Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25829 |
| ensemblid | ENSG00000198792.13 |
| hgncid | 1310 |
| symbol | TMEM184B |
| name | transmembrane protein 184B |
| refseq_nuc | NM_012264.5 |
| refseq_prot | NP_036396.2 |
| ensembl_nuc | ENST00000361906.8 |
| ensembl_prot | ENSP00000355210.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 38219291 |
| end | 38273010 |
| strand | - |
| ver | v1.2 |
| region | chr22:38219291-38273010 |
| region5000 | chr22:38214291-38278010 |
| regionname0 | TMEM184B_chr22_38219291_38273010 |
| regionname5000 | TMEM184B_chr22_38214291_38278010 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 407 | 353 | 90 | 64 | 143 | 14 | 40 | 104 | TMEM184B_chr22_38214291_38278010 | TMEM184B | MTVRG others(402): Show |
chr22 | 38214291 | 38278010 |
| a0002 | 0/0 | 407 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | MTVRG others(402): Show |
chr22 | 38214291 | 38278010 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1221 | 299 | 69 | 60 | 129 | 11 | 28 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0002 | 0/0 | 1221 | 16 | 5 | 0 | 1 | 0 | 10 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0003 | 0/0 | 1221 | 11 | 9 | 1 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0004 | 0/0 | 1221 | 8 | 4 | 2 | 1 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0005 | 0/0 | 1221 | 6 | 0 | 0 | 6 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0006 | 0/0 | 1221 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0007 | 0/0 | 1221 | 3 | 2 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0008 | 0/0 | 1221 | 3 | 0 | 0 | 0 | 3 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0001c0009 | 0/0 | 1221 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 | ||
| a0002c0010 | 0/0 | 1221 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATGAC others(1216): Show |
chr22 | 38214291 | 38278010 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3587 | 156 | 18 | 29 | 79 | 7 | 22 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0002 | 0/0 | 3587 | 78 | 7 | 22 | 40 | 3 | 6 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0003 | 0/0 | 3583 | 15 | 9 | 0 | 6 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3578): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0004 | 0/0 | 3587 | 11 | 10 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0006 | 0/0 | 3587 | 6 | 6 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0007 | 0/0 | 3587 | 6 | 0 | 6 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0009 | 0/0 | 3587 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0010 | 0/0 | 3588 | 2 | 1 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3583): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0012 | 0/0 | 3587 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0013 | 0/0 | 3587 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0014 | 0/0 | 3587 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0015 | 0/0 | 3587 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0016 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0020 | 0/0 | 3587 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0021 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0022 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0023 | 0/0 | 3587 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0024 | 0/0 | 3587 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0025 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0026 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0027 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0028 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0029 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0030 | 0/0 | 3587 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0031 | 0/0 | 3587 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0001t0033 | 0/1 | 3587 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ATTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0002t0003 | 0/0 | 3583 | 16 | 5 | 0 | 1 | 0 | 10 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3578): Show |
chr22 | 38214291 | 38278010 |
| a0001c0003t0001 | 0/0 | 3587 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0003t0005 | 0/0 | 3583 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3578): Show |
chr22 | 38214291 | 38278010 |
| a0001c0003t0018 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3578): Show |
chr22 | 38214291 | 38278010 |
| a0001c0003t0019 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3578): Show |
chr22 | 38214291 | 38278010 |
| a0001c0004t0008 | 0/0 | 3588 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3583): Show |
chr22 | 38214291 | 38278010 |
| a0001c0004t0011 | 0/0 | 3587 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0004t0017 | 0/0 | 3587 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0004t0032 | 0/0 | 3587 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0005t0001 | 0/0 | 3587 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0005t0002 | 0/0 | 3587 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0006t0002 | 0/0 | 3587 | 5 | 0 | 0 | 5 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0007t0001 | 0/0 | 3587 | 3 | 2 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0008t0002 | 0/0 | 3587 | 3 | 0 | 0 | 0 | 3 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0001c0009t0002 | 0/0 | 3587 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| a0002c0010t0002 | 0/0 | 3587 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | ACTCC others(3582): Show |
chr22 | 38214291 | 38278010 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0189 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0007g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0007g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0007g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0007g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0009g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0010g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0012g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0013g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0015g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0015g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0020g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0021g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0022g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0023g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0024g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0025g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0026g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0027g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0028g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0029g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0030g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0031g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0001t0033g0318 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0002t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0005g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0018g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0003t0019g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0004t0008g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0004t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0004t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0004t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0004t0011g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0004t0017g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0004t0032g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0005t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0005t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0005t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0006t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0006t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0006t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0006t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0006t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0007t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0007t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0007t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0008t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0008t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0008t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0009t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0001c0009t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| a0002c0010t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0008 | t0002 | g0049 | EUR | GBR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | GBR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | FIN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | FIN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00558 | hp1 | a0001 | c0006 | t0002 | g0206 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00639 | hp1 | a0001 | c0004 | t0032 | g0101 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00639 | hp2 | a0001 | c0004 | t0017 | g0026 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01074 | hp1 | a0001 | c0009 | t0002 | g0212 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0165 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0315 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01109 | hp1 | a0001 | c0003 | t0005 | g0070 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0270 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01496 | hp1 | a0001 | c0001 | t0024 | g0303 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01515 | hp1 | a0001 | c0008 | t0002 | g0046 | EUR | IBS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0256 | EUR | IBS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0306 | EUR | IBS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01517 | hp1 | a0001 | c0008 | t0002 | g0203 | EUR | IBS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | IBS | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01884 | hp2 | a0001 | c0001 | t0014 | g0095 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0299 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01934 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01981 | hp1 | a0001 | c0001 | t0007 | g0316 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0317 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02015 | hp1 | a0001 | c0006 | t0002 | g0169 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0163 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02083 | hp2 | a0001 | c0001 | t0030 | g0093 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02135 | hp1 | a0002 | c0010 | t0002 | g0196 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CDX | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0076 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02523 | hp2 | a0001 | c0005 | t0001 | g0107 | EAS | KHV | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02572 | hp1 | a0001 | c0003 | t0005 | g0071 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0109 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0187 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0164 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02818 | hp1 | a0001 | c0003 | t0005 | g0002 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02895 | hp1 | a0001 | c0001 | t0009 | g0271 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02895 | hp2 | a0001 | c0007 | t0001 | g0312 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02896 | hp1 | a0001 | c0003 | t0019 | g0073 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0218 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02897 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02897 | hp2 | a0001 | c0007 | t0001 | g0311 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02922 | hp1 | a0001 | c0003 | t0018 | g0074 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0100 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0025 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03041 | hp2 | a0001 | c0001 | t0026 | g0124 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03139 | hp1 | a0001 | c0004 | t0008 | g0181 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03195 | hp1 | a0001 | c0001 | t0028 | g0088 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03209 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03225 | hp1 | a0001 | c0003 | t0005 | g0002 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03225 | hp2 | a0001 | c0001 | t0025 | g0237 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0023 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03453 | hp1 | a0001 | c0001 | t0015 | g0314 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0193 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0313 | AFR | ESN | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03540 | hp2 | a0001 | c0001 | t0021 | g0122 | AFR | GWD | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03579 | hp1 | a0001 | c0003 | t0005 | g0002 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0222 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03669 | hp1 | a0001 | c0004 | t0011 | g0279 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0281 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0277 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03704 | hp1 | a0001 | c0002 | t0003 | g0276 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03710 | hp1 | a0001 | c0007 | t0001 | g0214 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0215 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0023 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0275 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0274 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0217 | SAS | STU | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CHB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | YRI | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | YRI | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18946 | hp2 | a0001 | c0006 | t0002 | g0209 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18951 | hp1 | a0001 | c0005 | t0001 | g0179 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18952 | hp2 | a0001 | c0001 | t0020 | g0136 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18966 | hp1 | a0001 | c0005 | t0001 | g0146 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18973 | hp1 | a0001 | c0006 | t0002 | g0207 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18978 | hp1 | a0001 | c0004 | t0011 | g0190 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18982 | hp2 | a0001 | c0006 | t0002 | g0052 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18987 | hp2 | a0001 | c0001 | t0010 | g0132 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18998 | hp1 | a0001 | c0001 | t0031 | g0202 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19030 | hp1 | a0001 | c0003 | t0005 | g0089 | AFR | LWK | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19030 | hp2 | a0001 | c0001 | t0022 | g0228 | AFR | LWK | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0002 | AFR | LWK | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | LWK | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19063 | hp2 | a0001 | c0002 | t0003 | g0308 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19065 | hp2 | a0001 | c0005 | t0002 | g0147 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19088 | hp1 | a0001 | c0005 | t0001 | g0149 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19240 | hp1 | a0001 | c0004 | t0008 | g0008 | AFR | YRI | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA19240 | hp2 | a0001 | c0003 | t0005 | g0072 | AFR | YRI | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20129 | hp1 | a0001 | c0001 | t0027 | g0186 | AFR | ASW | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0097 | AFR | ASW | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | TSI | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | GIH | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | GIH | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0082 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03471 | hp1 | a0001 | c0001 | t0029 | g0110 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | USA | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0220 | AFR | USA | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA18955 | hp2 | a0001 | c0005 | t0002 | g0148 | EAS | JPT | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20300 | hp1 | a0001 | c0009 | t0002 | g0201 | AFR | USA | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | LWK | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| NA21309 | hp2 | a0001 | c0004 | t0008 | g0008 | AFR | LWK | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0033 | g0318 | REF | REF | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0189 | REF | REF | TMEM184B_chr22_38214291_38278010 | TMEM184B | chr22 | 38214291 | 38278010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38221566 | C | G | 1 | a0002 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1127G>C | p.Trp376Ser | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1312/3587 | 1127/1224 | 376/407 | chr22 | 38221566 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38221697 | G | C | 1 | a0001c0009 | 2 | HG01074.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.996C>G | p.Pro332Pro | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1181/3587 | 996/1224 | 332/407 | chr22 | 38221697 | |||
| chr22:38224900 | G | T | 2 | a0001c0002 a0001c0004 |
24 | HG00639.hp1 HG00639.hp2 HG01884.hp1 others(21): Show |
synonymous_variant | LOW | c.867C>A | p.Thr289Thr | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/9 | 1052/3587 | 867/1224 | 289/407 | chr22 | 38224900 | |||
| chr22:38225449 | G | A | 1 | a0001c0003 | 11 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(8): Show |
synonymous_variant | LOW | c.762C>T | p.Ser254Ser | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 7/9 | 947/3587 | 762/1224 | 254/407 | chr22 | 38225449 | |||
| chr22:38226864 | G | A | 1 | a0001c0006 | 5 | HG00558.hp1 HG02015.hp1 NA18946.hp2 others(2): Show |
synonymous_variant | LOW | c.532C>T | p.Leu178Leu | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/9 | 717/3587 | 532/1224 | 178/407 | chr22 | 38226864 | |||
| chr22:38231333 | G | A | 1 | a0001c0008 | 3 | HG00140.hp1 HG01515.hp1 HG01517.hp1 |
splice_region_variant&synonymous_variant | LOW | c.360C>T | p.Ala120Ala | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 4/9 | 545/3587 | 360/1224 | 120/407 | chr22 | 38231333 | |||
| chr22:38246032 | G | A | 1 | a0001c0005 | 6 | HG02523.hp2 NA18951.hp1 NA18955.hp2 others(3): Show |
synonymous_variant | LOW | c.261C>T | p.Ile87Ile | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/9 | 446/3587 | 261/1224 | 87/407 | chr22 | 38246032 | |||
| chr22:38247794 | C | T | 2 | a0001c0002 a0001c0007 |
19 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
synonymous_variant | LOW | c.168G>A | p.Thr56Thr | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/9 | 353/3587 | 168/1224 | 56/407 | chr22 | 38247794 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38219526 | A | AT | 2 | a0001c0001t0010 a0001c0004t0008 |
6 | HG01891.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1942dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1942 | chr22 | 38219526 | ||||||
| chr22:38219529 | A | T | 31 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(28): Show |
254 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*1940T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1940 | chr22 | 38219529 | ||||||
| chr22:38219540 | A | G | 1 | a0001c0001t0023 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1929T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1929 | chr22 | 38219540 | ||||||
| chr22:38219603 | G | A | 1 | a0001c0001t0024 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1866C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1866 | chr22 | 38219603 | ||||||
| chr22:38219610 | C | T | 1 | a0001c0001t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1859G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1859 | chr22 | 38219610 | ||||||
| chr22:38219647 | C | T | 3 | a0001c0001t0009 a0001c0001t0014 a0001c0003t0018 |
6 | HG01243.hp1 HG01884.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1822 | chr22 | 38219647 | ||||||
| chr22:38219683 | C | T | 1 | a0001c0001t0022 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1786 | chr22 | 38219683 | ||||||
| chr22:38219847 | G | A | 1 | a0001c0001t0006 | 6 | HG02559.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1622C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1622 | chr22 | 38219847 | ||||||
| chr22:38219853 | C | G | 1 | a0001c0001t0028 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1616G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1616 | chr22 | 38219853 | ||||||
| chr22:38220138 | C | T | 1 | a0001c0001t0009 | 3 | HG01243.hp1 HG02895.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1331G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1331 | chr22 | 38220138 | ||||||
