Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55161 |
| ensemblid | ENSG00000109133.14 |
| hgncid | 25541 |
| symbol | TMEM33 |
| name | transmembrane protein 33 |
| refseq_nuc | NM_018126.3 |
| refseq_prot | NP_060596.2 |
| ensembl_nuc | ENST00000504986.6 |
| ensembl_prot | ENSP00000422473.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 41935429 |
| end | 41960803 |
| strand | + |
| ver | v1.2 |
| region | chr4:41935429-41960803 |
| region5000 | chr4:41930429-41965803 |
| regionname0 | TMEM33_chr4_41935429_41960803 |
| regionname5000 | TMEM33_chr4_41930429_41965803 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 247 | 196 | 84 | 46 | 29 | 6 | 29 | 19 | TMEM33_chr4_41930429_41965803 | TMEM33 | MADTT others(242): Show |
chr4 | 41930429 | 41965803 |
| a0002 | 0/0 | 247 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | MADTT others(242): Show |
chr4 | 41930429 | 41965803 |
| a0003 | 0/0 | 247 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | MADTT others(242): Show |
chr4 | 41930429 | 41965803 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 741 | 193 | 82 | 46 | 29 | 6 | 28 | TMEM33_chr4_41930429_41965803 | TMEM33 | ATGGC others(736): Show |
chr4 | 41930429 | 41965803 | ||
| a0001c0002 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | ATGGC others(736): Show |
chr4 | 41930429 | 41965803 | ||
| a0001c0005 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | ATGGC others(736): Show |
chr4 | 41930429 | 41965803 | ||
| a0001c0006 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | ATGGC others(736): Show |
chr4 | 41930429 | 41965803 | ||
| a0002c0004 | 0/0 | 741 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | ATGGC others(736): Show |
chr4 | 41930429 | 41965803 | ||
| a0003c0003 | 0/0 | 741 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | ATGGC others(736): Show |
chr4 | 41930429 | 41965803 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7405 | 65 | 7 | 21 | 19 | 3 | 14 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0002 | 0/0 | 7405 | 24 | 19 | 3 | 0 | 0 | 2 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0003 | 0/0 | 7406 | 18 | 9 | 6 | 1 | 1 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7401): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0004 | 0/0 | 7407 | 17 | 1 | 5 | 5 | 0 | 6 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0005 | 0/0 | 7407 | 12 | 12 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0006 | 0/0 | 7405 | 10 | 9 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0007 | 1/0 | 7404 | 6 | 5 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7399): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0008 | 0/0 | 7406 | 6 | 0 | 4 | 0 | 0 | 2 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7401): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0009 | 0/0 | 7407 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0010 | 0/0 | 7408 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7403): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0011 | 0/0 | 7405 | 3 | 0 | 2 | 0 | 1 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0012 | 0/0 | 7407 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0013 | 0/0 | 7402 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7397): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0014 | 0/0 | 7405 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0015 | 0/0 | 7417 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7412): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0016 | 0/0 | 7405 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0017 | 0/0 | 6921 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(6916): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0018 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(6917): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0019 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(6917): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0020 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0021 | 0/0 | 7408 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7403): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0022 | 0/0 | 7406 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7401): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0024 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0026 | 0/0 | 7405 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0027 | 0/0 | 7404 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7399): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0028 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0029 | 0/0 | 7405 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0030 | 0/0 | 7405 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0031 | 0/0 | 7406 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7401): Show |
chr4 | 41930429 | 41965803 |
| a0001c0001t0032 | 0/0 | 7405 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| a0001c0002t0023 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0005t0033 | 0/0 | 7407 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0001c0006t0012 | 0/0 | 7407 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7402): Show |
chr4 | 41930429 | 41965803 |
| a0002c0004t0025 | 0/0 | 7406 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7401): Show |
chr4 | 41930429 | 41965803 |
| a0003c0003t0001 | 0/0 | 7405 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | CTCCC others(7400): Show |
chr4 | 41930429 | 41965803 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 22 | 1 | 5 | 7 | 2 | 7 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0011 | 0/1 | 4 | 0 | 2 | 0 | 1 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0002 | 0/0 | 10 | 8 | 1 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0005g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0006g0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0006g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0007g0050 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0008g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0009g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0010g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0011g0008 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0012g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0012g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0013g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0014g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0015g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0015g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0016g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0017g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0018g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0019g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0021g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0022g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0024g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0026g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0027g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0028g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0029g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0030g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0031g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0002t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0005t0033g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0001c0006t0012g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0002c0004t0025g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0011 | g0008 | EUR | FIN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00642 | hp1 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | CHS | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00738 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01069 | hp1 | a0001 | c0001 | t0026 | g0010 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0008 