Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 130827 |
| ensemblid | ENSG00000170417.16 |
| hgncid | 26391 |
| symbol | TMEM182 |
| name | transmembrane protein 182 |
| refseq_nuc | NM_144632.5 |
| refseq_prot | NP_653233.5 |
| ensembl_nuc | ENST00000412401.3 |
| ensembl_prot | ENSP00000394178.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 102762031 |
| end | 102817679 |
| strand | + |
| ver | v1.2 |
| region | chr2:102762031-102817679 |
| region5000 | chr2:102757031-102822679 |
| regionname0 | TMEM182_chr2_102762031_102817679 |
| regionname5000 | TMEM182_chr2_102757031_102822679 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 229 | 354 | 86 | 66 | 146 | 16 | 39 | 106 | TMEM182_chr2_102757031_102822679 | TMEM182 | MRLNI others(224): Show |
chr2 | 102757031 | 102822679 |
| a0002 | 1/0 | 229 | 2 | 0 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | MRLNI others(224): Show |
chr2 | 102757031 | 102822679 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 687 | 353 | 86 | 66 | 146 | 15 | 39 | TMEM182_chr2_102757031_102822679 | TMEM182 | ATGAG others(682): Show |
chr2 | 102757031 | 102822679 | ||
| a0001c0003 | 0/0 | 687 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | ATGAG others(682): Show |
chr2 | 102757031 | 102822679 | ||
| a0002c0002 | 1/0 | 687 | 2 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | ATGAG others(682): Show |
chr2 | 102757031 | 102822679 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3588 | 108 | 16 | 32 | 37 | 8 | 14 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0002 | 0/0 | 3587 | 47 | 4 | 15 | 24 | 0 | 4 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0003 | 0/0 | 3590 | 42 | 10 | 3 | 24 | 2 | 3 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0004 | 0/0 | 3591 | 21 | 2 | 1 | 7 | 0 | 11 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3586): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0005 | 0/0 | 3591 | 16 | 5 | 2 | 9 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3586): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0006 | 0/0 | 3596 | 11 | 0 | 4 | 2 | 2 | 3 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3591): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0007 | 0/0 | 3593 | 10 | 0 | 1 | 7 | 2 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3588): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0008 | 0/0 | 3590 | 9 | 9 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0009 | 0/0 | 3588 | 8 | 3 | 0 | 5 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0010 | 0/0 | 3587 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0011 | 0/0 | 3594 | 7 | 0 | 0 | 7 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3589): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0012 | 0/0 | 3590 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0013 | 0/0 | 3590 | 5 | 0 | 4 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0014 | 0/0 | 3587 | 5 | 1 | 0 | 4 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0015 | 0/0 | 3587 | 4 | 2 | 1 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0016 | 0/0 | 3596 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3591): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0017 | 0/0 | 3597 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3592): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0018 | 0/0 | 3585 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3580): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0019 | 0/0 | 3587 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0020 | 0/0 | 3593 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3588): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0021 | 0/0 | 3599 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3594): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0022 | 0/0 | 3599 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3594): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0023 | 0/0 | 3597 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3592): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0024 | 0/0 | 3594 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3589): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0025 | 0/0 | 3588 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0026 | 0/0 | 3590 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0027 | 0/0 | 3587 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0028 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3588): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0029 | 0/0 | 3590 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0030 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3588): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0031 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0032 | 0/0 | 3593 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3588): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0033 | 0/0 | 3596 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3591): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0034 | 0/0 | 3587 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0035 | 0/0 | 3590 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0036 | 0/0 | 3599 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3594): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0037 | 0/0 | 3590 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0038 | 0/0 | 3593 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3588): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0039 | 0/0 | 3591 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3586): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0040 | 0/0 | 3591 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3586): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0041 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3589): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0042 | 0/0 | 3591 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3586): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0043 | 0/0 | 3588 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0044 | 0/0 | 3588 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0045 | 0/0 | 3588 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0046 | 0/0 | 3594 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3589): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0047 | 0/0 | 3594 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3589): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0048 | 0/0 | 3588 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| a0001c0001t0049 | 0/0 | 3590 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3585): Show |
chr2 | 102757031 | 102822679 |
| a0001c0003t0002 | 0/0 | 3587 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3582): Show |
chr2 | 102757031 | 102822679 |
| a0002c0002t0001 | 1/0 | 3588 | 2 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | GAATC others(3583): Show |
chr2 | 102757031 | 102822679 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0007 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0004 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0008g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0008g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0008g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0009g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0010g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0010g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0010g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0011g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0011g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0011g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0011g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0012g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0012g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0012g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0012g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0013g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0013g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0014g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0014g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0015g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0015g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0016g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0016g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0016g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0017g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0017g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0017g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0018g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0018g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0018g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0019g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0019g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0020g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0020g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0021g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0021g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0022g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0022g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0023g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0023g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0024g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0024g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0025g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0025g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0026g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0027g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0028g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0029g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0030g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0031g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0032g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0033g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0034g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0035g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0036g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0037g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0038g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0039g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0040g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0041g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0042g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0043g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0044g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0045g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0046g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0047g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0048g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0001t0049g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0002c0002t0001g0055 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0274 | EUR | GBR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00099 | hp2 | a0001 | c0001 | t0013 | g0028 | EUR | GBR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | GBR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0165 | EUR | FIN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0208 | EUR | FIN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0221 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0089 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00544 | hp2 | a0001 | c0001 | t0014 | g0204 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00621 | hp2 | a0001 | c0001 | t0014 | g0064 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00639 | hp2 | a0001 | c0001 | t0045 | g0083 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00673 | hp1 | a0001 | c0001 | t0018 | g0090 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00733 | hp2 | a0001 | c0001 | t0013 | g0014 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0031 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01071 | hp1 | a0001 | c0001 | t0046 | g0013 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01071 | hp2 | a0001 | c0001 | t0013 | g0014 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0014 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0211 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01346 | hp2 | a0001 | c0001 | t0013 | g0028 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0072 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01433 | hp2 | a0001 | c0001 | t0044 | g0071 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0220 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0030 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01515 | hp2 | a0001 | c0001 | t0006 | g0030 | EUR | IBS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01884 | hp2 | a0001 | c0001 | t0025 | g0253 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0015 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02055 | hp1 | a0001 | c0001 | t0024 | g0034 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0287 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02056 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02071 | hp1 | a0001 | c0001 | t0023 | g0235 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02071 | hp2 | a0001 | c0001 | t0023 | g0263 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02080 | hp1 | a0001 | c0001 | t0010 | g0183 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02083 | hp2 | a0001 | c0001 | t0018 | g0067 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02145 | hp2 | a0001 | c0001 | t0025 | g0036 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02155 | hp1 | a0001 | c0001 | t0007 | g0228 | EAS | CDX | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02155 | hp2 | a0001 | c0001 | t0011 | g0043 | EAS | CDX | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | CDX | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0120 | EAS | CDX | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02257 | hp1 | a0001 | c0001 | t0021 | g0275 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0033 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02258 | hp1 | a0001 | c0001 | t0009 | g0092 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02280 | hp2 | a0001 | c0001 | t0032 | g0254 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0280 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0088 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02523 | hp1 | a0001 | c0001 | t0010 | g0185 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0102 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02602 | hp2 | a0001 | c0001 | t0015 | g0031 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02622 | hp1 | a0001 | c0001 | t0037 | g0268 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0251 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0266 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0212 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02717 | hp2 | a0001 | c0001 | t0022 | g0271 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02723 | hp1 | a0001 | c0001 | t0036 | g0265 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0108 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0288 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02896 | hp1 | a0001 | c0001 | t0042 | g0032 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02896 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0032 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02922 | hp1 | a0001 | c0001 | t0049 | g0264 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02922 | hp2 | a0001 | c0001 | t0043 | g0161 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02965 | hp2 | a0001 | c0001 | t0016 | g0285 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0286 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0027 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0106 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03098 | hp2 | a0001 | c0001 | t0012 | g0255 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0010 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03195 | hp1 | a0001 | c0001 | t0033 | g0277 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03195 | hp2 | a0001 | c0001 | t0041 | g0094 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03209 | hp2 | a0001 | c0001 | t0048 | g0143 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0258 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0278 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03453 | hp2 | a0001 | c0001 | t0012 | g0256 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0242 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03486 | hp2 | a0001 | c0001 | t0030 | g0010 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03579 | hp1 | a0001 | c0001 | t0014 | g0239 