Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130733 |
| ensemblid | ENSG00000152154.12 |
| hgncid | 28517 |
| symbol | TMEM178A |
| name | transmembrane protein 178A |
| refseq_nuc | NM_152390.3 |
| refseq_prot | NP_689603.2 |
| ensembl_nuc | ENST00000281961.3 |
| ensembl_prot | ENSP00000281961.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 39665917 |
| end | 39717963 |
| strand | + |
| ver | v1.2 |
| region | chr2:39665917-39717963 |
| region5000 | chr2:39660917-39722963 |
| regionname0 | TMEM178A_chr2_39665917_39717963 |
| regionname5000 | TMEM178A_chr2_39660917_39722963 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 297 | 295 | 88 | 60 | 108 | 6 | 31 | 84 | TMEM178A_chr2_39660917_39722963 | TMEM178A | MEPRA others(292): Show |
chr2 | 39660917 | 39722963 |
| a0002 | 0/0 | 297 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | MEPRA others(292): Show |
chr2 | 39660917 | 39722963 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 891 | 293 | 87 | 60 | 107 | 6 | 31 | TMEM178A_chr2_39660917_39722963 | TMEM178A | ATGGA others(886): Show |
chr2 | 39660917 | 39722963 | ||
| a0001c0003 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | ATGGA others(886): Show |
chr2 | 39660917 | 39722963 | ||
| a0001c0004 | 0/0 | 891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | ATGGA others(886): Show |
chr2 | 39660917 | 39722963 | ||
| a0002c0002 | 0/0 | 891 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | ATGGA others(886): Show |
chr2 | 39660917 | 39722963 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1664 | 280 | 79 | 59 | 103 | 6 | 31 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1659): Show |
chr2 | 39660917 | 39722963 |
| a0001c0001t0002 | 0/0 | 1665 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1660): Show |
chr2 | 39660917 | 39722963 |
| a0001c0001t0003 | 0/0 | 1664 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1659): Show |
chr2 | 39660917 | 39722963 |
| a0001c0001t0004 | 0/0 | 1664 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1659): Show |
chr2 | 39660917 | 39722963 |
| a0001c0001t0005 | 0/0 | 1664 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1659): Show |
chr2 | 39660917 | 39722963 |
| a0001c0001t0006 | 0/0 | 1667 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1662): Show |
chr2 | 39660917 | 39722963 |
| a0001c0001t0007 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1660): Show |
chr2 | 39660917 | 39722963 |
| a0001c0003t0001 | 0/0 | 1664 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1659): Show |
chr2 | 39660917 | 39722963 |
| a0001c0004t0001 | 0/0 | 1664 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1659): Show |
chr2 | 39660917 | 39722963 |
| a0002c0002t0001 | 0/0 | 1664 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | GCATT others(1659): Show |
chr2 | 39660917 | 39722963 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0019 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | FIN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0088 | AFR | YRI | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18963 | hp1 | a0001 | c0004 | t0001 | g0023 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ASW | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | GIH | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | GIH | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | USA | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | USA | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | USA | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0138 | REF | REF | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0019 | REF | REF | TMEM178A_chr2_39660917_39722963 | TMEM178A | chr2 | 39660917 | 39722963 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39707093 | G | A | 1 | a0002 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.559G>A | p.Val187Ile | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/4 | 617/1664 | 559/894 | 187/297 | chr2 | 39707093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39666364 | C | T | 1 | a0001c0004 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.390C>T | p.Leu130Leu | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/4 | 448/1664 | 390/894 | 130/297 | chr2 | 39666364 | |||
| chr2:39707086 | C | T | 1 | a0001c0003 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.552C>T | p.Ala184Ala | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/4 | 610/1664 | 552/894 | 184/297 | chr2 | 39707086 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39717283 | C | T | 1 | a0001c0001t0007 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*32C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 32 | chr2 | 39717283 | ||||||
| chr2:39717330 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*79C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 79 | chr2 | 39717330 | ||||||
| chr2:39717331 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*80G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 80 | chr2 | 39717331 | ||||||
| chr2:39717332 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*81G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 81 | chr2 | 39717332 | ||||||
| chr2:39717334 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 83 | chr2 | 39717334 | ||||||
| chr2:39717340 | C | A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 89 | chr2 | 39717340 | ||||||
| chr2:39717341 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 90 | chr2 | 39717341 | ||||||
| chr2:39717344 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 93 | chr2 | 39717344 | ||||||
| chr2:39717345 | C | A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*94C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 94 | chr2 | 39717345 | ||||||
| chr2:39717346 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 95 | chr2 | 39717346 | ||||||
| chr2:39717347 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 96 | chr2 | 39717347 | ||||||
| chr2:39717348 | C | A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*97C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 97 | chr2 | 39717348 | ||||||
| chr2:39717349 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*98C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 98 | chr2 | 39717349 | ||||||
| chr2:39717351 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 100 | chr2 | 39717351 | ||||||
| chr2:39717354 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*103G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 103 | chr2 | 39717354 | ||||||
| chr2:39717355 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 104 | chr2 | 39717355 | ||||||
| chr2:39717356 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 105 | chr2 | 39717356 | ||||||
| chr2:39717358 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*107G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 107 | chr2 | 39717358 | ||||||
| chr2:39717359 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*108C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 108 | chr2 | 39717359 | ||||||
| chr2:39717360 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 109 | chr2 | 39717360 | ||||||
| chr2:39717362 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*111G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 111 | chr2 | 39717362 | ||||||
| chr2:39717363 | C | A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 112 | chr2 | 39717363 | ||||||
| chr2:39717364 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 113 | chr2 | 39717364 | ||||||
| chr2:39717365 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 114 | chr2 | 39717365 | ||||||
| chr2:39717369 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*118C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 118 | chr2 | 39717369 | ||||||
| chr2:39717371 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 120 | chr2 | 39717371 | ||||||
| chr2:39717372 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*121G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 121 | chr2 | 39717372 | ||||||
| chr2:39717373 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*122A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 122 | chr2 | 39717373 | ||||||
| chr2:39717376 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*125A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 125 | chr2 | 39717376 | ||||||
| chr2:39717377 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*126C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 126 | chr2 | 39717377 | ||||||
| chr2:39717379 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 128 | chr2 | 39717379 | ||||||
| chr2:39717382 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*131A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 131 | chr2 | 39717382 | ||||||
| chr2:39717383 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*132G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 132 | chr2 | 39717383 | ||||||
| chr2:39717384 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 133 | chr2 | 39717384 | ||||||
| chr2:39717385 | A | ATTGTTTT others(7): Show |
1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134_*135insTTGTTT others(8): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 135 | chr2 | 39717385 | ||||||
| chr2:39717387 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 136 | chr2 | 39717387 | ||||||
| chr2:39717389 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 138 | chr2 | 39717389 | ||||||
| chr2:39717393 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*142C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 142 | chr2 | 39717393 | ||||||
| chr2:39717394 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 143 | chr2 | 39717394 | ||||||
| chr2:39717396 | AACCTCCC others(4): Show |
A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*146_*156delACCTCC others(5): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 146 | chr2 | 39717396 | ||||||
| chr2:39717411 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*160C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 160 | chr2 | 39717411 | ||||||
| chr2:39717417 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*166A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 166 | chr2 | 39717417 | ||||||
| chr2:39717418 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 167 | chr2 | 39717418 | ||||||
| chr2:39717419 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 168 | chr2 | 39717419 | ||||||
| chr2:39717420 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 169 | chr2 | 39717420 | ||||||
| chr2:39717422 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*171A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 171 | chr2 | 39717422 | ||||||
| chr2:39717423 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 172 | chr2 | 39717423 | ||||||
| chr2:39717426 | C | A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 175 | chr2 | 39717426 | ||||||
| chr2:39717428 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 177 | chr2 | 39717428 | ||||||
| chr2:39717430 | G | A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 179 | chr2 | 39717430 | ||||||
| chr2:39717431 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 180 | chr2 | 39717431 | ||||||
| chr2:39717432 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*181A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 181 | chr2 | 39717432 | ||||||
| chr2:39717435 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*184C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 184 | chr2 | 39717435 | ||||||
| chr2:39717437 | A | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 186 | chr2 | 39717437 | ||||||
| chr2:39717438 | G | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 187 | chr2 | 39717438 | ||||||
| chr2:39717440 | G | A | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 189 | chr2 | 39717440 | ||||||
| chr2:39717441 | C | T | 1 | a0001c0001t0006 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*190C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 190 | chr2 | 39717441 | ||||||
| chr2:39717540 | A | G | 1 | a0001c0001t0003 | 2 | NA18946.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*289A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 289 | chr2 | 39717540 | ||||||
| chr2:39717543 | A | G | 1 | a0001c0001t0005 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 292 | chr2 | 39717543 | ||||||
| chr2:39717653 | T | C | 1 | a0001c0001t0004 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 402 | chr2 | 39717653 | ||||||
| chr2:39717781 | G | GT | 2 | a0001c0001t0002 a0001c0001t0007 |
8 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*543dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 4/4 | 544 | INFO_REALIGN_3_PRIME | chr2 | 39717781 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:39666578 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.400+204C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39666578 | |||||||
| chr2:39666645 | T | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0027 others(25): Show |
32 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.400+271T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39666645 | |||||||
| chr2:39666658 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+284C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39666658 | |||||||
| chr2:39666701 | T | A | 1 | a0001c0001t0002g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.400+327T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39666701 | |||||||
| chr2:39666799 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(92): Show |
115 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.400+425C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39666799 | |||||||
| chr2:39666807 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.400+433T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39666807 | |||||||
| chr2:39666861 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.400+487G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39666861 | |||||||
| chr2:39667021 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.400+647A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39667021 | |||||||
| chr2:39667133 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+759A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39667133 | |||||||
| chr2:39667328 | T | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+954T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39667328 | |||||||
| chr2:39667335 | AT | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0040 others(17): Show |
24 | HG00639.hp1 HG01243.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.400+977delT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39667335 | ||||||
| chr2:39667335 | ATT | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(120): Show |
146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.400+976_400+977del others(2): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39667335 | ||||||
| chr2:39667335 | ATTT | A | 11 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(8): Show |
11 | HG00544.hp2 HG02071.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.400+975_400+977del others(3): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39667335 | ||||||
| chr2:39667400 | T | G | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02572.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.400+1026T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39667400 | |||||||
| chr2:39667430 | A | T | 1 | a0001c0001t0001g0157 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.400+1056A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39667430 | |||||||
| chr2:39667450 | T | TA | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
172 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.400+1087dupA | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39667450 | ||||||
| chr2:39667538 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.400+1164C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39667538 | |||||||
| chr2:39667922 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.400+1548A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39667922 | |||||||
