Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100113407 |
| ensemblid | ENSG00000205269.6 |
| hgncid | 34244 |
| symbol | TMEM170B |
| name | transmembrane protein 170B |
| refseq_nuc | NM_001100829.3 |
| refseq_prot | NP_001094299.1 |
| ensembl_nuc | ENST00000379426.2 |
| ensembl_prot | ENSP00000368737.1 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 11537749 |
| end | 11583524 |
| strand | + |
| ver | v1.2 |
| region | chr6:11537749-11583524 |
| region5000 | chr6:11532749-11588524 |
| regionname0 | TMEM170B_chr6_11537749_11583524 |
| regionname5000 | TMEM170B_chr6_11532749_11588524 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 132 | 351 | 88 | 48 | 165 | 14 | 34 | 131 | TMEM170B_chr6_11532749_11588524 | TMEM170B | MKAEG others(127): Show |
chr6 | 11532749 | 11588524 |
| a0002 | 0/0 | 132 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | MKAER others(127): Show |
chr6 | 11532749 | 11588524 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 396 | 254 | 78 | 37 | 109 | 7 | 21 | TMEM170B_chr6_11532749_11588524 | TMEM170B | ATGAA others(391): Show |
chr6 | 11532749 | 11588524 | ||
| a0001c0002 | 0/0 | 396 | 94 | 8 | 10 | 56 | 7 | 13 | TMEM170B_chr6_11532749_11588524 | TMEM170B | ATGAA others(391): Show |
chr6 | 11532749 | 11588524 | ||
| a0001c0004 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | ATGAA others(391): Show |
chr6 | 11532749 | 11588524 | ||
| a0001c0005 | 0/0 | 396 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | ATGAA others(391): Show |
chr6 | 11532749 | 11588524 | ||
| a0001c0006 | 0/0 | 396 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | ATGAA others(391): Show |
chr6 | 11532749 | 11588524 | ||
| a0002c0003 | 0/0 | 396 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | ATGAA others(391): Show |
chr6 | 11532749 | 11588524 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 8891 | 98 | 18 | 19 | 51 | 2 | 7 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0003 | 0/0 | 8891 | 23 | 10 | 10 | 0 | 0 | 3 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0004 | 0/0 | 8890 | 22 | 0 | 1 | 19 | 0 | 2 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0005 | 0/0 | 8889 | 18 | 7 | 0 | 8 | 0 | 3 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8884): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0006 | 0/0 | 8891 | 10 | 9 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0007 | 0/0 | 8891 | 9 | 0 | 0 | 9 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0009 | 1/0 | 8891 | 7 | 5 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0010 | 0/0 | 8890 | 7 | 6 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0011 | 0/0 | 8891 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0012 | 0/0 | 8891 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0013 | 0/0 | 8889 | 5 | 1 | 1 | 1 | 2 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8884): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0015 | 0/0 | 8891 | 4 | 0 | 2 | 0 | 1 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0016 | 0/0 | 8890 | 4 | 0 | 0 | 0 | 1 | 3 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0017 | 0/0 | 8891 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0018 | 0/0 | 8891 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0019 | 0/0 | 8891 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0020 | 0/0 | 8890 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0021 | 0/0 | 8890 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0022 | 0/0 | 8891 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0023 | 0/0 | 8891 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0024 | 0/0 | 8891 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0026 | 0/0 | 8890 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0028 | 0/0 | 8891 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0029 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0030 | 0/0 | 8890 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0031 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0032 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0033 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0034 | 0/0 | 8891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0035 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0036 | 0/0 | 8891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0037 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0044 | 0/0 | 8890 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0045 | 0/0 | 8891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0046 | 0/0 | 8891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0048 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0001t0049 | 0/0 | 8890 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8885): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0002 | 0/0 | 8891 | 72 | 2 | 6 | 49 | 3 | 12 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0008 | 0/0 | 8891 | 8 | 0 | 4 | 0 | 4 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0014 | 0/0 | 8891 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0025 | 0/0 | 8891 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0038 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0039 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0040 | 0/0 | 8891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0041 | 0/0 | 8891 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0042 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0043 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0002t0050 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0004t0027 | 0/0 | 8891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0005t0047 | 0/0 | 8891 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0001c0006t0002 | 0/0 | 8891 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| a0002c0003t0001 | 0/0 | 8891 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | CCTCG others(8886): Show |
chr6 | 11532749 | 11588524 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/1 | 14 | 4 | 1 | 7 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 2 | 6 | 2 | 2 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0007 | 0/0 | 8 | 0 | 6 | 0 | 0 | 2 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0029 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0004g0004 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0004g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0019 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0006g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0007g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0009g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0009g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0010g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0010g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0010g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0011g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0011g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0012g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0012g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0013g0003 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0015g0017 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0016g0004 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0017g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0017g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0018g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0018g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0019g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0019g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0020g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0020g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0020g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0021g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0022g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0022g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0023g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0024g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0026g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0028g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0029g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0030g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0031g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0032g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0033g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0034g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0035g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0036g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0037g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0044g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0045g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0046g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0048g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0001t0049g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0001 | 0/0 | 29 | 0 | 1 | 23 | 1 | 4 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0023 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0008g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0008g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0008g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0008g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0008g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0008g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0014g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0014g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0025g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0038g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0039g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0040g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0041g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0042g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0043g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0002t0050g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0004t0027g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0005t0047g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0001c0006t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0030 | g0060 | EUR | GBR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00140 | hp2 | a0001 | c0001 | t0016 | g0004 | EUR | GBR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00280 | hp1 | a0001 | c0002 | t0008 | g0125 | EUR | FIN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00280 | hp2 | a0001 | c0001 | t0013 | g0003 | EUR | FIN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0108 | EUR | FIN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0001 | EUR | FIN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00597 | hp2 | a0001 | c0001 | t0017 | g0077 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00639 | hp2 | a0001 | c0002 | t0008 | g0088 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0074 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG00741 | hp2 | a0001 | c0001 | t0015 | g0017 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01074 | hp2 | a0001 | c0001 | t0013 | g0003 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0111 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0067 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0110 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01169 | hp2 | a0001 | c0002 | t0008 | g0037 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01192 | hp2 | a0001 | c0006 | t0002 | g0001 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0014 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01346 | hp1 | a0001 | c0002 | t0008 | g0113 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01433 | hp2 | a0001 | c0002 | t0008 | g0037 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01496 | hp2 | a0001 | c0001 | t0020 | g0004 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01515 | hp1 | a0001 | c0002 | t0008 | g0086 | EUR | IBS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0034 | EUR | IBS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01516 | hp2 | a0001 | c0001 | t0013 | g0003 | EUR | IBS | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0117 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02015 | hp1 | a0001 | c0001 | t0033 | g0002 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02027 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0034 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02040 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02055 | hp1 | a0001 | c0002 | t0014 | g0025 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0068 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02080 | hp1 | a0001 | c0001 | t0007 | g0150 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02080 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02132 | hp1 | a0001 | c0002 | t0038 | g0094 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | CDX | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02165 | hp2 | a0001 | c0001 | t0022 | g0144 | EAS | CDX | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02257 | hp1 | a0001 | c0001 | t0034 | g0127 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02300 | hp1 | a0001 | c0001 | t0015 | g0017 | AMR | PEL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0151 | EAS | KHV | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02615 | hp2 | a0001 | c0001 | t0020 | g0062 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02622 | hp1 | a0001 | c0001 | t0019 | g0031 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0036 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02647 | hp1 | a0001 | c0001 | t0021 | g0014 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0119 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02717 | hp2 | a0001 | c0001 | t0046 | g0069 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0090 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0031 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02895 | hp2 | a0001 | c0002 | t0014 | g0025 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02896 | hp2 | a0001 | c0004 | t0027 | g0055 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02922 | hp1 | a0001 | c0001 | t0021 | g0014 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02922 | hp2 | a0001 | c0002 | t0014 | g0025 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02970 | hp2 | a0001 | c0002 | t0014 | g0102 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0066 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0023 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03139 | hp1 | a0001 | c0001 | t0020 | g0059 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0044 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03195 | hp1 | a0001 | c0002 | t0014 | g0122 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0106 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03225 | hp2 | a0001 | c0001 | t0045 | g0081 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0121 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0082 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0118 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0036 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03490 | hp1 | a0001 | c0001 | t0016 | g0004 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03492 | hp2 | a0001 | c0002 | t0041 | g0076 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03579 | hp1 | a0001 | c0002 | t0040 | g0124 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0052 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03669 | hp2 | a0001 | c0001 | t0015 | g0017 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03688 | hp2 | a0001 | c0001 | t0028 | g0084 | SAS | STU | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0109 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0063 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0019 | SAS | PJL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0019 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03927 | hp1 | a0001 | c0001 | t0044 | g0064 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0107 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | STU | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0061 | SAS | STU | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0049 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG04204 | hp1 | a0001 | c0001 | t0016 | g0004 | SAS | STU | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | YRI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18522 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | YRI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | CHB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | CHB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | CHB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | YRI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18943 | hp2 | a0001 | c0001 | t0022 | g0027 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18944 | hp2 | a0002 | c0003 | t0001 | g0148 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18946 | hp1 | a0001 | c0001 | t0007 | g0152 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18951 | hp2 | a0001 | c0001 | t0024 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18952 | hp1 | a0001 | c0001 | t0037 | g0163 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18953 | hp2 | a0001 | c0001 | t0029 | g0141 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18954 | hp2 | a0001 | c0001 | t0018 | g0006 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18957 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18960 | hp1 | a0001 | c0001 | t0017 | g0078 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18961 | hp2 | a0001 | c0001 | t0018 | g0006 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18971 | hp1 | a0001 | c0001 | t0024 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18980 | hp1 | a0001 | c0001 | t0018 | g0136 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18981 | hp2 | a0001 | c0001 | t0032 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18992 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18998 | hp1 | a0001 | c0001 | t0023 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18998 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | LWK | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | LWK | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0120 | AFR | LWK | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0072 | AFR | LWK | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19055 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19057 | hp2 | a0001 | c0001 | t0048 | g0006 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19059 | hp2 | a0001 | c0002 | t0043 | g0114 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19060 | hp2 | a0001 | c0001 | t0031 | g0011 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19062 | hp1 | a0001 | c0001 | t0017 | g0079 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19062 | hp2 | a0001 | c0002 | t0025 | g0032 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19066 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19068 | hp1 | a0001 | c0002 | t0042 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19068 | hp2 | a0001 | c0001 | t0035 | g0003 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19075 | hp1 | a0001 | c0001 | t0026 | g0058 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19075 | hp2 | a0001 | c0002 | t0039 | g0126 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19082 | hp1 | a0001 | c0001 | t0049 | g0022 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19083 | hp2 | a0001 | c0001 | t0023 | g0153 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19088 | hp1 | a0001 | c0002 | t0025 | g0032 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19090 | hp2 | a0001 | c0002 | t0050 | g0001 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | YRI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA19240 | hp2 | a0001 | c0001 | t0036 | g0048 | AFR | YRI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0089 | AFR | ASW | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20752 | hp1 | a0001 | c0002 | t0008 | g0096 | EUR | TSI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20805 | hp1 | a0001 | c0001 | t0015 | g0017 | EUR | TSI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20805 | hp2 | a0001 | c0002 | t0008 | g0087 | EUR | TSI | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20905 | hp1 | a0001 | c0001 | t0016 | g0004 | SAS | GIH | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0112 | AMR | CLM | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0123 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0013 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0009 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | MSL | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | USA | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA20300 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | USA | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA21309 | hp1 | a0001 | c0005 | t0047 | g0075 | AFR | LWK | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0071 | REF | REF | TMEM170B_chr6_11532749_11588524 | TMEM170B | chr6 | 11532749 | 11588524 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:11538290 | G | A | 1 | a0002 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.13G>A | p.Gly5Arg | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | 542/8891 | 13/399 | 5/132 | chr6 | 11538290 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:11538301 | C | T | 2 | a0001c0002 a0001c0006 |
95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
synonymous_variant | LOW | c.24C>T | p.His8His | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | 553/8891 | 24/399 | 8/132 | chr6 | 11538301 | |||
| chr6:11538331 | C | G | 1 | a0001c0005 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.54C>G | p.Val18Val | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | 583/8891 | 54/399 | 18/132 | chr6 | 11538331 | |||
| chr6:11538331 | C | T | 1 | a0001c0006 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.54C>T | p.Val18Val | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | 583/8891 | 54/399 | 18/132 | chr6 | 11538331 | |||
| chr6:11565727 | A | G | 1 | a0001c0004 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.159A>G | p.Ala53Ala | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/3 | 688/8891 | 159/399 | 53/132 | chr6 | 11565727 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:11537969 | G | A | 1 | a0001c0001t0026 | 1 | NA19075.hp1 | 5_prime_UTR_variant | MODIFIER | c.-309G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | 309 | chr6 | 11537969 | ||||||
| chr6:11537992 | C | T | 1 | a0001c0002t0050 | 1 | NA19090.hp2 | 5_prime_UTR_variant | MODIFIER | c.-286C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | 286 | chr6 | 11537992 | ||||||
| chr6:11538061 | C | T | 1 | a0001c0001t0049 | 1 | NA19082.hp1 | 5_prime_UTR_variant | MODIFIER | c.-217C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | 217 | chr6 | 11538061 | ||||||
| chr6:11538156 | C | T | 1 | a0001c0001t0048 | 1 | NA19057.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-122C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/3 | chr6 | 11538156 | |||||||
| chr6:11575897 | T | C | 46 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(43): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*336T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 336 | chr6 | 11575897 | ||||||
| chr6:11575942 | T | C | 2 | a0001c0001t0005 a0001c0004t0027 |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*381T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 381 | chr6 | 11575942 | ||||||
| chr6:11576032 | G | A | 1 | a0001c0001t0028 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*471G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 471 | chr6 | 11576032 | ||||||
| chr6:11576439 | G | C | 1 | a0001c0001t0029 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*878G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 878 | chr6 | 11576439 | ||||||
| chr6:11576541 | A | G | 1 | a0001c0001t0045 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 980 | chr6 | 11576541 | ||||||
| chr6:11576700 | C | G | 7 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(4): Show |
33 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1139C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1139 | chr6 | 11576700 | ||||||
| chr6:11576819 | T | C | 1 | a0001c0001t0003 | 23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1258T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1258 | chr6 | 11576819 | ||||||
| chr6:11576852 | C | T | 13 | a0001c0001t0029 a0001c0002t0002 a0001c0002t0008 others(10): Show |
96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1291C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1291 | chr6 | 11576852 | ||||||
| chr6:11576868 | CA | C | 2 | a0001c0001t0010 a0001c0001t0021 |
10 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1311delA | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1311 | INFO_REALIGN_3_PRIME | chr6 | 11576868 | |||||
| chr6:11576970 | T | C | 1 | a0001c0001t0020 | 3 | HG01496.hp2 HG02615.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1409T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1409 | chr6 | 11576970 | ||||||
| chr6:11577233 | T | C | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1672T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1672 | chr6 | 11577233 | ||||||
| chr6:11577339 | A | G | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1778A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1778 | chr6 | 11577339 | ||||||
| chr6:11577459 | C | A | 1 | a0001c0002t0038 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1898C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 1898 | chr6 | 11577459 | ||||||
| chr6:11577635 | C | T | 1 | a0001c0001t0037 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2074C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 2074 | chr6 | 11577635 | ||||||
| chr6:11577785 | CT | C | 7 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(4): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2227delT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 2227 | INFO_REALIGN_3_PRIME | chr6 | 11577785 | |||||
| chr6:11577790 | C | A | 7 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(4): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2229C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 2229 | chr6 | 11577790 | ||||||
| chr6:11578031 | C | T | 2 | a0001c0001t0019 a0001c0001t0036 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2470C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 2470 | chr6 | 11578031 | ||||||
| chr6:11578124 | G | C | 1 | a0001c0001t0044 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2563G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 2563 | chr6 | 11578124 | ||||||
| chr6:11578317 | G | T | 6 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(3): Show |
32 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2756G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 2756 | chr6 | 11578317 | ||||||
| chr6:11578428 | C | G | 1 | a0001c0002t0043 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2867C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 2867 | chr6 | 11578428 | ||||||
| chr6:11578860 | G | A | 29 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(26): Show |
189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*3299G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3299 | chr6 | 11578860 | ||||||
| chr6:11578899 | T | G | 2 | a0001c0001t0007 a0001c0001t0031 |
10 | HG02027.hp2 HG02056.hp2 HG02080.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3338T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3338 | chr6 | 11578899 | ||||||
| chr6:11579010 | G | A | 1 | a0001c0001t0019 | 3 | HG02622.hp1 HG02886.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3449G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3449 | chr6 | 11579010 | ||||||
