Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 283521 |
| ensemblid | ENSG00000281106.4 |
| hgncid | 26737 |
| symbol | TMEM272 |
| name | transmembrane protein 272 |
| refseq_nuc | NM_001351003.2 |
| refseq_prot | NP_001337932.1 |
| ensembl_nuc | ENST00000629372.3 |
| ensembl_prot | ENSP00000490718.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 51813347 |
| end | 51845177 |
| strand | - |
| ver | v1.2 |
| region | chr13:51813347-51845177 |
| region5000 | chr13:51808347-51850177 |
| regionname0 | TMEM272_chr13_51813347_51845177 |
| regionname5000 | TMEM272_chr13_51808347_51850177 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 187 | 427 | 95 | 86 | 178 | 18 | 48 | 136 | TMEM272_chr13_51808347_51850177 | TMEM272 | MPGGL others(182): Show |
chr13 | 51808347 | 51850177 |
| a0002 | 0/0 | 187 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | TMEM272_chr13_51808347_51850177 | TMEM272 | MPGGL others(182): Show |
chr13 | 51808347 | 51850177 |
| a0003 | 0/0 | 187 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | MPGGL others(182): Show |
chr13 | 51808347 | 51850177 |
| a0004 | 0/0 | 187 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | MPGGL others(182): Show |
chr13 | 51808347 | 51850177 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 561 | 420 | 90 | 86 | 177 | 18 | 47 | TMEM272_chr13_51808347_51850177 | TMEM272 | ATGCC others(556): Show |
chr13 | 51808347 | 51850177 | ||
| a0001c0002 | 0/0 | 561 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ATGCC others(556): Show |
chr13 | 51808347 | 51850177 | ||
| a0001c0004 | 0/0 | 561 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | ATGCC others(556): Show |
chr13 | 51808347 | 51850177 | ||
| a0002c0003 | 0/0 | 561 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ATGCC others(556): Show |
chr13 | 51808347 | 51850177 | ||
| a0003c0006 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ATGCC others(556): Show |
chr13 | 51808347 | 51850177 | ||
| a0004c0005 | 0/0 | 561 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ATGCC others(556): Show |
chr13 | 51808347 | 51850177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4153 | 110 | 8 | 12 | 70 | 6 | 13 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0002 | 0/0 | 4153 | 88 | 6 | 17 | 51 | 4 | 10 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0003 | 0/1 | 4153 | 64 | 20 | 19 | 13 | 3 | 8 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0004 | 0/0 | 4153 | 25 | 0 | 0 | 25 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0005 | 0/0 | 4153 | 11 | 0 | 8 | 0 | 0 | 3 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0006 | 0/0 | 4161 | 10 | 2 | 8 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4156): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0007 | 0/0 | 4153 | 10 | 9 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0008 | 0/0 | 4153 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0009 | 0/0 | 4155 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4150): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0010 | 0/0 | 4153 | 6 | 2 | 3 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0011 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0012 | 0/0 | 4153 | 6 | 1 | 5 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0013 | 0/0 | 4157 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4152): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0014 | 0/0 | 4153 | 5 | 1 | 1 | 0 | 1 | 2 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0015 | 0/0 | 4153 | 5 | 0 | 5 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0016 | 0/0 | 4149 | 5 | 0 | 0 | 1 | 0 | 4 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4144): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0017 | 0/0 | 4153 | 4 | 0 | 0 | 0 | 2 | 2 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0018 | 0/0 | 4153 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0019 | 0/0 | 4153 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0020 | 0/0 | 4153 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0021 | 0/0 | 4153 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0022 | 0/0 | 4155 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4150): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0023 | 0/0 | 4153 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0024 | 0/0 | 4153 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0025 | 0/0 | 4153 | 2 | 1 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0026 | 0/0 | 4153 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0027 | 0/0 | 4151 | 2 | 1 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4146): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0028 | 0/0 | 4153 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0029 | 0/0 | 4163 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4158): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0030 | 0/0 | 4157 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4152): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0031 | 0/0 | 4155 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4150): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0032 | 0/0 | 4155 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4150): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0033 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0034 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0036 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0037 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0038 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0039 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0040 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0041 | 0/0 | 4153 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0042 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0043 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0044 | 0/0 | 4153 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0045 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0046 | 0/0 | 4143 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4138): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0047 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0048 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0049 | 0/0 | 4153 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0050 | 0/0 | 4151 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4146): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0051 | 0/0 | 4149 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4144): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0052 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0053 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0001t0054 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0002t0011 | 0/0 | 4153 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0001c0004t0001 | 0/0 | 4153 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0002c0003t0001 | 0/0 | 4153 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0003c0006t0001 | 0/0 | 4153 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| a0004c0005t0035 | 0/0 | 4153 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | ACGAG others(4148): Show |
chr13 | 51808347 | 51850177 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 0 | 0 | 19 | 1 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0002 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0003 | 0/0 | 7 | 1 | 1 | 4 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 0 | 0 | 0 | 5 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0009 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0303 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0006g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0006g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0007g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0008g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0009g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0009g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0010g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0010g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0010g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0010g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0012g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0012g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0012g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0013g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0013g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0014g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0014g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0014g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0015g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0015g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0015g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0016g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0016g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0016g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0016g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0017g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0017g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0018g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0018g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0018g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0018g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0019g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0019g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0019g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0020g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0021g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0022g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0022g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0023g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0023g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0024g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0024g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0025g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0025g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0026g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0026g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0027g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0027g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0028g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0028g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0029g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0030g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0031g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0032g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0033g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0034g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0036g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0037g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0038g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0039g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0040g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0041g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0042g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0043g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0044g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0045g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0046g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0047g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0048g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0049g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0050g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0051g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0052g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0053g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0001t0054g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0002t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0002t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0002t0011g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0002t0011g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0002t0011g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0001c0004t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0003c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| a0004c0005t0035g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0010 | g0046 | EUR | GBR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0082 | EUR | GBR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00140 | hp2 | a0001 | c0001 | t0022 | g0132 | EUR | GBR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | FIN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | FIN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00323 | hp2 | a0001 | c0001 | t0017 | g0115 | EUR | FIN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00438 | hp2 | a0001 | c0001 | t0054 | g0305 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00558 | hp2 | a0001 | c0001 | t0045 | g0089 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00735 | hp2 | a0001 | c0001 | t0015 | g0298 