| chr2:39668014 | T | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(4): Show |
7 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+1640T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668014 | |||||||
| chr2:39668067 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.400+1693G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668067 | |||||||
| chr2:39668276 | C | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.400+1902C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668276 | |||||||
| chr2:39668292 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.400+1918C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668292 | |||||||
| chr2:39668416 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
150 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.400+2042A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668416 | |||||||
| chr2:39668507 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.400+2133G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668507 | |||||||
| chr2:39668838 | G | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+2464G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668838 | |||||||
| chr2:39668909 | A | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02809.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.400+2535A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39668909 | |||||||
| chr2:39669303 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+2929C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39669303 | |||||||
| chr2:39669341 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02572.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.400+2967G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39669341 | |||||||
| chr2:39669537 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.400+3163A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39669537 | |||||||
| chr2:39669549 | A | T | 1 | a0001c0001t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.400+3175A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39669549 | |||||||
| chr2:39669660 | A | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
175 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.400+3286A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39669660 | |||||||
| chr2:39669979 | T | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
173 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.400+3605T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39669979 | |||||||
| chr2:39669990 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.400+3616C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39669990 | |||||||
| chr2:39670038 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.400+3664G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670038 | |||||||
| chr2:39670117 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.400+3743T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670117 | |||||||
| chr2:39670183 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.400+3809G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670183 | |||||||
| chr2:39670241 | G | A | 2 | a0001c0001t0001g0089 a0001c0003t0001g0088 |
2 | NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.400+3867G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670241 | |||||||
| chr2:39670372 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.400+3998G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670372 | |||||||
| chr2:39670385 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
176 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.400+4011A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670385 | |||||||
| chr2:39670545 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01069.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.400+4171G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670545 | |||||||
| chr2:39670551 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.400+4177G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670551 | |||||||
| chr2:39670849 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(10): Show |
16 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.400+4475T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39670849 | |||||||
| chr2:39671151 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.400+4777T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39671151 | |||||||
| chr2:39671213 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+4839T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39671213 | |||||||
| chr2:39671220 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.400+4846T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39671220 | |||||||
| chr2:39671340 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.400+4966C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39671340 | |||||||
| chr2:39671487 | A | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA18967.hp2 NA18994.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.400+5113A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39671487 | |||||||
| chr2:39671550 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0148 others(2): Show |
5 | HG01496.hp2 HG03017.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+5176G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39671550 | |||||||
| chr2:39671900 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.400+5526G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39671900 | |||||||
| chr2:39672105 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.400+5731T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672105 | |||||||
| chr2:39672225 | C | G | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+5851C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672225 | |||||||
| chr2:39672295 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(109): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.400+5921A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672295 | |||||||
| chr2:39672414 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG02109.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+6040C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672414 | |||||||
| chr2:39672422 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.400+6048T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672422 | |||||||
| chr2:39672495 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+6121A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672495 | |||||||
| chr2:39672531 | A | AT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(9): Show |
16 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.400+6165dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39672531 | ||||||
| chr2:39672700 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.400+6326T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672700 | |||||||
| chr2:39672701 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
10 | HG01928.hp2 HG01993.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.400+6327A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672701 | |||||||
| chr2:39672821 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+6447G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672821 | |||||||
| chr2:39672873 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0183 a0001c0001t0001g0184 |
4 | HG00280.hp2 HG00738.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+6499G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672873 | |||||||
| chr2:39672965 | T | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG02109.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.400+6591T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39672965 | |||||||
| chr2:39673134 | ACCTCAGA others(10): Show |
A | 1 | a0001c0001t0001g0240 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.400+6762_400+6778d others(19): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39673134 | ||||||
| chr2:39673186 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(107): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.400+6812C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673186 | |||||||
| chr2:39673197 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02809.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.400+6823T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673197 | |||||||
| chr2:39673237 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.400+6863G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673237 | |||||||
| chr2:39673260 | T | A | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
14 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(11): Show |
intron_variant | MODIFIER | c.400+6886T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673260 | |||||||
| chr2:39673352 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02809.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.400+6978C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673352 | |||||||
| chr2:39673545 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.400+7171C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673545 | |||||||
| chr2:39673751 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+7377G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673751 | |||||||
| chr2:39673760 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+7386G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673760 | |||||||
| chr2:39673856 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.400+7482C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39673856 | |||||||
| chr2:39674135 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.400+7761A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674135 | |||||||
| chr2:39674278 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG02572.hp2 HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.400+7904C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674278 | |||||||
| chr2:39674428 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+8054G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674428 | |||||||
| chr2:39674442 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.400+8068C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674442 | |||||||
| chr2:39674483 | G | T | 5 | a0001c0001t0001g0034 a0001c0001t0002g0036 a0001c0001t0002g0037 others(2): Show |
5 | HG02970.hp2 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+8109G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674483 | |||||||
| chr2:39674592 | A | T | 20 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(17): Show |
23 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.400+8218A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674592 | |||||||
| chr2:39674606 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(114): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.400+8232A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674606 | |||||||
| chr2:39674749 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+8375A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674749 | |||||||
| chr2:39674800 | T | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0185 others(1): Show |
4 | NA18942.hp2 NA18985.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+8426T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674800 | |||||||
| chr2:39674892 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.400+8518C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674892 | |||||||
| chr2:39674894 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0002g0036 others(4): Show |
7 | HG02622.hp1 HG02970.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+8520C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39674894 | |||||||
| chr2:39675116 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.400+8742C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675116 | |||||||
| chr2:39675294 | C | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
8 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+8920C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675294 | |||||||
| chr2:39675298 | T | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
175 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.400+8924T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675298 | |||||||
| chr2:39675346 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+8972C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675346 | |||||||
| chr2:39675408 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.400+9034T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675408 | |||||||
| chr2:39675415 | G | GCA | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
174 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.400+9042_400+9043d others(4): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39675415 | ||||||
| chr2:39675462 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0187 |
4 | HG01081.hp1 HG01167.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+9088T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675462 | |||||||
| chr2:39675470 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.400+9096C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675470 | |||||||
| chr2:39675488 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.400+9114C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675488 | |||||||
| chr2:39675512 | CCACCGAT others(4): Show |
C | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.400+9139_400+9149d others(13): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675512 | |||||||
| chr2:39675712 | A | AT | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+9348dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39675712 | ||||||
| chr2:39675838 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02109.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+9464G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675838 | |||||||
| chr2:39675897 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.400+9523A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39675897 | |||||||
| chr2:39676034 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(9): Show |
16 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.400+9660C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39676034 | |||||||
| chr2:39676245 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+9871A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39676245 | |||||||
| chr2:39676323 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
176 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.400+9949T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39676323 | |||||||
| chr2:39676436 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+10062A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39676436 | |||||||
| chr2:39676576 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.400+10202G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39676576 | |||||||
| chr2:39676897 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(93): Show |
116 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.400+10523G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39676897 | |||||||
| chr2:39677055 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
196 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.400+10681T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39677055 | |||||||
| chr2:39677147 | C | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+10773C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39677147 | |||||||
| chr2:39677238 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+10864C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39677238 | |||||||
| chr2:39677485 | A | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
27 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.400+11111A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39677485 | |||||||
| chr2:39677499 | A | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
197 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.400+11125A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39677499 | |||||||