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01081 | hp1 | a0001 | c0001 | t0011 | g0008 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01081 | hp2 | a0001 | c0001 | t0016 | g0041 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0010 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0007 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01257 | hp1 | a0001 | c0001 | t0008 | g0010 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0073 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0091 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0070 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02074 | hp2 | a0001 | c0001 | t0015 | g0032 | EAS | KHV | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02145 | hp2 | a0001 | c0001 | t0014 | g0023 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02572 | hp1 | a0001 | c0001 | t0019 | g0014 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02615 | hp1 | a0001 | c0001 | t0024 | g0088 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0021 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0038 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02723 | hp2 | a0001 | c0002 | t0023 | g0049 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02735 | hp2 | a0001 | c0006 | t0012 | g0035 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02738 | hp1 | a0001 | c0001 | t0031 | g0080 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0002 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0014 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0023 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02976 | hp2 | a0001 | c0001 | t0021 | g0021 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03017 | hp1 | a0001 | c0001 | t0012 | g0034 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | GWD | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03139 | hp1 | a0001 | c0001 | t0018 | g0014 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | ESN | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0029 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03225 | hp2 | a0001 | c0005 | t0033 | g0033 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03453 | hp2 | a0001 | c0001 | t0027 | g0030 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0063 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03492 | hp1 | a0001 | c0001 | t0030 | g0009 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0010 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04115 | hp2 | a0002 | c0004 | t0025 | g0092 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0079 | SAS | BEB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | BEB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0007 | AFR | YRI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | YRI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0087 | AFR | YRI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18948 | hp1 | a0001 | c0001 | t0032 | g0001 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18950 | hp1 | a0001 | c0001 | t0015 | g0019 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0029 | AFR | LWK | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | LWK | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19084 | hp2 | a0001 | c0001 | t0029 | g0009 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | YRI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA20805 | hp2 | a0001 | c0001 | t0022 | g0017 | EUR | TSI | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA20905 | hp1 | a0001 | c0001 | t0008 | g0090 | SAS | GIH | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01123 | hp1 | a0001 | c0001 | t0012 | g0019 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | MSL | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG06807 | hp1 | a0001 | c0001 | t0028 | g0030 | AFR | USA | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | USA | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | USA | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | USA | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | LWK | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0011 | REF | REF | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0050 | REF | REF | TMEM33_chr4_41930429_41965803 | TMEM33 | chr4 | 41930429 | 41965803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:41938630 | C | T | 1 | a0002 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.74C>T | p.Thr25Met | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 2/7 | 130/7404 | 74/744 | 25/247 | chr4 | 41938630 | |||
| chr4:41944806 | A | G | 1 | a0003 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.410A>G | p.Asn137Ser | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/7 | 466/7404 | 410/744 | 137/247 | chr4 | 41944806 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:41935499 | C | T | 1 | a0001c0006 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.15C>T | p.Thr5Thr | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/7 | 71/7404 | 15/744 | 5/247 | chr4 | 41935499 | |||
| chr4:41938604 | A | G | 1 | a0001c0005 | 1 | HG03225.hp2 | splice_region_variant&synonymous_variant | LOW | c.48A>G | p.Gln16Gln | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 2/7 | 104/7404 | 48/744 | 16/247 | chr4 | 41938604 | |||
| chr4:41943796 | T | C | 1 | a0001c0002 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.378T>C | p.Tyr126Tyr | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 4/7 | 434/7404 | 378/744 | 126/247 | chr4 | 41943796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:41935441 | C | T | 4 | a0001c0001t0012 a0001c0001t0015 a0001c0005t0033 others(1): Show |
6 | HG01123.hp1 HG02074.hp2 HG02735.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-44C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/7 | 44 | chr4 | 41935441 | ||||||
| chr4:41954234 | G | A | 2 | a0001c0001t0003 a0001c0001t0016 |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*35G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 35 | chr4 | 41954234 | ||||||
| chr4:41954238 | T | C | 2 | a0001c0001t0003 a0001c0001t0016 |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*39T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 39 | chr4 | 41954238 | ||||||
| chr4:41954296 | A | G | 2 | a0001c0001t0003 a0001c0001t0016 |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*97A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 97 | chr4 | 41954296 | ||||||
| chr4:41954396 | C | T | 7 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0029 others(4): Show |
72 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*197C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 197 | chr4 | 41954396 | ||||||
| chr4:41954447 | G | A | 10 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 others(7): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*248G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 248 | chr4 | 41954447 | ||||||
| chr4:41954489 | A | G | 1 | a0001c0001t0032 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 290 | chr4 | 41954489 | ||||||
| chr4:41954930 | G | A | 1 | a0001c0001t0006 | 10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*731G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 731 | chr4 | 41954930 | ||||||
| chr4:41955053 | C | T | 1 | a0001c0001t0011 | 3 | HG00280.hp1 HG01074.hp1 HG01081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*854C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 854 | chr4 | 41955053 | ||||||
| chr4:41955222 | T | C | 4 | a0001c0001t0012 a0001c0001t0015 a0001c0005t0033 others(1): Show |
6 | HG01123.hp1 HG02074.hp2 HG02735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1023T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1023 | chr4 | 41955222 | ||||||
| chr4:41955276 | A | C | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077A>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1077 | chr4 | 41955276 | ||||||
