Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 255488 |
| ensemblid | ENSG00000137393.10 |
| hgncid | 21578 |
| symbol | RNF144B |
| name | ring finger protein 144B |
| refseq_nuc | NM_182757.4 |
| refseq_prot | NP_877434.2 |
| ensembl_nuc | ENST00000259939.4 |
| ensembl_prot | ENSP00000259939.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 18387350 |
| end | 18468870 |
| strand | + |
| ver | v1.2 |
| region | chr6:18387350-18468870 |
| region5000 | chr6:18382350-18473870 |
| regionname0 | RNF144B_chr6_18387350_18468870 |
| regionname5000 | RNF144B_chr6_18382350_18473870 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 303 | 384 | 90 | 82 | 150 | 18 | 42 | 113 | RNF144B_chr6_18382350_18473870 | RNF144B | MGSAG others(298): Show |
chr6 | 18382350 | 18473870 |
| a0002 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | MGSAG others(298): Show |
chr6 | 18382350 | 18473870 |
| a0003 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | MGSAG others(298): Show |
chr6 | 18382350 | 18473870 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 909 | 380 | 90 | 81 | 149 | 16 | 42 | RNF144B_chr6_18382350_18473870 | RNF144B | ATGGG others(904): Show |
chr6 | 18382350 | 18473870 | ||
| a0001c0002 | 0/0 | 909 | 2 | 0 | 0 | 0 | 2 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | ATGGG others(904): Show |
chr6 | 18382350 | 18473870 | ||
| a0001c0003 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | ATGGG others(904): Show |
chr6 | 18382350 | 18473870 | ||
| a0001c0005 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | ATGGG others(904): Show |
chr6 | 18382350 | 18473870 | ||
| a0002c0004 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | ATGGG others(904): Show |
chr6 | 18382350 | 18473870 | ||
| a0003c0006 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | ATGGG others(904): Show |
chr6 | 18382350 | 18473870 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5037 | 31 | 0 | 2 | 28 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0002 | 0/0 | 5036 | 23 | 1 | 4 | 16 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0003 | 0/0 | 5033 | 17 | 0 | 0 | 16 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0004 | 0/0 | 5037 | 15 | 0 | 0 | 12 | 1 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0005 | 0/0 | 5033 | 15 | 1 | 6 | 6 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0006 | 0/0 | 5032 | 14 | 2 | 2 | 8 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0007 | 0/0 | 5028 | 13 | 1 | 7 | 1 | 3 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5023): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0008 | 0/0 | 5033 | 11 | 1 | 1 | 9 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0009 | 0/0 | 5031 | 9 | 2 | 0 | 6 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0010 | 0/0 | 5031 | 10 | 2 | 5 | 0 | 3 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0011 | 0/0 | 5036 | 9 | 1 | 8 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0012 | 0/0 | 5033 | 8 | 3 | 1 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0013 | 0/0 | 5036 | 8 | 4 | 0 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0014 | 0/0 | 5037 | 7 | 0 | 1 | 3 | 0 | 3 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0015 | 0/0 | 5033 | 7 | 0 | 3 | 3 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0016 | 0/0 | 5033 | 7 | 2 | 4 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0017 | 0/0 | 5032 | 6 | 3 | 1 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0018 | 0/0 | 5027 | 5 | 0 | 0 | 1 | 0 | 4 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5022): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0019 | 0/0 | 5036 | 5 | 2 | 2 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0020 | 0/0 | 5035 | 5 | 4 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0021 | 0/0 | 5035 | 5 | 4 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0022 | 0/0 | 5033 | 3 | 0 | 3 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0023 | 0/0 | 5038 | 5 | 0 | 0 | 5 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5033): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0024 | 0/0 | 5030 | 4 | 3 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5025): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0025 | 0/0 | 5031 | 3 | 0 | 0 | 3 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0026 | 0/0 | 5032 | 4 | 0 | 2 | 0 | 1 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0027 | 0/1 | 5036 | 4 | 0 | 2 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0028 | 0/0 | 5035 | 4 | 4 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0029 | 0/0 | 5037 | 4 | 0 | 3 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0030 | 0/0 | 5036 | 4 | 2 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0031 | 0/0 | 5037 | 4 | 0 | 0 | 4 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0032 | 0/0 | 5034 | 4 | 0 | 1 | 3 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5029): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0033 | 0/0 | 5030 | 3 | 3 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5025): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0034 | 0/0 | 5032 | 3 | 0 | 0 | 2 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0035 | 0/0 | 5028 | 3 | 0 | 0 | 1 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5023): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0036 | 0/0 | 5034 | 3 | 0 | 1 | 1 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5029): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0037 | 0/0 | 5032 | 3 | 0 | 1 | 1 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0038 | 0/0 | 5036 | 3 | 3 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0039 | 0/0 | 5033 | 3 | 2 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0040 | 1/0 | 5032 | 3 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0041 | 0/0 | 5036 | 3 | 1 | 1 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0042 | 0/0 | 5036 | 3 | 0 | 1 | 0 | 1 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0043 | 0/0 | 5033 | 2 | 0 | 0 | 0 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0044 | 0/0 | 5030 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5025): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0045 | 0/0 | 5028 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5023): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0046 | 0/0 | 5033 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0047 | 0/0 | 5037 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0048 | 0/0 | 5036 | 2 | 1 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0049 | 0/0 | 5033 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0050 | 0/0 | 5037 | 2 | 1 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0051 | 0/0 | 5036 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0052 | 0/0 | 5036 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0053 | 0/0 | 5033 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0054 | 0/0 | 5037 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0055 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0056 | 0/0 | 5033 | 2 | 0 | 1 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0057 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0058 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5023): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0059 | 0/0 | 5037 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0060 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0061 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0062 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5024): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0063 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0064 | 0/0 | 5030 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5025): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0065 | 0/0 | 5028 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5023): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0066 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0067 | 0/0 | 5032 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0068 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0069 | 0/0 | 5032 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0070 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0071 | 0/0 | 5025 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5020): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0072 | 0/0 | 5029 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5024): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0073 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0074 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0075 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0076 | 0/0 | 5037 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0077 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0079 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0080 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0081 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0082 | 0/0 | 5035 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0083 | 0/0 | 5035 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0084 | 0/0 | 5032 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5027): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0085 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0086 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0087 | 0/0 | 5036 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0088 | 0/0 | 5037 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0089 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0090 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5029): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0091 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0092 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0093 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0094 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5033): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0095 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0096 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0097 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5025): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0098 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5029): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0099 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5029): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0100 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5029): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0101 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0102 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0103 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0104 | 0/0 | 5035 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5030): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0105 | 0/0 | 5036 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5031): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0106 | 0/0 | 5034 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5029): Show |
chr6 | 18382350 | 18473870 |
| a0001c0001t0107 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0002t0022 | 0/0 | 5033 | 2 | 0 | 0 | 0 | 2 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5028): Show |
chr6 | 18382350 | 18473870 |
| a0001c0003t0025 | 0/0 | 5031 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0001c0005t0009 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5026): Show |
chr6 | 18382350 | 18473870 |
| a0002c0004t0078 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| a0003c0006t0055 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | GAGCT others(5032): Show |
chr6 | 18382350 | 18473870 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0004g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0005g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0007g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0010g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0011g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0012g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0014g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0015g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0016g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0017g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0018g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0019g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0020g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0021g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0022g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0022g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0022g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0023g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0024g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0025g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0025g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0025g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0026g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0027g0365 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0028g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0029g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0030g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0031g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0032g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0033g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0033g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0033g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0034g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0034g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0034g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0035g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0035g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0035g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0036g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0036g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0036g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0037g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0037g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0037g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0038g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0038g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0038g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0039g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0039g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0039g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0040g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0040g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0040g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0041g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0041g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0041g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0042g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0042g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0042g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0043g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0043g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0044g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0044g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0045g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0045g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0046g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0047g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0047g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0048g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0048g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0049g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0049g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0050g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0050g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0051g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0052g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0052g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0053g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0053g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0054g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0054g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0055g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0056g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0056g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0057g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0058g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0059g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0060g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0061g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0062g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0063g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0064g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0065g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0066g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0067g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0068g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0069g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0070g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0071g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0072g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0073g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0074g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0075g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0076g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0077g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0079g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0080g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0081g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0082g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0083g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0084g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0085g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0086g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0087g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0088g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0089g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0090g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0091g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0092g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0093g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0094g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0095g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0096g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0097g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0098g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0099g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0100g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0101g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0102g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0103g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0104g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0105g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0106g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0001t0107g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0002t0022g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0002t0022g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0003t0025g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0001c0005t0009g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0002c0004t0078g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| a0003c0006t0055g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0236 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0312 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00140 | hp1 | a0001 | c0001 | t0084 | g0111 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00140 | hp2 | a0001 | c0001 | t0071 | g0294 | EUR | GBR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00280 | hp1 | a0001 | c0001 | t0007 | g0232 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00280 | hp2 | a0001 | c0001 | t0010 | g0241 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00323 | hp1 | a0001 | c0001 | t0042 | g0075 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00323 | hp2 | a0001 | c0001 | t0029 | g0122 | EUR | FIN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00423 | hp1 | a0001 | c0001 | t0053 | g0205 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00438 | hp1 | a0001 | c0001 | t0089 | g0185 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00438 | hp2 | a0001 | c0001 | t0023 | g0046 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0360 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00609 | hp2 | a0001 | c0001 | t0034 | g0230 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00621 | hp2 | a0001 | c0001 | t0015 | g0339 | EAS | CHS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00639 | hp1 | a0001 | c0001 | t0007 | g0271 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00639 | hp2 | a0001 | c0001 | t0056 | g0054 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00642 | hp1 | a0001 | c0001 | t0017 | g0092 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0355 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00733 | hp1 | a0001 | c0001 | t0022 | g0160 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0240 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00735 | hp1 | a0001 | c0001 | t0059 | g0143 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00735 | hp2 | a0001 | c0001 | t0076 | g0363 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0243 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00738 | hp2 | a0001 | c0001 | t0039 | g0175 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00741 | hp1 | a0001 | c0001 | t0012 | g0193 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG00741 | hp2 | a0001 | c0001 | t0094 | g0210 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01069 | hp1 | a0001 | c0001 | t0010 | g0254 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01069 | hp2 | a0001 | c0001 | t0015 | g0367 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01070 | hp1 | a0001 | c0001 | t0016 | g0077 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01070 | hp2 | a0001 | c0001 | t0022 | g0217 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01071 | hp1 | a0001 | c0001 | t0016 | g0055 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01071 | hp2 | a0001 | c0001 | t0010 | g0010 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0344 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01074 | hp2 | a0001 | c0001 | t0015 | g0129 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01081 | hp1 | a0001 | c0001 | t0037 | g0137 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01099 | hp1 | a0001 | c0001 | t0022 | g0159 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01099 | hp2 | a0001 | c0001 | t0010 | g0234 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0293 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01106 | hp2 | a0001 | c0001 | t0015 | g0138 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0080 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01109 | hp2 | a0001 | c0001 | t0021 | g0196 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01167 | hp1 | a0001 | c0001 | t0029 | g0125 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01167 | hp2 | a0001 | c0001 | t0024 | g0291 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01168 | hp1 | a0001 | c0001 | t0046 | g0007 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01168 | hp2 | a0001 | c0001 | t0087 | g0123 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01169 | hp1 | a0001 | c0001 | t0046 | g0007 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01169 | hp2 | a0001 | c0001 | t0029 | g0121 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0237 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01175 | hp2 | a0001 | c0001 | t0029 | g0116 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01192 | hp1 | a0001 | c0001 | t0105 | g0067 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0032 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01243 | hp1 | a0001 | c0001 | t0027 | g0300 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01243 | hp2 | a0001 | c0001 | t0030 | g0163 | AMR | PUR | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01255 | hp1 | a0001 | c0001 | t0032 | g0208 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01255 | hp2 | a0001 | c0001 | t0041 | g0035 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0276 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01256 | hp2 | a0001 | c0001 | t0019 | g0006 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01257 | hp1 | a0001 | c0001 | t0052 | g0152 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01257 | hp2 | a0001 | c0001 | t0042 | g0094 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01258 | hp1 | a0001 | c0001 | t0019 | g0006 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01258 | hp2 | a0001 | c0001 | t0052 | g0151 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01261 | hp1 | a0001 | c0001 | t0016 | g0052 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01358 | hp1 | a0001 | c0001 | t0026 | g0260 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01361 | hp1 | a0001 | c0001 | t0014 | g0316 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01361 | hp2 | a0001 | c0001 | t0083 | g0127 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01433 | hp1 | a0001 | c0001 | t0106 | g0049 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01433 | hp2 | a0001 | c0001 | t0027 | g0357 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0317 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01496 | hp2 | a0001 | c0001 | t0020 | g0124 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01515 | hp1 | a0001 | c0002 | t0022 | g0182 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01515 | hp2 | a0001 | c0001 | t0082 | g0106 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0233 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01516 | hp2 | a0001 | c0001 | t0041 | g0059 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01517 | hp1 | a0001 | c0001 | t0007 | g0242 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01517 | hp2 | a0001 | c0002 | t0022 | g0194 | EUR | IBS | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01884 | hp1 | a0001 | c0001 | t0050 | g0213 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0290 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01891 | hp1 | a0001 | c0001 | t0062 | g0289 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01891 | hp2 | a0001 | c0001 | t0030 | g0197 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0301 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01928 | hp2 | a0001 | c0001 | t0073 | g0366 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0307 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01934 | hp2 | a0001 | c0003 | t0025 | g0248 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0245 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0319 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01975 | hp2 | a0001 | c0001 | t0026 | g0279 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01981 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01993 | hp1 | a0001 | c0001 | t0011 | g0318 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01993 | hp2 | a0001 | c0001 | t0060 | g0148 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02004 | hp1 | a0001 | c0001 | t0011 | g0368 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02055 | hp1 | a0001 | c0001 | t0058 | g0226 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02055 | hp2 | a0001 | c0001 | t0080 | g0103 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02056 | hp1 | a0001 | c0001 | t0012 | g0177 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02071 | hp1 | a0002 | c0004 | t0078 | g0311 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02074 | hp1 | a0001 | c0001 | t0079 | g0354 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0082 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02132 | hp1 | a0001 | c0001 | t0053 | g0204 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02145 | hp1 | a0001 | c0001 | t0012 | g0188 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02145 | hp2 | a0001 | c0001 | t0033 | g0283 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02148 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0309 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0362 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02155 | hp2 | a0001 | c0005 | t0009 | g0247 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02165 | hp2 | a0001 | c0001 | t0017 | g0033 | EAS | CDX | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02257 | hp1 | a0001 | c0001 | t0017 | g0005 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02258 | hp1 | a0001 | c0001 | t0020 | g0001 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02258 | hp2 | a0001 | c0001 | t0028 | g0104 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0305 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02280 | hp1 | a0001 | c0001 | t0103 | g0097 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02280 | hp2 | a0001 | c0001 | t0013 | g0086 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0231 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02293 | hp2 | a0001 | c0001 | t0036 | g0296 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0364 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0239 | AMR | PEL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02451 | hp1 | a0001 | c0001 | t0044 | g0265 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02451 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02523 | hp1 | a0001 | c0001 | t0015 | g0340 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02572 | hp1 | a0001 | c0001 | t0047 | g0110 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02572 | hp2 | a0001 | c0001 | t0049 | g0145 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02602 | hp1 | a0001 | c0001 | t0014 | g0136 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02602 | hp2 | a0001 | c0001 | t0007 | g0238 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02615 | hp1 | a0001 | c0001 | t0101 | g0024 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02615 | hp2 | a0001 | c0001 | t0024 | g0287 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0186 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02622 | hp2 | a0001 | c0001 | t0030 | g0170 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0117 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02630 | hp2 | a0001 | c0001 | t0041 | g0037 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02683 | hp1 | a0001 | c0001 | t0013 | g0095 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02683 | hp2 | a0001 | c0001 | t0048 | g0107 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02717 | hp1 | a0001 | c0001 | t0028 | g0109 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0091 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02723 | hp1 | a0001 | c0001 | t0104 | g0028 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02723 | hp2 | a0001 | c0001 | t0070 | g0225 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02735 | hp1 | a0001 | c0001 | t0077 | g0299 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02735 | hp2 | a0001 | c0001 | t0030 | g0201 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0346 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02738 | hp2 | a0001 | c0001 | t0042 | g0093 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02809 | hp1 | a0001 | c0001 | t0016 | g0053 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02809 | hp2 | a0001 | c0001 | t0067 | g0270 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02818 | hp1 | a0001 | c0001 | t0085 | g0118 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02818 | hp2 | a0001 | c0001 | t0066 | g0282 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02886 | hp1 | a0001 | c0001 | t0107 | g0025 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02886 | hp2 | a0001 | c0001 | t0028 | g0101 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02896 | hp1 | a0001 | c0001 | t0039 | g0150 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02896 | hp2 | a0001 | c0001 | t0044 | g0262 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02897 | hp1 | a0001 | c0001 | t0038 | g0102 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02897 | hp2 | a0001 | c0001 | t0039 | g0147 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0227 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02922 | hp2 | a0001 | c0001 | t0021 | g0218 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02965 | hp1 | a0001 | c0001 | t0092 | g0181 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0149 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02970 | hp1 | a0001 | c0001 | t0100 | g0023 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02970 | hp2 | a0001 | c0001 | t0021 | g0198 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02976 | hp1 | a0001 | c0001 | t0020 | g0001 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02976 | hp2 | a0001 | c0001 | t0038 | g0105 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03017 | hp1 | a0001 | c0001 | t0034 | g0269 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03017 | hp2 | a0001 | c0001 | t0014 | g0350 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0352 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03041 | hp2 | a0001 | c0001 | t0038 | g0144 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03098 | hp2 | a0001 | c0001 | t0096 | g0202 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03130 | hp1 | a0001 | c0001 | t0033 | g0284 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03130 | hp2 | a0001 | c0001 | t0099 | g0088 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03139 | hp1 | a0001 | c0001 | t0019 | g0146 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03139 | hp2 | a0001 | c0001 | t0028 | g0135 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03195 | hp1 | a0001 | c0001 | t0021 | g0195 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03195 | hp2 | a0001 | c0001 | t0040 | g0113 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03209 | hp1 | a0001 | c0001 | t0020 | g0128 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03209 | hp2 | a0001 | c0001 | t0054 | g0090 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03225 | hp1 | a0001 | c0001 | t0057 | g0228 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03225 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03239 | hp1 | a0001 | c0001 | t0015 | g0139 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03239 | hp2 | a0001 | c0001 | t0026 | g0261 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03453 | hp1 | a0001 | c0001 | t0040 | g0114 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03453 | hp2 | a0001 | c0001 | t0091 | g0214 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0356 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03486 | hp2 | a0001 | c0001 | t0017 | g0005 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03490 | hp1 | a0001 | c0001 | t0009 | g0249 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0013 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03491 | hp1 | a0001 | c0001 | t0043 | g0141 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03491 | hp2 | a0001 | c0001 | t0018 | g0266 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0013 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03492 | hp2 | a0001 | c0001 | t0043 | g0142 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03516 | hp2 | a0001 | c0001 | t0021 | g0179 | AFR | ESN | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03540 | hp1 | a0001 | c0001 | t0054 | g0019 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03540 | hp2 | a0001 | c0001 | t0102 | g0085 | AFR | GWD | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03579 | hp1 | a0001 | c0001 | t0098 | g0206 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0219 | AFR | MSL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03654 | hp1 | a0001 | c0001 | t0061 | g0119 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03654 | hp2 | a0001 | c0001 | t0019 | g0108 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03669 | hp1 | a0001 | c0001 | t0068 | g0278 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0280 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0268 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0158 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03710 | hp2 | a0001 | c0001 | t0035 | g0267 | SAS | PJL | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03834 | hp1 | a0001 | c0001 | t0027 | g0130 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0295 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0132 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG03942 | hp2 | a0001 | c0001 | t0006 | g0157 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04115 | hp1 | a0001 | c0001 | t0035 | g0264 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04115 | hp2 | a0001 | c0001 | t0012 | g0199 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04184 | hp1 | a0001 | c0001 | t0064 | g0369 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04184 | hp2 | a0001 | c0001 | t0036 | g0331 | SAS | BEB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04199 | hp1 | a0001 | c0001 | t0037 | g0328 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0187 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04204 | hp1 | a0001 | c0001 | t0056 | g0060 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04204 | hp2 | a0001 | c0001 | t0074 | g0140 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04228 | hp1 | a0001 | c0001 | t0018 | g0253 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | STU | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0192 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0288 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18747 | hp2 | a0001 | c0001 | t0008 | g0081 | EAS | CHB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18906 | hp1 | a0001 | c0001 | t0063 | g0012 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18906 | hp2 | a0001 | c0001 | t0093 | g0180 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18939 | hp1 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18939 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18941 | hp1 | a0001 | c0001 | t0055 | g0079 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18941 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18944 | hp2 | a0001 | c0001 | t0045 | g0255 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18945 | hp2 | a0001 | c0001 | t0025 | g0277 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18948 | hp1 | a0001 | c0001 | t0023 | g0068 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18948 | hp2 | a0001 | c0001 | t0025 | g0275 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18949 | hp2 | a0001 | c0001 | t0097 | g0221 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18951 | hp1 | a0001 | c0001 | t0016 | g0070 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18951 | hp2 | a0001 | c0001 | t0014 | g0322 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0302 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18956 | hp2 | a0001 | c0001 | t0023 | g0026 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18959 | hp2 | a0003 | c0006 | t0055 | g0071 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0353 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18962 | hp2 | a0001 | c0001 | t0031 | g0209 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18964 | hp2 | a0001 | c0001 | t0013 | g0040 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18965 | hp1 | a0001 | c0001 | t0032 | g0200 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18969 | hp1 | a0001 | c0001 | t0012 | g0017 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18969 | hp2 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18971 | hp2 | a0001 | c0001 | t0018 | g0258 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18972 | hp1 | a0001 | c0001 | t0037 | g0333 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18975 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18981 | hp1 | a0001 | c0001 | t0032 | g0191 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18982 | hp2 | a0001 | c0001 | t0009 | g0229 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18984 | hp1 | a0001 | c0001 | t0015 | g0329 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18985 | hp2 | a0001 | c0001 | t0008 | g0036 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18986 | hp1 | a0001 | c0001 | t0013 | g0031 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18989 | hp2 | a0001 | c0001 | t0025 | g0273 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18991 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18994 | hp2 | a0001 | c0001 | t0014 | g0349 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18995 | hp2 | a0001 | c0001 | t0045 | g0256 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19000 | hp1 | a0001 | c0001 | t0036 | g0330 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19000 | hp2 | a0001 | c0001 | t0034 | g0246 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19004 | hp2 | a0001 | c0001 | t0095 | g0224 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19009 | hp1 | a0001 | c0001 | t0013 | g0030 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19011 | hp1 | a0001 | c0001 | t0075 | g0321 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0096 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19043 | hp2 | a0001 | c0001 | t0051 | g0009 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0351 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19054 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19056 | hp1 | a0001 | c0001 | t0031 | g0211 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19057 | hp2 | a0001 | c0001 | t0009 | g0251 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0155 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19060 | hp1 | a0001 | c0001 | t0032 | g0166 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19060 | hp2 | a0001 | c0001 | t0031 | g0161 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19064 | hp1 | a0001 | c0001 | t0035 | g0257 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0361 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19076 | hp2 | a0001 | c0001 | t0008 | g0041 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19079 | hp1 | a0001 | c0001 | t0031 | g0168 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19080 | hp1 | a0001 | c0001 | t0012 | g0018 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0359 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19081 | hp2 | a0001 | c0001 | t0009 | g0252 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19082 | hp2 | a0001 | c0001 | t0023 | g0065 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19083 | hp2 | a0001 | c0001 | t0069 | g0274 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19084 | hp1 | a0001 | c0001 | t0023 | g0029 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0358 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0332 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19088 | hp1 | a0001 | c0001 | t0017 | g0069 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19091 | hp1 | a0001 | c0001 | t0009 | g0250 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA19240 | hp2 | a0001 | c0001 | t0065 | g0286 | AFR | YRI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20129 | hp1 | a0001 | c0001 | t0047 | g0133 | AFR | ASW | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0244 | AFR | ASW | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20752 | hp1 | a0001 | c0001 | t0026 | g0259 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20752 | hp2 | a0001 | c0001 | t0088 | g0115 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20805 | hp1 | a0001 | c0001 | t0010 | g0235 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20805 | hp2 | a0001 | c0001 | t0050 | g0162 | EUR | TSI | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20905 | hp1 | a0001 | c0001 | t0072 | g0272 | SAS | GIH | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20905 | hp2 | a0001 | c0001 | t0014 | g0310 | SAS | GIH | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG01123 | hp2 | a0001 | c0001 | t0011 | g0314 | AMR | CLM | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02109 | hp1 | a0001 | c0001 | t0033 | g0281 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02109 | hp2 | a0001 | c0001 | t0049 | g0120 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02559 | hp1 | a0001 | c0001 | t0090 | g0178 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG02559 | hp2 | a0001 | c0001 | t0081 | g0126 | AFR | ACB | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG06807 | hp1 | a0001 | c0001 | t0051 | g0009 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0089 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20300 | hp1 | a0001 | c0001 | t0086 | g0001 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA20300 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | USA | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA21309 | hp1 | a0001 | c0001 | t0048 | g0100 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0087 | AFR | LWK | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0027 | g0365 | REF | REF | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0040 | g0112 | REF | REF | RNF144B_chr6_18382350_18473870 | RNF144B | chr6 | 18382350 | 18473870 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18399610 | C | T | 1 | a0003 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.76C>T | p.Pro26Ser | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/8 | 393/5032 | 76/912 | 26/303 | chr6 | 18399610 | |||
| chr6:18459713 | A | G | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.643A>G | p.Lys215Glu | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/8 | 960/5032 | 643/912 | 215/303 | chr6 | 18459713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18399606 | G | A | 1 | a0001c0002 | 2 | HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.72G>A | p.Pro24Pro | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/8 | 389/5032 | 72/912 | 24/303 | chr6 | 18399606 | |||
| chr6:18459670 | C | A | 1 | a0001c0003 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.600C>A | p.Ile200Ile | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/8 | 917/5032 | 600/912 | 200/303 | chr6 | 18459670 | |||
| chr6:18459688 | C | T | 1 | a0001c0005 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.618C>T | p.Cys206Cys | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/8 | 935/5032 | 618/912 | 206/303 | chr6 | 18459688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18387446 | T | C | 2 | a0001c0001t0057 a0001c0001t0058 |
2 | HG02055.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-221T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12089 | chr6 | 18387446 | ||||||
| chr6:18387452 | T | C | 3 | a0001c0001t0043 a0001c0001t0059 a0001c0001t0060 |
4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-215T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12083 | chr6 | 18387452 | ||||||
| chr6:18387461 | A | G | 21 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0013 others(18): Show |
89 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
5_prime_UTR_variant | MODIFIER | c.-206A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12074 | chr6 | 18387461 | ||||||
| chr6:18387521 | G | A | 1 | a0001c0001t0061 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-146G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 12014 | chr6 | 18387521 | ||||||
| chr6:18387537 | CTCCTG | C | 27 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0010 others(24): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
5_prime_UTR_variant | MODIFIER | c.-126_-122delTGTCC | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 11990 | INFO_REALIGN_3_PRIME | chr6 | 18387537 | |||||
| chr6:18387584 | A | C | 23 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0012 others(20): Show |
79 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-83A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | 11951 | chr6 | 18387584 | ||||||
| chr6:18387600 | C | T | 1 | a0001c0001t0045 | 2 | NA18944.hp2 NA18995.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-67C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/8 | chr6 | 18387600 | |||||||
| chr6:18399519 | T | C | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(62): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
5_prime_UTR_variant | MODIFIER | c.-16T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/8 | 16 | chr6 | 18399519 | ||||||
| chr6:18465450 | G | A | 2 | a0001c0001t0089 a0001c0001t0090 |
2 | HG00438.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*383G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 383 | chr6 | 18465450 | ||||||
| chr6:18465479 | G | A | 106 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(103): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*412G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 412 | chr6 | 18465479 | ||||||
| chr6:18465636 | G | A | 9 | a0001c0001t0024 a0001c0001t0028 a0001c0001t0062 others(6): Show |
15 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*569G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 569 | chr6 | 18465636 | ||||||
| chr6:18465727 | G | C | 1 | a0001c0001t0073 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 660 | chr6 | 18465727 | ||||||
| chr6:18465785 | A | G | 1 | a0001c0001t0058 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 718 | chr6 | 18465785 | ||||||
| chr6:18465873 | G | A | 2 | a0001c0001t0091 a0001c0001t0099 |
2 | HG03130.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*806G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 806 | chr6 | 18465873 | ||||||
| chr6:18466177 | G | A | 8 | a0001c0001t0038 a0001c0001t0064 a0001c0001t0074 others(5): Show |
10 | HG01515.hp2 HG02559.hp2 HG02897.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1110 | chr6 | 18466177 | ||||||
| chr6:18466382 | T | C | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1315T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1315 | chr6 | 18466382 | ||||||
| chr6:18466383 | T | C | 1 | a0001c0001t0065 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1316T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1316 | chr6 | 18466383 | ||||||
| chr6:18466446 | A | T | 106 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(103): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*1379A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1379 | chr6 | 18466446 | ||||||
| chr6:18466451 | G | C | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1384G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1384 | chr6 | 18466451 | ||||||
| chr6:18466519 | C | T | 25 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(22): Show |
80 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1452C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1452 | chr6 | 18466519 | ||||||
| chr6:18466587 | C | T | 1 | a0001c0001t0070 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1520C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1520 | chr6 | 18466587 | ||||||
| chr6:18466632 | G | A | 1 | a0001c0001t0094 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1565G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1565 | chr6 | 18466632 | ||||||
| chr6:18466877 | G | A | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1810G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1810 | chr6 | 18466877 | ||||||
| chr6:18466929 | A | G | 2 | a0001c0001t0026 a0002c0004t0078 |
5 | HG01358.hp1 HG01975.hp2 HG02071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1862A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1862 | chr6 | 18466929 | ||||||
| chr6:18466973 | T | C | 2 | a0001c0001t0066 a0001c0001t0083 |
2 | HG01361.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1906T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1906 | chr6 | 18466973 | ||||||
| chr6:18467009 | C | A | 5 | a0001c0001t0022 a0001c0001t0046 a0001c0001t0056 others(2): Show |
10 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1942C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1942 | chr6 | 18467009 | ||||||
| chr6:18467025 | CAT | C | 25 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(22): Show |
80 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1959_*1960delAT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 1959 | chr6 | 18467025 | ||||||
| chr6:18467097 | C | G | 1 | a0001c0001t0053 | 2 | HG00423.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2030C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2030 | chr6 | 18467097 | ||||||
| chr6:18467225 | T | C | 106 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(103): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*2158T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2158 | chr6 | 18467225 | ||||||
| chr6:18467291 | G | A | 16 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(13): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*2224G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2224 | chr6 | 18467291 | ||||||
| chr6:18467303 | G | T | 9 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0042 others(6): Show |
22 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2236G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2236 | chr6 | 18467303 | ||||||
| chr6:18467351 | A | G | 106 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(103): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*2284A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2284 | chr6 | 18467351 | ||||||
| chr6:18467395 | C | CTTT | 3 | a0001c0001t0052 a0001c0001t0077 a0001c0001t0079 |
4 | HG01257.hp1 HG01258.hp2 HG02074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2330_*2332dupTTT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2333 | INFO_REALIGN_3_PRIME | chr6 | 18467395 | |||||
| chr6:18467400 | G | GTTT | 41 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(38): Show |
119 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2350_*2352dupTTT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2353 | INFO_REALIGN_3_PRIME | chr6 | 18467400 | |||||
| chr6:18467400 | G | GTTTT | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*2349_*2352dupTTTT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2353 | INFO_REALIGN_3_PRIME | chr6 | 18467400 | |||||
| chr6:18467400 | G | GTTTTT | 14 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0026 others(11): Show |
30 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2348_*2352dupTTTT others(1): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2353 | INFO_REALIGN_3_PRIME | chr6 | 18467400 | |||||
| chr6:18467400 | G | T | 3 | a0001c0001t0052 a0001c0001t0077 a0001c0001t0079 |
4 | HG01257.hp1 HG01258.hp2 HG02074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2333G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2333 | chr6 | 18467400 | ||||||
| chr6:18467408 | T | TG | 8 | a0001c0001t0007 a0001c0001t0012 a0001c0001t0015 others(5): Show |
42 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2341_*2342insG | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2342 | chr6 | 18467408 | ||||||
| chr6:18467422 | C | T | 1 | a0001c0001t0085 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2355C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2355 | chr6 | 18467422 | ||||||
| chr6:18467647 | A | AT | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0011 others(22): Show |
99 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2585dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2586 | INFO_REALIGN_3_PRIME | chr6 | 18467647 | |||||
| chr6:18467653 | A | T | 105 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(102): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*2586A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2586 | chr6 | 18467653 | ||||||
| chr6:18467688 | C | T | 3 | a0001c0001t0049 a0001c0001t0098 a0001c0001t0107 |
4 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2621C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2621 | chr6 | 18467688 | ||||||
| chr6:18467723 | C | T | 1 | a0001c0001t0096 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2656C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2656 | chr6 | 18467723 | ||||||
| chr6:18467880 | A | G | 4 | a0001c0001t0038 a0001c0001t0092 a0001c0001t0093 others(1): Show |
6 | HG02897.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2813A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2813 | chr6 | 18467880 | ||||||
| chr6:18467883 | C | T | 15 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0023 others(12): Show |
76 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2816C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2816 | chr6 | 18467883 | ||||||
| chr6:18467988 | G | A | 1 | a0001c0001t0058 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2921G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 2921 | chr6 | 18467988 | ||||||
| chr6:18468123 | CA | C | 9 | a0001c0001t0024 a0001c0001t0028 a0001c0001t0062 others(6): Show |
15 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3058delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3058 | INFO_REALIGN_3_PRIME | chr6 | 18468123 | |||||
| chr6:18468138 | G | T | 9 | a0001c0001t0011 a0001c0001t0025 a0001c0001t0042 others(6): Show |
22 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3071G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3071 | chr6 | 18468138 | ||||||
| chr6:18468176 | T | C | 9 | a0001c0001t0024 a0001c0001t0028 a0001c0001t0062 others(6): Show |
15 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3109T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3109 | chr6 | 18468176 | ||||||
| chr6:18468233 | C | T | 106 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(103): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
3_prime_UTR_variant | MODIFIER | c.*3166C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3166 | chr6 | 18468233 | ||||||
| chr6:18468267 | A | C | 1 | a0001c0001t0057 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3200A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3200 | chr6 | 18468267 | ||||||
| chr6:18468384 | G | A | 2 | a0001c0001t0055 a0003c0006t0055 |
2 | NA18941.hp1 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3317G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3317 | chr6 | 18468384 | ||||||
| chr6:18468578 | C | T | 1 | a0001c0001t0075 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3511C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3511 | chr6 | 18468578 | ||||||
| chr6:18468736 | A | G | 1 | a0001c0001t0081 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3669A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3669 | chr6 | 18468736 | ||||||
| chr6:18468750 | T | A | 14 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0024 others(11): Show |
29 | HG01109.hp2 HG01167.hp2 HG01496.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3683T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 8/8 | 3683 | chr6 | 18468750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:18387664 | G | C | 1 | a0001c0001t0001g0016 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-37+34G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387664 | |||||||
| chr6:18387722 | A | C | 78 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(75): Show |
83 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-37+92A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387722 | |||||||
| chr6:18387864 | C | T | 2 | a0001c0001t0007g0293 a0001c0001t0071g0294 |
2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-37+234C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387864 | |||||||
| chr6:18387871 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-37+241A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387871 | |||||||
| chr6:18387890 | G | A | 2 | a0001c0001t0012g0017 a0001c0001t0012g0018 |
2 | NA18969.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-37+260G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18387890 | |||||||
| chr6:18388062 | G | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(84): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+432G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388062 | |||||||
| chr6:18388139 | T | C | 6 | a0001c0001t0028g0101 a0001c0001t0028g0104 a0001c0001t0038g0102 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37+509T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388139 | |||||||
| chr6:18388314 | C | G | 150 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(147): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-37+684C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388314 | |||||||
| chr6:18388608 | C | T | 1 | a0001c0001t0095g0224 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-37+978C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388608 | |||||||
| chr6:18388775 | C | A | 4 | a0001c0001t0010g0227 a0001c0001t0057g0228 a0001c0001t0058g0226 others(1): Show |
4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+1145C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18388775 | |||||||
| chr6:18388806 | A | AT | 68 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(65): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-37+1187dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18388806 | ||||||
| chr6:18388806 | AT | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(84): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+1187delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18388806 | ||||||
| chr6:18389070 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-37+1440C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389070 | |||||||
| chr6:18389079 | G | A | 1 | a0001c0001t0036g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37+1449G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389079 | |||||||
| chr6:18389132 | C | T | 1 | a0001c0001t0011g0368 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-37+1502C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389132 | |||||||
| chr6:18389258 | A | G | 4 | a0001c0001t0003g0220 a0001c0001t0003g0222 a0001c0001t0003g0223 others(1): Show |
4 | NA18949.hp2 NA18964.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37+1628A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389258 | |||||||
| chr6:18389539 | G | C | 1 | a0001c0001t0054g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-37+1909G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389539 | |||||||
| chr6:18389602 | C | A | 57 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(54): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-37+1972C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389602 | |||||||
| chr6:18389680 | C | G | 343 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(340): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.-37+2050C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389680 | |||||||
| chr6:18389868 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37+2238T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389868 | |||||||
| chr6:18389970 | A | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(84): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+2340A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18389970 | |||||||
| chr6:18390406 | T | C | 1 | a0001c0001t0082g0106 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-37+2776T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390406 | |||||||
| chr6:18390442 | T | C | 4 | a0001c0001t0010g0227 a0001c0001t0057g0228 a0001c0001t0058g0226 others(1): Show |
4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+2812T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390442 | |||||||
| chr6:18390574 | A | C | 1 | a0001c0001t0015g0367 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-37+2944A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390574 | |||||||
| chr6:18390692 | A | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(84): Show |
90 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.-37+3062A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390692 | |||||||
| chr6:18390705 | C | T | 1 | a0001c0001t0018g0280 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-37+3075C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390705 | |||||||
| chr6:18390801 | G | A | 1 | a0001c0001t0013g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-37+3171G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18390801 | |||||||
| chr6:18391015 | A | G | 1 | a0001c0001t0006g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-37+3385A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391015 | |||||||
| chr6:18391160 | C | G | 78 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(75): Show |
80 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-37+3530C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391160 | |||||||
| chr6:18391202 | C | T | 4 | a0001c0001t0010g0227 a0001c0001t0057g0228 a0001c0001t0058g0226 others(1): Show |
4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37+3572C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391202 | |||||||
| chr6:18391513 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-37+3883A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391513 | |||||||
| chr6:18391683 | C | T | 1 | a0001c0001t0073g0366 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-37+4053C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391683 | |||||||
| chr6:18391817 | G | A | 18 | a0001c0001t0002g0134 a0001c0001t0004g0131 a0001c0001t0004g0132 others(15): Show |
20 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37+4187G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391817 | |||||||
| chr6:18391872 | A | G | 2 | a0001c0001t0015g0139 a0001c0001t0074g0140 |
2 | HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-37+4242A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391872 | |||||||
| chr6:18391910 | T | C | 1 | a0001c0001t0102g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-37+4280T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391910 | |||||||
| chr6:18391995 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-37+4365C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18391995 | |||||||
| chr6:18392035 | T | TA | 53 | a0001c0001t0001g0078 a0001c0001t0003g0153 a0001c0001t0003g0220 others(50): Show |
54 | HG00609.hp2 HG00639.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.-37+4432dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | ||||||
| chr6:18392035 | T | TAA | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(82): Show |
88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-37+4431_-37+4432d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | ||||||
| chr6:18392035 | TA | T | 36 | a0001c0001t0002g0134 a0001c0001t0002g0303 a0001c0001t0003g0215 others(33): Show |
38 | HG00323.hp2 HG01070.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-37+4432delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | ||||||
| chr6:18392035 | TAA | T | 66 | a0001c0001t0002g0014 a0001c0001t0002g0306 a0001c0001t0002g0308 others(63): Show |
71 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-37+4431_-37+4432d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | ||||||
| chr6:18392035 | TAAAAAAA others(2): Show |
T | 15 | a0001c0001t0008g0098 a0001c0001t0013g0086 a0001c0001t0013g0087 others(12): Show |
16 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37+4424_-37+4432d others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18392035 | ||||||
| chr6:18392489 | A | C | 1 | a0001c0001t0028g0104 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-37+4859A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392489 | |||||||
| chr6:18392573 | G | C | 149 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-37+4943G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392573 | |||||||
| chr6:18392795 | G | C | 57 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(54): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.-37+5165G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392795 | |||||||
| chr6:18392851 | A | G | 18 | a0001c0001t0002g0134 a0001c0001t0004g0131 a0001c0001t0004g0132 others(15): Show |
20 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-37+5221A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392851 | |||||||
| chr6:18392855 | A | T | 7 | a0001c0001t0009g0288 a0001c0001t0024g0012 a0001c0001t0024g0287 others(4): Show |
7 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37+5225A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392855 | |||||||
| chr6:18392936 | T | A | 1 | a0001c0001t0001g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-37+5306T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18392936 | |||||||
| chr6:18393040 | G | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37+5410G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393040 | |||||||
| chr6:18393097 | G | A | 3 | a0001c0001t0002g0297 a0001c0001t0002g0306 a0001c0001t0011g0307 |
3 | HG01123.hp1 HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-37+5467G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393097 | |||||||
| chr6:18393119 | C | CA | 13 | a0001c0001t0013g0086 a0001c0001t0013g0087 a0001c0001t0013g0089 others(10): Show |
14 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37+5506dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18393119 | ||||||
| chr6:18393119 | CA | C | 164 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(161): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-37+5506delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18393119 | ||||||
| chr6:18393147 | G | A | 1 | a0001c0001t0007g0232 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-37+5517G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393147 | |||||||
| chr6:18393181 | G | C | 1 | a0001c0001t0081g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-37+5551G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393181 | |||||||
| chr6:18393241 | A | G | 2 | a0001c0001t0057g0228 a0001c0001t0058g0226 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-37+5611A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393241 | |||||||
| chr6:18393375 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-37+5745T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393375 | |||||||
| chr6:18393409 | C | T | 2 | a0001c0001t0051g0009 a0001c0001t0091g0214 |
3 | HG03453.hp2 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-37+5779C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393409 | |||||||
| chr6:18393635 | G | C | 1 | a0001c0001t0002g0308 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-36-5864G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393635 | |||||||
| chr6:18393647 | G | A | 4 | a0001c0001t0010g0227 a0001c0001t0057g0228 a0001c0001t0058g0226 others(1): Show |
4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-5852G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393647 | |||||||
| chr6:18393829 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-36-5670C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393829 | |||||||
| chr6:18393944 | C | T | 4 | a0001c0001t0043g0141 a0001c0001t0043g0142 a0001c0001t0059g0143 others(1): Show |
4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-5555C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18393944 | |||||||
