Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55858 |
| ensemblid | ENSG00000134851.13 |
| hgncid | 30760 |
| symbol | TMEM165 |
| name | transmembrane protein 165 |
| refseq_nuc | NM_018475.5 |
| refseq_prot | NP_060945.2 |
| ensembl_nuc | ENST00000381334.10 |
| ensembl_prot | ENSP00000370736.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 55395957 |
| end | 55426175 |
| strand | + |
| ver | v1.2 |
| region | chr4:55395957-55426175 |
| region5000 | chr4:55390957-55431175 |
| regionname0 | TMEM165_chr4_55395957_55426175 |
| regionname5000 | TMEM165_chr4_55390957_55431175 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 324 | 380 | 93 | 72 | 158 | 15 | 40 | 124 | TMEM165_chr4_55390957_55431175 | TMEM165 | MAAAA others(319): Show |
chr4 | 55390957 | 55431175 |
| a0002 | 0/0 | 324 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | MAAAA others(319): Show |
chr4 | 55390957 | 55431175 |
| a0003 | 0/0 | 324 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | MAAAA others(319): Show |
chr4 | 55390957 | 55431175 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 972 | 275 | 83 | 50 | 105 | 8 | 29 | TMEM165_chr4_55390957_55431175 | TMEM165 | ATGGC others(967): Show |
chr4 | 55390957 | 55431175 | ||
| a0001c0002 | 1/1 | 972 | 103 | 10 | 20 | 53 | 7 | 11 | TMEM165_chr4_55390957_55431175 | TMEM165 | ATGGC others(967): Show |
chr4 | 55390957 | 55431175 | ||
| a0001c0003 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | ATGGC others(967): Show |
chr4 | 55390957 | 55431175 | ||
| a0001c0005 | 0/0 | 972 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | ATGGC others(967): Show |
chr4 | 55390957 | 55431175 | ||
| a0002c0004 | 0/0 | 972 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | ATGGC others(967): Show |
chr4 | 55390957 | 55431175 | ||
| a0003c0006 | 0/0 | 972 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | ATGGC others(967): Show |
chr4 | 55390957 | 55431175 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1931 | 42 | 39 | 2 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0002 | 0/0 | 1929 | 127 | 17 | 30 | 68 | 2 | 10 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1924): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0003 | 0/0 | 1931 | 79 | 4 | 15 | 36 | 6 | 18 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0004 | 0/0 | 1931 | 9 | 9 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0005 | 0/0 | 1931 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0006 | 0/0 | 1931 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0008 | 0/0 | 1931 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0009 | 0/0 | 1931 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0012 | 0/0 | 1931 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0013 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1924): Show |
chr4 | 55390957 | 55431175 |
| a0001c0001t0014 | 0/0 | 1929 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1924): Show |
chr4 | 55390957 | 55431175 |
| a0001c0002t0001 | 1/1 | 1931 | 97 | 9 | 18 | 51 | 6 | 11 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0002t0007 | 0/0 | 1931 | 4 | 1 | 2 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0002t0010 | 0/0 | 1963 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1958): Show |
chr4 | 55390957 | 55431175 |
| a0001c0002t0011 | 0/0 | 1931 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0003t0001 | 0/0 | 1931 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0001c0005t0002 | 0/0 | 1929 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1924): Show |
chr4 | 55390957 | 55431175 |
| a0002c0004t0003 | 0/0 | 1931 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| a0003c0006t0015 | 0/0 | 1931 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | GACTC others(1926): Show |
chr4 | 55390957 | 55431175 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0001 | 0/0 | 15 | 0 | 5 | 9 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0007 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0012g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0001t0014g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0002 | 0/0 | 13 | 0 | 4 | 8 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0003 | 0/0 | 7 | 0 | 3 | 2 | 2 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0006 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0035 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0007g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0007g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0002t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0003t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0001c0005t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0002c0004t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| a0003c0006t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0277 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0251 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0268 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00323 | hp2 | a0002 | c0004 | t0003 | g0020 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00733 | hp1 | a0001 | c0001 | t0014 | g0010 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0234 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01081 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01168 | hp2 | a0001 | c0001 | t0012 | g0219 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01192 | hp1 | a0001 | c0002 | t0007 | g0200 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0153 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01255 | hp1 | a0001 | c0005 | t0002 | g0030 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01256 | hp1 | a0001 | c0002 | t0007 | g0159 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0239 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01515 | hp2 | a0001 | c0002 | t0007 | g0157 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0043 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0274 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0048 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0213 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0185 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0204 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0212 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0039 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0252 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0246 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0195 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0223 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0152 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18612 | hp1 | a0001 | c0002 | t0011 | g0187 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18954 | hp1 | a0001 | c0002 | t0010 | g0188 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0207 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19043 | hp2 | a0001 | c0002 | t0007 | g0158 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19059 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19090 | hp2 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | ASW | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ASW | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0035 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0190 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0189 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0229 | SAS | GIH | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | GIH | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0205 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| NA21309 | hp2 | a0003 | c0006 | t0015 | g0203 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0035 | REF | REF | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0156 | REF | REF | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55396365 | C | G | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.176C>G | p.Ala59Gly | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 409/1931 | 176/975 | 59/324 | chr4 | 55396365 | |||
| chr4:55411728 | G | A | 1 | a0002 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.322G>A | p.Glu108Lys | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/6 | 555/1931 | 322/975 | 108/324 | chr4 | 55411728 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55396207 | A | G | 4 | a0001c0001 a0001c0005 a0002c0004 others(1): Show |
278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
synonymous_variant | LOW | c.18A>G | p.Pro6Pro | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 251/1931 | 18/975 | 6/324 | chr4 | 55396207 | |||
| chr4:55411700 | C | T | 1 | a0001c0003 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.294C>T | p.Val98Val | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/6 | 527/1931 | 294/975 | 98/324 | chr4 | 55411700 | |||
| chr4:55411790 | C | T | 1 | a0001c0005 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.384C>T | p.Thr128Thr | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/6 | 617/1931 | 384/975 | 128/324 | chr4 | 55411790 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55396043 | T | C | 1 | a0001c0001t0005 | 7 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-147T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 147 | chr4 | 55396043 | ||||||
| chr4:55396160 | C | T | 1 | a0003c0006t0015 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 30 | chr4 | 55396160 | ||||||
| chr4:55425453 | CAA | C | 4 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0014 others(1): Show |
130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2_*3delAA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 2 | chr4 | 55425453 | ||||||
| chr4:55425556 | A | G | 1 | a0001c0001t0014 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 104 | chr4 | 55425556 | ||||||
| chr4:55425578 | C | CCCATTAT others(25): Show |
1 | a0001c0002t0010 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128_*159dupCATTAT others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 160 | INFO_REALIGN_3_PRIME | chr4 | 55425578 | |||||
| chr4:55425584 | A | C | 1 | a0001c0002t0007 | 4 | HG01192.hp1 HG01256.hp1 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*132A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 132 | chr4 | 55425584 | ||||||
| chr4:55425605 | T | C | 2 | a0001c0001t0006 a0001c0001t0008 |
6 | HG01243.hp2 HG02647.hp1 HG03471.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*153T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 153 | chr4 | 55425605 | ||||||
| chr4:55425688 | A | G | 1 | a0001c0001t0012 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 236 | chr4 | 55425688 | ||||||
| chr4:55425704 | T | C | 1 | a0001c0001t0008 | 2 | HG01243.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 252 | chr4 | 55425704 | ||||||
| chr4:55425725 | T | G | 1 | a0001c0002t0011 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*273T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 273 | chr4 | 55425725 | ||||||
| chr4:55425934 | A | T | 3 | a0001c0001t0003 a0001c0001t0012 a0002c0004t0003 |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 482 | chr4 | 55425934 | ||||||
| chr4:55425946 | T | C | 1 | a0001c0001t0004 | 9 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*494T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 494 | chr4 | 55425946 | ||||||
| chr4:55425957 | T | A | 1 | a0001c0001t0009 | 2 | HG01884.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*505T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 505 | chr4 | 55425957 | ||||||
| chr4:55426079 | A | C | 1 | a0001c0001t0013 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*627A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 627 | chr4 | 55426079 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:55396435 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.207+39C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396435 | |||||||
| chr4:55396457 | C | G | 1 | a0001c0001t0003g0277 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.207+61C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396457 | |||||||
| chr4:55396472 | C | T | 1 | a0001c0001t0003g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.207+76C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396472 | |||||||
| chr4:55396574 | C | G | 70 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(67): Show |
87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.207+178C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396574 | |||||||
| chr4:55396635 | C | T | 6 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0213 others(3): Show |
6 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+239C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396635 | |||||||
| chr4:55396697 | C | G | 7 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0005g0206 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+301C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396697 | |||||||
| chr4:55396945 | C | A | 1 | a0001c0001t0003g0217 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.207+549C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396945 | |||||||
| chr4:55396960 | G | A | 7 | a0001c0001t0005g0204 a0001c0001t0005g0205 a0001c0001t0005g0206 others(4): Show |
7 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+564G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396960 | |||||||
| chr4:55396966 | G | C | 1 | a0001c0001t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.207+570G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396966 | |||||||
| chr4:55396968 | G | T | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+572G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396968 | |||||||
| chr4:55397213 | A | G | 1 | a0001c0001t0003g0040 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.207+817A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397213 | |||||||
| chr4:55397236 | G | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.207+840G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397236 | |||||||
| chr4:55397267 | C | T | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+871C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397267 | |||||||
| chr4:55397376 | T | G | 2 | a0001c0001t0009g0047 a0001c0001t0009g0048 |
2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.207+980T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397376 | |||||||
| chr4:55397463 | C | T | 1 | a0001c0001t0003g0275 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+1067C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397463 | |||||||
| chr4:55397494 | GA | G | 8 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0004g0211 others(5): Show |
8 | HG01517.hp2 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+1111delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397494 | ||||||
| chr4:55397562 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.207+1166T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397562 | |||||||
| chr4:55397836 | T | C | 1 | a0001c0001t0003g0218 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.207+1440T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397836 | |||||||
| chr4:55397910 | A | AT | 5 | a0001c0001t0001g0023 a0001c0001t0001g0202 a0001c0002t0001g0009 others(2): Show |
9 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+1528dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397910 | ||||||
| chr4:55397910 | AT | A | 17 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 others(14): Show |