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03579 | hp2 | a0001 | c0001 | t0028 | g0281 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03669 | hp1 | a0001 | c0001 | t0039 | g0099 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0104 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03710 | hp1 | a0001 | c0001 | t0006 | g0238 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03710 | hp2 | a0001 | c0001 | t0027 | g0002 | SAS | PJL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0117 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0194 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0037 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0100 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0109 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04204 | hp1 | a0001 | c0001 | t0038 | g0015 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0101 | SAS | STU | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | YRI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18612 | hp1 | a0001 | c0001 | t0014 | g0176 | EAS | CHB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18747 | hp1 | a0001 | c0001 | t0011 | g0136 | EAS | CHB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | YRI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0270 | AFR | YRI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18941 | hp1 | a0001 | c0001 | t0035 | g0224 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0095 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18944 | hp2 | a0001 | c0001 | t0034 | g0186 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18951 | hp1 | a0001 | c0001 | t0009 | g0097 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18954 | hp1 | a0001 | c0001 | t0007 | g0215 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18954 | hp2 | a0001 | c0001 | t0011 | g0118 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18956 | hp2 | a0001 | c0001 | t0017 | g0160 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18957 | hp1 | a0001 | c0001 | t0011 | g0137 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18957 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18962 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18963 | hp1 | a0001 | c0001 | t0009 | g0096 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0105 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18966 | hp1 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18966 | hp2 | a0001 | c0001 | t0009 | g0098 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18972 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0087 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18980 | hp2 | a0001 | c0001 | t0019 | g0008 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18983 | hp1 | a0001 | c0001 | t0011 | g0115 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18987 | hp2 | a0001 | c0001 | t0010 | g0201 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18988 | hp2 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18991 | hp1 | a0001 | c0001 | t0011 | g0227 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18993 | hp1 | a0001 | c0001 | t0026 | g0195 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18993 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18995 | hp1 | a0001 | c0001 | t0019 | g0192 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19006 | hp2 | a0001 | c0001 | t0010 | g0008 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19009 | hp1 | a0001 | c0001 | t0017 | g0044 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19010 | hp2 | a0001 | c0001 | t0009 | g0093 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | LWK | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | LWK | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0091 | AFR | LWK | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19043 | hp2 | a0001 | c0001 | t0047 | g0041 | AFR | LWK | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19056 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19056 | hp2 | a0001 | c0001 | t0005 | g0086 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19062 | hp2 | a0001 | c0001 | t0014 | g0205 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0248 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19072 | hp2 | a0001 | c0001 | t0017 | g0116 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19074 | hp1 | a0001 | c0001 | t0010 | g0198 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19077 | hp2 | a0001 | c0001 | t0005 | g0085 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19079 | hp1 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | YRI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | YRI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA20752 | hp1 | a0001 | c0001 | t0007 | g0273 | EUR | TSI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0269 | EUR | TSI | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0027 | SAS | GIH | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02486 | hp1 | a0001 | c0001 | t0031 | g0252 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02559 | hp1 | a0001 | c0001 | t0012 | g0257 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG02559 | hp2 | a0001 | c0001 | t0024 | g0035 | AFR | ACB | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0241 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | MSL | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG06807 | hp1 | a0001 | c0001 | t0016 | g0284 | AFR | USA | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | USA | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18955 | hp1 | a0001 | c0001 | t0018 | g0068 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA20300 | hp1 | a0001 | c0001 | t0021 | g0276 | AFR | USA | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA20300 | hp2 | a0001 | c0001 | t0040 | g0122 | AFR | USA | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | LWK | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| NA21309 | hp2 | a0001 | c0001 | t0029 | g0283 | AFR | LWK | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0142 | REF | REF | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0055 | REF | REF | TMEM182_chr2_102757031_102822679 | TMEM182 | chr2 | 102757031 | 102822679 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102814945 | T | C | 1 | a0001 | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
missense_variant | MODERATE | c.667T>C | p.Trp223Arg | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 854/3588 | 667/690 | 223/229 | chr2 | 102814945 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102764375 | G | A | 1 | a0001c0003 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.279G>A | p.Pro93Pro | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/5 | 466/3588 | 279/690 | 93/229 | chr2 | 102764375 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102762040 | G | A | 3 | a0001c0001t0010 a0001c0001t0026 a0001c0001t0027 |
9 | HG02080.hp1 HG02523.hp1 HG03710.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-178G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 1/5 | 178 | chr2 | 102762040 | ||||||
| chr2:102762047 | C | T | 1 | a0001c0001t0049 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-171C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 1/5 | 171 | chr2 | 102762047 | ||||||
| chr2:102762101 | T | C | 1 | a0001c0001t0013 | 5 | HG00099.hp2 HG00733.hp2 HG01071.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-117T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 1/5 | 117 | chr2 | 102762101 | ||||||
| chr2:102762122 | CT | C | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(28): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-80delT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 1/5 | 80 | INFO_REALIGN_3_PRIME | chr2 | 102762122 | |||||
| chr2:102762200 | G | A | 1 | a0001c0001t0039 | 1 | HG03669.hp1 | 5_prime_UTR_variant | MODIFIER | c.-18G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 1/5 | 18 | chr2 | 102762200 | ||||||
| chr2:102815115 | C | T | 1 | a0001c0001t0038 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 147 | chr2 | 102815115 | ||||||
| chr2:102815146 | C | T | 1 | a0001c0001t0048 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*178C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 178 | chr2 | 102815146 | ||||||
| chr2:102815468 | A | G | 1 | a0001c0001t0037 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 500 | chr2 | 102815468 | ||||||
| chr2:102815544 | A | C | 1 | a0001c0001t0047 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*576A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 576 | chr2 | 102815544 | ||||||
| chr2:102815607 | G | A | 2 | a0001c0001t0024 a0001c0001t0028 |
3 | HG02055.hp1 HG02559.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*639G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 639 | chr2 | 102815607 | ||||||
| chr2:102815754 | C | T | 1 | a0001c0001t0027 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*786C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 786 | chr2 | 102815754 | ||||||
| chr2:102815859 | T | C | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(39): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*891T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 891 | chr2 | 102815859 | ||||||
| chr2:102815878 | A | G | 18 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(15): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*910A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 910 | chr2 | 102815878 | ||||||
| chr2:102815895 | G | A | 1 | a0001c0001t0019 | 2 | NA18980.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 927 | chr2 | 102815895 | ||||||
| chr2:102815904 | A | T | 1 | a0001c0001t0034 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*936A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 936 | chr2 | 102815904 | ||||||
| chr2:102816039 | C | G | 1 | a0001c0001t0043 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1071C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1071 | chr2 | 102816039 | ||||||
| chr2:102816266 | C | T | 8 | a0001c0001t0012 a0001c0001t0021 a0001c0001t0025 others(5): Show |
15 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1298C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1298 | chr2 | 102816266 | ||||||
| chr2:102816510 | C | CAAT | 14 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(11): Show |
107 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1578_*1580dupTAA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1581 | INFO_REALIGN_3_PRIME | chr2 | 102816510 | |||||
| chr2:102816510 | C | CAATAAT | 11 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0020 others(8): Show |
28 | HG00099.hp1 HG00438.hp2 HG00741.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1575_*1580dupTAAT others(2): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1581 | INFO_REALIGN_3_PRIME | chr2 | 102816510 | |||||
| chr2:102816510 | C | CAATAATA others(2): Show |
4 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0017 others(1): Show |
18 | HG01167.hp1 HG01169.hp1 HG01496.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1572_*1580dupTAAT others(5): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1581 | INFO_REALIGN_3_PRIME | chr2 | 102816510 | |||||
| chr2:102816510 | C | CAATAATA others(5): Show |
3 | a0001c0001t0021 a0001c0001t0022 a0001c0001t0036 |
5 | HG02257.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1569_*1580dupTAAT others(8): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1581 | INFO_REALIGN_3_PRIME | chr2 | 102816510 | |||||
| chr2:102816510 | CAAT | C | 1 | a0001c0001t0018 | 3 | HG00673.hp1 HG02083.hp2 NA18955.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1578_*1580delTAA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1578 | INFO_REALIGN_3_PRIME | chr2 | 102816510 | |||||
| chr2:102816548 | A | ATAATAAT others(3): Show |
1 | a0001c0001t0023 | 2 | HG02071.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1580_*1581insTAAT others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1581 | chr2 | 102816548 | ||||||
| chr2:102816637 | C | G | 1 | a0001c0001t0035 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1669C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1669 | chr2 | 102816637 | ||||||
| chr2:102816698 | T | C | 1 | a0001c0001t0044 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1730T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1730 | chr2 | 102816698 | ||||||
| chr2:102816786 | A | G | 1 | a0001c0001t0045 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1818A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1818 | chr2 | 102816786 | ||||||
| chr2:102816833 | C | G | 8 | a0001c0001t0012 a0001c0001t0021 a0001c0001t0025 others(5): Show |
15 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1865C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1865 | chr2 | 102816833 | ||||||
| chr2:102816885 | G | A | 1 | a0001c0001t0029 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1917G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 1917 | chr2 | 102816885 | ||||||
| chr2:102817059 | C | T | 3 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0029 |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2091C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 2091 | chr2 | 102817059 | ||||||
| chr2:102817083 | A | G | 1 | a0001c0001t0036 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2115A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 2115 | chr2 | 102817083 | ||||||
| chr2:102817165 | T | A | 32 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(29): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*2197T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 5/5 | 2197 | chr2 | 102817165 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:102762398 | C | G | 156 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(153): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.132+49C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 1/4 | chr2 | 102762398 | |||||||
| chr2:102762541 | A | G | 1 | a0001c0001t0017g0160 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.133-46A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 1/4 | chr2 | 102762541 | |||||||
| chr2:102762754 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0005g0159 |
2 | NA19010.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.232+68A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102762754 | |||||||
| chr2:102762840 | C | A | 53 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(50): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.232+154C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102762840 | |||||||
| chr2:102762929 | T | C | 2 | a0001c0001t0014g0204 a0001c0001t0014g0205 |
2 | HG00544.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.232+243T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102762929 | |||||||
| chr2:102763135 | T | A | 155 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(152): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.232+449T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102763135 | |||||||
| chr2:102763135 | T | TA | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.232+456dupA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | 102763135 | ||||||
| chr2:102763300 | T | C | 54 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(51): Show |
64 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.232+614T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102763300 | |||||||
| chr2:102763389 | T | C | 2 | a0001c0001t0024g0034 a0001c0001t0024g0035 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.232+703T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102763389 | |||||||
| chr2:102763426 | A | G | 1 | a0001c0001t0029g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.232+740A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102763426 | |||||||
| chr2:102763443 | T | C | 2 | a0001c0001t0014g0204 a0001c0001t0014g0205 |
2 | HG00544.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.232+757T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102763443 | |||||||
| chr2:102763690 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.233-639G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102763690 | |||||||
| chr2:102763775 | G | T | 8 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(5): Show |
11 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-554G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102763775 | |||||||
| chr2:102764057 | C | T | 1 | a0001c0001t0017g0160 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.233-272C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102764057 | |||||||
| chr2:102764094 | T | G | 10 | a0001c0001t0001g0259 a0001c0001t0003g0029 a0001c0001t0012g0251 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.233-235T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102764094 | |||||||