| chr6:18394058 | C | G | 76 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(73): Show |
81 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-36-5441C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394058 | |||||||
| chr6:18394177 | T | C | 2 | a0001c0001t0057g0228 a0001c0001t0058g0226 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-36-5322T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394177 | |||||||
| chr6:18394297 | T | C | 1 | a0001c0001t0010g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-36-5202T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394297 | |||||||
| chr6:18394496 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-5003G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394496 | |||||||
| chr6:18394523 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-36-4976G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394523 | |||||||
| chr6:18394562 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(65): Show |
70 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-36-4937C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394562 | |||||||
| chr6:18394592 | C | T | 1 | a0001c0001t0050g0213 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-36-4907C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394592 | |||||||
| chr6:18394613 | GA | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(101): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-36-4872delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18394613 | ||||||
| chr6:18394614 | A | G | 74 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(71): Show |
79 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-36-4885A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394614 | |||||||
| chr6:18394615 | A | G | 1 | a0001c0001t0005g0305 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-36-4884A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394615 | |||||||
| chr6:18394692 | C | G | 2 | a0001c0001t0015g0139 a0001c0001t0074g0140 |
2 | HG03239.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-36-4807C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394692 | |||||||
| chr6:18394753 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-36-4746T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394753 | |||||||
| chr6:18394761 | C | T | 16 | a0001c0001t0008g0098 a0001c0001t0013g0086 a0001c0001t0013g0087 others(13): Show |
17 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-36-4738C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394761 | |||||||
| chr6:18394898 | T | A | 4 | a0001c0001t0043g0141 a0001c0001t0043g0142 a0001c0001t0059g0143 others(1): Show |
4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-4601T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394898 | |||||||
| chr6:18394904 | G | A | 1 | a0001c0001t0025g0277 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-36-4595G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394904 | |||||||
| chr6:18394952 | T | C | 1 | a0001c0001t0031g0161 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-36-4547T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18394952 | |||||||
| chr6:18395000 | G | C | 154 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-36-4499G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395000 | |||||||
| chr6:18395091 | G | A | 5 | a0001c0001t0013g0095 a0001c0001t0017g0096 a0001c0001t0042g0093 others(2): Show |
5 | HG01257.hp2 HG02280.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-4408G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395091 | |||||||
| chr6:18395359 | C | T | 1 | a0001c0001t0008g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-36-4140C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395359 | |||||||
| chr6:18395386 | G | A | 2 | a0001c0001t0005g0301 a0001c0001t0005g0309 |
2 | HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-36-4113G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395386 | |||||||
| chr6:18395439 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-36-4060T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395439 | |||||||
| chr6:18395566 | T | C | 1 | a0001c0001t0008g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-36-3933T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395566 | |||||||
| chr6:18395578 | C | CT | 170 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(167): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-36-3909dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 18395578 | ||||||
| chr6:18395798 | A | G | 1 | a0001c0001t0037g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-36-3701A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18395798 | |||||||
| chr6:18396086 | C | T | 166 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-36-3413C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396086 | |||||||
| chr6:18396122 | G | A | 5 | a0001c0001t0009g0285 a0001c0001t0033g0281 a0001c0001t0033g0283 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36-3377G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396122 | |||||||
| chr6:18396194 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-3305A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396194 | |||||||
| chr6:18396230 | A | T | 4 | a0001c0001t0010g0227 a0001c0001t0057g0228 a0001c0001t0058g0226 others(1): Show |
4 | HG02055.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-3269A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396230 | |||||||
| chr6:18396352 | C | T | 1 | a0001c0001t0070g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-36-3147C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396352 | |||||||
| chr6:18396375 | A | T | 73 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(70): Show |
74 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-36-3124A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396375 | |||||||
| chr6:18396458 | C | T | 166 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-36-3041C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396458 | |||||||
| chr6:18396554 | G | A | 1 | a0001c0001t0003g0164 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-36-2945G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396554 | |||||||
| chr6:18396665 | T | C | 1 | a0001c0001t0001g0003 | 2 | NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-36-2834T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396665 | |||||||
| chr6:18396806 | C | A | 1 | a0001c0001t0013g0086 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-36-2693C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396806 | |||||||
| chr6:18396888 | C | T | 2 | a0001c0001t0014g0136 a0001c0001t0037g0137 |
2 | HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-36-2611C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396888 | |||||||
| chr6:18396899 | C | T | 166 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-36-2600C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396899 | |||||||
| chr6:18396964 | G | A | 1 | a0001c0001t0048g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-36-2535G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396964 | |||||||
| chr6:18396986 | G | A | 1 | a0001c0001t0010g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-36-2513G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18396986 | |||||||
| chr6:18397018 | A | G | 1 | a0001c0001t0011g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-36-2481A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397018 | |||||||
| chr6:18397298 | G | A | 4 | a0001c0001t0043g0141 a0001c0001t0043g0142 a0001c0001t0059g0143 others(1): Show |
4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36-2201G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397298 | |||||||
| chr6:18397359 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-36-2140C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397359 | |||||||
| chr6:18397569 | C | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-1930C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397569 | |||||||
| chr6:18397592 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-1907G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397592 | |||||||
| chr6:18397698 | T | G | 6 | a0001c0001t0002g0297 a0001c0001t0002g0306 a0001c0001t0004g0312 others(3): Show |
6 | HG00099.hp2 HG01123.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.-36-1801T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397698 | |||||||
| chr6:18397756 | G | A | 1 | a0001c0001t0002g0306 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-36-1743G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18397756 | |||||||
| chr6:18398041 | C | T | 1 | a0001c0001t0054g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-36-1458C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398041 | |||||||
| chr6:18398104 | T | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(234): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-36-1395T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398104 | |||||||
| chr6:18398122 | C | A | 2 | a0001c0001t0052g0151 a0001c0001t0052g0152 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-36-1377C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398122 | |||||||
| chr6:18398148 | C | T | 1 | a0001c0001t0054g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-36-1351C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398148 | |||||||
| chr6:18398160 | G | A | 1 | a0001c0001t0102g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-36-1339G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398160 | |||||||
| chr6:18398164 | C | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-36-1335C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398164 | |||||||
| chr6:18398287 | G | T | 1 | a0001c0001t0011g0364 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-36-1212G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398287 | |||||||
| chr6:18398579 | A | C | 5 | a0001c0001t0013g0095 a0001c0001t0017g0096 a0001c0001t0042g0093 others(2): Show |
5 | HG01257.hp2 HG02280.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-36-920A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398579 | |||||||
| chr6:18398646 | G | A | 12 | a0001c0001t0002g0313 a0001c0001t0002g0315 a0001c0001t0005g0301 others(9): Show |
14 | HG01069.hp2 HG01123.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-36-853G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398646 | |||||||
| chr6:18398669 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-36-830C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398669 | |||||||
| chr6:18398732 | G | T | 16 | a0001c0001t0008g0098 a0001c0001t0013g0086 a0001c0001t0013g0087 others(13): Show |
17 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-36-767G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398732 | |||||||
| chr6:18398934 | C | T | 166 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-36-565C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18398934 | |||||||
| chr6:18399163 | C | T | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(234): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-36-336C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18399163 | |||||||
| chr6:18399335 | G | A | 1 | a0001c0001t0104g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-36-164G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 1/7 | chr6 | 18399335 | |||||||
| chr6:18399992 | C | A | 9 | a0001c0001t0002g0298 a0001c0001t0002g0320 a0001c0001t0002g0323 others(6): Show |
9 | HG00423.hp2 HG02080.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+293C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18399992 | |||||||
| chr6:18399999 | C | T | 14 | a0001c0001t0008g0098 a0001c0001t0013g0087 a0001c0001t0013g0089 others(11): Show |
15 | HG00642.hp1 HG01257.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+300C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18399999 | |||||||
| chr6:18400042 | C | T | 164 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(161): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.165+343C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400042 | |||||||
| chr6:18400046 | C | T | 1 | a0001c0001t0013g0086 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.165+347C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400046 | |||||||
| chr6:18400047 | G | A | 1 | a0001c0001t0068g0278 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.165+348G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400047 | |||||||
| chr6:18400147 | C | T | 1 | a0001c0001t0010g0276 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.165+448C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400147 | |||||||
| chr6:18400272 | CA | C | 166 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.165+590delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18400272 | ||||||
| chr6:18400312 | C | G | 166 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.165+613C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400312 | |||||||
| chr6:18400330 | C | G | 1 | a0001c0001t0034g0246 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.165+631C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400330 | |||||||
| chr6:18400740 | C | T | 3 | a0001c0001t0002g0297 a0001c0001t0002g0306 a0001c0001t0011g0307 |
3 | HG01123.hp1 HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.165+1041C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18400740 | |||||||
| chr6:18401102 | T | A | 1 | a0001c0001t0083g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.165+1403T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401102 | |||||||
| chr6:18401150 | A | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(144): Show |
154 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.165+1451A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401150 | |||||||
| chr6:18401194 | G | A | 1 | a0001c0001t0023g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.165+1495G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401194 | |||||||
| chr6:18401332 | T | A | 151 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(148): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.165+1633T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401332 | |||||||
| chr6:18401377 | T | G | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(67): Show |
72 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.165+1678T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401377 | |||||||
| chr6:18401632 | T | C | 1 | a0001c0001t0046g0007 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.165+1933T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18401632 | |||||||
| chr6:18401856 | CCCCAGGG others(773): Show |
C | 237 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(234): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.165+2161_165+2940d others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18401856 | ||||||
| chr6:18402718 | C | A | 2 | a0001c0001t0005g0013 a0001c0001t0036g0331 |
3 | HG03490.hp2 HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.165+3019C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402718 | |||||||
| chr6:18402761 | T | A | 14 | a0001c0001t0008g0098 a0001c0001t0013g0086 a0001c0001t0013g0087 others(11): Show |
14 | HG01257.hp2 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+3062T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402761 | |||||||
| chr6:18402764 | G | T | 1 | a0001c0001t0030g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+3065G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402764 | |||||||
| chr6:18402884 | A | G | 1 | a0001c0001t0082g0106 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.165+3185A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402884 | |||||||
| chr6:18402950 | G | A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(162): Show |
173 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.165+3251G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402950 | |||||||
| chr6:18402973 | C | T | 1 | a0001c0001t0054g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+3274C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18402973 | |||||||
| chr6:18403028 | A | G | 76 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0298 others(73): Show |
81 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.165+3329A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403028 | |||||||
| chr6:18403045 | G | A | 17 | a0001c0001t0002g0134 a0001c0001t0004g0131 a0001c0001t0004g0132 others(14): Show |
19 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.165+3346G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403045 | |||||||
| chr6:18403109 | T | C | 1 | a0001c0001t0054g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+3410T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403109 | |||||||
| chr6:18403479 | T | G | 1 | a0001c0001t0054g0019 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.165+3780T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403479 | |||||||
| chr6:18403496 | C | T | 4 | a0001c0001t0043g0141 a0001c0001t0043g0142 a0001c0001t0059g0143 others(1): Show |
4 | HG00735.hp1 HG01993.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+3797C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403496 | |||||||
| chr6:18403566 | T | C | 1 | a0001c0001t0002g0315 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.165+3867T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403566 | |||||||
| chr6:18403711 | G | A | 10 | a0001c0001t0009g0285 a0001c0001t0017g0005 a0001c0001t0017g0092 others(7): Show |
11 | HG00642.hp1 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+4012G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403711 | |||||||
| chr6:18403773 | G | T | 1 | a0001c0001t0017g0069 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.165+4074G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403773 | |||||||
| chr6:18403789 | A | G | 101 | a0001c0001t0001g0084 a0001c0001t0002g0014 a0001c0001t0002g0134 others(98): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.165+4090A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403789 | |||||||
| chr6:18403817 | C | T | 4 | a0001c0001t0028g0135 a0001c0001t0047g0133 a0001c0001t0081g0126 others(1): Show |
4 | HG01361.hp2 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+4118C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403817 | |||||||
| chr6:18403902 | C | A | 210 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(207): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.165+4203C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403902 | |||||||
| chr6:18403912 | A | G | 3 | a0001c0001t0013g0087 a0001c0001t0099g0088 a0001c0001t0102g0085 |
3 | HG03130.hp2 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.165+4213A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403912 | |||||||
| chr6:18403937 | C | A | 6 | a0001c0001t0003g0165 a0001c0001t0003g0167 a0001c0001t0003g0215 others(3): Show |
6 | HG00621.hp1 HG02040.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+4238C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18403937 | |||||||
| chr6:18404219 | C | T | 17 | a0001c0001t0001g0003 a0001c0001t0004g0304 a0001c0001t0005g0309 others(14): Show |
18 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.165+4520C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404219 | |||||||
| chr6:18404261 | C | G | 1 | a0001c0001t0044g0265 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.165+4562C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404261 | |||||||
| chr6:18404706 | G | GA | 63 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(60): Show |
68 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.165+5015dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18404706 | ||||||
| chr6:18404781 | A | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.165+5082A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404781 | |||||||
| chr6:18404813 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(125): Show |
132 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.165+5114C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404813 | |||||||
| chr6:18404886 | T | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(210): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.165+5187T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404886 | |||||||
| chr6:18404913 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(210): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.165+5214A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404913 | |||||||
| chr6:18404957 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(210): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.165+5258T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18404957 | |||||||
| chr6:18405070 | G | A | 336 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.165+5371G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405070 | |||||||
| chr6:18405117 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(210): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.165+5418T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405117 | |||||||
| chr6:18405150 | T | A | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+5451T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405150 | |||||||
| chr6:18405150 | T | TTTA | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(75): Show |
82 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.165+5475_165+5477d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | ||||||
| chr6:18405150 | T | TTTATTA | 54 | a0001c0001t0002g0356 a0001c0001t0003g0167 a0001c0001t0003g0203 others(51): Show |
56 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.165+5472_165+5477d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | ||||||
| chr6:18405150 | T | TTTATTAT others(2): Show |
5 | a0001c0001t0032g0200 a0001c0001t0041g0035 a0001c0001t0042g0075 others(2): Show |
5 | HG00323.hp1 HG01255.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+5469_165+5477d others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | ||||||
| chr6:18405150 | T | TTTATTAT others(5): Show |
56 | a0001c0001t0003g0008 a0001c0001t0003g0165 a0001c0001t0003g0183 others(53): Show |
58 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.165+5466_165+5477d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | ||||||
| chr6:18405150 | T | TTTATTAT others(8): Show |
17 | a0001c0001t0003g0176 a0001c0001t0005g0335 a0001c0001t0008g0034 others(14): Show |
17 | HG00738.hp2 HG01361.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+5463_165+5477d others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | ||||||
| chr6:18405150 | T | TTTATTAT others(14): Show |
1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+5457_165+5477d others(23): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | ||||||
| chr6:18405150 | TTTA | T | 117 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(114): Show |
123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.165+5475_165+5477d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405150 | ||||||
| chr6:18405174 | A | ATTATTAT others(11): Show |
4 | a0001c0001t0009g0285 a0001c0001t0033g0281 a0001c0001t0033g0283 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+5477_165+5478i others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405174 | ||||||
| chr6:18405174 | A | ATTATTAT others(8): Show |
1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+5477_165+5478i others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405174 | ||||||
| chr6:18405174 | A | ATTATTAT others(2): Show |
2 | a0001c0001t0010g0227 a0001c0001t0019g0006 |
3 | HG01256.hp2 HG01258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.165+5477_165+5478i others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18405174 | ||||||
| chr6:18405177 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.165+5478G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405177 | |||||||
| chr6:18405180 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.165+5481A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405180 | |||||||
| chr6:18405266 | C | G | 2 | a0001c0001t0076g0363 a0001c0001t0105g0067 |
2 | HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.165+5567C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405266 | |||||||
| chr6:18405319 | A | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(212): Show |
223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+5620A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405319 | |||||||
| chr6:18405426 | C | T | 1 | a0001c0001t0012g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.165+5727C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405426 | |||||||
| chr6:18405540 | G | A | 338 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(335): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.165+5841G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405540 | |||||||
| chr6:18405553 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(128): Show |
135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.165+5854A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405553 | |||||||
| chr6:18405576 | C | A | 7 | a0001c0001t0009g0285 a0001c0001t0010g0227 a0001c0001t0016g0091 others(4): Show |
8 | HG01256.hp2 HG01258.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+5877C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405576 | |||||||
| chr6:18405619 | T | C | 1 | a0001c0001t0048g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.165+5920T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405619 | |||||||
| chr6:18405654 | C | T | 1 | a0001c0001t0047g0133 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.165+5955C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405654 | |||||||
| chr6:18405771 | G | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0072 |
2 | NA18940.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.165+6072G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405771 | |||||||
| chr6:18405772 | A | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0072 |
2 | NA18940.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.165+6073A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405772 | |||||||
| chr6:18405774 | G | A | 1 | a0001c0001t0018g0266 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.165+6075G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405774 | |||||||
| chr6:18405864 | A | G | 1 | a0001c0001t0013g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+6165A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18405864 | |||||||
| chr6:18406084 | A | G | 1 | a0001c0001t0098g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165+6385A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406084 | |||||||
| chr6:18406156 | G | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+6457G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406156 | |||||||
| chr6:18406269 | A | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+6570A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406269 | |||||||
| chr6:18406405 | G | A | 1 | a0001c0001t0013g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+6706G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406405 | |||||||
| chr6:18406433 | A | G | 4 | a0001c0001t0009g0011 a0001c0001t0009g0229 a0001c0001t0009g0251 others(1): Show |
5 | NA18939.hp2 NA18941.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+6734A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406433 | |||||||
| chr6:18406457 | A | AGT | 90 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0021 others(87): Show |
92 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.165+6801_165+6802d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | A | AGTGT | 20 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0061 others(17): Show |
20 | HG00140.hp2 HG00735.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+6799_165+6802d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | A | AGTGTGT | 8 | a0001c0001t0004g0295 a0001c0001t0006g0154 a0001c0001t0006g0169 others(5): Show |
9 | HG01261.hp2 HG01993.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6797_165+6802d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | A | AGTGTGTG others(1): Show |
23 | a0001c0001t0001g0083 a0001c0001t0003g0153 a0001c0001t0004g0332 others(20): Show |
24 | HG00642.hp1 HG01081.hp1 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.165+6795_165+6802d others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | A | AGTGTGTG others(3): Show |
6 | a0001c0001t0004g0304 a0001c0001t0018g0268 a0001c0001t0030g0163 others(3): Show |
6 | HG01243.hp2 HG02132.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+6793_165+6802d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0013g0086 a0001c0001t0013g0087 a0001c0001t0018g0266 others(1): Show |
4 | HG02280.hp2 HG03225.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+6791_165+6802d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0053g0205 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.165+6789_165+6802d others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | A | AGTGTGTG others(9): Show |
3 | a0001c0001t0013g0020 a0001c0001t0018g0258 a0001c0001t0054g0090 |
3 | HG03209.hp2 HG03516.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.165+6787_165+6802d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGT | A | 15 | a0001c0001t0001g0003 a0001c0001t0004g0359 a0001c0001t0005g0352 others(12): Show |
17 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+6801_165+6802d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGT | A | 16 | a0001c0001t0008g0098 a0001c0001t0009g0288 a0001c0001t0024g0012 others(13): Show |
16 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+6799_165+6802d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGT | A | 9 | a0001c0001t0002g0303 a0001c0001t0002g0308 a0001c0001t0002g0325 others(6): Show |
9 | HG00140.hp1 HG03669.hp1 HG04115.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6797_165+6802d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGTG others(1): Show |
A | 67 | a0001c0001t0002g0134 a0001c0001t0002g0298 a0001c0001t0002g0306 others(64): Show |
70 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.165+6795_165+6802d others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGTG others(3): Show |
A | 73 | a0001c0001t0002g0297 a0001c0001t0003g0008 a0001c0001t0003g0176 others(70): Show |
76 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.165+6793_165+6802d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0070g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+6791_165+6802d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0042 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.165+6789_165+6802d others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0013g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.165+6787_165+6802d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGTG others(11): Show |
A | 1 | a0001c0001t0019g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+6785_165+6802d others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406457 | AGTGTGTG others(13): Show |
A | 5 | a0001c0001t0002g0014 a0001c0001t0004g0015 a0001c0001t0013g0030 others(2): Show |
7 | HG00408.hp2 NA18971.hp1 NA18986.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+6783_165+6802d others(22): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18406457 | ||||||
| chr6:18406504 | G | T | 76 | a0001c0001t0003g0008 a0001c0001t0003g0176 a0001c0001t0003g0183 others(73): Show |
79 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.165+6805G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406504 | |||||||
| chr6:18406507 | G | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+6808G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406507 | |||||||
| chr6:18406623 | G | A | 337 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(334): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.165+6924G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406623 | |||||||
| chr6:18406749 | C | G | 1 | a0001c0001t0098g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.165+7050C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406749 | |||||||
| chr6:18406974 | C | T | 2 | a0001c0001t0002g0134 a0001c0001t0002g0346 |
2 | HG02738.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.165+7275C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406974 | |||||||
| chr6:18406995 | G | A | 1 | a0001c0001t0019g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+7296G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18406995 | |||||||
| chr6:18407068 | T | C | 14 | a0001c0001t0008g0098 a0001c0001t0009g0288 a0001c0001t0024g0012 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+7369T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407068 | |||||||
| chr6:18407085 | G | T | 70 | a0001c0001t0003g0008 a0001c0001t0003g0176 a0001c0001t0003g0183 others(67): Show |
73 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.165+7386G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407085 | |||||||
| chr6:18407091 | A | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+7392A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407091 | |||||||
| chr6:18407170 | A | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(212): Show |
223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.165+7471A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407170 | |||||||
| chr6:18407322 | G | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(127): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.165+7623G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407322 | |||||||
| chr6:18407359 | T | C | 51 | a0001c0001t0003g0008 a0001c0001t0003g0176 a0001c0001t0003g0183 others(48): Show |
53 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.165+7660T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407359 | |||||||
| chr6:18407483 | A | G | 1 | a0001c0001t0015g0367 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.165+7784A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407483 | |||||||
| chr6:18407487 | A | T | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(206): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.165+7788A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407487 | |||||||
| chr6:18407512 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+7813T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407512 | |||||||
| chr6:18407675 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.165+7976A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407675 | |||||||
| chr6:18407868 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+8169T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407868 | |||||||
| chr6:18407901 | G | A | 1 | a0001c0001t0091g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165+8202G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407901 | |||||||
| chr6:18407966 | TTTTC | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+8279_165+8282d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407966 | ||||||
| chr6:18407984 | C | CT | 13 | a0001c0001t0009g0229 a0001c0001t0009g0288 a0001c0001t0010g0276 others(10): Show |
13 | HG01167.hp2 HG01256.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+8302dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407984 | ||||||
| chr6:18407984 | C | CTT | 60 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(57): Show |
64 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.165+8301_165+8302d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407984 | ||||||
| chr6:18407984 | CTT | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(209): Show |
219 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.165+8301_165+8302d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18407984 | ||||||
| chr6:18407986 | T | C | 1 | a0001c0002t0022g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+8287T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407986 | |||||||