| chr6:11579054 | C | T | 1 | a0001c0001t0045 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3493C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3493 | chr6 | 11579054 | ||||||
| chr6:11579178 | T | C | 2 | a0001c0001t0005 a0001c0004t0027 |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3617T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3617 | chr6 | 11579178 | ||||||
| chr6:11579297 | A | G | 1 | a0001c0001t0017 | 3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3736A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3736 | chr6 | 11579297 | ||||||
| chr6:11579431 | G | T | 7 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(4): Show |
33 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3870G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3870 | chr6 | 11579431 | ||||||
| chr6:11579496 | G | A | 16 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0013 others(13): Show |
132 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*3935G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3935 | chr6 | 11579496 | ||||||
| chr6:11579545 | T | G | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3984T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 3984 | chr6 | 11579545 | ||||||
| chr6:11579586 | A | G | 1 | a0001c0001t0016 | 4 | HG00140.hp2 HG03490.hp1 HG04204.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4025A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 4025 | chr6 | 11579586 | ||||||
| chr6:11579628 | A | G | 1 | a0001c0001t0003 | 23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4067A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 4067 | chr6 | 11579628 | ||||||
| chr6:11579835 | A | C | 1 | a0001c0001t0003 | 23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4274A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 4274 | chr6 | 11579835 | ||||||
| chr6:11580044 | C | T | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4483C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 4483 | chr6 | 11580044 | ||||||
| chr6:11580091 | C | T | 1 | a0001c0001t0035 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4530C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 4530 | chr6 | 11580091 | ||||||
| chr6:11580092 | G | A | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4531G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 4531 | chr6 | 11580092 | ||||||
| chr6:11580190 | T | G | 1 | a0001c0001t0032 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4629T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 4629 | chr6 | 11580190 | ||||||
| chr6:11580664 | G | A | 2 | a0001c0001t0018 a0001c0001t0022 |
5 | HG02165.hp2 NA18943.hp2 NA18954.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5103G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5103 | chr6 | 11580664 | ||||||
| chr6:11580743 | A | C | 2 | a0001c0001t0005 a0001c0004t0027 |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*5182A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5182 | chr6 | 11580743 | ||||||
| chr6:11580752 | A | G | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*5191A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5191 | chr6 | 11580752 | ||||||
| chr6:11580767 | T | A | 2 | a0001c0001t0019 a0001c0001t0036 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5206T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5206 | chr6 | 11580767 | ||||||
| chr6:11580779 | C | T | 1 | a0001c0002t0025 | 2 | NA19062.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5218C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5218 | chr6 | 11580779 | ||||||
| chr6:11580885 | A | G | 1 | a0001c0001t0034 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5324A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5324 | chr6 | 11580885 | ||||||
| chr6:11580963 | G | T | 7 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(4): Show |
33 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5402G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5402 | chr6 | 11580963 | ||||||
| chr6:11581141 | T | C | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*5580T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5580 | chr6 | 11581141 | ||||||
| chr6:11581181 | A | G | 1 | a0001c0001t0012 | 5 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5620A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5620 | chr6 | 11581181 | ||||||
| chr6:11581243 | C | T | 1 | a0001c0002t0042 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5682C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5682 | chr6 | 11581243 | ||||||
| chr6:11581362 | T | G | 8 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(5): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*5801T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5801 | chr6 | 11581362 | ||||||
| chr6:11581544 | G | A | 1 | a0001c0002t0014 | 5 | HG02055.hp1 HG02895.hp2 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5983G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 5983 | chr6 | 11581544 | ||||||
| chr6:11581642 | G | C | 1 | a0001c0001t0021 | 3 | HG02647.hp1 HG02922.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6081G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6081 | chr6 | 11581642 | ||||||
| chr6:11581660 | C | G | 1 | a0001c0001t0015 | 4 | HG00741.hp2 HG02300.hp1 HG03669.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6099C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6099 | chr6 | 11581660 | ||||||
| chr6:11581730 | A | G | 1 | a0001c0001t0036 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6169A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6169 | chr6 | 11581730 | ||||||
| chr6:11581757 | A | G | 9 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(6): Show |
35 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*6196A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6196 | chr6 | 11581757 | ||||||
| chr6:11581807 | T | C | 1 | a0001c0001t0046 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6246T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6246 | chr6 | 11581807 | ||||||
| chr6:11582059 | T | A | 13 | a0001c0001t0011 a0001c0001t0029 a0001c0002t0002 others(10): Show |
100 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*6498T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6498 | chr6 | 11582059 | ||||||
| chr6:11582214 | A | G | 10 | a0001c0001t0004 a0001c0001t0016 a0001c0001t0020 others(7): Show |
36 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*6653A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6653 | chr6 | 11582214 | ||||||
| chr6:11582399 | A | T | 50 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(47): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*6838A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6838 | chr6 | 11582399 | ||||||
| chr6:11582447 | A | G | 1 | a0001c0001t0018 | 3 | NA18954.hp2 NA18961.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6886A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6886 | chr6 | 11582447 | ||||||
| chr6:11582458 | G | T | 1 | a0001c0001t0033 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6897G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6897 | chr6 | 11582458 | ||||||
| chr6:11582471 | C | A | 1 | a0001c0001t0023 | 2 | NA18998.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6910C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6910 | chr6 | 11582471 | ||||||
| chr6:11582514 | CTA | C | 2 | a0001c0001t0005 a0001c0001t0013 |
23 | HG00280.hp2 HG01074.hp2 HG01516.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*6957_*6958delAT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 6957 | INFO_REALIGN_3_PRIME | chr6 | 11582514 | |||||
| chr6:11582700 | T | C | 1 | a0001c0002t0039 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7139T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 7139 | chr6 | 11582700 | ||||||
| chr6:11582775 | G | A | 1 | a0001c0001t0024 | 2 | NA18951.hp2 NA18971.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7214G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 7214 | chr6 | 11582775 | ||||||
| chr6:11583508 | T | G | 1 | a0001c0002t0008 | 8 | HG00280.hp1 HG00639.hp2 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7947T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 3/3 | 7947 | chr6 | 11583508 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:11538395 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.97+21G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11538395 | |||||||
| chr6:11538595 | G | A | 1 | a0001c0001t0006g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.97+221G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11538595 | |||||||
| chr6:11538604 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.97+230G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11538604 | |||||||
| chr6:11538627 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.97+253C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11538627 | |||||||
| chr6:11538839 | A | G | 13 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0164 others(10): Show |
22 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.97+465A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11538839 | |||||||
| chr6:11538960 | C | T | 1 | a0001c0001t0006g0012 | 5 | HG02145.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+586C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11538960 | |||||||
| chr6:11539009 | G | A | 1 | a0001c0001t0036g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97+635G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11539009 | |||||||
| chr6:11539104 | G | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
130 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.97+730G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11539104 | |||||||
| chr6:11539302 | A | T | 1 | a0001c0002t0039g0126 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.97+928A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11539302 | |||||||
| chr6:11539416 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.97+1042A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11539416 | |||||||
| chr6:11539602 | C | T | 2 | a0001c0002t0008g0037 a0001c0002t0008g0125 |
3 | HG00280.hp1 HG01169.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.97+1228C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11539602 | |||||||
| chr6:11539661 | C | T | 1 | a0001c0001t0037g0163 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.97+1287C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11539661 | |||||||
| chr6:11540027 | G | A | 1 | a0001c0002t0002g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.97+1653G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540027 | |||||||
| chr6:11540176 | T | C | 28 | a0001c0001t0001g0021 a0001c0001t0004g0004 a0001c0001t0004g0008 others(25): Show |
56 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.97+1802T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540176 | |||||||
| chr6:11540195 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG02896.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.97+1821G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540195 | |||||||
| chr6:11540304 | A | G | 2 | a0001c0001t0004g0008 a0001c0001t0004g0065 |
7 | HG00408.hp2 HG02083.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+1930A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540304 | |||||||
| chr6:11540357 | C | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.97+1983C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540357 | |||||||
| chr6:11540393 | G | A | 13 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(10): Show |
20 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+2019G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540393 | |||||||
| chr6:11540554 | C | T | 1 | a0001c0002t0040g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.97+2180C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540554 | |||||||
| chr6:11540565 | A | G | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+2191A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540565 | |||||||
| chr6:11540626 | A | C | 1 | a0001c0002t0014g0122 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.97+2252A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11540626 | |||||||
| chr6:11541150 | A | G | 1 | a0001c0002t0002g0121 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.97+2776A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541150 | |||||||
| chr6:11541168 | G | T | 5 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+2794G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541168 | |||||||
| chr6:11541444 | T | A | 1 | a0001c0002t0041g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.97+3070T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541444 | |||||||
| chr6:11541491 | T | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+3117T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541491 | |||||||
| chr6:11541508 | G | A | 13 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(10): Show |
20 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+3134G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541508 | |||||||
| chr6:11541645 | C | T | 13 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(10): Show |
20 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+3271C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541645 | |||||||
| chr6:11541741 | G | A | 13 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(10): Show |
20 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+3367G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541741 | |||||||
| chr6:11541857 | C | G | 8 | a0001c0001t0006g0046 a0001c0001t0006g0073 a0001c0001t0006g0074 others(5): Show |
14 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.97+3483C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541857 | |||||||
| chr6:11541861 | G | A | 17 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(14): Show |
27 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.97+3487G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11541861 | |||||||