| chr2:102764195 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.233-134G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102764195 | |||||||
| chr2:102764212 | A | C | 8 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(5): Show |
11 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.233-117A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102764212 | |||||||
| chr2:102764294 | A | G | 2 | a0001c0001t0003g0249 a0001c0001t0003g0250 |
2 | NA18990.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.233-35A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 2/4 | chr2 | 102764294 | |||||||
| chr2:102764532 | G | A | 1 | a0001c0001t0029g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331+105G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102764532 | |||||||
| chr2:102764539 | C | G | 76 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(73): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.331+112C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102764539 | |||||||
| chr2:102764758 | G | A | 159 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(156): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.331+331G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102764758 | |||||||
| chr2:102764822 | G | T | 134 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(131): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.331+395G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102764822 | |||||||
| chr2:102765054 | G | A | 136 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(133): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.331+627G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765054 | |||||||
| chr2:102765091 | TAGTC | T | 3 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0029g0283 |
3 | HG03130.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.331+667_331+670del others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102765091 | ||||||
| chr2:102765286 | TTGCAATC others(7): Show |
T | 3 | a0001c0001t0024g0034 a0001c0001t0024g0035 a0001c0001t0025g0036 |
3 | HG02055.hp1 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.331+862_331+875del others(14): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102765286 | ||||||
| chr2:102765291 | A | G | 156 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(153): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.331+864A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765291 | |||||||
| chr2:102765306 | G | A | 3 | a0001c0001t0024g0034 a0001c0001t0024g0035 a0001c0001t0025g0036 |
3 | HG02055.hp1 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.331+879G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765306 | |||||||
| chr2:102765312 | C | G | 3 | a0001c0001t0024g0034 a0001c0001t0024g0035 a0001c0001t0025g0036 |
3 | HG02055.hp1 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.331+885C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765312 | |||||||
| chr2:102765358 | T | C | 160 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(157): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.331+931T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765358 | |||||||
| chr2:102765528 | A | G | 58 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(55): Show |
69 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.331+1101A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765528 | |||||||
| chr2:102765546 | A | G | 21 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(18): Show |
30 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.331+1119A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765546 | |||||||
| chr2:102765639 | C | T | 58 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(55): Show |
69 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.331+1212C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765639 | |||||||
| chr2:102765731 | G | A | 8 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(5): Show |
11 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+1304G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765731 | |||||||
| chr2:102765763 | T | C | 70 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(67): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.331+1336T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765763 | |||||||
| chr2:102765786 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.331+1359C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765786 | |||||||
| chr2:102765966 | T | C | 58 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(55): Show |
69 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.331+1539T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102765966 | |||||||
| chr2:102766183 | A | G | 1 | a0001c0001t0029g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331+1756A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102766183 | |||||||
| chr2:102766634 | C | T | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+2207C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102766634 | |||||||
| chr2:102766672 | T | C | 157 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(154): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.331+2245T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102766672 | |||||||
| chr2:102766767 | G | C | 1 | a0001c0001t0012g0251 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.331+2340G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102766767 | |||||||
| chr2:102766829 | A | G | 10 | a0001c0001t0001g0259 a0001c0001t0003g0029 a0001c0001t0012g0251 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.331+2402A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102766829 | |||||||
| chr2:102766988 | A | C | 3 | a0001c0001t0024g0034 a0001c0001t0024g0035 a0001c0001t0025g0036 |
3 | HG02055.hp1 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.331+2561A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102766988 | |||||||
| chr2:102767011 | T | G | 1 | a0001c0001t0003g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.331+2584T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767011 | |||||||
| chr2:102767036 | G | C | 1 | a0001c0001t0005g0042 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.331+2609G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767036 | |||||||
| chr2:102767168 | T | G | 10 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0008g0010 others(7): Show |
13 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.331+2741T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767168 | |||||||
| chr2:102767192 | A | G | 159 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(156): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.331+2765A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767192 | |||||||
| chr2:102767486 | T | C | 10 | a0001c0001t0001g0259 a0001c0001t0003g0029 a0001c0001t0012g0251 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.331+3059T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767486 | |||||||
| chr2:102767514 | A | G | 2 | a0001c0001t0014g0204 a0001c0001t0014g0205 |
2 | HG00544.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.331+3087A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767514 | |||||||
| chr2:102767528 | G | T | 4 | a0001c0001t0007g0031 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG00099.hp1 HG00741.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+3101G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767528 | |||||||
| chr2:102767726 | A | G | 70 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(67): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.331+3299A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102767726 | |||||||
| chr2:102768006 | C | T | 10 | a0001c0001t0001g0259 a0001c0001t0003g0029 a0001c0001t0012g0251 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.331+3579C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768006 | |||||||
| chr2:102768008 | G | A | 3 | a0001c0001t0024g0034 a0001c0001t0024g0035 a0001c0001t0025g0036 |
3 | HG02055.hp1 HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.331+3581G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768008 | |||||||
| chr2:102768159 | C | T | 70 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(67): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.331+3732C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768159 | |||||||
| chr2:102768205 | G | A | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+3778G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768205 | |||||||
| chr2:102768529 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.331+4102A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768529 | |||||||
| chr2:102768536 | A | AC | 70 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(67): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.331+4109_331+4110i others(3): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768536 | |||||||
| chr2:102768546 | A | C | 1 | a0001c0001t0033g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+4119A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768546 | |||||||
| chr2:102768561 | A | C | 158 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(155): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.331+4134A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768561 | |||||||
| chr2:102768561 | A | T | 1 | a0001c0001t0007g0248 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.331+4134A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768561 | |||||||
| chr2:102768585 | C | G | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+4158C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768585 | |||||||
| chr2:102768679 | C | T | 4 | a0001c0001t0007g0031 a0001c0001t0007g0273 a0001c0001t0007g0274 others(1): Show |
4 | HG00099.hp1 HG00741.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+4252C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102768679 | |||||||
| chr2:102769026 | T | C | 1 | a0001c0001t0004g0037 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.331+4599T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769026 | |||||||
| chr2:102769042 | G | C | 1 | a0001c0001t0043g0161 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.331+4615G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769042 | |||||||
| chr2:102769105 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.331+4678A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769105 | |||||||
| chr2:102769209 | G | A | 2 | a0001c0001t0011g0043 a0001c0001t0017g0044 |
2 | HG02155.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.331+4782G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769209 | |||||||
| chr2:102769218 | G | C | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | NA18972.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.331+4791G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769218 | |||||||
| chr2:102769310 | A | G | 1 | a0001c0001t0003g0272 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.331+4883A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769310 | |||||||
| chr2:102769349 | C | T | 70 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(67): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.331+4922C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769349 | |||||||
| chr2:102769389 | A | T | 1 | a0001c0001t0005g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.331+4962A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769389 | |||||||
| chr2:102769485 | G | T | 20 | a0001c0001t0001g0259 a0001c0001t0003g0029 a0001c0001t0008g0010 others(17): Show |
24 | HG00544.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.331+5058G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769485 | |||||||
| chr2:102769624 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01167.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.331+5197G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769624 | |||||||
| chr2:102769698 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.331+5271A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769698 | |||||||
| chr2:102769766 | C | T | 58 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(55): Show |
69 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.331+5339C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769766 | |||||||
| chr2:102769837 | G | A | 11 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(8): Show |
14 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.331+5410G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769837 | |||||||
| chr2:102769909 | C | T | 58 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(55): Show |
69 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.331+5482C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769909 | |||||||
| chr2:102769938 | C | G | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.331+5511C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102769938 | |||||||
| chr2:102770095 | T | C | 3 | a0001c0001t0002g0260 a0001c0001t0002g0261 a0001c0001t0029g0283 |
3 | HG03130.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.331+5668T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770095 | |||||||
| chr2:102770217 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.331+5790C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770217 | |||||||
| chr2:102770344 | A | G | 139 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(136): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.331+5917A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770344 | |||||||
| chr2:102770434 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.331+6007C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770434 | |||||||
| chr2:102770470 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.331+6043G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770470 | |||||||
| chr2:102770497 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.331+6070C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770497 | |||||||
| chr2:102770702 | A | G | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+6275A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770702 | |||||||
| chr2:102770823 | C | T | 8 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(5): Show |
11 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+6396C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770823 | |||||||
| chr2:102770867 | ACATTTGG others(4): Show |
A | 2 | a0001c0001t0011g0136 a0001c0001t0011g0137 |
2 | NA18747.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.331+6441_331+6451d others(13): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102770867 | |||||||
| chr2:102771066 | G | A | 156 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(153): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.331+6639G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771066 | |||||||
| chr2:102771259 | C | T | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+6832C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771259 | |||||||
| chr2:102771403 | G | C | 1 | a0001c0001t0002g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.331+6976G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771403 | |||||||
| chr2:102771478 | C | A | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+7051C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771478 | |||||||
| chr2:102771605 | G | A | 1 | a0001c0001t0048g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.331+7178G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771605 | |||||||
| chr2:102771644 | G | A | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+7217G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771644 | |||||||
| chr2:102771708 | T | G | 160 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(157): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.331+7281T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771708 | |||||||
| chr2:102771746 | A | G | 1 | a0001c0001t0003g0246 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.331+7319A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771746 | |||||||
| chr2:102771799 | G | A | 3 | a0001c0001t0001g0259 a0001c0001t0025g0253 a0001c0001t0031g0252 |
3 | HG01884.hp1 HG01884.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.331+7372G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102771799 | |||||||
| chr2:102772056 | T | C | 1 | a0001c0003t0002g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.331+7629T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772056 | |||||||
| chr2:102772135 | C | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0124 others(14): Show |
19 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.331+7708C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772135 | |||||||
| chr2:102772181 | T | C | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.331+7754T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772181 | |||||||
| chr2:102772318 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.331+7891G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772318 | |||||||