| chr2:39677757 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02109.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+11383C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39677757 | |||||||
| chr2:39677963 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.400+11589A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39677963 | |||||||
| chr2:39678046 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+11672G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678046 | |||||||
| chr2:39678086 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.400+11712T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678086 | |||||||
| chr2:39678106 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.400+11732A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678106 | |||||||
| chr2:39678166 | G | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(111): Show |
134 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.400+11792G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678166 | |||||||
| chr2:39678272 | C | G | 23 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): Show |
26 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.400+11898C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678272 | |||||||
| chr2:39678460 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.400+12086C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678460 | |||||||
| chr2:39678518 | A | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(20): Show |
26 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.400+12144A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678518 | |||||||
| chr2:39678670 | G | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(12): Show |
18 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.400+12296G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678670 | |||||||
| chr2:39678716 | A | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
198 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.400+12342A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678716 | |||||||
| chr2:39678726 | T | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
27 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.400+12352T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678726 | |||||||
| chr2:39678883 | C | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
24 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.400+12509C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678883 | |||||||
| chr2:39678890 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0187 |
4 | HG01081.hp1 HG01167.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+12516C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678890 | |||||||
| chr2:39678904 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.400+12530A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39678904 | |||||||
| chr2:39679178 | G | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+12804G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679178 | |||||||
| chr2:39679340 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0058 |
5 | HG02717.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+12966G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679340 | |||||||
| chr2:39679396 | T | TA | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(114): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.400+13031dupA | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39679396 | ||||||
| chr2:39679469 | A | ACTTC | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13095_400+1309 others(8): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679469 | |||||||
| chr2:39679474 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13100A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679474 | |||||||
| chr2:39679476 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13102A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679476 | |||||||
| chr2:39679477 | T | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13103T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679477 | |||||||
| chr2:39679480 | G | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13106G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679480 | |||||||
| chr2:39679481 | T | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13107T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679481 | |||||||
| chr2:39679482 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13108G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679482 | |||||||
| chr2:39679483 | T | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13109T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679483 | |||||||
| chr2:39679485 | T | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13111T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679485 | |||||||
| chr2:39679486 | A | AGAGGC | 3 | a0001c0001t0001g0013 a0001c0001t0001g0049 a0001c0001t0001g0050 |
4 | HG00544.hp1 NA18947.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+13112_400+1311 others(9): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679486 | |||||||
| chr2:39679577 | G | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+13203G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679577 | |||||||
| chr2:39679636 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.400+13262G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679636 | |||||||
| chr2:39679675 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+13301G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679675 | |||||||
| chr2:39679887 | T | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(8): Show |
15 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.400+13513T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679887 | |||||||
| chr2:39679991 | C | T | 1 | a0001c0001t0006g0171 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.400+13617C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39679991 | |||||||
| chr2:39680064 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.400+13690T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680064 | |||||||
| chr2:39680102 | TTACTC | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(9): Show |
16 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.400+13730_400+1373 others(9): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39680102 | ||||||
| chr2:39680295 | A | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG02109.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.400+13921A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680295 | |||||||
| chr2:39680457 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.400+14083G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680457 | |||||||
| chr2:39680476 | A | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02809.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.400+14102A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680476 | |||||||
| chr2:39680541 | T | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.400+14167T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680541 | |||||||
| chr2:39680649 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+14275A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680649 | |||||||
| chr2:39680716 | G | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02109.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+14342G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680716 | |||||||
| chr2:39680754 | C | CT | 24 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
27 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.400+14388dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39680754 | ||||||
| chr2:39680764 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.400+14390T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39680764 | |||||||
| chr2:39680946 | CTTTAA | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
8 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+14581_400+1458 others(9): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39680946 | ||||||
| chr2:39681164 | CTT | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+14792_400+1479 others(6): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39681164 | ||||||
| chr2:39681184 | G | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(95): Show |
118 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.400+14810G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681184 | |||||||
| chr2:39681213 | T | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
19 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.400+14839T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681213 | |||||||
| chr2:39681278 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
194 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.400+14904T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681278 | |||||||
| chr2:39681427 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.400+15053G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681427 | |||||||
| chr2:39681582 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.400+15208T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681582 | |||||||
| chr2:39681726 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.400+15352G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681726 | |||||||
| chr2:39681869 | T | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
19 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.400+15495T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681869 | |||||||
| chr2:39681872 | G | C | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+15498G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681872 | |||||||
| chr2:39681927 | A | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
177 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.400+15553A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681927 | |||||||
| chr2:39681977 | G | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
149 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.400+15603G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681977 | |||||||
| chr2:39681992 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.400+15618T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39681992 | |||||||
| chr2:39682090 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.400+15716T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682090 | |||||||
| chr2:39682091 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0143 |
3 | NA18941.hp1 NA19004.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.400+15717A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682091 | |||||||
| chr2:39682198 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.400+15824G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682198 | |||||||
| chr2:39682301 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.400+15927A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682301 | |||||||
| chr2:39682381 | G | GT | 16 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(13): Show |
19 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.400+16019dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39682381 | ||||||
| chr2:39682381 | GT | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(9): Show |
16 | HG01361.hp2 HG01496.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.400+16019delT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39682381 | ||||||
| chr2:39682394 | A | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
8 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.400+16020A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682394 | |||||||
| chr2:39682447 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
12 | HG01928.hp2 HG01993.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+16073G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682447 | |||||||
| chr2:39682447 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.400+16073G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682447 | |||||||
| chr2:39682504 | T | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
24 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.400+16130T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682504 | |||||||
| chr2:39682548 | A | T | 1 | a0001c0001t0002g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.400+16174A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682548 | |||||||
| chr2:39682594 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.400+16220C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682594 | |||||||
| chr2:39682809 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(123): Show |
150 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.400+16435C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682809 | |||||||
| chr2:39682972 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0002g0036 a0001c0001t0002g0037 others(2): Show |
5 | HG02622.hp1 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+16598C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682972 | |||||||
| chr2:39682985 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0002g0036 a0001c0001t0002g0037 others(2): Show |
5 | HG02622.hp1 HG03195.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+16611C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39682985 | |||||||
| chr2:39683061 | A | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
27 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(24): Show |
intron_variant | MODIFIER | c.400+16687A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39683061 | |||||||
| chr2:39683083 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG00408.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.400+16709G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39683083 | |||||||
| chr2:39683685 | G | A | 9 | a0001c0001t0001g0034 a0001c0001t0001g0045 a0001c0001t0001g0178 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+17311G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39683685 | |||||||
| chr2:39683710 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.400+17336C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39683710 | |||||||
| chr2:39684011 | T | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG01175.hp2 HG01258.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.400+17637T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684011 | |||||||
| chr2:39684074 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.400+17700T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684074 | |||||||
| chr2:39684189 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.400+17815T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684189 | |||||||
| chr2:39684196 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
197 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.400+17822T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684196 | |||||||
| chr2:39684275 | T | A | 1 | a0001c0001t0001g0106 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.400+17901T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684275 | |||||||
| chr2:39684356 | A | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(18): Show |
24 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.400+17982A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684356 | |||||||
| chr2:39684398 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(94): Show |
117 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.400+18024A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684398 | |||||||
| chr2:39684630 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0071 a0001c0001t0001g0238 |
4 | HG02132.hp2 NA18963.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+18256A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684630 | |||||||
| chr2:39684684 | C | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG02109.hp2 HG03041.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+18310C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684684 | |||||||
| chr2:39684795 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.400+18421A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684795 | |||||||