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0021 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01069 | hp2 | a0001 | c0001 | t0012 | g0044 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0044 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01099 | hp1 | a0001 | c0001 | t0015 | g0021 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0024 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01168 | hp2 | a0001 | c0001 | t0010 | g0183 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01169 | hp1 | a0001 | c0001 | t0012 | g0024 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01175 | hp2 | a0001 | c0001 | t0030 | g0103 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0247 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01243 | hp1 | a0001 | c0001 | t0021 | g0023 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01255 | hp1 | a0001 | c0001 | t0012 | g0043 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0124 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01346 | hp1 | a0001 | c0001 | t0014 | g0144 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01358 | hp1 | a0001 | c0001 | t0022 | g0197 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0075 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0011 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | IBS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01516 | hp2 | a0001 | c0001 | t0017 | g0027 | EUR | IBS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0048 | EUR | IBS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0176 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01884 | hp2 | a0001 | c0001 | t0037 | g0164 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0166 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01891 | hp2 | a0001 | c0001 | t0008 | g0239 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0060 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01943 | hp2 | a0001 | c0001 | t0015 | g0021 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01975 | hp1 | a0001 | c0001 | t0026 | g0268 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01978 | hp1 | a0001 | c0001 | t0044 | g0096 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01993 | hp1 | a0001 | c0001 | t0010 | g0292 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0073 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0257 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0264 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02015 | hp2 | a0003 | c0006 | t0001 | g0294 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0259 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02135 | hp2 | a0001 | c0001 | t0038 | g0228 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0011 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02148 | hp2 | a0001 | c0001 | t0005 | g0061 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CDX | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02165 | hp2 | a0001 | c0001 | t0048 | g0226 | EAS | CDX | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02257 | hp1 | a0001 | c0001 | t0024 | g0070 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0049 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02258 | hp1 | a0001 | c0001 | t0040 | g0194 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02273 | hp1 | a0001 | c0001 | t0050 | g0091 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02280 | hp1 | a0001 | c0001 | t0039 | g0279 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0011 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02300 | hp1 | a0001 | c0001 | t0026 | g0071 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02572 | hp2 | a0001 | c0001 | t0043 | g0063 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02602 | hp2 | a0001 | c0001 | t0014 | g0094 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0180 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0193 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0175 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02647 | hp2 | a0001 | c0001 | t0019 | g0037 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02698 | hp1 | a0001 | c0001 | t0005 | g0235 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02717 | hp1 | a0001 | c0001 | t0053 | g0137 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0191 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02723 | hp2 | a0001 | c0001 | t0047 | g0150 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0295 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0288 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0189 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0045 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02886 | hp2 | a0001 | c0001 | t0018 | g0172 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0304 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02896 | hp2 | a0001 | c0002 | t0011 | g0270 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02897 | hp2 | a0001 | c0002 | t0011 | g0269 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02970 | hp1 | a0001 | c0001 | t0018 | g0173 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02976 | hp1 | a0001 | c0001 | t0018 | g0158 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03041 | hp2 | a0001 | c0001 | t0020 | g0019 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0043 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0178 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0068 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0186 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03195 | hp2 | a0004 | c0005 | t0035 | g0202 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03209 | hp1 | a0001 | c0001 | t0052 | g0062 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03209 | hp2 | a0001 | c0001 | t0033 | g0238 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0045 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0192 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03453 | hp2 | a0001 | c0001 | t0031 | g0188 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0023 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0195 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03491 | hp1 | a0001 | c0001 | t0016 | g0025 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03492 | hp2 | a0001 | c0001 | t0016 | g0025 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0187 | AFR | ESN | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03540 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03540 | hp2 | a0001 | c0002 | t0011 | g0161 | AFR | GWD | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03579 | hp2 | a0001 | c0002 | t0011 | g0067 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03654 | hp1 | a0001 | c0001 | t0017 | g0027 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03654 | hp2 | a0001 | c0001 | t0049 | g0128 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03688 | hp1 | a0001 | c0001 | t0051 | g0206 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03831 | hp2 | a0001 | c0001 | t0041 | g0281 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0051 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03942 | hp1 | a0001 | c0001 | t0023 | g0106 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04115 | hp2 | a0001 | c0001 | t0017 | g0085 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0231 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04199 | hp1 | a0001 | c0001 | t0027 | g0170 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04204 | hp1 | a0001 | c0001 | t0016 | g0290 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0287 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG04228 | hp2 | a0001 | c0001 | t0016 | g0289 | SAS | STU | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | CHB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18747 | hp2 | a0001 | c0004 | t0001 | g0051 | EAS | CHB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18906 | hp1 | a0001 | c0001 | t0029 | g0167 | AFR | YRI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | YRI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18942 | hp1 | a0001 | c0001 | t0036 | g0261 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18943 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18951 | hp2 | a0001 | c0001 | t0009 | g0296 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18966 | hp1 | a0002 | c0003 | t0001 | g0125 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18969 | hp1 | a0001 | c0001 | t0032 | g0214 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18983 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18999 | hp2 | a0001 | c0001 | t0025 | g0293 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0301 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19030 | hp1 | a0001 | c0001 | t0019 | g0037 | AFR | LWK | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | LWK | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19043 | hp1 | a0001 | c0001 | t0013 | g0148 | AFR | LWK | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19043 | hp2 | a0001 | c0001 | t0042 | g0190 | AFR | LWK | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19074 | hp1 | a0001 | c0001 | t0016 | g0123 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19075 | hp2 | a0001 | c0001 | t0046 | g0099 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19080 | hp2 | a0001 | c0001 | t0028 | g0227 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19087 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19088 | hp1 | a0001 | c0001 | t0009 | g0237 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19088 | hp2 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19089 | hp2 | a0001 | c0001 | t0028 | g0098 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19090 | hp1 | a0001 | c0001 | t0023 | g0224 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0277 | AFR | YRI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20129 | hp1 | a0001 | c0001 | t0034 | g0131 | AFR | ASW | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0299 | AFR | ASW | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20752 | hp2 | a0001 | c0001 | t0014 | g0174 | EUR | TSI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0242 | EUR | TSI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0034 | EUR | TSI | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | GIH | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20905 | hp2 | a0001 | c0001 | t0014 | g0083 | SAS | GIH | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0049 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | MSL | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | USA | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| HG06807 | hp2 | a0001 | c0001 | t0027 | g0276 | AFR | USA | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20300 | hp1 | a0001 | c0001 | t0024 | g0069 | AFR | USA | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA20300 | hp2 | a0001 | c0002 | t0011 | g0182 | AFR | USA | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA21309 | hp1 | a0001 | c0001 | t0014 | g0143 | AFR | LWK | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0303 | REF | REF | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0157 | REF | REF | TMEM272_chr13_51808347_51850177 | TMEM272 | chr13 | 51808347 | 51850177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51816915 | A | G | 1 | a0002 | 3 | HG02071.hp2 NA18953.hp1 NA18966.hp1 |
missense_variant | MODERATE | c.400T>C | p.Phe134Leu | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 585/4153 | 400/564 | 134/187 | chr13 | 51816915 | |||
| chr13:51817085 | C | T | 1 | a0004 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.230G>A | p.Arg77Lys | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 415/4153 | 230/564 | 77/187 | chr13 | 51817085 | |||
| chr13:51826608 | G | C | 1 | a0003 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.76C>G | p.Leu26Val | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/5 | 261/4153 | 76/564 | 26/187 | chr13 | 51826608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51816853 | G | A | 1 | a0001c0002 | 5 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(2): Show |
synonymous_variant | LOW | c.462C>T | p.Val154Val | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 647/4153 | 462/564 | 154/187 | chr13 | 51816853 | |||
| chr13:51816954 | G | A | 1 | a0001c0004 | 2 | HG03927.hp2 NA18747.hp2 |
synonymous_variant | LOW | c.361C>T | p.Leu121Leu | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 546/4153 | 361/564 | 121/187 | chr13 | 51816954 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51813494 | G | A | 1 | a0001c0001t0041 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3257C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 3257 | chr13 | 51813494 | ||||||
| chr13:51813609 | C | T | 3 | a0001c0001t0018 a0001c0001t0024 a0001c0001t0031 |
7 | HG02257.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3142G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 3142 | chr13 | 51813609 | ||||||
| chr13:51813691 | A | G | 4 | a0001c0001t0011 a0001c0001t0012 a0001c0002t0011 others(1): Show |