| chr4:41955414 | A | G | 10 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 others(7): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1215A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1215 | chr4 | 41955414 | ||||||
| chr4:41955965 | G | C | 8 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 others(5): Show |
13 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1766G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1766 | chr4 | 41955965 | ||||||
| chr4:41955969 | G | GT | 11 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 others(8): Show |
16 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1777dupT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1778 | INFO_REALIGN_3_PRIME | chr4 | 41955969 | |||||
| chr4:41955977 | G | T | 16 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(13): Show |
44 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1778G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1778 | chr4 | 41955977 | ||||||
| chr4:41956000 | CAG | C | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0019 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1804_*1805delAG | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1804 | INFO_REALIGN_3_PRIME | chr4 | 41956000 | |||||
| chr4:41956108 | G | T | 1 | a0001c0001t0010 | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1909G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1909 | chr4 | 41956108 | ||||||
| chr4:41956133 | A | G | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0019 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1934A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 1934 | chr4 | 41956133 | ||||||
| chr4:41956218 | G | C | 3 | a0001c0001t0012 a0001c0001t0015 a0001c0006t0012 |
5 | HG01123.hp1 HG02074.hp2 HG02735.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2019G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 2019 | chr4 | 41956218 | ||||||
| chr4:41956253 | G | A | 1 | a0001c0001t0024 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 2054 | chr4 | 41956253 | ||||||
| chr4:41956355 | C | T | 2 | a0001c0001t0004 a0001c0001t0022 |
18 | HG01074.hp2 HG01106.hp1 HG01109.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2156C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 2156 | chr4 | 41956355 | ||||||
| chr4:41956522 | T | C | 3 | a0001c0001t0008 a0001c0001t0026 a0002c0004t0025 |
8 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2323T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 2323 | chr4 | 41956522 | ||||||
| chr4:41956982 | T | C | 1 | a0002c0004t0025 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2783T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 2783 | chr4 | 41956982 | ||||||
| chr4:41957176 | G | T | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2977G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 2977 | chr4 | 41957176 | ||||||
| chr4:41957225 | A | T | 3 | a0001c0001t0012 a0001c0001t0015 a0001c0006t0012 |
5 | HG01123.hp1 HG02074.hp2 HG02735.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3026A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3026 | chr4 | 41957225 | ||||||
| chr4:41957267 | G | GT | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(10): Show |
131 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*3085dupT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3086 | INFO_REALIGN_3_PRIME | chr4 | 41957267 | |||||
| chr4:41957267 | G | GTT | 11 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(8): Show |
35 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*3084_*3085dupTT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3086 | INFO_REALIGN_3_PRIME | chr4 | 41957267 | |||||
| chr4:41957267 | G | GTTT | 7 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0018 others(4): Show |
21 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3083_*3085dupTTT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3086 | INFO_REALIGN_3_PRIME | chr4 | 41957267 | |||||
| chr4:41957611 | T | A | 10 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 others(7): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3412T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3412 | chr4 | 41957611 | ||||||
| chr4:41957728 | T | C | 10 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 others(7): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3529T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3529 | chr4 | 41957728 | ||||||
| chr4:41957734 | C | G | 1 | a0002c0004t0025 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3535C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3535 | chr4 | 41957734 | ||||||
| chr4:41957822 | G | A | 1 | a0001c0001t0010 | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3623G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3623 | chr4 | 41957822 | ||||||
| chr4:41957907 | C | T | 2 | a0001c0001t0008 a0001c0001t0026 |
7 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3708C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3708 | chr4 | 41957907 | ||||||
| chr4:41958117 | A | G | 10 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0015 others(7): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3918A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3918 | chr4 | 41958117 | ||||||
| chr4:41958126 | T | C | 1 | a0001c0001t0029 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3927T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3927 | chr4 | 41958126 | ||||||
| chr4:41958160 | G | A | 2 | a0001c0001t0017 a0001c0001t0018 |
2 | HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3961G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3961 | chr4 | 41958160 | ||||||
| chr4:41958189 | T | A | 1 | a0001c0001t0030 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3990T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 3990 | chr4 | 41958189 | ||||||
| chr4:41958255 | C | G | 3 | a0001c0001t0006 a0001c0001t0014 a0001c0002t0023 |
13 | HG01167.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4056C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4056 | chr4 | 41958255 | ||||||
| chr4:41958324 | T | C | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(16): Show |
57 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*4125T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4125 | chr4 | 41958324 | ||||||
| chr4:41958467 | C | CACCGAAA others(3): Show |
1 | a0001c0001t0015 | 2 | HG02074.hp2 NA18950.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4268_*4269insACCG others(6): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4269 | chr4 | 41958467 | ||||||
| chr4:41958498 | T | G | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0019 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4299T>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4299 | chr4 | 41958498 | ||||||
| chr4:41958499 | C | T | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0019 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4300C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4300 | chr4 | 41958499 | ||||||
| chr4:41958500 | AGATGTGT others(477): Show |
A | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0019 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4302_*4785del | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4302 | chr4 | 41958500 | ||||||
| chr4:41958590 | C | T | 6 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0016 others(3): Show |
34 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4391C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4391 | chr4 | 41958590 | ||||||
| chr4:41958609 | A | T | 2 | a0001c0001t0003 a0001c0001t0016 |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4410A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4410 | chr4 | 41958609 | ||||||
| chr4:41958637 | G | A | 1 | a0001c0001t0010 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4438G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4438 | chr4 | 41958637 | ||||||
| chr4:41958698 | CTCTTTTT others(1): Show |
