15:41466300 | C | T | 1 | a0001c0001t0003g0161 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.889+48C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466300 | |||||||
| chr15:41466696 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.889+444C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466696 | |||||||
| chr15:41466804 | G | A | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.889+552G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466804 | |||||||
| chr15:41466959 | G | A | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.889+707G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466959 | |||||||
| chr15:41466969 | T | G | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.889+717T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466969 | |||||||
| chr15:41467342 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.889+1090G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467342 | |||||||
| chr15:41467477 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0124 |
2 | NA18953.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.889+1225G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467477 | |||||||
| chr15:41467592 | G | A | 1 | a0001c0002t0015g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889+1340G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467592 | |||||||
| chr15:41467639 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.889+1387C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467639 | |||||||
| chr15:41467891 | A | G | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1639A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467891 | |||||||
| chr15:41467919 | C | G | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1667C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467919 | |||||||
| chr15:41468030 | T | C | 1 | a0001c0002t0015g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889+1778T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468030 | |||||||
| chr15:41468164 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.889+1912C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468164 | |||||||
| chr15:41468185 | A | C | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1933A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468185 | |||||||
| chr15:41468186 | TAATAACG others(165): Show |
T | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1935_890-1899d others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468186 | |||||||
| chr15:41468202 | C | T | 2 | a0001c0001t0005g0211 a0001c0001t0005g0212 |
2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.889+1950C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468202 | |||||||
| chr15:41468341 | G | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.890-1916G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468341 | |||||||
| chr15:41468419 | A | G | 88 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.890-1838A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468419 | |||||||
| chr15:41468469 | C | T | 1 | a0001c0001t0005g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.890-1788C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468469 | |||||||
| chr15:41468507 | A | C | 29 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(26): Show |
30 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.890-1750A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468507 | |||||||
| chr15:41468508 | G | A | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.890-1749G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468508 | |||||||
| chr15:41468511 | G | A | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.890-1746G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468511 | |||||||
| chr15:41468519 | A | G | 12 | a0001c0001t0004g0177 a0001c0001t0004g0178 a0001c0001t0004g0180 others(9): Show |
12 | HG01928.hp2 HG01975.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.890-1738A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468519 | |||||||
| chr15:41468534 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.890-1723G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468534 | |||||||
| chr15:41468538 | T | C | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.890-1719T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468538 | |||||||
| chr15:41468592 | C | G | 23 | a0001c0001t0002g0101 a0001c0001t0003g0020 a0001c0001t0003g0021 others(20): Show |
23 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.890-1665C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468592 | |||||||
| chr15:41468592 | C | T | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.890-1665C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468592 | |||||||
| chr15:41468595 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0016g0145 others(2): Show |
5 | HG02451.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-1662G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468595 | |||||||
| chr15:41468596 | T | C | 10 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0004g0191 others(7): Show |
10 | HG01496.hp1 HG01981.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.890-1661T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468596 | |||||||
| chr15:41468608 | C | T | 1 | a0001c0001t0006g0137 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.890-1649C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468608 | |||||||
| chr15:41468609 | A | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0020 a0001c0001t0003g0021 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.890-1648A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468609 | |||||||
| chr15:41468904 | C | G | 1 | a0001c0001t0011g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.890-1353C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468904 | |||||||
| chr15:41469125 | C | CCTGA | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.890-1130_890-1129i others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr15 | 41469125 | ||||||
| chr15:41469134 | G | T | 89 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.890-1123G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469134 | |||||||
| chr15:41469339 | T | A | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.890-918T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469339 | |||||||
| chr15:41469604 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.890-653C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469604 | |||||||
| chr15:41469611 | C | T | 55 | a0001c0001t0001g0009 a0001c0001t0004g0004 a0001c0001t0004g0176 others(52): Show |
56 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.890-646C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469611 | |||||||
| chr15:41469725 | A | G | 1 | a0001c0001t0002g0144 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.890-532A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469725 | |||||||
| chr15:41469786 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.890-471A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469786 | |||||||
| chr15:41469827 | A | G | 1 | a0001c0003t0004g0188 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.890-430A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469827 | |||||||
| chr15:41469931 | A | G | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.890-326A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469931 | |||||||
| chr15:41470112 | C | T | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.890-145C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41470112 | |||||||
| chr15:41470148 | G | A | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.890-109G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41470148 | |||||||
| chr15:41470433 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025+41G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470433 | |||||||