13 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3060T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 3060 | chr13 | 51813691 | ||||||
| chr13:51813837 | A | C | 2 | a0001c0001t0016 a0001c0001t0051 |
6 | HG03491.hp1 HG03492.hp2 HG03688.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2914T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2914 | chr13 | 51813837 | ||||||
| chr13:51813840 | T | G | 1 | a0001c0001t0034 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2911A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2911 | chr13 | 51813840 | ||||||
| chr13:51814102 | C | T | 1 | a0001c0001t0032 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2649G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2649 | chr13 | 51814102 | ||||||
| chr13:51814328 | G | A | 2 | a0001c0001t0007 a0001c0001t0037 |
11 | HG01192.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2423C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2423 | chr13 | 51814328 | ||||||
| chr13:51814376 | C | T | 2 | a0001c0001t0005 a0001c0001t0044 |
12 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2375G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2375 | chr13 | 51814376 | ||||||
| chr13:51814517 | T | C | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(39): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
3_prime_UTR_variant | MODIFIER | c.*2234A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2234 | chr13 | 51814517 | ||||||
| chr13:51814518 | G | A | 2 | a0001c0001t0026 a0001c0001t0050 |
3 | HG01975.hp1 HG02273.hp1 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2233C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2233 | chr13 | 51814518 | ||||||
| chr13:51814542 | A | T | 1 | a0001c0001t0043 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2209T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2209 | chr13 | 51814542 | ||||||
| chr13:51814629 | T | C | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(11): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2122A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 2122 | chr13 | 51814629 | ||||||
| chr13:51815013 | G | C | 1 | a0001c0001t0020 | 3 | HG02145.hp1 HG03041.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1738C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1738 | chr13 | 51815013 | ||||||
| chr13:51815031 | C | T | 2 | a0001c0001t0019 a0001c0001t0039 |
5 | HG02280.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1720G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1720 | chr13 | 51815031 | ||||||
| chr13:51815040 | G | C | 1 | a0001c0001t0017 | 4 | HG00323.hp2 HG01516.hp2 HG03654.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1711C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1711 | chr13 | 51815040 | ||||||
| chr13:51815211 | C | T | 39 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(36): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*1540G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1540 | chr13 | 51815211 | ||||||
| chr13:51815305 | C | T | 1 | a0001c0001t0033 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1446G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1446 | chr13 | 51815305 | ||||||
| chr13:51815429 | G | A | 1 | a0001c0001t0045 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1322C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1322 | chr13 | 51815429 | ||||||
| chr13:51815452 | G | C | 1 | a0001c0001t0042 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1299C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1299 | chr13 | 51815452 | ||||||
| chr13:51815572 | T | C | 1 | a0001c0001t0012 | 6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1179A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1179 | chr13 | 51815572 | ||||||
| chr13:51815607 | G | A | 19 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(16): Show |
105 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1144C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1144 | chr13 | 51815607 | ||||||
| chr13:51815632 | G | A | 2 | a0001c0001t0016 a0001c0001t0051 |
6 | HG03491.hp1 HG03492.hp2 HG03688.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1119C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1119 | chr13 | 51815632 | ||||||
| chr13:51815668 | ATACAAAA others(3): Show |
A | 1 | a0001c0001t0046 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073_*1082delGAAT others(6): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1073 | chr13 | 51815668 | ||||||
| chr13:51815670 | AC | A | 1 | a0001c0001t0002 | 4 | HG00741.hp1 HG01433.hp2 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1080delG | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 1080 | chr13 | 51815670 | ||||||
| chr13:51815758 | G | T | 2 | a0001c0001t0004 a0001c0001t0038 |
26 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*993C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 993 | chr13 | 51815758 | ||||||
| chr13:51815809 | C | T | 1 | a0001c0001t0037 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 942 | chr13 | 51815809 | ||||||
| chr13:51815912 | C | T | 1 | a0001c0001t0036 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*839G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 839 | chr13 | 51815912 | ||||||
| chr13:51815952 | A | C | 1 | a0001c0001t0054 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 799 | chr13 | 51815952 | ||||||
| chr13:51816069 | C | T | 1 | a0001c0001t0024 | 2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*682G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 682 | chr13 | 51816069 | ||||||
| chr13:51816077 | T | C | 1 | a0001c0001t0047 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*674A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 674 | chr13 | 51816077 | ||||||
| chr13:51816205 | G | A | 1 | a0001c0001t0048 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 546 | chr13 | 51816205 | ||||||
| chr13:51816386 | C | G | 1 | a0004c0005t0035 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 365 | chr13 | 51816386 | ||||||
| chr13:51816467 | C | T | 9 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0022 others(6): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*284G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 284 | chr13 | 51816467 | ||||||
| chr13:51816494 | T | C | 1 | a0001c0001t0049 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*257A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 257 | chr13 | 51816494 | ||||||
| chr13:51816653 | C | CTG | 4 | a0001c0001t0009 a0001c0001t0022 a0001c0001t0031 others(1): Show |
10 | HG00140.hp2 HG01358.hp1 HG03453.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*96_*97dupCA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 97 | chr13 | 51816653 | ||||||
| chr13:51816653 | C | CTGTG | 2 | a0001c0001t0013 a0001c0001t0030 |
6 | HG01175.hp2 HG02630.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*94_*97dupCACA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 97 | chr13 | 51816653 | ||||||
| chr13:51816653 | C | CTGTGTGT others(1): Show |
1 | a0001c0001t0006 | 10 | HG01106.hp2 HG01257.hp2 HG01496.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*90_*97dupCACACACA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 97 | chr13 | 51816653 | ||||||
| chr13:51816653 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0029 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88_*97dupCACACACA others(2): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 97 | chr13 | 51816653 | ||||||
| chr13:51816653 | CTG | C | 2 | a0001c0001t0027 a0001c0001t0050 |
3 | HG02273.hp1 HG04199.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*96_*97delCA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 96 | chr13 | 51816653 | ||||||
| chr13:51816653 | CTGTG | C | 2 | a0001c0001t0016 a0001c0001t0051 |
6 | HG03491.hp1 HG03492.hp2 HG03688.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*94_*97delCACA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 94 | chr13 | 51816653 | ||||||
| chr13:51816676 | T | C | 3 | a0001c0001t0028 a0001c0001t0052 a0001c0001t0053 |
4 | HG02717.hp1 HG03209.hp1 NA19080.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*75A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 5/5 | 75 | chr13 | 51816676 | ||||||
| chr13:51845073 | G | A | 1 | a0001c0001t0054 | 1 | HG00438.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-81C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/5 | chr13 | 51845073 | |||||||
| chr13:51845156 | C | T | 1 | a0001c0001t0021 | 2 | HG01243.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-164G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/5 | 6626 | chr13 | 51845156 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51817178 | T | C | 3 | a0001c0001t0012g0024 a0001c0001t0012g0043 a0001c0001t0012g0044 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-65A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817178 | |||||||
| chr13:51817189 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.202-76C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817189 | |||||||
| chr13:51817205 | C | T | 168 | a0001c0001t0001g0081 a0001c0001t0001g0159 a0001c0001t0002g0002 others(165): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.202-92G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817205 | |||||||
| chr13:51817360 | G | A | 1 | a0001c0004t0001g0051 | 2 | HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.202-247C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817360 | |||||||
| chr13:51817531 | C | G | 62 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0006 others(59): Show |
96 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.202-418G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817531 | |||||||
| chr13:51817711 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.202-598C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817711 | |||||||
| chr13:51817751 | T | G | 1 | a0001c0001t0002g0086 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.202-638A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817751 | |||||||
| chr13:51817924 | C | A | 1 | a0001c0001t0053g0137 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.202-811G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817924 | |||||||
| chr13:51817966 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.202-853C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51817966 | |||||||
| chr13:51818020 | T | C | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | NA18985.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.202-907A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818020 | |||||||
| chr13:51818025 | A | G | 197 | a0001c0001t0001g0081 a0001c0001t0001g0159 a0001c0001t0001g0220 others(194): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.202-912T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818025 | |||||||
| chr13:51818039 | T | G | 3 | a0001c0001t0012g0024 a0001c0001t0012g0043 a0001c0001t0012g0044 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.202-926A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818039 | |||||||
| chr13:51818137 | T | C | 8 | a0001c0001t0005g0010 a0001c0001t0005g0060 a0001c0001t0005g0061 others(5): Show |
11 | HG01109.hp1 HG01255.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.202-1024A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818137 | |||||||
| chr13:51818173 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.202-1060C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818173 | |||||||
| chr13:51818406 | T | C | 181 | a0001c0001t0001g0081 a0001c0001t0001g0159 a0001c0001t0002g0002 others(178): Show |
251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.202-1293A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818406 | |||||||
| chr13:51818827 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.202-1714G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818827 | |||||||
| chr13:51818981 | A | G | 39 | a0001c0001t0001g0220 a0001c0001t0002g0002 a0001c0001t0002g0006 others(36): Show |
54 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.202-1868T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51818981 | |||||||
| chr13:51819059 | T | A | 1 | a0001c0001t0002g0152 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.202-1946A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819059 | |||||||
| chr13:51819072 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.202-1959C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819072 | |||||||
| chr13:51819101 | G | A | 1 | a0001c0001t0011g0187 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.202-1988C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819101 | |||||||
| chr13:51819112 | T | G | 1 | a0001c0001t0003g0297 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.202-1999A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819112 | |||||||
| chr13:51819399 | G | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0222 a0001c0001t0001g0252 others(1): Show |
6 | NA18942.hp1 NA18952.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.202-2286C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819399 | |||||||