| chr2:102772430 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.331+8003G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772430 | |||||||
| chr2:102772441 | C | G | 1 | a0001c0001t0004g0123 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.331+8014C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772441 | |||||||
| chr2:102772463 | C | T | 89 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(86): Show |
101 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.331+8036C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772463 | |||||||
| chr2:102772467 | G | T | 1 | a0001c0001t0047g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.331+8040G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772467 | |||||||
| chr2:102772601 | G | A | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+8174G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772601 | |||||||
| chr2:102772605 | AGGGTTCT others(5): Show |
A | 1 | a0001c0001t0040g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.331+8181_331+8192d others(14): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102772605 | ||||||
| chr2:102772682 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0135 |
2 | HG02129.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.331+8255C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772682 | |||||||
| chr2:102772744 | T | C | 2 | a0001c0001t0024g0034 a0001c0001t0024g0035 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.331+8317T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772744 | |||||||
| chr2:102772904 | C | G | 1 | a0001c0001t0022g0271 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+8477C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102772904 | |||||||
| chr2:102772939 | G | GGT | 48 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0259 others(45): Show |
53 | HG00140.hp2 HG00544.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.331+8537_331+8538d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102772939 | ||||||
| chr2:102773136 | A | G | 2 | a0001c0001t0003g0244 a0001c0001t0003g0245 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.331+8709A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773136 | |||||||
| chr2:102773333 | A | G | 185 | a0001c0001t0001g0121 a0001c0001t0001g0199 a0001c0001t0001g0200 others(182): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.331+8906A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773333 | |||||||
| chr2:102773355 | G | C | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+8928G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773355 | |||||||
| chr2:102773355 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.331+8928G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773355 | |||||||
| chr2:102773374 | G | A | 184 | a0001c0001t0001g0121 a0001c0001t0001g0199 a0001c0001t0001g0200 others(181): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.331+8947G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773374 | |||||||
| chr2:102773541 | A | AG | 199 | a0001c0001t0001g0121 a0001c0001t0001g0162 a0001c0001t0001g0163 others(196): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.331+9115dupG | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102773541 | ||||||
| chr2:102773650 | TGA | T | 17 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0124 others(14): Show |
19 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.331+9227_331+9228d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102773650 | ||||||
| chr2:102773685 | A | G | 1 | a0001c0001t0018g0090 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.331+9258A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773685 | |||||||
| chr2:102773710 | T | C | 2 | a0001c0001t0003g0206 a0001c0001t0003g0207 |
2 | HG02040.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.331+9283T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773710 | |||||||
| chr2:102773802 | T | C | 3 | a0001c0001t0002g0047 a0001c0001t0024g0034 a0001c0001t0024g0035 |
3 | HG02055.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.331+9375T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773802 | |||||||
| chr2:102773861 | C | T | 25 | a0001c0001t0001g0259 a0001c0001t0008g0010 a0001c0001t0008g0033 others(22): Show |
28 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.331+9434C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773861 | |||||||
| chr2:102773881 | G | C | 1 | a0001c0001t0022g0271 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.331+9454G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773881 | |||||||
| chr2:102773984 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.331+9557T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102773984 | |||||||
| chr2:102774171 | A | G | 1 | a0001c0001t0009g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.331+9744A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774171 | |||||||
| chr2:102774250 | C | CT | 49 | a0001c0001t0001g0133 a0001c0001t0001g0138 a0001c0001t0001g0156 others(46): Show |
52 | HG00408.hp1 HG01884.hp1 HG01884.hp2 others(49): Show |
intron_variant | MODIFIER | c.331+9845dupT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102774250 | ||||||
| chr2:102774250 | C | CTTT | 87 | a0001c0001t0001g0157 a0001c0001t0003g0004 a0001c0001t0003g0009 others(84): Show |
100 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.331+9843_331+9845d others(5): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102774250 | ||||||
| chr2:102774250 | C | CTTTT | 14 | a0001c0001t0003g0207 a0001c0001t0003g0232 a0001c0001t0003g0233 others(11): Show |
14 | HG00140.hp1 HG00621.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.331+9842_331+9845d others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102774250 | ||||||
| chr2:102774272 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.331+9845T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774272 | |||||||
| chr2:102774423 | T | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0144 others(3): Show |
10 | HG00733.hp1 HG01106.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.331+9996T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774423 | |||||||
| chr2:102774454 | G | T | 1 | a0001c0001t0003g0231 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.331+10027G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774454 | |||||||
| chr2:102774487 | G | C | 1 | a0001c0001t0004g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.331+10060G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774487 | |||||||
| chr2:102774502 | T | A | 1 | a0001c0001t0004g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.331+10075T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774502 | |||||||
| chr2:102774696 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.331+10269C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774696 | |||||||
| chr2:102774755 | A | G | 1 | a0001c0001t0003g0230 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.331+10328A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774755 | |||||||
| chr2:102774833 | G | A | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+10406G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774833 | |||||||
| chr2:102774957 | T | C | 1 | a0001c0001t0003g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.331+10530T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102774957 | |||||||
| chr2:102775106 | C | T | 1 | a0001c0001t0010g0198 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.331+10679C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775106 | |||||||
| chr2:102775180 | C | T | 196 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(193): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.331+10753C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775180 | |||||||
| chr2:102775334 | A | G | 198 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(195): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.331+10907A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775334 | |||||||
| chr2:102775377 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.331+10950C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775377 | |||||||
| chr2:102775419 | C | T | 2 | a0001c0001t0024g0034 a0001c0001t0024g0035 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.331+10992C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775419 | |||||||
| chr2:102775644 | C | T | 58 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(55): Show |
69 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.331+11217C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775644 | |||||||
| chr2:102775673 | T | TAGGCAAC others(14): Show |
15 | a0001c0001t0001g0259 a0001c0001t0012g0032 a0001c0001t0012g0251 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.331+11250_331+1127 others(25): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102775673 | ||||||
| chr2:102775732 | T | C | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.331+11305T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775732 | |||||||
| chr2:102775838 | T | G | 2 | a0001c0001t0006g0210 a0001c0001t0006g0211 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.331+11411T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102775838 | |||||||
| chr2:102776028 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.331+11601A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776028 | |||||||
| chr2:102776151 | C | T | 2 | a0001c0001t0015g0241 a0001c0001t0015g0242 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.331+11724C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776151 | |||||||
| chr2:102776343 | A | G | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.331+11916A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776343 | |||||||
| chr2:102776348 | C | G | 200 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(197): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.331+11921C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776348 | |||||||
| chr2:102776582 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.331+12155C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776582 | |||||||
| chr2:102776615 | A | G | 2 | a0001c0001t0006g0210 a0001c0001t0006g0211 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.331+12188A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776615 | |||||||
| chr2:102776726 | G | A | 10 | a0001c0001t0002g0007 a0001c0001t0002g0167 a0001c0001t0002g0174 others(7): Show |
13 | HG00741.hp1 HG01928.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.331+12299G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776726 | |||||||
| chr2:102776741 | A | G | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.331+12314A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776741 | |||||||
| chr2:102776773 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.331+12346A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776773 | |||||||
| chr2:102776862 | C | T | 2 | a0001c0001t0006g0229 a0001c0001t0007g0228 |
2 | HG02056.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.331+12435C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776862 | |||||||
| chr2:102776863 | A | G | 101 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.331+12436A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776863 | |||||||
| chr2:102776896 | C | G | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.331+12469C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776896 | |||||||
| chr2:102776913 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.331+12486C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776913 | |||||||
| chr2:102776919 | T | C | 1 | a0001c0001t0002g0174 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.331+12492T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776919 | |||||||
| chr2:102776957 | G | A | 1 | a0001c0001t0032g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.331+12530G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102776957 | |||||||
| chr2:102777012 | A | G | 1 | a0001c0001t0045g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.331+12585A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777012 | |||||||
| chr2:102777030 | G | A | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.331+12603G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777030 | |||||||
| chr2:102777068 | TA | T | 101 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.331+12651delA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102777068 | ||||||
| chr2:102777201 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.331+12774T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777201 | |||||||
| chr2:102777206 | A | C | 196 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(193): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.331+12779A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777206 | |||||||
| chr2:102777274 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.331+12847G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777274 | |||||||
| chr2:102777282 | C | A | 26 | a0001c0001t0003g0110 a0001c0001t0004g0018 a0001c0001t0004g0037 others(23): Show |
27 | HG00544.hp1 HG01106.hp2 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.331+12855C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777282 | |||||||
| chr2:102777423 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.331+12996G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777423 | |||||||
| chr2:102777577 | G | A | 1 | a0001c0001t0009g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.331+13150G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777577 | |||||||
| chr2:102777589 | C | T | 1 | a0001c0001t0024g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.331+13162C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777589 | |||||||
| chr2:102777672 | G | T | 2 | a0001c0001t0015g0241 a0001c0001t0015g0242 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.331+13245G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777672 | |||||||
| chr2:102777802 | A | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(55): Show |
69 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.331+13375A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777802 | |||||||
| chr2:102777937 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | NA18943.hp2 NA18972.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.331+13510G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777937 | |||||||
| chr2:102777962 | T | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0124 |
3 | HG00738.hp1 HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.331+13535T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777962 | |||||||
| chr2:102777988 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.331+13561T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102777988 | |||||||
| chr2:102778037 | A | T | 196 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(193): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.331+13610A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778037 | |||||||
| chr2:102778086 | C | T | 5 | a0001c0001t0005g0042 a0001c0001t0005g0081 a0001c0001t0005g0082 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+13659C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778086 | |||||||
| chr2:102778174 | T | A | 200 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(197): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.331+13747T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778174 | |||||||
| chr2:102778180 | C | T | 196 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(193): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.331+13753C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778180 | |||||||
| chr2:102778250 | C | T | 3 | a0001c0001t0007g0031 a0001c0001t0007g0274 a0001c0001t0015g0031 |
3 | HG00099.hp1 HG00741.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.331+13823C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778250 | |||||||
| chr2:102778304 | A | T | 1 | a0001c0001t0033g0277 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.331+13877A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778304 | |||||||
| chr2:102778455 | T | A | 1 | a0001c0001t0004g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.331+14028T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778455 | |||||||
| chr2:102778676 | C | G | 1 | a0001c0001t0020g0288 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.331+14249C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778676 | |||||||
| chr2:102778701 | CATG | C | 3 | a0001c0001t0003g0015 a0001c0001t0015g0015 a0001c0001t0038g0015 |
3 | HG01952.hp2 HG01975.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.331+14275_331+1427 others(7): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778701 | |||||||