| chr6:18407987 | T | C | 1 | a0003c0006t0055g0071 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.165+8288T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18407987 | |||||||
| chr6:18408001 | T | C | 3 | a0001c0001t0049g0120 a0001c0001t0051g0009 a0001c0001t0098g0206 |
4 | HG02109.hp2 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+8302T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408001 | |||||||
| chr6:18408092 | C | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+8393C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408092 | |||||||
| chr6:18408135 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+8436T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408135 | |||||||
| chr6:18408145 | C | T | 19 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0007g0238 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+8446C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408145 | |||||||
| chr6:18408186 | T | C | 5 | a0001c0001t0013g0020 a0001c0001t0013g0086 a0001c0001t0013g0089 others(2): Show |
5 | HG01243.hp2 HG02280.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+8487T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408186 | |||||||
| chr6:18408187 | G | A | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+8488G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408187 | |||||||
| chr6:18408192 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+8493T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408192 | |||||||
| chr6:18408284 | T | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+8585T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408284 | |||||||
| chr6:18408317 | T | G | 3 | a0001c0001t0034g0269 a0001c0001t0059g0143 a0001c0001t0060g0148 |
3 | HG00735.hp1 HG01993.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.165+8618T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408317 | |||||||
| chr6:18408511 | A | C | 11 | a0001c0001t0009g0288 a0001c0001t0024g0012 a0001c0001t0024g0287 others(8): Show |
11 | HG01167.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.165+8812A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408511 | |||||||
| chr6:18408544 | G | A | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+8845G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408544 | |||||||
| chr6:18408546 | A | C | 1 | a0001c0001t0032g0200 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.165+8847A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408546 | |||||||
| chr6:18408660 | G | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(206): Show |
216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.165+8961G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408660 | |||||||
| chr6:18408698 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(127): Show |
134 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.165+8999G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408698 | |||||||
| chr6:18408772 | T | A | 70 | a0001c0001t0003g0008 a0001c0001t0003g0176 a0001c0001t0003g0183 others(67): Show |
73 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.165+9073T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408772 | |||||||
| chr6:18408772 | T | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(143): Show |
151 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.165+9073T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18408772 | |||||||
| chr6:18408938 | G | GT | 62 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(59): Show |
67 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.165+9257dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18408938 | ||||||
| chr6:18408938 | GT | G | 26 | a0001c0001t0003g0153 a0001c0001t0004g0304 a0001c0001t0004g0332 others(23): Show |
26 | HG01256.hp1 HG01261.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.165+9257delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18408938 | ||||||
| chr6:18408938 | GTTTTTT | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(208): Show |
219 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.165+9252_165+9257d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18408938 | ||||||
| chr6:18409042 | T | C | 1 | a0001c0001t0062g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.165+9343T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409042 | |||||||
| chr6:18409073 | G | A | 1 | a0001c0001t0005g0358 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.165+9374G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409073 | |||||||
| chr6:18409091 | A | G | 10 | a0001c0001t0007g0231 a0001c0001t0007g0243 a0001c0001t0007g0244 others(7): Show |
10 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+9392A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409091 | |||||||
| chr6:18409246 | C | T | 1 | a0001c0001t0006g0173 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.165+9547C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409246 | |||||||
| chr6:18409247 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165+9548G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409247 | |||||||
| chr6:18409298 | A | G | 1 | a0001c0001t0038g0105 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.165+9599A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409298 | |||||||
| chr6:18409302 | C | T | 1 | a0001c0001t0004g0131 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.165+9603C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409302 | |||||||
| chr6:18409303 | G | A | 1 | a0001c0001t0007g0293 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.165+9604G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409303 | |||||||
| chr6:18409353 | G | A | 217 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(214): Show |
225 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.165+9654G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409353 | |||||||
| chr6:18409375 | C | CA | 8 | a0001c0001t0013g0020 a0001c0001t0014g0350 a0001c0001t0017g0092 others(5): Show |
8 | HG00140.hp1 HG00642.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+9704dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | C | CAA | 40 | a0001c0001t0002g0297 a0001c0001t0002g0298 a0001c0001t0002g0303 others(37): Show |
41 | HG01074.hp1 HG01081.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.165+9703_165+9704d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | C | CAAA | 49 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0306 others(46): Show |
54 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.165+9702_165+9704d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | C | CAAAA | 17 | a0001c0001t0003g0153 a0001c0001t0004g0332 a0001c0001t0005g0301 others(14): Show |
17 | HG01261.hp2 HG01891.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.165+9701_165+9704d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | CA | C | 12 | a0001c0001t0001g0044 a0001c0001t0003g0167 a0001c0001t0005g0355 others(9): Show |
12 | HG00621.hp1 HG00642.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+9704delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | CAA | C | 44 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0002g0356 others(41): Show |
45 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.165+9703_165+9704d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | CAAA | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(88): Show |
95 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.165+9702_165+9704d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | CAAAA | C | 12 | a0001c0001t0004g0359 a0001c0001t0007g0238 a0001c0001t0007g0239 others(9): Show |
13 | HG00099.hp1 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+9701_165+9704d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409375 | CAAAAA | C | 8 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0007g0240 others(5): Show |
8 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+9700_165+9704d others(7): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409375 | ||||||
| chr6:18409402 | A | AG | 17 | a0001c0001t0003g0184 a0001c0001t0003g0187 a0001c0001t0003g0220 others(14): Show |
17 | HG00438.hp1 HG00738.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+9703_165+9704i others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409402 | |||||||
| chr6:18409402 | A | G | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(197): Show |
208 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.165+9703A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409402 | |||||||
| chr6:18409429 | G | T | 1 | a0001c0001t0091g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.165+9730G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409429 | |||||||
| chr6:18409463 | C | A | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+9764C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409463 | |||||||
| chr6:18409492 | G | C | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+9793G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409492 | |||||||
| chr6:18409560 | C | A | 1 | a0001c0002t0022g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+9861C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409560 | |||||||
| chr6:18409561 | C | CT | 39 | a0001c0001t0002g0346 a0001c0001t0003g0153 a0001c0001t0004g0304 others(36): Show |
39 | HG00735.hp2 HG01175.hp1 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.165+9881dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | ||||||
| chr6:18409561 | C | CTTT | 18 | a0001c0001t0019g0146 a0001c0001t0019g0149 a0001c0001t0020g0001 others(15): Show |
19 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.165+9879_165+9881d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | ||||||
| chr6:18409561 | C | CTTTT | 15 | a0001c0001t0009g0285 a0001c0001t0010g0227 a0001c0001t0019g0006 others(12): Show |
16 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+9878_165+9881d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | ||||||
| chr6:18409561 | C | CTTTTT | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(155): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.165+9877_165+9881d others(7): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | ||||||
| chr6:18409561 | C | CTTTTTT | 23 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0047 others(20): Show |
23 | HG00423.hp1 HG00621.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.165+9876_165+9881d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18409561 | ||||||
| chr6:18409762 | A | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+10063A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409762 | |||||||
| chr6:18409856 | C | T | 1 | a0001c0001t0018g0266 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.165+10157C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409856 | |||||||
| chr6:18409861 | C | T | 70 | a0001c0001t0003g0008 a0001c0001t0003g0176 a0001c0001t0003g0183 others(67): Show |
73 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.165+10162C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409861 | |||||||
| chr6:18409922 | G | A | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.165+10223G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409922 | |||||||
| chr6:18409987 | G | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(213): Show |
224 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.165+10288G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18409987 | |||||||
| chr6:18410047 | A | G | 1 | a0001c0001t0083g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.165+10348A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410047 | |||||||
| chr6:18410194 | G | A | 2 | a0001c0001t0024g0287 a0001c0001t0028g0101 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.165+10495G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410194 | |||||||
| chr6:18410219 | C | T | 14 | a0001c0001t0008g0098 a0001c0001t0009g0288 a0001c0001t0024g0012 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+10520C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410219 | |||||||
| chr6:18410390 | A | G | 358 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(355): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.165+10691A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410390 | |||||||
| chr6:18410546 | GT | G | 11 | a0001c0001t0011g0364 a0001c0001t0025g0273 a0001c0001t0025g0275 others(8): Show |
11 | HG00323.hp1 HG01257.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+10848delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410546 | |||||||
| chr6:18410550 | G | T | 99 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(96): Show |
104 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.165+10851G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410550 | |||||||
| chr6:18410693 | T | TA | 61 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(58): Show |
66 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.165+11001dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18410693 | ||||||
| chr6:18410753 | G | C | 5 | a0001c0001t0006g0174 a0001c0001t0017g0005 a0001c0001t0017g0092 others(2): Show |
6 | HG00642.hp1 HG01081.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11054G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410753 | |||||||
| chr6:18410755 | C | CGGTACAG others(17): Show |
1 | a0001c0002t0022g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+11057_165+1108 others(28): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18410755 | ||||||
| chr6:18410757 | G | A | 24 | a0001c0001t0003g0153 a0001c0001t0004g0304 a0001c0001t0004g0332 others(21): Show |
24 | HG01261.hp2 HG01928.hp1 HG02004.hp2 others(21): Show |
intron_variant | MODIFIER | c.165+11058G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410757 | |||||||
| chr6:18410907 | A | G | 3 | a0001c0001t0034g0269 a0001c0001t0059g0143 a0001c0001t0060g0148 |
3 | HG00735.hp1 HG01993.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.165+11208A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410907 | |||||||
| chr6:18410982 | T | C | 5 | a0001c0001t0081g0126 a0001c0001t0083g0127 a0001c0001t0092g0181 others(2): Show |
5 | HG01361.hp2 HG02559.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+11283T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18410982 | |||||||
| chr6:18410994 | C | CT | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+11304dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18410994 | ||||||
| chr6:18411077 | C | T | 1 | a0001c0001t0005g0301 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.165+11378C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411077 | |||||||
| chr6:18411089 | G | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+11390G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411089 | |||||||
| chr6:18411150 | A | G | 7 | a0001c0001t0009g0285 a0001c0001t0010g0227 a0001c0001t0016g0091 others(4): Show |
8 | HG01256.hp2 HG01258.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+11451A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411150 | |||||||
| chr6:18411173 | C | T | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(210): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.165+11474C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411173 | |||||||
| chr6:18411174 | G | T | 1 | a0001c0002t0022g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.165+11475G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411174 | |||||||
| chr6:18411211 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(204): Show |
214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.165+11512C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411211 | |||||||
| chr6:18411230 | G | A | 1 | a0001c0001t0006g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.165+11531G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411230 | |||||||
| chr6:18411241 | C | T | 1 | a0001c0001t0019g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+11542C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411241 | |||||||
| chr6:18411276 | C | G | 1 | a0001c0001t0004g0327 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.165+11577C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411276 | |||||||
| chr6:18411334 | T | TG | 366 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(363): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.165+11635_165+1163 others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411334 | |||||||
| chr6:18411361 | G | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+11662G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411361 | |||||||
| chr6:18411378 | C | A | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+11679C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411378 | |||||||
| chr6:18411380 | T | C | 1 | a0001c0001t0066g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.165+11681T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411380 | |||||||
| chr6:18411456 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.165+11757A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411456 | |||||||
| chr6:18411460 | T | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+11761T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411460 | |||||||
| chr6:18411462 | C | CAT | 4 | a0001c0001t0016g0091 a0001c0001t0026g0279 a0001c0001t0054g0019 others(1): Show |
4 | HG01975.hp2 HG02071.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+11798_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | C | CATATAT | 3 | a0001c0001t0026g0259 a0001c0001t0026g0260 a0001c0001t0107g0025 |
3 | HG01358.hp1 HG02886.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.165+11794_165+1179 others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | C | CATATATA others(3): Show |
1 | a0001c0001t0101g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.165+11790_165+1179 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | CATATAT | C | 7 | a0001c0001t0002g0356 a0001c0001t0004g0359 a0001c0001t0015g0129 others(4): Show |
7 | HG00438.hp2 HG01074.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+11794_165+1179 others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | CATATATA others(1): Show |
C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0022 others(74): Show |
81 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.165+11792_165+1179 others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | CATATATA others(3): Show |
C | 15 | a0001c0001t0011g0364 a0001c0001t0017g0033 a0001c0001t0025g0273 others(12): Show |
15 | HG01167.hp1 HG01257.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.165+11790_165+1179 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | CATATATA others(5): Show |
C | 45 | a0001c0001t0002g0297 a0001c0001t0002g0306 a0001c0001t0002g0315 others(42): Show |
47 | HG01123.hp1 HG01175.hp1 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.165+11788_165+1179 others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | CATATATA others(7): Show |
C | 14 | a0001c0001t0007g0233 a0001c0001t0007g0242 a0001c0001t0010g0236 others(11): Show |
14 | HG00099.hp1 HG01168.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+11786_165+1179 others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411462 | CATATATA others(9): Show |
C | 1 | a0001c0001t0008g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+11784_165+1179 others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411462 | ||||||
| chr6:18411478 | TATATATA others(8): Show |
T | 1 | a0001c0001t0062g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.165+11780_165+1179 others(19): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411478 | |||||||
| chr6:18411480 | TATATATA others(6): Show |
T | 12 | a0001c0001t0007g0232 a0001c0001t0007g0239 a0001c0001t0007g0240 others(9): Show |
13 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+11782_165+1179 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411480 | |||||||
| chr6:18411480 | TATATATA others(8): Show |
T | 2 | a0001c0001t0009g0288 a0001c0001t0024g0290 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.165+11782_165+1179 others(19): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411480 | |||||||
| chr6:18411481 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0320 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.165+11784_165+1180 others(22): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411481 | ||||||
| chr6:18411481 | ATATATAT others(13): Show |
A | 3 | a0001c0001t0001g0048 a0001c0001t0023g0068 a0001c0001t0060g0148 |
3 | HG01993.hp2 HG02132.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.165+11784_165+1180 others(24): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411481 | ||||||
| chr6:18411481 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0034g0269 a0001c0001t0059g0143 |
2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.165+11784_165+1180 others(25): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411481 | ||||||
| chr6:18411482 | TATATATA | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0073 others(4): Show |
7 | HG04184.hp1 NA18949.hp1 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+11784_165+1179 others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | |||||||
| chr6:18411482 | TATATATA others(2): Show |
T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(6): Show |
9 | HG00558.hp1 HG01169.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+11784_165+1179 others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | |||||||
| chr6:18411482 | TATATATA others(4): Show |
T | 1 | a0001c0001t0006g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.165+11784_165+1179 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | |||||||
| chr6:18411482 | TATATATA others(6): Show |
T | 1 | a0001c0001t0024g0291 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.165+11784_165+1179 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411482 | |||||||
| chr6:18411484 | TATATATA | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02040.hp1 HG02165.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+11786_165+1179 others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411484 | |||||||
| chr6:18411484 | TATATATA others(2): Show |
T | 3 | a0001c0001t0016g0077 a0001c0001t0042g0093 a0003c0006t0055g0071 |
3 | HG01070.hp1 HG02738.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.165+11786_165+1179 others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411484 | |||||||
| chr6:18411484 | TATATATA others(4): Show |
T | 2 | a0001c0001t0037g0333 a0001c0001t0042g0075 |
2 | HG00323.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.165+11786_165+1179 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411484 | |||||||
| chr6:18411485 | ATATATAT others(6): Show |
A | 3 | a0001c0001t0002g0313 a0001c0001t0002g0341 a0001c0001t0013g0031 |
3 | HG01943.hp2 NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.165+11788_165+1180 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411485 | ||||||
| chr6:18411486 | TATATATA | T | 3 | a0001c0001t0006g0174 a0001c0001t0056g0060 a0001c0001t0106g0049 |
3 | HG01433.hp1 HG03098.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+11788_165+1179 others(11): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411486 | |||||||
| chr6:18411486 | TATATATA others(2): Show |
T | 9 | a0001c0001t0003g0203 a0001c0001t0005g0352 a0001c0001t0005g0358 others(6): Show |
9 | HG00140.hp2 HG02132.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+11788_165+1179 others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411486 | |||||||
| chr6:18411486 | TATATATA others(4): Show |
T | 3 | a0001c0001t0019g0149 a0001c0001t0038g0105 a0001c0001t0038g0144 |
3 | HG02965.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.165+11788_165+1179 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411486 | |||||||
| chr6:18411487 | A | AT | 6 | a0001c0001t0003g0008 a0001c0001t0003g0216 a0001c0001t0005g0335 others(3): Show |
6 | NA18942.hp1 NA18975.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11789dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | ||||||
| chr6:18411487 | A | T | 3 | a0001c0001t0003g0176 a0001c0001t0008g0034 a0001c0001t0023g0046 |
3 | HG00438.hp2 NA18991.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.165+11788A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411487 | |||||||
| chr6:18411487 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0002g0014 a0001c0001t0036g0330 |
2 | NA19000.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.165+11790_165+1180 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | ||||||
| chr6:18411487 | ATATATAT others(5): Show |
A | 24 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0298 others(21): Show |
26 | HG00408.hp2 HG00621.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.165+11790_165+1180 others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | ||||||
| chr6:18411487 | ATATATAT others(6): Show |
A | 7 | a0001c0001t0002g0324 a0001c0001t0002g0325 a0001c0001t0002g0334 others(4): Show |
7 | HG02523.hp1 HG02723.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+11790_165+1180 others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411487 | ||||||
| chr6:18411489 | A | AT | 13 | a0001c0001t0003g0183 a0001c0001t0003g0187 a0001c0001t0005g0351 others(10): Show |
13 | HG01106.hp1 HG01175.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+11791dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | ||||||
| chr6:18411489 | A | ATT | 4 | a0001c0001t0003g0220 a0001c0001t0003g0222 a0001c0001t0003g0223 others(1): Show |
4 | NA18949.hp2 NA18964.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+11791_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | ||||||
| chr6:18411489 | A | T | 18 | a0001c0001t0001g0061 a0001c0001t0001g0066 a0001c0001t0001g0072 others(15): Show |
18 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+11790A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411489 | |||||||
| chr6:18411489 | ATATATAT others(3): Show |
A | 4 | a0001c0001t0020g0001 a0001c0001t0044g0262 a0001c0001t0085g0118 others(1): Show |
4 | HG02818.hp1 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+11792_165+1180 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | ||||||
| chr6:18411489 | ATATATAT others(4): Show |
A | 5 | a0001c0001t0002g0303 a0001c0001t0005g0344 a0001c0001t0020g0001 others(2): Show |
5 | HG01074.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+11792_165+1180 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | ||||||
| chr6:18411489 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0034g0230 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.165+11792_165+1180 others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411489 | ||||||
| chr6:18411491 | A | ATT | 6 | a0001c0001t0012g0192 a0001c0001t0012g0193 a0001c0001t0016g0080 others(3): Show |
6 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11793_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411491 | ||||||
| chr6:18411491 | A | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(73): Show |
78 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.165+11792A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411491 | |||||||
| chr6:18411491 | ATATATAT others(1): Show |
A | 9 | a0001c0001t0013g0020 a0001c0001t0013g0086 a0001c0001t0013g0089 others(6): Show |
9 | HG01243.hp2 HG02280.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+11794_165+1180 others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411491 | ||||||
| chr6:18411493 | A | ATT | 3 | a0001c0001t0039g0147 a0001c0001t0039g0150 a0001c0001t0072g0272 |
3 | HG02896.hp1 HG02897.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.165+11795_165+1179 others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411493 | ||||||
| chr6:18411493 | A | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(116): Show |
124 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.165+11794A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411493 | |||||||
| chr6:18411495 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0022g0159 a0001c0001t0022g0160 |
2 | HG00733.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.165+11797_165+1179 others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411495 | ||||||
| chr6:18411495 | A | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(204): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.165+11796A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411495 | |||||||
| chr6:18411497 | A | ATATATAT others(9): Show |
1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.165+11799_165+1180 others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411497 | ||||||
| chr6:18411497 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0022g0194 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.165+11812_165+1182 others(15): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18411497 | ||||||
| chr6:18411497 | A | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(240): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.165+11798A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411497 | |||||||
| chr6:18411499 | T | A | 6 | a0001c0001t0026g0259 a0001c0001t0026g0279 a0001c0001t0047g0110 others(3): Show |
6 | HG01975.hp2 HG02071.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11800T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411499 | |||||||
| chr6:18411501 | T | A | 1 | a0001c0001t0026g0259 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.165+11802T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411501 | |||||||
| chr6:18411592 | C | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(211): Show |
222 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.165+11893C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411592 | |||||||
| chr6:18411659 | G | A | 5 | a0001c0001t0025g0273 a0001c0001t0025g0275 a0001c0001t0025g0277 others(2): Show |
5 | NA18945.hp2 NA18948.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+11960G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411659 | |||||||
| chr6:18411787 | C | T | 3 | a0001c0001t0034g0269 a0001c0001t0059g0143 a0001c0001t0060g0148 |
3 | HG00735.hp1 HG01993.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.165+12088C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411787 | |||||||
| chr6:18411795 | A | G | 1 | a0001c0001t0074g0140 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.165+12096A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411795 | |||||||
| chr6:18411797 | C | T | 1 | a0001c0001t0019g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.165+12098C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411797 | |||||||
| chr6:18411834 | G | A | 99 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(96): Show |
104 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.165+12135G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18411834 | |||||||
| chr6:18412104 | G | T | 1 | a0001c0001t0060g0148 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.165+12405G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412104 | |||||||
| chr6:18412148 | A | G | 1 | a0001c0001t0079g0354 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.165+12449A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412148 | |||||||
| chr6:18412176 | A | G | 1 | a0001c0001t0030g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.165+12477A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412176 | |||||||
| chr6:18412238 | C | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(72): Show |
77 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.165+12539C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412238 | |||||||
| chr6:18412247 | C | G | 5 | a0001c0001t0081g0126 a0001c0001t0083g0127 a0001c0001t0092g0181 others(2): Show |
5 | HG01361.hp2 HG02559.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+12548C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412247 | |||||||
| chr6:18412346 | A | G | 3 | a0001c0001t0038g0102 a0001c0001t0038g0105 a0001c0001t0038g0144 |
3 | HG02897.hp1 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.165+12647A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412346 | |||||||
| chr6:18412410 | A | G | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.165+12711A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412410 | |||||||
| chr6:18412559 | CA | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(210): Show |
221 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.165+12867delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18412559 | ||||||
| chr6:18412678 | T | C | 19 | a0001c0001t0007g0232 a0001c0001t0007g0233 a0001c0001t0007g0238 others(16): Show |
20 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+12979T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412678 | |||||||
| chr6:18412795 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(83): Show |
88 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.165+13096A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412795 | |||||||
| chr6:18412858 | G | A | 1 | a0001c0001t0001g0003 | 2 | NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.165+13159G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412858 | |||||||
| chr6:18412993 | A | G | 1 | a0001c0001t0019g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.165+13294A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18412993 | |||||||
| chr6:18413013 | A | G | 1 | a0001c0001t0013g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+13314A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413013 | |||||||
| chr6:18413207 | A | AT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(69): Show |
75 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.165+13516dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18413207 | ||||||
| chr6:18413397 | T | A | 2 | a0001c0001t0064g0369 a0001c0001t0082g0106 |
2 | HG01515.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.165+13698T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413397 | |||||||
| chr6:18413437 | TG | T | 12 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(9): Show |
13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+13740delG | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18413437 | ||||||
| chr6:18413444 | G | A | 2 | a0001c0001t0030g0201 a0001c0001t0084g0111 |
2 | HG00140.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.165+13745G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413444 | |||||||
| chr6:18413663 | T | A | 2 | a0001c0001t0066g0282 a0001c0001t0083g0127 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-13918T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413663 | |||||||
| chr6:18413758 | T | C | 20 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(17): Show |
20 | HG01261.hp2 HG02004.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.166-13823T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413758 | |||||||
| chr6:18413801 | T | C | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-13780T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413801 | |||||||
| chr6:18413953 | T | G | 1 | a0001c0001t0001g0292 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.166-13628T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18413953 | |||||||
| chr6:18414061 | C | G | 1 | a0001c0001t0070g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.166-13520C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414061 | |||||||
| chr6:18414093 | G | A | 2 | a0001c0001t0020g0124 a0001c0001t0021g0195 |
2 | HG01496.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.166-13488G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414093 | |||||||
| chr6:18414240 | A | T | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.166-13341A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414240 | |||||||
| chr6:18414458 | G | A | 1 | a0001c0001t0023g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.166-13123G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414458 | |||||||