| chr22:38220141 | G | A | 1 | a0001c0001t0025 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1328C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1328 | chr22 | 38220141 | ||||||
| chr22:38220198 | C | T | 1 | a0001c0001t0021 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1271 | chr22 | 38220198 | ||||||
| chr22:38220262 | T | C | 2 | a0001c0004t0011 a0001c0004t0017 |
3 | HG00639.hp2 HG03669.hp1 NA18978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1207A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1207 | chr22 | 38220262 | ||||||
| chr22:38220378 | C | G | 3 | a0001c0001t0013 a0001c0001t0027 a0001c0001t0029 |
4 | HG02622.hp1 HG03471.hp1 NA20129.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1091G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1091 | chr22 | 38220378 | ||||||
| chr22:38220453 | G | A | 2 | a0001c0001t0003 a0001c0002t0003 |
31 | HG00673.hp1 HG01884.hp1 HG01891.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1016C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 1016 | chr22 | 38220453 | ||||||
| chr22:38220487 | C | T | 1 | a0001c0001t0020 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*982G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 982 | chr22 | 38220487 | ||||||
| chr22:38220499 | C | T | 1 | a0001c0001t0012 | 2 | HG03209.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*970G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 970 | chr22 | 38220499 | ||||||
| chr22:38220787 | G | A | 1 | a0001c0003t0019 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*682C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 682 | chr22 | 38220787 | ||||||
| chr22:38220918 | G | A | 1 | a0001c0001t0026 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*551C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 551 | chr22 | 38220918 | ||||||
| chr22:38221005 | G | A | 5 | a0001c0001t0004 a0001c0001t0027 a0001c0001t0028 others(2): Show |
18 | HG00639.hp1 HG01099.hp2 HG02109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*464C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 464 | chr22 | 38221005 | ||||||
| chr22:38221106 | G | A | 1 | a0001c0001t0029 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*363C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 363 | chr22 | 38221106 | ||||||
| chr22:38221168 | G | A | 1 | a0001c0001t0030 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 301 | chr22 | 38221168 | ||||||
| chr22:38221234 | T | C | 1 | a0001c0001t0031 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*235A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 235 | chr22 | 38221234 | ||||||
| chr22:38221291 | T | C | 2 | a0001c0004t0008 a0001c0004t0032 |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*178A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 178 | chr22 | 38221291 | ||||||
| chr22:38221326 | T | C | 24 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(21): Show |
164 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*143A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 143 | chr22 | 38221326 | ||||||
| chr22:38221331 | TGTGA | T | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0005 others(2): Show |
41 | HG00673.hp1 HG01109.hp1 HG01884.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*134_*137delTCAC | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 9/9 | 134 | chr22 | 38221331 | ||||||
| chr22:38272922 | G | A | 1 | a0001c0001t0015 | 2 | HG03453.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-97C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/9 | 24961 | chr22 | 38272922 | ||||||
| chr22:38272968 | C | T | 1 | a0001c0004t0017 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-143G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/9 | 25007 | chr22 | 38272968 | ||||||
| chr22:38272994 | C | A | 2 | a0001c0001t0001 a0001c0001t0004 |
2 | HG01109.hp2 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-169G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/9 | 25033 | chr22 | 38272994 | ||||||
| chr22:38273000 | C | T | 1 | a0001c0001t0016 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-175G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/9 | 25039 | chr22 | 38273000 | ||||||
| chr22:38273009 | G | A | 1 | a0001c0001t0007 | 6 | HG01074.hp2 HG01106.hp2 HG01934.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-184C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/9 | 25048 | chr22 | 38273009 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:38221716 | G | A | 33 | a0001c0001t0003g0003 a0001c0001t0003g0018 a0001c0001t0003g0030 others(30): Show |
41 | HG00673.hp1 HG01109.hp1 HG01884.hp1 others(38): Show |
splice_region_variant&intron_variant | LOW | c.983-6C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38221716 | |||||||
| chr22:38221762 | G | A | 1 | a0001c0003t0018g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.983-52C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38221762 | |||||||
| chr22:38221783 | C | T | 1 | a0001c0001t0025g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.983-73G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38221783 | |||||||
| chr22:38222120 | T | C | 39 | a0001c0001t0003g0003 a0001c0001t0003g0018 a0001c0001t0003g0030 others(36): Show |
48 | HG00673.hp1 HG01109.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.983-410A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222120 | |||||||
| chr22:38222127 | C | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0085 others(15): Show |
22 | HG00673.hp1 HG01884.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.983-417G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222127 | |||||||
| chr22:38222142 | C | T | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.983-432G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222142 | |||||||
| chr22:38222175 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.983-465T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222175 | |||||||
| chr22:38222353 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.983-643G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222353 | |||||||
| chr22:38222458 | G | C | 33 | a0001c0001t0003g0003 a0001c0001t0003g0018 a0001c0001t0003g0030 others(30): Show |
41 | HG00673.hp1 HG01109.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.983-748C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222458 | |||||||
| chr22:38222597 | G | C | 1 | a0001c0001t0001g0310 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.983-887C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222597 | |||||||
| chr22:38222786 | C | A | 1 | a0001c0001t0004g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.983-1076G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222786 | |||||||
| chr22:38222814 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.983-1104G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222814 | |||||||
| chr22:38222869 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.983-1159C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38222869 | |||||||
| chr22:38223209 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.983-1499G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38223209 | |||||||
| chr22:38223210 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.983-1500C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38223210 | |||||||
| chr22:38223524 | G | C | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.982+1261C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38223524 | |||||||
| chr22:38223580 | A | G | 6 | a0001c0001t0001g0267 a0001c0001t0006g0081 a0001c0001t0006g0082 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.982+1205T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38223580 | |||||||
| chr22:38223809 | C | A | 1 | a0001c0001t0002g0061 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.982+976G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38223809 | |||||||
| chr22:38223986 | C | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0113 |
2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.982+799G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38223986 | |||||||
| chr22:38224002 | T | G | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.982+783A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224002 | |||||||
| chr22:38224050 | G | A | 100 | a0001c0001t0001g0178 a0001c0001t0001g0283 a0001c0001t0001g0296 others(97): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.982+735C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224050 | |||||||
| chr22:38224117 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0114 |
2 | NA18979.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.982+668G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224117 | |||||||
| chr22:38224125 | C | CT | 27 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(24): Show |
32 | HG00673.hp1 HG00741.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.982+659dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224125 | |||||||
| chr22:38224169 | G | A | 3 | a0001c0002t0003g0215 a0001c0002t0003g0217 a0001c0002t0003g0274 |
3 | HG03834.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.982+616C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224169 | |||||||
| chr22:38224172 | A | G | 3 | a0001c0002t0003g0215 a0001c0002t0003g0217 a0001c0002t0003g0274 |
3 | HG03834.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.982+613T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224172 | |||||||
| chr22:38224248 | C | G | 3 | a0001c0004t0011g0190 a0001c0004t0011g0279 a0001c0004t0017g0026 |
3 | HG00639.hp2 HG03669.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.982+537G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224248 | |||||||
| chr22:38224263 | C | T | 25 | a0001c0001t0001g0188 a0001c0001t0001g0267 a0001c0001t0001g0310 others(22): Show |
26 | HG01109.hp2 HG01243.hp1 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.982+522G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224263 | |||||||
| chr22:38224328 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.982+457T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224328 | |||||||
| chr22:38224389 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.982+396A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224389 | |||||||
| chr22:38224403 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.982+382G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224403 | |||||||
| chr22:38224405 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.982+380A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224405 | |||||||
| chr22:38224410 | G | A | 14 | a0001c0001t0001g0267 a0001c0001t0004g0117 a0001c0001t0004g0118 others(11): Show |
14 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.982+375C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224410 | |||||||
| chr22:38224519 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.982+266T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224519 | |||||||
| chr22:38224643 | T | C | 1 | a0001c0003t0018g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.982+142A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224643 | |||||||
| chr22:38224661 | T | C | 4 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0184 others(1): Show |
4 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+124A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224661 | |||||||
| chr22:38224695 | C | G | 22 | a0001c0001t0001g0036 a0001c0001t0001g0269 a0001c0001t0016g0025 others(19): Show |
25 | HG00639.hp1 HG00639.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.982+90G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224695 | |||||||
| chr22:38224737 | G | A | 1 | a0001c0001t0009g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.982+48C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224737 | |||||||
| chr22:38224742 | C | T | 1 | a0001c0001t0003g0182 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.982+43G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 8/8 | chr22 | 38224742 | |||||||
| chr22:38224996 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0167 a0001c0001t0001g0168 others(6): Show |
11 | HG01433.hp2 HG02080.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.788-17C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 7/8 | chr22 | 38224996 | |||||||
| chr22:38225034 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.788-55G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 7/8 | chr22 | 38225034 | |||||||
| chr22:38225142 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.788-163C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 7/8 | chr22 | 38225142 | |||||||
| chr22:38225230 | G | C | 17 | a0001c0002t0003g0014 a0001c0002t0003g0023 a0001c0002t0003g0076 others(14): Show |
19 | HG00639.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.787+194C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 7/8 | chr22 | 38225230 | |||||||
| chr22:38225602 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.618-9G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38225602 | |||||||
| chr22:38225809 | C | T | 1 | a0001c0001t0002g0258 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.618-216G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38225809 | |||||||
| chr22:38225919 | G | A | 1 | a0001c0005t0002g0148 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.618-326C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38225919 | |||||||
| chr22:38225965 | C | T | 2 | a0001c0007t0001g0311 a0001c0007t0001g0312 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.618-372G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38225965 | |||||||
| chr22:38225978 | CT | C | 8 | a0001c0001t0001g0310 a0001c0001t0003g0018 a0001c0001t0003g0096 others(5): Show |
9 | HG01433.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.618-386delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38225978 | |||||||
| chr22:38226010 | GCT | G | 29 | a0001c0001t0001g0267 a0001c0001t0001g0310 a0001c0001t0003g0018 others(26): Show |
31 | HG01099.hp2 HG01109.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.618-419_618-418del others(2): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226010 | |||||||
| chr22:38226040 | C | T | 1 | a0001c0004t0008g0181 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.618-447G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226040 | |||||||
| chr22:38226076 | C | CT | 20 | a0001c0001t0001g0126 a0001c0001t0001g0267 a0001c0001t0002g0067 others(17): Show |
21 | HG01099.hp2 HG01109.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.618-484dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226076 | |||||||
| chr22:38226076 | C | CTT | 10 | a0001c0001t0001g0310 a0001c0001t0003g0018 a0001c0001t0003g0096 others(7): Show |
11 | HG01433.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.618-485_618-484dup others(2): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226076 | |||||||
| chr22:38226076 | CT | C | 10 | a0001c0001t0001g0036 a0001c0001t0001g0159 a0001c0001t0001g0233 others(7): Show |
10 | HG01070.hp2 HG01167.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.618-484delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226076 | |||||||
| chr22:38226122 | C | G | 3 | a0001c0002t0003g0215 a0001c0002t0003g0217 a0001c0002t0003g0274 |
3 | HG03834.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.618-529G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226122 | |||||||
| chr22:38226205 | G | A | 7 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(4): Show |
8 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+574C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226205 | |||||||
| chr22:38226236 | C | T | 1 | a0001c0003t0018g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.617+543G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226236 | |||||||
| chr22:38226241 | G | C | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.617+538C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226241 | |||||||
| chr22:38226330 | G | A | 4 | a0001c0001t0002g0295 a0001c0001t0004g0015 a0001c0001t0004g0165 others(1): Show |
5 | HG00733.hp2 HG01099.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+449C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226330 | |||||||
| chr22:38226417 | T | A | 5 | a0001c0006t0002g0052 a0001c0006t0002g0169 a0001c0006t0002g0206 others(2): Show |
5 | HG00558.hp1 HG02015.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+362A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226417 | |||||||
| chr22:38226513 | T | C | 53 | a0001c0001t0001g0267 a0001c0001t0001g0310 a0001c0001t0003g0018 others(50): Show |
59 | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.617+266A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226513 | |||||||
| chr22:38226580 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.617+199T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226580 | |||||||
| chr22:38226591 | C | A | 96 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0001t0001g0283 others(93): Show |
99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.617+188G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226591 | |||||||
| chr22:38226592 | G | A | 1 | a0001c0005t0001g0179 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.617+187C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226592 | |||||||
| chr22:38226603 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0016g0025 |
2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.617+176G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226603 | |||||||
| chr22:38226678 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.617+101A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226678 | |||||||
| chr22:38226769 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.617+10G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 6/8 | chr22 | 38226769 | |||||||
| chr22:38226898 | TGGA | T | 19 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(16): Show |
23 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.526-31_526-29delTC others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38226898 | |||||||
| chr22:38226902 | G | C | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.526-32C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38226902 | |||||||
| chr22:38226977 | T | C | 15 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(12): Show |
15 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.526-107A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38226977 | |||||||
| chr22:38226998 | A | AGGGATGG others(10): Show |
8 | a0001c0001t0001g0310 a0001c0001t0003g0018 a0001c0001t0003g0096 others(5): Show |
9 | HG01433.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-145_526-129dup others(17): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38226998 | |||||||
| chr22:38227012 | G | A | 1 | a0002c0010t0002g0196 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.526-142C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227012 | |||||||
| chr22:38227076 | G | A | 1 | a0001c0001t0031g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.526-206C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227076 | |||||||
| chr22:38227116 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.526-246G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227116 | |||||||
| chr22:38227120 | G | C | 1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.526-250C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227120 | |||||||
| chr22:38227136 | A | G | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.526-266T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227136 | |||||||
| chr22:38227254 | A | G | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-384T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227254 | |||||||
| chr22:38227268 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.526-398C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227268 | |||||||
| chr22:38227306 | G | A | 93 | a0001c0001t0001g0178 a0001c0001t0001g0204 a0001c0001t0001g0283 others(90): Show |
96 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.526-436C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227306 | |||||||
| chr22:38227318 | G | A | 1 | a0001c0001t0027g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.526-448C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227318 | |||||||
| chr22:38227348 | G | A | 1 | a0001c0002t0003g0308 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.526-478C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227348 | |||||||
| chr22:38227429 | C | T | 1 | a0001c0001t0021g0122 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.526-559G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227429 | |||||||
| chr22:38227479 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.526-609C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227479 | |||||||
| chr22:38227663 | T | C | 7 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(4): Show |
10 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.526-793A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227663 | |||||||