| chr2:102778704 | GTTA | G | 193 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(190): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.331+14282_331+1428 others(7): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102778704 | ||||||
| chr2:102778707 | A | G | 3 | a0001c0001t0003g0015 a0001c0001t0015g0015 a0001c0001t0038g0015 |
3 | HG01952.hp2 HG01975.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.331+14280A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778707 | |||||||
| chr2:102778751 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.331+14324C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778751 | |||||||
| chr2:102778834 | C | T | 200 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(197): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.331+14407C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778834 | |||||||
| chr2:102778913 | C | T | 196 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(193): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.331+14486C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778913 | |||||||
| chr2:102778929 | T | C | 101 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.331+14502T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102778929 | |||||||
| chr2:102779086 | G | A | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.331+14659G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779086 | |||||||
| chr2:102779149 | A | T | 2 | a0001c0001t0014g0204 a0001c0001t0014g0205 |
2 | HG00544.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.331+14722A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779149 | |||||||
| chr2:102779478 | T | C | 3 | a0001c0001t0012g0251 a0001c0001t0012g0255 a0001c0001t0012g0256 |
3 | HG02622.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.331+15051T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779478 | |||||||
| chr2:102779689 | A | AT | 19 | a0001c0001t0002g0196 a0001c0001t0002g0260 a0001c0001t0002g0261 others(16): Show |
22 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.331+15275dupT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102779689 | ||||||
| chr2:102779704 | A | G | 1 | a0001c0001t0004g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.331+15277A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779704 | |||||||
| chr2:102779763 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(223): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.331+15336A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779763 | |||||||
| chr2:102779767 | C | A | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+15340C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779767 | |||||||
| chr2:102779777 | A | C | 1 | a0001c0001t0011g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.331+15350A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779777 | |||||||
| chr2:102779832 | A | G | 1 | a0001c0001t0041g0094 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.331+15405A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779832 | |||||||
| chr2:102779971 | G | C | 200 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(197): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.331+15544G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102779971 | |||||||
| chr2:102780015 | T | A | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.331+15588T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102780015 | |||||||
| chr2:102780049 | A | AT | 28 | a0001c0001t0003g0110 a0001c0001t0004g0089 a0001c0001t0004g0104 others(25): Show |
29 | HG00099.hp1 HG00544.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.331+15638dupT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102780049 | ||||||
| chr2:102780049 | AT | A | 14 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(11): Show |
14 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.331+15638delT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102780049 | ||||||
| chr2:102780138 | C | A | 200 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(197): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.331+15711C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102780138 | |||||||
| chr2:102780424 | C | G | 198 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(195): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.331+15997C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102780424 | |||||||
| chr2:102780548 | C | A | 1 | a0001c0001t0012g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.331+16121C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102780548 | |||||||
| chr2:102780568 | T | A | 2 | a0001c0001t0014g0204 a0001c0001t0014g0205 |
2 | HG00544.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.331+16141T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102780568 | |||||||
| chr2:102781007 | C | T | 1 | a0001c0001t0005g0080 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.331+16580C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102781007 | |||||||
| chr2:102781495 | A | G | 1 | a0001c0001t0003g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.332-16368A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102781495 | |||||||
| chr2:102781660 | A | G | 1 | a0001c0001t0017g0116 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.332-16203A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102781660 | |||||||
| chr2:102781875 | G | A | 194 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(191): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.332-15988G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102781875 | |||||||
| chr2:102782096 | G | A | 99 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(96): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.332-15767G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782096 | |||||||
| chr2:102782102 | T | C | 2 | a0001c0001t0014g0204 a0001c0001t0014g0205 |
2 | HG00544.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.332-15761T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782102 | |||||||
| chr2:102782175 | C | T | 1 | a0001c0001t0003g0267 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.332-15688C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782175 | |||||||
| chr2:102782176 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.332-15687G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782176 | |||||||
| chr2:102782307 | CAA | C | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-15555_332-1555 others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782307 | |||||||
| chr2:102782504 | C | T | 1 | a0001c0001t0003g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.332-15359C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782504 | |||||||
| chr2:102782530 | G | A | 2 | a0001c0001t0009g0092 a0001c0001t0009g0106 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.332-15333G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782530 | |||||||
| chr2:102782574 | A | G | 3 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0048g0143 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.332-15289A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782574 | |||||||
| chr2:102782676 | A | G | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-15187A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782676 | |||||||
| chr2:102782784 | T | C | 197 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(194): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.332-15079T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782784 | |||||||
| chr2:102782873 | T | G | 4 | a0001c0001t0003g0232 a0001c0001t0003g0233 a0001c0001t0003g0234 others(1): Show |
4 | HG02071.hp1 NA18970.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-14990T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782873 | |||||||
| chr2:102782967 | A | G | 1 | a0001c0001t0029g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-14896A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782967 | |||||||
| chr2:102782997 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.332-14866A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102782997 | |||||||
| chr2:102783482 | C | T | 76 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(73): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.332-14381C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102783482 | |||||||
| chr2:102783725 | T | C | 1 | a0001c0001t0004g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.332-14138T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102783725 | |||||||
| chr2:102783917 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.332-13946C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102783917 | |||||||
| chr2:102783926 | C | T | 1 | a0001c0001t0011g0115 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.332-13937C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102783926 | |||||||
| chr2:102783973 | T | TA | 18 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(15): Show |
27 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-13889dupA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102783973 | ||||||
| chr2:102784014 | C | A | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(221): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.332-13849C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784014 | |||||||
| chr2:102784069 | G | A | 1 | a0001c0001t0011g0043 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.332-13794G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784069 | |||||||
| chr2:102784222 | G | A | 101 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.332-13641G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784222 | |||||||
| chr2:102784356 | C | CT | 98 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(95): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.332-13496dupT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102784356 | ||||||
| chr2:102784554 | G | A | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-13309G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784554 | |||||||
| chr2:102784559 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.332-13304G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784559 | |||||||
| chr2:102784655 | C | T | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | NA18972.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.332-13208C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784655 | |||||||
| chr2:102784909 | T | C | 1 | a0001c0001t0010g0180 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.332-12954T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784909 | |||||||
| chr2:102784912 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.332-12951A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102784912 | |||||||
| chr2:102785007 | T | C | 53 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.332-12856T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102785007 | |||||||
| chr2:102785365 | A | C | 2 | a0001c0001t0014g0204 a0001c0001t0014g0205 |
2 | HG00544.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.332-12498A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102785365 | |||||||
| chr2:102785395 | T | G | 8 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(5): Show |
11 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.332-12468T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102785395 | |||||||
| chr2:102785738 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.332-12125C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102785738 | |||||||
| chr2:102785844 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.332-12019A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102785844 | |||||||
| chr2:102786041 | AT | A | 179 | a0001c0001t0001g0019 a0001c0001t0001g0259 a0001c0001t0002g0002 others(176): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.332-11803delT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102786041 | ||||||
| chr2:102786041 | ATT | A | 13 | a0001c0001t0002g0181 a0001c0001t0002g0261 a0001c0001t0004g0108 others(10): Show |
13 | HG02735.hp2 HG02896.hp1 HG02897.hp2 others(10): Show |
intron_variant | MODIFIER | c.332-11804_332-1180 others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102786041 | ||||||
| chr2:102786210 | G | GT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(46): Show |
60 | HG00621.hp1 HG00639.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.332-11631dupT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102786210 | ||||||
| chr2:102786210 | G | GTT | 21 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0048 others(18): Show |
30 | HG00438.hp1 HG00558.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.332-11632_332-1163 others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102786210 | ||||||
| chr2:102786210 | G | GTTT | 46 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0002g0002 others(43): Show |
56 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.332-11633_332-1163 others(7): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102786210 | ||||||
| chr2:102786210 | G | GTTTT | 23 | a0001c0001t0001g0259 a0001c0001t0002g0008 a0001c0001t0002g0047 others(20): Show |
24 | HG01109.hp2 HG01258.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.332-11634_332-1163 others(8): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102786210 | ||||||
| chr2:102786210 | GT | G | 11 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0003g0240 others(8): Show |
13 | HG00280.hp2 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.332-11631delT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102786210 | ||||||
| chr2:102786261 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.332-11602C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786261 | |||||||
| chr2:102786262 | G | A | 1 | a0001c0001t0025g0253 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.332-11601G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786262 | |||||||
| chr2:102786307 | T | C | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-11556T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786307 | |||||||
| chr2:102786401 | G | C | 1 | a0001c0001t0002g0196 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.332-11462G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786401 | |||||||
| chr2:102786508 | C | T | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-11355C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786508 | |||||||
| chr2:102786509 | A | G | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-11354A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786509 | |||||||
| chr2:102786548 | C | T | 1 | a0001c0001t0007g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.332-11315C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786548 | |||||||
| chr2:102786941 | T | A | 3 | a0001c0001t0025g0036 a0001c0001t0025g0253 a0001c0001t0031g0252 |
3 | HG01884.hp2 HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.332-10922T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102786941 | |||||||
| chr2:102787185 | A | C | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.332-10678A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787185 | |||||||
| chr2:102787189 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0048g0143 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.332-10674G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787189 | |||||||
| chr2:102787210 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.332-10653G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787210 | |||||||
| chr2:102787236 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.332-10627G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787236 | |||||||
| chr2:102787245 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.332-10618A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787245 | |||||||
| chr2:102787359 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.332-10504C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787359 | |||||||
| chr2:102787368 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(15): Show |
27 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.332-10495A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787368 | |||||||
| chr2:102787782 | A | C | 101 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.332-10081A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787782 | |||||||
| chr2:102787889 | G | A | 1 | a0001c0001t0029g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-9974G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787889 | |||||||
| chr2:102787951 | G | C | 1 | a0001c0001t0005g0074 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-9912G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787951 | |||||||
| chr2:102787952 | C | G | 1 | a0001c0001t0005g0074 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-9911C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787952 | |||||||