18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+1528delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397910 | ||||||
| chr4:55397910 | ATTT | A | 172 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(169): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.207+1526_207+1528d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397910 | ||||||
| chr4:55398026 | G | A | 1 | a0001c0001t0004g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+1630G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398026 | |||||||
| chr4:55398040 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.207+1644G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398040 | |||||||
| chr4:55398049 | G | T | 1 | a0001c0001t0006g0199 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.207+1653G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398049 | |||||||
| chr4:55398161 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.207+1765C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398161 | |||||||
| chr4:55398328 | T | C | 2 | a0001c0001t0002g0220 a0001c0001t0012g0219 |
2 | HG01168.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.207+1932T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398328 | |||||||
| chr4:55398348 | ACAACAG | A | 6 | a0001c0001t0005g0205 a0001c0001t0005g0206 a0001c0001t0005g0207 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+1955_207+1960d others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55398348 | ||||||
| chr4:55398505 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.207+2109T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398505 | |||||||
| chr4:55398586 | C | G | 146 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(143): Show |
214 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.207+2190C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398586 | |||||||
| chr4:55398599 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+2203A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398599 | |||||||
| chr4:55398612 | A | G | 3 | a0001c0001t0002g0129 a0001c0001t0002g0130 a0001c0001t0013g0131 |
3 | NA18954.hp2 NA19081.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.207+2216A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398612 | |||||||
| chr4:55398729 | A | G | 6 | a0001c0001t0005g0205 a0001c0001t0005g0206 a0001c0001t0005g0207 others(3): Show |
6 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+2333A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398729 | |||||||
| chr4:55398774 | C | G | 172 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(169): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.207+2378C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398774 | |||||||
| chr4:55398887 | AAC | A | 163 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(160): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.207+2493_207+2494d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55398887 | ||||||
| chr4:55398888 | AC | A | 8 | a0001c0001t0002g0032 a0001c0001t0002g0068 a0001c0001t0002g0077 others(5): Show |
9 | HG01978.hp1 HG02280.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+2493delC | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398888 | |||||||
| chr4:55398920 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.207+2524A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398920 | |||||||
| chr4:55399130 | T | G | 1 | a0001c0002t0001g0166 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.207+2734T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399130 | |||||||
| chr4:55399327 | C | G | 1 | a0001c0001t0002g0032 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.207+2931C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399327 | |||||||
| chr4:55399400 | T | G | 19 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(16): Show |
20 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.207+3004T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399400 | |||||||
| chr4:55399494 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.207+3098T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399494 | |||||||
| chr4:55400013 | CT | C | 6 | a0001c0001t0003g0221 a0001c0001t0003g0222 a0001c0001t0004g0211 others(3): Show |
6 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+3631delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400013 | ||||||
| chr4:55400045 | A | G | 16 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0132 others(13): Show |
18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+3649A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400045 | |||||||
| chr4:55400131 | C | T | 72 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(69): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.207+3735C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400131 | |||||||
| chr4:55400167 | A | G | 72 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(69): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.207+3771A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400167 | |||||||
| chr4:55400172 | A | T | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3776A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400172 | |||||||
| chr4:55400182 | A | T | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3786A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400182 | |||||||
| chr4:55400184 | A | T | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3788A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400184 | |||||||
| chr4:55400184 | AAT | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
12 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+3790_207+3791d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400184 | ||||||
| chr4:55400187 | A | T | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3791A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400187 | |||||||
| chr4:55400221 | T | TATTA | 268 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(265): Show |
359 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.207+3828_207+3831d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400221 | ||||||
| chr4:55400223 | T | A | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3827T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400223 | |||||||
| chr4:55400226 | A | T | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3830A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400226 | |||||||
| chr4:55400236 | G | A | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3840G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400236 | |||||||
| chr4:55400243 | A | ATAT | 46 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0033 others(43): Show |
57 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.207+3851_207+3853d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400243 | ||||||
| chr4:55400244 | T | TATAATA | 8 | a0001c0001t0003g0223 a0001c0001t0003g0224 a0001c0001t0003g0225 others(5): Show |
8 | HG01168.hp2 HG03491.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3850_207+3851i others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400244 | ||||||
| chr4:55400244 | T | TATTATAA others(2): Show |
212 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(209): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.207+3854_207+3855i others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400244 | ||||||
| chr4:55400246 | T | TTA | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG02145.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.207+3854_207+3855d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400246 | ||||||
| chr4:55400256 | TTAATATA | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0003g0230 |
3 | HG02809.hp1 HG03130.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.207+3875_207+3881d others(9): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400256 | ||||||
| chr4:55400258 | A | AATATATA others(24): Show |
1 | a0001c0001t0001g0023 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.207+3874_207+3904d others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400258 | ||||||
| chr4:55400258 | A | T | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3862A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400258 | |||||||
| chr4:55400265 | A | AATATATA others(17): Show |
1 | a0001c0001t0003g0231 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.207+3881_207+3904d others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400265 | ||||||
| chr4:55400265 | A | AATATATA others(48): Show |
4 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(1): Show |
4 | HG01175.hp2 HG01346.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+3918_207+3919i others(57): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400265 | ||||||
| chr4:55400265 | A | T | 1 | a0001c0001t0003g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3869A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400265 | |||||||
| chr4:55400272 | A | AATATAAT others(24): Show |
1 | a0001c0001t0002g0056 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.207+3892_207+3893i others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | ||||||
| chr4:55400272 | A | AATATAAT others(12): Show |
1 | a0001c0002t0001g0198 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.207+3893_207+3911d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | ||||||
| chr4:55400272 | A | AATATAAT others(21): Show |
1 | a0001c0001t0002g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+3877_207+3904d others(30): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | ||||||
| chr4:55400272 | A | AATATAAT others(55): Show |
1 | a0001c0001t0002g0032 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.207+3904_207+3905i others(64): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | ||||||
| chr4:55400272 | A | AATATAAT others(24): Show |
130 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(127): Show |
192 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.207+3888_207+3918d others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | ||||||
| chr4:55400272 | A | AATATAAT others(36): Show |
1 | a0001c0001t0002g0128 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.207+3911_207+3912i others(45): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | ||||||
| chr4:55400273 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
8 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3877A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400273 | |||||||
| chr4:55400277 | A | T | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+3881A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400277 | |||||||
| chr4:55400278 | ATAT | A | 24 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0133 others(21): Show |
27 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+3886_207+3888d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400278 | ||||||
| chr4:55400281 | T | TTATATAT others(21): Show |
2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | HG02015.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.207+3889_207+3916d others(30): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400281 | ||||||
| chr4:55400284 | T | TATATTAT others(5): Show |
1 | a0001c0001t0002g0061 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.207+3907_207+3918d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400284 | ||||||
| chr4:55400284 | TATATTAT others(5): Show |
T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+3907_207+3918d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400284 | ||||||
| chr4:55400289 | TATATATA others(12): Show |
T | 4 | a0001c0001t0003g0260 a0001c0001t0003g0261 a0001c0001t0003g0262 others(1): Show |
4 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3898_207+3916d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400289 | ||||||
| chr4:55400296 | A | AATATTAT others(24): Show |
9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0005g0204 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+3916_207+3917i others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400296 | ||||||
| chr4:55400297 | ATAT | A | 2 | a0001c0001t0001g0202 a0001c0001t0003g0040 |
3 | HG02280.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.207+3905_207+3907d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400297 | ||||||
| chr4:55400309 | A | ATATTATA others(24): Show |
1 | a0001c0001t0002g0127 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.207+3918_207+3919i others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400309 | ||||||
| chr4:55400319 | T | C | 72 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(69): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.207+3923T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400319 | |||||||
| chr4:55400323 | TTA | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
8 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3934_207+3935d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400323 | ||||||
| chr4:55400333 | TATA | T | 63 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(60): Show |
80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.207+3941_207+3943d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400333 | ||||||
| chr4:55400337 | A | T | 4 | a0001c0001t0003g0217 a0001c0001t0003g0230 a0001c0001t0003g0268 others(1): Show |
4 | HG00280.hp2 HG01192.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3941A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400337 | |||||||
| chr4:55400339 | ATTAATTA others(1): Show |
A | 4 | a0001c0001t0003g0217 a0001c0001t0003g0230 a0001c0001t0003g0268 others(1): Show |
4 | HG00280.hp2 HG01192.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3944_207+3951d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400339 | |||||||
| chr4:55400376 | TATA | T | 222 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(219): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.207+3991_207+3993d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400376 | ||||||
| chr4:55400458 | T | A | 1 | a0001c0001t0003g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.207+4062T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400458 | |||||||
| chr4:55400534 | CTCACGCC others(2347): Show |
C | 16 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0132 others(13): Show |
18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+4156_207+6509d others(2): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400534 | ||||||
| chr4:55400557 | C | T | 146 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(143): Show |
214 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.207+4161C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400557 | |||||||
| chr4:55400627 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.207+4231C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400627 | |||||||
| chr4:55400636 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.207+4240A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400636 | |||||||
| chr4:55400715 | A | C | 242 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0034 others(239): Show |
330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.207+4319A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400715 | |||||||
| chr4:55400844 | A | G | 1 | a0001c0001t0003g0275 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+4448A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400844 | |||||||