| chr6:18414560 | C | T | 1 | a0001c0001t0004g0326 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.166-13021C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18414560 | |||||||
| chr6:18415154 | T | A | 2 | a0001c0001t0066g0282 a0001c0001t0083g0127 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.166-12427T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415154 | |||||||
| chr6:18415163 | T | C | 1 | a0002c0004t0078g0311 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.166-12418T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415163 | |||||||
| chr6:18415275 | C | T | 1 | a0001c0001t0010g0276 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.166-12306C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415275 | |||||||
| chr6:18415298 | A | G | 1 | a0001c0001t0066g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.166-12283A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415298 | |||||||
| chr6:18415341 | T | C | 4 | a0001c0001t0027g0130 a0001c0001t0027g0300 a0001c0001t0027g0357 others(1): Show |
4 | HG01243.hp1 HG01433.hp2 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-12240T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415341 | |||||||
| chr6:18415347 | C | T | 1 | a0001c0001t0042g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.166-12234C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415347 | |||||||
| chr6:18415378 | G | A | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-12203G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415378 | |||||||
| chr6:18415385 | T | C | 1 | a0001c0001t0076g0363 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.166-12196T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415385 | |||||||
| chr6:18415386 | G | A | 19 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(16): Show |
21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-12195G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415386 | |||||||
| chr6:18415445 | C | T | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-12136C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415445 | |||||||
| chr6:18415482 | T | C | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-12099T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415482 | |||||||
| chr6:18415482 | T | G | 79 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(76): Show |
82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.166-12099T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415482 | |||||||
| chr6:18415495 | C | G | 118 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(115): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.166-12086C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415495 | |||||||
| chr6:18415640 | C | G | 1 | a0001c0001t0047g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.166-11941C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415640 | |||||||
| chr6:18415766 | A | G | 1 | a0001c0001t0032g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.166-11815A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415766 | |||||||
| chr6:18415777 | A | G | 1 | a0001c0001t0023g0068 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.166-11804A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415777 | |||||||
| chr6:18415898 | G | A | 13 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(10): Show |
14 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-11683G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18415898 | |||||||
| chr6:18416013 | G | T | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-11568G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416013 | |||||||
| chr6:18416137 | CAGTT | C | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-11442_166-1143 others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18416137 | ||||||
| chr6:18416206 | A | T | 118 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(115): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.166-11375A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416206 | |||||||
| chr6:18416384 | G | T | 78 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(75): Show |
81 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.166-11197G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416384 | |||||||
| chr6:18416461 | C | T | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-11120C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416461 | |||||||
| chr6:18416539 | A | G | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-11042A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416539 | |||||||
| chr6:18416565 | C | G | 1 | a0001c0001t0079g0354 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.166-11016C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416565 | |||||||
| chr6:18416612 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.166-10969A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416612 | |||||||
| chr6:18416613 | A | G | 2 | a0001c0001t0089g0185 a0001c0001t0090g0178 |
2 | HG00438.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.166-10968A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416613 | |||||||
| chr6:18416646 | G | A | 6 | a0001c0001t0005g0013 a0001c0001t0005g0344 a0001c0001t0008g0032 others(3): Show |
7 | HG00140.hp2 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-10935G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416646 | |||||||
| chr6:18416868 | T | C | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-10713T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416868 | |||||||
| chr6:18416972 | A | C | 1 | a0001c0001t0101g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.166-10609A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18416972 | |||||||
| chr6:18417066 | T | C | 1 | a0001c0001t0012g0192 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-10515T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417066 | |||||||
| chr6:18417260 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.166-10321T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417260 | |||||||
| chr6:18417264 | A | G | 1 | a0001c0001t0050g0213 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-10317A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417264 | |||||||
| chr6:18417302 | C | G | 1 | a0001c0001t0002g0341 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.166-10279C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417302 | |||||||
| chr6:18417335 | G | C | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-10246G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417335 | |||||||
| chr6:18417456 | G | T | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-10125G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417456 | |||||||
| chr6:18417501 | G | A | 1 | a0001c0001t0002g0341 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.166-10080G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417501 | |||||||
| chr6:18417566 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0292 |
3 | NA18747.hp1 NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.166-10015G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417566 | |||||||
| chr6:18417612 | T | G | 2 | a0001c0001t0005g0353 a0001c0001t0079g0354 |
2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.166-9969T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417612 | |||||||
| chr6:18417898 | A | G | 2 | a0001c0001t0005g0013 a0001c0001t0036g0331 |
3 | HG03490.hp2 HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.166-9683A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417898 | |||||||
| chr6:18417934 | G | C | 1 | a0001c0001t0002g0297 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.166-9647G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417934 | |||||||
| chr6:18417959 | G | A | 40 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(37): Show |
42 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.166-9622G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417959 | |||||||
| chr6:18417979 | T | C | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-9602T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18417979 | |||||||
| chr6:18418005 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.166-9576C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418005 | |||||||
| chr6:18418112 | T | C | 1 | a0001c0001t0008g0036 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.166-9469T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418112 | |||||||
| chr6:18418152 | G | A | 1 | a0001c0001t0070g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.166-9429G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418152 | |||||||
| chr6:18418165 | A | G | 1 | a0001c0001t0030g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.166-9416A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418165 | |||||||
| chr6:18418376 | A | G | 1 | a0001c0001t0004g0326 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.166-9205A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418376 | |||||||
| chr6:18418385 | A | G | 19 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(16): Show |
21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-9196A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418385 | |||||||
| chr6:18418477 | T | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(260): Show |
274 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.166-9104T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418477 | |||||||
| chr6:18418495 | A | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(141): Show |
149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.166-9086A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418495 | |||||||
| chr6:18418574 | T | A | 1 | a0001c0001t0070g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.166-9007T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418574 | |||||||
| chr6:18418577 | G | A | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-9004G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418577 | |||||||
| chr6:18418658 | G | A | 4 | a0001c0001t0016g0052 a0001c0001t0016g0053 a0001c0001t0016g0055 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-8923G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418658 | |||||||
| chr6:18418717 | A | G | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-8864A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418717 | |||||||
| chr6:18418838 | A | C | 89 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(86): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.166-8743A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418838 | |||||||
| chr6:18418842 | A | G | 1 | a0001c0001t0033g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.166-8739A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418842 | |||||||
| chr6:18418963 | A | G | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-8618A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18418963 | |||||||
| chr6:18419087 | A | G | 1 | a0001c0001t0003g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.166-8494A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419087 | |||||||
| chr6:18419208 | C | T | 8 | a0001c0001t0038g0102 a0001c0001t0038g0105 a0001c0001t0038g0144 others(5): Show |
8 | HG01515.hp2 HG02559.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-8373C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419208 | |||||||
| chr6:18419318 | G | A | 6 | a0001c0001t0020g0001 a0001c0001t0021g0179 a0001c0001t0021g0218 others(3): Show |
7 | HG02258.hp1 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-8263G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419318 | |||||||
| chr6:18419459 | G | A | 4 | a0001c0001t0049g0120 a0001c0001t0049g0145 a0001c0001t0098g0206 others(1): Show |
4 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-8122G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419459 | |||||||
| chr6:18419562 | G | A | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(346): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.166-8019G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419562 | |||||||
| chr6:18419713 | G | C | 73 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(70): Show |
76 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.166-7868G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419713 | |||||||
| chr6:18419840 | T | C | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-7741T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419840 | |||||||
| chr6:18419995 | A | G | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-7586A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18419995 | |||||||
| chr6:18420134 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.166-7447G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420134 | |||||||
| chr6:18420155 | C | T | 1 | a0001c0001t0030g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.166-7426C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420155 | |||||||
| chr6:18420158 | A | AT | 151 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(148): Show |
158 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.166-7413dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18420158 | ||||||
| chr6:18420158 | A | ATT | 124 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(121): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.166-7414_166-7413d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18420158 | ||||||
| chr6:18420158 | A | ATTT | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(80): Show |
86 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.166-7415_166-7413d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18420158 | ||||||
| chr6:18420215 | C | A | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-7366C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420215 | |||||||
| chr6:18420278 | A | T | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-7303A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420278 | |||||||
| chr6:18420483 | G | A | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-7098G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420483 | |||||||
| chr6:18420527 | C | A | 5 | a0001c0001t0002g0303 a0001c0001t0002g0308 a0001c0001t0002g0347 others(2): Show |
5 | NA18940.hp2 NA18965.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-7054C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420527 | |||||||
| chr6:18420566 | T | C | 1 | a0001c0001t0024g0290 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.166-7015T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420566 | |||||||
| chr6:18420789 | G | A | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.166-6792G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420789 | |||||||
| chr6:18420849 | C | T | 1 | a0001c0001t0037g0328 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.166-6732C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18420849 | |||||||
| chr6:18421079 | A | T | 1 | a0001c0001t0012g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.166-6502A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421079 | |||||||
| chr6:18421123 | C | T | 2 | a0001c0001t0005g0353 a0001c0001t0079g0354 |
2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.166-6458C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421123 | |||||||
| chr6:18421270 | TTA | T | 3 | a0001c0001t0002g0348 a0001c0001t0026g0260 a0001c0001t0026g0261 |
3 | HG01358.hp1 HG03239.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.166-6308_166-6307d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421270 | ||||||
| chr6:18421271 | T | TAC | 18 | a0001c0001t0002g0014 a0001c0001t0002g0297 a0001c0001t0002g0303 others(15): Show |
18 | HG00140.hp1 HG01123.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-6309_166-6308i others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | T | TACAC | 29 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0298 others(26): Show |
29 | HG00408.hp2 HG00423.hp2 HG02083.hp2 others(26): Show |
intron_variant | MODIFIER | c.166-6309_166-6308i others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | T | TACACAC | 9 | a0001c0001t0002g0308 a0001c0001t0002g0325 a0001c0001t0009g0011 others(6): Show |
9 | HG01243.hp2 HG02602.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-6309_166-6308i others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | T | TACACACA others(1): Show |
3 | a0001c0001t0009g0252 a0001c0001t0009g0285 a0001c0001t0019g0149 |
3 | HG02965.hp2 NA19081.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.166-6309_166-6308i others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | T | TACACACA others(3): Show |
1 | a0001c0001t0002g0356 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-6309_166-6308i others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | T | TACACACA others(5): Show |
1 | a0001c0001t0019g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.166-6309_166-6308i others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | T | TACACACA others(9): Show |
1 | a0001c0005t0009g0247 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.166-6309_166-6308i others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | TATACACA others(9): Show |
T | 97 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(94): Show |
100 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.166-6308_166-6293d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | TATACACA others(11): Show |
T | 44 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(41): Show |
47 | HG00323.hp1 HG00642.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.166-6308_166-6291d others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421271 | TATACACA others(13): Show |
T | 13 | a0001c0001t0020g0001 a0001c0001t0020g0117 a0001c0001t0020g0124 others(10): Show |
14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-6308_166-6289d others(22): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421271 | ||||||
| chr6:18421273 | T | C | 69 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(66): Show |
72 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.166-6308T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421273 | |||||||
| chr6:18421273 | T | TAC | 18 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0050 others(15): Show |
21 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.166-6266_166-6265d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | ||||||
| chr6:18421273 | T | TACAC | 6 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0010g0227 others(3): Show |
6 | HG01256.hp1 HG02922.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-6268_166-6265d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | ||||||
| chr6:18421273 | TAC | T | 28 | a0001c0001t0004g0132 a0001c0001t0004g0304 a0001c0001t0004g0326 others(25): Show |
28 | HG00639.hp1 HG01167.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.166-6266_166-6265d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | ||||||
| chr6:18421273 | TACAC | T | 19 | a0001c0001t0004g0015 a0001c0001t0007g0231 a0001c0001t0007g0233 others(16): Show |
20 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.166-6268_166-6265d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | ||||||
| chr6:18421273 | TACACAC | T | 8 | a0001c0001t0004g0360 a0001c0001t0007g0232 a0001c0001t0027g0130 others(5): Show |
8 | HG00280.hp1 HG00558.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-6270_166-6265d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421273 | ||||||
| chr6:18421313 | C | T | 1 | a0001c0001t0056g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.166-6268C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421313 | |||||||
| chr6:18421315 | C | T | 154 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(151): Show |
161 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.166-6266C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421315 | |||||||
| chr6:18421315 | CAT | C | 3 | a0001c0001t0010g0235 a0001c0001t0068g0278 a0001c0001t0076g0363 |
3 | HG00735.hp2 HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.166-6258_166-6257d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18421315 | ||||||
| chr6:18421317 | T | C | 13 | a0001c0001t0001g0045 a0001c0001t0002g0298 a0001c0001t0010g0010 others(10): Show |
14 | HG00099.hp1 HG00280.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-6264T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421317 | |||||||
| chr6:18421319 | T | C | 1 | a0001c0001t0010g0234 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.166-6262T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421319 | |||||||
| chr6:18421571 | C | T | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-6010C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421571 | |||||||
| chr6:18421582 | A | G | 1 | a0001c0001t0014g0302 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.166-5999A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421582 | |||||||
| chr6:18421611 | C | T | 1 | a0001c0001t0006g0154 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.166-5970C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421611 | |||||||
| chr6:18421745 | G | A | 2 | a0001c0001t0040g0113 a0001c0001t0040g0114 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.166-5836G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421745 | |||||||
| chr6:18421797 | C | T | 1 | a0001c0001t0101g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.166-5784C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18421797 | |||||||
| chr6:18422226 | A | G | 2 | a0001c0001t0027g0130 a0001c0001t0048g0107 |
2 | HG02683.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.166-5355A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422226 | |||||||
| chr6:18422242 | G | T | 56 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.166-5339G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422242 | |||||||
| chr6:18422318 | T | C | 89 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(86): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.166-5263T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422318 | |||||||
| chr6:18422421 | G | A | 351 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(348): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.166-5160G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422421 | |||||||
| chr6:18422574 | C | CT | 4 | a0001c0001t0016g0091 a0001c0001t0033g0281 a0001c0001t0033g0283 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-5005dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422574 | ||||||
| chr6:18422617 | C | T | 1 | a0001c0001t0028g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.166-4964C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18422617 | |||||||
| chr6:18422951 | C | CA | 68 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0298 others(65): Show |
72 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.166-4615dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422951 | ||||||
| chr6:18422951 | C | CAA | 18 | a0001c0001t0002g0297 a0001c0001t0002g0308 a0001c0001t0002g0315 others(15): Show |
18 | HG00140.hp1 HG01358.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.166-4616_166-4615d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422951 | ||||||
| chr6:18422951 | CA | C | 155 | a0001c0001t0001g0058 a0001c0001t0003g0008 a0001c0001t0003g0153 others(152): Show |
163 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.166-4615delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18422951 | ||||||
| chr6:18423174 | C | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(99): Show |
105 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.166-4407C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423174 | |||||||
| chr6:18423189 | G | A | 3 | a0001c0001t0005g0335 a0001c0001t0005g0336 a0001c0001t0005g0337 |
3 | NA18975.hp1 NA18982.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.166-4392G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423189 | |||||||
| chr6:18423334 | A | T | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.166-4247A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423334 | |||||||
| chr6:18423357 | T | C | 1 | a0001c0001t0089g0185 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.166-4224T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423357 | |||||||
| chr6:18423358 | T | C | 1 | a0001c0001t0008g0082 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.166-4223T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423358 | |||||||
| chr6:18423395 | T | C | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-4186T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423395 | |||||||
| chr6:18423419 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.166-4162C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423419 | |||||||
| chr6:18423436 | A | G | 79 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(76): Show |
82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.166-4145A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423436 | |||||||
| chr6:18423517 | A | G | 13 | a0001c0001t0010g0227 a0001c0001t0033g0281 a0001c0001t0033g0283 others(10): Show |
14 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-4064A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423517 | |||||||
| chr6:18423561 | G | A | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-4020G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423561 | |||||||
| chr6:18423577 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-4004G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423577 | |||||||
| chr6:18423766 | C | CT | 86 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(83): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.166-3815_166-3814i others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423766 | |||||||
| chr6:18423767 | C | A | 86 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(83): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.166-3814C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423767 | |||||||
| chr6:18423847 | A | G | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-3734A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18423847 | |||||||
| chr6:18424038 | G | T | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-3543G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424038 | |||||||
| chr6:18424047 | G | A | 3 | a0001c0001t0029g0121 a0001c0001t0029g0125 a0001c0001t0041g0059 |
3 | HG01167.hp1 HG01169.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.166-3534G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424047 | |||||||
| chr6:18424068 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(261): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.166-3513A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424068 | |||||||
| chr6:18424077 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-3504G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424077 | |||||||
| chr6:18424170 | G | T | 1 | a0001c0001t0094g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-3411G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424170 | |||||||
| chr6:18424171 | A | T | 1 | a0001c0001t0094g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-3410A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424171 | |||||||
| chr6:18424199 | G | T | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-3382G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424199 | |||||||
| chr6:18424349 | A | G | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-3232A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424349 | |||||||
| chr6:18424370 | A | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.166-3211A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424370 | |||||||
| chr6:18424374 | C | T | 1 | a0001c0001t0094g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.166-3207C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424374 | |||||||
| chr6:18424385 | G | A | 1 | a0001c0001t0009g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.166-3196G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424385 | |||||||
| chr6:18424495 | A | G | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-3086A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424495 | |||||||
| chr6:18424609 | GA | G | 16 | a0001c0001t0014g0136 a0001c0001t0014g0350 a0001c0001t0026g0259 others(13): Show |
16 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-2970delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18424609 | ||||||
| chr6:18424648 | C | G | 2 | a0001c0001t0007g0245 a0001c0001t0007g0271 |
2 | HG00639.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.166-2933C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424648 | |||||||
| chr6:18424691 | T | C | 1 | a0001c0001t0020g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.166-2890T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424691 | |||||||
| chr6:18424783 | T | TAAG | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(261): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.166-2796_166-2794d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18424783 | ||||||
| chr6:18424951 | C | A | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-2630C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424951 | |||||||
| chr6:18424970 | A | G | 4 | a0001c0001t0038g0102 a0001c0001t0038g0105 a0001c0001t0038g0144 others(1): Show |
4 | HG02897.hp1 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-2611A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18424970 | |||||||
| chr6:18425056 | G | GGTGT | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-2510_166-2507d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18425056 | ||||||
| chr6:18425056 | G | T | 1 | a0001c0001t0045g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.166-2525G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425056 | |||||||
| chr6:18425056 | GGT | G | 37 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(34): Show |
39 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.166-2508_166-2507d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18425056 | ||||||
| chr6:18425064 | T | A | 3 | a0001c0001t0064g0369 a0001c0001t0074g0140 a0001c0001t0082g0106 |
3 | HG01515.hp2 HG04184.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.166-2517T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425064 | |||||||
| chr6:18425079 | A | C | 351 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(348): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.166-2502A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425079 | |||||||
| chr6:18425109 | G | A | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2472G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425109 | |||||||
| chr6:18425135 | C | T | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.166-2446C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425135 | |||||||
| chr6:18425184 | T | C | 30 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(27): Show |
32 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.166-2397T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425184 | |||||||
| chr6:18425472 | G | C | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-2109G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425472 | |||||||
| chr6:18425723 | A | G | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-1858A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425723 | |||||||
| chr6:18425725 | A | G | 6 | a0001c0001t0002g0297 a0001c0001t0002g0306 a0001c0001t0002g0313 others(3): Show |
6 | HG01123.hp1 HG01361.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-1856A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425725 | |||||||
| chr6:18425751 | C | T | 12 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(9): Show |
13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-1830C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425751 | |||||||
| chr6:18425912 | T | C | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-1669T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425912 | |||||||
| chr6:18425989 | A | T | 1 | a0001c0001t0062g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.166-1592A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18425989 | |||||||
| chr6:18426093 | G | A | 4 | a0001c0001t0010g0227 a0001c0001t0051g0009 a0001c0001t0058g0226 others(1): Show |
5 | HG02055.hp1 HG02922.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-1488G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426093 | |||||||
| chr6:18426168 | G | A | 1 | a0001c0001t0072g0272 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.166-1413G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426168 | |||||||
| chr6:18426181 | T | C | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.166-1400T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426181 | |||||||
| chr6:18426193 | A | C | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-1388A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426193 | |||||||
| chr6:18426316 | A | G | 1 | a0001c0001t0100g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.166-1265A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426316 | |||||||
| chr6:18426344 | T | C | 66 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(63): Show |
70 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.166-1237T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426344 | |||||||
| chr6:18426365 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-1216G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426365 | |||||||
| chr6:18426377 | A | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(221): Show |
232 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.166-1204A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426377 | |||||||
| chr6:18426390 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-1191G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426390 | |||||||
| chr6:18426470 | T | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.166-1111T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426470 | |||||||
| chr6:18426494 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0004g0362 |
2 | HG02015.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.166-1087G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426494 | |||||||
| chr6:18426506 | T | C | 12 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(9): Show |
13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-1075T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426506 | |||||||
| chr6:18426744 | CTTTTTTC others(25): Show |
C | 12 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(9): Show |
13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-789_166-758del others(32): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18426744 | ||||||
| chr6:18426792 | GTCTTCTC others(25): Show |
G | 1 | a0001c0001t0047g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.166-773_166-742del others(32): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18426792 | ||||||
| chr6:18426794 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-787C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426794 | |||||||
| chr6:18426896 | C | T | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-685C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18426896 | |||||||
| chr6:18426967 | G | GAGA | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-612_166-611ins others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18426967 | ||||||
| chr6:18427021 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-560G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427021 | |||||||
| chr6:18427081 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-500T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427081 | |||||||
| chr6:18427101 | A | G | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-480A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427101 | |||||||