| chr2:102787953 | T | C | 1 | a0001c0001t0005g0074 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.332-9910T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787953 | |||||||
| chr2:102787963 | T | G | 7 | a0001c0001t0003g0009 a0001c0001t0003g0015 a0001c0001t0003g0213 others(4): Show |
10 | HG00673.hp2 HG01952.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.332-9900T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102787963 | |||||||
| chr2:102788042 | A | T | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-9821A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788042 | |||||||
| chr2:102788083 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.332-9780A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788083 | |||||||
| chr2:102788120 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.332-9743G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788120 | |||||||
| chr2:102788158 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.332-9705G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788158 | |||||||
| chr2:102788165 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.332-9698G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788165 | |||||||
| chr2:102788221 | C | T | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-9642C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788221 | |||||||
| chr2:102788254 | G | C | 91 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(88): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.332-9609G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788254 | |||||||
| chr2:102788326 | G | A | 1 | a0001c0001t0006g0030 | 2 | HG01496.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.332-9537G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788326 | |||||||
| chr2:102788521 | CTAT | C | 193 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(190): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.332-9336_332-9334d others(5): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102788521 | ||||||
| chr2:102788608 | C | T | 14 | a0001c0001t0012g0032 a0001c0001t0012g0251 a0001c0001t0012g0255 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-9255C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788608 | |||||||
| chr2:102788775 | G | A | 1 | a0001c0001t0003g0214 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.332-9088G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102788775 | |||||||
| chr2:102789070 | A | G | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-8793A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102789070 | |||||||
| chr2:102789268 | T | C | 1 | a0001c0001t0023g0263 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.332-8595T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102789268 | |||||||
| chr2:102789270 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.332-8593A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102789270 | |||||||
| chr2:102789750 | C | A | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.332-8113C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102789750 | |||||||
| chr2:102789816 | CA | C | 99 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(96): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.332-8046delA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102789816 | |||||||
| chr2:102789986 | C | G | 1 | a0001c0001t0002g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.332-7877C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102789986 | |||||||
| chr2:102789988 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.332-7875C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102789988 | |||||||
| chr2:102790011 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.332-7852A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102790011 | |||||||
| chr2:102790240 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(221): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.332-7623T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102790240 | |||||||
| chr2:102790594 | A | G | 9 | a0001c0001t0012g0251 a0001c0001t0012g0255 a0001c0001t0012g0256 others(6): Show |
9 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.332-7269A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102790594 | |||||||
| chr2:102790608 | A | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0270 a0001c0001t0037g0268 others(1): Show |
4 | HG02622.hp1 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-7255A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102790608 | |||||||
| chr2:102790630 | G | T | 1 | a0001c0001t0032g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.332-7233G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102790630 | |||||||
| chr2:102790705 | C | G | 99 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(96): Show |
112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.332-7158C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102790705 | |||||||
| chr2:102791127 | A | G | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-6736A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102791127 | |||||||
| chr2:102791381 | A | G | 1 | a0001c0001t0002g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.332-6482A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102791381 | |||||||
| chr2:102791485 | A | G | 1 | a0001c0001t0025g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.332-6378A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102791485 | |||||||
| chr2:102791508 | T | C | 5 | a0001c0001t0005g0042 a0001c0001t0005g0081 a0001c0001t0005g0082 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-6355T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102791508 | |||||||
| chr2:102791591 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.332-6272A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102791591 | |||||||
| chr2:102791642 | A | G | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.332-6221A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102791642 | |||||||
| chr2:102791976 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.332-5887A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102791976 | |||||||
| chr2:102792041 | T | TAC | 30 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(27): Show |
43 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.332-5792_332-5791d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102792041 | ||||||
| chr2:102792041 | T | TACAC | 7 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0012g0032 others(4): Show |
7 | HG02004.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.332-5794_332-5791d others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102792041 | ||||||
| chr2:102792041 | TAC | T | 139 | a0001c0001t0001g0076 a0001c0001t0001g0153 a0001c0001t0001g0162 others(136): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.332-5792_332-5791d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102792041 | ||||||
| chr2:102792041 | TACAC | T | 12 | a0001c0001t0005g0081 a0001c0001t0008g0010 a0001c0001t0008g0033 others(9): Show |
15 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-5794_332-5791d others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102792041 | ||||||
| chr2:102792234 | G | A | 1 | a0001c0001t0029g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.332-5629G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102792234 | |||||||
| chr2:102792354 | A | G | 8 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(5): Show |
11 | HG01891.hp1 HG02257.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.332-5509A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102792354 | |||||||
| chr2:102792436 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.332-5427A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102792436 | |||||||
| chr2:102792454 | G | T | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.332-5409G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102792454 | |||||||
| chr2:102792586 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.332-5277G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102792586 | |||||||
| chr2:102792620 | G | A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0169 a0001c0001t0002g0171 |
4 | HG00558.hp2 NA18972.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-5243G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102792620 | |||||||
| chr2:102792957 | T | A | 1 | a0001c0001t0011g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.332-4906T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102792957 | |||||||
| chr2:102792996 | CGCTGCCT others(10): Show |
C | 2 | a0001c0001t0025g0036 a0001c0001t0031g0252 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.332-4861_332-4845d others(19): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr2 | 102792996 | ||||||
| chr2:102793028 | C | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0048g0143 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.332-4835C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793028 | |||||||
| chr2:102793168 | A | G | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-4695A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793168 | |||||||
| chr2:102793226 | C | T | 76 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(73): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.332-4637C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793226 | |||||||
| chr2:102793269 | G | A | 1 | a0001c0001t0010g0183 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.332-4594G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793269 | |||||||
| chr2:102793297 | T | C | 1 | a0001c0001t0007g0216 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.332-4566T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793297 | |||||||
| chr2:102793424 | C | T | 2 | a0001c0001t0003g0244 a0001c0001t0003g0245 |
2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.332-4439C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793424 | |||||||
| chr2:102793538 | C | T | 62 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.332-4325C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793538 | |||||||
| chr2:102793602 | A | G | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-4261A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793602 | |||||||
| chr2:102793659 | T | C | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-4204T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793659 | |||||||
| chr2:102793698 | G | C | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-4165G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102793698 | |||||||
| chr2:102794020 | T | C | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-3843T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102794020 | |||||||
| chr2:102794034 | C | T | 53 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(50): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.332-3829C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102794034 | |||||||
| chr2:102794038 | C | G | 1 | a0001c0001t0008g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.332-3825C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102794038 | |||||||
| chr2:102794334 | A | T | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-3529A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102794334 | |||||||
| chr2:102794565 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.332-3298C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102794565 | |||||||
| chr2:102794823 | G | A | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-3040G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102794823 | |||||||
| chr2:102795093 | C | T | 101 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.332-2770C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795093 | |||||||
| chr2:102795268 | T | G | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-2595T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795268 | |||||||
| chr2:102795359 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.332-2504G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795359 | |||||||
| chr2:102795360 | T | G | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-2503T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795360 | |||||||
| chr2:102795455 | T | A | 1 | a0001c0001t0017g0044 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.332-2408T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795455 | |||||||
| chr2:102795458 | G | A | 1 | a0001c0001t0032g0254 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.332-2405G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795458 | |||||||
| chr2:102795497 | T | C | 1 | a0001c0001t0002g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.332-2366T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795497 | |||||||
| chr2:102795601 | C | T | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-2262C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795601 | |||||||
| chr2:102795677 | G | A | 1 | a0001c0001t0003g0110 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.332-2186G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795677 | |||||||
| chr2:102795777 | G | A | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-2086G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795777 | |||||||
| chr2:102795905 | A | G | 1 | a0001c0001t0025g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.332-1958A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795905 | |||||||
| chr2:102795966 | G | T | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-1897G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102795966 | |||||||
| chr2:102796113 | A | G | 3 | a0001c0001t0018g0067 a0001c0001t0018g0068 a0001c0001t0018g0090 |
3 | HG00673.hp1 HG02083.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.332-1750A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102796113 | |||||||
| chr2:102796270 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.332-1593T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102796270 | |||||||
| chr2:102796358 | T | C | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.332-1505T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102796358 | |||||||
| chr2:102796504 | A | G | 5 | a0001c0001t0005g0042 a0001c0001t0005g0081 a0001c0001t0005g0082 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-1359A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102796504 | |||||||
| chr2:102796537 | G | A | 15 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(12): Show |
18 | HG01891.hp1 HG02055.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.332-1326G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102796537 | |||||||
| chr2:102796853 | C | A | 2 | a0001c0001t0001g0158 a0001c0001t0005g0159 |
2 | NA19010.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.332-1010C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102796853 | |||||||
| chr2:102796888 | T | A | 1 | a0001c0001t0047g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.332-975T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102796888 | |||||||
| chr2:102797144 | C | G | 1 | a0001c0001t0006g0030 | 2 | HG01496.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.332-719C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797144 | |||||||
| chr2:102797199 | T | C | 26 | a0001c0001t0003g0110 a0001c0001t0004g0018 a0001c0001t0004g0037 others(23): Show |
27 | HG00544.hp1 HG01106.hp2 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.332-664T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797199 | |||||||
| chr2:102797285 | T | C | 2 | a0001c0001t0003g0217 a0001c0001t0003g0218 |
2 | NA18942.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.332-578T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797285 | |||||||
| chr2:102797394 | C | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0066 a0001c0001t0001g0141 |
3 | HG00408.hp2 NA18612.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.332-469C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797394 | |||||||
| chr2:102797434 | T | G | 1 | a0001c0001t0003g0219 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.332-429T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797434 | |||||||
| chr2:102797790 | C | T | 1 | a0001c0001t0005g0087 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.332-73C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797790 | |||||||
| chr2:102797805 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.332-58G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797805 | |||||||
| chr2:102797832 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.332-31T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 3/4 | chr2 | 102797832 | |||||||
| chr2:102798016 | T | C | 5 | a0001c0001t0005g0042 a0001c0001t0005g0081 a0001c0001t0005g0082 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+16T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102798016 | |||||||
| chr2:102798104 | C | G | 1 | a0001c0001t0009g0106 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.469+104C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102798104 | |||||||