| chr4:55401015 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.207+4619T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401015 | |||||||
| chr4:55401060 | GAGGGGGG others(6): Show |
G | 1 | a0001c0001t0003g0272 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.207+4665_207+4677d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401060 | |||||||
| chr4:55401234 | T | C | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+4838T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401234 | |||||||
| chr4:55401306 | C | T | 80 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0011 others(77): Show |
111 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.207+4910C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401306 | |||||||
| chr4:55401656 | C | T | 3 | a0001c0001t0002g0014 a0001c0001t0002g0070 a0001c0001t0002g0126 |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+5260C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401656 | |||||||
| chr4:55401720 | C | T | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+5324C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401720 | |||||||
| chr4:55401732 | C | T | 3 | a0001c0002t0001g0002 a0001c0002t0001g0144 a0001c0002t0001g0198 |
3 | HG00609.hp1 NA18950.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.207+5336C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401732 | |||||||
| chr4:55401839 | G | C | 1 | a0001c0002t0001g0002 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.207+5443G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401839 | |||||||
| chr4:55401854 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.207+5458C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401854 | |||||||
| chr4:55401882 | C | T | 1 | a0001c0003t0001g0002 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.207+5486C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401882 | |||||||
| chr4:55402119 | C | CAAAAA | 14 | a0001c0001t0001g0054 a0001c0001t0001g0161 a0001c0001t0001g0162 others(11): Show |
15 | HG00558.hp2 HG02015.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+5731_207+5735d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402119 | C | CAAAAAA | 162 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(159): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.207+5730_207+5735d others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402119 | C | CAAAAAAA | 10 | a0001c0001t0001g0034 a0001c0001t0002g0029 a0001c0001t0002g0063 others(7): Show |
10 | HG01175.hp2 HG02723.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+5729_207+5735d others(9): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402119 | C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0004g0164 others(11): Show |
14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.207+5728_207+5735d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402119 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0023 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.207+5735_207+5736i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402119 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0023 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.207+5735_207+5736i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402119 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0004g0215 a0001c0001t0009g0048 |
2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.207+5735_207+5736i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402119 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0202 a0001c0001t0009g0047 |
2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.207+5735_207+5736i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | ||||||
| chr4:55402124 | A | AAAAAAAA others(36): Show |
1 | a0001c0001t0004g0163 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+5735_207+5736i others(45): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402124 | ||||||
| chr4:55402173 | T | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.207+5777T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402173 | |||||||
| chr4:55402243 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.207+5847A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402243 | |||||||
| chr4:55402268 | TAAC | T | 173 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(170): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.207+5875_207+5877d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402268 | ||||||
| chr4:55402340 | T | C | 173 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(170): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.207+5944T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402340 | |||||||
| chr4:55402388 | C | CGTGT | 7 | a0001c0001t0001g0147 a0001c0001t0006g0199 a0001c0001t0008g0152 others(4): Show |
7 | HG02109.hp1 HG02647.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+6005_207+6008d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402388 | ||||||
| chr4:55402388 | CGTGT | C | 2 | a0001c0001t0003g0021 a0001c0001t0003g0040 |
3 | HG02280.hp2 HG03669.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.207+6005_207+6008d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402388 | ||||||
| chr4:55402397 | GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.207+6003_207+6020d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402397 | ||||||
| chr4:55402399 | GTGTGTAT others(1): Show |
G | 10 | a0001c0001t0001g0022 a0001c0001t0003g0007 a0001c0001t0003g0021 others(7): Show |
11 | HG01361.hp1 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6005_207+6012d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | ||||||
| chr4:55402399 | GTGTGTAT others(3): Show |
G | 38 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0020 others(35): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.207+6005_207+6014d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | ||||||
| chr4:55402399 | GTGTGTAT others(5): Show |
G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0258 others(14): Show |
18 | HG00140.hp1 HG01069.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.207+6005_207+6016d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | ||||||
| chr4:55402399 | GTGTGTAT others(7): Show |
G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
5 | HG02055.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6005_207+6018d others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | ||||||
| chr4:55402403 | G | A | 104 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(101): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.207+6007G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402403 | |||||||
| chr4:55402403 | G | GTGTATA | 3 | a0001c0002t0001g0004 a0001c0002t0001g0166 a0001c0002t0001g0195 |
3 | HG03710.hp2 HG03834.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTATAT others(3): Show |
2 | a0001c0002t0001g0173 a0001c0002t0001g0184 |
2 | HG04184.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTATAT others(5): Show |
2 | a0001c0002t0001g0002 a0001c0002t0001g0193 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTATAT others(7): Show |
1 | a0001c0002t0001g0018 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.207+6008_207+6009i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTA | 11 | a0001c0001t0006g0149 a0001c0001t0006g0150 a0001c0001t0006g0151 others(8): Show |
11 | HG00558.hp1 HG00738.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTAT others(1): Show |
8 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0017 others(5): Show |
10 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTAT others(3): Show |
7 | a0001c0002t0001g0002 a0001c0002t0001g0006 a0001c0002t0001g0038 others(4): Show |
8 | HG00597.hp1 HG02698.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTAT others(5): Show |
6 | a0001c0002t0001g0144 a0001c0002t0001g0172 a0001c0002t0001g0179 others(3): Show |
6 | HG00621.hp2 HG02027.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTAT others(7): Show |
2 | a0001c0002t0001g0002 a0001c0002t0010g0188 |
2 | HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTAT others(9): Show |
1 | a0001c0002t0001g0016 | 2 | NA18998.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTGT others(1): Show |
3 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0017 |
3 | HG00735.hp2 HG02083.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTGT others(3): Show |
1 | a0001c0002t0001g0017 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0008g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.207+6008_207+6009i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTGT others(3): Show |
1 | a0001c0002t0001g0180 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | G | GTGTGTGT others(5): Show |
1 | a0001c0002t0001g0002 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.207+6008_207+6009i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | GTA | G | 4 | a0001c0001t0001g0034 a0001c0001t0005g0205 a0001c0001t0005g0207 others(1): Show |
5 | HG02258.hp2 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+6037_207+6038d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402403 | GTATA | G | 4 | a0001c0001t0001g0278 a0001c0001t0004g0216 a0001c0001t0005g0210 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6035_207+6038d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | ||||||
| chr4:55402405 | A | G | 31 | a0001c0001t0001g0023 a0001c0001t0001g0147 a0001c0001t0001g0148 others(28): Show |
42 | HG00609.hp1 HG01123.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.207+6009A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402405 | |||||||
| chr4:55402407 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
11 | HG00609.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6011A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402407 | |||||||
| chr4:55402409 | A | G | 4 | a0001c0001t0001g0034 a0001c0001t0001g0148 a0001c0001t0004g0216 others(1): Show |
5 | HG02258.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+6013A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402409 | |||||||
| chr4:55402411 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0004g0216 |
3 | HG02258.hp2 HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.207+6015A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402411 | |||||||
| chr4:55402417 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0002g0001 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.207+6023_207+6043d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402417 | ||||||
| chr4:55402419 | ATATATAT others(10): Show |
A | 1 | a0001c0002t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+6025_207+6041d others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | ||||||
| chr4:55402419 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0056 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.207+6025_207+6042d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | ||||||
| chr4:55402419 | ATATATAT others(13): Show |
A | 9 | a0001c0001t0002g0001 a0001c0001t0002g0029 a0001c0001t0002g0063 others(6): Show |
10 | HG00609.hp2 HG01175.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6025_207+6044d others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | ||||||
| chr4:55402419 | ATATATAT others(14): Show |
A | 30 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(27): Show |
39 | HG01167.hp2 HG01346.hp1 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.207+6025_207+6045d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | ||||||
| chr4:55402419 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0011 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.207+6025_207+6046d others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | ||||||
| chr4:55402421 | ATATATAT others(10): Show |
A | 1 | a0001c0002t0001g0002 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.207+6027_207+6043d others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | ||||||
| chr4:55402421 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207+6027_207+6044d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | ||||||
| chr4:55402421 | ATATATAT others(13): Show |
A | 10 | a0001c0001t0002g0008 a0001c0001t0002g0013 a0001c0001t0002g0032 others(7): Show |
10 | HG01433.hp2 HG02809.hp2 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6027_207+6046d others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | ||||||
| chr4:55402421 | ATATATAT others(14): Show |
A | 36 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(33): Show |
45 | HG00438.hp1 HG00544.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.207+6027_207+6047d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | ||||||
| chr4:55402421 | ATATATAT others(15): Show |
A | 9 | a0001c0001t0002g0001 a0001c0001t0002g0058 a0001c0001t0002g0080 others(6): Show |
9 | HG00099.hp2 HG00280.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+6027_207+6048d others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | ||||||
| chr4:55402421 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0002g0001 a0001c0001t0003g0021 |
2 | HG01257.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.207+6027_207+6049d others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | ||||||
| chr4:55402423 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207+6029_207+6046d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | ||||||
| chr4:55402423 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0113 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.207+6029_207+6047d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | ||||||
| chr4:55402423 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0002g0008 a0001c0001t0002g0026 a0001c0001t0002g0111 others(1): Show |
4 | HG00558.hp2 HG01261.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6029_207+6048d others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | ||||||
| chr4:55402423 | ATATATAT others(14): Show |
A | 8 | a0001c0001t0002g0026 a0001c0001t0002g0088 a0001c0001t0002g0094 others(5): Show |
8 | HG00621.hp1 HG00673.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+6029_207+6049d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | ||||||
| chr4:55402423 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0002g0108 a0001c0001t0003g0253 |
2 | NA18948.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.207+6029_207+6050d others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | ||||||
| chr4:55402425 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+6031_207+6047d others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402425 | ||||||
| chr4:55402425 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0112 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.207+6031_207+6049d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402425 | ||||||
| chr4:55402427 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0005g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207+6033_207+6045d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402427 | ||||||
| chr4:55402429 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.207+6035_207+6045d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402429 | ||||||
| chr4:55402431 | A | T | 2 | a0001c0001t0005g0208 a0001c0001t0005g0210 |
2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.207+6035A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402431 | |||||||
| chr4:55402433 | A | T | 8 | a0001c0001t0001g0023 a0001c0001t0004g0164 a0001c0001t0005g0208 others(5): Show |