C | 3 | a0001c0001t0008 a0001c0001t0026 a0002c0004t0025 |
8 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4501_*4508delCTTT others(4): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4501 | INFO_REALIGN_3_PRIME | chr4 | 41958698 | |||||
| chr4:41958700 | C | CT | 6 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(3): Show |
17 | HG01099.hp2 HG01243.hp2 HG01516.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4527dupT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | C | CTTT | 2 | a0001c0001t0005 a0001c0001t0024 |
9 | HG02451.hp2 HG02486.hp2 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4525_*4527dupTTT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | C | CTTTTTTT others(7): Show |
1 | a0001c0005t0033 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4514_*4527dupTTTT others(10): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0015 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4513_*4527dupTTTT others(11): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0012 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4512_*4527dupTTTT others(12): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0015 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4511_*4527dupTTTT others(13): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | C | CTTTTTTT others(11): Show |
1 | a0001c0006t0012 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4510_*4527dupTTTT others(14): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0012 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4507_*4527dupTTTT others(17): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4528 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | CT | C | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 |
11 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4527delT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4527 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4518_*4527delTTTT others(6): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4518 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958700 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4516_*4527delTTTT others(8): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4516 | INFO_REALIGN_3_PRIME | chr4 | 41958700 | |||||
| chr4:41958811 | C | T | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4612C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4612 | chr4 | 41958811 | ||||||
| chr4:41958854 | G | A | 2 | a0001c0001t0005 a0001c0001t0028 |
2 | HG06807.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4655G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4655 | chr4 | 41958854 | ||||||
| chr4:41958986 | G | T | 3 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0019 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4787G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 4787 | chr4 | 41958986 | ||||||
| chr4:41959342 | C | CTA | 3 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0022 |
23 | HG00738.hp2 HG01074.hp2 HG01106.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5148_*5149dupTA | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 5150 | INFO_REALIGN_3_PRIME | chr4 | 41959342 | |||||
| chr4:41959404 | CAA | C | 1 | a0001c0001t0013 | 2 | HG03209.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5206_*5207delAA | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 5206 | chr4 | 41959404 | ||||||
| chr4:41959474 | A | G | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5275A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 5275 | chr4 | 41959474 | ||||||
| chr4:41960248 | G | A | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02622.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6049G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 6049 | chr4 | 41960248 | ||||||
| chr4:41960474 | C | A | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(16): Show |
57 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*6275C>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 7/7 | 6275 | chr4 | 41960474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:41935649 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.45+120G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41935649 | |||||||
| chr4:41935670 | G | C | 15 | a0001c0001t0002g0036 a0001c0001t0010g0020 a0001c0001t0010g0037 others(12): Show |
16 | HG01099.hp2 HG01123.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.45+141G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41935670 | |||||||
| chr4:41935741 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.45+212C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41935741 | |||||||
| chr4:41936357 | A | G | 2 | a0001c0001t0020g0021 a0001c0001t0021g0021 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.45+828A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936357 | |||||||
| chr4:41936437 | G | A | 8 | a0001c0001t0012g0019 a0001c0001t0012g0034 a0001c0001t0015g0019 others(5): Show |
8 | HG01123.hp1 HG02074.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+908G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936437 | |||||||
| chr4:41936469 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.45+940A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936469 | |||||||
| chr4:41936520 | G | A | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(7): Show |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+991G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936520 | |||||||
| chr4:41936543 | AAAAC | A | 36 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(33): Show |
57 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.45+1036_45+1039del others(4): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 41936543 | ||||||
| chr4:41936596 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.45+1067C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936596 | |||||||
| chr4:41936647 | C | G | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+1118C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936647 | |||||||
| chr4:41936655 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.45+1126C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936655 | |||||||
| chr4:41936731 | G | C | 36 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(33): Show |
57 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.45+1202G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936731 | |||||||
| chr4:41936981 | A | G | 6 | a0001c0001t0012g0019 a0001c0001t0012g0034 a0001c0001t0015g0019 others(3): Show |
6 | HG01123.hp1 HG02074.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+1452A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41936981 | |||||||
| chr4:41937043 | A | G | 3 | a0001c0001t0017g0014 a0001c0001t0018g0014 a0001c0001t0019g0014 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.45+1514A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41937043 | |||||||
| chr4:41937055 | A | AT | 15 | a0001c0001t0001g0082 a0001c0001t0002g0081 a0001c0001t0003g0005 others(12): Show |
31 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.46-1532dupT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 41937055 | ||||||
| chr4:41937055 | A | ATT | 5 | a0001c0001t0003g0006 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
9 | HG00673.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-1533_46-1532dup others(2): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 41937055 | ||||||
| chr4:41937103 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-1499T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41937103 | |||||||
| chr4:41937294 | G | T | 2 | a0001c0001t0010g0020 a0001c0001t0010g0038 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.46-1308G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41937294 | |||||||
| chr4:41937412 | C | G | 1 | a0001c0001t0031g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.46-1190C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41937412 | |||||||