| chr6:11542007 | A | G | 1 | a0001c0001t0005g0057 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.97+3633A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542007 | |||||||
| chr6:11542016 | AAAT | A | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
133 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.97+3651_97+3653del others(3): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11542016 | ||||||
| chr6:11542051 | T | G | 21 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(18): Show |
29 | HG00597.hp2 HG01891.hp2 HG02015.hp2 others(26): Show |
intron_variant | MODIFIER | c.97+3677T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542051 | |||||||
| chr6:11542185 | G | A | 1 | a0001c0001t0034g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97+3811G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542185 | |||||||
| chr6:11542208 | T | G | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+3834T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542208 | |||||||
| chr6:11542237 | A | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+3863A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542237 | |||||||
| chr6:11542277 | C | T | 2 | a0001c0001t0003g0007 a0001c0001t0003g0173 |
9 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+3903C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542277 | |||||||
| chr6:11542349 | T | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.97+3975T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542349 | |||||||
| chr6:11542403 | A | G | 73 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(70): Show |
125 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.97+4029A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542403 | |||||||
| chr6:11542444 | T | C | 4 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 others(1): Show |
4 | HG00597.hp2 HG03225.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+4070T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542444 | |||||||
| chr6:11542448 | A | G | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+4074A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542448 | |||||||
| chr6:11542479 | A | G | 1 | a0001c0001t0005g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.97+4105A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542479 | |||||||
| chr6:11542489 | AGGACTGA others(4): Show |
A | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+4125_97+4135del others(11): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11542489 | ||||||
| chr6:11542596 | T | G | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+4222T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542596 | |||||||
| chr6:11542785 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.97+4411T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542785 | |||||||
| chr6:11542804 | C | T | 4 | a0001c0001t0011g0026 a0001c0001t0011g0123 a0001c0001t0019g0031 others(1): Show |
7 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+4430C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542804 | |||||||
| chr6:11542911 | T | C | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+4537T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542911 | |||||||
| chr6:11542958 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.97+4584A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11542958 | |||||||
| chr6:11543062 | C | A | 16 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(13): Show |
27 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.97+4688C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543062 | |||||||
| chr6:11543062 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.97+4688C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543062 | |||||||
| chr6:11543109 | A | G | 77 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(74): Show |
128 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.97+4735A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543109 | |||||||
| chr6:11543255 | A | G | 3 | a0001c0002t0002g0115 a0001c0002t0002g0116 a0001c0002t0043g0114 |
3 | NA18990.hp2 NA19003.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.97+4881A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543255 | |||||||
| chr6:11543359 | G | A | 1 | a0001c0001t0009g0066 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.97+4985G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543359 | |||||||
| chr6:11543569 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.97+5195A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543569 | |||||||
| chr6:11543596 | A | G | 1 | a0001c0001t0044g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97+5222A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543596 | |||||||
| chr6:11543746 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97+5372T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543746 | |||||||
| chr6:11543812 | T | C | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.97+5438T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11543812 | |||||||
| chr6:11544217 | T | G | 1 | a0001c0002t0040g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.97+5843T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544217 | |||||||
| chr6:11544424 | G | T | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+6050G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544424 | |||||||
| chr6:11544438 | T | G | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+6064T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544438 | |||||||
| chr6:11544467 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+6093C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544467 | |||||||
| chr6:11544496 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97+6122G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544496 | |||||||
| chr6:11544568 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+6194C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544568 | |||||||
| chr6:11544598 | A | C | 54 | a0001c0001t0028g0084 a0001c0002t0002g0001 a0001c0002t0002g0015 others(51): Show |
96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.97+6224A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544598 | |||||||
| chr6:11544649 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97+6275A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544649 | |||||||
| chr6:11544683 | C | T | 1 | a0001c0001t0007g0157 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.97+6309C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544683 | |||||||
| chr6:11544927 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.97+6553T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11544927 | |||||||
| chr6:11544949 | GT | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+6585delT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11544949 | ||||||
| chr6:11545002 | A | C | 1 | a0001c0002t0008g0113 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.97+6628A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545002 | |||||||
| chr6:11545254 | G | A | 1 | a0001c0001t0007g0132 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.97+6880G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545254 | |||||||
| chr6:11545264 | T | TTC | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0005g0050 others(2): Show |
6 | HG02257.hp2 HG02622.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+6906_97+6907dup others(2): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545264 | ||||||
| chr6:11545264 | T | TTCTCTC | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+6902_97+6907dup others(6): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545264 | ||||||
| chr6:11545278 | C | CTGTGTGT others(7): Show |
1 | a0001c0002t0002g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.97+6905_97+6906ins others(14): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545278 | ||||||
| chr6:11545278 | CTCTG | C | 1 | a0001c0001t0005g0020 | 3 | HG02015.hp2 NA19005.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.97+6906_97+6909del others(4): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545278 | ||||||
| chr6:11545280 | C | CTCTCTG | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(6): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTCTGT others(7): Show |
3 | a0001c0001t0003g0080 a0001c0001t0003g0171 a0001c0001t0003g0172 |
3 | HG02486.hp2 HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(14): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTCTGT others(11): Show |
5 | a0001c0001t0003g0007 a0001c0001t0003g0166 a0001c0001t0003g0173 others(2): Show |
11 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(18): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTCTGT others(13): Show |
8 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0164 others(5): Show |
10 | HG00741.hp1 HG01071.hp2 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(20): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTG | 4 | a0001c0001t0005g0030 a0001c0001t0005g0051 a0001c0001t0005g0053 others(1): Show |
5 | HG02572.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(4): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTGTGT others(1): Show |
3 | a0001c0001t0017g0078 a0001c0001t0017g0079 a0001c0004t0027g0055 |
3 | HG02896.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(8): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTGTGT others(3): Show |
1 | a0001c0001t0017g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.97+6907_97+6908ins others(10): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTGTGT others(7): Show |
2 | a0001c0002t0008g0087 a0001c0002t0008g0088 |
2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(14): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTCTGTGT others(11): Show |
2 | a0001c0002t0002g0023 a0001c0002t0002g0089 |
2 | HG01109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.97+6907_97+6908ins others(18): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTG | 5 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0043 others(2): Show |
8 | HG01175.hp2 HG01496.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6936_97+6937dup others(2): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(1): Show |
4 | a0001c0001t0012g0036 a0001c0001t0012g0117 a0001c0001t0012g0118 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+6930_97+6937dup others(8): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(3): Show |
1 | a0001c0002t0002g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.97+6928_97+6937dup others(10): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(5): Show |
3 | a0001c0002t0002g0001 a0001c0002t0002g0111 a0001c0006t0002g0001 |
4 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+6926_97+6937dup others(12): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(7): Show |
9 | a0001c0001t0011g0120 a0001c0002t0002g0049 a0001c0002t0002g0083 others(6): Show |
9 | HG01167.hp2 HG01358.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+6924_97+6937dup others(14): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(9): Show |
10 | a0001c0002t0002g0001 a0001c0002t0002g0015 a0001c0002t0002g0033 others(7): Show |
12 | HG00323.hp1 HG01433.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.97+6922_97+6937dup others(16): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(11): Show |
21 | a0001c0002t0002g0001 a0001c0002t0002g0015 a0001c0002t0002g0023 others(18): Show |
34 | HG00609.hp1 HG01169.hp2 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.97+6920_97+6937dup others(18): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(13): Show |
9 | a0001c0002t0002g0001 a0001c0002t0002g0024 a0001c0002t0002g0034 others(6): Show |
17 | HG00558.hp2 HG01346.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.97+6918_97+6937dup others(20): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(15): Show |
8 | a0001c0002t0002g0001 a0001c0002t0002g0015 a0001c0002t0002g0023 others(5): Show |
8 | HG03017.hp2 HG03710.hp1 HG03834.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6916_97+6937dup others(22): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(17): Show |
2 | a0001c0002t0002g0001 a0001c0002t0002g0015 |
5 | NA18945.hp2 NA18962.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+6914_97+6937dup others(24): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | CTGTGTGT others(21): Show |
1 | a0001c0002t0008g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.97+6910_97+6937dup others(28): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545280 | ||||||
| chr6:11545280 | C | G | 9 | a0001c0001t0001g0021 a0001c0001t0007g0011 a0001c0001t0007g0132 others(6): Show |
12 | HG01123.hp2 HG02027.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+6906C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545280 | |||||||
| chr6:11545282 | G | C | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0038 others(20): Show |
47 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.97+6908G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545282 | |||||||
| chr6:11545284 | G | C | 13 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(10): Show |
32 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.97+6910G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545284 | |||||||
| chr6:11545349 | G | A | 53 | a0001c0002t0002g0001 a0001c0002t0002g0015 a0001c0002t0002g0023 others(50): Show |
95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.97+6975G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545349 | |||||||
| chr6:11545533 | C | T | 53 | a0001c0002t0002g0001 a0001c0002t0002g0015 a0001c0002t0002g0023 others(50): Show |
95 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.97+7159C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545533 | |||||||
| chr6:11545678 | C | T | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+7304C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545678 | |||||||
| chr6:11545709 | A | T | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+7335A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545709 | |||||||