| chr2:39684822 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.400+18448C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684822 | |||||||
| chr2:39684838 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.400+18464C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684838 | |||||||
| chr2:39684895 | C | T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+18521C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684895 | |||||||
| chr2:39684996 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0002g0051 |
2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.400+18622T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39684996 | |||||||
| chr2:39685079 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.400+18705A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685079 | |||||||
| chr2:39685143 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.400+18769A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685143 | |||||||
| chr2:39685298 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.401-18783A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685298 | |||||||
| chr2:39685537 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.401-18544G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685537 | |||||||
| chr2:39685560 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.401-18521A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685560 | |||||||
| chr2:39685925 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-18156C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685925 | |||||||
| chr2:39685928 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.401-18153A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685928 | |||||||
| chr2:39685946 | C | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(9): Show |
16 | HG01361.hp2 HG01496.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.401-18135C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39685946 | |||||||
| chr2:39686056 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-18025G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39686056 | |||||||
| chr2:39686137 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.401-17944T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39686137 | |||||||
| chr2:39686178 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-17903C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39686178 | |||||||
| chr2:39686229 | C | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0142 a0001c0001t0002g0141 |
3 | HG01099.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.401-17852C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39686229 | |||||||
| chr2:39686415 | G | GT | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(15): Show |
21 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(18): Show |
intron_variant | MODIFIER | c.401-17656dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686415 | ||||||
| chr2:39686693 | G | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.401-17388G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39686693 | |||||||
| chr2:39686868 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02809.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.401-17213C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39686868 | |||||||
| chr2:39686916 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-17165G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39686916 | |||||||
| chr2:39686963 | ATG | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0103 others(3): Show |
6 | HG00140.hp2 HG01123.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-17066_401-1706 others(6): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTG | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0014 others(52): Show |
69 | HG00408.hp2 HG00639.hp2 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.401-17068_401-1706 others(8): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTG | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0030 others(17): Show |
22 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.401-17070_401-1706 others(10): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTGT others(1): Show |
A | 34 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0034 others(31): Show |
35 | HG00438.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.401-17072_401-1706 others(12): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTGT others(3): Show |
A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(82): Show |
105 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.401-17074_401-1706 others(14): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTGT others(5): Show |
A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(22): Show |
33 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.401-17076_401-1706 others(16): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTGT others(7): Show |
A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.401-17078_401-1706 others(18): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTGT others(9): Show |
A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG02809.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-17080_401-1706 others(20): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTGT others(11): Show |
A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0142 a0001c0001t0002g0141 |
3 | HG01099.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.401-17082_401-1706 others(22): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39686963 | ATGTGTGT others(13): Show |
A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
5 | HG02109.hp1 HG02559.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-17084_401-1706 others(24): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39686963 | ||||||
| chr2:39687051 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-17030C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687051 | |||||||
| chr2:39687052 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(110): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.401-17029G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687052 | |||||||
| chr2:39687077 | C | A | 6 | a0001c0001t0001g0027 a0001c0001t0002g0036 a0001c0001t0002g0037 others(3): Show |
6 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-17004C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687077 | |||||||
| chr2:39687111 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(9): Show |
16 | HG01361.hp2 HG01496.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.401-16970G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687111 | |||||||
| chr2:39687200 | C | A | 1 | a0001c0001t0001g0202 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.401-16881C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687200 | |||||||
| chr2:39687206 | G | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(31): Show |
41 | HG00738.hp2 HG01361.hp2 HG01496.hp1 others(38): Show |
intron_variant | MODIFIER | c.401-16875G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687206 | |||||||
| chr2:39687365 | C | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0028 others(21): Show |
28 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-16716C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687365 | |||||||
| chr2:39687434 | C | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(12): Show |
18 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.401-16647C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687434 | |||||||
| chr2:39687466 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0109 others(2): Show |
7 | HG02015.hp2 NA18941.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-16615G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687466 | |||||||
| chr2:39687541 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(64): Show |
80 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.401-16540A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687541 | |||||||
| chr2:39687554 | A | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02486.hp2 HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.401-16527A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687554 | |||||||
| chr2:39687675 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.401-16406T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687675 | |||||||
| chr2:39687830 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.401-16251A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687830 | |||||||
| chr2:39687927 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-16154A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687927 | |||||||
| chr2:39687980 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-16101T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39687980 | |||||||
| chr2:39688133 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0039 |
2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.401-15948C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688133 | |||||||
| chr2:39688528 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0028 others(21): Show |
28 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.401-15553G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688528 | |||||||
| chr2:39688657 | T | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
40 | HG00738.hp2 HG01361.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.401-15424T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688657 | |||||||
| chr2:39688667 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.401-15414T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688667 | |||||||
| chr2:39688880 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-15201T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688880 | |||||||
| chr2:39688964 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.401-15117T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688964 | |||||||
| chr2:39688971 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-15110A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688971 | |||||||
| chr2:39688987 | G | A | 1 | a0001c0001t0002g0077 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.401-15094G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39688987 | |||||||
| chr2:39689077 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG01243.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.401-15004A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689077 | |||||||
| chr2:39689104 | A | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
20 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.401-14977A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689104 | |||||||
| chr2:39689141 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.401-14940G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689141 | |||||||
| chr2:39689181 | A | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(1): Show |
4 | HG02809.hp2 HG03453.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-14900A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689181 | |||||||
| chr2:39689191 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-14890A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689191 | |||||||
| chr2:39689201 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.401-14880G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689201 | |||||||
| chr2:39689315 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.401-14766G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689315 | |||||||
| chr2:39689406 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-14675A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689406 | |||||||
| chr2:39689546 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.401-14535T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689546 | |||||||
| chr2:39689892 | G | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
40 | HG00738.hp2 HG01361.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.401-14189G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689892 | |||||||
| chr2:39689910 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(6): Show |
13 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-14171C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689910 | |||||||
| chr2:39689970 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0178 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.401-14111G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39689970 | |||||||
| chr2:39690021 | G | C | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
40 | HG00738.hp2 HG01361.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.401-14060G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690021 | |||||||
| chr2:39690035 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(6): Show |
13 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-14046G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690035 | |||||||
| chr2:39690050 | C | T | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.401-14031C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690050 | |||||||
| chr2:39690075 | A | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0230 |
2 | HG01433.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.401-14006A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690075 | |||||||
| chr2:39690093 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.401-13988A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690093 | |||||||
| chr2:39690343 | C | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(6): Show |
13 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-13738C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690343 | |||||||
| chr2:39690419 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.401-13662A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690419 | |||||||
| chr2:39690435 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(6): Show |
13 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-13646G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690435 | |||||||
| chr2:39690566 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(23): Show |
33 | HG00738.hp2 HG01361.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.401-13515A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690566 | |||||||
| chr2:39690645 | A | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.401-13436A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690645 | |||||||
| chr2:39690688 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-13393C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690688 | |||||||
| chr2:39690955 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.401-13126G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690955 | |||||||
| chr2:39690992 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.401-13089C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39690992 | |||||||
| chr2:39691021 | T | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(6): Show |
13 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-13060T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691021 | |||||||
| chr2:39691059 | G | C | 6 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-13022G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691059 | |||||||
| chr2:39691217 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.401-12864C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691217 | |||||||
| chr2:39691227 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.401-12854C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691227 | |||||||
| chr2:39691302 | G | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-12779G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691302 | |||||||
| chr2:39691389 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.401-12692A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691389 | |||||||
| chr2:39691428 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.401-12653C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691428 | |||||||