| chr22:38227708 | G | A | 44 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(41): Show |
51 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.526-838C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227708 | |||||||
| chr22:38227728 | C | T | 6 | a0001c0001t0001g0188 a0001c0001t0009g0193 a0001c0001t0009g0270 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-858G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227728 | |||||||
| chr22:38227744 | C | A | 14 | a0001c0002t0003g0014 a0001c0002t0003g0023 a0001c0002t0003g0076 others(11): Show |
16 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.526-874G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227744 | |||||||
| chr22:38227847 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.526-977G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227847 | |||||||
| chr22:38227864 | G | T | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.526-994C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227864 | |||||||
| chr22:38227878 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.526-1008C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227878 | |||||||
| chr22:38227927 | A | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0208 |
2 | NA18948.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.526-1057T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38227927 | |||||||
| chr22:38228084 | T | C | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526-1214A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228084 | |||||||
| chr22:38228085 | G | A | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526-1215C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228085 | |||||||
| chr22:38228222 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.526-1352T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228222 | |||||||
| chr22:38228348 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.526-1478C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228348 | |||||||
| chr22:38228376 | A | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-1506T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228376 | |||||||
| chr22:38228392 | G | A | 6 | a0001c0001t0001g0188 a0001c0001t0009g0193 a0001c0001t0009g0270 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.526-1522C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228392 | |||||||
| chr22:38228406 | A | AAGC | 161 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(158): Show |
172 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.526-1539_526-1537d others(5): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228406 | |||||||
| chr22:38228406 | AAGC | A | 11 | a0001c0001t0001g0273 a0001c0001t0001g0283 a0001c0001t0001g0296 others(8): Show |
12 | HG01069.hp2 HG01071.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-1539_526-1537d others(5): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228406 | |||||||
| chr22:38228432 | C | G | 1 | a0001c0001t0002g0260 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.526-1562G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228432 | |||||||
| chr22:38228549 | G | A | 1 | a0001c0006t0002g0206 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.526-1679C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228549 | |||||||
| chr22:38228702 | G | A | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.526-1832C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228702 | |||||||
| chr22:38228753 | C | T | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-1883G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228753 | |||||||
| chr22:38228781 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.525+1888G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228781 | |||||||
| chr22:38228914 | G | C | 17 | a0001c0002t0003g0014 a0001c0002t0003g0023 a0001c0002t0003g0076 others(14): Show |
19 | HG00639.hp2 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.525+1755C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38228914 | |||||||
| chr22:38229027 | A | C | 113 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(110): Show |
117 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.525+1642T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229027 | |||||||
| chr22:38229054 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.525+1615C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229054 | |||||||
| chr22:38229089 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.525+1580C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229089 | |||||||
| chr22:38229113 | C | G | 1 | a0001c0001t0001g0223 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.525+1556G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229113 | |||||||
| chr22:38229210 | C | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0252 |
3 | HG00597.hp2 HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.525+1459G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229210 | |||||||
| chr22:38229249 | C | T | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+1420G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229249 | |||||||
| chr22:38229309 | T | C | 3 | a0001c0002t0003g0023 a0001c0002t0003g0276 a0001c0002t0003g0277 |
4 | HG03239.hp1 HG03688.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.525+1360A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229309 | |||||||
| chr22:38229312 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0180 others(4): Show |
8 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.525+1357G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229312 | |||||||
| chr22:38229371 | C | T | 16 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(13): Show |
17 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.525+1298G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229371 | |||||||
| chr22:38229398 | A | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(312): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.525+1271T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229398 | |||||||
| chr22:38229474 | C | T | 7 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(4): Show |
10 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1195G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229474 | |||||||
| chr22:38229540 | C | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0123 a0001c0001t0002g0069 others(1): Show |
4 | HG02145.hp1 HG02647.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+1129G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229540 | |||||||
| chr22:38229551 | C | T | 7 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(4): Show |
10 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.525+1118G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229551 | |||||||
| chr22:38229589 | TCAGCCCA others(335): Show |
T | 1 | a0001c0001t0001g0135 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.525+738_525+1079de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229589 | |||||||
| chr22:38229608 | C | T | 5 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+1061G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229608 | |||||||
| chr22:38229609 | A | G | 7 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0009g0270 others(4): Show |
8 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+1060T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229609 | |||||||
| chr22:38229609 | AGCTGGAT others(107): Show |
A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0054 a0001c0001t0006g0084 |
3 | HG02615.hp2 NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.525+946_525+1059de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229609 | |||||||
| chr22:38229609 | AGCTGGAT others(164): Show |
A | 6 | a0001c0001t0001g0221 a0001c0001t0009g0193 a0001c0001t0026g0124 others(3): Show |
6 | HG00639.hp2 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+889_525+1059de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229609 | |||||||
| chr22:38229609 | AGCTGGAT others(221): Show |
A | 3 | a0001c0001t0003g0182 a0001c0001t0003g0183 a0001c0001t0003g0184 |
3 | HG02109.hp2 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.525+832_525+1059de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229609 | |||||||
| chr22:38229609 | AGCTGGAT others(620): Show |
A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0292 |
2 | HG00438.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.525+433_525+1059de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229609 | |||||||
| chr22:38229646 | T | C | 5 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+1023A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229646 | |||||||
| chr22:38229646 | TCAGCCCA others(50): Show |
T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(10): Show |
14 | HG01433.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.525+966_525+1022de others(58): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229646 | |||||||
| chr22:38229646 | TCAGCCCA others(278): Show |
T | 24 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(21): Show |
29 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.525+738_525+1022de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229646 | |||||||
| chr22:38229646 | TCAGCCCA others(392): Show |
T | 1 | a0001c0001t0003g0129 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.525+624_525+1022de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229646 | |||||||
| chr22:38229665 | T | C | 24 | a0001c0001t0001g0138 a0001c0001t0001g0172 a0001c0001t0001g0188 others(21): Show |
26 | HG00609.hp2 HG01099.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.525+1004A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229665 | |||||||
| chr22:38229665 | TGGCTGGA others(221): Show |
T | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.525+776_525+1003de others(1): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229665 | |||||||
| chr22:38229677 | CAAGGCTA others(279): Show |
C | 1 | a0001c0001t0001g0172 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.525+706_525+991del | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229677 | |||||||
| chr22:38229703 | C | T | 20 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(17): Show |
22 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.525+966G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229703 | |||||||
| chr22:38229703 | CCAGCCCA others(50): Show |
C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0140 |
3 | HG01070.hp1 HG01192.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.525+909_525+965del others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229703 | |||||||
| chr22:38229703 | CCAGCCCA others(107): Show |
C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0055 others(6): Show |
12 | HG02040.hp1 HG02055.hp1 NA18941.hp1 others(9): Show |
intron_variant | MODIFIER | c.525+852_525+965del | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229703 | |||||||
| chr22:38229723 | G | A | 6 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(3): Show |
9 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+946C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229723 | |||||||
| chr22:38229760 | T | C | 15 | a0001c0001t0001g0310 a0001c0002t0003g0014 a0001c0002t0003g0023 others(12): Show |
17 | HG01433.hp2 HG01884.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.525+909A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229760 | |||||||
| chr22:38229817 | T | C | 27 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0054 others(24): Show |
30 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.525+852A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229817 | |||||||
| chr22:38229817 | TCAGCCCA others(107): Show |
T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0204 a0001c0001t0001g0239 others(12): Show |
17 | HG00438.hp2 HG00642.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.525+738_525+851del | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229817 | |||||||
| chr22:38229874 | T | C | 3 | a0001c0001t0004g0117 a0001c0001t0006g0084 a0001c0005t0001g0179 |
3 | HG02615.hp2 HG02630.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.525+795A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229874 | |||||||
| chr22:38229874 | T | TCAGCCCA others(50): Show |
1 | a0001c0001t0001g0001 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.525+738_525+794dup others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229874 | |||||||
| chr22:38229874 | TCAGCCCA others(50): Show |
T | 1 | a0001c0001t0002g0199 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.525+738_525+794del others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229874 | |||||||
| chr22:38229931 | C | CCAGCCCA others(50): Show |
82 | a0001c0001t0001g0178 a0001c0001t0001g0283 a0001c0001t0001g0296 others(79): Show |
85 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.525+681_525+737dup others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229931 | |||||||
| chr22:38229931 | C | CCAGCCCA others(107): Show |
1 | a0001c0001t0002g0048 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.525+737_525+738ins others(114): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229931 | |||||||
| chr22:38229931 | C | CCAGCCCA others(335): Show |
3 | a0001c0001t0001g0036 a0001c0001t0002g0086 a0001c0001t0002g0087 |
3 | HG00544.hp1 HG02165.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.525+737_525+738ins others(342): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229931 | |||||||
| chr22:38229931 | C | T | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+738G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229931 | |||||||
| chr22:38229931 | CCAGCCCA others(50): Show |
C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0003g0102 |
4 | HG01891.hp1 HG01934.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+681_525+737del others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229931 | |||||||
| chr22:38229958 | TTGCCAAG others(221): Show |
T | 1 | a0001c0001t0002g0155 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.525+483_525+710del | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229958 | |||||||
| chr22:38229988 | T | C | 5 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(2): Show |
5 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+681A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229988 | |||||||
| chr22:38229988 | TCAGCCCA others(50): Show |
T | 9 | a0001c0001t0001g0120 a0001c0001t0001g0123 a0001c0001t0001g0180 others(6): Show |
9 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+624_525+680del others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38229988 | |||||||
| chr22:38230045 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.525+624G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230045 | |||||||
| chr22:38230045 | CCAGCCCA others(50): Show |
C | 7 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0006g0084 others(4): Show |
7 | HG01081.hp1 HG02615.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+567_525+623del others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230045 | |||||||
| chr22:38230072 | TTGCCAAG others(107): Show |
T | 1 | a0001c0001t0001g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.525+483_525+596del | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230072 | |||||||
| chr22:38230100 | G | GGCCAGCC others(221): Show |
1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.525+568_525+569ins others(228): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230100 | |||||||
| chr22:38230102 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0310 a0001c0001t0002g0086 others(4): Show |
7 | HG00544.hp1 HG01433.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+567A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230102 | |||||||
| chr22:38230102 | T | TCAGCCCA others(50): Show |
7 | a0001c0001t0004g0116 a0001c0001t0004g0117 a0001c0001t0004g0118 others(4): Show |
7 | HG02109.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+510_525+566dup others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230102 | |||||||
| chr22:38230102 | T | TCAGCCCA others(107): Show |
1 | a0001c0001t0001g0080 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.525+566_525+567ins others(114): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230102 | |||||||
| chr22:38230129 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.525+540A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230129 | |||||||
| chr22:38230129 | T | TTGCCAAG others(50): Show |
2 | a0001c0001t0001g0269 a0001c0001t0016g0025 |
2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.525+539_525+540ins others(57): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230129 | |||||||
| chr22:38230157 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0002g0216 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.525+512C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230157 | |||||||
| chr22:38230159 | C | CCAGCCCA others(107): Show |
1 | a0001c0001t0001g0020 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.525+509_525+510ins others(114): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230159 | |||||||
| chr22:38230159 | C | CCAGCCCA others(392): Show |
1 | a0001c0001t0001g0231 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.525+509_525+510ins others(399): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230159 | |||||||
| chr22:38230159 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0002g0216 a0001c0001t0022g0228 |
3 | HG01433.hp2 HG04115.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.525+510G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230159 | |||||||
| chr22:38230178 | C | CGGCTGGA others(164): Show |
6 | a0001c0001t0001g0267 a0001c0001t0006g0081 a0001c0001t0006g0082 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+490_525+491ins others(171): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230178 | |||||||
| chr22:38230178 | C | T | 8 | a0001c0001t0009g0193 a0001c0003t0005g0002 a0001c0003t0005g0070 others(5): Show |
11 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.525+491G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230178 | |||||||
| chr22:38230186 | C | T | 43 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(40): Show |
49 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.525+483G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230186 | |||||||
| chr22:38230224 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.525+445C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230224 | |||||||
| chr22:38230235 | C | T | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.525+434G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230235 | |||||||
| chr22:38230272 | A | G | 54 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
60 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.525+397T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230272 | |||||||
| chr22:38230550 | G | T | 45 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(42): Show |
54 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.525+119C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230550 | |||||||
| chr22:38230552 | C | G | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.525+117G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230552 | |||||||
| chr22:38230607 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.525+62C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 5/8 | chr22 | 38230607 | |||||||
| chr22:38230786 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.450-42T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 4/8 | chr22 | 38230786 | |||||||
| chr22:38230928 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.450-184C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 4/8 | chr22 | 38230928 | |||||||
| chr22:38231086 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.449+158C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 4/8 | chr22 | 38231086 | |||||||
| chr22:38231142 | C | T | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.449+102G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 4/8 | chr22 | 38231142 | |||||||
| chr22:38231423 | A | G | 5 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0239 others(2): Show |
5 | HG00735.hp1 HG01081.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.359-89T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38231423 | |||||||
| chr22:38231470 | T | C | 24 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(21): Show |
28 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.359-136A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38231470 | |||||||
| chr22:38231738 | C | T | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.359-404G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38231738 | |||||||
| chr22:38231884 | G | T | 14 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(11): Show |
15 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.359-550C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38231884 | |||||||