| chr13:51819403 | G | A | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.202-2290C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819403 | |||||||
| chr13:51819438 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.202-2325G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819438 | |||||||
| chr13:51819524 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.202-2411C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819524 | |||||||
| chr13:51819853 | G | A | 1 | a0001c0001t0022g0132 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.201+2202C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819853 | |||||||
| chr13:51819885 | C | G | 1 | a0001c0001t0001g0052 | 2 | NA18970.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.201+2170G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819885 | |||||||
| chr13:51819895 | T | A | 1 | a0001c0001t0040g0194 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.201+2160A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51819895 | |||||||
| chr13:51820113 | A | G | 4 | a0001c0001t0011g0187 a0001c0001t0012g0024 a0001c0001t0012g0043 others(1): Show |
7 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.201+1942T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820113 | |||||||
| chr13:51820133 | A | T | 68 | a0001c0001t0001g0220 a0001c0001t0002g0002 a0001c0001t0002g0003 others(65): Show |
102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.201+1922T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820133 | |||||||
| chr13:51820204 | T | C | 186 | a0001c0001t0001g0081 a0001c0001t0001g0159 a0001c0001t0001g0220 others(183): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.201+1851A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820204 | |||||||
| chr13:51820208 | G | A | 5 | a0001c0001t0016g0025 a0001c0001t0016g0123 a0001c0001t0016g0289 others(2): Show |
6 | HG03491.hp1 HG03492.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.201+1847C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820208 | |||||||
| chr13:51820452 | A | C | 1 | a0001c0001t0003g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.201+1603T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820452 | |||||||
| chr13:51820461 | C | T | 1 | a0001c0001t0003g0218 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.201+1594G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820461 | |||||||
| chr13:51820466 | G | A | 1 | a0001c0001t0004g0108 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.201+1589C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820466 | |||||||
| chr13:51820537 | C | T | 1 | a0001c0001t0006g0186 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.201+1518G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820537 | |||||||
| chr13:51820779 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.201+1276C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820779 | |||||||
| chr13:51820837 | T | A | 5 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(2): Show |
5 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.201+1218A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51820837 | |||||||
| chr13:51821001 | T | C | 13 | a0001c0001t0002g0076 a0001c0001t0003g0074 a0001c0001t0006g0011 others(10): Show |
16 | HG01361.hp2 HG01496.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.201+1054A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821001 | |||||||
| chr13:51821002 | T | C | 3 | a0001c0002t0011g0161 a0001c0002t0011g0269 a0001c0002t0011g0270 |
3 | HG02896.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.201+1053A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821002 | |||||||
| chr13:51821173 | C | T | 5 | a0001c0001t0005g0288 a0001c0001t0016g0025 a0001c0001t0016g0123 others(2): Show |
6 | HG02738.hp2 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.201+882G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821173 | |||||||
| chr13:51821174 | T | G | 11 | a0001c0001t0010g0189 a0001c0001t0013g0045 a0001c0001t0013g0068 others(8): Show |
14 | HG01884.hp1 HG02145.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.201+881A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821174 | |||||||
| chr13:51821200 | C | T | 1 | a0001c0001t0024g0070 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.201+855G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821200 | |||||||
| chr13:51821201 | G | A | 1 | a0001c0001t0003g0057 | 2 | HG00738.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.201+854C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821201 | |||||||
| chr13:51821226 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.201+829C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821226 | |||||||
| chr13:51821306 | T | C | 3 | a0001c0001t0013g0045 a0001c0001t0013g0068 a0001c0001t0013g0175 |
4 | HG02630.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+749A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821306 | |||||||
| chr13:51821668 | C | CA | 14 | a0001c0001t0001g0031 a0001c0001t0001g0081 a0001c0001t0001g0159 others(11): Show |
16 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.201+386dupT | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821668 | |||||||
| chr13:51821668 | C | CAA | 25 | a0001c0001t0002g0107 a0001c0001t0002g0110 a0001c0001t0003g0199 others(22): Show |
37 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.201+385_201+386dup others(2): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821668 | |||||||
| chr13:51821676 | AAAAAAAA others(6): Show |
A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0223 a0001c0001t0001g0225 |
3 | HG02027.hp2 NA19075.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.201+366_201+378del others(13): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821676 | |||||||
| chr13:51821686 | AAGCAAAA others(11): Show |
A | 8 | a0001c0001t0001g0163 a0001c0001t0001g0243 a0001c0001t0001g0271 others(5): Show |
10 | HG00639.hp1 HG01243.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.201+351_201+368del others(18): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821686 | |||||||
| chr13:51821687 | AGCAAAAA others(9): Show |
A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(21): Show |
34 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.201+352_201+367del others(16): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821687 | |||||||
| chr13:51821687 | AGCAAAAA others(10): Show |
A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(201): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.201+351_201+367del others(17): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821687 | |||||||
| chr13:51821687 | AGCAAAAA others(12): Show |
A | 1 | a0001c0001t0010g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.201+349_201+367del others(19): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821687 | |||||||
| chr13:51821701 | AAGC | A | 50 | a0001c0001t0001g0081 a0001c0001t0001g0159 a0001c0001t0002g0066 others(47): Show |
63 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.201+351_201+353del others(3): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821701 | |||||||
| chr13:51821702 | AGC | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0223 a0001c0001t0001g0225 |
3 | HG02027.hp2 NA19075.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.201+351_201+352del others(2): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821702 | |||||||
| chr13:51821704 | C | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(21): Show |
34 | HG00423.hp1 HG00558.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.201+351G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821704 | |||||||
| chr13:51821707 | C | A | 1 | a0001c0001t0010g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.201+348G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821707 | |||||||
| chr13:51821806 | A | G | 1 | a0001c0002t0011g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.201+249T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821806 | |||||||
| chr13:51821848 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.201+207G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51821848 | |||||||
| chr13:51822036 | G | A | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.201+19C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51822036 | |||||||
| chr13:51822054 | C | T | 2 | a0001c0001t0003g0160 a0001c0001t0047g0150 |
2 | HG02615.hp2 HG02723.hp2 |
splice_donor_variant&intron_variant | HIGH | c.201+1G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 4/4 | chr13 | 51822054 | |||||||
| chr13:51822317 | G | A | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-180C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822317 | |||||||
| chr13:51822336 | C | G | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-199G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822336 | |||||||
| chr13:51822623 | G | A | 1 | a0001c0004t0001g0051 | 2 | HG03927.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.119-486C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822623 | |||||||
| chr13:51822692 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.119-555A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822692 | |||||||
| chr13:51822731 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(79): Show |
133 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.119-594G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822731 | |||||||
| chr13:51822735 | C | T | 1 | a0001c0001t0014g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.119-598G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822735 | |||||||
| chr13:51822783 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.119-646C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822783 | |||||||
| chr13:51822881 | G | A | 3 | a0001c0001t0002g0110 a0001c0001t0004g0109 a0001c0001t0004g0112 |
3 | NA18947.hp2 NA18984.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.119-744C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51822881 | |||||||
| chr13:51823263 | A | C | 1 | a0001c0001t0003g0295 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.119-1126T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823263 | |||||||
| chr13:51823463 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.119-1326A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823463 | |||||||
| chr13:51823478 | A | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(99): Show |
159 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.119-1341T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823478 | |||||||
| chr13:51823582 | G | A | 5 | a0001c0001t0018g0172 a0001c0001t0018g0173 a0001c0001t0018g0191 others(2): Show |
5 | HG02723.hp1 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-1445C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823582 | |||||||
| chr13:51823678 | T | G | 1 | a0001c0001t0025g0176 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.119-1541A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823678 | |||||||
| chr13:51823696 | T | A | 11 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0003g0074 others(8): Show |
15 | HG01361.hp2 HG01496.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.119-1559A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823696 | |||||||
| chr13:51823771 | G | A | 26 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0003g0005 others(23): Show |
43 | HG00323.hp1 HG00597.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.119-1634C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823771 | |||||||
| chr13:51823853 | C | T | 1 | a0001c0001t0003g0181 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.119-1716G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823853 | |||||||
| chr13:51823943 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.119-1806C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823943 | |||||||
| chr13:51823966 | T | C | 1 | a0001c0001t0010g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.119-1829A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51823966 | |||||||
| chr13:51824046 | T | C | 1 | a0001c0001t0047g0150 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.119-1909A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51824046 | |||||||
| chr13:51824194 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.119-2057G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51824194 | |||||||
| chr13:51824499 | T | G | 3 | a0001c0001t0003g0179 a0001c0001t0008g0178 a0001c0001t0008g0180 |
3 | HG02486.hp2 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.118+2067A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51824499 | |||||||
| chr13:51824562 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118+2004C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51824562 | |||||||
| chr13:51824801 | A | C | 34 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0003g0005 others(31): Show |
51 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.118+1765T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51824801 | |||||||
| chr13:51824841 | T | C | 1 | a0001c0001t0028g0098 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.118+1725A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51824841 | |||||||