| chr6:18427186 | C | T | 1 | a0001c0001t0050g0213 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.166-395C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427186 | |||||||
| chr6:18427207 | A | G | 1 | a0001c0001t0100g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.166-374A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427207 | |||||||
| chr6:18427256 | A | AT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.166-314dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18427256 | ||||||
| chr6:18427256 | AT | A | 16 | a0001c0001t0013g0087 a0001c0001t0014g0136 a0001c0001t0014g0350 others(13): Show |
16 | HG00140.hp1 HG01358.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.166-314delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18427256 | ||||||
| chr6:18427256 | ATT | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-315_166-314del others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 18427256 | ||||||
| chr6:18427321 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.166-260T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427321 | |||||||
| chr6:18427445 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-136G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427445 | |||||||
| chr6:18427522 | T | C | 13 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(10): Show |
14 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-59T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427522 | |||||||
| chr6:18427553 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.166-28C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 2/7 | chr6 | 18427553 | |||||||
| chr6:18427824 | G | T | 92 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(89): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.270+139G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427824 | |||||||
| chr6:18427877 | C | T | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.270+192C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427877 | |||||||
| chr6:18427886 | T | C | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.270+201T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427886 | |||||||
| chr6:18427940 | A | G | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+255A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427940 | |||||||
| chr6:18427946 | C | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+261C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18427946 | |||||||
| chr6:18428011 | T | C | 2 | a0001c0001t0013g0030 a0001c0001t0013g0031 |
2 | NA18986.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.270+326T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428011 | |||||||
| chr6:18428101 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+416G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428101 | |||||||
| chr6:18428102 | T | G | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.270+417T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428102 | |||||||
| chr6:18428115 | T | A | 2 | a0001c0001t0014g0136 a0001c0001t0014g0350 |
2 | HG02602.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.270+430T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428115 | |||||||
| chr6:18428198 | C | T | 1 | a0001c0001t0014g0310 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.270+513C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428198 | |||||||
| chr6:18428199 | T | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(250): Show |
264 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.270+514T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428199 | |||||||
| chr6:18428247 | C | A | 79 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(76): Show |
82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.270+562C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428247 | |||||||
| chr6:18428280 | T | C | 1 | a0001c0001t0021g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.270+595T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428280 | |||||||
| chr6:18428307 | A | G | 315 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(312): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.270+622A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428307 | |||||||
| chr6:18428467 | C | G | 16 | a0001c0001t0014g0136 a0001c0001t0014g0350 a0001c0001t0026g0259 others(13): Show |
16 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.270+782C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428467 | |||||||
| chr6:18428485 | A | ATG | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+801_270+802ins others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18428485 | ||||||
| chr6:18428513 | C | T | 1 | a0001c0001t0005g0352 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.270+828C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428513 | |||||||
| chr6:18428514 | G | A | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+829G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428514 | |||||||
| chr6:18428549 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.270+864A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428549 | |||||||
| chr6:18428627 | G | A | 92 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(89): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.270+942G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428627 | |||||||
| chr6:18428755 | C | T | 13 | a0001c0001t0020g0001 a0001c0001t0020g0117 a0001c0001t0020g0124 others(10): Show |
14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.270+1070C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428755 | |||||||
| chr6:18428824 | C | T | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+1139C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428824 | |||||||
| chr6:18428825 | A | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+1140A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428825 | |||||||
| chr6:18428849 | A | G | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.270+1164A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18428849 | |||||||
| chr6:18429062 | G | A | 1 | a0001c0001t0014g0322 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.270+1377G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429062 | |||||||
| chr6:18429202 | A | G | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+1517A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429202 | |||||||
| chr6:18429229 | A | G | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.270+1544A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429229 | |||||||
| chr6:18429342 | T | C | 2 | a0001c0001t0006g0169 a0001c0001t0017g0069 |
2 | NA19011.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.270+1657T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429342 | |||||||
| chr6:18429344 | CTTTG | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.270+1663_270+1666d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18429344 | ||||||
| chr6:18429483 | T | G | 91 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(88): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.270+1798T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429483 | |||||||
| chr6:18429496 | T | C | 38 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(35): Show |
39 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.270+1811T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429496 | |||||||
| chr6:18429580 | T | C | 86 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(83): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.270+1895T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429580 | |||||||
| chr6:18429597 | AC | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.270+1915delC | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18429597 | ||||||
| chr6:18429612 | A | G | 1 | a0001c0001t0032g0191 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.270+1927A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429612 | |||||||
| chr6:18429627 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+1942G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429627 | |||||||
| chr6:18429689 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2004G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429689 | |||||||
| chr6:18429860 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2175C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429860 | |||||||
| chr6:18429881 | G | A | 37 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(34): Show |
39 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.270+2196G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429881 | |||||||
| chr6:18429885 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2200G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429885 | |||||||
| chr6:18429974 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2289G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18429974 | |||||||
| chr6:18430004 | A | G | 1 | a0001c0001t0006g0169 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.270+2319A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430004 | |||||||
| chr6:18430084 | GA | G | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2400delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430084 | |||||||
| chr6:18430258 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2573C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430258 | |||||||
| chr6:18430356 | T | C | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+2671T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430356 | |||||||
| chr6:18430486 | TTC | T | 357 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(354): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.270+2821_270+2822d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18430486 | ||||||
| chr6:18430586 | C | T | 1 | a0001c0001t0010g0227 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.270+2901C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430586 | |||||||
| chr6:18430657 | AT | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(225): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.270+2987delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18430657 | ||||||
| chr6:18430663 | T | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.270+2978T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430663 | |||||||
| chr6:18430700 | G | A | 3 | a0001c0001t0010g0241 a0001c0001t0076g0363 a0001c0001t0105g0067 |
3 | HG00280.hp2 HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.270+3015G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430700 | |||||||
| chr6:18430720 | A | C | 2 | a0001c0001t0053g0204 a0001c0001t0053g0205 |
2 | HG00423.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.270+3035A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430720 | |||||||
| chr6:18430731 | C | T | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+3046C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430731 | |||||||
| chr6:18430787 | G | C | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+3102G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430787 | |||||||
| chr6:18430788 | AATAG | A | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+3105_270+3108d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18430788 | ||||||
| chr6:18430852 | C | T | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.270+3167C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430852 | |||||||
| chr6:18430879 | T | C | 1 | a0001c0001t0008g0034 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.270+3194T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18430879 | |||||||
| chr6:18431005 | G | A | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3320G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431005 | |||||||
| chr6:18431008 | T | C | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3323T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431008 | |||||||
| chr6:18431048 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3363C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431048 | |||||||
| chr6:18431199 | C | G | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3514C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431199 | |||||||
| chr6:18431225 | C | CA | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3549dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18431225 | ||||||
| chr6:18431242 | TA | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+3567delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18431242 | ||||||
| chr6:18431423 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.270+3738A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431423 | |||||||
| chr6:18431429 | A | G | 1 | a0001c0001t0002g0334 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.270+3744A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431429 | |||||||
| chr6:18431464 | A | C | 168 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(165): Show |
176 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.270+3779A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431464 | |||||||
| chr6:18431519 | C | T | 351 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(348): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.270+3834C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431519 | |||||||
| chr6:18431572 | A | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+3887A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431572 | |||||||
| chr6:18431663 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.270+3978A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431663 | |||||||
| chr6:18431666 | C | G | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.270+3981C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431666 | |||||||
| chr6:18431674 | T | C | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(347): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.270+3989T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431674 | |||||||
| chr6:18431841 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4156C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431841 | |||||||
| chr6:18431960 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4275T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431960 | |||||||
| chr6:18431985 | G | A | 1 | a0001c0001t0002g0298 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.270+4300G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18431985 | |||||||
| chr6:18432012 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4327G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432012 | |||||||
| chr6:18432130 | T | C | 1 | a0001c0001t0047g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.270+4445T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432130 | |||||||
| chr6:18432181 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4496T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432181 | |||||||
| chr6:18432237 | C | T | 5 | a0001c0001t0005g0305 a0001c0001t0005g0317 a0001c0001t0005g0351 others(2): Show |
5 | HG01496.hp1 HG01928.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.270+4552C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432237 | |||||||
| chr6:18432315 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(91): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.270+4630C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432315 | |||||||
| chr6:18432316 | G | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(9): Show |
13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.270+4631G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432316 | |||||||
| chr6:18432349 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.270+4664G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432349 | |||||||
| chr6:18432355 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.270+4670C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432355 | |||||||
| chr6:18432482 | T | C | 1 | a0001c0001t0003g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.270+4797T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432482 | |||||||
| chr6:18432498 | A | G | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.270+4813A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432498 | |||||||
| chr6:18432538 | C | A | 1 | a0001c0001t0005g0337 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.270+4853C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432538 | |||||||
| chr6:18432631 | T | C | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.270+4946T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432631 | |||||||
| chr6:18432870 | G | C | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5185G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18432870 | |||||||
| chr6:18433128 | C | T | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5443C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433128 | |||||||
| chr6:18433224 | T | A | 2 | a0001c0001t0014g0310 a0001c0001t0019g0108 |
2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.270+5539T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433224 | |||||||
| chr6:18433360 | A | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5675A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433360 | |||||||
| chr6:18433438 | A | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5753A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433438 | |||||||
| chr6:18433504 | A | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.270+5819A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433504 | |||||||
| chr6:18433568 | A | G | 2 | a0001c0001t0015g0329 a0001c0001t0016g0070 |
2 | NA18951.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.270+5883A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433568 | |||||||
| chr6:18433676 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.270+5991C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433676 | |||||||
| chr6:18433859 | G | A | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5825G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433859 | |||||||
| chr6:18433867 | C | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5817C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433867 | |||||||
| chr6:18433918 | G | A | 42 | a0001c0001t0003g0190 a0001c0001t0007g0263 a0001c0001t0007g0293 others(39): Show |
45 | HG00323.hp1 HG00609.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.271-5766G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433918 | |||||||
| chr6:18433922 | A | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5762A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433922 | |||||||
| chr6:18433969 | C | A | 2 | a0001c0001t0010g0227 a0001c0001t0051g0009 |
3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.271-5715C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433969 | |||||||
| chr6:18433993 | G | A | 20 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(17): Show |
20 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-5691G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18433993 | |||||||
| chr6:18434005 | C | T | 351 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(348): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.271-5679C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434005 | |||||||
| chr6:18434101 | A | T | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5583A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434101 | |||||||
| chr6:18434204 | T | G | 2 | a0001c0001t0034g0269 a0001c0001t0059g0143 |
2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.271-5480T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434204 | |||||||
| chr6:18434224 | G | A | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-5460G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434224 | |||||||
| chr6:18434235 | T | A | 1 | a0001c0001t0015g0139 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.271-5449T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434235 | |||||||
| chr6:18434359 | T | C | 1 | a0001c0001t0026g0279 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.271-5325T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434359 | |||||||
| chr6:18434366 | G | A | 92 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(89): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-5318G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434366 | |||||||
| chr6:18434366 | GA | G | 20 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(17): Show |
20 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-5317delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434366 | |||||||
| chr6:18434445 | G | A | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-5239G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434445 | |||||||
| chr6:18434470 | G | T | 1 | a0001c0001t0008g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.271-5214G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434470 | |||||||
| chr6:18434576 | T | C | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.271-5108T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434576 | |||||||
| chr6:18434621 | T | TTTTG | 5 | a0001c0001t0010g0227 a0001c0001t0011g0318 a0001c0001t0051g0009 others(2): Show |
6 | HG01993.hp1 HG02055.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-5051_271-5048d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18434621 | ||||||
| chr6:18434633 | G | GTTTT | 35 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(32): Show |
37 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.271-5047_271-5044d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18434633 | ||||||
| chr6:18434690 | C | T | 1 | a0001c0001t0003g0203 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.271-4994C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434690 | |||||||
| chr6:18434753 | C | T | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4931C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434753 | |||||||
| chr6:18434807 | G | C | 1 | a0001c0001t0062g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.271-4877G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434807 | |||||||
| chr6:18434903 | A | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4781A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434903 | |||||||
| chr6:18434925 | T | C | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4759T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434925 | |||||||
| chr6:18434982 | A | G | 1 | a0001c0001t0011g0364 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.271-4702A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434982 | |||||||
| chr6:18434998 | A | G | 2 | a0001c0002t0022g0182 a0001c0002t0022g0194 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.271-4686A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18434998 | |||||||
| chr6:18435041 | T | C | 1 | a0001c0001t0062g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.271-4643T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435041 | |||||||
| chr6:18435089 | G | A | 2 | a0001c0001t0020g0001 a0001c0001t0086g0001 |
3 | HG02258.hp1 HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.271-4595G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435089 | |||||||
| chr6:18435096 | T | C | 92 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(89): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-4588T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435096 | |||||||
| chr6:18435136 | A | G | 3 | a0001c0001t0002g0356 a0001c0001t0009g0285 a0001c0001t0019g0149 |
3 | HG02965.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.271-4548A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435136 | |||||||
| chr6:18435304 | G | A | 351 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(348): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.271-4380G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435304 | |||||||
| chr6:18435406 | A | G | 1 | a0001c0001t0006g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.271-4278A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435406 | |||||||
| chr6:18435409 | GAATA | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4270_271-4267d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18435409 | ||||||
| chr6:18435447 | A | C | 2 | a0001c0001t0042g0094 a0001c0001t0052g0152 |
2 | HG01257.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.271-4237A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435447 | |||||||
| chr6:18435483 | AG | A | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-4200delG | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435483 | |||||||
| chr6:18435559 | C | A | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-4125C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435559 | |||||||
| chr6:18435573 | A | C | 10 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(7): Show |
10 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-4111A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435573 | |||||||
| chr6:18435779 | A | C | 1 | a0001c0001t0037g0333 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.271-3905A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435779 | |||||||
| chr6:18435787 | C | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-3897C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435787 | |||||||
| chr6:18435837 | C | A | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-3847C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435837 | |||||||
| chr6:18435885 | G | C | 4 | a0001c0001t0010g0227 a0001c0001t0051g0009 a0001c0001t0058g0226 others(1): Show |
5 | HG02055.hp1 HG02922.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3799G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435885 | |||||||
| chr6:18435888 | G | T | 79 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(76): Show |
82 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.271-3796G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435888 | |||||||
| chr6:18435889 | G | A | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.271-3795G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435889 | |||||||
| chr6:18435892 | G | A | 1 | a0001c0001t0007g0243 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.271-3792G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435892 | |||||||
| chr6:18435957 | G | T | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.271-3727G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18435957 | |||||||
| chr6:18436058 | T | TA | 24 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(21): Show |
25 | HG01261.hp2 HG02004.hp2 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.271-3613dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436058 | ||||||
| chr6:18436058 | TA | T | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.271-3613delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436058 | ||||||
| chr6:18436281 | A | G | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-3403A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436281 | |||||||
| chr6:18436294 | T | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.271-3390T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436294 | |||||||
| chr6:18436312 | C | T | 10 | a0001c0001t0009g0288 a0001c0001t0013g0020 a0001c0001t0013g0086 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-3372C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436312 | |||||||
| chr6:18436318 | C | T | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-3366C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436318 | |||||||
| chr6:18436344 | G | A | 92 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(89): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-3340G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436344 | |||||||
| chr6:18436519 | G | A | 3 | a0001c0001t0002g0014 a0001c0001t0013g0030 a0001c0001t0013g0031 |
4 | HG00408.hp2 NA18986.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3165G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436519 | |||||||
| chr6:18436807 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(92): Show |
98 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.271-2877A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436807 | |||||||
| chr6:18436851 | G | C | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-2833G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18436851 | |||||||
| chr6:18436905 | G | GTT | 20 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(17): Show |
20 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.271-2770_271-2769d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436905 | ||||||
| chr6:18436905 | G | GTTT | 20 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(17): Show |
23 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.271-2771_271-2769d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436905 | ||||||
| chr6:18436905 | GT | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(296): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.271-2769delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 18436905 | ||||||
| chr6:18437167 | A | C | 1 | a0001c0001t0001g0078 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.271-2517A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437167 | |||||||
| chr6:18437245 | C | G | 2 | a0001c0001t0006g0172 a0001c0001t0006g0173 |
2 | HG02071.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.271-2439C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437245 | |||||||
| chr6:18437328 | A | G | 1 | a0001c0001t0006g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.271-2356A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437328 | |||||||
| chr6:18437376 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0013g0030 a0001c0001t0013g0031 |
4 | HG00408.hp2 NA18986.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2308C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437376 | |||||||
| chr6:18437384 | G | A | 22 | a0001c0001t0004g0131 a0001c0001t0004g0338 a0001c0001t0007g0231 others(19): Show |
22 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-2300G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437384 | |||||||
| chr6:18437391 | T | C | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-2293T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437391 | |||||||
| chr6:18437534 | A | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(68): Show |
74 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.271-2150A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437534 | |||||||
| chr6:18437576 | G | A | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-2108G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437576 | |||||||
| chr6:18437603 | T | C | 22 | a0001c0001t0004g0131 a0001c0001t0004g0338 a0001c0001t0007g0231 others(19): Show |
22 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.271-2081T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437603 | |||||||
| chr6:18437614 | C | T | 1 | a0001c0001t0023g0065 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.271-2070C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437614 | |||||||
| chr6:18437615 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.271-2069G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437615 | |||||||
| chr6:18437717 | A | G | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1967A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437717 | |||||||
| chr6:18437789 | C | A | 7 | a0001c0001t0038g0102 a0001c0001t0038g0105 a0001c0001t0038g0144 others(4): Show |
7 | HG01515.hp2 HG02897.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-1895C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437789 | |||||||
| chr6:18437801 | A | G | 1 | a0001c0001t0081g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.271-1883A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437801 | |||||||
| chr6:18437835 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1849C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437835 | |||||||
| chr6:18437843 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1841T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18437843 | |||||||
| chr6:18438047 | G | T | 1 | a0001c0001t0016g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.271-1637G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438047 | |||||||
| chr6:18438061 | A | T | 2 | a0001c0001t0012g0017 a0001c0001t0012g0018 |
2 | NA18969.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.271-1623A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438061 | |||||||
| chr6:18438094 | G | A | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1590G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438094 | |||||||
| chr6:18438256 | G | A | 92 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(89): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-1428G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438256 | |||||||
| chr6:18438274 | C | T | 4 | a0001c0001t0091g0214 a0001c0001t0092g0181 a0001c0001t0093g0180 others(1): Show |
4 | HG02965.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-1410C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438274 | |||||||
| chr6:18438361 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1323C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438361 | |||||||
| chr6:18438367 | A | G | 118 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(115): Show |
123 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.271-1317A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438367 | |||||||
| chr6:18438453 | A | G | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271-1231A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438453 | |||||||
| chr6:18438497 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1187C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438497 | |||||||
| chr6:18438601 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-1083G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438601 | |||||||
| chr6:18438645 | T | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(71): Show |
77 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.271-1039T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438645 | |||||||
| chr6:18438731 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.271-953G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438731 | |||||||
| chr6:18438796 | T | C | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.271-888T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438796 | |||||||
| chr6:18438876 | T | G | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.271-808T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18438876 | |||||||
| chr6:18439308 | T | G | 40 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0010g0227 others(37): Show |
43 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.271-376T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439308 | |||||||
| chr6:18439327 | A | G | 88 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(85): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.271-357A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439327 | |||||||
| chr6:18439404 | G | C | 1 | a0001c0001t0014g0310 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.271-280G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439404 | |||||||
| chr6:18439443 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.271-241T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439443 | |||||||
| chr6:18439508 | T | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.271-176T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439508 | |||||||
| chr6:18439580 | G | T | 1 | a0001c0001t0100g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.271-104G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 3/7 | chr6 | 18439580 | |||||||
| chr6:18439788 | A | G | 2 | a0001c0001t0010g0227 a0001c0001t0051g0009 |
3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331+44A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18439788 | |||||||