| chr2:39691462 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG02818.hp1 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.401-12619G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691462 | |||||||
| chr2:39691632 | T | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
20 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.401-12449T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691632 | |||||||
| chr2:39691775 | A | G | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
203 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.401-12306A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691775 | |||||||
| chr2:39691966 | A | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | HG02109.hp2 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.401-12115A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39691966 | |||||||
| chr2:39692169 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.401-11912A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692169 | |||||||
| chr2:39692534 | T | C | 2 | a0001c0001t0001g0023 a0001c0004t0001g0023 |
2 | NA18945.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.401-11547T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692534 | |||||||
| chr2:39692587 | A | T | 6 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-11494A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692587 | |||||||
| chr2:39692596 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
196 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.401-11485A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692596 | |||||||
| chr2:39692628 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-11453T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692628 | |||||||
| chr2:39692676 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02055.hp1 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-11405G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692676 | |||||||
| chr2:39692686 | G | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.401-11395G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692686 | |||||||
| chr2:39692780 | A | G | 5 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0148 others(2): Show |
5 | HG01496.hp2 HG03017.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-11301A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692780 | |||||||
| chr2:39692790 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
8 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.401-11291C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39692790 | |||||||
| chr2:39693039 | G | T | 1 | a0001c0001t0001g0173 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.401-11042G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693039 | |||||||
| chr2:39693045 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401-11036C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693045 | |||||||
| chr2:39693095 | T | C | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
9 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.401-10986T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693095 | |||||||
| chr2:39693103 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-10978G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693103 | |||||||
| chr2:39693121 | A | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.401-10960A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693121 | |||||||
| chr2:39693162 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.401-10919A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693162 | |||||||
| chr2:39693209 | C | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(16): Show |
22 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.401-10872C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693209 | |||||||
| chr2:39693447 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-10634G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693447 | |||||||
| chr2:39693649 | G | A | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(30): Show |
40 | HG00738.hp2 HG01361.hp2 HG01496.hp1 others(37): Show |
intron_variant | MODIFIER | c.401-10432G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693649 | |||||||
| chr2:39693706 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.401-10375G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693706 | |||||||
| chr2:39693707 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0002g0051 a0001c0001t0002g0077 |
3 | HG02145.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.401-10374A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693707 | |||||||
| chr2:39693803 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(5): Show |
12 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.401-10278C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693803 | |||||||
| chr2:39693878 | T | C | 1 | a0001c0001t0001g0014 | 2 | HG01928.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.401-10203T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693878 | |||||||
| chr2:39693890 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(8): Show |
15 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.401-10191C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39693890 | |||||||
| chr2:39693966 | C | CT | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(7): Show |
14 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.401-10100dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39693966 | ||||||
| chr2:39694004 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-10077A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39694004 | |||||||
| chr2:39694161 | G | GTAA | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
14 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.401-9897_401-9895d others(5): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39694161 | ||||||
| chr2:39694161 | G | GTAATAA | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(98): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.401-9900_401-9895d others(8): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39694161 | ||||||
| chr2:39694161 | G | GTAATAAT others(2): Show |
9 | a0001c0001t0001g0052 a0001c0001t0001g0188 a0001c0001t0001g0198 others(6): Show |
9 | HG00642.hp1 HG01258.hp2 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.401-9903_401-9895d others(11): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39694161 | ||||||
| chr2:39694161 | G | GTAATAAT others(5): Show |
6 | a0001c0001t0001g0027 a0001c0001t0002g0036 a0001c0001t0002g0037 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-9906_401-9895d others(14): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39694161 | ||||||
| chr2:39694161 | G | GTAATAAT others(8): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0159 |
2 | HG02647.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.401-9909_401-9895d others(17): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39694161 | ||||||
| chr2:39694161 | G | GTAATAAT others(11): Show |
1 | a0001c0001t0001g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.401-9912_401-9895d others(20): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39694161 | ||||||
| chr2:39694193 | G | T | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0027 others(34): Show |
41 | HG00738.hp2 HG01106.hp1 HG01361.hp2 others(38): Show |
intron_variant | MODIFIER | c.401-9888G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39694193 | |||||||
| chr2:39694226 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.401-9855A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39694226 | |||||||
| chr2:39694589 | A | G | 16 | a0001c0001t0001g0027 a0001c0001t0001g0083 a0001c0001t0001g0085 others(13): Show |
16 | HG01106.hp1 HG02145.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.401-9492A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39694589 | |||||||
| chr2:39694748 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.401-9333T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39694748 | |||||||
| chr2:39694830 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.401-9251A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39694830 | |||||||
| chr2:39694965 | C | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-9116C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39694965 | |||||||
| chr2:39695171 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.401-8910G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39695171 | |||||||
| chr2:39695417 | T | C | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(12): Show |
18 | HG00738.hp2 HG01928.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.401-8664T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39695417 | |||||||
| chr2:39695501 | A | C | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.401-8580A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39695501 | |||||||
| chr2:39695606 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.401-8475A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39695606 | |||||||
| chr2:39695618 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.401-8463G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39695618 | |||||||
| chr2:39695759 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02647.hp1 HG03195.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.401-8322A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39695759 | |||||||
| chr2:39696340 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-7741A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696340 | |||||||
| chr2:39696542 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-7539G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696542 | |||||||
| chr2:39696750 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-7331A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696750 | |||||||
| chr2:39696912 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02809.hp2 HG03453.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-7169C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696912 | |||||||
| chr2:39696940 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.401-7141C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696940 | |||||||
| chr2:39696973 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.401-7108C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696973 | |||||||
| chr2:39696981 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-7100T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696981 | |||||||
| chr2:39696999 | A | T | 7 | a0001c0001t0001g0027 a0001c0001t0002g0036 a0001c0001t0002g0037 others(4): Show |
7 | HG02145.hp2 HG02622.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-7082A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39696999 | |||||||
| chr2:39697042 | C | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0095 others(3): Show |
6 | HG02647.hp1 HG03041.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-7039C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39697042 | |||||||
| chr2:39697426 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.401-6655T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39697426 | |||||||
| chr2:39697479 | CA | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0053 others(7): Show |
14 | HG01361.hp2 HG01496.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.401-6600delA | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39697479 | ||||||
| chr2:39697509 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.401-6572A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39697509 | |||||||
| chr2:39697601 | C | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0027 others(20): Show |
27 | HG01106.hp1 HG01361.hp2 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.401-6480C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39697601 | |||||||
| chr2:39697917 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.401-6164T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39697917 | |||||||
| chr2:39697944 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0178 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.401-6137C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39697944 | |||||||
| chr2:39698052 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
6 | HG00738.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-6029G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698052 | |||||||
| chr2:39698114 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0002g0026 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.401-5967T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698114 | |||||||
| chr2:39698129 | C | T | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0028 others(27): Show |
34 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.401-5952C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698129 | |||||||
| chr2:39698145 | A | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0052 others(21): Show |
28 | HG01106.hp1 HG01361.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.401-5936A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698145 | |||||||
| chr2:39698152 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.401-5929A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698152 | |||||||
| chr2:39698164 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.401-5917A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698164 | |||||||
| chr2:39698217 | T | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0040 others(7): Show |
14 | HG00544.hp1 HG01243.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.401-5864T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698217 | |||||||
| chr2:39698227 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0142 |
2 | HG01099.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.401-5854G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698227 | |||||||
| chr2:39698260 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0062 others(2): Show |
8 | HG01074.hp1 HG01255.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.401-5821C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698260 | |||||||
| chr2:39698261 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.401-5820G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698261 | |||||||
| chr2:39698264 | T | G | 2 | a0001c0001t0001g0096 a0001c0001t0002g0026 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.401-5817T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698264 | |||||||
| chr2:39698286 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-5795T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698286 | |||||||
| chr2:39698592 | A | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
195 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.401-5489A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698592 | |||||||
| chr2:39698651 | G | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(13): Show |
18 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.401-5430G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698651 | |||||||
| chr2:39698693 | G | T | 27 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
29 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.401-5388G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698693 | |||||||
| chr2:39698694 | C | T | 27 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
29 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.401-5387C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698694 | |||||||
| chr2:39698698 | A | AT | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(90): Show |
111 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.401-5371dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39698698 | ||||||
| chr2:39698698 | AT | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(18): Show |
23 | HG01361.hp2 HG01496.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.401-5371delT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39698698 | ||||||
| chr2:39698798 | T | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0132 |
2 | HG02523.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.401-5283T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698798 | |||||||