| chr13:51824907 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(100): Show |
160 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.118+1659G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51824907 | |||||||
| chr13:51825139 | A | T | 6 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+1427T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825139 | |||||||
| chr13:51825205 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(99): Show |
159 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.118+1361G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825205 | |||||||
| chr13:51825212 | T | G | 1 | a0001c0002t0011g0269 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.118+1354A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825212 | |||||||
| chr13:51825421 | T | G | 5 | a0001c0001t0003g0038 a0001c0001t0003g0139 a0001c0001t0003g0151 others(2): Show |
7 | HG02622.hp2 HG02647.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+1145A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825421 | |||||||
| chr13:51825524 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.118+1042C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825524 | |||||||
| chr13:51825619 | T | G | 3 | a0001c0001t0002g0050 a0001c0001t0002g0079 a0001c0001t0002g0254 |
4 | HG00673.hp2 NA19063.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+947A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825619 | |||||||
| chr13:51825635 | GT | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(259): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.118+930delA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825635 | |||||||
| chr13:51825635 | GTT | G | 11 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0304 others(8): Show |
13 | HG01168.hp2 HG01891.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+929_118+930del others(2): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825635 | |||||||
| chr13:51825640 | T | A | 1 | a0001c0001t0008g0049 | 2 | HG02109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.118+926A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825640 | |||||||
| chr13:51825669 | C | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(278): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.118+897G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825669 | |||||||
| chr13:51825676 | C | T | 1 | a0001c0001t0007g0041 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.118+890G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825676 | |||||||
| chr13:51825716 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.118+850G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825716 | |||||||
| chr13:51825721 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0200 |
2 | HG01074.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.118+845C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825721 | |||||||
| chr13:51825856 | G | A | 9 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0008g0049 others(6): Show |
11 | HG01891.hp2 HG01975.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.118+710C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825856 | |||||||
| chr13:51825879 | G | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0156 a0001c0001t0001g0262 others(1): Show |
5 | NA18955.hp2 NA18970.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+687C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51825879 | |||||||
| chr13:51826055 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.118+511A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826055 | |||||||
| chr13:51826105 | G | A | 1 | a0001c0001t0046g0099 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.118+461C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826105 | |||||||
| chr13:51826137 | G | GAAAAAA | 4 | a0001c0001t0003g0198 a0001c0001t0003g0304 a0001c0001t0008g0239 others(1): Show |
4 | HG01891.hp2 HG02896.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.118+428_118+429ins others(6): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826137 | |||||||
| chr13:51826138 | C | A | 6 | a0001c0001t0003g0198 a0001c0001t0003g0304 a0001c0001t0008g0049 others(3): Show |
7 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+428G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826138 | C | CA | 21 | a0001c0001t0001g0080 a0001c0001t0001g0100 a0001c0001t0002g0056 others(18): Show |
31 | HG00323.hp1 HG01070.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.118+427dupT | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826138 | C | CAA | 14 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0003g0074 others(11): Show |
18 | HG01361.hp2 HG01496.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.118+426_118+427dup others(2): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826138 | C | CAAA | 6 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+425_118+427dup others(3): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826138 | C | CAAAA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(74): Show |
127 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.118+424_118+427dup others(4): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826138 | C | CAAAAA | 22 | a0001c0001t0001g0052 a0001c0001t0001g0077 a0001c0001t0001g0217 others(19): Show |
26 | HG01123.hp1 HG01192.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.118+423_118+427dup others(5): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826138 | CA | C | 29 | a0001c0001t0001g0081 a0001c0001t0001g0159 a0001c0001t0001g0274 others(26): Show |
37 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.118+427delT | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826138 | CAAAAA | C | 3 | a0001c0001t0012g0024 a0001c0001t0012g0043 a0001c0001t0012g0044 |
6 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+423_118+427del others(5): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826138 | |||||||
| chr13:51826357 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0244 others(2): Show |
6 | HG00099.hp2 HG01069.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+209G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826357 | |||||||
| chr13:51826362 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(138): Show |
206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.118+204G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826362 | |||||||
| chr13:51826371 | C | A | 1 | a0001c0001t0005g0075 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.118+195G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826371 | |||||||
| chr13:51826415 | A | G | 1 | a0004c0005t0035g0202 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.118+151T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826415 | |||||||
| chr13:51826479 | A | G | 1 | a0001c0001t0020g0019 | 3 | HG02145.hp1 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.118+87T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 3/4 | chr13 | 51826479 | |||||||
| chr13:51826700 | T | G | 1 | a0001c0001t0003g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.59-75A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51826700 | |||||||
| chr13:51826812 | C | T | 17 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0003g0074 others(14): Show |
22 | HG01361.hp2 HG01496.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.59-187G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51826812 | |||||||
| chr13:51826850 | C | T | 2 | a0001c0001t0003g0119 a0001c0001t0003g0242 |
2 | HG01099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.59-225G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51826850 | |||||||
| chr13:51826897 | CT | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0003g0074 others(8): Show |
15 | HG01361.hp2 HG01496.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-273delA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51826897 | |||||||
| chr13:51826967 | G | A | 141 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0080 others(138): Show |
201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.59-342C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51826967 | |||||||
| chr13:51827070 | A | G | 2 | a0001c0001t0002g0066 a0004c0005t0035g0202 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.59-445T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827070 | |||||||
| chr13:51827217 | A | G | 6 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-592T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827217 | |||||||
| chr13:51827405 | T | C | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-780A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827405 | |||||||
| chr13:51827475 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0267 |
2 | NA18967.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.59-850C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827475 | |||||||
| chr13:51827481 | T | C | 2 | a0001c0001t0002g0152 a0001c0001t0004g0168 |
2 | HG02132.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.59-856A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827481 | |||||||
| chr13:51827578 | CAG | C | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-955_59-954delCT | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827578 | |||||||
| chr13:51827668 | G | C | 1 | a0001c0001t0003g0055 | 2 | NA18955.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.59-1043C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827668 | |||||||
| chr13:51827700 | T | C | 6 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-1075A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827700 | |||||||
| chr13:51827753 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(99): Show |
160 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.59-1128A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827753 | |||||||
| chr13:51827832 | C | T | 1 | a0001c0001t0004g0168 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.59-1207G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827832 | |||||||
| chr13:51827886 | T | C | 38 | a0001c0001t0001g0121 a0001c0001t0001g0159 a0001c0001t0002g0047 others(35): Show |
47 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.59-1261A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827886 | |||||||
| chr13:51827922 | C | T | 1 | a0001c0001t0016g0025 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.59-1297G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51827922 | |||||||
| chr13:51828042 | G | A | 76 | a0001c0001t0001g0029 a0001c0001t0001g0080 a0001c0001t0001g0090 others(73): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.59-1417C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828042 | |||||||
| chr13:51828069 | G | C | 1 | a0001c0001t0052g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-1444C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828069 | |||||||
| chr13:51828128 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(100): Show |
158 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.59-1503T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828128 | |||||||
| chr13:51828190 | A | G | 1 | a0001c0001t0003g0299 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-1565T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828190 | |||||||
| chr13:51828265 | TGTG | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0200 a0001c0001t0001g0201 |
3 | HG01074.hp2 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.59-1643_59-1641del others(3): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828265 | |||||||
| chr13:51828307 | C | T | 5 | a0001c0001t0003g0198 a0001c0001t0008g0049 a0001c0001t0008g0239 others(2): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-1682G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828307 | |||||||
| chr13:51828363 | C | A | 5 | a0001c0001t0003g0198 a0001c0001t0008g0049 a0001c0001t0008g0239 others(2): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-1738G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828363 | |||||||
| chr13:51828364 | G | A | 2 | a0001c0001t0003g0304 a0001c0001t0021g0023 |
3 | HG01243.hp1 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.59-1739C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828364 | |||||||
| chr13:51828617 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0117 a0001c0001t0001g0136 others(2): Show |
6 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-1992G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828617 | |||||||
| chr13:51828632 | G | C | 1 | a0001c0001t0043g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-2007C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828632 | |||||||
| chr13:51828728 | G | T | 8 | a0001c0001t0001g0156 a0001c0001t0005g0288 a0001c0001t0016g0025 others(5): Show |
11 | HG02145.hp1 HG02738.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-2103C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828728 | |||||||
| chr13:51828743 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.59-2118C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828743 | |||||||
| chr13:51828775 | C | A | 17 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0003g0074 others(14): Show |