| chr4:41937494 | A | AT | 13 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0012g0019 others(10): Show |
13 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.46-1099dupT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr4 | 41937494 | ||||||
| chr4:41937600 | T | C | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(7): Show |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.46-1002T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41937600 | |||||||
| chr4:41937624 | A | T | 1 | a0001c0001t0004g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.46-978A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41937624 | |||||||
| chr4:41937778 | C | A | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-824C>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41937778 | |||||||
| chr4:41938115 | C | A | 42 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(39): Show |
70 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.46-487C>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41938115 | |||||||
| chr4:41938559 | G | A | 36 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(33): Show |
57 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.46-43G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 1/6 | chr4 | 41938559 | |||||||
| chr4:41938750 | A | G | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.140+54A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 2/6 | chr4 | 41938750 | |||||||
| chr4:41938822 | C | T | 1 | a0002c0004t0025g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.140+126C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 2/6 | chr4 | 41938822 | |||||||
| chr4:41938826 | C | A | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.140+130C>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 2/6 | chr4 | 41938826 | |||||||
| chr4:41938961 | A | G | 4 | a0001c0001t0008g0010 a0001c0001t0008g0090 a0001c0001t0008g0091 others(1): Show |
7 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-235A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 2/6 | chr4 | 41938961 | |||||||
| chr4:41939033 | T | TA | 4 | a0001c0001t0008g0010 a0001c0001t0008g0090 a0001c0001t0008g0091 others(1): Show |
7 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-162dupA | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr4 | 41939033 | ||||||
| chr4:41939490 | T | C | 1 | a0002c0004t0025g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.328+107T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41939490 | |||||||
| chr4:41939491 | C | T | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.328+108C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41939491 | |||||||
| chr4:41939720 | G | C | 6 | a0001c0001t0012g0019 a0001c0001t0012g0034 a0001c0001t0015g0019 others(3): Show |
6 | HG01123.hp1 HG02074.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+337G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41939720 | |||||||
| chr4:41939956 | C | T | 1 | a0002c0004t0025g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.328+573C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41939956 | |||||||
| chr4:41940010 | G | A | 1 | a0001c0001t0015g0032 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.328+627G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940010 | |||||||
| chr4:41940045 | T | TC | 7 | a0001c0001t0003g0006 a0001c0001t0003g0039 a0001c0001t0003g0043 others(4): Show |
12 | HG01891.hp1 HG02257.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.328+663dupC | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940045 | ||||||
| chr4:41940046 | C | CCTT | 3 | a0001c0001t0017g0014 a0001c0001t0018g0014 a0001c0001t0019g0014 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.328+663_328+664ins others(3): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940046 | |||||||
| chr4:41940046 | C | CCTTTTTT others(2): Show |
5 | a0001c0001t0006g0047 a0001c0001t0008g0010 a0001c0001t0008g0090 others(2): Show |
8 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.328+663_328+664ins others(9): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940046 | |||||||
| chr4:41940046 | C | CCTTTTTT others(3): Show |
3 | a0001c0001t0006g0007 a0001c0001t0006g0048 a0001c0001t0008g0091 |
7 | HG01167.hp2 HG01981.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+663_328+664ins others(10): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940046 | |||||||
| chr4:41940046 | C | CCTTTTTT others(4): Show |
1 | a0001c0001t0006g0015 | 3 | HG02257.hp2 HG03453.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.328+663_328+664ins others(11): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940046 | |||||||
| chr4:41940046 | C | CCTTTTTT others(6): Show |
1 | a0001c0001t0014g0023 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.328+663_328+664ins others(13): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940046 | |||||||
| chr4:41940046 | C | CCTTTTTT others(15): Show |
1 | a0001c0001t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.328+663_328+664ins others(22): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940046 | |||||||
| chr4:41940046 | C | CCTTTTTT others(17): Show |
1 | a0001c0001t0003g0044 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.328+663_328+664ins others(24): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940046 | |||||||
| chr4:41940046 | C | CT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
52 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.328+687dupT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940046 | ||||||
| chr4:41940046 | C | CTT | 34 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0046 others(31): Show |
55 | HG00738.hp2 HG01074.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.328+686_328+687dup others(2): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940046 | ||||||
| chr4:41940046 | C | CTTT | 6 | a0001c0001t0002g0013 a0001c0001t0004g0077 a0001c0001t0004g0078 others(3): Show |
9 | HG01109.hp2 HG01175.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.328+685_328+687dup others(3): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940046 | ||||||
| chr4:41940046 | CT | C | 5 | a0001c0001t0005g0087 a0001c0001t0012g0034 a0001c0001t0027g0030 others(2): Show |
5 | HG03017.hp1 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.328+687delT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940046 | ||||||
| chr4:41940046 | CTTTTT | C | 4 | a0001c0001t0003g0005 a0001c0001t0003g0022 a0001c0001t0003g0042 others(1): Show |
9 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.328+683_328+687del others(5): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940046 | ||||||
| chr4:41940047 | T | C | 7 | a0001c0001t0005g0004 a0001c0001t0005g0018 a0001c0001t0012g0019 others(4): Show |
15 | HG01123.hp1 HG01884.hp1 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.328+664T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940047 | |||||||
| chr4:41940048 | T | C | 5 | a0001c0001t0005g0087 a0001c0001t0012g0034 a0001c0001t0027g0030 others(2): Show |
5 | HG03017.hp1 HG03225.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.328+665T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940048 | |||||||
| chr4:41940052 | T | C | 4 | a0001c0001t0003g0005 a0001c0001t0003g0022 a0001c0001t0003g0042 others(1): Show |
9 | HG00735.hp1 HG00738.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.328+669T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940052 | |||||||
| chr4:41940317 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.328+934T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940317 | |||||||
| chr4:41940391 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.328+1008G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940391 | |||||||
| chr4:41940542 | C | T | 1 | a0001c0001t0010g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328+1159C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940542 | |||||||