9 | HG00597.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+6037A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402433 | |||||||
| chr4:55402433 | ATTTTTTT others(2): Show |
A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(6): Show |
10 | HG01168.hp2 HG02559.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6063_207+6071d others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | ||||||
| chr4:55402433 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0003g0226 a0001c0001t0003g0232 a0001c0001t0003g0238 others(2): Show |
5 | HG00642.hp2 HG01070.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6062_207+6071d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | ||||||
| chr4:55402433 | ATTTTTTT others(4): Show |
A | 40 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0020 others(37): Show |
50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.207+6061_207+6071d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | ||||||
| chr4:55402433 | ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0003g0005 a0001c0001t0003g0236 a0001c0001t0003g0239 |
4 | HG01361.hp1 HG03688.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+6060_207+6071d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | ||||||
| chr4:55402433 | ATTTTTTT others(6): Show |
A | 6 | a0001c0001t0003g0021 a0001c0001t0003g0040 a0001c0001t0003g0243 others(3): Show |
6 | HG01175.hp1 HG03017.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+6059_207+6071d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | ||||||
| chr4:55402433 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0003g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.207+6058_207+6071d others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | ||||||
| chr4:55402434 | T | TA | 26 | a0001c0001t0006g0149 a0001c0001t0006g0151 a0001c0001t0006g0199 others(23): Show |
33 | HG00438.hp2 HG00733.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.207+6038_207+6039i others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | |||||||
| chr4:55402434 | T | TATATA | 6 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0006 others(3): Show |
12 | HG00099.hp1 HG01123.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+6038_207+6039i others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | |||||||
| chr4:55402434 | T | TATATATA others(4): Show |
3 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0001g0170 |
3 | HG01069.hp2 HG01071.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.207+6038_207+6039i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | |||||||
| chr4:55402434 | T | TATATATA others(6): Show |
1 | a0001c0002t0001g0183 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.207+6038_207+6039i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | |||||||
| chr4:55402434 | T | TATATATA others(8): Show |
1 | a0001c0002t0001g0019 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.207+6038_207+6039i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | |||||||
| chr4:55402434 | T | TATATATA others(10): Show |
1 | a0001c0002t0001g0002 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.207+6038_207+6039i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | |||||||
| chr4:55402434 | T | TATATATA others(16): Show |
1 | a0001c0002t0001g0019 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.207+6038_207+6039i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | |||||||
| chr4:55402435 | T | A | 19 | a0001c0001t0001g0147 a0001c0001t0006g0150 a0001c0001t0008g0153 others(16): Show |
23 | HG00558.hp1 HG00621.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.207+6039T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402435 | |||||||
| chr4:55402436 | T | A | 31 | a0001c0001t0006g0149 a0001c0001t0006g0151 a0001c0001t0006g0199 others(28): Show |
44 | HG00438.hp2 HG00738.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.207+6040T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402436 | |||||||
| chr4:55402437 | T | A | 4 | a0001c0002t0001g0002 a0001c0002t0001g0019 a0001c0002t0001g0180 others(1): Show |
4 | HG00558.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+6041T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402437 | |||||||
| chr4:55402438 | T | A | 13 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0006 others(10): Show |
13 | HG02027.hp2 HG02129.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.207+6042T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402438 | |||||||
| chr4:55402439 | T | A | 3 | a0001c0001t0001g0162 a0001c0002t0001g0019 a0001c0002t0001g0180 |
3 | HG00558.hp1 HG02622.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.207+6043T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402439 | |||||||
| chr4:55402440 | T | A | 1 | a0001c0002t0001g0016 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.207+6044T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402440 | |||||||
| chr4:55402534 | G | C | 1 | a0001c0001t0001g0034 | 2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.207+6138G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402534 | |||||||
| chr4:55402552 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.207+6156A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402552 | |||||||
| chr4:55402681 | C | T | 1 | a0001c0001t0003g0221 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.207+6285C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402681 | |||||||
| chr4:55402699 | C | T | 1 | a0001c0002t0001g0160 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+6303C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402699 | |||||||
| chr4:55402795 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0006g0149 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+6406_207+6413d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0034 a0001c0001t0001g0148 a0001c0001t0001g0161 others(13): Show |
16 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.207+6405_207+6413d others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0055 a0001c0001t0005g0205 |
2 | HG01261.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.207+6404_207+6413d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.207+6403_207+6413d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(6): Show |
10 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG01168.hp2 HG02055.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6401_207+6413d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(7): Show |
42 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(39): Show |
53 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.207+6400_207+6413d others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(8): Show |
78 | a0001c0001t0001g0022 a0001c0001t0002g0001 a0001c0001t0002g0008 others(75): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.207+6413_207+6414i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(9): Show |
42 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(39): Show |
47 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.207+6413_207+6414i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(10): Show |
7 | a0001c0001t0002g0057 a0001c0001t0002g0114 a0001c0001t0002g0116 others(4): Show |
7 | HG00323.hp2 HG03453.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+6413_207+6414i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0003g0040 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.207+6413_207+6414i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0003g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.207+6413_207+6414i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402795 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0031 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.207+6413_207+6414i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | ||||||
| chr4:55402875 | T | G | 1 | a0001c0001t0003g0040 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.207+6479T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402875 | |||||||
| chr4:55402892 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.207+6496C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402892 | |||||||
| chr4:55402912 | C | T | 1 | a0001c0001t0003g0229 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.207+6516C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402912 | |||||||
| chr4:55403178 | A | C | 1 | a0001c0001t0005g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207+6782A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403178 | |||||||
| chr4:55403210 | G | A | 1 | a0001c0002t0001g0168 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.207+6814G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403210 | |||||||
| chr4:55403335 | G | GCAGGTAT others(325): Show |
11 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
12 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.207+6959_207+6960i others(334): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403335 | ||||||
| chr4:55403335 | G | GCAGGTAT others(326): Show |
10 | a0001c0001t0001g0202 a0001c0001t0005g0210 a0001c0001t0006g0149 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6959_207+6960i others(335): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403335 | ||||||
| chr4:55403389 | G | T | 1 | a0001c0001t0002g0031 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.207+6993G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403389 | |||||||
| chr4:55403492 | C | CT | 205 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(202): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.207+7101dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403492 | ||||||
| chr4:55403492 | C | CTT | 11 | a0001c0001t0001g0202 a0001c0001t0002g0014 a0001c0001t0002g0126 others(8): Show |
15 | HG00280.hp2 HG00558.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+7100_207+7101d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403492 | ||||||
| chr4:55403496 | T | C | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+7100T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403496 | |||||||
| chr4:55403497 | TC | T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0005g0204 others(5): Show |
8 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+7102delC | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403497 | |||||||
| chr4:55403498 | C | T | 248 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(245): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.207+7102C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403498 | |||||||
| chr4:55403516 | A | C | 145 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(142): Show |
213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.207+7120A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403516 | |||||||
| chr4:55403518 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.207+7122T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403518 | |||||||
| chr4:55403576 | T | A | 5 | a0001c0001t0003g0232 a0001c0001t0006g0149 a0001c0001t0006g0150 others(2): Show |
5 | HG01070.hp2 HG02647.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+7180T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403576 | |||||||
| chr4:55403576 | T | TA | 219 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(216): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.207+7187dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403576 | ||||||
| chr4:55403706 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.207+7310C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403706 | |||||||
| chr4:55403812 | A | G | 66 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(63): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.207+7416A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403812 | |||||||
| chr4:55403830 | T | G | 1 | a0001c0002t0001g0173 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.207+7434T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403830 | |||||||
| chr4:55403985 | TCTTAA | T | 146 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(143): Show |
214 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.207+7593_207+7597d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403985 | ||||||
| chr4:55403998 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+7602A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403998 | |||||||
| chr4:55404045 | C | CT | 7 | a0001c0001t0004g0146 a0001c0001t0004g0164 a0001c0001t0004g0212 others(4): Show |
7 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-7552dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | ||||||
| chr4:55404045 | CT | C | 13 | a0001c0001t0001g0034 a0001c0001t0001g0133 a0001c0001t0001g0147 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-7552delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | ||||||
| chr4:55404045 | CTT | C | 12 | a0001c0001t0001g0055 a0001c0001t0001g0143 a0001c0001t0001g0161 others(9): Show |
12 | HG01261.hp1 HG01891.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-7553_208-7552d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | ||||||
| chr4:55404045 | CTTT | C | 219 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(216): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.208-7554_208-7552d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | ||||||
| chr4:55404050 | T | C | 12 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-7564T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404050 | |||||||
| chr4:55404160 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.208-7454C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404160 | |||||||
| chr4:55404177 | A | AT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0054 a0001c0001t0001g0055 others(11): Show |
15 | HG01261.hp1 HG01943.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-7425dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404177 | ||||||
| chr4:55404200 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.208-7414T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404200 | |||||||
| chr4:55404206 | T | C | 257 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0033 others(254): Show |
347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.208-7408T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404206 | |||||||
| chr4:55404206 | T | G | 1 | a0001c0001t0002g0123 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.208-7408T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404206 | |||||||
| chr4:55404253 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-7361G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404253 | |||||||
| chr4:55404305 | A | G | 219 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(216): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.208-7309A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404305 | |||||||
| chr4:55404464 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.208-7150C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404464 | |||||||
| chr4:55404606 | AT | A | 38 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(35): Show |
41 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.208-6996delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404606 | ||||||
| chr4:55404606 | ATTTTT | A | 10 | a0001c0001t0002g0030 a0001c0001t0002g0115 a0001c0001t0002g0116 others(7): Show |
10 | HG01255.hp1 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-7000_208-6996d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404606 | ||||||