| chr6:11545737 | T | TTA | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.97+7363_97+7364ins others(2): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545737 | |||||||
| chr6:11545773 | C | T | 1 | a0001c0002t0002g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.97+7399C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545773 | |||||||
| chr6:11545789 | C | T | 1 | a0001c0001t0036g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97+7415C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545789 | |||||||
| chr6:11545843 | T | TA | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(182): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.97+7479dupA | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11545843 | ||||||
| chr6:11545873 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.97+7499G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545873 | |||||||
| chr6:11545943 | C | A | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+7569C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11545943 | |||||||
| chr6:11546012 | T | TA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
196 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.97+7661dupA | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11546012 | ||||||
| chr6:11546012 | T | TAA | 10 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0135 others(7): Show |
16 | HG00597.hp1 HG01109.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+7660_97+7661dup others(2): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11546012 | ||||||
| chr6:11546012 | TAAAAAAA others(2): Show |
T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+7653_97+7661del others(9): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11546012 | ||||||
| chr6:11546149 | TG | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+7778delG | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11546149 | ||||||
| chr6:11546170 | A | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.97+7796A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546170 | |||||||
| chr6:11546245 | A | ATTTTTTT others(1): Show |
11 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(8): Show |
18 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+7873_97+7880dup others(8): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11546245 | ||||||
| chr6:11546263 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
133 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.97+7889A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546263 | |||||||
| chr6:11546264 | A | G | 54 | a0001c0001t0028g0084 a0001c0002t0002g0001 a0001c0002t0002g0015 others(51): Show |
96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.97+7890A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546264 | |||||||
| chr6:11546303 | T | G | 1 | a0001c0002t0040g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.97+7929T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546303 | |||||||
| chr6:11546365 | GTTAAAAC | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0173 |
9 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+7998_97+8004del others(7): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11546365 | ||||||
| chr6:11546369 | A | G | 1 | a0001c0001t0004g0004 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.97+7995A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546369 | |||||||
| chr6:11546453 | A | G | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+8079A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546453 | |||||||
| chr6:11546459 | G | A | 1 | a0001c0001t0036g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97+8085G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546459 | |||||||
| chr6:11546608 | T | C | 1 | a0001c0001t0010g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97+8234T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546608 | |||||||
| chr6:11546647 | C | G | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+8273C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546647 | |||||||
| chr6:11546867 | A | C | 1 | a0001c0001t0004g0065 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.97+8493A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546867 | |||||||
| chr6:11546964 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97+8590C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11546964 | |||||||
| chr6:11547015 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.97+8641G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547015 | |||||||
| chr6:11547286 | G | A | 1 | a0001c0002t0014g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.97+8912G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547286 | |||||||
| chr6:11547403 | A | G | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+9029A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547403 | |||||||
| chr6:11547413 | G | GA | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+9045dupA | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11547413 | ||||||
| chr6:11547427 | A | G | 1 | a0001c0001t0005g0057 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.97+9053A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547427 | |||||||
| chr6:11547634 | T | C | 8 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(5): Show |
9 | HG00597.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+9260T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547634 | |||||||
| chr6:11547667 | G | A | 1 | a0001c0001t0006g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+9293G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547667 | |||||||
| chr6:11547691 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.97+9317T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547691 | |||||||
| chr6:11547807 | C | T | 8 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(5): Show |
9 | HG00597.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+9433C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11547807 | |||||||
| chr6:11548269 | A | G | 7 | a0001c0002t0002g0083 a0001c0002t0002g0107 a0001c0002t0002g0108 others(4): Show |
7 | HG00323.hp1 HG01081.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+9895A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548269 | |||||||
| chr6:11548290 | G | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
133 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.97+9916G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548290 | |||||||
| chr6:11548318 | A | T | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+9944A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548318 | |||||||
| chr6:11548326 | T | A | 8 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(5): Show |
9 | HG00597.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+9952T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548326 | |||||||
| chr6:11548378 | A | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
133 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.97+10004A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548378 | |||||||
| chr6:11548485 | A | G | 1 | a0001c0001t0004g0063 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.97+10111A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548485 | |||||||
| chr6:11548491 | G | A | 1 | a0001c0001t0005g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.97+10117G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548491 | |||||||
| chr6:11548510 | C | CAG | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+10136_97+10137i others(4): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548510 | |||||||
| chr6:11548522 | C | T | 1 | a0001c0002t0002g0101 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.97+10148C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548522 | |||||||
| chr6:11548679 | T | G | 1 | a0001c0001t0015g0017 | 4 | HG00741.hp2 HG02300.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+10305T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548679 | |||||||
| chr6:11548695 | T | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.97+10321T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548695 | |||||||
| chr6:11548810 | A | G | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.97+10436A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548810 | |||||||
| chr6:11548813 | T | A | 5 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+10439T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11548813 | |||||||
| chr6:11549086 | A | G | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+10712A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549086 | |||||||
| chr6:11549309 | GACTA | G | 16 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(13): Show |
25 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.97+10940_97+10943d others(6): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11549309 | ||||||
| chr6:11549412 | C | T | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+11038C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549412 | |||||||
| chr6:11549415 | G | A | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+11041G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549415 | |||||||
| chr6:11549445 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+11071C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549445 | |||||||
| chr6:11549459 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+11085C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549459 | |||||||
| chr6:11549511 | AAGTT | A | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+11140_97+11143d others(6): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11549511 | ||||||
| chr6:11549534 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.97+11160G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549534 | |||||||
| chr6:11549595 | G | A | 1 | a0001c0002t0002g0085 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.97+11221G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549595 | |||||||
| chr6:11549649 | C | T | 5 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+11275C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549649 | |||||||
| chr6:11549662 | C | CA | 8 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0002t0002g0024 others(5): Show |
11 | HG00280.hp1 HG00639.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+11301dupA | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11549662 | ||||||
| chr6:11549682 | A | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+11308A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549682 | |||||||
| chr6:11549785 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0162 |
3 | NA18946.hp2 NA18991.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.97+11411G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11549785 | |||||||
| chr6:11550027 | G | A | 1 | a0001c0001t0009g0068 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.97+11653G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550027 | |||||||
| chr6:11550131 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
132 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.97+11757C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550131 | |||||||
| chr6:11550174 | A | AT | 17 | a0001c0001t0001g0135 a0001c0001t0005g0018 a0001c0001t0005g0019 others(14): Show |
25 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.97+11816dupT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11550174 | ||||||
| chr6:11550174 | AT | A | 77 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(74): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.97+11816delT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11550174 | ||||||
| chr6:11550234 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.97+11860G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550234 | |||||||
| chr6:11550235 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.97+11861C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550235 | |||||||
| chr6:11550290 | C | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+11916C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550290 | |||||||
| chr6:11550291 | G | A | 1 | a0001c0002t0002g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97+11917G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550291 | |||||||
| chr6:11550338 | T | C | 1 | a0001c0001t0017g0077 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.97+11964T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550338 | |||||||
| chr6:11550508 | C | T | 1 | a0001c0001t0034g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97+12134C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550508 | |||||||
| chr6:11550515 | T | TATGATTC others(311): Show |
1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+12150_97+12151i others(320): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11550515 | ||||||
| chr6:11550516 | A | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+12142A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550516 | |||||||
| chr6:11550752 | T | C | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97+12378T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550752 | |||||||
| chr6:11550759 | C | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+12385C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550759 | |||||||
| chr6:11550817 | A | G | 16 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(13): Show |
27 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.97+12443A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550817 | |||||||
| chr6:11550999 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.97+12625T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11550999 | |||||||
| chr6:11551434 | T | C | 1 | a0001c0002t0002g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.97+13060T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11551434 | |||||||
| chr6:11551645 | A | G | 7 | a0001c0001t0007g0011 a0001c0001t0007g0132 a0001c0001t0007g0150 others(4): Show |