| chr2:102798105 | A | G | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.469+105A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102798105 | |||||||
| chr2:102798134 | CACTA | C | 61 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(58): Show |
72 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.469+140_469+143del others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102798134 | ||||||
| chr2:102798372 | C | T | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.469+372C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102798372 | |||||||
| chr2:102798526 | A | G | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.469+526A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102798526 | |||||||
| chr2:102798766 | G | A | 62 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(59): Show |
73 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.469+766G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102798766 | |||||||
| chr2:102798773 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.469+773G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102798773 | |||||||
| chr2:102799002 | G | A | 1 | a0001c0001t0012g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.469+1002G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799002 | |||||||
| chr2:102799013 | C | T | 76 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(73): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.469+1013C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799013 | |||||||
| chr2:102799035 | G | A | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.469+1035G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799035 | |||||||
| chr2:102799150 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.469+1150A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799150 | |||||||
| chr2:102799225 | G | T | 3 | a0001c0001t0012g0251 a0001c0001t0012g0255 a0001c0001t0012g0256 |
3 | HG02622.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.469+1225G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799225 | |||||||
| chr2:102799365 | G | A | 1 | a0001c0003t0002g0165 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.469+1365G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799365 | |||||||
| chr2:102799412 | C | T | 1 | a0001c0001t0047g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469+1412C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799412 | |||||||
| chr2:102799457 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469+1457T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799457 | |||||||
| chr2:102799529 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0017 |
5 | HG01257.hp2 HG01258.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1529T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799529 | |||||||
| chr2:102799617 | T | A | 3 | a0001c0001t0006g0210 a0001c0001t0006g0211 a0001c0001t0006g0220 |
3 | HG01167.hp1 HG01169.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.469+1617T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799617 | |||||||
| chr2:102799641 | G | A | 1 | a0001c0001t0029g0283 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469+1641G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799641 | |||||||
| chr2:102799696 | G | A | 61 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(58): Show |
72 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.469+1696G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799696 | |||||||
| chr2:102799747 | C | A | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.469+1747C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799747 | |||||||
| chr2:102799870 | C | G | 2 | a0001c0001t0006g0030 a0001c0001t0006g0269 |
3 | HG01496.hp2 HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.469+1870C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102799870 | |||||||
| chr2:102800019 | T | TA | 8 | a0001c0001t0004g0212 a0001c0001t0008g0280 a0001c0001t0016g0284 others(5): Show |
8 | HG02055.hp2 HG02451.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.469+2030dupA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800019 | ||||||
| chr2:102800078 | T | C | 1 | a0001c0001t0008g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.469+2078T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800078 | |||||||
| chr2:102800239 | C | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
6 | HG01167.hp2 HG01891.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+2239C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800239 | |||||||
| chr2:102800386 | A | G | 101 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(98): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.469+2386A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800386 | |||||||
| chr2:102800563 | A | C | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.469+2563A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800563 | |||||||
| chr2:102800658 | C | CT | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0020g0286 others(3): Show |
6 | HG02886.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+2668dupT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800658 | ||||||
| chr2:102800797 | T | TTG | 59 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(56): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.469+2841_469+2842d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | T | TTGTG | 13 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0139 others(10): Show |
14 | HG00639.hp2 HG00642.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.469+2839_469+2842d others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | T | TTGTGTG | 6 | a0001c0001t0001g0001 a0001c0001t0001g0063 a0001c0001t0003g0004 others(3): Show |
6 | HG00140.hp1 HG00438.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+2837_469+2842d others(8): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | TTG | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(52): Show |
63 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.469+2841_469+2842d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | TTGTG | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(17): Show |
21 | HG00323.hp1 HG00558.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.469+2839_469+2842d others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | TTGTGTG | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(44): Show |
55 | HG00280.hp1 HG00408.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.469+2837_469+2842d others(8): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | TTGTGTGT others(1): Show |
T | 8 | a0001c0001t0001g0259 a0001c0001t0002g0260 a0001c0001t0002g0261 others(5): Show |
8 | HG01884.hp1 HG02258.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.469+2835_469+2842d others(10): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0190 |
2 | HG01981.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.469+2833_469+2842d others(12): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0002g0002 a0001c0001t0004g0037 a0001c0001t0007g0225 |
3 | HG03942.hp2 NA18959.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.469+2831_469+2842d others(14): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800797 | TTGTGTGT others(17): Show |
T | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.469+2819_469+2842d others(26): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800797 | ||||||
| chr2:102800831 | G | A | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+2831G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800831 | |||||||
| chr2:102800841 | GT | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0011g0118 |
3 | HG00738.hp2 HG01934.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.469+2844delT | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102800841 | ||||||
| chr2:102800842 | T | TG | 4 | a0001c0001t0001g0005 a0001c0001t0001g0062 a0001c0001t0005g0074 others(1): Show |
4 | HG02683.hp2 HG03471.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+2842_469+2843i others(3): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800842 | |||||||
| chr2:102800844 | T | G | 1 | a0001c0001t0015g0241 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.469+2844T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800844 | |||||||
| chr2:102800908 | C | T | 191 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(188): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.469+2908C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102800908 | |||||||
| chr2:102801245 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(294): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.469+3245A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801245 | |||||||
| chr2:102801310 | C | G | 1 | a0001c0001t0047g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469+3310C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801310 | |||||||
| chr2:102801481 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.469+3481G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801481 | |||||||
| chr2:102801500 | C | T | 75 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(72): Show |
86 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.469+3500C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801500 | |||||||
| chr2:102801565 | C | T | 1 | a0001c0001t0047g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469+3565C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801565 | |||||||
| chr2:102801822 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.469+3822G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801822 | |||||||
| chr2:102801863 | T | G | 1 | a0001c0001t0047g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469+3863T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801863 | |||||||
| chr2:102801895 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.469+3895T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102801895 | |||||||
| chr2:102802100 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.469+4100C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802100 | |||||||
| chr2:102802296 | G | A | 1 | a0001c0001t0007g0273 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.469+4296G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802296 | |||||||
| chr2:102802379 | C | T | 3 | a0001c0001t0022g0266 a0001c0001t0022g0271 a0001c0001t0036g0265 |
3 | HG02630.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.469+4379C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802379 | |||||||
| chr2:102802584 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.469+4584C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802584 | |||||||
| chr2:102802736 | C | G | 52 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0008 others(49): Show |
63 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.469+4736C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802736 | |||||||
| chr2:102802788 | T | A | 76 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(73): Show |
87 | HG00280.hp1 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.469+4788T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802788 | |||||||
| chr2:102802799 | C | A | 1 | a0001c0001t0023g0263 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.469+4799C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802799 | |||||||
| chr2:102802836 | T | C | 1 | a0001c0001t0047g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.469+4836T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802836 | |||||||
| chr2:102802944 | T | C | 1 | a0001c0001t0021g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.469+4944T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102802944 | |||||||
| chr2:102803199 | C | T | 3 | a0001c0001t0012g0251 a0001c0001t0012g0255 a0001c0001t0012g0256 |
3 | HG02622.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.469+5199C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803199 | |||||||
| chr2:102803200 | A | G | 191 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(188): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.469+5200A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803200 | |||||||
| chr2:102803239 | A | G | 14 | a0001c0001t0012g0032 a0001c0001t0012g0251 a0001c0001t0012g0255 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.469+5239A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803239 | |||||||
| chr2:102803310 | G | A | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.469+5310G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803310 | |||||||
| chr2:102803413 | A | G | 9 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(6): Show |
12 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.469+5413A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803413 | |||||||
| chr2:102803698 | G | A | 192 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.469+5698G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803698 | |||||||
| chr2:102803772 | G | A | 178 | a0001c0001t0001g0259 a0001c0001t0002g0002 a0001c0001t0002g0007 others(175): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.469+5772G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803772 | |||||||
| chr2:102803821 | G | A | 1 | a0001c0001t0031g0252 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.469+5821G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803821 | |||||||
| chr2:102803848 | T | C | 6 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(3): Show |
6 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.469+5848T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803848 | |||||||
| chr2:102803922 | G | A | 14 | a0001c0001t0012g0032 a0001c0001t0012g0251 a0001c0001t0012g0255 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.469+5922G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102803922 | |||||||
| chr2:102804001 | A | G | 1 | a0001c0001t0037g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.469+6001A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102804001 | |||||||
| chr2:102804021 | C | G | 1 | a0001c0001t0003g0218 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.469+6021C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102804021 | |||||||
| chr2:102804392 | T | C | 117 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(114): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.469+6392T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102804392 | |||||||
| chr2:102804590 | T | A | 3 | a0001c0001t0012g0251 a0001c0001t0012g0255 a0001c0001t0012g0256 |
3 | HG02622.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.469+6590T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102804590 | |||||||
| chr2:102804743 | A | G | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+6743A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102804743 | |||||||
| chr2:102804835 | C | T | 4 | a0001c0001t0005g0065 a0001c0001t0005g0074 a0001c0001t0005g0085 others(1): Show |
4 | NA18956.hp1 NA18974.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+6835C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102804835 | |||||||
| chr2:102804959 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(15): Show |
27 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.469+6959A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102804959 | |||||||
| chr2:102805109 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.469+7109A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102805109 | |||||||
| chr2:102805404 | G | A | 2 | a0001c0001t0002g0188 a0001c0001t0002g0202 |
2 | NA18985.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.469+7404G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102805404 | |||||||
| chr2:102805466 | A | G | 5 | a0001c0001t0012g0032 a0001c0001t0021g0275 a0001c0001t0021g0276 others(2): Show |
5 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+7466A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102805466 | |||||||
| chr2:102805541 | G | A | 3 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0048g0143 |
3 | HG02258.hp2 HG03209.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.469+7541G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102805541 | |||||||
| chr2:102805608 | C | CA | 19 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0057 others(16): Show |
22 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.469+7621dupA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102805608 | ||||||
| chr2:102805608 | CA | C | 6 | a0001c0001t0001g0107 a0001c0001t0001g0154 a0001c0001t0001g0163 others(3): Show |
6 | HG00140.hp2 HG01168.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.469+7621delA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102805608 | ||||||
| chr2:102805724 | C | T | 3 | a0001c0001t0018g0067 a0001c0001t0018g0068 a0001c0001t0018g0090 |
3 | HG00673.hp1 HG02083.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.469+7724C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102805724 | |||||||