| chr22:38231899 | C | G | 1 | a0001c0001t0002g0257 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.359-565G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38231899 | |||||||
| chr22:38231978 | C | A | 6 | a0001c0001t0001g0267 a0001c0001t0006g0081 a0001c0001t0006g0082 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-644G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38231978 | |||||||
| chr22:38232138 | A | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(27): Show |
35 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.359-804T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232138 | |||||||
| chr22:38232162 | G | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-828C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232162 | |||||||
| chr22:38232242 | T | C | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.359-908A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232242 | |||||||
| chr22:38232254 | A | T | 2 | a0001c0001t0013g0109 a0001c0001t0029g0110 |
2 | HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.359-920T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232254 | |||||||
| chr22:38232266 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0006g0084 |
2 | HG01433.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.359-932G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232266 | |||||||
| chr22:38232300 | C | A | 206 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(203): Show |
223 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.359-966G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232300 | |||||||
| chr22:38232382 | T | G | 206 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(203): Show |
223 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.359-1048A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232382 | |||||||
| chr22:38232458 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.359-1124C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232458 | |||||||
| chr22:38232460 | G | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-1126C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232460 | |||||||
| chr22:38232578 | G | A | 100 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0051 others(97): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.359-1244C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232578 | |||||||
| chr22:38232637 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0160 |
3 | HG00323.hp2 HG01256.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.359-1303C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232637 | |||||||
| chr22:38232664 | C | T | 1 | a0001c0001t0027g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.359-1330G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232664 | |||||||
| chr22:38232668 | A | G | 1 | a0001c0001t0027g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.359-1334T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232668 | |||||||
| chr22:38232718 | G | T | 6 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(3): Show |
9 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.359-1384C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232718 | |||||||
| chr22:38232722 | T | C | 6 | a0001c0001t0001g0269 a0001c0001t0016g0025 a0001c0004t0008g0008 others(3): Show |
7 | HG00639.hp1 HG01243.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.359-1388A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232722 | |||||||
| chr22:38232733 | A | G | 115 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0047 others(112): Show |
118 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.359-1399T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232733 | |||||||
| chr22:38232853 | C | T | 2 | a0001c0001t0014g0095 a0001c0001t0026g0124 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.359-1519G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232853 | |||||||
| chr22:38232978 | A | G | 2 | a0001c0001t0014g0095 a0001c0001t0026g0124 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.359-1644T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38232978 | |||||||
| chr22:38233095 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-1761G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233095 | |||||||
| chr22:38233388 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.359-2054C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233388 | |||||||
| chr22:38233454 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.359-2120C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233454 | |||||||
| chr22:38233513 | T | C | 145 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(142): Show |
153 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.359-2179A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233513 | |||||||
| chr22:38233590 | C | G | 2 | a0001c0001t0002g0191 a0001c0001t0002g0208 |
2 | NA18948.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.359-2256G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233590 | |||||||
| chr22:38233597 | C | A | 1 | a0001c0001t0002g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.359-2263G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233597 | |||||||
| chr22:38233735 | C | T | 1 | a0001c0001t0013g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.359-2401G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233735 | |||||||
| chr22:38233747 | A | AT | 111 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0047 others(108): Show |
114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.359-2414dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233747 | |||||||
| chr22:38233760 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.359-2426C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233760 | |||||||
| chr22:38233801 | G | A | 5 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0155 others(2): Show |
5 | HG02083.hp1 NA18948.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-2467C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233801 | |||||||
| chr22:38233893 | T | C | 145 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(142): Show |
153 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.359-2559A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233893 | |||||||
| chr22:38233992 | C | T | 2 | a0001c0001t0014g0095 a0001c0001t0026g0124 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.359-2658G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38233992 | |||||||
| chr22:38234028 | C | CA | 142 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(139): Show |
150 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.359-2695dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234028 | |||||||
| chr22:38234069 | G | A | 3 | a0001c0004t0011g0190 a0001c0004t0011g0279 a0001c0004t0017g0026 |
3 | HG00639.hp2 HG03669.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.359-2735C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234069 | |||||||
| chr22:38234121 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.359-2787A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234121 | |||||||
| chr22:38234266 | T | C | 206 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(203): Show |
223 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.359-2932A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234266 | |||||||
| chr22:38234281 | C | T | 142 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(139): Show |
150 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.359-2947G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234281 | |||||||
| chr22:38234324 | C | T | 7 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(4): Show |
8 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-2990G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234324 | |||||||
| chr22:38234457 | C | A | 1 | a0001c0001t0002g0034 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.359-3123G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234457 | |||||||
| chr22:38234604 | CCTGGGAC others(3): Show |
C | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-3280_359-3271d others(12): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234604 | |||||||
| chr22:38234665 | A | C | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.359-3331T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234665 | |||||||
| chr22:38234760 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.359-3426G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234760 | |||||||
| chr22:38234776 | TTAAG | T | 3 | a0001c0001t0002g0155 a0001c0001t0002g0191 a0001c0001t0002g0208 |
3 | HG02083.hp1 NA18948.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.359-3446_359-3443d others(6): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234776 | |||||||
| chr22:38234780 | G | A | 1 | a0001c0001t0024g0303 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.359-3446C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234780 | |||||||
| chr22:38234941 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0113 |
2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.359-3607C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234941 | |||||||
| chr22:38234950 | G | A | 197 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(194): Show |
213 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.359-3616C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38234950 | |||||||
| chr22:38235095 | A | G | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.359-3761T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235095 | |||||||
| chr22:38235309 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.359-3975C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235309 | |||||||
| chr22:38235389 | G | C | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.359-4055C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235389 | |||||||
| chr22:38235514 | A | C | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.359-4180T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235514 | |||||||
| chr22:38235531 | C | G | 2 | a0001c0001t0003g0018 a0001c0001t0003g0162 |
3 | HG02258.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.359-4197G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235531 | |||||||
| chr22:38235585 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.359-4251A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235585 | |||||||
| chr22:38235662 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.359-4328G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235662 | |||||||
| chr22:38235673 | C | T | 22 | a0001c0001t0003g0096 a0001c0001t0003g0099 a0001c0001t0003g0182 others(19): Show |
24 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.359-4339G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235673 | |||||||
| chr22:38235762 | T | C | 206 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(203): Show |
223 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.359-4428A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235762 | |||||||
| chr22:38235826 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.359-4492C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235826 | |||||||
| chr22:38235842 | C | T | 24 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(21): Show |
27 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.359-4508G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235842 | |||||||
| chr22:38235843 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-4509C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235843 | |||||||
| chr22:38235872 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.359-4538A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235872 | |||||||
| chr22:38235899 | C | T | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.359-4565G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38235899 | |||||||
| chr22:38236198 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-4864C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38236198 | |||||||
| chr22:38236203 | A | C | 1 | a0001c0001t0001g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.359-4869T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38236203 | |||||||
| chr22:38236341 | G | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0162 |
3 | HG02258.hp2 HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.359-5007C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38236341 | |||||||
| chr22:38236466 | T | C | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.359-5132A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38236466 | |||||||
| chr22:38236476 | T | C | 1 | a0001c0001t0002g0260 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.359-5142A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38236476 | |||||||
| chr22:38236744 | C | T | 22 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(19): Show |
25 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.359-5410G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38236744 | |||||||
| chr22:38236782 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18945.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.359-5448C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38236782 | |||||||
| chr22:38237013 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.359-5679G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237013 | |||||||
| chr22:38237174 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.359-5840C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237174 | |||||||
| chr22:38237180 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.359-5846C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237180 | |||||||
| chr22:38237196 | C | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0197 a0001c0001t0001g0210 |
3 | HG01175.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.359-5862G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237196 | |||||||
| chr22:38237312 | G | A | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.359-5978C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237312 | |||||||
| chr22:38237320 | G | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(27): Show |
40 | HG00438.hp2 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.359-5986C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237320 | |||||||
| chr22:38237398 | T | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.359-6064A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237398 | |||||||
| chr22:38237414 | C | T | 7 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(4): Show |
8 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-6080G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237414 | |||||||
| chr22:38237419 | G | A | 111 | a0001c0001t0001g0017 a0001c0001t0001g0047 a0001c0001t0001g0051 others(108): Show |
114 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.359-6085C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237419 | |||||||
| chr22:38237639 | T | C | 3 | a0001c0004t0011g0190 a0001c0004t0011g0279 a0001c0004t0017g0026 |
3 | HG00639.hp2 HG03669.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.359-6305A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237639 | |||||||
| chr22:38237641 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.359-6307C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237641 | |||||||
| chr22:38237650 | G | A | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.359-6316C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237650 | |||||||
| chr22:38237653 | C | T | 10 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(7): Show |
12 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.359-6319G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237653 | |||||||
| chr22:38237660 | A | C | 205 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(202): Show |
222 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.359-6326T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237660 | |||||||
| chr22:38237704 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.359-6370G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237704 | |||||||
| chr22:38237741 | G | A | 9 | a0001c0001t0001g0075 a0001c0001t0001g0120 a0001c0001t0001g0123 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.359-6407C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237741 | |||||||
| chr22:38237801 | CT | C | 9 | a0001c0001t0001g0047 a0001c0001t0002g0058 a0001c0001t0002g0306 others(6): Show |
11 | HG00639.hp1 HG01516.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.359-6468delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237801 | |||||||
| chr22:38237818 | T | A | 19 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(16): Show |
22 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.359-6484A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237818 | |||||||
| chr22:38237818 | T | TA | 4 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0152 others(1): Show |
4 | HG02615.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-6485dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237818 | |||||||
| chr22:38237823 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.359-6489C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237823 | |||||||
| chr22:38237830 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-6496G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237830 | |||||||
| chr22:38237868 | G | A | 17 | a0001c0002t0003g0014 a0001c0002t0003g0023 a0001c0002t0003g0076 others(14): Show |
19 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.359-6534C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237868 | |||||||
| chr22:38237986 | G | C | 1 | a0001c0001t0002g0034 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.359-6652C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237986 | |||||||
| chr22:38237988 | T | C | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-6654A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38237988 | |||||||
| chr22:38238106 | C | T | 6 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-6772G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238106 | |||||||
| chr22:38238227 | CT | C | 8 | a0001c0001t0001g0161 a0001c0001t0001g0261 a0001c0001t0002g0037 others(5): Show |
8 | HG01070.hp2 HG01257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.359-6894delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238227 | |||||||
| chr22:38238260 | C | T | 188 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(185): Show |
203 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.359-6926G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238260 | |||||||
| chr22:38238261 | G | A | 2 | a0001c0001t0014g0095 a0001c0001t0026g0124 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.359-6927C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238261 | |||||||
| chr22:38238288 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-6954G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238288 | |||||||
| chr22:38238289 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.359-6955C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238289 | |||||||
| chr22:38238294 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0009g0193 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.359-6960G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238294 | |||||||
| chr22:38238328 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.359-6994G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238328 | |||||||
| chr22:38238376 | C | T | 2 | a0001c0001t0002g0090 a0001c0001t0002g0205 |
2 | NA18612.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.359-7042G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238376 | |||||||
| chr22:38238382 | C | T | 198 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(195): Show |
215 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.359-7048G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238382 | |||||||
| chr22:38238467 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.359-7133C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238467 | |||||||
| chr22:38238516 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.359-7182C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238516 | |||||||
| chr22:38238644 | T | C | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+7291A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238644 | |||||||
| chr22:38238897 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.358+7038A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238897 | |||||||
| chr22:38238956 | C | A | 1 | a0001c0001t0001g0302 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.358+6979G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38238956 | |||||||
| chr22:38239030 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+6905G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239030 | |||||||
| chr22:38239238 | T | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0138 a0001c0001t0001g0252 others(6): Show |
10 | HG00597.hp2 HG00621.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+6697A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239238 | |||||||