| chr2:39698953 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.401-5128T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39698953 | |||||||
| chr2:39699026 | AT | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0062 others(6): Show |
12 | HG01074.hp1 HG01074.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.401-5038delT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39699026 | ||||||
| chr2:39699178 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-4903A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699178 | |||||||
| chr2:39699297 | G | A | 5 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(2): Show |
5 | HG01106.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.401-4784G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699297 | |||||||
| chr2:39699333 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-4748T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699333 | |||||||
| chr2:39699375 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-4706C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699375 | |||||||
| chr2:39699397 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.401-4684G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699397 | |||||||
| chr2:39699398 | T | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02647.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.401-4683T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699398 | |||||||
| chr2:39699534 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.401-4547G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699534 | |||||||
| chr2:39699754 | C | T | 14 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(11): Show |
14 | HG00738.hp2 HG02055.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.401-4327C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699754 | |||||||
| chr2:39699759 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0121 |
2 | NA18946.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.401-4322T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699759 | |||||||
| chr2:39699907 | G | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(7): Show |
10 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.401-4174G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699907 | |||||||
| chr2:39699936 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.401-4145C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39699936 | |||||||
| chr2:39700743 | A | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(13): Show |
18 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.401-3338A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39700743 | |||||||
| chr2:39700826 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-3255T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39700826 | |||||||
| chr2:39700928 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0049 |
3 | NA18947.hp2 NA18970.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.401-3153G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39700928 | |||||||
| chr2:39700994 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0182 others(9): Show |
17 | HG01106.hp2 HG01934.hp2 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.401-3087A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39700994 | |||||||
| chr2:39700995 | C | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(102): Show |
123 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.401-3086C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39700995 | |||||||
| chr2:39701055 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(101): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.401-3026A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701055 | |||||||
| chr2:39701074 | G | GA | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-3000dupA | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39701074 | ||||||
| chr2:39701253 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-2828C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701253 | |||||||
| chr2:39701314 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0141 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.401-2767G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701314 | |||||||
| chr2:39701377 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.401-2704G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701377 | |||||||
| chr2:39701445 | A | G | 4 | a0001c0001t0001g0133 a0001c0001t0001g0166 a0001c0001t0001g0221 others(1): Show |
4 | HG00438.hp2 HG02129.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-2636A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701445 | |||||||
| chr2:39701482 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.401-2599G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701482 | |||||||
| chr2:39701528 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-2553C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701528 | |||||||
| chr2:39701582 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.401-2499A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701582 | |||||||
| chr2:39701632 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-2449T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701632 | |||||||
| chr2:39701705 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.401-2376G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701705 | |||||||
| chr2:39701733 | G | T | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
12 | HG02630.hp2 HG02717.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.401-2348G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701733 | |||||||
| chr2:39701844 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.401-2237C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701844 | |||||||
| chr2:39701858 | T | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
8 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.401-2223T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701858 | |||||||
| chr2:39701959 | T | G | 1 | a0001c0001t0001g0192 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.401-2122T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701959 | |||||||
| chr2:39701969 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.401-2112G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39701969 | |||||||
| chr2:39702063 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.401-2018A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702063 | |||||||
| chr2:39702100 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-1981C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702100 | |||||||
| chr2:39702111 | G | T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG02109.hp2 HG02630.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-1970G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702111 | |||||||
| chr2:39702209 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-1872G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702209 | |||||||
| chr2:39702243 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401-1838A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702243 | |||||||
| chr2:39702440 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.401-1641C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702440 | |||||||
| chr2:39702540 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-1541C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702540 | |||||||
| chr2:39702616 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-1465C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702616 | |||||||
| chr2:39702646 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401-1435C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702646 | |||||||
| chr2:39702671 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-1410A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702671 | |||||||
| chr2:39702674 | TA | T | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(12): Show |
15 | HG01169.hp2 HG02109.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.401-1394delA | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 39702674 | ||||||
| chr2:39702773 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0212 a0001c0001t0001g0226 |
3 | HG03831.hp1 NA18956.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.401-1308G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702773 | |||||||
| chr2:39702784 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.401-1297C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702784 | |||||||
| chr2:39702875 | A | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0062 others(3): Show |
9 | HG01074.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.401-1206A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702875 | |||||||
| chr2:39702985 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.401-1096C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39702985 | |||||||
| chr2:39703001 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.401-1080T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703001 | |||||||
| chr2:39703005 | G | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
12 | HG02109.hp2 HG02630.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.401-1076G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703005 | |||||||
| chr2:39703051 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
207 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.401-1030A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703051 | |||||||
| chr2:39703083 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0098 others(5): Show |
10 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.401-998C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703083 | |||||||
| chr2:39703084 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(115): Show |
140 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.401-997A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703084 | |||||||
| chr2:39703137 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(228): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.401-944T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703137 | |||||||
| chr2:39703156 | A | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-925A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703156 | |||||||
| chr2:39703166 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.401-915G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703166 | |||||||
| chr2:39703195 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.401-886C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703195 | |||||||
| chr2:39703283 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.401-798A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703283 | |||||||
| chr2:39703285 | A | G | 23 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0052 others(20): Show |
27 | HG00741.hp1 HG01109.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.401-796A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703285 | |||||||
| chr2:39703615 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.401-466A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703615 | |||||||
| chr2:39703644 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(3): Show |
8 | HG01361.hp2 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.401-437C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703644 | |||||||
| chr2:39703735 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.401-346C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703735 | |||||||
| chr2:39703846 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0028 others(33): Show |
40 | HG00741.hp1 HG01109.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.401-235G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39703846 | |||||||
| chr2:39704062 | G | T | 1 | a0001c0001t0001g0243 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.401-19G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 1/3 | chr2 | 39704062 | |||||||
| chr2:39704245 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.514+51A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39704245 | |||||||
| chr2:39704316 | A | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0098 others(5): Show |
10 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.514+122A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39704316 | |||||||
| chr2:39704445 | G | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.514+251G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39704445 | |||||||
| chr2:39704664 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.514+470A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39704664 | |||||||
| chr2:39704798 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.514+604C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39704798 | |||||||
| chr2:39704803 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.514+609C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39704803 | |||||||
| chr2:39704892 | G | T | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.514+698G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39704892 | |||||||
| chr2:39705123 | A | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0089 a0001c0001t0001g0098 others(5): Show |
10 | HG00741.hp1 HG01109.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.514+929A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705123 | |||||||
| chr2:39705290 | T | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0104 a0001c0001t0002g0026 |
3 | HG02109.hp2 HG03579.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.514+1096T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705290 | |||||||
| chr2:39705290 | T | G | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.514+1096T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705290 | |||||||
| chr2:39705351 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.514+1157A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705351 | |||||||
| chr2:39705416 | T | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.514+1222T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705416 | |||||||
| chr2:39705431 | G | T | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.514+1237G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705431 | |||||||
| chr2:39705543 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.514+1349C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705543 | |||||||
| chr2:39705667 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(90): Show |
111 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.515-1382G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705667 | |||||||
| chr2:39705685 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.515-1364A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705685 | |||||||
| chr2:39705699 | T | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(10): Show |
15 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.515-1350T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705699 | |||||||
| chr2:39705722 | G | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
204 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.515-1327G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705722 | |||||||
| chr2:39705745 | C | G | 2 | a0001c0001t0001g0096 a0001c0001t0002g0026 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.515-1304C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705745 | |||||||
| chr2:39705754 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.515-1295A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705754 | |||||||
| chr2:39705784 | C | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | NA18967.hp2 NA18994.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.515-1265C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705784 | |||||||
| chr2:39705810 | G | A | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
12 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.515-1239G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705810 | |||||||