| chr4:55404611 | T | A | 211 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(208): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.208-7003T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404611 | |||||||
| chr4:55404617 | T | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6997T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404617 | |||||||
| chr4:55404689 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.208-6925C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404689 | |||||||
| chr4:55404832 | T | A | 11 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
12 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-6782T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404832 | |||||||
| chr4:55404896 | A | G | 1 | a0001c0001t0004g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.208-6718A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404896 | |||||||
| chr4:55404924 | T | G | 1 | a0001c0001t0003g0233 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.208-6690T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404924 | |||||||
| chr4:55404977 | GCACCC | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6634_208-6630d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404977 | ||||||
| chr4:55405086 | C | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-6528C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405086 | |||||||
| chr4:55405250 | G | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
12 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-6364G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405250 | |||||||
| chr4:55405498 | A | G | 1 | a0001c0001t0002g0029 | 2 | NA18971.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.208-6116A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405498 | |||||||
| chr4:55405562 | A | G | 1 | a0001c0001t0002g0114 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.208-6052A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405562 | |||||||
| chr4:55405566 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0005g0204 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-6048A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405566 | |||||||
| chr4:55405775 | G | T | 9 | a0001c0001t0004g0146 a0001c0001t0004g0163 a0001c0001t0004g0164 others(6): Show |
9 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-5839G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405775 | |||||||
| chr4:55405894 | C | G | 12 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-5720C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405894 | |||||||
| chr4:55405959 | T | G | 1 | a0001c0001t0003g0231 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.208-5655T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405959 | |||||||
| chr4:55406129 | C | T | 1 | a0001c0001t0005g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208-5485C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406129 | |||||||
| chr4:55406236 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208-5378C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406236 | |||||||
| chr4:55406483 | C | T | 9 | a0001c0001t0004g0146 a0001c0001t0004g0163 a0001c0001t0004g0164 others(6): Show |
9 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-5131C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406483 | |||||||
| chr4:55406487 | A | G | 1 | a0001c0001t0004g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.208-5127A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406487 | |||||||
| chr4:55406507 | A | G | 1 | a0001c0001t0005g0204 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208-5107A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406507 | |||||||
| chr4:55406520 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.208-5094T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406520 | |||||||
| chr4:55406559 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-5055G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406559 | |||||||
| chr4:55406696 | G | C | 67 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(64): Show |
84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.208-4918G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406696 | |||||||
| chr4:55406845 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-4769A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406845 | |||||||
| chr4:55406955 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.208-4659C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406955 | |||||||
| chr4:55406979 | T | C | 1 | a0001c0001t0005g0205 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208-4635T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406979 | |||||||
| chr4:55407119 | G | A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0074 |
2 | NA18948.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.208-4495G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407119 | |||||||
| chr4:55407120 | G | C | 51 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0020 others(48): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.208-4494G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407120 | |||||||
| chr4:55407142 | A | C | 1 | a0001c0001t0002g0122 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-4472A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407142 | |||||||
| chr4:55407285 | T | C | 2 | a0001c0001t0002g0030 a0001c0005t0002g0030 |
2 | HG01255.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.208-4329T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407285 | |||||||
| chr4:55407625 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-3989T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407625 | |||||||
| chr4:55407721 | G | C | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-3893G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407721 | |||||||
| chr4:55407928 | T | A | 1 | a0001c0001t0004g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.208-3686T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407928 | |||||||
| chr4:55407965 | G | A | 97 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(94): Show |
130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.208-3649G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407965 | |||||||
| chr4:55408140 | G | A | 173 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(170): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.208-3474G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408140 | |||||||
| chr4:55408163 | C | T | 172 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(169): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.208-3451C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408163 | |||||||
| chr4:55408164 | G | A | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-3450G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408164 | |||||||
| chr4:55408174 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0005g0204 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-3440G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408174 | |||||||
| chr4:55408304 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-3310G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408304 | |||||||
| chr4:55408506 | A | G | 16 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0132 others(13): Show |
18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.208-3108A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408506 | |||||||
| chr4:55408533 | T | TAAAAAAT others(3): Show |
1 | a0001c0001t0003g0272 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.208-3080_208-3071d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55408533 | ||||||
| chr4:55408597 | T | A | 221 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(218): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.208-3017T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408597 | |||||||
| chr4:55408862 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-2752C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408862 | |||||||
| chr4:55408922 | C | CT | 212 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(209): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.208-2678dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55408922 | ||||||
| chr4:55408998 | T | C | 2 | a0001c0001t0009g0047 a0001c0001t0009g0048 |
2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.208-2616T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408998 | |||||||
| chr4:55409053 | G | A | 6 | a0001c0001t0006g0149 a0001c0001t0006g0150 a0001c0001t0006g0151 others(3): Show |
6 | HG01243.hp2 HG02647.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-2561G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409053 | |||||||
| chr4:55409063 | G | T | 97 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(94): Show |
130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.208-2551G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409063 | |||||||
| chr4:55409067 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 |
5 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-2547G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409067 | |||||||
| chr4:55409197 | T | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG03239.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.208-2417T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409197 | |||||||
| chr4:55409567 | T | C | 1 | a0001c0002t0001g0154 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.208-2047T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409567 | |||||||
| chr4:55409574 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-2040T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409574 | |||||||
| chr4:55409590 | T | G | 1 | a0001c0001t0002g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-2024T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409590 | |||||||
| chr4:55409658 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.208-1956G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409658 | |||||||
| chr4:55409694 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.208-1920G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409694 | |||||||
| chr4:55409780 | A | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.208-1834A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409780 | |||||||
| chr4:55409901 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 |
5 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-1713G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409901 | |||||||
| chr4:55409961 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-1653C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409961 | |||||||
| chr4:55410167 | T | C | 145 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(142): Show |
213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.208-1447T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410167 | |||||||
| chr4:55410311 | C | T | 68 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(65): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.208-1303C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410311 | |||||||
| chr4:55410372 | AATGACAG others(18): Show |
A | 1 | a0001c0001t0003g0272 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.208-1241_208-1217d others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410372 | |||||||
| chr4:55410464 | A | G | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-1150A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410464 | |||||||
| chr4:55410466 | G | A | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-1148G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410466 | |||||||
| chr4:55410551 | G | A | 1 | a0001c0001t0009g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208-1063G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410551 | |||||||
| chr4:55410602 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.208-1012G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410602 | |||||||
| chr4:55410608 | C | T | 2 | a0001c0001t0009g0047 a0001c0001t0009g0048 |
2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.208-1006C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410608 | |||||||
| chr4:55410701 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.208-913G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410701 | |||||||
| chr4:55410728 | C | T | 68 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(65): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.208-886C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410728 | |||||||
| chr4:55410759 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.208-855G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410759 | |||||||
| chr4:55410859 | G | A | 1 | a0001c0001t0003g0040 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.208-755G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410859 | |||||||
| chr4:55411044 | A | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-570A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411044 | |||||||
| chr4:55411064 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.208-550G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411064 | |||||||
| chr4:55411130 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0122 |
2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.208-484G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411130 | |||||||
| chr4:55411134 | C | CA | 8 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0081 others(5): Show |
8 | HG01175.hp2 HG01978.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-463dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55411134 | ||||||
| chr4:55411134 | CA | C | 8 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0141 others(5): Show |
8 | HG01261.hp1 HG02886.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-463delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55411134 | ||||||
| chr4:55411151 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-463A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411151 | |||||||
| chr4:55411179 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-435G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411179 | |||||||
| chr4:55411384 | C | T | 1 | a0001c0001t0003g0275 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.208-230C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411384 | |||||||
| chr4:55411449 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-165C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411449 | |||||||
| chr4:55411554 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.208-60G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411554 | |||||||
| chr4:55411868 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.433+29C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55411868 | |||||||
| chr4:55411967 | A | G | 1 | a0001c0001t0003g0268 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.433+128A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55411967 | |||||||
| chr4:55411970 | TTTTCCTT others(8): Show |
T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.433+148_433+162del others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55411970 | ||||||
| chr4:55412132 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.433+293C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412132 | |||||||
| chr4:55412161 | G | A | 1 | a0001c0002t0001g0172 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.433+322G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412161 | |||||||