| chr4:41940701 | C | T | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(7): Show |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.328+1318C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41940701 | |||||||
| chr4:41940807 | C | CA | 22 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0067 others(19): Show |
37 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.328+1447dupA | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940807 | ||||||
| chr4:41940807 | C | CAA | 10 | a0001c0001t0003g0039 a0001c0001t0003g0042 a0001c0001t0005g0004 others(7): Show |
16 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.328+1446_328+1447d others(4): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41940807 | ||||||
| chr4:41941020 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.328+1637A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41941020 | |||||||
| chr4:41941084 | T | A | 6 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(3): Show |
7 | HG02572.hp1 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.328+1701T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41941084 | |||||||
| chr4:41941301 | G | T | 1 | a0001c0002t0023g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.328+1918G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41941301 | |||||||
| chr4:41941540 | G | A | 3 | a0001c0001t0004g0026 a0001c0001t0004g0069 a0001c0001t0004g0077 |
4 | HG01106.hp1 HG01175.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+2157G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41941540 | |||||||
| chr4:41941737 | A | G | 1 | a0001c0001t0005g0018 | 3 | HG01884.hp1 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.329-2010A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41941737 | |||||||
| chr4:41941863 | T | C | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.329-1884T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41941863 | |||||||
| chr4:41941972 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG00621.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.329-1775C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41941972 | |||||||
| chr4:41942007 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-1740T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942007 | |||||||
| chr4:41942259 | A | T | 2 | a0001c0001t0020g0021 a0001c0001t0021g0021 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.329-1488A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942259 | |||||||
| chr4:41942369 | A | G | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(7): Show |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.329-1378A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942369 | |||||||
| chr4:41942370 | T | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0081 a0001c0001t0002g0084 others(1): Show |
5 | HG01255.hp1 HG02723.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.329-1377T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942370 | |||||||
| chr4:41942406 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.329-1341A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942406 | |||||||
| chr4:41942427 | A | G | 1 | a0001c0001t0014g0023 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.329-1320A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942427 | |||||||
| chr4:41942455 | A | G | 3 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.329-1292A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942455 | |||||||
| chr4:41942651 | AT | A | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(7): Show |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.329-1084delT | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41942651 | ||||||
| chr4:41942651 | ATT | A | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.329-1085_329-1084d others(4): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41942651 | ||||||
| chr4:41942944 | G | A | 1 | a0002c0004t0025g0092 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.329-803G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942944 | |||||||
| chr4:41942970 | G | T | 1 | a0001c0001t0002g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329-777G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41942970 | |||||||
| chr4:41943042 | A | G | 22 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(19): Show |
42 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.329-705A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943042 | |||||||
| chr4:41943109 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.329-638A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943109 | |||||||
| chr4:41943253 | A | G | 42 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(39): Show |
70 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.329-494A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943253 | |||||||
| chr4:41943275 | A | G | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.329-472A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943275 | |||||||
| chr4:41943323 | G | A | 1 | a0001c0005t0033g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.329-424G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943323 | |||||||
| chr4:41943498 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.329-249C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943498 | |||||||
| chr4:41943520 | T | C | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.329-227T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943520 | |||||||
| chr4:41943525 | C | CA | 44 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0051 others(41): Show |
74 | HG00621.hp2 HG00642.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.329-210dupA | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr4 | 41943525 | ||||||
| chr4:41943584 | G | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0054 |
4 | HG00280.hp2 HG01069.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-163G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943584 | |||||||
| chr4:41943620 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.329-127A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 3/6 | chr4 | 41943620 | |||||||
| chr4:41943996 | A | G | 6 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(3): Show |
13 | HG01167.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.396+182A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 4/6 | chr4 | 41943996 | |||||||
| chr4:41944075 | A | T | 36 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(33): Show |
57 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.396+261A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 4/6 | chr4 | 41944075 | |||||||
| chr4:41944228 | T | C | 1 | a0001c0001t0014g0023 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.396+414T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 4/6 | chr4 | 41944228 | |||||||
| chr4:41944635 | A | G | 4 | a0001c0001t0005g0004 a0001c0001t0005g0018 a0001c0001t0005g0089 others(1): Show |
12 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.397-158A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 4/6 | chr4 | 41944635 | |||||||
| chr4:41945113 | G | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(3): Show |
13 | HG01167.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+187G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945113 | |||||||
| chr4:41945114 | A | G | 6 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(3): Show |
13 | HG01167.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+188A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945114 | |||||||
| chr4:41945119 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(3): Show |
13 | HG01167.hp2 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.530+193G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945119 | |||||||
| chr4:41945285 | C | G | 3 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.530+359C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945285 | |||||||