10 | HG02027.hp2 HG02056.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+13271A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11551645 | |||||||
| chr6:11551832 | G | A | 1 | a0001c0001t0029g0141 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.97+13458G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11551832 | |||||||
| chr6:11552063 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-13603C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552063 | |||||||
| chr6:11552120 | A | G | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-13546A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552120 | |||||||
| chr6:11552137 | G | A | 14 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(11): Show |
23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-13529G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552137 | |||||||
| chr6:11552173 | T | G | 1 | a0001c0001t0003g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.98-13493T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552173 | |||||||
| chr6:11552176 | T | A | 1 | a0001c0002t0002g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.98-13490T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552176 | |||||||
| chr6:11552559 | TTCA | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-13105_98-13103d others(5): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11552559 | ||||||
| chr6:11552644 | G | A | 4 | a0001c0001t0012g0036 a0001c0001t0012g0117 a0001c0001t0012g0118 others(1): Show |
5 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-13022G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552644 | |||||||
| chr6:11552675 | C | T | 1 | a0001c0001t0020g0062 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.98-12991C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552675 | |||||||
| chr6:11552678 | A | T | 1 | a0001c0001t0004g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.98-12988A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552678 | |||||||
| chr6:11552831 | G | A | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-12835G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11552831 | |||||||
| chr6:11553247 | C | A | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-12419C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553247 | |||||||
| chr6:11553273 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.98-12393A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553273 | |||||||
| chr6:11553350 | A | G | 1 | a0001c0001t0006g0046 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.98-12316A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553350 | |||||||
| chr6:11553513 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.98-12153A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553513 | |||||||
| chr6:11553665 | A | G | 1 | a0001c0002t0002g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.98-12001A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553665 | |||||||
| chr6:11553692 | T | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-11974T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553692 | |||||||
| chr6:11553774 | T | C | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-11892T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553774 | |||||||
| chr6:11553832 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.98-11834T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553832 | |||||||
| chr6:11553932 | A | C | 1 | a0001c0002t0002g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.98-11734A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553932 | |||||||
| chr6:11553948 | T | C | 55 | a0001c0001t0028g0084 a0001c0001t0029g0141 a0001c0002t0002g0001 others(52): Show |
97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.98-11718T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553948 | |||||||
| chr6:11553961 | G | A | 1 | a0001c0002t0008g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98-11705G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11553961 | |||||||
| chr6:11554042 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-11624C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554042 | |||||||
| chr6:11554119 | T | C | 1 | a0001c0001t0012g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.98-11547T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554119 | |||||||
| chr6:11554155 | A | T | 2 | a0001c0002t0002g0099 a0001c0002t0002g0101 |
2 | NA18966.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.98-11511A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554155 | |||||||
| chr6:11554177 | A | G | 1 | a0001c0001t0030g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.98-11489A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554177 | |||||||
| chr6:11554235 | T | C | 1 | a0001c0001t0022g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.98-11431T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554235 | |||||||
| chr6:11554665 | A | C | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-11001A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554665 | |||||||
| chr6:11554676 | T | C | 14 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(11): Show |
23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-10990T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554676 | |||||||
| chr6:11554708 | C | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.98-10958C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554708 | |||||||
| chr6:11554743 | C | G | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-10923C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554743 | |||||||
| chr6:11554752 | A | G | 55 | a0001c0001t0028g0084 a0001c0001t0029g0141 a0001c0002t0002g0001 others(52): Show |
97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.98-10914A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554752 | |||||||
| chr6:11554810 | T | C | 2 | a0001c0001t0003g0007 a0001c0001t0003g0173 |
9 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-10856T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11554810 | |||||||
| chr6:11555210 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0018g0006 others(2): Show |
10 | HG00621.hp2 HG02083.hp1 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-10456T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555210 | |||||||
| chr6:11555307 | C | A | 1 | a0001c0002t0002g0107 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.98-10359C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555307 | |||||||
| chr6:11555339 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-10327C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555339 | |||||||
| chr6:11555422 | T | C | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-10244T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555422 | |||||||
| chr6:11555488 | A | C | 1 | a0001c0001t0010g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.98-10178A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555488 | |||||||
| chr6:11555496 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-10170C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555496 | |||||||
| chr6:11555570 | A | G | 1 | a0001c0002t0041g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.98-10096A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555570 | |||||||
| chr6:11555645 | A | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-10021A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555645 | |||||||
| chr6:11555679 | G | A | 55 | a0001c0001t0028g0084 a0001c0001t0029g0141 a0001c0002t0002g0001 others(52): Show |
97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.98-9987G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555679 | |||||||
| chr6:11555747 | A | G | 1 | a0001c0001t0003g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.98-9919A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555747 | |||||||
| chr6:11555754 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.98-9912G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555754 | |||||||
| chr6:11555854 | T | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-9812T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11555854 | |||||||
| chr6:11555858 | TAAAGACT others(313): Show |
T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(182): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.98-9792_98-9473del | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11555858 | ||||||
| chr6:11556267 | G | A | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-9399G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11556267 | |||||||
| chr6:11556554 | C | T | 14 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(11): Show |
23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-9112C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11556554 | |||||||
| chr6:11556670 | C | T | 1 | a0001c0002t0002g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.98-8996C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11556670 | |||||||
| chr6:11556756 | C | T | 1 | a0001c0002t0002g0097 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.98-8910C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11556756 | |||||||
| chr6:11556877 | C | G | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98-8789C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11556877 | |||||||
| chr6:11556910 | C | T | 1 | a0001c0001t0020g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.98-8756C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11556910 | |||||||
| chr6:11556978 | A | G | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-8688A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11556978 | |||||||
| chr6:11557109 | T | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-8557T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11557109 | |||||||
| chr6:11557361 | A | G | 1 | a0001c0001t0005g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.98-8305A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11557361 | |||||||
| chr6:11557506 | A | T | 16 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(13): Show |
27 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.98-8160A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11557506 | |||||||
| chr6:11557872 | T | C | 14 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(11): Show |
23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-7794T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11557872 | |||||||
| chr6:11557996 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0013g0044 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.98-7670A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11557996 | |||||||
| chr6:11558260 | G | A | 2 | a0001c0001t0009g0068 a0001c0001t0046g0069 |
2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.98-7406G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11558260 | |||||||
| chr6:11558508 | A | G | 1 | a0001c0005t0047g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-7158A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11558508 | |||||||
| chr6:11558534 | C | T | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-7132C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11558534 | |||||||
| chr6:11558636 | C | T | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-7030C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11558636 | |||||||
| chr6:11558749 | TACCCCAT others(3): Show |
T | 1 | a0001c0001t0001g0154 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.98-6915_98-6906del others(10): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11558749 | ||||||
| chr6:11558792 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.98-6874G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11558792 | |||||||
| chr6:11558803 | A | G | 5 | a0001c0002t0008g0086 a0001c0002t0008g0087 a0001c0002t0008g0088 others(2): Show |
5 | HG00639.hp2 HG01346.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-6863A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11558803 | |||||||
| chr6:11559014 | G | A | 16 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(13): Show |
27 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.98-6652G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559014 | |||||||
| chr6:11559033 | C | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-6633C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559033 | |||||||
| chr6:11559142 | A | G | 8 | a0001c0001t0006g0046 a0001c0001t0006g0073 a0001c0001t0006g0074 others(5): Show |
14 | HG00735.hp1 HG01243.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.98-6524A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559142 | |||||||
| chr6:11559192 | C | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.98-6474C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559192 | |||||||
| chr6:11559216 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0047 others(4): Show |
13 | HG00558.hp1 HG00609.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-6450C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559216 | |||||||
| chr6:11559267 | G | C | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-6399G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559267 | |||||||
| chr6:11559274 | G | A | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-6392G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559274 | |||||||
| chr6:11559308 | C | T | 1 | a0001c0002t0002g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.98-6358C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559308 | |||||||
| chr6:11559378 | T | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-6288T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559378 | |||||||
| chr6:11559600 | A | G | 1 | a0001c0001t0003g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.98-6066A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559600 | |||||||
| chr6:11559658 | T | G | 14 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(11): Show |
23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.98-6008T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559658 | |||||||