| chr22:38239305 | AG | A | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+6629delC | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239305 | |||||||
| chr22:38239353 | C | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(25): Show |
33 | HG00673.hp1 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.358+6582G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239353 | |||||||
| chr22:38239480 | T | C | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+6455A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239480 | |||||||
| chr22:38239487 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0009g0193 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.358+6448G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239487 | |||||||
| chr22:38239614 | C | T | 1 | a0001c0005t0001g0146 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.358+6321G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239614 | |||||||
| chr22:38239642 | C | T | 4 | a0001c0002t0003g0014 a0001c0002t0003g0076 a0001c0002t0003g0163 others(1): Show |
5 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.358+6293G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239642 | |||||||
| chr22:38239673 | C | T | 203 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(200): Show |
220 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.358+6262G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239673 | |||||||
| chr22:38239695 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.358+6240C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239695 | |||||||
| chr22:38239919 | T | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0125 others(10): Show |
15 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.358+6016A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239919 | |||||||
| chr22:38239926 | A | G | 3 | a0001c0004t0011g0190 a0001c0004t0011g0279 a0001c0004t0017g0026 |
3 | HG00639.hp2 HG03669.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.358+6009T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239926 | |||||||
| chr22:38239942 | A | AT | 6 | a0001c0001t0002g0037 a0001c0001t0002g0211 a0001c0002t0003g0163 others(3): Show |
6 | HG02055.hp2 NA18946.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+5992dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38239942 | |||||||
| chr22:38240123 | C | G | 2 | a0001c0001t0009g0270 a0001c0001t0009g0271 |
2 | HG01243.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.358+5812G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240123 | |||||||
| chr22:38240177 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.358+5758C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240177 | |||||||
| chr22:38240206 | T | A | 1 | a0001c0001t0013g0097 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.358+5729A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240206 | |||||||
| chr22:38240277 | C | T | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.358+5658G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240277 | |||||||
| chr22:38240390 | A | G | 10 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(7): Show |
12 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.358+5545T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240390 | |||||||
| chr22:38240722 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0188 a0001c0001t0009g0270 others(4): Show |
8 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.358+5213C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240722 | |||||||
| chr22:38240730 | G | GCA | 6 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+5204_358+5205i others(4): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240730 | |||||||
| chr22:38240731 | G | A | 6 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+5204C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240731 | |||||||
| chr22:38240732 | C | A | 6 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+5203G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240732 | |||||||
| chr22:38240732 | C | CA | 24 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0104 others(21): Show |
24 | HG00544.hp1 HG00544.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.358+5202dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240732 | |||||||
| chr22:38240732 | CA | C | 32 | a0001c0001t0001g0051 a0001c0001t0001g0105 a0001c0001t0001g0123 others(29): Show |
38 | HG00621.hp1 HG00642.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.358+5202delT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240732 | |||||||
| chr22:38240732 | CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0017g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.358+5192_358+5202d others(13): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240732 | |||||||
| chr22:38240732 | CAAAAAAA others(5): Show |
C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(27): Show |
35 | HG00673.hp1 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.358+5191_358+5202d others(14): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240732 | |||||||
| chr22:38240781 | AG | A | 6 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(3): Show |
6 | HG01243.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+5153delC | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240781 | |||||||
| chr22:38240789 | G | A | 41 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(38): Show |
48 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.358+5146C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38240789 | |||||||
| chr22:38241128 | A | T | 2 | a0001c0001t0009g0270 a0001c0001t0009g0271 |
2 | HG01243.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.358+4807T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241128 | |||||||
| chr22:38241163 | G | A | 2 | a0001c0007t0001g0311 a0001c0007t0001g0312 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.358+4772C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241163 | |||||||
| chr22:38241524 | C | CA | 23 | a0001c0001t0001g0126 a0001c0001t0001g0141 a0001c0001t0001g0151 others(20): Show |
25 | HG00639.hp2 HG00673.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.358+4410dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241524 | |||||||
| chr22:38241524 | CA | C | 121 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0054 others(118): Show |
126 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.358+4410delT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241524 | |||||||
| chr22:38241524 | CAA | C | 9 | a0001c0001t0001g0055 a0001c0001t0001g0283 a0001c0001t0001g0296 others(6): Show |
10 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+4409_358+4410d others(4): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241524 | |||||||
| chr22:38241576 | TCTGTCAG others(7): Show |
T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+4345_358+4358d others(16): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241576 | |||||||
| chr22:38241670 | A | G | 207 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
224 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.358+4265T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241670 | |||||||
| chr22:38241759 | C | CT | 7 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(4): Show |
10 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+4175dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241759 | |||||||
| chr22:38241802 | T | C | 175 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0047 others(172): Show |
186 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.358+4133A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241802 | |||||||
| chr22:38241836 | G | A | 207 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
224 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.358+4099C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241836 | |||||||
| chr22:38241879 | G | A | 2 | a0001c0001t0002g0191 a0001c0001t0002g0208 |
2 | NA18948.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.358+4056C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241879 | |||||||
| chr22:38241883 | C | CA | 20 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0083 others(17): Show |
21 | HG01891.hp2 HG01934.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.358+4051dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAA | 15 | a0001c0001t0001g0188 a0001c0001t0003g0018 a0001c0001t0003g0096 others(12): Show |
17 | HG01099.hp2 HG01243.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.358+4050_358+4051d others(4): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAA | 6 | a0001c0001t0001g0269 a0001c0001t0016g0025 a0001c0003t0005g0002 others(3): Show |
9 | HG01243.hp2 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.358+4047_358+4051d others(7): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAA | 6 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0027g0186 others(3): Show |
6 | HG01109.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+4046_358+4051d others(8): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA | 11 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(8): Show |
11 | HG01109.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+4045_358+4051d others(9): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0002g0045 a0001c0001t0002g0185 a0001c0001t0015g0313 |
3 | HG02717.hp2 HG03516.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.358+4042_358+4051d others(12): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(4): Show |
16 | a0001c0001t0001g0047 a0001c0001t0001g0283 a0001c0001t0002g0032 others(13): Show |
17 | HG00438.hp1 HG01255.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.358+4041_358+4051d others(13): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(5): Show |
40 | a0001c0001t0001g0055 a0001c0001t0001g0178 a0001c0001t0001g0296 others(37): Show |
42 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.358+4040_358+4051d others(14): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(6): Show |
28 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0197 others(25): Show |
28 | HG00544.hp2 HG00642.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.358+4039_358+4051d others(15): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(7): Show |
10 | a0001c0001t0001g0054 a0001c0001t0001g0156 a0001c0001t0002g0037 others(7): Show |
10 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.358+4038_358+4051d others(16): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0060 a0001c0001t0002g0154 |
2 | HG00597.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.358+4037_358+4051d others(17): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0094 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.358+4036_358+4051d others(18): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0002g0216 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.358+4051_358+4052i others(38): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | CA | C | 20 | a0001c0001t0001g0127 a0001c0001t0001g0168 a0001c0001t0001g0175 others(17): Show |
23 | HG01169.hp1 HG01884.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.358+4051delT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241883 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0006g0081 a0001c0001t0006g0082 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.358+4042_358+4051d others(12): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241883 | |||||||
| chr22:38241897 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0002g0177 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.358+4037_358+4038i others(15): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241897 | |||||||
| chr22:38241942 | T | C | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+3993A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38241942 | |||||||
| chr22:38242012 | A | AT | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(310): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
intron_variant | MODIFIER | c.358+3922dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242012 | |||||||
| chr22:38242065 | C | T | 128 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0051 others(125): Show |
134 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.358+3870G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242065 | |||||||
| chr22:38242215 | C | A | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+3720G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242215 | |||||||
| chr22:38242220 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0010g0299 |
2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.358+3715G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242220 | |||||||
| chr22:38242228 | G | A | 128 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0051 others(125): Show |
134 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.358+3707C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242228 | |||||||
| chr22:38242243 | G | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+3692C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242243 | |||||||
| chr22:38242286 | G | A | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+3649C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242286 | |||||||
| chr22:38242296 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.358+3639G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242296 | |||||||
| chr22:38242312 | C | CA | 12 | a0001c0001t0001g0055 a0001c0001t0001g0075 a0001c0001t0001g0104 others(9): Show |
13 | HG00639.hp1 HG00639.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+3622dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242312 | |||||||
| chr22:38242431 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.358+3504A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242431 | |||||||
| chr22:38242591 | T | C | 163 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0051 others(160): Show |
173 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.358+3344A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242591 | |||||||
| chr22:38242607 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+3328G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242607 | |||||||
| chr22:38242655 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0016g0025 |
2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.358+3280C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242655 | |||||||
| chr22:38242661 | C | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+3274G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242661 | |||||||
| chr22:38242891 | G | A | 100 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0051 others(97): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.358+3044C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242891 | |||||||
| chr22:38242989 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+2946C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38242989 | |||||||
| chr22:38243048 | C | CA | 51 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0075 others(48): Show |
54 | HG01243.hp1 HG01346.hp1 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.358+2886dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243048 | |||||||
| chr22:38243048 | C | CAA | 129 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0051 others(126): Show |
137 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.358+2885_358+2886d others(4): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243048 | |||||||
| chr22:38243084 | G | A | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+2851C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243084 | |||||||
| chr22:38243151 | G | A | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+2784C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243151 | |||||||
| chr22:38243158 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+2777C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243158 | |||||||
| chr22:38243308 | C | T | 124 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0051 others(121): Show |
130 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.358+2627G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243308 | |||||||
| chr22:38243587 | C | G | 1 | a0001c0001t0007g0316 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.358+2348G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243587 | |||||||
| chr22:38243614 | T | G | 2 | a0001c0001t0001g0298 a0001c0001t0010g0299 |
2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.358+2321A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243614 | |||||||
| chr22:38243694 | C | T | 1 | a0001c0002t0003g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.358+2241G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243694 | |||||||
| chr22:38243729 | G | A | 22 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(19): Show |
25 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.358+2206C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243729 | |||||||
| chr22:38243744 | G | A | 7 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(4): Show |
10 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.358+2191C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243744 | |||||||
| chr22:38243918 | T | C | 1 | a0001c0001t0003g0129 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.358+2017A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243918 | |||||||
| chr22:38243923 | G | A | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.358+2012C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243923 | |||||||
| chr22:38243995 | G | A | 10 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(7): Show |
12 | HG01099.hp2 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.358+1940C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38243995 | |||||||
| chr22:38244199 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+1736G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244199 | |||||||
| chr22:38244306 | A | G | 207 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(204): Show |
224 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.358+1629T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244306 | |||||||
| chr22:38244437 | A | G | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+1498T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244437 | |||||||
| chr22:38244455 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.358+1480C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244455 | |||||||
| chr22:38244520 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.358+1415C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244520 | |||||||
| chr22:38244526 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.358+1409T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244526 | |||||||
| chr22:38244617 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+1318G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244617 | |||||||
| chr22:38244736 | G | A | 1 | a0001c0001t0022g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.358+1199C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244736 | |||||||
| chr22:38244815 | C | A | 6 | a0001c0001t0001g0267 a0001c0001t0006g0081 a0001c0001t0006g0082 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+1120G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244815 | |||||||
| chr22:38244824 | T | C | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+1111A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244824 | |||||||
| chr22:38244835 | A | G | 208 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(205): Show |
226 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.358+1100T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244835 | |||||||
| chr22:38244854 | G | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0001g0227 |
4 | HG02145.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358+1081C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244854 | |||||||
| chr22:38244979 | G | T | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+956C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38244979 | |||||||
| chr22:38245017 | G | C | 1 | a0001c0002t0003g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.358+918C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245017 | |||||||
| chr22:38245034 | C | A | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358+901G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245034 | |||||||
| chr22:38245059 | C | G | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+876G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245059 | |||||||
| chr22:38245187 | G | A | 1 | a0001c0001t0025g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.358+748C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245187 | |||||||
| chr22:38245257 | CCCTGCCT others(115): Show |
C | 3 | a0001c0001t0001g0134 a0001c0001t0002g0133 a0001c0001t0028g0088 |
3 | HG00733.hp1 HG01346.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.358+556_358+677del | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245257 | |||||||
| chr22:38245270 | G | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+665C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245270 | |||||||