| chr6:18439802 | C | T | 5 | a0001c0001t0002g0334 a0001c0001t0009g0011 a0001c0001t0009g0229 others(2): Show |
6 | NA18939.hp2 NA18941.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+58C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18439802 | |||||||
| chr6:18439982 | T | C | 65 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(62): Show |
68 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.331+238T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18439982 | |||||||
| chr6:18440016 | A | G | 19 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(16): Show |
21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.331+272A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440016 | |||||||
| chr6:18440069 | A | G | 13 | a0001c0001t0020g0001 a0001c0001t0020g0117 a0001c0001t0020g0124 others(10): Show |
14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+325A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440069 | |||||||
| chr6:18440081 | C | T | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+337C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440081 | |||||||
| chr6:18440162 | A | G | 1 | a0001c0001t0041g0035 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.331+418A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440162 | |||||||
| chr6:18440269 | C | CTT | 64 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(61): Show |
67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+525_331+526ins others(2): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440269 | |||||||
| chr6:18440377 | G | C | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+633G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440377 | |||||||
| chr6:18440409 | A | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.331+665A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440409 | |||||||
| chr6:18440436 | G | C | 64 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(61): Show |
67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+692G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440436 | |||||||
| chr6:18440525 | A | G | 1 | a0001c0001t0006g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.331+781A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440525 | |||||||
| chr6:18440663 | GA | G | 64 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(61): Show |
67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+927delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440663 | ||||||
| chr6:18440672 | C | T | 1 | a0001c0001t0041g0035 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.331+928C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440672 | |||||||
| chr6:18440680 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(91): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.331+936G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440680 | |||||||
| chr6:18440710 | T | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(91): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.331+966T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440710 | |||||||
| chr6:18440723 | G | GGTT | 350 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(347): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.331+980_331+982dup others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440723 | ||||||
| chr6:18440729 | T | C | 1 | a0001c0001t0015g0329 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.331+985T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440729 | |||||||
| chr6:18440795 | G | GT | 189 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(186): Show |
196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.331+1065dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440795 | ||||||
| chr6:18440810 | A | T | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(155): Show |
164 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.331+1066A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440810 | |||||||
| chr6:18440811 | A | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(131): Show |
140 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.331+1067A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440811 | |||||||
| chr6:18440836 | T | C | 65 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(62): Show |
68 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.331+1092T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440836 | |||||||
| chr6:18440891 | C | CA | 7 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(4): Show |
7 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.331+1158dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440891 | ||||||
| chr6:18440891 | C | CAA | 44 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(41): Show |
46 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(43): Show |
intron_variant | MODIFIER | c.331+1157_331+1158d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440891 | ||||||
| chr6:18440891 | C | CAAA | 64 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(61): Show |
67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+1156_331+1158d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18440891 | ||||||
| chr6:18440980 | T | G | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+1236T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18440980 | |||||||
| chr6:18441101 | T | C | 37 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(34): Show |
39 | HG00323.hp1 HG00741.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.331+1357T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441101 | |||||||
| chr6:18441105 | T | C | 56 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(53): Show |
59 | HG00408.hp2 HG00423.hp2 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.331+1361T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441105 | |||||||
| chr6:18441214 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+1470C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441214 | |||||||
| chr6:18441296 | T | C | 2 | a0001c0001t0015g0339 a0001c0001t0015g0340 |
2 | HG00621.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.331+1552T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441296 | |||||||
| chr6:18441331 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+1587T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441331 | |||||||
| chr6:18441377 | A | G | 64 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(61): Show |
67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+1633A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441377 | |||||||
| chr6:18441393 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(128): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.331+1649G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441393 | |||||||
| chr6:18441575 | CT | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+1837delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18441575 | ||||||
| chr6:18441696 | T | C | 1 | a0001c0001t0003g0167 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.331+1952T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441696 | |||||||
| chr6:18441723 | G | T | 1 | a0001c0001t0049g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.331+1979G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441723 | |||||||
| chr6:18441752 | G | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2008G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441752 | |||||||
| chr6:18441825 | G | A | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331+2081G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18441825 | |||||||
| chr6:18442086 | G | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2342G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442086 | |||||||
| chr6:18442248 | G | C | 1 | a0001c0001t0077g0299 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.331+2504G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442248 | |||||||
| chr6:18442259 | A | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2515A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442259 | |||||||
| chr6:18442325 | G | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2581G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442325 | |||||||
| chr6:18442366 | G | A | 1 | a0001c0001t0005g0358 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.331+2622G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442366 | |||||||
| chr6:18442385 | C | T | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331+2641C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442385 | |||||||
| chr6:18442541 | T | G | 2 | a0001c0001t0050g0162 a0001c0001t0088g0115 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.331+2797T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442541 | |||||||
| chr6:18442554 | A | G | 1 | a0001c0001t0062g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.331+2810A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442554 | |||||||
| chr6:18442573 | C | T | 3 | a0001c0001t0010g0241 a0001c0001t0076g0363 a0001c0001t0105g0067 |
3 | HG00280.hp2 HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.331+2829C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442573 | |||||||
| chr6:18442617 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.331+2873C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442617 | |||||||
| chr6:18442723 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+2979C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442723 | |||||||
| chr6:18442728 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.331+2984A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442728 | |||||||
| chr6:18442805 | G | C | 3 | a0001c0001t0016g0080 a0001c0001t0043g0141 a0001c0001t0043g0142 |
3 | HG01109.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.331+3061G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442805 | |||||||
| chr6:18442969 | T | C | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+3225T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442969 | |||||||
| chr6:18442988 | G | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3244G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18442988 | |||||||
| chr6:18443027 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3283T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443027 | |||||||
| chr6:18443160 | T | C | 1 | a0001c0001t0031g0161 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.331+3416T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443160 | |||||||
| chr6:18443169 | G | A | 1 | a0001c0001t0006g0155 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.331+3425G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443169 | |||||||
| chr6:18443290 | T | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3546T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443290 | |||||||
| chr6:18443316 | G | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3572G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443316 | |||||||
| chr6:18443326 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.331+3582G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443326 | |||||||
| chr6:18443459 | A | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3715A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443459 | |||||||
| chr6:18443593 | G | A | 3 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 |
3 | HG02109.hp1 HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.331+3849G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443593 | |||||||
| chr6:18443615 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3871G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443615 | |||||||
| chr6:18443705 | A | G | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.331+3961A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443705 | |||||||
| chr6:18443706 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3962C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443706 | |||||||
| chr6:18443729 | C | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+3985C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443729 | |||||||
| chr6:18443828 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.331+4084T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443828 | |||||||
| chr6:18443942 | A | G | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+4198A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18443942 | |||||||
| chr6:18444045 | T | C | 11 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(8): Show |
11 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.331+4301T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444045 | |||||||
| chr6:18444151 | C | T | 1 | a0001c0001t0031g0211 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.331+4407C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444151 | |||||||
| chr6:18444157 | A | T | 2 | a0001c0001t0018g0268 a0001c0001t0018g0280 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.331+4413A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444157 | |||||||
| chr6:18444158 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+4414T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444158 | |||||||
| chr6:18444201 | G | A | 12 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(9): Show |
13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.331+4457G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444201 | |||||||
| chr6:18444244 | G | A | 64 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(61): Show |
67 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.331+4500G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444244 | |||||||
| chr6:18444389 | C | T | 1 | a0001c0001t0019g0006 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.331+4645C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444389 | |||||||
| chr6:18444468 | T | TG | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.331+4724_331+4725i others(3): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444468 | |||||||
| chr6:18444673 | T | TA | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+4937dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18444673 | ||||||
| chr6:18444703 | CT | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+4963delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18444703 | ||||||
| chr6:18444719 | A | C | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+4975A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444719 | |||||||
| chr6:18444790 | C | A | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+5046C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444790 | |||||||
| chr6:18444803 | T | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5059T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444803 | |||||||
| chr6:18444846 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5102C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444846 | |||||||
| chr6:18444877 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5133C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444877 | |||||||
| chr6:18444953 | A | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5209A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444953 | |||||||
| chr6:18444997 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5253C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18444997 | |||||||
| chr6:18445016 | CTTTTAGT others(5): Show |
C | 1 | a0001c0001t0002g0320 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.331+5276_331+5287d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445016 | ||||||
| chr6:18445024 | G | GT | 39 | a0001c0001t0004g0338 a0001c0001t0007g0263 a0001c0001t0007g0293 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.331+5287dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445024 | ||||||
| chr6:18445084 | A | AT | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5347dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445084 | ||||||
| chr6:18445119 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.331+5375T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445119 | |||||||
| chr6:18445189 | C | T | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+5445C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445189 | |||||||
| chr6:18445274 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5530G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445274 | |||||||
| chr6:18445308 | T | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5564T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445308 | |||||||
| chr6:18445351 | G | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(141): Show |
149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.331+5607G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445351 | |||||||
| chr6:18445519 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.331+5775C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445519 | |||||||
| chr6:18445563 | A | G | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.331+5819A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445563 | |||||||
| chr6:18445608 | T | A | 1 | a0001c0001t0035g0267 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.331+5864T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445608 | |||||||
| chr6:18445661 | A | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5917A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445661 | |||||||
| chr6:18445688 | G | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(141): Show |
149 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.331+5944G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445688 | |||||||
| chr6:18445727 | C | T | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+5983C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445727 | |||||||
| chr6:18445743 | A | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+5999A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445743 | |||||||
| chr6:18445816 | T | G | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.331+6072T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445816 | |||||||
| chr6:18445839 | C | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6095C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445839 | |||||||
| chr6:18445863 | G | T | 12 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(9): Show |
13 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.331+6119G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445863 | |||||||
| chr6:18445936 | A | G | 1 | a0001c0001t0013g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.331+6192A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18445936 | |||||||
| chr6:18445982 | GCACTC | G | 2 | a0001c0001t0010g0227 a0001c0001t0051g0009 |
3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.331+6243_331+6247d others(7): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18445982 | ||||||
| chr6:18446020 | T | C | 90 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(87): Show |
95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.331+6276T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446020 | |||||||
| chr6:18446029 | A | C | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.331+6285A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446029 | |||||||
| chr6:18446113 | G | C | 1 | a0001c0001t0002g0315 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.331+6369G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446113 | |||||||
| chr6:18446145 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6401G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446145 | |||||||
| chr6:18446207 | A | C | 359 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(356): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.331+6463A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446207 | |||||||
| chr6:18446253 | T | C | 19 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(16): Show |
21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.331+6509T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446253 | |||||||
| chr6:18446277 | T | TA | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6539dupA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446277 | ||||||
| chr6:18446359 | T | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.331+6615T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446359 | |||||||
| chr6:18446516 | G | A | 80 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(77): Show |
83 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.331+6772G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446516 | |||||||
| chr6:18446530 | A | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+6786A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446530 | |||||||
| chr6:18446567 | TACTATGG others(25): Show |
T | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331+6824_331+6855d others(34): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446567 | |||||||
| chr6:18446619 | C | T | 1 | a0001c0001t0008g0039 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.331+6875C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446619 | |||||||
| chr6:18446637 | A | G | 2 | a0001c0001t0041g0037 a0001c0001t0104g0028 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.331+6893A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446637 | |||||||
| chr6:18446735 | G | A | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+6991G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446735 | |||||||
| chr6:18446739 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(105): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.331+6995C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446739 | |||||||
| chr6:18446746 | G | T | 5 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(2): Show |
5 | HG01261.hp2 HG02004.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+7002G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446746 | |||||||
| chr6:18446840 | G | GGT | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(85): Show |
94 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.331+7129_331+7130d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | G | GGTGT | 20 | a0001c0001t0002g0298 a0001c0001t0002g0320 a0001c0001t0002g0323 others(17): Show |
20 | HG00140.hp1 HG00423.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.331+7127_331+7130d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | G | GGTGTGT | 11 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0063 others(8): Show |
11 | HG01884.hp1 HG02040.hp1 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+7125_331+7130d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | G | GGTGTGTG others(9): Show |
2 | a0001c0001t0033g0281 a0001c0001t0033g0284 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.331+7115_331+7130d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | G | GGTGTGTG others(11): Show |
1 | a0001c0001t0033g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.331+7113_331+7130d others(20): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | GGTGT | G | 9 | a0001c0001t0002g0303 a0001c0001t0002g0308 a0001c0001t0002g0348 others(6): Show |
9 | HG01361.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.331+7127_331+7130d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | GGTGTGT | G | 14 | a0001c0001t0002g0347 a0001c0001t0020g0001 a0001c0001t0020g0117 others(11): Show |
15 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.331+7125_331+7130d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | GGTGTGTG others(3): Show |
G | 115 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(112): Show |
120 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.331+7121_331+7130d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446840 | GGTGTGTG others(5): Show |
G | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.331+7119_331+7130d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18446840 | ||||||
| chr6:18446865 | G | C | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.331+7121G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18446865 | |||||||
| chr6:18447379 | T | C | 353 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(350): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.331+7635T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447379 | |||||||
| chr6:18447473 | G | A | 5 | a0001c0001t0002g0303 a0001c0001t0002g0308 a0001c0001t0002g0347 others(2): Show |
5 | NA18940.hp2 NA18965.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+7729G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447473 | |||||||
| chr6:18447521 | G | A | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.331+7777G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447521 | |||||||
| chr6:18447624 | G | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.331+7880G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447624 | |||||||
| chr6:18447794 | G | A | 1 | a0001c0001t0015g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.331+8050G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447794 | |||||||
| chr6:18447853 | T | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+8109T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447853 | |||||||
| chr6:18447890 | A | G | 1 | a0001c0001t0002g0334 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.331+8146A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18447890 | |||||||
| chr6:18448218 | G | A | 13 | a0001c0001t0020g0001 a0001c0001t0020g0117 a0001c0001t0020g0124 others(10): Show |
14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+8474G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448218 | |||||||
| chr6:18448290 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.331+8546T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448290 | |||||||
| chr6:18448317 | C | T | 1 | a0001c0001t0013g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331+8573C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448317 | |||||||
| chr6:18448345 | G | T | 5 | a0001c0001t0009g0288 a0001c0001t0013g0020 a0001c0001t0013g0086 others(2): Show |
5 | HG02280.hp2 HG03209.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+8601G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448345 | |||||||
| chr6:18448598 | T | C | 37 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(34): Show |
39 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.332-8557T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448598 | |||||||
| chr6:18448672 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-8483T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448672 | |||||||
| chr6:18448680 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.332-8475G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448680 | |||||||
| chr6:18448688 | G | GCA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(94): Show |
101 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.332-8439_332-8438d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448688 | G | GCACA | 21 | a0001c0001t0001g0042 a0001c0001t0009g0011 a0001c0001t0009g0229 others(18): Show |
22 | HG00140.hp1 HG00621.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.332-8441_332-8438d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448688 | G | GCACACA | 48 | a0001c0001t0001g0064 a0001c0001t0002g0134 a0001c0001t0002g0297 others(45): Show |
49 | HG00423.hp2 HG01123.hp1 HG01243.hp2 others(46): Show |
intron_variant | MODIFIER | c.332-8443_332-8438d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448688 | G | GCACACAC others(1): Show |
9 | a0001c0001t0002g0014 a0001c0001t0002g0303 a0001c0001t0002g0342 others(6): Show |
10 | HG00408.hp2 HG02809.hp2 HG03225.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-8445_332-8438d others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448688 | G | GCACACAC others(3): Show |
2 | a0001c0001t0010g0227 a0001c0001t0051g0009 |
3 | HG02922.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.332-8447_332-8438d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448688 | G | GCACACAC others(5): Show |
1 | a0001c0001t0013g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-8449_332-8438d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448688 | GCA | G | 5 | a0001c0001t0031g0211 a0001c0001t0049g0120 a0001c0001t0049g0145 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-8439_332-8438d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448688 | GCACACA | G | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.332-8443_332-8438d others(8): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448688 | ||||||
| chr6:18448716 | A | ACACACAC others(1): Show |
11 | a0001c0001t0010g0010 a0001c0001t0010g0234 a0001c0001t0010g0235 others(8): Show |
12 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.332-8438_332-8437i others(10): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18448716 | ||||||
| chr6:18448718 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0072g0272 |
2 | NA19083.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.332-8437C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448718 | |||||||
| chr6:18448785 | C | T | 1 | a0001c0001t0095g0224 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.332-8370C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448785 | |||||||
| chr6:18448795 | T | C | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-8360T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448795 | |||||||
| chr6:18448910 | C | T | 1 | a0001c0001t0014g0349 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.332-8245C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18448910 | |||||||
| chr6:18449025 | T | A | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-8130T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449025 | |||||||
| chr6:18449269 | T | C | 1 | a0001c0001t0037g0328 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.332-7886T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449269 | |||||||
| chr6:18449376 | G | A | 1 | a0001c0001t0002g0323 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.332-7779G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449376 | |||||||
| chr6:18449592 | T | A | 2 | a0001c0001t0027g0130 a0001c0001t0048g0107 |
2 | HG02683.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.332-7563T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449592 | |||||||
| chr6:18449653 | A | C | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-7502A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449653 | |||||||
| chr6:18449697 | G | GTA | 85 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(82): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.332-7443_332-7442d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | ||||||
| chr6:18449697 | G | GTATATAT others(3): Show |
17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.332-7451_332-7442d others(12): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | ||||||
| chr6:18449697 | G | GTATATAT others(5): Show |
2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-7453_332-7442d others(14): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | ||||||
| chr6:18449697 | G | GTATATAT others(7): Show |
17 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(14): Show |
19 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.332-7455_332-7442d others(16): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | ||||||
| chr6:18449697 | G | GTATATAT others(9): Show |
2 | a0001c0001t0025g0273 a0001c0001t0025g0277 |
2 | NA18945.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.332-7457_332-7442d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18449697 | ||||||
| chr6:18449745 | G | A | 1 | a0001c0001t0010g0235 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.332-7410G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449745 | |||||||
| chr6:18449750 | C | T | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-7405C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449750 | |||||||
| chr6:18449877 | G | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-7278G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449877 | |||||||
| chr6:18449968 | A | C | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.332-7187A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449968 | |||||||
| chr6:18449968 | A | T | 2 | a0001c0001t0043g0141 a0001c0001t0043g0142 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.332-7187A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449968 | |||||||
| chr6:18449986 | G | A | 1 | a0001c0001t0016g0070 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.332-7169G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449986 | |||||||
| chr6:18449990 | T | C | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-7165T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18449990 | |||||||
| chr6:18450039 | A | G | 1 | a0001c0001t0009g0249 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.332-7116A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450039 | |||||||
| chr6:18450057 | T | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-7098T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450057 | |||||||
| chr6:18450078 | G | A | 3 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 |
3 | HG02109.hp1 HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.332-7077G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450078 | |||||||
| chr6:18450255 | C | G | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-6900C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450255 | |||||||
| chr6:18450304 | G | C | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-6851G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450304 | |||||||
| chr6:18450304 | G | GT | 26 | a0001c0001t0002g0297 a0001c0001t0002g0306 a0001c0001t0002g0313 others(23): Show |
26 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.332-6839dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18450304 | ||||||
| chr6:18450304 | G | GTT | 19 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(16): Show |
21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.332-6840_332-6839d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18450304 | ||||||
| chr6:18450376 | C | T | 20 | a0001c0001t0007g0231 a0001c0001t0007g0232 a0001c0001t0007g0233 others(17): Show |
20 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.332-6779C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450376 | |||||||
| chr6:18450383 | C | T | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-6772C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450383 | |||||||
| chr6:18450440 | C | T | 1 | a0001c0001t0040g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.332-6715C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450440 | |||||||
| chr6:18450450 | A | G | 4 | a0001c0001t0015g0329 a0001c0001t0015g0339 a0001c0001t0015g0340 others(1): Show |
4 | HG00621.hp2 HG02523.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-6705A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450450 | |||||||
| chr6:18450550 | C | T | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.332-6605C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450550 | |||||||
| chr6:18450689 | A | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-6466A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450689 | |||||||
| chr6:18450720 | A | G | 1 | a0002c0004t0078g0311 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.332-6435A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450720 | |||||||
| chr6:18450829 | C | T | 36 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(33): Show |
38 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.332-6326C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450829 | |||||||
| chr6:18450897 | A | T | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-6258A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18450897 | |||||||
| chr6:18451022 | A | G | 13 | a0001c0001t0020g0001 a0001c0001t0020g0117 a0001c0001t0020g0124 others(10): Show |