| chr4:55412221 | G | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.433+382G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412221 | |||||||
| chr4:55412332 | T | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0084 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.433+493T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412332 | |||||||
| chr4:55412349 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.433+510G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412349 | |||||||
| chr4:55412393 | C | CA | 13 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0161 others(10): Show |
14 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.433+578dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412393 | C | CAAA | 13 | a0001c0001t0001g0259 a0001c0001t0002g0030 a0001c0001t0002g0062 others(10): Show |
13 | HG01175.hp2 HG01255.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.433+576_433+578dup others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412393 | C | CAAAA | 118 | a0001c0001t0001g0022 a0001c0001t0001g0055 a0001c0001t0002g0001 others(115): Show |
180 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.433+575_433+578dup others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412393 | C | CAAAAA | 65 | a0001c0001t0001g0054 a0001c0001t0001g0258 a0001c0001t0002g0025 others(62): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.433+574_433+578dup others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412393 | C | CAAAAAA | 13 | a0001c0001t0002g0085 a0001c0001t0003g0041 a0001c0001t0003g0222 others(10): Show |
16 | HG00642.hp2 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.433+573_433+578dup others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412393 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0052 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.433+569_433+578dup others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412393 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.433+567_433+578dup others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412393 | CA | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0036 others(14): Show |
20 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.433+578delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | ||||||
| chr4:55412714 | C | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.433+875C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412714 | |||||||
| chr4:55412983 | A | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+1144A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412983 | |||||||
| chr4:55412987 | A | T | 13 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(10): Show |
14 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.433+1148A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412987 | |||||||
| chr4:55412991 | T | A | 73 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(70): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.433+1152T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412991 | |||||||
| chr4:55413170 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 |
5 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+1331G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413170 | |||||||
| chr4:55413302 | ATTTTTAT others(9): Show |
A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.433+1477_433+1492d others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55413302 | ||||||
| chr4:55413318 | C | CT | 6 | a0001c0001t0006g0149 a0001c0001t0006g0150 a0001c0001t0006g0151 others(3): Show |
6 | HG01243.hp2 HG02647.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.433+1484dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55413318 | ||||||
| chr4:55413357 | C | A | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.433+1518C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413357 | |||||||
| chr4:55413363 | G | A | 26 | a0001c0001t0003g0007 a0001c0001t0003g0020 a0001c0001t0003g0041 others(23): Show |
32 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.433+1524G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413363 | |||||||
| chr4:55413385 | A | G | 221 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(218): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.433+1546A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413385 | |||||||
| chr4:55413522 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.433+1683G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413522 | |||||||
| chr4:55413561 | C | T | 1 | a0001c0001t0002g0028 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.433+1722C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413561 | |||||||
| chr4:55413708 | A | G | 80 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0011 others(77): Show |
111 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.433+1869A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413708 | |||||||
| chr4:55413774 | A | T | 9 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.433+1935A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413774 | |||||||
| chr4:55413804 | A | T | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433+1965A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413804 | |||||||
| chr4:55413805 | C | G | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433+1966C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413805 | |||||||
| chr4:55413861 | T | C | 1 | a0001c0002t0001g0183 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.433+2022T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413861 | |||||||
| chr4:55413993 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.433+2154G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413993 | |||||||
| chr4:55414021 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.433+2182C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414021 | |||||||
| chr4:55414066 | A | T | 218 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(215): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.433+2227A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414066 | |||||||
| chr4:55414095 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433+2256C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414095 | |||||||
| chr4:55414104 | T | G | 2 | a0001c0002t0001g0178 a0001c0002t0001g0184 |
2 | NA18949.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.433+2265T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414104 | |||||||
| chr4:55414121 | C | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0005g0204 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.433+2282C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414121 | |||||||
| chr4:55414224 | T | C | 259 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(256): Show |
350 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.433+2385T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414224 | |||||||
| chr4:55414296 | T | TA | 221 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(218): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.433+2457_433+2458i others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414296 | |||||||
| chr4:55414306 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.433+2467T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414306 | |||||||
| chr4:55414432 | A | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0121 |
2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.433+2593A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414432 | |||||||
| chr4:55414504 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.434-2568G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414504 | |||||||
| chr4:55414750 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.434-2322A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414750 | |||||||
| chr4:55414991 | T | A | 1 | a0001c0002t0001g0155 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.434-2081T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414991 | |||||||
| chr4:55415082 | T | C | 1 | a0001c0002t0001g0185 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.434-1990T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415082 | |||||||
| chr4:55415153 | A | G | 80 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0011 others(77): Show |
111 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.434-1919A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415153 | |||||||
| chr4:55415172 | C | G | 2 | a0001c0002t0007g0158 a0001c0002t0007g0159 |
2 | HG01256.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.434-1900C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415172 | |||||||
| chr4:55415290 | T | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0237 |
3 | NA18942.hp1 NA18981.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.434-1782T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415290 | |||||||
| chr4:55415317 | G | A | 73 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(70): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.434-1755G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415317 | |||||||
| chr4:55415398 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434-1674C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415398 | |||||||
| chr4:55415454 | C | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0005g0204 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.434-1618C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415454 | |||||||
| chr4:55415466 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.434-1606C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415466 | |||||||
| chr4:55415468 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434-1604G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415468 | |||||||
| chr4:55415602 | C | T | 12 | a0001c0001t0001g0015 a0001c0002t0001g0003 a0001c0002t0001g0015 others(9): Show |
19 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.434-1470C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415602 | |||||||
| chr4:55415847 | TTTTC | T | 7 | a0001c0001t0004g0163 a0001c0001t0004g0211 a0001c0001t0004g0212 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-1213_434-1210d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55415847 | ||||||
| chr4:55415863 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.434-1209T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415863 | |||||||
| chr4:55416135 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0009g0047 a0001c0001t0009g0048 |
3 | HG01884.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.434-937A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416135 | |||||||
| chr4:55416280 | A | G | 1 | a0001c0002t0007g0159 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.434-792A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416280 | |||||||
| chr4:55416330 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434-742G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416330 | |||||||
| chr4:55416485 | T | G | 1 | a0003c0006t0015g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.434-587T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416485 | |||||||
| chr4:55416507 | T | A | 1 | a0001c0002t0001g0037 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.434-565T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416507 | |||||||
| chr4:55416823 | AGGAAGAT others(15): Show |
A | 4 | a0001c0001t0002g0091 a0001c0001t0002g0105 a0001c0001t0002g0106 others(1): Show |
4 | NA18747.hp2 NA18950.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-245_434-224del others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55416823 | ||||||
| chr4:55416918 | G | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
8 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.434-154G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416918 | |||||||
| chr4:55417534 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.610-269T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 3/5 | chr4 | 55417534 | |||||||
| chr4:55417584 | G | C | 1 | a0001c0002t0001g0173 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.610-219G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 3/5 | chr4 | 55417584 | |||||||
| chr4:55417739 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.610-64T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 3/5 | chr4 | 55417739 | |||||||
| chr4:55418436 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.792+451A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418436 | |||||||
| chr4:55418462 | T | G | 1 | a0001c0001t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.792+477T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418462 | |||||||
| chr4:55418464 | C | T | 181 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0050 others(178): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.792+479C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418464 | |||||||
| chr4:55418479 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.792+494G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418479 | |||||||
| chr4:55418521 | GA | G | 5 | a0001c0001t0002g0129 a0001c0001t0003g0040 a0001c0001t0003g0242 others(2): Show |
6 | HG01169.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+550delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55418521 | ||||||
| chr4:55418608 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.792+623C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418608 | |||||||
| chr4:55418683 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.792+698C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418683 | |||||||
| chr4:55418768 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.792+783C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418768 | |||||||
| chr4:55418891 | A | C | 1 | a0001c0001t0002g0220 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.792+906A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418891 | |||||||
| chr4:55418915 | C | G | 51 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0020 others(48): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.792+930C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418915 | |||||||
| chr4:55418999 | T | G | 226 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(223): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.792+1014T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418999 | |||||||
| chr4:55419010 | A | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG02055.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+1025A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419010 | |||||||
| chr4:55419059 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.792+1074A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419059 | |||||||
| chr4:55419138 | C | T | 226 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(223): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.792+1153C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419138 | |||||||
| chr4:55419239 | A | T | 1 | a0001c0001t0002g0104 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.792+1254A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419239 | |||||||
| chr4:55419598 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.792+1613A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419598 | |||||||
| chr4:55419710 | T | G | 12 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
13 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.792+1725T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419710 | |||||||