| chr22:38245276 | A | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+659T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245276 | |||||||
| chr22:38245378 | T | C | 1 | a0001c0003t0018g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.358+557A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245378 | |||||||
| chr22:38245401 | G | GAGAAGCG others(54): Show |
1 | a0001c0001t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.358+473_358+533dup others(61): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245401 | |||||||
| chr22:38245401 | GAGAAGCG others(54): Show |
G | 1 | a0001c0001t0001g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.358+473_358+533del others(61): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245401 | |||||||
| chr22:38245426 | C | T | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+509G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245426 | |||||||
| chr22:38245478 | G | C | 1 | a0001c0001t0004g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.358+457C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245478 | |||||||
| chr22:38245506 | T | C | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.358+429A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245506 | |||||||
| chr22:38245540 | GGGAGGGC others(54): Show |
G | 2 | a0001c0001t0007g0316 a0001c0001t0012g0019 |
3 | HG01981.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.358+334_358+394del others(61): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245540 | |||||||
| chr22:38245547 | CCCTTGCT others(115): Show |
C | 1 | a0001c0004t0011g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.358+266_358+387del | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245547 | |||||||
| chr22:38245608 | CCCTTGCT others(54): Show |
C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(27): Show |
35 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.358+266_358+326del others(61): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245608 | |||||||
| chr22:38245701 | G | A | 7 | a0001c0001t0004g0116 a0001c0001t0004g0117 a0001c0001t0004g0118 others(4): Show |
7 | HG02109.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.358+234C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245701 | |||||||
| chr22:38245891 | C | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+44G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245891 | |||||||
| chr22:38245892 | C | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+43G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 3/8 | chr22 | 38245892 | |||||||
| chr22:38246116 | T | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0123 |
2 | HG02145.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.193-16A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38246116 | |||||||
| chr22:38246248 | G | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-148C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38246248 | |||||||
| chr22:38246337 | T | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(127): Show |
137 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.193-237A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38246337 | |||||||
| chr22:38246376 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0238 |
2 | HG01081.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.193-276G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38246376 | |||||||
| chr22:38246488 | A | G | 172 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0040 others(169): Show |
184 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.193-388T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38246488 | |||||||
| chr22:38246611 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.193-511G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38246611 | |||||||
| chr22:38247033 | G | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0161 |
2 | NA18945.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.192+737C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247033 | |||||||
| chr22:38247034 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.192+736C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247034 | |||||||
| chr22:38247069 | T | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.192+701A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247069 | |||||||
| chr22:38247164 | G | C | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+606C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247164 | |||||||
| chr22:38247179 | C | A | 1 | a0001c0001t0002g0295 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.192+591G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247179 | |||||||
| chr22:38247311 | G | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(25): Show |
33 | HG00673.hp1 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.192+459C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247311 | |||||||
| chr22:38247335 | G | T | 1 | a0001c0001t0001g0006 | 2 | NA19009.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.192+435C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247335 | |||||||
| chr22:38247411 | C | T | 1 | a0001c0001t0001g0010 | 2 | NA18964.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.192+359G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247411 | |||||||
| chr22:38247414 | C | T | 31 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(28): Show |
36 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.192+356G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247414 | |||||||
| chr22:38247428 | C | T | 22 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(19): Show |
25 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.192+342G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247428 | |||||||
| chr22:38247611 | A | G | 1 | a0001c0001t0022g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192+159T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 2/8 | chr22 | 38247611 | |||||||
| chr22:38248157 | C | T | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58-138G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248157 | |||||||
| chr22:38248186 | C | G | 8 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58-167G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248186 | |||||||
| chr22:38248189 | T | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(100): Show |
106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-58-170A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248189 | |||||||
| chr22:38248204 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-58-185G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248204 | |||||||
| chr22:38248321 | A | C | 6 | a0001c0001t0001g0267 a0001c0001t0006g0081 a0001c0001t0006g0082 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58-302T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248321 | |||||||
| chr22:38248511 | C | G | 2 | a0001c0007t0001g0311 a0001c0007t0001g0312 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-58-492G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248511 | |||||||
| chr22:38248596 | T | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0161 |
2 | NA18945.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-58-577A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248596 | |||||||
| chr22:38248640 | C | A | 1 | a0001c0001t0004g0165 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-58-621G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248640 | |||||||
| chr22:38248645 | C | A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0310 a0001c0001t0012g0019 others(4): Show |
8 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-626G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248645 | |||||||
| chr22:38248664 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0016g0025 |
2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-58-645A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248664 | |||||||
| chr22:38248708 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0034 |
3 | NA18612.hp2 NA18993.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-58-689C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248708 | |||||||
| chr22:38248766 | G | A | 1 | a0001c0002t0003g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-58-747C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248766 | |||||||
| chr22:38248829 | G | A | 1 | a0001c0001t0002g0291 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-58-810C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248829 | |||||||
| chr22:38248894 | C | T | 22 | a0001c0001t0001g0267 a0001c0001t0004g0117 a0001c0001t0004g0118 others(19): Show |
26 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-58-875G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38248894 | |||||||
| chr22:38249049 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-58-1030G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249049 | |||||||
| chr22:38249050 | G | A | 29 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0310 others(26): Show |
33 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-58-1031C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249050 | |||||||
| chr22:38249051 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-1032G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249051 | |||||||
| chr22:38249063 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-58-1044G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249063 | |||||||
| chr22:38249218 | C | T | 6 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(3): Show |
9 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58-1199G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249218 | |||||||
| chr22:38249428 | G | C | 1 | a0001c0001t0002g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-58-1409C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249428 | |||||||
| chr22:38249484 | C | T | 8 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58-1465G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249484 | |||||||
| chr22:38249714 | C | T | 6 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0200 others(3): Show |
6 | HG00735.hp2 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58-1695G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249714 | |||||||
| chr22:38249744 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-58-1725T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249744 | |||||||
| chr22:38249762 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-58-1743G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249762 | |||||||
| chr22:38249890 | T | G | 30 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0310 others(27): Show |
34 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58-1871A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249890 | |||||||
| chr22:38249969 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-58-1950G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38249969 | |||||||
| chr22:38250011 | T | A | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58-1992A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250011 | |||||||
| chr22:38250045 | C | A | 1 | a0001c0001t0002g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-58-2026G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250045 | |||||||
| chr22:38250057 | G | A | 208 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(205): Show |
226 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.-58-2038C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250057 | |||||||
| chr22:38250174 | G | C | 2 | a0001c0001t0002g0257 a0001c0001t0002g0258 |
2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-58-2155C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250174 | |||||||
| chr22:38250178 | C | T | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-58-2159G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250178 | |||||||
| chr22:38250196 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-58-2177G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250196 | |||||||
| chr22:38250199 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0014g0095 |
2 | HG01433.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-58-2180G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250199 | |||||||
| chr22:38250254 | G | A | 1 | a0001c0001t0002g0260 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-58-2235C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250254 | |||||||
| chr22:38250350 | C | A | 2 | a0001c0001t0006g0081 a0001c0001t0006g0082 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-58-2331G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250350 | |||||||
| chr22:38250379 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-58-2360C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250379 | |||||||
| chr22:38250411 | G | T | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-58-2392C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250411 | |||||||
| chr22:38250454 | C | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(96): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-58-2435G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250454 | |||||||
| chr22:38250588 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-58-2569A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250588 | |||||||
| chr22:38250734 | T | TG | 7 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(4): Show |
8 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-2716dupC | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250734 | |||||||
| chr22:38250770 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-58-2751C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250770 | |||||||
| chr22:38250822 | A | G | 30 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0310 others(27): Show |
34 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58-2803T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250822 | |||||||
| chr22:38250842 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-58-2823C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250842 | |||||||
| chr22:38250894 | G | A | 30 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0310 others(27): Show |
34 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58-2875C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250894 | |||||||
| chr22:38250957 | C | G | 20 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0210 others(17): Show |
20 | HG00558.hp1 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-58-2938G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38250957 | |||||||
| chr22:38251136 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(9): Show |
13 | HG01891.hp1 HG01891.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.-58-3117G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251136 | |||||||
| chr22:38251188 | A | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-3169T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251188 | |||||||
| chr22:38251209 | C | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(27): Show |
35 | HG00673.hp1 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-58-3190G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251209 | |||||||
| chr22:38251352 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-58-3333C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251352 | |||||||
| chr22:38251400 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-3381C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251400 | |||||||
| chr22:38251449 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-58-3430C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251449 | |||||||
| chr22:38251633 | A | G | 208 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(205): Show |
226 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.-58-3614T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251633 | |||||||
| chr22:38251707 | G | A | 27 | a0001c0001t0001g0267 a0001c0001t0001g0310 a0001c0001t0004g0116 others(24): Show |
31 | HG01109.hp1 HG01109.hp2 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.-58-3688C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251707 | |||||||
| chr22:38251776 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-58-3757G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251776 | |||||||
| chr22:38251896 | G | GT | 59 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0017 others(56): Show |
67 | HG00639.hp2 HG00673.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.-58-3878dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251896 | |||||||
| chr22:38251896 | G | GTTT | 22 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0118 others(19): Show |
25 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-58-3880_-58-3878d others(5): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251896 | |||||||
| chr22:38251896 | G | GTTTT | 7 | a0001c0001t0001g0269 a0001c0001t0001g0310 a0001c0001t0004g0117 others(4): Show |
8 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-3881_-58-3878d others(6): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251896 | |||||||
| chr22:38251896 | GT | G | 12 | a0001c0001t0001g0020 a0001c0001t0001g0091 a0001c0001t0001g0175 others(9): Show |
14 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.-58-3878delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251896 | |||||||
| chr22:38251995 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0273 |
2 | HG06807.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-58-3976C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38251995 | |||||||
| chr22:38252003 | CTCCCACC others(4): Show |
C | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-58-3995_-58-3985d others(13): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252003 | |||||||
| chr22:38252052 | T | G | 30 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0310 others(27): Show |
34 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58-4033A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252052 | |||||||
| chr22:38252062 | A | AT | 35 | a0001c0001t0001g0017 a0001c0001t0001g0111 a0001c0001t0001g0267 others(32): Show |
40 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.-58-4044dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252062 | |||||||
| chr22:38252103 | A | C | 4 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0008g0181 others(1): Show |
5 | HG00639.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58-4084T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252103 | |||||||
| chr22:38252113 | G | A | 30 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0310 others(27): Show |
34 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58-4094C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252113 | |||||||
| chr22:38252155 | G | T | 3 | a0001c0001t0001g0269 a0001c0001t0016g0025 a0001c0001t0022g0228 |
3 | HG01243.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-58-4136C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252155 | |||||||
| chr22:38252289 | G | A | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-58-4270C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252289 | |||||||
| chr22:38252592 | GT | G | 8 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58-4574delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252592 | |||||||
| chr22:38252706 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0060 |
2 | HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.-58-4687G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252706 | |||||||
| chr22:38252743 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-58-4724T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252743 | |||||||
| chr22:38252768 | C | G | 1 | a0001c0001t0001g0013 | 2 | NA18964.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-58-4749G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252768 | |||||||
| chr22:38252836 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-58-4817T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252836 | |||||||
| chr22:38252869 | A | G | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-4850T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252869 | |||||||
| chr22:38252955 | ACATGGTG others(6): Show |
A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0310 a0001c0001t0012g0019 others(4): Show |
8 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-4949_-58-4937d others(15): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252955 | |||||||
| chr22:38252957 | A | G | 1 | a0001c0001t0027g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-58-4938T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38252957 | |||||||
| chr22:38253071 | G | A | 1 | a0001c0001t0002g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-58-5052C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253071 | |||||||
| chr22:38253091 | G | A | 1 | a0001c0001t0009g0271 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-58-5072C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253091 | |||||||
| chr22:38253097 | G | A | 7 | a0001c0001t0001g0269 a0001c0001t0001g0310 a0001c0001t0012g0019 others(4): Show |