21 | HG01361.hp2 HG01496.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.59-2150G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828775 | |||||||
| chr13:51828797 | C | T | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2172G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828797 | |||||||
| chr13:51828827 | G | A | 1 | a0001c0001t0043g0063 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-2202C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828827 | |||||||
| chr13:51828857 | G | A | 1 | a0001c0001t0010g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59-2232C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51828857 | |||||||
| chr13:51829069 | A | C | 1 | a0001c0001t0002g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.59-2444T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829069 | |||||||
| chr13:51829124 | CA | C | 8 | a0001c0001t0001g0156 a0001c0001t0005g0288 a0001c0001t0016g0025 others(5): Show |
11 | HG02145.hp1 HG02738.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-2500delT | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829124 | |||||||
| chr13:51829136 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(271): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.59-2511C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829136 | |||||||
| chr13:51829295 | T | C | 4 | a0001c0002t0011g0067 a0001c0002t0011g0161 a0001c0002t0011g0269 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-2670A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829295 | |||||||
| chr13:51829506 | T | G | 1 | a0001c0001t0020g0019 | 3 | HG02145.hp1 HG03041.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.59-2881A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829506 | |||||||
| chr13:51829519 | C | T | 2 | a0001c0001t0002g0086 a0001c0001t0002g0208 |
2 | NA18951.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.59-2894G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829519 | |||||||
| chr13:51829521 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(97): Show |
154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.59-2896T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829521 | |||||||
| chr13:51829663 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-3038G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829663 | |||||||
| chr13:51829853 | T | TA | 16 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0003g0074 others(13): Show |
20 | HG01361.hp2 HG01496.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-3229dupT | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829853 | |||||||
| chr13:51829896 | T | C | 1 | a0001c0001t0003g0018 | 3 | HG02055.hp2 HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.59-3271A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829896 | |||||||
| chr13:51829989 | T | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(96): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.59-3364A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51829989 | |||||||
| chr13:51830187 | T | C | 6 | a0001c0001t0003g0198 a0001c0001t0003g0304 a0001c0001t0008g0049 others(3): Show |
7 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-3562A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830187 | |||||||
| chr13:51830477 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.59-3852A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830477 | |||||||
| chr13:51830678 | C | T | 1 | a0001c0001t0004g0263 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59-4053G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830678 | |||||||
| chr13:51830770 | A | G | 3 | a0001c0001t0017g0027 a0001c0001t0017g0085 a0001c0001t0017g0115 |
4 | HG00323.hp2 HG01516.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-4145T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830770 | |||||||
| chr13:51830849 | C | T | 2 | a0001c0001t0010g0065 a0001c0001t0043g0063 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.59-4224G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830849 | |||||||
| chr13:51830923 | C | T | 2 | a0001c0001t0002g0152 a0001c0001t0004g0168 |
2 | HG02132.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.59-4298G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830923 | |||||||
| chr13:51830924 | G | A | 1 | a0001c0001t0052g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.59-4299C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830924 | |||||||
| chr13:51830951 | GAGGTCGA others(20): Show |
G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0200 |
2 | HG01074.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.59-4353_59-4327del others(27): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51830951 | |||||||
| chr13:51831115 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(102): Show |
160 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.59-4490T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831115 | |||||||
| chr13:51831138 | C | A | 1 | a0001c0001t0004g0301 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.59-4513G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831138 | |||||||
| chr13:51831364 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.59-4739A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831364 | |||||||
| chr13:51831432 | A | G | 7 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(4): Show |
7 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.59-4807T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831432 | |||||||
| chr13:51831655 | G | T | 6 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-5030C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831655 | |||||||
| chr13:51831767 | T | C | 10 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0304 others(7): Show |
12 | HG01891.hp2 HG01975.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-5142A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831767 | |||||||
| chr13:51831825 | A | G | 1 | a0001c0001t0013g0068 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-5200T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831825 | |||||||
| chr13:51831854 | G | A | 8 | a0001c0001t0001g0156 a0001c0001t0005g0288 a0001c0001t0016g0025 others(5): Show |
11 | HG02145.hp1 HG02738.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.59-5229C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51831854 | |||||||
| chr13:51832002 | G | A | 1 | a0001c0001t0010g0292 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.59-5377C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832002 | |||||||
| chr13:51832268 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(88): Show |
143 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.59-5643A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832268 | |||||||
| chr13:51832313 | A | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(287): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.59-5688T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832313 | |||||||
| chr13:51832417 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(88): Show |
143 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.59-5792A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832417 | |||||||
| chr13:51832528 | A | T | 1 | a0001c0001t0003g0084 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.59-5903T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832528 | |||||||
| chr13:51832657 | G | A | 2 | a0001c0001t0002g0066 a0004c0005t0035g0202 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.58+5816C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832657 | |||||||
| chr13:51832678 | C | T | 6 | a0001c0001t0003g0198 a0001c0001t0003g0304 a0001c0001t0008g0049 others(3): Show |
7 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+5795G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832678 | |||||||
| chr13:51832681 | G | T | 1 | a0001c0001t0001g0026 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.58+5792C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832681 | |||||||
| chr13:51832708 | C | T | 30 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0003g0005 others(27): Show |
49 | HG00323.hp1 HG00597.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.58+5765G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832708 | |||||||
| chr13:51832784 | C | A | 6 | a0001c0001t0003g0198 a0001c0001t0003g0304 a0001c0001t0008g0049 others(3): Show |
7 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+5689G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832784 | |||||||
| chr13:51832870 | T | C | 1 | a0001c0001t0052g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.58+5603A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832870 | |||||||
| chr13:51832960 | C | A | 6 | a0001c0001t0003g0198 a0001c0001t0003g0304 a0001c0001t0008g0049 others(3): Show |
7 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+5513G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832960 | |||||||
| chr13:51832998 | A | G | 8 | a0001c0001t0001g0156 a0001c0001t0005g0288 a0001c0001t0016g0025 others(5): Show |
11 | HG02145.hp1 HG02738.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+5475T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51832998 | |||||||
| chr13:51833085 | G | C | 5 | a0001c0001t0003g0198 a0001c0001t0008g0049 a0001c0001t0008g0239 others(2): Show |
6 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+5388C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833085 | |||||||
| chr13:51833125 | A | G | 3 | a0001c0001t0002g0240 a0001c0001t0002g0278 a0001c0001t0003g0184 |
3 | HG02258.hp2 HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58+5348T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833125 | |||||||
| chr13:51833132 | C | T | 1 | a0001c0001t0031g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.58+5341G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833132 | |||||||
| chr13:51833327 | A | G | 12 | a0001c0001t0001g0026 a0001c0001t0001g0120 a0001c0001t0003g0074 others(9): Show |
16 | HG01361.hp2 HG01496.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.58+5146T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833327 | |||||||
| chr13:51833410 | AG | A | 7 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(4): Show |
7 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+5062delC | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833410 | |||||||
| chr13:51833469 | T | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(262): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.58+5004A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833469 | |||||||
| chr13:51833766 | G | A | 2 | a0001c0001t0002g0066 a0004c0005t0035g0202 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.58+4707C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833766 | |||||||
| chr13:51833979 | C | T | 1 | a0001c0001t0006g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+4494G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51833979 | |||||||
| chr13:51834040 | G | A | 7 | a0001c0001t0010g0189 a0001c0001t0018g0172 a0001c0001t0018g0173 others(4): Show |
7 | HG02723.hp1 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+4433C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834040 | |||||||
| chr13:51834059 | C | A | 1 | a0001c0001t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.58+4414G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834059 | |||||||
| chr13:51834204 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4269C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834204 | |||||||
| chr13:51834204 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.58+4269C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834204 | |||||||
| chr13:51834206 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0002g0152 a0001c0001t0004g0168 |
4 | HG01516.hp1 HG01517.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4267T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834206 | |||||||
| chr13:51834428 | T | C | 1 | a0001c0001t0023g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.58+4045A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834428 | |||||||
| chr13:51834599 | G | A | 11 | a0001c0001t0001g0120 a0001c0001t0003g0074 a0001c0001t0006g0011 others(8): Show |
14 | HG01361.hp2 HG01496.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.58+3874C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834599 | |||||||
| chr13:51834646 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58+3827G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51834646 | |||||||
| chr13:51835101 | T | C | 168 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(165): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.58+3372A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835101 | |||||||
| chr13:51835186 | G | A | 1 | a0001c0001t0005g0060 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.58+3287C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835186 | |||||||
| chr13:51835220 | TTTTC | T | 133 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(130): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.58+3249_58+3252del others(4): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835220 | |||||||