| chr4:41945400 | T | A | 2 | a0001c0001t0010g0020 a0001c0001t0010g0038 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.530+474T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945400 | |||||||
| chr4:41945400 | T | C | 12 | a0001c0001t0010g0037 a0001c0001t0012g0019 a0001c0001t0012g0034 others(9): Show |
12 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.530+474T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945400 | |||||||
| chr4:41945547 | A | G | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+621A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945547 | |||||||
| chr4:41945575 | T | C | 5 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(2): Show |
11 | HG01167.hp2 HG02257.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.530+649T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945575 | |||||||
| chr4:41945695 | G | A | 2 | a0001c0001t0020g0021 a0001c0001t0021g0021 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.530+769G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945695 | |||||||
| chr4:41945906 | A | G | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+980A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945906 | |||||||
| chr4:41945973 | CA | C | 67 | a0001c0001t0001g0031 a0001c0001t0002g0002 a0001c0001t0002g0013 others(64): Show |
112 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(109): Show |
intron_variant | MODIFIER | c.530+1065delA | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 41945973 | ||||||
| chr4:41945993 | A | G | 11 | a0001c0001t0008g0010 a0001c0001t0008g0090 a0001c0001t0008g0091 others(8): Show |
14 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.530+1067A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945993 | |||||||
| chr4:41945997 | G | C | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(7): Show |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+1071G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41945997 | |||||||
| chr4:41946016 | T | C | 4 | a0001c0001t0003g0006 a0001c0001t0003g0039 a0001c0001t0003g0043 others(1): Show |
8 | HG00673.hp2 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.530+1090T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946016 | |||||||
| chr4:41946047 | T | A | 6 | a0001c0001t0012g0019 a0001c0001t0012g0034 a0001c0001t0015g0019 others(3): Show |
6 | HG01123.hp1 HG02074.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+1121T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946047 | |||||||
| chr4:41946200 | G | A | 1 | a0001c0001t0004g0072 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.530+1274G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946200 | |||||||
| chr4:41946202 | C | T | 1 | a0001c0001t0010g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.530+1276C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946202 | |||||||
| chr4:41946256 | G | A | 10 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(7): Show |
19 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.530+1330G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946256 | |||||||
| chr4:41946539 | A | G | 1 | a0001c0006t0012g0035 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.530+1613A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946539 | |||||||
| chr4:41946616 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.530+1690C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946616 | |||||||
| chr4:41946821 | G | A | 42 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(39): Show |
70 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.530+1895G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41946821 | |||||||
| chr4:41947016 | G | T | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.530+2090G>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947016 | |||||||
| chr4:41947234 | CA | C | 27 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0039 others(24): Show |
44 | HG00673.hp2 HG00738.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.531-2053delA | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr4 | 41947234 | ||||||
| chr4:41947244 | A | G | 1 | a0003c0003t0001g0061 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.531-2058A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947244 | |||||||
| chr4:41947293 | T | G | 4 | a0001c0001t0004g0017 a0001c0001t0004g0063 a0001c0001t0004g0078 others(1): Show |
5 | HG01109.hp2 HG02698.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.531-2009T>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947293 | |||||||
| chr4:41947311 | C | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0075 a0001c0001t0007g0083 others(1): Show |
4 | HG03041.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-1991C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947311 | |||||||
| chr4:41947416 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.531-1886C>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947416 | |||||||
| chr4:41947466 | C | A | 1 | a0001c0002t0023g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.531-1836C>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947466 | |||||||
| chr4:41947484 | A | G | 3 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-1818A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947484 | |||||||
| chr4:41947513 | A | G | 42 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(39): Show |
70 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.531-1789A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947513 | |||||||
| chr4:41947649 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.531-1653A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41947649 | |||||||
| chr4:41948310 | A | G | 3 | a0001c0001t0017g0014 a0001c0001t0018g0014 a0001c0001t0019g0014 |
3 | HG02572.hp1 HG02896.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.531-992A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948310 | |||||||
| chr4:41948363 | T | A | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.531-939T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948363 | |||||||
| chr4:41948367 | T | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-935T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948367 | |||||||
| chr4:41948438 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.531-864T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948438 | |||||||
| chr4:41948472 | A | T | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.531-830A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948472 | |||||||
| chr4:41948481 | G | A | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.531-821G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948481 | |||||||
| chr4:41948591 | T | C | 2 | a0001c0001t0009g0070 a0001c0001t0009g0073 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.531-711T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948591 | |||||||
| chr4:41948672 | A | G | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.531-630A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948672 | |||||||
| chr4:41948799 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.531-503T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948799 | |||||||
| chr4:41948939 | T | C | 6 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(3): Show |
7 | HG02572.hp1 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.531-363T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41948939 | |||||||
| chr4:41949233 | T | C | 36 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(33): Show |
57 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.531-69T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41949233 | |||||||
| chr4:41949267 | T | G | 3 | a0001c0001t0005g0087 a0001c0001t0027g0030 a0001c0001t0028g0030 |
3 | HG03453.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.531-35T>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41949267 | |||||||