8 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-5078C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253097 | |||||||
| chr22:38253136 | A | C | 129 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(126): Show |
136 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-58-5117T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253136 | |||||||
| chr22:38253137 | G | A | 8 | a0001c0001t0001g0269 a0001c0001t0001g0310 a0001c0001t0006g0084 others(5): Show |
9 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-58-5118C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253137 | |||||||
| chr22:38253147 | C | T | 129 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(126): Show |
136 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.-58-5128G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253147 | |||||||
| chr22:38253184 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0014g0095 |
2 | HG01433.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-58-5165G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253184 | |||||||
| chr22:38253196 | C | A | 4 | a0001c0002t0003g0014 a0001c0002t0003g0076 a0001c0002t0003g0163 others(1): Show |
5 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58-5177G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253196 | |||||||
| chr22:38253368 | G | A | 30 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0310 others(27): Show |
34 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.-58-5349C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253368 | |||||||
| chr22:38253390 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-58-5371G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253390 | |||||||
| chr22:38253497 | G | C | 15 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(12): Show |
15 | HG01109.hp2 HG02109.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-58-5478C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253497 | |||||||
| chr22:38253508 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-58-5489A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253508 | |||||||
| chr22:38253550 | A | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0260 |
3 | HG01069.hp1 HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.-58-5531T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253550 | |||||||
| chr22:38253582 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-58-5563T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253582 | |||||||
| chr22:38253626 | T | C | 3 | a0001c0001t0001g0269 a0001c0001t0016g0025 a0001c0001t0022g0228 |
3 | HG01243.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-58-5607A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253626 | |||||||
| chr22:38253777 | C | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(96): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-58-5758G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253777 | |||||||
| chr22:38253805 | A | C | 11 | a0001c0001t0003g0018 a0001c0001t0003g0096 a0001c0001t0003g0099 others(8): Show |
13 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-58-5786T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253805 | |||||||
| chr22:38253928 | C | G | 22 | a0001c0001t0001g0267 a0001c0001t0004g0116 a0001c0001t0004g0117 others(19): Show |
25 | HG01109.hp1 HG01109.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-58-5909G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38253928 | |||||||
| chr22:38254158 | G | T | 1 | a0001c0001t0002g0272 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-58-6139C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254158 | |||||||
| chr22:38254204 | C | CA | 14 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0077 others(11): Show |
16 | HG00673.hp1 HG01169.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.-58-6186dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254204 | |||||||
| chr22:38254204 | C | CAAA | 82 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(79): Show |
85 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-58-6188_-58-6186d others(5): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254204 | |||||||
| chr22:38254204 | C | CAAAA | 14 | a0001c0001t0001g0296 a0001c0001t0002g0037 a0001c0001t0002g0058 others(11): Show |
14 | HG00558.hp1 HG00733.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.-58-6189_-58-6186d others(6): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254204 | |||||||
| chr22:38254204 | CA | C | 18 | a0001c0001t0001g0130 a0001c0001t0001g0269 a0001c0001t0001g0310 others(15): Show |
20 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-58-6186delT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254204 | |||||||
| chr22:38254232 | A | T | 1 | a0001c0001t0001g0126 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-58-6213T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254232 | |||||||
| chr22:38254291 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-58-6272C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254291 | |||||||
| chr22:38254323 | G | C | 2 | a0001c0007t0001g0311 a0001c0007t0001g0312 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-58-6304C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254323 | |||||||
| chr22:38254325 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-58-6306G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254325 | |||||||
| chr22:38254340 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-6321G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254340 | |||||||
| chr22:38254482 | C | T | 28 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0022 others(25): Show |
33 | HG00673.hp1 HG00741.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.-58-6463G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254482 | |||||||
| chr22:38254507 | G | A | 11 | a0001c0001t0001g0017 a0001c0001t0001g0075 a0001c0001t0001g0120 others(8): Show |
12 | HG01891.hp2 HG01934.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-58-6488C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254507 | |||||||
| chr22:38254638 | A | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(96): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-58-6619T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254638 | |||||||
| chr22:38254659 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-58-6640C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254659 | |||||||
| chr22:38254725 | C | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(96): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-58-6706G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254725 | |||||||
| chr22:38254758 | G | A | 8 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58-6739C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254758 | |||||||
| chr22:38254851 | C | CT | 10 | a0001c0001t0001g0077 a0001c0001t0001g0125 a0001c0001t0001g0267 others(7): Show |
11 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58-6833dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254851 | |||||||
| chr22:38254851 | C | CTT | 8 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(5): Show |
9 | HG00639.hp1 HG01243.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58-6834_-58-6833d others(4): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254851 | |||||||
| chr22:38254851 | CT | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(98): Show |
104 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.-58-6833delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254851 | |||||||
| chr22:38254878 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-58-6859C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38254878 | |||||||
| chr22:38255032 | T | G | 3 | a0001c0001t0001g0269 a0001c0001t0016g0025 a0001c0001t0022g0228 |
3 | HG01243.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-58-7013A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255032 | |||||||
| chr22:38255062 | C | T | 3 | a0001c0004t0011g0190 a0001c0004t0011g0279 a0001c0004t0017g0026 |
3 | HG00639.hp2 HG03669.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-58-7043G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255062 | |||||||
| chr22:38255095 | G | T | 1 | a0001c0001t0004g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-58-7076C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255095 | |||||||
| chr22:38255346 | G | T | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-58-7327C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255346 | |||||||
| chr22:38255451 | C | T | 1 | a0001c0001t0027g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-58-7432G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255451 | |||||||
| chr22:38255578 | C | T | 6 | a0001c0001t0001g0267 a0001c0001t0006g0081 a0001c0001t0006g0082 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58-7559G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255578 | |||||||
| chr22:38255886 | G | A | 18 | a0001c0001t0003g0162 a0001c0002t0003g0014 a0001c0002t0003g0023 others(15): Show |
20 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-58-7867C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255886 | |||||||
| chr22:38255901 | A | C | 1 | a0001c0001t0002g0282 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-58-7882T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255901 | |||||||
| chr22:38255906 | G | T | 4 | a0001c0001t0001g0269 a0001c0001t0012g0019 a0001c0001t0016g0025 others(1): Show |
5 | HG01243.hp2 HG02976.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-58-7887C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38255906 | |||||||
| chr22:38256036 | A | G | 6 | a0001c0001t0001g0267 a0001c0001t0006g0081 a0001c0001t0006g0082 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58-8017T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256036 | |||||||
| chr22:38256058 | T | C | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-58-8039A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256058 | |||||||
| chr22:38256168 | T | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0004g0266 |
4 | HG01099.hp2 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-8149A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256168 | |||||||
| chr22:38256216 | C | CT | 205 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(202): Show |
223 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.-58-8198dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256216 | |||||||
| chr22:38256269 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-58-8250C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256269 | |||||||
| chr22:38256301 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0009g0270 a0001c0001t0009g0271 others(1): Show |
4 | HG01243.hp1 HG02630.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-8282G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256301 | |||||||
| chr22:38256307 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-58-8288C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256307 | |||||||
| chr22:38256333 | C | G | 114 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0040 others(111): Show |
118 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-58-8314G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256333 | |||||||
| chr22:38256349 | G | C | 1 | a0001c0001t0001g0176 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-58-8330C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256349 | |||||||
| chr22:38256406 | T | G | 27 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0004g0116 others(24): Show |
31 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.-58-8387A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256406 | |||||||
| chr22:38256525 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-58-8506C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256525 | |||||||
| chr22:38256542 | G | T | 2 | a0001c0001t0003g0162 a0001c0002t0003g0163 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-58-8523C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256542 | |||||||
| chr22:38256560 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(96): Show |
102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-58-8541A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256560 | |||||||
| chr22:38256634 | T | C | 1 | a0001c0003t0018g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-58-8615A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256634 | |||||||
| chr22:38256889 | T | C | 1 | a0001c0001t0007g0317 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-58-8870A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256889 | |||||||
| chr22:38256943 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-58-8924C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256943 | |||||||
| chr22:38256977 | G | GT | 8 | a0001c0001t0001g0197 a0001c0001t0001g0230 a0001c0001t0001g0231 others(5): Show |
8 | HG01106.hp1 HG01175.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58-8959dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256977 | |||||||
| chr22:38256977 | G | GTTT | 16 | a0001c0001t0004g0116 a0001c0001t0004g0117 a0001c0001t0004g0118 others(13): Show |
19 | HG01109.hp1 HG02109.hp1 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58-8961_-58-8959d others(5): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256977 | |||||||
| chr22:38256977 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0022g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-58-8969_-58-8959d others(13): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256977 | |||||||
| chr22:38256977 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-58-8970_-58-8959d others(14): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256977 | |||||||
| chr22:38256977 | GT | G | 8 | a0001c0001t0001g0178 a0001c0001t0001g0226 a0001c0001t0002g0066 others(5): Show |
8 | HG01069.hp1 HG01169.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-8959delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38256977 | |||||||
| chr22:38257058 | G | A | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-58-9039C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257058 | |||||||
| chr22:38257153 | T | C | 1 | a0001c0002t0003g0308 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-58-9134A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257153 | |||||||
| chr22:38257206 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0114 others(1): Show |
6 | HG02040.hp1 NA18941.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58-9187G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257206 | |||||||
| chr22:38257234 | AT | A | 17 | a0001c0001t0003g0162 a0001c0002t0003g0014 a0001c0002t0003g0023 others(14): Show |
19 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-58-9216delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257234 | |||||||
| chr22:38257321 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-58-9302A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257321 | |||||||
| chr22:38257382 | T | C | 1 | a0001c0001t0028g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-58-9363A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257382 | |||||||
| chr22:38257416 | A | G | 2 | a0001c0001t0002g0272 a0001c0001t0004g0266 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-58-9397T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257416 | |||||||
| chr22:38257520 | C | T | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-58-9501G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257520 | |||||||
| chr22:38257521 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-58-9502C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257521 | |||||||
| chr22:38257569 | G | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0047 others(95): Show |
101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-58-9550C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257569 | |||||||
| chr22:38257619 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-58-9600C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257619 | |||||||
| chr22:38257635 | T | A | 1 | a0001c0001t0002g0306 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-58-9616A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257635 | |||||||
| chr22:38257683 | T | C | 102 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0040 others(99): Show |
106 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-58-9664A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257683 | |||||||
| chr22:38257845 | T | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0060 |
2 | HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.-58-9826A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257845 | |||||||
| chr22:38257869 | A | G | 32 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0278 others(29): Show |
37 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-58-9850T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38257869 | |||||||
| chr22:38258095 | A | T | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-58-10076T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258095 | |||||||
| chr22:38258108 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-58-10089G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258108 | |||||||
| chr22:38258158 | C | T | 21 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(18): Show |
25 | HG01109.hp1 HG01433.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.-58-10139G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258158 | |||||||
| chr22:38258240 | C | T | 10 | a0001c0001t0001g0269 a0001c0001t0001g0278 a0001c0001t0016g0025 others(7): Show |
11 | HG00639.hp1 HG00639.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58-10221G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258240 | |||||||
| chr22:38258272 | T | C | 1 | a0001c0001t0001g0013 | 2 | NA18964.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-58-10253A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258272 | |||||||
| chr22:38258299 | A | ATTT | 9 | a0001c0002t0003g0023 a0001c0002t0003g0215 a0001c0002t0003g0217 others(6): Show |
10 | HG03239.hp1 HG03654.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58-10281_-58-1028 others(7): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258299 | |||||||
| chr22:38258300 | A | AT | 16 | a0001c0001t0001g0091 a0001c0001t0001g0108 a0001c0001t0001g0229 others(13): Show |
16 | HG01109.hp2 HG02056.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-58-10282dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258300 | |||||||
| chr22:38258300 | A | ATT | 5 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(2): Show |
8 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-58-10283_-58-1028 others(6): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258300 | |||||||
| chr22:38258300 | A | ATTT | 11 | a0001c0001t0001g0269 a0001c0001t0001g0278 a0001c0001t0016g0025 others(8): Show |
12 | HG00639.hp1 HG00639.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-58-10284_-58-1028 others(7): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258300 | |||||||
| chr22:38258300 | A | T | 10 | a0001c0002t0003g0023 a0001c0002t0003g0215 a0001c0002t0003g0217 others(7): Show |
11 | HG02523.hp2 HG03239.hp1 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58-10281T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258300 | |||||||
| chr22:38258300 | AT | A | 16 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(13): Show |
16 | HG00323.hp2 HG00741.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-58-10282delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258300 | |||||||
| chr22:38258423 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-58-10404A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258423 | |||||||
| chr22:38258431 | G | A | 5 | a0001c0001t0003g0162 a0001c0002t0003g0014 a0001c0002t0003g0076 others(2): Show |
6 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58-10412C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258431 | |||||||
| chr22:38258520 | G | A | 4 | a0001c0001t0001g0298 a0001c0001t0004g0015 a0001c0001t0004g0165 others(1): Show |
5 | HG01099.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-58-10501C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258520 | |||||||
| chr22:38258600 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-58-10581C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258600 | |||||||
| chr22:38258647 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0009g0193 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-58-10628G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258647 | |||||||
| chr22:38258744 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-58-10725G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258744 | |||||||
| chr22:38258806 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-58-10787G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258806 | |||||||
| chr22:38258878 | C | T | 1 | a0001c0001t0003g0018 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-58-10859G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38258878 | |||||||
| chr22:38259011 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0002g0027 a0001c0001t0002g0061 others(3): Show |