| chr13:51835225 | TTTC | T | 15 | a0001c0001t0001g0081 a0001c0001t0001g0156 a0001c0001t0002g0066 others(12): Show |
18 | HG02145.hp1 HG02738.hp2 HG02896.hp2 others(15): Show |
intron_variant | MODIFIER | c.58+3245_58+3247del others(3): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835225 | |||||||
| chr13:51835227 | T | C | 4 | a0001c0001t0001g0163 a0001c0001t0001g0243 a0001c0001t0001g0271 others(1): Show |
4 | HG02258.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3246A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835227 | |||||||
| chr13:51835228 | C | CT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(80): Show |
132 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.58+3244dupA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835228 | |||||||
| chr13:51835293 | C | T | 32 | a0001c0001t0001g0033 a0001c0001t0001g0121 a0001c0001t0002g0122 others(29): Show |
52 | HG00323.hp1 HG00597.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.58+3180G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835293 | |||||||
| chr13:51835371 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(282): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.58+3102A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835371 | |||||||
| chr13:51835416 | C | A | 1 | a0001c0001t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.58+3057G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835416 | |||||||
| chr13:51835459 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.58+3014G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835459 | |||||||
| chr13:51835492 | G | C | 2 | a0001c0001t0010g0065 a0001c0001t0043g0063 |
2 | HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58+2981C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835492 | |||||||
| chr13:51835503 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.58+2970G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835503 | |||||||
| chr13:51835590 | A | T | 1 | a0001c0001t0003g0212 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.58+2883T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835590 | |||||||
| chr13:51835724 | A | C | 194 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(191): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.58+2749T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835724 | |||||||
| chr13:51835859 | T | G | 1 | a0001c0001t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.58+2614A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835859 | |||||||
| chr13:51835984 | T | C | 107 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0026 others(104): Show |
149 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.58+2489A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51835984 | |||||||
| chr13:51836092 | T | C | 1 | a0001c0001t0001g0283 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.58+2381A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836092 | |||||||
| chr13:51836271 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.58+2202G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836271 | |||||||
| chr13:51836325 | T | C | 1 | a0001c0001t0003g0299 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.58+2148A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836325 | |||||||
| chr13:51836375 | G | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0026 others(58): Show |
100 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.58+2098C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836375 | |||||||
| chr13:51836539 | G | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG02056.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.58+1934C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836539 | |||||||
| chr13:51836683 | G | A | 2 | a0001c0001t0003g0059 a0001c0001t0003g0287 |
3 | HG01978.hp2 HG02293.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.58+1790C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836683 | |||||||
| chr13:51836728 | G | A | 1 | a0001c0001t0012g0044 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.58+1745C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836728 | |||||||
| chr13:51836784 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.58+1689T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836784 | |||||||
| chr13:51836920 | A | G | 1 | a0001c0001t0007g0162 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.58+1553T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836920 | |||||||
| chr13:51836938 | A | G | 1 | a0001c0001t0051g0206 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.58+1535T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51836938 | |||||||
| chr13:51837080 | G | A | 17 | a0001c0001t0001g0185 a0001c0001t0001g0271 a0001c0001t0002g0066 others(14): Show |
17 | HG01891.hp1 HG02258.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.58+1393C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837080 | |||||||
| chr13:51837165 | G | A | 1 | a0001c0001t0005g0061 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.58+1308C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837165 | |||||||
| chr13:51837216 | G | A | 41 | a0001c0001t0001g0185 a0001c0001t0001g0271 a0001c0001t0002g0020 others(38): Show |
52 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.58+1257C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837216 | |||||||
| chr13:51837357 | T | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0141 |
2 | NA18948.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.58+1116A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837357 | |||||||
| chr13:51837526 | G | A | 7 | a0001c0001t0002g0072 a0001c0001t0003g0074 a0001c0001t0005g0075 others(4): Show |
10 | HG00280.hp1 HG01361.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+947C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837526 | |||||||
| chr13:51837606 | T | C | 1 | a0001c0001t0039g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.58+867A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837606 | |||||||
| chr13:51837690 | A | G | 30 | a0001c0001t0001g0159 a0001c0001t0001g0200 a0001c0001t0001g0201 others(27): Show |
37 | HG01074.hp2 HG01106.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.58+783T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837690 | |||||||
| chr13:51837997 | T | A | 3 | a0001c0001t0002g0278 a0001c0001t0008g0277 a0001c0001t0039g0279 |
3 | HG02280.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58+476A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51837997 | |||||||
| chr13:51838175 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0022g0132 a0001c0001t0022g0197 others(1): Show |
6 | HG00140.hp2 HG00741.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+298C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51838175 | |||||||
| chr13:51838232 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58+241G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51838232 | |||||||
| chr13:51838385 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.58+88T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 2/4 | chr13 | 51838385 | |||||||
| chr13:51838611 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-23-58A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51838611 | |||||||
| chr13:51838667 | C | T | 1 | a0001c0001t0052g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-23-114G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51838667 | |||||||
| chr13:51838756 | C | T | 1 | a0001c0001t0002g0205 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-23-203G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51838756 | |||||||
| chr13:51838813 | T | C | 1 | a0001c0001t0001g0052 | 2 | NA18970.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.-23-260A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51838813 | |||||||
| chr13:51838941 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-23-388G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51838941 | |||||||
| chr13:51839016 | A | G | 41 | a0001c0001t0001g0159 a0001c0001t0001g0163 a0001c0001t0001g0200 others(38): Show |
53 | HG00280.hp1 HG01074.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.-23-463T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839016 | |||||||
| chr13:51839058 | G | C | 1 | a0001c0001t0001g0267 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-23-505C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839058 | |||||||
| chr13:51839059 | C | G | 1 | a0001c0001t0001g0267 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-23-506G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839059 | |||||||
| chr13:51839060 | G | C | 1 | a0001c0001t0001g0267 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-23-507C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839060 | |||||||
| chr13:51839155 | G | A | 1 | a0001c0001t0003g0134 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-23-602C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839155 | |||||||
| chr13:51839431 | CTCCATGG others(11): Show |
C | 1 | a0001c0001t0052g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-23-896_-23-879del others(18): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839431 | |||||||
| chr13:51839445 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(92): Show |
145 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-23-892C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839445 | |||||||
| chr13:51839456 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-23-903G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839456 | |||||||
| chr13:51839522 | C | T | 1 | a0001c0001t0003g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-23-969G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839522 | |||||||
| chr13:51839665 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-23-1112C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839665 | |||||||
| chr13:51839690 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-23-1137C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839690 | |||||||
| chr13:51839775 | G | A | 5 | a0001c0001t0001g0053 a0001c0001t0002g0278 a0001c0001t0008g0277 others(2): Show |
6 | HG02280.hp1 HG06807.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1222C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839775 | |||||||
| chr13:51839852 | A | T | 6 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0304 others(3): Show |
8 | HG01243.hp1 HG01975.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23-1299T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839852 | |||||||
| chr13:51839859 | T | G | 2 | a0001c0001t0024g0069 a0001c0001t0024g0070 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-23-1306A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839859 | |||||||
| chr13:51839885 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0016 others(258): Show |
378 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(375): Show |
intron_variant | MODIFIER | c.-23-1332A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839885 | |||||||
| chr13:51839894 | T | G | 21 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0250 others(18): Show |
24 | HG00280.hp2 HG00438.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-23-1341A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51839894 | |||||||
| chr13:51840007 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-23-1454G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840007 | |||||||
| chr13:51840020 | T | A | 1 | a0001c0001t0026g0268 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-23-1467A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840020 | |||||||
| chr13:51840025 | C | T | 3 | a0001c0001t0005g0288 a0001c0001t0016g0289 a0001c0001t0016g0290 |
3 | HG02738.hp2 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-23-1472G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840025 | |||||||
| chr13:51840328 | C | T | 1 | a0001c0001t0052g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-23-1775G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840328 | |||||||
| chr13:51840497 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-23-1944A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840497 | |||||||
| chr13:51840563 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(70): Show |
121 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-23-2010G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840563 | |||||||
| chr13:51840667 | T | C | 3 | a0001c0001t0024g0069 a0001c0001t0024g0070 a0001c0002t0011g0067 |
3 | HG02257.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-23-2114A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840667 | |||||||
| chr13:51840869 | C | T | 1 | a0001c0001t0007g0155 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-23-2316G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840869 | |||||||
| chr13:51840899 | C | T | 1 | a0001c0002t0011g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-23-2346G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840899 | |||||||