14 | HG01109.hp2 HG01496.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-6133A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451022 | |||||||
| chr6:18451266 | G | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.332-5889G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451266 | |||||||
| chr6:18451326 | T | A | 1 | a0001c0001t0006g0219 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.332-5829T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451326 | |||||||
| chr6:18451501 | T | C | 13 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(10): Show |
13 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-5654T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451501 | |||||||
| chr6:18451519 | G | T | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-5636G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451519 | |||||||
| chr6:18451554 | A | C | 1 | a0001c0001t0003g0190 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.332-5601A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451554 | |||||||
| chr6:18451732 | C | T | 1 | a0001c0001t0002g0342 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.332-5423C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451732 | |||||||
| chr6:18451760 | T | G | 1 | a0001c0001t0002g0348 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.332-5395T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451760 | |||||||
| chr6:18451771 | A | T | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.332-5384A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451771 | |||||||
| chr6:18451888 | G | A | 1 | a0001c0001t0047g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.332-5267G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18451888 | |||||||
| chr6:18452004 | A | C | 2 | a0001c0001t0027g0300 a0001c0001t0027g0357 |
2 | HG01243.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.332-5151A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452004 | |||||||
| chr6:18452023 | T | G | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-5132T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452023 | |||||||
| chr6:18452135 | A | C | 1 | a0001c0001t0003g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.332-5020A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452135 | |||||||
| chr6:18452380 | T | C | 1 | a0001c0001t0081g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.332-4775T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452380 | |||||||
| chr6:18452387 | C | T | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-4768C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452387 | |||||||
| chr6:18452423 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-4732G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452423 | |||||||
| chr6:18452504 | G | A | 1 | a0001c0001t0048g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.332-4651G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452504 | |||||||
| chr6:18452650 | A | T | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-4505A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452650 | |||||||
| chr6:18452659 | T | A | 1 | a0001c0001t0013g0040 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.332-4496T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452659 | |||||||
| chr6:18452739 | TA | T | 5 | a0001c0001t0002g0303 a0001c0001t0002g0308 a0001c0001t0002g0347 others(2): Show |
5 | NA18940.hp2 NA18965.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-4414delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18452739 | ||||||
| chr6:18452952 | T | A | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-4203T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18452952 | |||||||
| chr6:18453029 | G | T | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-4126G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453029 | |||||||
| chr6:18453124 | CTCTT | C | 19 | a0001c0001t0011g0002 a0001c0001t0011g0314 a0001c0001t0011g0318 others(16): Show |
21 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.332-4027_332-4024d others(6): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453124 | ||||||
| chr6:18453137 | C | CT | 67 | a0001c0001t0002g0324 a0001c0001t0006g0189 a0001c0001t0007g0263 others(64): Show |
70 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.332-3999dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | ||||||
| chr6:18453137 | C | CTT | 62 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(59): Show |
65 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.332-4000_332-3999d others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | ||||||
| chr6:18453137 | C | CTTT | 15 | a0001c0001t0003g0184 a0001c0001t0005g0301 a0001c0001t0005g0305 others(12): Show |
15 | HG00438.hp1 HG01255.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-4001_332-3999d others(5): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | ||||||
| chr6:18453137 | CT | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(88): Show |
94 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.332-3999delT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | ||||||
| chr6:18453137 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0041g0037 a0001c0001t0104g0028 |
2 | HG02630.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.332-4009_332-3999d others(13): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18453137 | ||||||
| chr6:18453359 | G | A | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-3796G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453359 | |||||||
| chr6:18453385 | G | A | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-3770G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453385 | |||||||
| chr6:18453386 | C | T | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-3769C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453386 | |||||||
| chr6:18453422 | G | A | 1 | a0001c0001t0017g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.332-3733G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453422 | |||||||
| chr6:18453430 | A | C | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-3725A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453430 | |||||||
| chr6:18453538 | C | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.332-3617C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453538 | |||||||
| chr6:18453588 | T | C | 1 | a0001c0001t0062g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.332-3567T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453588 | |||||||
| chr6:18453658 | G | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.332-3497G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453658 | |||||||
| chr6:18453669 | G | A | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.332-3486G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453669 | |||||||
| chr6:18453790 | G | A | 1 | a0001c0001t0033g0283 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.332-3365G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453790 | |||||||
| chr6:18453851 | T | A | 1 | a0001c0001t0085g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.332-3304T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453851 | |||||||
| chr6:18453932 | A | G | 17 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0012g0186 others(14): Show |
17 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.332-3223A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18453932 | |||||||
| chr6:18454060 | C | G | 2 | a0001c0001t0006g0157 a0001c0001t0018g0266 |
2 | HG03491.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.332-3095C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454060 | |||||||
| chr6:18454096 | T | G | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-3059T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454096 | |||||||
| chr6:18454179 | T | C | 1 | a0001c0001t0008g0032 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.332-2976T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454179 | |||||||
| chr6:18454264 | T | C | 1 | a0001c0001t0004g0360 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.332-2891T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454264 | |||||||
| chr6:18454294 | G | T | 1 | a0001c0001t0004g0326 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.332-2861G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454294 | |||||||
| chr6:18454354 | A | G | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-2801A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454354 | |||||||
| chr6:18454574 | A | T | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-2581A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454574 | |||||||
| chr6:18454612 | T | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(262): Show |
275 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.332-2543T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454612 | |||||||
| chr6:18454640 | T | C | 1 | a0001c0001t0004g0131 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.332-2515T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454640 | |||||||
| chr6:18454654 | G | A | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.332-2501G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454654 | |||||||
| chr6:18454660 | T | TGCCATAG others(9): Show |
1 | a0001c0001t0013g0087 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-2478_332-2463d others(18): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18454660 | ||||||
| chr6:18454738 | T | G | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-2417T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454738 | |||||||
| chr6:18454814 | G | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-2341G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18454814 | |||||||
| chr6:18455093 | A | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(142): Show |
150 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.332-2062A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455093 | |||||||
| chr6:18455316 | A | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(90): Show |
96 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.332-1839A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455316 | |||||||
| chr6:18455342 | T | A | 2 | a0001c0001t0092g0181 a0001c0001t0093g0180 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.332-1813T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455342 | |||||||
| chr6:18455383 | G | C | 80 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(77): Show |
83 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.332-1772G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455383 | |||||||
| chr6:18455404 | G | A | 1 | a0001c0001t0013g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.332-1751G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455404 | |||||||
| chr6:18455610 | C | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-1545C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455610 | |||||||
| chr6:18455683 | G | C | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-1472G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455683 | |||||||
| chr6:18455710 | G | A | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-1445G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455710 | |||||||
| chr6:18455730 | G | C | 1 | a0001c0001t0010g0241 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.332-1425G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455730 | |||||||
| chr6:18455750 | CA | C | 9 | a0001c0001t0003g0008 a0001c0001t0003g0164 a0001c0001t0003g0184 others(6): Show |
10 | HG00558.hp2 NA18942.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-1402delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 18455750 | ||||||
| chr6:18455771 | G | T | 1 | a0001c0001t0045g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.332-1384G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455771 | |||||||
| chr6:18455814 | A | C | 9 | a0001c0001t0003g0008 a0001c0001t0003g0164 a0001c0001t0003g0184 others(6): Show |
10 | HG00558.hp2 NA18942.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-1341A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18455814 | |||||||
| chr6:18456124 | C | G | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.332-1031C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456124 | |||||||
| chr6:18456164 | C | T | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.332-991C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456164 | |||||||
| chr6:18456190 | G | A | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-965G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456190 | |||||||
| chr6:18456390 | A | G | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-765A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456390 | |||||||
| chr6:18456587 | C | T | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.332-568C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456587 | |||||||
| chr6:18456610 | A | T | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.332-545A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456610 | |||||||
| chr6:18456732 | G | C | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.332-423G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456732 | |||||||
| chr6:18456779 | G | A | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.332-376G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456779 | |||||||
| chr6:18456839 | G | A | 2 | a0001c0001t0034g0269 a0001c0001t0059g0143 |
2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.332-316G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456839 | |||||||
| chr6:18456890 | T | C | 39 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(36): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.332-265T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456890 | |||||||
| chr6:18456996 | G | A | 13 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(10): Show |
13 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-159G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18456996 | |||||||
| chr6:18457022 | C | T | 1 | a0001c0001t0101g0024 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.332-133C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18457022 | |||||||
| chr6:18457024 | G | C | 2 | a0001c0001t0039g0147 a0001c0001t0039g0150 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.332-131G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 4/7 | chr6 | 18457024 | |||||||
| chr6:18457463 | G | A | 1 | a0001c0001t0030g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.536+104G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457463 | |||||||
| chr6:18457543 | C | A | 38 | a0001c0001t0007g0263 a0001c0001t0007g0293 a0001c0001t0011g0002 others(35): Show |
40 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.536+184C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457543 | |||||||
| chr6:18457560 | A | T | 1 | a0001c0001t0008g0041 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.536+201A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457560 | |||||||
| chr6:18457587 | G | A | 1 | a0001c0001t0034g0230 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.536+228G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457587 | |||||||
| chr6:18457606 | G | T | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.536+247G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457606 | |||||||
| chr6:18457660 | C | A | 353 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(350): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.536+301C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457660 | |||||||
| chr6:18457801 | A | G | 1 | a0001c0001t0096g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.536+442A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457801 | |||||||
| chr6:18457896 | A | G | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.536+537A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457896 | |||||||
| chr6:18457930 | G | GT | 17 | a0001c0001t0005g0351 a0001c0001t0007g0239 a0001c0001t0008g0036 others(14): Show |
17 | HG01243.hp1 HG01515.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.536+580dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 18457930 | ||||||
| chr6:18457935 | T | G | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.536+576T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457935 | |||||||
| chr6:18457940 | G | T | 1 | a0001c0001t0103g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.536+581G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18457940 | |||||||
| chr6:18458014 | T | A | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.536+655T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458014 | |||||||
| chr6:18458030 | T | C | 182 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(179): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.536+671T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458030 | |||||||
| chr6:18458063 | G | A | 1 | a0001c0001t0008g0032 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.536+704G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458063 | |||||||
| chr6:18458125 | A | T | 1 | a0001c0001t0023g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.536+766A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458125 | |||||||
| chr6:18458263 | G | A | 2 | a0001c0001t0003g0008 a0001c0001t0003g0164 |
3 | HG00558.hp2 NA19004.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.536+904G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458263 | |||||||
| chr6:18458305 | T | C | 14 | a0001c0001t0014g0136 a0001c0001t0014g0350 a0001c0001t0026g0259 others(11): Show |
14 | HG00140.hp1 HG01358.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.536+946T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458305 | |||||||
| chr6:18458356 | T | C | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.536+997T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458356 | |||||||
| chr6:18458406 | C | T | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.536+1047C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458406 | |||||||
| chr6:18458446 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.536+1087T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458446 | |||||||
| chr6:18458530 | C | G | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(106): Show |
112 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.537-1077C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458530 | |||||||
| chr6:18458541 | A | G | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-1066A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458541 | |||||||
| chr6:18458567 | C | T | 12 | a0001c0001t0003g0165 a0001c0001t0003g0167 a0001c0001t0003g0203 others(9): Show |
12 | HG00621.hp1 HG02040.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.537-1040C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458567 | |||||||
| chr6:18458980 | A | C | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-627A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18458980 | |||||||
| chr6:18459029 | C | G | 10 | a0001c0001t0009g0288 a0001c0001t0013g0020 a0001c0001t0013g0086 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.537-578C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459029 | |||||||
| chr6:18459088 | T | TCACCTAT others(10): Show |
3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-516_537-515ins others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 18459088 | ||||||
| chr6:18459093 | C | G | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.537-514C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459093 | |||||||
| chr6:18459168 | G | A | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.537-439G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459168 | |||||||
| chr6:18459191 | A | G | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.537-416A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459191 | |||||||
| chr6:18459250 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-357G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459250 | |||||||
| chr6:18459255 | A | T | 1 | a0001c0001t0012g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.537-352A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459255 | |||||||
| chr6:18459269 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.537-338G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459269 | |||||||
| chr6:18459395 | G | GTAAT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.537-209_537-206dup others(4): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr6 | 18459395 | ||||||
| chr6:18459449 | G | A | 1 | a0001c0001t0065g0286 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.537-158G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459449 | |||||||
| chr6:18459505 | A | C | 89 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(86): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.537-102A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 5/7 | chr6 | 18459505 | |||||||
| chr6:18459972 | T | A | 93 | a0001c0001t0003g0008 a0001c0001t0003g0153 a0001c0001t0003g0164 others(90): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.681+221T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18459972 | |||||||
| chr6:18460088 | C | A | 1 | a0001c0001t0047g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.681+337C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460088 | |||||||
| chr6:18460096 | T | C | 1 | a0001c0001t0003g0216 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.681+345T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460096 | |||||||
| chr6:18460257 | A | G | 1 | a0001c0001t0058g0226 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.681+506A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460257 | |||||||
| chr6:18460346 | G | A | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+595G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460346 | |||||||
| chr6:18460365 | A | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(91): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.681+614A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460365 | |||||||
| chr6:18460505 | A | T | 6 | a0001c0001t0007g0231 a0001c0001t0007g0243 a0001c0001t0007g0244 others(3): Show |
6 | HG00639.hp1 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+754A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460505 | |||||||
| chr6:18460581 | C | T | 1 | a0001c0001t0057g0228 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.681+830C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460581 | |||||||
| chr6:18460588 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.681+837C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460588 | |||||||
| chr6:18460611 | T | C | 1 | a0001c0001t0016g0091 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.681+860T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460611 | |||||||
| chr6:18460614 | A | G | 353 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(350): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.681+863A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460614 | |||||||
| chr6:18460753 | T | C | 353 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(350): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.681+1002T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460753 | |||||||
| chr6:18460800 | TA | T | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+1054delA | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18460800 | ||||||
| chr6:18460865 | G | T | 1 | a0001c0001t0037g0333 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.681+1114G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460865 | |||||||
| chr6:18460890 | A | T | 5 | a0001c0001t0016g0052 a0001c0001t0016g0053 a0001c0001t0016g0055 others(2): Show |
5 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+1139A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460890 | |||||||
| chr6:18460927 | A | C | 13 | a0001c0001t0033g0281 a0001c0001t0033g0283 a0001c0001t0033g0284 others(10): Show |
13 | HG01515.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.681+1176A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18460927 | |||||||
| chr6:18461113 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.681+1362T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461113 | |||||||
| chr6:18461233 | G | T | 2 | a0001c0001t0066g0282 a0001c0001t0083g0127 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.681+1482G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461233 | |||||||
| chr6:18461236 | C | T | 2 | a0001c0001t0015g0129 a0001c0001t0015g0138 |
2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.681+1485C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461236 | |||||||
| chr6:18461302 | A | G | 2 | a0001c0001t0053g0204 a0001c0001t0053g0205 |
2 | HG00423.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.681+1551A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461302 | |||||||
| chr6:18461590 | C | T | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.682-1701C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461590 | |||||||
| chr6:18461622 | G | T | 1 | a0001c0001t0015g0367 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.682-1669G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461622 | |||||||
| chr6:18461761 | G | A | 2 | a0001c0001t0058g0226 a0001c0001t0065g0286 |
2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.682-1530G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461761 | |||||||
| chr6:18461854 | G | A | 26 | a0001c0001t0006g0154 a0001c0001t0006g0155 a0001c0001t0006g0156 others(23): Show |
27 | HG00642.hp1 HG01081.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.682-1437G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461854 | |||||||
| chr6:18461867 | A | G | 1 | a0001c0001t0081g0126 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.682-1424A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461867 | |||||||
| chr6:18461871 | A | G | 2 | a0001c0001t0019g0146 a0001c0001t0057g0228 |
2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.682-1420A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461871 | |||||||
| chr6:18461940 | G | GGTGTAGT others(8): Show |
1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1350_682-1349i others(17): Show |
RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18461940 | ||||||
| chr6:18461956 | A | T | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1335A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18461956 | |||||||
| chr6:18462022 | T | C | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1269T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462022 | |||||||
| chr6:18462024 | C | T | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1267C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462024 | |||||||
| chr6:18462027 | T | G | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1264T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462027 | |||||||
| chr6:18462028 | C | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1263C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462028 | |||||||
| chr6:18462037 | T | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1254T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462037 | |||||||
| chr6:18462057 | T | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1234T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462057 | |||||||
| chr6:18462058 | C | T | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1233C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462058 | |||||||
| chr6:18462059 | T | C | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1232T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462059 | |||||||
| chr6:18462061 | A | T | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1230A>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462061 | |||||||
| chr6:18462069 | C | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1222C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462069 | |||||||
| chr6:18462071 | T | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1220T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462071 | |||||||
| chr6:18462071 | T | C | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.682-1220T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462071 | |||||||
| chr6:18462078 | G | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1213G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462078 | |||||||
| chr6:18462082 | G | T | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1209G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462082 | |||||||
| chr6:18462083 | T | C | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1208T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462083 | |||||||
| chr6:18462084 | G | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1207G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462084 | |||||||
| chr6:18462087 | A | G | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1204A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462087 | |||||||
| chr6:18462088 | C | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1203C>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462088 | |||||||
| chr6:18462089 | A | G | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1202A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462089 | |||||||
| chr6:18462092 | T | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1199T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462092 | |||||||
| chr6:18462094 | A | C | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1197A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462094 | |||||||
| chr6:18462114 | T | G | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1177T>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462114 | |||||||
| chr6:18462125 | T | A | 352 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(349): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.682-1166T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462125 | |||||||
| chr6:18462145 | C | T | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1146C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462145 | |||||||
| chr6:18462146 | T | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1145T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462146 | |||||||
| chr6:18462147 | A | C | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1144A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462147 | |||||||
| chr6:18462150 | T | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1141T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462150 | |||||||
| chr6:18462152 | T | A | 1 | a0001c0001t0009g0252 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.682-1139T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462152 | |||||||
| chr6:18462261 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.682-1030G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462261 | |||||||
| chr6:18462457 | C | T | 3 | a0001c0001t0016g0091 a0001c0001t0058g0226 a0001c0001t0065g0286 |
3 | HG02055.hp1 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.682-834C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462457 | |||||||
| chr6:18462560 | C | T | 1 | a0001c0001t0004g0015 | 2 | NA18971.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.682-731C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462560 | |||||||
| chr6:18462622 | T | C | 1 | a0001c0001t0004g0360 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.682-669T>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462622 | |||||||
| chr6:18462648 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.682-643C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462648 | |||||||
| chr6:18462662 | G | GT | 133 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(130): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.682-616dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18462662 | ||||||
| chr6:18462697 | A | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(313): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.682-594A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462697 | |||||||
| chr6:18462848 | G | C | 1 | a0001c0001t0005g0336 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.682-443G>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462848 | |||||||
| chr6:18462879 | C | T | 1 | a0001c0001t0039g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.682-412C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18462879 | |||||||
| chr6:18463012 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.682-279G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463012 | |||||||
| chr6:18463034 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.682-257A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463034 | |||||||
| chr6:18463040 | T | A | 73 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(70): Show |
76 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.682-251T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463040 | |||||||
| chr6:18463056 | C | CT | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(91): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.682-226dupT | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 18463056 | ||||||
| chr6:18463063 | T | A | 2 | a0001c0001t0091g0214 a0001c0001t0099g0088 |
2 | HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.682-228T>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463063 | |||||||
| chr6:18463129 | C | G | 180 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(177): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.682-162C>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463129 | |||||||
| chr6:18463155 | G | T | 2 | a0001c0001t0002g0134 a0001c0001t0002g0346 |
2 | HG02738.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.682-136G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 6/7 | chr6 | 18463155 | |||||||
| chr6:18463402 | C | T | 88 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(85): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.771+22C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463402 | |||||||
| chr6:18463592 | A | G | 355 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(352): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.771+212A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463592 | |||||||
| chr6:18463718 | A | G | 1 | a0001c0001t0015g0367 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.771+338A>G | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463718 | |||||||
| chr6:18463719 | G | A | 20 | a0001c0001t0011g0002 a0001c0001t0011g0307 a0001c0001t0011g0314 others(17): Show |
22 | HG00323.hp1 HG01123.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.771+339G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463719 | |||||||
| chr6:18463968 | G | A | 2 | a0001c0001t0066g0282 a0001c0001t0083g0127 |
2 | HG01361.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.771+588G>A | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18463968 | |||||||
| chr6:18464320 | C | T | 1 | a0001c0001t0004g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.772-607C>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464320 | |||||||
| chr6:18464417 | G | T | 74 | a0001c0001t0002g0014 a0001c0001t0002g0134 a0001c0001t0002g0297 others(71): Show |
78 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.772-510G>T | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464417 | |||||||
| chr6:18464676 | A | C | 1 | a0001c0001t0005g0335 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.772-251A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464676 | |||||||
| chr6:18464878 | A | C | 1 | a0001c0001t0047g0133 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.772-49A>C | RNF144B | ENSG00000137393.10 | transcript | ENST00000259939.4 | protein_coding | 7/7 | chr6 | 18464878 |