| chr4:41949281 | G | A | 1 | a0001c0001t0014g0023 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.531-21G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 5/6 | chr4 | 41949281 | |||||||
| chr4:41949452 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.614+67A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41949452 | |||||||
| chr4:41949535 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.614+150T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41949535 | |||||||
| chr4:41949777 | A | G | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.614+392A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41949777 | |||||||
| chr4:41950857 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.614+1472A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41950857 | |||||||
| chr4:41951011 | T | A | 1 | a0001c0001t0001g0012 | 4 | HG02074.hp1 NA18941.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.614+1626T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951011 | |||||||
| chr4:41951062 | C | T | 4 | a0001c0001t0008g0010 a0001c0001t0008g0090 a0001c0001t0008g0091 others(1): Show |
7 | HG00642.hp1 HG01069.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.614+1677C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951062 | |||||||
| chr4:41951064 | CTT | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
71 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.614+1685_614+1686d others(4): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 41951064 | ||||||
| chr4:41951125 | G | A | 19 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(16): Show |
39 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.614+1740G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951125 | |||||||
| chr4:41951198 | C | G | 1 | a0001c0001t0006g0048 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.614+1813C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951198 | |||||||
| chr4:41951259 | T | C | 14 | a0001c0001t0010g0020 a0001c0001t0010g0037 a0001c0001t0010g0038 others(11): Show |
15 | HG01123.hp1 HG02074.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.614+1874T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951259 | |||||||
| chr4:41951262 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0028 |
4 | HG03017.hp2 HG03688.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.614+1877T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951262 | |||||||
| chr4:41951440 | C | A | 1 | a0001c0001t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.614+2055C>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951440 | |||||||
| chr4:41951465 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.614+2080C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951465 | |||||||
| chr4:41951527 | C | T | 1 | a0001c0001t0005g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.614+2142C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951527 | |||||||
| chr4:41951589 | G | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.614+2204G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951589 | |||||||
| chr4:41951646 | A | G | 1 | a0001c0006t0012g0035 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.614+2261A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951646 | |||||||
| chr4:41951753 | C | T | 2 | a0001c0001t0020g0021 a0001c0001t0021g0021 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.615-2317C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951753 | |||||||
| chr4:41951788 | C | G | 1 | a0001c0001t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.615-2282C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951788 | |||||||
| chr4:41951858 | T | C | 1 | a0001c0001t0031g0080 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.615-2212T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41951858 | |||||||
| chr4:41952073 | A | C | 1 | a0001c0001t0010g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.615-1997A>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41952073 | |||||||
| chr4:41952157 | A | G | 42 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(39): Show |
70 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.615-1913A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41952157 | |||||||
| chr4:41952256 | C | T | 1 | a0001c0002t0023g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.615-1814C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41952256 | |||||||
| chr4:41952275 | A | T | 1 | a0001c0001t0010g0037 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.615-1795A>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41952275 | |||||||
| chr4:41952941 | C | T | 1 | a0001c0001t0003g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.615-1129C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41952941 | |||||||
| chr4:41953057 | T | A | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.615-1013T>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953057 | |||||||
| chr4:41953168 | A | G | 1 | a0001c0002t0023g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.615-902A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953168 | |||||||
| chr4:41953231 | T | C | 42 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(39): Show |
70 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.615-839T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953231 | |||||||
| chr4:41953241 | G | A | 2 | a0001c0001t0020g0021 a0001c0001t0021g0021 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.615-829G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953241 | |||||||
| chr4:41953261 | A | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.615-809A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953261 | |||||||
| chr4:41953280 | C | G | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.615-790C>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953280 | |||||||
| chr4:41953342 | G | C | 1 | a0001c0005t0033g0033 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.615-728G>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953342 | |||||||
| chr4:41953386 | C | T | 7 | a0001c0001t0005g0004 a0001c0001t0005g0018 a0001c0001t0005g0087 others(4): Show |
15 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.615-684C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953386 | |||||||
| chr4:41953475 | C | T | 2 | a0001c0001t0010g0020 a0001c0001t0010g0038 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.615-595C>T | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953475 | |||||||
| chr4:41953502 | A | G | 3 | a0001c0001t0005g0087 a0001c0001t0027g0030 a0001c0001t0028g0030 |
3 | HG03453.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.615-568A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953502 | |||||||
| chr4:41953627 | T | G | 2 | a0001c0001t0020g0021 a0001c0001t0021g0021 |
2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.615-443T>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953627 | |||||||
| chr4:41953652 | T | C | 4 | a0001c0001t0006g0007 a0001c0001t0006g0015 a0001c0001t0006g0047 others(1): Show |
10 | HG01167.hp2 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.615-418T>C | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953652 | |||||||
| chr4:41953666 | G | A | 22 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0022 others(19): Show |
42 | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.615-404G>A | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953666 | |||||||
| chr4:41953957 | A | G | 1 | a0001c0001t0008g0090 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.615-113A>G | TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | chr4 | 41953957 | |||||||
| chr4:41953964 | CTTCAAT | C | 1 | a0001c0001t0014g0023 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.615-103_615-98delC others(5): Show |
TMEM33 | ENSG00000109133.14 | transcript | ENST00000504986.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr4 | 41953964 |