| chr6:11559698 | A | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-5968A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559698 | |||||||
| chr6:11559836 | T | C | 2 | a0001c0001t0011g0026 a0001c0001t0011g0123 |
4 | HG02109.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-5830T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559836 | |||||||
| chr6:11559929 | T | C | 40 | a0001c0001t0029g0141 a0001c0002t0002g0001 a0001c0002t0002g0015 others(37): Show |
79 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.98-5737T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11559929 | |||||||
| chr6:11560189 | C | T | 3 | a0001c0001t0010g0009 a0001c0001t0010g0014 a0001c0001t0021g0014 |
9 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-5477C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560189 | |||||||
| chr6:11560203 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.98-5463C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560203 | |||||||
| chr6:11560330 | AT | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.98-5320delT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11560330 | ||||||
| chr6:11560391 | C | G | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98-5275C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560391 | |||||||
| chr6:11560582 | T | TA | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(103): Show |
194 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(191): Show |
intron_variant | MODIFIER | c.98-5067dupA | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11560582 | ||||||
| chr6:11560582 | T | TAA | 50 | a0001c0001t0019g0082 a0001c0001t0028g0084 a0001c0001t0029g0141 others(47): Show |
89 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.98-5068_98-5067dup others(2): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11560582 | ||||||
| chr6:11560582 | TA | T | 5 | a0001c0001t0011g0026 a0001c0001t0011g0123 a0001c0001t0017g0077 others(2): Show |
7 | HG00597.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-5067delA | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11560582 | ||||||
| chr6:11560597 | A | AG | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-5069_98-5068ins others(1): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560597 | |||||||
| chr6:11560620 | AT | A | 1 | a0001c0001t0006g0012 | 5 | HG02145.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-5045delT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560620 | |||||||
| chr6:11560673 | A | G | 1 | a0001c0002t0002g0095 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.98-4993A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560673 | |||||||
| chr6:11560722 | A | AAGAT | 109 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(106): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.98-4942_98-4941ins others(4): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11560722 | ||||||
| chr6:11560737 | C | T | 1 | a0001c0001t0005g0020 | 3 | HG02015.hp2 NA19005.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.98-4929C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560737 | |||||||
| chr6:11560848 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.98-4818T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11560848 | |||||||
| chr6:11561331 | G | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-4335G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11561331 | |||||||
| chr6:11561380 | T | C | 1 | a0001c0002t0002g0091 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.98-4286T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11561380 | |||||||
| chr6:11561511 | A | G | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-4155A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11561511 | |||||||
| chr6:11561636 | G | A | 2 | a0001c0001t0010g0014 a0001c0001t0021g0014 |
4 | HG01243.hp1 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-4030G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11561636 | |||||||
| chr6:11561721 | GAA | G | 2 | a0001c0001t0012g0036 a0001c0001t0012g0117 |
3 | HG01891.hp2 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.98-3943_98-3942del others(2): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11561721 | ||||||
| chr6:11561857 | T | C | 2 | a0001c0001t0019g0031 a0001c0001t0019g0082 |
3 | HG02622.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.98-3809T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11561857 | |||||||
| chr6:11561991 | T | G | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98-3675T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11561991 | |||||||
| chr6:11562015 | A | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-3651A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562015 | |||||||
| chr6:11562046 | T | A | 3 | a0001c0002t0002g0015 a0001c0002t0002g0092 a0001c0002t0002g0104 |
6 | NA18944.hp1 NA18945.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-3620T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562046 | |||||||
| chr6:11562071 | A | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
132 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.98-3595A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562071 | |||||||
| chr6:11562140 | A | C | 3 | a0001c0001t0006g0046 a0001c0001t0006g0073 a0001c0001t0006g0074 |
3 | HG00735.hp1 HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-3526A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562140 | |||||||
| chr6:11562170 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.98-3496C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562170 | |||||||
| chr6:11562177 | T | C | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-3489T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562177 | |||||||
| chr6:11562181 | C | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-3485C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562181 | |||||||
| chr6:11562408 | T | C | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-3258T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562408 | |||||||
| chr6:11562498 | A | G | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-3168A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562498 | |||||||
| chr6:11562506 | C | T | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.98-3160C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562506 | |||||||
| chr6:11562717 | A | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-2949A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562717 | |||||||
| chr6:11562776 | A | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(62): Show |
128 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.98-2890A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562776 | |||||||
| chr6:11562784 | C | T | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-2882C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11562784 | |||||||
| chr6:11563018 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.98-2648T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563018 | |||||||
| chr6:11563041 | G | A | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.98-2625G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563041 | |||||||
| chr6:11563060 | G | C | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.98-2606G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563060 | |||||||
| chr6:11563096 | A | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-2570A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563096 | |||||||
| chr6:11563204 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.98-2462C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563204 | |||||||
| chr6:11563205 | G | A | 3 | a0001c0002t0014g0025 a0001c0002t0014g0102 a0001c0002t0014g0122 |
5 | HG02055.hp1 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-2461G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563205 | |||||||
| chr6:11563262 | G | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-2404G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563262 | |||||||
| chr6:11563421 | T | G | 16 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(13): Show |
27 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.98-2245T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563421 | |||||||
| chr6:11563445 | T | G | 1 | a0001c0002t0002g0049 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.98-2221T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563445 | |||||||
| chr6:11563474 | G | T | 1 | a0001c0001t0005g0052 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.98-2192G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563474 | |||||||
| chr6:11563537 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.98-2129C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563537 | |||||||
| chr6:11563568 | G | A | 51 | a0001c0001t0029g0141 a0001c0002t0002g0001 a0001c0002t0002g0015 others(48): Show |
93 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.98-2098G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563568 | |||||||
| chr6:11563702 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0156 |
3 | HG02027.hp1 NA19004.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.98-1964C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563702 | |||||||
| chr6:11563829 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0149 |
3 | HG01167.hp1 HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.98-1837G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11563829 | |||||||
| chr6:11564103 | T | G | 16 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(13): Show |
27 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.98-1563T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11564103 | |||||||
| chr6:11564149 | GAGTT | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-1516_98-1513del others(4): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11564149 | |||||||
| chr6:11564567 | A | G | 2 | a0001c0001t0004g0022 a0001c0001t0049g0022 |
3 | NA18990.hp1 NA19005.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.98-1099A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11564567 | |||||||
| chr6:11564643 | T | C | 1 | a0001c0001t0007g0150 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.98-1023T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11564643 | |||||||
| chr6:11564712 | T | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-954T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11564712 | |||||||
| chr6:11564811 | A | G | 5 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-855A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11564811 | |||||||
| chr6:11565008 | C | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-658C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565008 | |||||||
| chr6:11565023 | G | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0041 others(12): Show |
34 | HG00280.hp2 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.98-643G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565023 | |||||||
| chr6:11565122 | A | G | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-544A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565122 | |||||||
| chr6:11565134 | C | CT | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.98-531dupT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr6 | 11565134 | ||||||
| chr6:11565134 | C | T | 1 | a0001c0001t0003g0173 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.98-532C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565134 | |||||||
| chr6:11565271 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG01070.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.98-395A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565271 | |||||||
| chr6:11565336 | G | A | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-330G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565336 | |||||||
| chr6:11565417 | C | T | 9 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(6): Show |
16 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.98-249C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565417 | |||||||
| chr6:11565481 | C | T | 1 | a0001c0001t0007g0152 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.98-185C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565481 | |||||||
| chr6:11565569 | C | A | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.98-97C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 1/2 | chr6 | 11565569 | |||||||
| chr6:11566166 | A | G | 2 | a0001c0001t0019g0031 a0001c0001t0019g0082 |
3 | HG02622.hp1 HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.268+330A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566166 | |||||||
| chr6:11566170 | A | T | 1 | a0001c0002t0002g0121 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.268+334A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566170 | |||||||
| chr6:11566172 | G | A | 1 | a0001c0002t0002g0121 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.268+336G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566172 | |||||||
| chr6:11566173 | C | T | 8 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(5): Show |
9 | HG00597.hp2 HG01891.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+337C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566173 | |||||||
| chr6:11566197 | A | G | 1 | a0001c0001t0026g0058 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.268+361A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566197 | |||||||
| chr6:11566330 | G | T | 1 | a0001c0002t0002g0097 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.268+494G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566330 | |||||||
| chr6:11566546 | C | T | 1 | a0001c0002t0002g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.268+710C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566546 | |||||||
| chr6:11566628 | T | C | 1 | a0001c0002t0025g0032 | 2 | NA19062.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.268+792T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566628 | |||||||
| chr6:11566748 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0013g0044 |