| chr15:41470650 | C | CT | 26 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0041 others(23): Show |
26 | HG00140.hp2 HG00423.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1025+284dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr15 | 41470650 | ||||||
| chr15:41470650 | CT | C | 78 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0003g0005 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1025+284delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr15 | 41470650 | ||||||
| chr15:41470650 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1025+271_1025+284d others(16): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr15 | 41470650 | ||||||
| chr15:41470656 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(2): Show |
5 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+264T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470656 | |||||||
| chr15:41470657 | T | C | 1 | a0001c0001t0009g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1025+265T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470657 | |||||||
| chr15:41470681 | C | T | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1025+289C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470681 | |||||||
| chr15:41470720 | A | G | 24 | a0001c0001t0001g0009 a0001c0001t0005g0207 a0001c0001t0005g0208 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1025+328A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470720 | |||||||
| chr15:41470880 | G | A | 4 | a0001c0001t0006g0098 a0001c0001t0006g0117 a0001c0001t0006g0123 others(1): Show |
4 | HG00544.hp2 NA18961.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-292G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470880 | |||||||
| chr15:41471366 | T | C | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1203+17T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471366 | |||||||
| chr15:41471590 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1203+241C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471590 | |||||||
| chr15:41471721 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0063 |
2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1203+372C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471721 | |||||||
| chr15:41471721 | C | T | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1203+372C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471721 | |||||||
| chr15:41471898 | T | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG02145.hp1 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1203+549T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471898 | |||||||
| chr15:41471981 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0007g0065 |
3 | HG00741.hp1 HG03654.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1203+632C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471981 | |||||||
| chr15:41472011 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1203+662G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472011 | |||||||
| chr15:41472215 | T | G | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1203+866T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472215 | |||||||
| chr15:41472324 | A | G | 89 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1203+975A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472324 | |||||||
| chr15:41472356 | G | A | 1 | a0001c0001t0014g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1203+1007G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472356 | |||||||
| chr15:41472378 | T | C | 3 | a0001c0001t0016g0145 a0001c0001t0016g0146 a0001c0001t0026g0147 |
3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1203+1029T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472378 | |||||||
| chr15:41472502 | C | T | 7 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0215 others(4): Show |
7 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203+1153C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472502 | |||||||
| chr15:41472503 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1203+1154G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472503 | |||||||
| chr15:41472675 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1203+1326G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472675 | |||||||
| chr15:41472705 | CT | C | 5 | a0001c0001t0003g0163 a0001c0001t0013g0027 a0001c0001t0013g0201 others(2): Show |
5 | HG00323.hp2 NA18955.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203+1371delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr15 | 41472705 | ||||||
| chr15:41472903 | G | T | 1 | a0001c0001t0003g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1203+1554G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472903 | |||||||
| chr15:41472922 | T | C | 10 | a0001c0001t0003g0005 a0001c0001t0003g0167 a0001c0001t0003g0168 others(7): Show |
10 | HG00642.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203+1573T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472922 | |||||||
| chr15:41472931 | A | G | 10 | a0001c0001t0003g0005 a0001c0001t0003g0167 a0001c0001t0003g0168 others(7): Show |
10 | HG00642.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203+1582A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472931 | |||||||
| chr15:41473038 | G | T | 1 | a0001c0001t0005g0221 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1204-1582G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473038 | |||||||
| chr15:41473072 | C | T | 6 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0007g0054 others(3): Show |
6 | HG02451.hp1 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1204-1548C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473072 | |||||||
| chr15:41473086 | T | C | 1 | a0001c0001t0003g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1204-1534T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473086 | |||||||
| chr15:41473156 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1204-1464C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473156 | |||||||
| chr15:41473278 | C | T | 1 | a0001c0001t0007g0037 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1204-1342C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473278 | |||||||
| chr15:41473279 | G | A | 1 | a0001c0001t0004g0190 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1204-1341G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473279 | |||||||
| chr15:41473442 | G | GT | 12 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
12 | HG00639.hp1 HG00741.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1204-1162dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr15 | 41473442 | ||||||
| chr15:41473442 | GT | G | 26 | a0001c0001t0001g0009 a0001c0001t0001g0031 a0001c0001t0005g0207 others(23): Show |
26 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1204-1162delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr15 | 41473442 | ||||||
| chr15:41473620 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1204-1000C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473620 | |||||||
| chr15:41473762 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-858C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473762 | |||||||
| chr15:41473906 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1204-714A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473906 | |||||||
| chr15:41474225 | A | G | 5 | a0001c0001t0006g0112 a0001c0001t0006g0115 a0001c0001t0006g0121 others(2): Show |
5 | HG01168.hp2 HG02293.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1204-395A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41474225 | |||||||
| chr15:41474344 | C | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-276C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41474344 | |||||||
| chr15:41474599 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1204-21C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41474599 | |||||||