| chr2:102805896 | T | C | 132 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(129): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.469+7896T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102805896 | |||||||
| chr2:102806213 | A | G | 1 | a0001c0001t0021g0275 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.469+8213A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102806213 | |||||||
| chr2:102806471 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.470-8277G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102806471 | |||||||
| chr2:102806534 | A | T | 8 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(5): Show |
11 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.470-8214A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102806534 | |||||||
| chr2:102806649 | G | A | 1 | a0001c0001t0012g0258 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.470-8099G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102806649 | |||||||
| chr2:102806659 | T | TTAA | 3 | a0001c0001t0002g0202 a0001c0001t0004g0113 a0001c0001t0004g0114 |
3 | NA18985.hp1 NA18993.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.470-8070_470-8068d others(5): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102806659 | ||||||
| chr2:102806718 | C | T | 15 | a0001c0001t0012g0032 a0001c0001t0012g0251 a0001c0001t0012g0255 others(12): Show |
15 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.470-8030C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102806718 | |||||||
| chr2:102806854 | A | G | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0003g0214 others(1): Show |
4 | HG02040.hp2 HG02135.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-7894A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102806854 | |||||||
| chr2:102807123 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.470-7625A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102807123 | |||||||
| chr2:102807447 | A | G | 1 | a0001c0001t0005g0086 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.470-7301A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102807447 | |||||||
| chr2:102807692 | T | C | 4 | a0001c0001t0005g0065 a0001c0001t0005g0074 a0001c0001t0005g0085 others(1): Show |
4 | NA18956.hp1 NA18974.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-7056T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102807692 | |||||||
| chr2:102807783 | A | C | 1 | a0001c0001t0014g0064 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.470-6965A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102807783 | |||||||
| chr2:102808198 | C | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0114 |
2 | NA18993.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.470-6550C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102808198 | |||||||
| chr2:102808698 | A | C | 103 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(100): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.470-6050A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102808698 | |||||||
| chr2:102808955 | A | C | 1 | a0001c0001t0003g0262 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.470-5793A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102808955 | |||||||
| chr2:102809218 | A | G | 132 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(129): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.470-5530A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809218 | |||||||
| chr2:102809401 | G | A | 103 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(100): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.470-5347G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809401 | |||||||
| chr2:102809425 | G | A | 4 | a0001c0001t0006g0229 a0001c0001t0007g0221 a0001c0001t0007g0228 others(1): Show |
4 | HG00438.hp2 HG02056.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-5323G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809425 | |||||||
| chr2:102809600 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.470-5148G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809600 | |||||||
| chr2:102809607 | C | G | 1 | a0001c0001t0037g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.470-5141C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809607 | |||||||
| chr2:102809640 | C | T | 5 | a0001c0001t0001g0149 a0001c0001t0003g0009 a0001c0001t0003g0213 others(2): Show |
8 | HG00673.hp2 HG02004.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-5108C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809640 | |||||||
| chr2:102809663 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.470-5085A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809663 | |||||||
| chr2:102809718 | C | T | 2 | a0001c0001t0013g0014 a0001c0001t0013g0028 |
5 | HG00099.hp2 HG00733.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-5030C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809718 | |||||||
| chr2:102809818 | G | A | 1 | a0001c0001t0003g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.470-4930G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809818 | |||||||
| chr2:102809830 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.470-4918C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809830 | |||||||
| chr2:102809965 | C | A | 1 | a0001c0001t0003g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.470-4783C>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809965 | |||||||
| chr2:102809967 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.470-4781A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102809967 | |||||||
| chr2:102810129 | T | TA | 5 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0169 others(2): Show |
7 | HG00558.hp2 HG02074.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.470-4610dupA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102810129 | ||||||
| chr2:102810130 | A | T | 6 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
6 | HG01167.hp2 HG01891.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-4618A>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810130 | |||||||
| chr2:102810412 | T | C | 1 | a0001c0001t0012g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.470-4336T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810412 | |||||||
| chr2:102810471 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.470-4277C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810471 | |||||||
| chr2:102810701 | T | G | 1 | a0001c0001t0004g0113 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.470-4047T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810701 | |||||||
| chr2:102810735 | A | C | 3 | a0001c0001t0014g0176 a0001c0001t0014g0204 a0001c0001t0014g0205 |
3 | HG00544.hp2 NA18612.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.470-4013A>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810735 | |||||||
| chr2:102810779 | T | C | 1 | a0001c0001t0003g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.470-3969T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810779 | |||||||
| chr2:102810860 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.470-3888G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810860 | |||||||
| chr2:102810966 | C | G | 1 | a0001c0001t0003g0245 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.470-3782C>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102810966 | |||||||
| chr2:102811058 | C | CA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(113): Show |
144 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.470-3666dupA | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102811058 | ||||||
| chr2:102811058 | C | CAA | 126 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(123): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.470-3667_470-3666d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102811058 | ||||||
| chr2:102811058 | C | CAAA | 19 | a0001c0001t0003g0029 a0001c0001t0003g0110 a0001c0001t0003g0243 others(16): Show |
23 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.470-3668_470-3666d others(5): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102811058 | ||||||
| chr2:102811343 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0017 |
5 | HG01257.hp2 HG01258.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-3405G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102811343 | |||||||
| chr2:102811423 | C | T | 1 | a0001c0001t0002g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.470-3325C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102811423 | |||||||
| chr2:102811530 | T | A | 1 | a0001c0001t0004g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.470-3218T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102811530 | |||||||
| chr2:102811592 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0014g0239 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.470-3156A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102811592 | |||||||
| chr2:102811740 | T | G | 1 | a0001c0001t0010g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.470-3008T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102811740 | |||||||
| chr2:102811751 | G | A | 9 | a0001c0001t0012g0251 a0001c0001t0012g0255 a0001c0001t0012g0256 others(6): Show |
9 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-2997G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102811751 | |||||||
| chr2:102811889 | G | A | 14 | a0001c0001t0012g0032 a0001c0001t0012g0251 a0001c0001t0012g0255 others(11): Show |
14 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.470-2859G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102811889 | |||||||
| chr2:102812384 | T | TAC | 15 | a0001c0001t0001g0073 a0001c0001t0001g0147 a0001c0001t0001g0155 others(12): Show |
15 | HG00544.hp1 HG01167.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.470-2319_470-2318d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | T | TACAC | 7 | a0001c0001t0001g0016 a0001c0001t0001g0164 a0001c0001t0003g0213 others(4): Show |
8 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-2321_470-2318d others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TAC | T | 55 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0060 others(52): Show |
68 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.470-2319_470-2318d others(4): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TACAC | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(40): Show |
52 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.470-2321_470-2318d others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TACACAC | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0013 others(54): Show |
68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.470-2323_470-2318d others(8): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TACACACA others(1): Show |
T | 41 | a0001c0001t0001g0150 a0001c0001t0002g0002 a0001c0001t0002g0007 others(38): Show |
51 | HG00408.hp1 HG00558.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.470-2325_470-2318d others(10): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TACACACA others(3): Show |
T | 4 | a0001c0001t0001g0062 a0001c0001t0002g0260 a0001c0001t0002g0261 others(1): Show |
4 | HG02258.hp1 HG02683.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-2327_470-2318d others(12): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TACACACA others(5): Show |
T | 5 | a0001c0001t0005g0042 a0001c0001t0005g0081 a0001c0001t0005g0082 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-2329_470-2318d others(14): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TACACACA others(7): Show |
T | 3 | a0001c0001t0024g0034 a0001c0001t0024g0035 a0001c0001t0028g0281 |
3 | HG02055.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.470-2331_470-2318d others(16): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812384 | TACACACA others(15): Show |
T | 5 | a0001c0001t0016g0284 a0001c0001t0016g0285 a0001c0001t0016g0287 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-2339_470-2318d others(24): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812384 | ||||||
| chr2:102812425 | A | ACACG | 7 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(4): Show |
10 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-2320_470-2319i others(6): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102812425 | ||||||
| chr2:102812520 | G | A | 100 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(97): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.470-2228G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102812520 | |||||||
| chr2:102812706 | T | C | 1 | a0001c0001t0008g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.470-2042T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102812706 | |||||||
| chr2:102812863 | C | T | 1 | a0001c0001t0004g0212 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.470-1885C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102812863 | |||||||
| chr2:102812972 | G | A | 7 | a0001c0001t0008g0010 a0001c0001t0008g0033 a0001c0001t0008g0278 others(4): Show |
10 | HG01891.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.470-1776G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102812972 | |||||||
| chr2:102813095 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0129 |
2 | HG00280.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.470-1653C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102813095 | |||||||
| chr2:102813179 | T | G | 9 | a0001c0001t0002g0007 a0001c0001t0002g0167 a0001c0001t0002g0174 others(6): Show |
12 | HG00741.hp1 HG01928.hp1 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.470-1569T>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102813179 | |||||||
| chr2:102813196 | A | G | 1 | a0001c0001t0003g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.470-1552A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102813196 | |||||||
| chr2:102813237 | C | T | 103 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(100): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.470-1511C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102813237 | |||||||
| chr2:102813269 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.470-1479A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102813269 | |||||||
| chr2:102813428 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG02735.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.470-1320A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102813428 | |||||||
| chr2:102813767 | C | T | 5 | a0001c0001t0005g0042 a0001c0001t0005g0081 a0001c0001t0005g0082 others(2): Show |
5 | HG02451.hp2 HG02895.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-981C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102813767 | |||||||
| chr2:102814086 | G | GTA | 9 | a0001c0001t0002g0047 a0001c0001t0002g0193 a0001c0001t0002g0260 others(6): Show |
9 | HG02258.hp1 HG03098.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.470-644_470-643dup others(2): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102814086 | ||||||
| chr2:102814086 | GTA | G | 112 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(109): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.470-644_470-643del others(2): Show |
TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr2 | 102814086 | ||||||
| chr2:102814124 | C | T | 1 | a0002c0002t0001g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.470-624C>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814124 | |||||||
| chr2:102814125 | G | T | 1 | a0001c0001t0003g0243 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.470-623G>T | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814125 | |||||||
| chr2:102814162 | G | A | 1 | a0001c0001t0005g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.470-586G>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814162 | |||||||
| chr2:102814251 | G | C | 1 | a0001c0001t0002g0261 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.470-497G>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814251 | |||||||
| chr2:102814463 | T | C | 111 | a0001c0001t0003g0004 a0001c0001t0003g0009 a0001c0001t0003g0015 others(108): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.470-285T>C | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814463 | |||||||
| chr2:102814485 | T | A | 3 | a0001c0001t0022g0266 a0001c0001t0022g0271 a0001c0001t0036g0265 |
3 | HG02630.hp2 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.470-263T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814485 | |||||||
| chr2:102814590 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0130 |
2 | HG00323.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.470-158A>G | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814590 | |||||||
| chr2:102814630 | T | A | 1 | a0001c0001t0041g0094 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.470-118T>A | TMEM182 | ENSG00000170417.16 | transcript | ENST00000412401.3 | protein_coding | 4/4 | chr2 | 102814630 |