4 | HG02896.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+912C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566748 | |||||||
| chr6:11566791 | G | A | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.268+955G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566791 | |||||||
| chr6:11566874 | G | A | 12 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(9): Show |
19 | HG02015.hp2 HG02040.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.268+1038G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566874 | |||||||
| chr6:11566880 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.268+1044C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11566880 | |||||||
| chr6:11567065 | G | A | 1 | a0001c0001t0005g0030 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.268+1229G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567065 | |||||||
| chr6:11567233 | T | A | 55 | a0001c0001t0028g0084 a0001c0001t0029g0141 a0001c0002t0002g0001 others(52): Show |
97 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.268+1397T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567233 | |||||||
| chr6:11567247 | AC | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0133 a0001c0001t0001g0137 others(2): Show |
13 | HG00597.hp1 HG00621.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.268+1413delC | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 11567247 | ||||||
| chr6:11567250 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0133 a0001c0001t0001g0137 others(2): Show |
13 | HG00597.hp1 HG00621.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.268+1414G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567250 | |||||||
| chr6:11567251 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0133 a0001c0001t0001g0137 others(2): Show |
13 | HG00597.hp1 HG00621.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.268+1415G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567251 | |||||||
| chr6:11567252 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0133 a0001c0001t0001g0137 others(2): Show |
13 | HG00597.hp1 HG00621.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.268+1416G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567252 | |||||||
| chr6:11567253 | T | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0133 a0001c0001t0001g0137 others(2): Show |
13 | HG00597.hp1 HG00621.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.268+1417T>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567253 | |||||||
| chr6:11567258 | C | G | 1 | a0001c0002t0038g0094 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.268+1422C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567258 | |||||||
| chr6:11567421 | T | C | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+1585T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567421 | |||||||
| chr6:11567468 | T | C | 2 | a0001c0002t0002g0099 a0001c0002t0002g0101 |
2 | NA18966.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.268+1632T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567468 | |||||||
| chr6:11567559 | A | G | 14 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(11): Show |
23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.268+1723A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567559 | |||||||
| chr6:11567591 | G | T | 1 | a0001c0005t0047g0075 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.268+1755G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567591 | |||||||
| chr6:11567724 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(182): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.268+1888G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567724 | |||||||
| chr6:11567725 | G | C | 28 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(25): Show |
46 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.268+1889G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567725 | |||||||
| chr6:11567784 | A | G | 3 | a0001c0002t0002g0015 a0001c0002t0002g0092 a0001c0002t0002g0104 |
6 | NA18944.hp1 NA18945.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+1948A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567784 | |||||||
| chr6:11567984 | C | T | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.268+2148C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11567984 | |||||||
| chr6:11568420 | A | G | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.268+2584A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11568420 | |||||||
| chr6:11568429 | GTA | G | 108 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(105): Show |
189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.268+2605_268+2606d others(4): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 11568429 | ||||||
| chr6:11568610 | A | G | 2 | a0001c0001t0003g0169 a0001c0001t0003g0170 |
2 | HG02818.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.268+2774A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11568610 | |||||||
| chr6:11569156 | T | C | 1 | a0001c0001t0006g0070 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.268+3320T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569156 | |||||||
| chr6:11569169 | G | A | 108 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(105): Show |
189 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.268+3333G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569169 | |||||||
| chr6:11569236 | T | C | 1 | a0001c0001t0003g0166 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.268+3400T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569236 | |||||||
| chr6:11569318 | G | A | 1 | a0001c0001t0006g0070 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.268+3482G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569318 | |||||||
| chr6:11569367 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.268+3531C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569367 | |||||||
| chr6:11569514 | G | A | 54 | a0001c0001t0029g0141 a0001c0002t0002g0001 a0001c0002t0002g0015 others(51): Show |
96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.268+3678G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569514 | |||||||
| chr6:11569581 | T | C | 1 | a0001c0001t0044g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.268+3745T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569581 | |||||||
| chr6:11569591 | T | G | 1 | a0001c0001t0005g0018 | 3 | HG02132.hp2 NA18967.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.268+3755T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569591 | |||||||
| chr6:11569618 | T | C | 1 | a0001c0002t0002g0108 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.268+3782T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569618 | |||||||
| chr6:11569762 | A | G | 1 | a0001c0001t0003g0168 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.268+3926A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11569762 | |||||||
| chr6:11570046 | C | T | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.268+4210C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570046 | |||||||
| chr6:11570198 | G | A | 1 | a0001c0001t0045g0081 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.268+4362G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570198 | |||||||
| chr6:11570244 | C | T | 14 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(11): Show |
33 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.268+4408C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570244 | |||||||
| chr6:11570305 | G | C | 1 | a0001c0001t0005g0054 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.268+4469G>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570305 | |||||||
| chr6:11570379 | T | C | 3 | a0001c0001t0017g0077 a0001c0001t0017g0078 a0001c0001t0017g0079 |
3 | HG00597.hp2 NA18960.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.268+4543T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570379 | |||||||
| chr6:11570641 | G | A | 1 | a0001c0001t0004g0061 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.269-4790G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570641 | |||||||
| chr6:11570670 | A | G | 7 | a0001c0002t0002g0083 a0001c0002t0002g0107 a0001c0002t0002g0108 others(4): Show |
7 | HG00323.hp1 HG01081.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-4761A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570670 | |||||||
| chr6:11570870 | A | G | 14 | a0001c0001t0005g0018 a0001c0001t0005g0019 a0001c0001t0005g0020 others(11): Show |
23 | HG02015.hp2 HG02040.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.269-4561A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570870 | |||||||
| chr6:11570967 | A | G | 3 | a0001c0002t0002g0015 a0001c0002t0002g0092 a0001c0002t0002g0104 |
6 | NA18944.hp1 NA18945.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-4464A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11570967 | |||||||
| chr6:11571175 | CT | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(164): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.269-4242delT | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 11571175 | ||||||
| chr6:11571175 | CTT | C | 6 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(3): Show |
7 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-4243_269-4242d others(4): Show |
TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr6 | 11571175 | ||||||
| chr6:11571512 | G | T | 13 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(10): Show |
32 | HG00140.hp2 HG00408.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.269-3919G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11571512 | |||||||
| chr6:11571640 | T | C | 14 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(11): Show |
23 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.269-3791T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11571640 | |||||||
| chr6:11571850 | A | G | 1 | a0001c0001t0001g0138 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.269-3581A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11571850 | |||||||
| chr6:11571985 | T | G | 15 | a0001c0001t0004g0004 a0001c0001t0004g0008 a0001c0001t0004g0022 others(12): Show |
34 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.269-3446T>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11571985 | |||||||
| chr6:11572022 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.269-3409C>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11572022 | |||||||
| chr6:11572444 | A | G | 1 | a0001c0001t0011g0120 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.269-2987A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11572444 | |||||||
| chr6:11572510 | T | C | 1 | a0001c0001t0005g0030 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.269-2921T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11572510 | |||||||
| chr6:11572517 | T | C | 1 | a0001c0001t0044g0064 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.269-2914T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11572517 | |||||||
| chr6:11572584 | G | T | 28 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0080 others(25): Show |
46 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.269-2847G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11572584 | |||||||
| chr6:11572746 | G | A | 2 | a0001c0001t0045g0081 a0001c0002t0008g0086 |
2 | HG01515.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.269-2685G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11572746 | |||||||
| chr6:11572863 | A | T | 1 | a0001c0001t0001g0138 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.269-2568A>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11572863 | |||||||
| chr6:11573045 | T | C | 5 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-2386T>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11573045 | |||||||
| chr6:11573904 | G | A | 5 | a0001c0001t0011g0120 a0001c0001t0012g0036 a0001c0001t0012g0117 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-1527G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11573904 | |||||||
| chr6:11574107 | C | T | 3 | a0001c0001t0019g0031 a0001c0001t0019g0082 a0001c0001t0036g0048 |
4 | HG02622.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.269-1324C>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574107 | |||||||
| chr6:11574129 | G | A | 54 | a0001c0001t0029g0141 a0001c0002t0002g0001 a0001c0002t0002g0015 others(51): Show |
96 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.269-1302G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574129 | |||||||
| chr6:11574141 | C | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
133 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.269-1290C>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574141 | |||||||
| chr6:11574293 | A | G | 1 | a0001c0001t0003g0168 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.269-1138A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574293 | |||||||
| chr6:11574414 | A | C | 1 | a0001c0001t0005g0057 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.269-1017A>C | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574414 | |||||||
| chr6:11574450 | A | G | 1 | a0001c0001t0005g0057 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.269-981A>G | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574450 | |||||||
| chr6:11574471 | G | A | 1 | a0001c0002t0002g0106 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.269-960G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574471 | |||||||
| chr6:11574642 | G | T | 1 | a0001c0001t0020g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.269-789G>T | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11574642 | |||||||
| chr6:11575074 | G | A | 1 | a0001c0004t0027g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.269-357G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11575074 | |||||||
| chr6:11575128 | G | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0029 a0001c0001t0003g0164 others(2): Show |
14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-303G>A | TMEM170B | ENSG00000205269.6 | transcript | ENST00000379426.2 | protein_coding | 2/2 | chr6 | 11575128 |