| chr15:41475117 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1287-408C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 9/17 | chr15 | 41475117 | |||||||
| chr15:41475157 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287-368A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 9/17 | chr15 | 41475157 | |||||||
| chr15:41475359 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1287-166A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 9/17 | chr15 | 41475359 | |||||||
| chr15:41476057 | G | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1482+238G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476057 | |||||||
| chr15:41476096 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1482+277G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476096 | |||||||
| chr15:41476137 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1483-309A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476137 | |||||||
| chr15:41476138 | A | G | 4 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(1): Show |
4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-308A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476138 | |||||||
| chr15:41476780 | C | A | 1 | a0001c0001t0011g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1560+257C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 12/17 | chr15 | 41476780 | |||||||
| chr15:41476830 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1560+307A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 12/17 | chr15 | 41476830 | |||||||
| chr15:41477724 | C | G | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1740+209C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41477724 | |||||||
| chr15:41477754 | T | A | 2 | a0001c0001t0004g0179 a0001c0001t0004g0189 |
2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1740+239T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41477754 | |||||||
| chr15:41477790 | C | G | 3 | a0001c0001t0016g0145 a0001c0001t0016g0146 a0001c0001t0026g0147 |
3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1740+275C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41477790 | |||||||
| chr15:41478024 | T | C | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1740+509T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478024 | |||||||
| chr15:41478138 | C | T | 1 | a0001c0001t0004g0191 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1741-410C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478138 | |||||||
| chr15:41478305 | G | A | 15 | a0001c0001t0005g0207 a0001c0001t0005g0208 a0001c0001t0005g0209 others(12): Show |
15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1741-243G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478305 | |||||||
| chr15:41478357 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1741-191C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478357 | |||||||
| chr15:41478410 | T | TA | 8 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0008g0017 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741-123dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr15 | 41478410 | ||||||
| chr15:41478441 | C | CT | 20 | a0001c0001t0002g0038 a0001c0001t0002g0103 a0001c0001t0005g0207 others(17): Show |
20 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1741-95dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr15 | 41478441 | ||||||
| chr15:41478943 | C | CT | 24 | a0001c0001t0001g0073 a0001c0001t0002g0135 a0001c0001t0003g0167 others(21): Show |
24 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1819-142dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr15 | 41478943 | ||||||
| chr15:41479393 | G | A | 89 | a0001c0001t0001g0009 a0001c0001t0003g0005 a0001c0001t0003g0020 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1914+195G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479393 | |||||||
| chr15:41479432 | A | G | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1914+234A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479432 | |||||||
| chr15:41479483 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1914+285C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479483 | |||||||
| chr15:41479487 | G | A | 7 | a0001c0001t0003g0023 a0001c0001t0003g0148 a0001c0001t0003g0157 others(4): Show |
7 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1914+289G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479487 | |||||||
| chr15:41479626 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1914+428G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479626 | |||||||
| chr15:41479627 | G | C | 1 | a0001c0001t0005g0220 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1914+429G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479627 | |||||||
| chr15:41479642 | C | A | 1 | a0001c0001t0003g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1914+444C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479642 | |||||||
| chr15:41479730 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1915-484G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479730 | |||||||
| chr15:41479732 | G | A | 1 | a0001c0001t0004g0182 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1915-482G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479732 | |||||||
| chr15:41479780 | G | A | 3 | a0001c0001t0011g0197 a0001c0001t0011g0198 a0001c0001t0011g0199 |
3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1915-434G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479780 | |||||||
| chr15:41479818 | G | A | 28 | a0001c0001t0004g0004 a0001c0001t0004g0176 a0001c0001t0004g0177 others(25): Show |
29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1915-396G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479818 | |||||||
| chr15:41479864 | C | CA | 7 | a0001c0001t0001g0058 a0001c0001t0001g0072 a0001c0001t0002g0139 others(4): Show |
7 | HG00544.hp2 HG01081.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1915-333dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr15 | 41479864 | ||||||
| chr15:41479864 | CA | C | 55 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0102 others(52): Show |
56 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1915-333delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr15 | 41479864 | ||||||
| chr15:41479979 | C | T | 2 | a0001c0001t0006g0112 a0001c0001t0021g0134 |
2 | HG02293.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1915-235C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479979 | |||||||
| chr15:41480004 | A | C | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1915-210A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480004 | |||||||
| chr15:41480010 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1915-204G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480010 | |||||||
| chr15:41480141 | G | A | 3 | a0001c0001t0011g0026 a0001c0001t0014g0196 a0001c0001t0014g0206 |
3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1915-73G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480141 | |||||||
| chr15:41480176 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1915-38T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480176 | |||||||
| chr15:41480425 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0009g0007 a0001c0001t0009g0008 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2026+100G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480425 | |||||||
| chr15:41480466 | T | C | 12 | a0001c0001t0001g0094 a0001c0001t0005g0207 a0001c0001t0005g0208 others(9): Show |
12 | HG01496.hp1 HG01891.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2027-115T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480466 | |||||||
| chr15:41480495 | G | A | 23 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2027-86G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480495 | |||||||
| chr15:41480554 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2027-27C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480554 |