| chr13:51840934 | A | G | 1 | a0001c0001t0004g0204 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-23-2381T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840934 | |||||||
| chr13:51840989 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-23-2436A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51840989 | |||||||
| chr13:51841109 | C | T | 25 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0002g0056 others(22): Show |
38 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-23-2556G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841109 | |||||||
| chr13:51841128 | AG | A | 6 | a0001c0001t0001g0026 a0001c0001t0005g0010 a0001c0001t0005g0060 others(3): Show |
12 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23-2576delC | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841128 | |||||||
| chr13:51841168 | T | C | 7 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0002g0169 others(4): Show |
7 | HG01074.hp2 HG02132.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23-2615A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841168 | |||||||
| chr13:51841176 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-23-2623G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841176 | |||||||
| chr13:51841215 | CAG | C | 5 | a0001c0001t0003g0038 a0001c0001t0003g0138 a0001c0001t0003g0139 others(2): Show |
7 | HG02647.hp2 HG02717.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23-2664_-23-2663d others(4): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841215 | |||||||
| chr13:51841319 | G | T | 9 | a0001c0001t0001g0154 a0001c0001t0002g0152 a0001c0001t0003g0018 others(6): Show |
13 | HG01106.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23-2766C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841319 | |||||||
| chr13:51841345 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-23-2792G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841345 | |||||||
| chr13:51841411 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-23-2858G>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841411 | |||||||
| chr13:51841534 | T | C | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-2981A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841534 | |||||||
| chr13:51841537 | C | T | 1 | a0001c0001t0003g0287 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-23-2984G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841537 | |||||||
| chr13:51841639 | C | T | 1 | a0001c0001t0013g0045 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23-3086G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841639 | |||||||
| chr13:51841671 | A | G | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-3118T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841671 | |||||||
| chr13:51841681 | A | C | 2 | a0001c0001t0012g0043 a0001c0001t0012g0044 |
4 | HG01069.hp2 HG01071.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-3128T>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841681 | |||||||
| chr13:51841753 | C | T | 1 | a0001c0001t0012g0024 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-23-3200G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841753 | |||||||
| chr13:51841815 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-24+3201T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841815 | |||||||
| chr13:51841871 | C | T | 1 | a0001c0001t0003g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-24+3145G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841871 | |||||||
| chr13:51841893 | A | G | 3 | a0001c0001t0001g0271 a0001c0002t0011g0269 a0001c0002t0011g0270 |
3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-24+3123T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841893 | |||||||
| chr13:51841941 | G | A | 1 | a0001c0001t0002g0039 | 2 | NA18977.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-24+3075C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841941 | |||||||
| chr13:51841984 | C | T | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+3032G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51841984 | |||||||
| chr13:51842036 | A | AAC | 26 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0002g0056 others(23): Show |
39 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-24+2978_-24+2979d others(4): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842036 | |||||||
| chr13:51842067 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-24+2949A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842067 | |||||||
| chr13:51842081 | T | C | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+2935A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842081 | |||||||
| chr13:51842222 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-24+2794C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842222 | |||||||
| chr13:51842228 | G | C | 1 | a0001c0001t0003g0142 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-24+2788C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842228 | |||||||
| chr13:51842299 | CATT | C | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+2714_-24+2716d others(5): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842299 | |||||||
| chr13:51842347 | A | G | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+2669T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842347 | |||||||
| chr13:51842396 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-24+2620T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842396 | |||||||
| chr13:51842431 | G | A | 100 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0028 others(97): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.-24+2585C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842431 | |||||||
| chr13:51842433 | A | G | 2 | a0001c0001t0024g0069 a0001c0001t0024g0070 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-24+2583T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842433 | |||||||
| chr13:51842621 | AT | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0250 others(18): Show |
24 | HG00280.hp2 HG00438.hp1 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.-24+2394delA | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842621 | |||||||
| chr13:51842631 | T | C | 3 | a0001c0001t0001g0271 a0001c0002t0011g0269 a0001c0002t0011g0270 |
3 | HG02896.hp2 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-24+2385A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842631 | |||||||
| chr13:51842776 | T | G | 26 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0002g0056 others(23): Show |
39 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-24+2240A>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842776 | |||||||
| chr13:51842794 | T | C | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+2222A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842794 | |||||||
| chr13:51842866 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0010g0065 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-24+2150A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842866 | |||||||
| chr13:51842894 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0013g0148 |
2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-24+2122C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842894 | |||||||
| chr13:51842919 | T | A | 1 | a0001c0001t0003g0286 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-24+2097A>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842919 | |||||||
| chr13:51842936 | G | T | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+2080C>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51842936 | |||||||
| chr13:51843220 | A | T | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+1796T>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843220 | |||||||
| chr13:51843402 | T | C | 36 | a0001c0001t0001g0185 a0001c0001t0002g0020 a0001c0001t0002g0047 others(33): Show |
46 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.-24+1614A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843402 | |||||||
| chr13:51843450 | A | G | 1 | a0001c0001t0013g0068 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-24+1566T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843450 | |||||||
| chr13:51843509 | T | C | 3 | a0001c0001t0002g0145 a0001c0001t0014g0143 a0001c0001t0014g0144 |
3 | HG00733.hp2 HG01346.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-24+1507A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843509 | |||||||
| chr13:51843591 | G | A | 3 | a0001c0001t0001g0272 a0001c0001t0002g0066 a0001c0001t0010g0065 |
3 | HG02965.hp1 HG03098.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-24+1425C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843591 | |||||||
| chr13:51843718 | C | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG01074.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-24+1298G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843718 | |||||||
| chr13:51843802 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-24+1214A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843802 | |||||||
| chr13:51843814 | T | C | 5 | a0001c0001t0002g0066 a0001c0001t0003g0198 a0001c0001t0003g0199 others(2): Show |
6 | HG01975.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+1202A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843814 | |||||||
| chr13:51843834 | G | A | 22 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0002g0056 others(19): Show |
31 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-24+1182C>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843834 | |||||||
| chr13:51843870 | G | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG01074.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-24+1146C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843870 | |||||||
| chr13:51843928 | G | C | 1 | a0004c0005t0035g0202 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-24+1088C>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51843928 | |||||||
| chr13:51844036 | C | A | 2 | a0001c0001t0002g0066 a0001c0001t0010g0065 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-24+980G>T | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844036 | |||||||
| chr13:51844080 | T | C | 8 | a0001c0001t0001g0026 a0001c0001t0002g0147 a0001c0001t0005g0010 others(5): Show |
14 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-24+936A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844080 | |||||||
| chr13:51844108 | T | C | 2 | a0001c0001t0002g0007 a0001c0001t0002g0273 |
6 | HG02071.hp1 HG02135.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24+908A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844108 | |||||||
| chr13:51844130 | A | G | 111 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0028 others(108): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.-24+886T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844130 | |||||||
| chr13:51844199 | A | AACATATA others(39): Show |
1 | a0001c0002t0011g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-24+816_-24+817ins others(46): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844199 | |||||||
| chr13:51844203 | T | TATATATA others(37): Show |
2 | a0001c0001t0003g0304 a0001c0001t0008g0284 |
2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-24+812_-24+813ins others(44): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844203 | |||||||
| chr13:51844203 | T | TATATATA others(35): Show |
84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0022 others(81): Show |
131 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.-24+771_-24+812dup others(42): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844203 | |||||||
| chr13:51844203 | T | TATATATA others(77): Show |
7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0002g0278 others(4): Show |
8 | HG01167.hp2 HG02280.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.-24+812_-24+813ins others(84): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844203 | |||||||
| chr13:51844203 | T | TATATATA others(119): Show |
4 | a0001c0001t0001g0280 a0001c0001t0001g0282 a0001c0001t0001g0283 others(1): Show |
4 | HG03490.hp2 HG03831.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+812_-24+813ins others(126): Show |
TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844203 | |||||||
| chr13:51844248 | A | G | 2 | a0001c0001t0002g0066 a0001c0001t0010g0065 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-24+768T>C | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844248 | |||||||
| chr13:51844462 | T | C | 26 | a0001c0001t0001g0300 a0001c0001t0001g0302 a0001c0001t0002g0056 others(23): Show |
39 | HG00323.hp1 HG00597.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.-24+554A>G | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844462 | |||||||
| chr13:51844482 | C | T | 3 | a0001c0001t0007g0064 a0001c0001t0043g0063 a0001c0001t0052g0062 |
3 | HG02109.hp2 HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-24+534G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844482 | |||||||
| chr13:51844665 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0005g0010 a0001c0001t0005g0060 others(3): Show |
12 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-24+351G>A | TMEM272 | ENSG00000281106.4 | transcript | ENST00000629372.3 | protein_coding | 1/4 | chr13 | 51844665 |