| chr2:39705938 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0002g0026 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.515-1111G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705938 | |||||||
| chr2:39705985 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.515-1064A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39705985 | |||||||
| chr2:39706043 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-1006T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706043 | |||||||
| chr2:39706044 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-1005T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706044 | |||||||
| chr2:39706045 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.515-1004A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706045 | |||||||
| chr2:39706046 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-1003A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706046 | |||||||
| chr2:39706048 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-1001A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706048 | |||||||
| chr2:39706049 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-1000A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706049 | |||||||
| chr2:39706050 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-999A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706050 | |||||||
| chr2:39706051 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-998A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706051 | |||||||
| chr2:39706054 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-995A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706054 | |||||||
| chr2:39706055 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-994G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706055 | |||||||
| chr2:39706057 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-992A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706057 | |||||||
| chr2:39706058 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.515-991A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706058 | |||||||
| chr2:39706126 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.515-923C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706126 | |||||||
| chr2:39706127 | T | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(130): Show |
158 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.515-922T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706127 | |||||||
| chr2:39706153 | T | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.515-896T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706153 | |||||||
| chr2:39706154 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.515-895A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706154 | |||||||
| chr2:39706442 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.515-607A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706442 | |||||||
| chr2:39706456 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.515-593C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706456 | |||||||
| chr2:39706458 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.515-591C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706458 | |||||||
| chr2:39706480 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01069.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.515-569A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706480 | |||||||
| chr2:39706624 | C | CT | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
199 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.515-417dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 39706624 | ||||||
| chr2:39706787 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.515-262G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706787 | |||||||
| chr2:39706826 | C | T | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
14 | HG02109.hp2 HG02630.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.515-223C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706826 | |||||||
| chr2:39706846 | T | G | 1 | a0001c0001t0001g0213 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.515-203T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 2/3 | chr2 | 39706846 | |||||||
| chr2:39707199 | C | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.652+13C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707199 | |||||||
| chr2:39707207 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0239 |
3 | HG02015.hp1 NA18956.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.652+21C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707207 | |||||||
| chr2:39707243 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.652+57C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707243 | |||||||
| chr2:39707358 | G | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(12): Show |
15 | HG02109.hp2 HG02630.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.652+172G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707358 | |||||||
| chr2:39707387 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.652+201T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707387 | |||||||
| chr2:39707508 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(3): Show |
8 | HG01361.hp2 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.652+322G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707508 | |||||||
| chr2:39707567 | G | A | 1 | a0001c0001t0007g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.652+381G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707567 | |||||||
| chr2:39707761 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.652+575C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39707761 | |||||||
| chr2:39708136 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.652+950G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708136 | |||||||
| chr2:39708173 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.652+987G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708173 | |||||||
| chr2:39708409 | A | AT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(85): Show |
110 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.652+1250dupT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39708409 | ||||||
| chr2:39708409 | A | ATT | 29 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0034 others(26): Show |
31 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.652+1249_652+1250d others(4): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39708409 | ||||||
| chr2:39708409 | AT | A | 26 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0029 others(23): Show |
27 | HG01074.hp2 HG01099.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.652+1250delT | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39708409 | ||||||
| chr2:39708409 | ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(3): Show |
8 | HG01361.hp2 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.652+1242_652+1250d others(11): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39708409 | ||||||
| chr2:39708511 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.652+1325C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708511 | |||||||
| chr2:39708543 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.652+1357C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708543 | |||||||
| chr2:39708545 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.652+1359T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708545 | |||||||
| chr2:39708565 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+1379C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708565 | |||||||
| chr2:39708566 | G | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(89): Show |
110 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.652+1380G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708566 | |||||||
| chr2:39708579 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0153 others(1): Show |
4 | HG02809.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.652+1393C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708579 | |||||||
| chr2:39708585 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.652+1399A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708585 | |||||||
| chr2:39708603 | G | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0062 others(3): Show |
9 | HG01074.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.652+1417G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708603 | |||||||
| chr2:39708638 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+1452C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708638 | |||||||
| chr2:39708639 | G | A | 12 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0040 others(9): Show |
12 | HG00738.hp2 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.652+1453G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708639 | |||||||
| chr2:39708663 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.652+1477C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708663 | |||||||
| chr2:39708664 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.652+1478G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708664 | |||||||
| chr2:39708665 | C | T | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
12 | HG02630.hp2 HG02717.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.652+1479C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708665 | |||||||
| chr2:39708751 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.652+1565T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708751 | |||||||
| chr2:39708843 | G | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+1657G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708843 | |||||||
| chr2:39708901 | G | T | 1 | a0001c0001t0006g0171 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.652+1715G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708901 | |||||||
| chr2:39708993 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.652+1807G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39708993 | |||||||
| chr2:39709007 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.652+1821G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709007 | |||||||
| chr2:39709074 | C | A | 1 | a0001c0003t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.652+1888C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709074 | |||||||
| chr2:39709091 | A | T | 1 | a0001c0001t0001g0240 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.652+1905A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709091 | |||||||
| chr2:39709128 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(3): Show |
8 | HG01361.hp2 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.652+1942C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709128 | |||||||
| chr2:39709129 | G | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+1943G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709129 | |||||||
| chr2:39709166 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0075 |
2 | HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.652+1980G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709166 | |||||||
| chr2:39709191 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.652+2005C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709191 | |||||||
| chr2:39709206 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.652+2020C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709206 | |||||||
| chr2:39709380 | C | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
30 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.652+2194C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709380 | |||||||
| chr2:39709502 | A | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(8): Show |
11 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+2316A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709502 | |||||||
| chr2:39709548 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02145.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.652+2362T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709548 | |||||||
| chr2:39709597 | G | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0055 others(3): Show |
8 | HG01361.hp2 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.652+2411G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709597 | |||||||
| chr2:39709708 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.652+2522T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709708 | |||||||
| chr2:39709723 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.652+2537T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39709723 | |||||||
| chr2:39710193 | A | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 |
5 | HG02451.hp2 HG02559.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.652+3007A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39710193 | |||||||
| chr2:39710404 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.652+3218T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39710404 | |||||||
| chr2:39710647 | T | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0153 others(1): Show |
4 | HG02809.hp2 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.652+3461T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39710647 | |||||||
| chr2:39710745 | C | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.652+3559C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39710745 | |||||||
| chr2:39710879 | G | C | 15 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(12): Show |
15 | HG02630.hp2 HG02717.hp2 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.652+3693G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39710879 | |||||||
| chr2:39710925 | A | G | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.652+3739A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39710925 | |||||||
| chr2:39710926 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.652+3740T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39710926 | |||||||
| chr2:39711159 | C | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 |
3 | NA18940.hp2 NA18979.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.652+3973C>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39711159 | |||||||
| chr2:39711373 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.652+4187T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39711373 | |||||||
| chr2:39711460 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.652+4274C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39711460 | |||||||
| chr2:39711657 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0187 |
4 | HG01081.hp1 HG01167.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.652+4471A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39711657 | |||||||
| chr2:39711711 | T | G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG02647.hp1 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.652+4525T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39711711 | |||||||
| chr2:39711739 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.652+4553C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39711739 | |||||||
| chr2:39711814 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.652+4628C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39711814 | |||||||
| chr2:39712041 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0199 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.652+4855_652+4856i others(13): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712041 | |||||||
| chr2:39712041 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0001g0185 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.652+4855_652+4856i others(15): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712041 | |||||||
| chr2:39712041 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0001g0086 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.652+4855_652+4856i others(17): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712041 | |||||||
| chr2:39712041 | T | TGTGTGTG others(12): Show |
1 | a0001c0001t0001g0181 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.652+4855_652+4856i others(21): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712041 | |||||||