| chr4:55419723 | G | C | 2 | a0001c0002t0001g0170 a0001c0002t0001g0186 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.792+1738G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419723 | |||||||
| chr4:55419957 | G | A | 1 | a0001c0001t0002g0270 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.792+1972G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419957 | |||||||
| chr4:55420021 | G | T | 97 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(94): Show |
130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.792+2036G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420021 | |||||||
| chr4:55420062 | C | T | 1 | a0001c0002t0007g0200 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.792+2077C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420062 | |||||||
| chr4:55420098 | G | GA | 36 | a0001c0001t0002g0115 a0001c0001t0003g0007 a0001c0001t0003g0020 others(33): Show |
47 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.792+2122dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420098 | G | GAAAAA | 10 | a0001c0001t0002g0030 a0001c0001t0002g0124 a0001c0001t0003g0005 others(7): Show |
15 | HG01255.hp1 HG02615.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.792+2118_792+2122d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420098 | G | GAAAAAAA others(1): Show |
13 | a0001c0001t0002g0012 a0001c0001t0002g0027 a0001c0001t0002g0060 others(10): Show |
16 | HG01175.hp2 HG01346.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+2115_792+2122d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420098 | G | GAAAAAAA others(2): Show |
6 | a0001c0001t0002g0011 a0001c0001t0002g0025 a0001c0001t0002g0061 others(3): Show |
9 | HG02273.hp2 NA18955.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2114_792+2122d others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420098 | G | GAAAAAAA others(4): Show |
6 | a0001c0001t0002g0026 a0001c0001t0002g0096 a0001c0001t0002g0105 others(3): Show |
7 | HG00673.hp1 HG04204.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420098 | G | GAAAAAAA others(6): Show |
2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | NA18971.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420098 | G | GAAAAAAA others(11): Show |
1 | a0001c0001t0002g0092 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420098 | GAA | G | 10 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
10 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+2121_792+2122d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | ||||||
| chr4:55420106 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0098 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0002g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0008 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0071 a0001c0002t0001g0002 |
2 | HG00544.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(15): Show |
2 | a0001c0002t0001g0006 a0001c0002t0001g0190 |
2 | HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(8): Show |
2 | a0001c0001t0002g0010 a0001c0002t0001g0173 |
2 | HG03195.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0002g0008 a0001c0002t0001g0194 |
2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(14): Show |
1 | a0001c0002t0001g0002 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(16): Show |
1 | a0001c0002t0001g0002 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0002g0081 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(20): Show |
1 | a0001c0002t0001g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(29): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0144 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(11): Show |
1 | a0001c0002t0001g0019 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0002 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(15): Show |
1 | a0001c0002t0001g0193 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(17): Show |
1 | a0001c0002t0001g0002 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(6): Show |
4 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0049 others(1): Show |
4 | HG00738.hp2 HG02129.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(8): Show |
3 | a0001c0001t0002g0001 a0001c0001t0002g0056 a0001c0002t0001g0195 |
3 | HG03710.hp2 NA18986.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(10): Show |
3 | a0001c0001t0002g0001 a0001c0002t0001g0002 a0001c0002t0001g0185 |
3 | HG00609.hp2 HG02129.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0002g0013 a0001c0002t0001g0182 |
2 | HG02027.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(14): Show |
4 | a0001c0001t0002g0086 a0001c0002t0001g0004 a0001c0002t0001g0006 others(1): Show |
4 | HG00544.hp1 NA18983.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0014g0010 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0166 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0002g0032 a0001c0001t0002g0077 |
2 | HG01891.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0031 a0001c0002t0001g0174 |
3 | HG00738.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0014 a0001c0002t0001g0004 |
2 | HG01952.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(11): Show |
3 | a0001c0002t0001g0002 a0001c0002t0001g0175 a0001c0002t0001g0181 |
5 | HG00609.hp1 HG01243.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(13): Show |
2 | a0001c0002t0001g0009 a0001c0002t0001g0189 |
2 | HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(15): Show |
2 | a0001c0002t0001g0006 a0001c0002t0001g0180 |
2 | HG01123.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(17): Show |
1 | a0001c0002t0001g0037 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0002 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(28): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(4): Show |
8 | a0001c0001t0002g0001 a0001c0001t0002g0028 a0001c0001t0002g0067 others(5): Show |
9 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(6): Show |
12 | a0001c0001t0002g0013 a0001c0001t0002g0028 a0001c0001t0002g0072 others(9): Show |
12 | HG00438.hp2 HG01081.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(8): Show |
4 | a0001c0001t0002g0089 a0001c0001t0002g0127 a0001c0002t0001g0004 others(1): Show |
4 | HG00438.hp1 NA18947.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(10): Show |
5 | a0001c0001t0002g0103 a0001c0002t0001g0004 a0001c0002t0001g0018 others(2): Show |
7 | HG00621.hp2 HG02015.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(12): Show |
7 | a0001c0001t0002g0079 a0001c0002t0001g0006 a0001c0002t0001g0016 others(4): Show |
7 | HG02109.hp2 HG03453.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(14): Show |
2 | a0001c0002t0001g0016 a0001c0002t0001g0178 |
2 | NA18949.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0179 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(3): Show |
5 | a0001c0001t0002g0001 a0001c0001t0002g0076 a0001c0001t0002g0101 others(2): Show |
6 | HG00280.hp2 HG01358.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0001 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0117 |
2 | HG01257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(11): Show |
3 | a0001c0001t0002g0121 a0001c0002t0001g0018 a0001c0002t0001g0191 |
3 | HG02895.hp2 NA18961.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(15): Show |
1 | a0001c0002t0001g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(4): Show |
8 | a0001c0001t0002g0001 a0001c0001t0002g0066 a0001c0001t0002g0084 others(5): Show |
9 | HG00280.hp1 HG00621.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(6): Show |
4 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0002t0001g0145 others(1): Show |
5 | HG02083.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0002g0058 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(10): Show |
6 | a0001c0001t0002g0059 a0001c0001t0013g0131 a0001c0002t0001g0006 others(3): Show |
6 | HG04184.hp2 NA18959.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0002g0090 a0001c0002t0001g0002 a0001c0002t0001g0176 |
3 | HG02074.hp2 HG02717.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(14): Show |
3 | a0001c0001t0003g0246 a0001c0002t0001g0002 a0001c0002t0001g0009 |
3 | HG00642.hp1 HG03710.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(16): Show |
2 | a0001c0002t0001g0002 a0001c0002t0001g0172 |
2 | HG02027.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(22): Show |
1 | a0001c0002t0001g0019 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(31): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0002g0029 a0001c0001t0002g0091 |
2 | NA19068.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0002 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0002g0014 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAT others(4): Show |
2 | a0001c0001t0002g0013 a0001c0001t0002g0100 |
2 | NA18943.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAT others(8): Show |
1 | a0001c0002t0001g0019 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAAAT others(14): Show |
1 | a0001c0001t0002g0014 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0002g0070 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | AAATATAT others(12): Show |
1 | a0001c0001t0003g0245 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | ||||||
| chr4:55420106 | A | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0136 |
2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.792+2121A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420106 | |||||||
| chr4:55420107 | AT | A | 33 | a0001c0001t0001g0024 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
34 | HG01070.hp2 HG01167.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.792+2123delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420107 | |||||||
| chr4:55420107 | ATAT | A | 4 | a0001c0001t0003g0040 a0001c0001t0003g0252 a0001c0001t0003g0275 others(1): Show |
5 | HG02145.hp1 HG02280.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+2123_792+2125d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420107 | |||||||
| chr4:55420108 | T | A | 73 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0051 others(70): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.792+2123T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420108 | |||||||
| chr4:55420110 | T | A | 86 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0052 others(83): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.792+2125T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420110 | |||||||
| chr4:55420112 | T | A | 47 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0052 others(44): Show |
56 | HG01069.hp1 HG01070.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.792+2127T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420112 | |||||||
| chr4:55420114 | T | A | 15 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0002g0057 others(12): Show |
16 | HG01255.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+2129T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420114 | |||||||
| chr4:55420116 | T | A | 3 | a0001c0001t0002g0057 a0001c0001t0002g0115 a0001c0002t0001g0198 |
3 | HG03041.hp1 HG03927.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.792+2131T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420116 | |||||||
| chr4:55420118 | T | A | 1 | a0001c0002t0001g0198 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.792+2133T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420118 | |||||||
| chr4:55420119 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.792+2134A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420119 | |||||||
| chr4:55420120 | TAC | T | 3 | a0001c0001t0001g0033 a0001c0001t0003g0262 a0001c0001t0006g0150 |
4 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+2137_792+2138d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420120 | ||||||
| chr4:55420122 | C | T | 251 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0036 others(248): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.792+2137C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420122 | |||||||
| chr4:55420123 | A | T | 10 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
10 | HG02257.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+2138A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420123 | |||||||
| chr4:55420127 | A | T | 22 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0132 others(19): Show |
24 | HG01243.hp2 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.792+2142A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420127 | |||||||
| chr4:55420131 | T | A | 216 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(213): Show |
300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.792+2146T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420131 | |||||||
| chr4:55420134 | TTTATTTA others(4): Show |
T | 1 | a0001c0001t0002g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.792+2152_792+2162d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420134 | ||||||
| chr4:55420135 | T | A | 213 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(210): Show |
296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.792+2150T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420135 | |||||||
| chr4:55420139 | T | A | 154 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(151): Show |
218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.792+2154T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420139 | |||||||
| chr4:55420141 | ATTTAT | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2164_792+2168d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420141 | ||||||
| chr4:55420142 | TTTA | T | 6 | a0001c0001t0003g0224 a0001c0001t0003g0225 a0001c0001t0003g0227 others(3): Show |
6 | HG01168.hp2 HG03491.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+2160_792+2162d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420142 | ||||||
| chr4:55420143 | T | A | 97 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(94): Show |
127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.792+2158T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420143 | |||||||
| chr4:55420145 | AT | A | 171 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0036 others(168): Show |
232 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.792+2164delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420145 | ||||||
| chr4:55420146 | T | A | 8 | a0001c0001t0002g0057 a0001c0001t0002g0126 a0001c0001t0003g0224 others(5): Show |
8 | HG01168.hp2 HG02148.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+2161T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420146 | |||||||
| chr4:55420146 | T | TA | 74 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0014 others(71): Show |
99 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.792+2161_792+2162i others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420146 | |||||||
| chr4:55420146 | T | TTTA | 5 | a0001c0001t0001g0022 a0001c0001t0001g0258 a0001c0001t0001g0259 others(2): Show |
7 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+2163_792+2164i others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420146 | ||||||
| chr4:55420146 | T | TTTATTTA others(4): Show |
2 | a0001c0001t0001g0023 a0001c0001t0005g0204 |
3 | HG02647.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.792+2163_792+2164i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420146 | ||||||
| chr4:55420148 | T | A | 7 | a0001c0001t0002g0088 a0001c0001t0002g0096 a0001c0001t0002g0106 others(4): Show |