| chr2:39712041 | T | TTG | 18 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0041 others(15): Show |
22 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.652+4891_652+4892d others(4): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTG | 52 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
70 | HG00140.hp2 HG00408.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.652+4889_652+4892d others(6): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTGTG | 16 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0018 others(13): Show |
22 | HG01074.hp1 HG01099.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.652+4887_652+4892d others(8): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTGTGT others(1): Show |
11 | a0001c0001t0001g0072 a0001c0001t0001g0113 a0001c0001t0001g0115 others(8): Show |
11 | HG01081.hp2 HG02015.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.652+4885_652+4892d others(10): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTGTGT others(3): Show |
18 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0034 others(15): Show |
21 | HG00438.hp1 HG00642.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.652+4883_652+4892d others(12): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTGTGT others(5): Show |
57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(54): Show |
69 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.652+4881_652+4892d others(14): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTGTGT others(7): Show |
17 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0052 others(14): Show |
20 | HG00738.hp1 HG01081.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.652+4879_652+4892d others(16): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTGTGT others(9): Show |
7 | a0001c0001t0001g0188 a0001c0001t0001g0207 a0001c0001t0001g0216 others(4): Show |
7 | HG01243.hp1 HG03540.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.652+4877_652+4892d others(18): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0003g0206 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.652+4875_652+4892d others(20): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | TTG | T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG02630.hp2 HG02717.hp2 HG02897.hp1 others(10): Show |
intron_variant | MODIFIER | c.652+4891_652+4892d others(4): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712041 | TTGTG | T | 6 | a0001c0001t0001g0031 a0001c0001t0002g0037 a0001c0001t0002g0038 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.652+4889_652+4892d others(6): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712041 | ||||||
| chr2:39712083 | G | A | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.652+4897G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712083 | |||||||
| chr2:39712133 | G | A | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-4877G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712133 | |||||||
| chr2:39712162 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.653-4848G>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712162 | |||||||
| chr2:39712344 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.653-4666G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712344 | |||||||
| chr2:39712366 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0127 |
3 | NA18940.hp2 NA18979.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.653-4644G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712366 | |||||||
| chr2:39712396 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(28): Show |
33 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.653-4614T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712396 | |||||||
| chr2:39712662 | C | CCT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0053 a0001c0001t0001g0054 others(10): Show |
15 | HG01106.hp1 HG02109.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.653-4327_653-4326d others(4): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712662 | ||||||
| chr2:39712662 | CCTCT | C | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-4329_653-4326d others(6): Show |
TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39712662 | ||||||
| chr2:39712831 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.653-4179A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712831 | |||||||
| chr2:39712867 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.653-4143C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712867 | |||||||
| chr2:39712969 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.653-4041C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712969 | |||||||
| chr2:39712970 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.653-4040G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39712970 | |||||||
| chr2:39713014 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.653-3996C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713014 | |||||||
| chr2:39713030 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.653-3980A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713030 | |||||||
| chr2:39713031 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0001g0065 |
3 | HG00738.hp2 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.653-3979C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713031 | |||||||
| chr2:39713178 | A | G | 23 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
25 | HG01361.hp2 HG01496.hp1 HG02630.hp2 others(22): Show |
intron_variant | MODIFIER | c.653-3832A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713178 | |||||||
| chr2:39713279 | T | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG02809.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.653-3731T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713279 | |||||||
| chr2:39713368 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
192 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.653-3642T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713368 | |||||||
| chr2:39713373 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.653-3637T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713373 | |||||||
| chr2:39713448 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.653-3562C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713448 | |||||||
| chr2:39713464 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
11 | HG01361.hp2 HG01496.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.653-3546A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713464 | |||||||
| chr2:39713924 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.653-3086A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713924 | |||||||
| chr2:39713945 | G | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0015 others(50): Show |
58 | HG00738.hp2 HG01074.hp1 HG01255.hp1 others(55): Show |
intron_variant | MODIFIER | c.653-3065G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39713945 | |||||||
| chr2:39714057 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0142 |
2 | HG01099.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.653-2953T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714057 | |||||||
| chr2:39714066 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.653-2944T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714066 | |||||||
| chr2:39714165 | C | T | 12 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(9): Show |
12 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.653-2845C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714165 | |||||||
| chr2:39714247 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.653-2763A>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714247 | |||||||
| chr2:39714248 | T | C | 23 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(20): Show |
23 | HG01884.hp2 HG02145.hp2 HG02630.hp2 others(20): Show |
intron_variant | MODIFIER | c.653-2762T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714248 | |||||||
| chr2:39714250 | G | T | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-2760G>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714250 | |||||||
| chr2:39714269 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.653-2741C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714269 | |||||||
| chr2:39714354 | C | CA | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-2646dupA | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 39714354 | ||||||
| chr2:39714383 | A | G | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
219 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.653-2627A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714383 | |||||||
| chr2:39714384 | A | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
219 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.653-2626A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714384 | |||||||
| chr2:39714386 | A | G | 1 | a0001c0001t0001g0008 | 3 | HG00639.hp2 HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.653-2624A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714386 | |||||||
| chr2:39714517 | C | T | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-2493C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714517 | |||||||
| chr2:39714637 | A | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0015 others(19): Show |
27 | HG01074.hp1 HG01255.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.653-2373A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714637 | |||||||
| chr2:39714649 | C | T | 23 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(20): Show |
23 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.653-2361C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714649 | |||||||
| chr2:39714798 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0056 others(14): Show |
19 | HG01361.hp2 HG01496.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.653-2212G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714798 | |||||||
| chr2:39714806 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0234 |
2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.653-2204T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714806 | |||||||
| chr2:39714844 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0031 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.653-2166T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714844 | |||||||
| chr2:39714937 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.653-2073A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714937 | |||||||
| chr2:39714995 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0002g0026 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.653-2015T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39714995 | |||||||
| chr2:39715066 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.653-1944T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715066 | |||||||
| chr2:39715168 | T | G | 2 | a0001c0001t0001g0096 a0001c0001t0002g0026 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.653-1842T>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715168 | |||||||
| chr2:39715170 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.653-1840A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715170 | |||||||
| chr2:39715433 | A | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0152 |
3 | HG02818.hp1 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.653-1577A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715433 | |||||||
| chr2:39715556 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.653-1454A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715556 | |||||||
| chr2:39715675 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0141 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.653-1335C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715675 | |||||||
| chr2:39715688 | A | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0062 others(2): Show |
8 | HG01074.hp1 HG01255.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.653-1322A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715688 | |||||||
| chr2:39715720 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0041 others(7): Show |
14 | HG00544.hp1 HG00639.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.653-1290G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715720 | |||||||
| chr2:39715725 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0065 |
2 | HG00738.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.653-1285C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715725 | |||||||
| chr2:39715726 | G | A | 1 | a0001c0001t0006g0171 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.653-1284G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715726 | |||||||
| chr2:39715791 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.653-1219A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715791 | |||||||
| chr2:39715830 | C | T | 11 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0153 others(8): Show |
11 | HG01884.hp2 HG02145.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.653-1180C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715830 | |||||||
| chr2:39715852 | A | G | 11 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0153 others(8): Show |
11 | HG01884.hp2 HG02145.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.653-1158A>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715852 | |||||||
| chr2:39715869 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.653-1141C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715869 | |||||||
| chr2:39715926 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0136 |
2 | HG00140.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.653-1084G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715926 | |||||||
| chr2:39715939 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.653-1071T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715939 | |||||||
| chr2:39715998 | G | A | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-1012G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39715998 | |||||||
| chr2:39716004 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.653-1006C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716004 | |||||||
| chr2:39716047 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.653-963T>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716047 | |||||||
| chr2:39716163 | C | T | 7 | a0001c0001t0002g0036 a0001c0001t0002g0037 a0001c0001t0002g0038 others(4): Show |
7 | HG01884.hp2 HG02145.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-847C>T | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716163 | |||||||
| chr2:39716177 | C | G | 13 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(10): Show |
13 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.653-833C>G | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716177 | |||||||
| chr2:39716206 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0001g0155 |
2 | HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.653-804T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716206 | |||||||
| chr2:39716361 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.653-649T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716361 | |||||||
| chr2:39716643 | G | A | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
14 | HG02630.hp2 HG02717.hp2 HG02965.hp1 others(11): Show |
intron_variant | MODIFIER | c.653-367G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716643 | |||||||
| chr2:39716861 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02145.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.653-149T>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716861 | |||||||
| chr2:39716915 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
196 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.653-95G>A | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716915 | |||||||
| chr2:39716927 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.653-83A>C | TMEM178A | ENSG00000152154.12 | transcript | ENST00000281961.3 | protein_coding | 3/3 | chr2 | 39716927 |