7 | HG00621.hp1 HG04204.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2163T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420148 | |||||||
| chr4:55420172 | C | T | 1 | a0001c0001t0005g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.792+2187C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420172 | |||||||
| chr4:55420215 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.792+2230T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420215 | |||||||
| chr4:55420258 | G | T | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0161 others(8): Show |
11 | HG01261.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.792+2273G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420258 | |||||||
| chr4:55420306 | C | T | 1 | a0001c0002t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.792+2321C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420306 | |||||||
| chr4:55420329 | ATAGACTC others(25): Show |
A | 1 | a0001c0002t0010g0188 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.792+2345_792+2376d others(34): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420329 | |||||||
| chr4:55420394 | T | G | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.792+2409T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420394 | |||||||
| chr4:55420446 | A | T | 226 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(223): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.792+2461A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420446 | |||||||
| chr4:55420533 | A | G | 2 | a0001c0001t0003g0238 a0001c0001t0003g0239 |
2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.792+2548A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420533 | |||||||
| chr4:55420550 | T | C | 269 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(266): Show |
360 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.792+2565T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420550 | |||||||
| chr4:55420568 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(7): Show |
11 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.792+2583A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420568 | |||||||
| chr4:55420701 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.792+2716A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420701 | |||||||
| chr4:55420769 | C | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(6): Show |
9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+2784C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420769 | |||||||
| chr4:55420911 | A | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(6): Show |
9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+2926A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420911 | |||||||
| chr4:55421145 | C | T | 16 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0132 others(13): Show |
18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.792+3160C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421145 | |||||||
| chr4:55421166 | C | CA | 19 | a0001c0001t0001g0023 a0001c0001t0001g0132 a0001c0001t0001g0143 others(16): Show |
21 | HG00642.hp2 HG01175.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.792+3203dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | ||||||
| chr4:55421166 | C | CAA | 5 | a0001c0001t0001g0015 a0001c0001t0001g0202 a0001c0001t0003g0237 others(2): Show |
6 | HG00673.hp2 HG01099.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+3202_792+3203d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | ||||||
| chr4:55421166 | CA | C | 26 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(23): Show |
28 | HG01123.hp2 HG01167.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.792+3203delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | ||||||
| chr4:55421166 | CAAAAA | C | 136 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(133): Show |
204 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.792+3199_792+3203d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | ||||||
| chr4:55421284 | A | G | 2 | a0001c0002t0001g0018 a0001c0002t0001g0182 |
4 | HG02027.hp1 NA19062.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-3254A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421284 | |||||||
| chr4:55421297 | C | CT | 33 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 others(30): Show |
37 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.793-3220dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | ||||||
| chr4:55421297 | C | CTT | 11 | a0001c0001t0003g0005 a0001c0001t0003g0237 a0001c0001t0003g0240 others(8): Show |
16 | NA18612.hp1 NA18939.hp1 NA18959.hp2 others(13): Show |
intron_variant | MODIFIER | c.793-3221_793-3220d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | ||||||
| chr4:55421297 | CT | C | 33 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0033 others(30): Show |
38 | HG01070.hp2 HG01099.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.793-3220delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | ||||||
| chr4:55421297 | CTT | C | 10 | a0001c0001t0001g0034 a0001c0001t0001g0148 a0001c0001t0006g0149 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.793-3221_793-3220d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | ||||||
| chr4:55421300 | T | C | 3 | a0001c0002t0001g0039 a0001c0002t0001g0170 a0001c0002t0001g0186 |
4 | HG02965.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-3238T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421300 | |||||||
| chr4:55421301 | T | C | 1 | a0001c0002t0001g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.793-3237T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421301 | |||||||
| chr4:55421391 | C | T | 1 | a0001c0001t0003g0254 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.793-3147C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421391 | |||||||
| chr4:55421522 | T | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.793-3016T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421522 | |||||||
| chr4:55421709 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793-2829C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421709 | |||||||
| chr4:55421876 | A | G | 1 | a0001c0001t0012g0219 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.793-2662A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421876 | |||||||
| chr4:55421915 | GA | G | 271 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0023 others(268): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.793-2612delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421915 | ||||||
| chr4:55421958 | A | C | 178 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0051 others(175): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.793-2580A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421958 | |||||||
| chr4:55422317 | G | A | 5 | a0001c0002t0001g0169 a0001c0002t0001g0179 a0001c0002t0001g0180 others(2): Show |
5 | NA18954.hp1 NA18959.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-2221G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422317 | |||||||
| chr4:55422361 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793-2177G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422361 | |||||||
| chr4:55422363 | T | G | 1 | a0001c0001t0002g0100 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.793-2175T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422363 | |||||||
| chr4:55422510 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.793-2028G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422510 | |||||||
| chr4:55422576 | C | G | 65 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0020 others(62): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.793-1962C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422576 | |||||||
| chr4:55422656 | A | AT | 13 | a0001c0001t0001g0033 a0001c0001t0001g0132 a0001c0001t0001g0133 others(10): Show |
14 | HG01243.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.793-1872dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55422656 | ||||||
| chr4:55422656 | A | T | 1 | a0001c0001t0001g0202 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793-1882A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422656 | |||||||
| chr4:55422660 | T | A | 2 | a0001c0001t0009g0047 a0001c0001t0009g0048 |
2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.793-1878T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422660 | |||||||
| chr4:55422915 | C | T | 5 | a0001c0002t0001g0018 a0001c0002t0001g0178 a0001c0002t0001g0182 others(2): Show |
7 | HG02027.hp1 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-1623C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422915 | |||||||
| chr4:55423200 | G | T | 2 | a0001c0001t0004g0146 a0001c0001t0004g0164 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.793-1338G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423200 | |||||||
| chr4:55423212 | C | A | 254 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(251): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.793-1326C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423212 | |||||||
| chr4:55423233 | C | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(6): Show |
9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-1305C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423233 | |||||||
| chr4:55423339 | G | A | 21 | a0001c0001t0001g0034 a0001c0001t0001g0147 a0001c0001t0001g0148 others(18): Show |
22 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.793-1199G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423339 | |||||||
| chr4:55423344 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.793-1194G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423344 | |||||||
| chr4:55423425 | T | TAAAG | 8 | a0001c0001t0001g0036 a0001c0001t0001g0136 a0001c0001t0001g0137 others(5): Show |
9 | HG02572.hp1 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-1113_793-1112i others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423425 | |||||||
| chr4:55423426 | C | T | 8 | a0001c0001t0001g0036 a0001c0001t0001g0136 a0001c0001t0001g0137 others(5): Show |
9 | HG02572.hp1 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-1112C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423426 | |||||||
| chr4:55423569 | C | T | 4 | a0001c0001t0003g0043 a0001c0001t0003g0221 a0001c0001t0003g0234 others(1): Show |
5 | HG00140.hp2 HG01069.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-969C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423569 | |||||||
| chr4:55423611 | C | T | 147 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(144): Show |
215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-927C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423611 | |||||||
| chr4:55423612 | A | G | 233 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0036 others(230): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.793-926A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423612 | |||||||
| chr4:55423618 | T | C | 145 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(142): Show |
213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.793-920T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423618 | |||||||
| chr4:55423619 | C | T | 1 | a0001c0002t0001g0198 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.793-919C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423619 | |||||||
| chr4:55423662 | A | G | 2 | a0001c0001t0009g0047 a0001c0001t0009g0048 |
2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.793-876A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423662 | |||||||
| chr4:55423832 | A | G | 254 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(251): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.793-706A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423832 | |||||||
| chr4:55423885 | CTGGT | C | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0070 others(7): Show |
14 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.793-650_793-647del others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55423885 | ||||||
| chr4:55423890 | T | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0070 others(7): Show |
14 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.793-648T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423890 | |||||||
| chr4:55424053 | A | G | 254 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0034 others(251): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.793-485A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424053 | |||||||
| chr4:55424134 | G | T | 2 | a0001c0001t0002g0030 a0001c0005t0002g0030 |
2 | HG01255.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.793-404G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424134 | |||||||
| chr4:55424270 | T | C | 147 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(144): Show |
215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-268T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424270 | |||||||
| chr4:55424329 | C | T | 147 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(144): Show |
215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-209C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424329 | |||||||
| chr4:55424391 | C | T | 147 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(144): Show |
215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-147C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424391 | |||||||
| chr4:55424406 | T | C | 145 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0010 others(142): Show |
213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.793-132T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424406 | |||||||
| chr4:55424463 | C | T | 3 | a0001c0001t0003g0226 a0001c0001t0003g0227 a0001c0001t0003g0228 |
3 | HG03491.hp2 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.793-75C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424463 | |||||||
| chr4:55424773 | T | TAATA | 147 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(144): Show |
215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.898+131_898+132ins others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 55424773 | ||||||
| chr4:55424948 | A | G | 1 | a0001c0001t0003g0257 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.898+305A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55424948 | |||||||
| chr4:55424957 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0165 others(6): Show |
9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.898+314A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55424957 | |||||||
| chr4:55424989 | G | A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0074 |
2 | NA18948.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.898+346G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55424989 | |||||||
| chr4:55425281 | G | T | 1 | a0001c0001t0002g0056 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.899-95G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55425281 | |||||||
| chr4:55425312 | C | T | 99 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(96): Show |
132 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.899-64C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55425312 | |||||||
| chr4:55425361 | T | C | 99 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0001 others(96): Show |
132 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.899-15T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55425361 |