7 | NA18955.hp1 NA18962.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.-58-10992C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259011 | |||||||
| chr22:38259287 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-58-11268A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259287 | |||||||
| chr22:38259537 | C | T | 3 | a0001c0004t0008g0008 a0001c0004t0008g0100 a0001c0004t0032g0101 |
4 | HG00639.hp1 HG02922.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58-11518G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259537 | |||||||
| chr22:38259565 | C | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(118): Show |
145 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.-58-11546G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259565 | |||||||
| chr22:38259569 | A | G | 21 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(18): Show |
23 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-58-11550T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259569 | |||||||
| chr22:38259580 | A | G | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0003t0018g0074 |
3 | HG02896.hp2 HG02897.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-58-11561T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259580 | |||||||
| chr22:38259591 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(120): Show |
147 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-58-11572G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259591 | |||||||
| chr22:38259616 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-58-11597T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259616 | |||||||
| chr22:38259688 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-58-11669T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259688 | |||||||
| chr22:38259724 | A | G | 4 | a0001c0001t0001g0098 a0001c0001t0003g0096 a0001c0001t0003g0099 others(1): Show |
4 | HG02886.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58-11705T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259724 | |||||||
| chr22:38259900 | A | G | 141 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0035 others(138): Show |
149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-58-11881T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259900 | |||||||
| chr22:38259901 | GAGTAGCT others(7650): Show |
G | 1 | a0001c0001t0002g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-59+5326_-58-11883 others(3): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259901 | |||||||
| chr22:38259939 | C | CT | 8 | a0001c0001t0001g0231 a0001c0001t0001g0254 a0001c0001t0001g0262 others(5): Show |
8 | HG00741.hp2 HG01243.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.-58-11921dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259939 | |||||||
| chr22:38259939 | CT | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
106 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.-58-11921delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259939 | |||||||
| chr22:38259939 | CTT | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
140 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-58-11922_-58-1192 others(6): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38259939 | |||||||
| chr22:38260168 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-58-12149T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260168 | |||||||
| chr22:38260187 | C | T | 6 | a0001c0001t0001g0236 a0001c0001t0001g0238 a0001c0001t0001g0239 others(3): Show |
6 | HG00735.hp1 HG01081.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58-12168G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260187 | |||||||
| chr22:38260188 | G | A | 1 | a0001c0001t0031g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-58-12169C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260188 | |||||||
| chr22:38260237 | T | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(257): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.-58-12218A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260237 | |||||||
| chr22:38260351 | C | T | 1 | a0001c0001t0003g0018 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-58-12332G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260351 | |||||||
| chr22:38260508 | C | A | 2 | a0001c0001t0001g0188 a0001c0001t0014g0187 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-59+12376G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260508 | |||||||
| chr22:38260662 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-59+12222G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260662 | |||||||
| chr22:38260679 | A | G | 212 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(209): Show |
227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.-59+12205T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260679 | |||||||
| chr22:38260747 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0086 a0001c0001t0002g0087 others(2): Show |
6 | HG00544.hp1 HG00639.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-59+12137C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38260747 | |||||||
| chr22:38261185 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-59+11699C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261185 | |||||||
| chr22:38261388 | C | T | 6 | a0001c0001t0002g0007 a0001c0001t0002g0086 a0001c0001t0002g0087 others(3): Show |
7 | HG00544.hp1 HG00639.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.-59+11496G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261388 | |||||||
| chr22:38261395 | G | A | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+11489C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261395 | |||||||
| chr22:38261438 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-59+11446T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261438 | |||||||
| chr22:38261452 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-59+11432T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261452 | |||||||
| chr22:38261665 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-59+11219C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261665 | |||||||
| chr22:38261852 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-59+11032G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261852 | |||||||
| chr22:38261962 | G | T | 1 | a0001c0001t0015g0313 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-59+10922C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261962 | |||||||
| chr22:38261992 | A | AT | 24 | a0001c0001t0001g0188 a0001c0001t0002g0007 a0001c0001t0002g0086 others(21): Show |
28 | HG00544.hp1 HG00639.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-59+10891dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38261992 | |||||||
| chr22:38262049 | G | A | 31 | a0001c0001t0001g0268 a0001c0001t0001g0278 a0001c0001t0001g0283 others(28): Show |
33 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-59+10835C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262049 | |||||||
| chr22:38262151 | C | A | 1 | a0001c0001t0016g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-59+10733G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262151 | |||||||
| chr22:38262160 | C | T | 1 | a0001c0001t0016g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-59+10724G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262160 | |||||||
| chr22:38262193 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-59+10691G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262193 | |||||||
| chr22:38262255 | G | A | 1 | a0001c0001t0031g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-59+10629C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262255 | |||||||
| chr22:38262288 | T | G | 1 | a0001c0001t0001g0141 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-59+10596A>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262288 | |||||||
| chr22:38262307 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-59+10577C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262307 | |||||||
| chr22:38262409 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-59+10475C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262409 | |||||||
| chr22:38262527 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0004g0266 |
2 | HG01109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-59+10357C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262527 | |||||||
| chr22:38262571 | G | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(112): Show |
125 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-59+10313C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262571 | |||||||
| chr22:38262622 | G | A | 33 | a0001c0001t0001g0268 a0001c0001t0001g0278 a0001c0001t0001g0283 others(30): Show |
35 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-59+10262C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262622 | |||||||
| chr22:38262627 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0077 others(43): Show |
49 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.-59+10257G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262627 | |||||||
| chr22:38262696 | C | A | 4 | a0001c0001t0001g0188 a0001c0001t0002g0185 a0001c0001t0014g0187 others(1): Show |
4 | HG02630.hp1 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-59+10188G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262696 | |||||||
| chr22:38262950 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0004g0266 |
2 | HG01109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-59+9934A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262950 | |||||||
| chr22:38262994 | T | C | 186 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(183): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-59+9890A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38262994 | |||||||
| chr22:38263024 | T | C | 1 | a0001c0001t0002g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-59+9860A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263024 | |||||||
| chr22:38263104 | T | C | 24 | a0001c0001t0001g0188 a0001c0001t0002g0007 a0001c0001t0002g0086 others(21): Show |
28 | HG00544.hp1 HG00639.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-59+9780A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263104 | |||||||
| chr22:38263106 | T | C | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+9778A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263106 | |||||||
| chr22:38263183 | G | A | 1 | a0001c0001t0016g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-59+9701C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263183 | |||||||
| chr22:38263193 | G | A | 4 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0013g0109 others(1): Show |
5 | HG01099.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+9691C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263193 | |||||||
| chr22:38263239 | T | A | 1 | a0001c0001t0010g0132 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-59+9645A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263239 | |||||||
| chr22:38263316 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0002g0094 |
2 | HG01257.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-59+9568G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263316 | |||||||
| chr22:38263348 | C | A | 1 | a0001c0001t0003g0018 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-59+9536G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263348 | |||||||
| chr22:38263376 | T | A | 2 | a0001c0009t0002g0201 a0001c0009t0002g0212 |
2 | HG01074.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-59+9508A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263376 | |||||||
| chr22:38263552 | C | T | 6 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(3): Show |
9 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-59+9332G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263552 | |||||||
| chr22:38263577 | C | A | 1 | a0001c0001t0010g0132 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-59+9307G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263577 | |||||||
| chr22:38263644 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-59+9240C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263644 | |||||||
| chr22:38263728 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0013g0109 a0001c0001t0029g0110 |
4 | HG02622.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-59+9156G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263728 | |||||||
| chr22:38263772 | C | G | 1 | a0001c0002t0003g0281 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-59+9112G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263772 | |||||||
| chr22:38263801 | T | A | 1 | a0001c0001t0010g0132 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-59+9083A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263801 | |||||||
| chr22:38263812 | G | C | 2 | a0001c0001t0003g0162 a0001c0002t0003g0163 |
2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-59+9072C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263812 | |||||||
| chr22:38263813 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-59+9071A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263813 | |||||||
| chr22:38263829 | C | G | 115 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(112): Show |
125 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-59+9055G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263829 | |||||||
| chr22:38263836 | G | A | 94 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(91): Show |
100 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-59+9048C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263836 | |||||||
| chr22:38263859 | C | A | 3 | a0001c0001t0001g0041 a0001c0001t0002g0048 a0001c0001t0002g0057 |
3 | HG01261.hp1 HG01952.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-59+9025G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263859 | |||||||
| chr22:38263890 | T | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(113): Show |
126 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-59+8994A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263890 | |||||||
| chr22:38263978 | T | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0238 |
2 | HG01081.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-59+8906A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38263978 | |||||||
| chr22:38264088 | A | G | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-59+8796T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264088 | |||||||
| chr22:38264089 | G | A | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-59+8795C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264089 | |||||||
| chr22:38264090 | C | G | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-59+8794G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264090 | |||||||
| chr22:38264273 | C | T | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+8611G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264273 | |||||||
| chr22:38264389 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-59+8495C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264389 | |||||||
| chr22:38264404 | G | A | 1 | a0001c0001t0006g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-59+8480C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264404 | |||||||
| chr22:38264405 | T | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(95): Show |
104 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-59+8479A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264405 | |||||||
| chr22:38264560 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(214): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.-59+8324C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264560 | |||||||
| chr22:38264591 | T | A | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-59+8293A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264591 | |||||||
| chr22:38264727 | G | C | 1 | a0001c0001t0001g0168 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-59+8157C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264727 | |||||||
| chr22:38264865 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(95): Show |
104 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-59+8019G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264865 | |||||||
| chr22:38264885 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0161 |
2 | NA18945.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-59+7999C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38264885 | |||||||
| chr22:38265380 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-59+7504C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265380 | |||||||
| chr22:38265501 | G | A | 1 | a0001c0001t0014g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-59+7383C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265501 | |||||||
| chr22:38265503 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-59+7381C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265503 | |||||||
| chr22:38265559 | T | C | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG00597.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.-59+7325A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265559 | |||||||
| chr22:38265560 | C | G | 1 | a0001c0001t0003g0003 | 2 | NA19066.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-59+7324G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265560 | |||||||
| chr22:38265742 | C | T | 1 | a0001c0001t0026g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-59+7142G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265742 | |||||||
| chr22:38265854 | A | C | 170 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(167): Show |
177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-59+7030T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265854 | |||||||
| chr22:38265857 | G | A | 1 | a0001c0001t0003g0129 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-59+7027C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265857 | |||||||
| chr22:38265860 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0054 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-59+7024C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265860 | |||||||
| chr22:38265895 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-59+6989C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265895 | |||||||
| chr22:38265955 | G | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(312): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.-59+6929C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265955 | |||||||
| chr22:38265956 | A | G | 1 | a0001c0001t0012g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-59+6928T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38265956 | |||||||
| chr22:38266157 | G | A | 176 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(173): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-59+6727C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266157 | |||||||
| chr22:38266214 | G | A | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+6670C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266214 | |||||||
| chr22:38266254 | C | G | 2 | a0001c0001t0001g0192 a0001c0001t0009g0193 |
2 | HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-59+6630G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266254 | |||||||
| chr22:38266278 | A | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(205): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-59+6606T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266278 | |||||||
| chr22:38266337 | G | A | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+6547C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266337 | |||||||
| chr22:38266390 | T | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(64): Show |
68 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-59+6494A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266390 | |||||||
| chr22:38266481 | C | T | 1 | a0001c0001t0003g0003 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-59+6403G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266481 | |||||||
| chr22:38266850 | G | A | 34 | a0001c0001t0001g0268 a0001c0001t0001g0278 a0001c0001t0001g0283 others(31): Show |
36 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.-59+6034C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38266850 | |||||||
| chr22:38267040 | A | G | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+5844T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267040 | |||||||
| chr22:38267059 | G | C | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+5825C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267059 | |||||||
| chr22:38267083 | CA | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(100): Show |
110 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-59+5800delT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267083 | |||||||
| chr22:38267147 | C | T | 4 | a0001c0001t0004g0015 a0001c0001t0004g0165 a0001c0001t0013g0109 others(1): Show |
5 | HG01099.hp2 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+5737G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267147 | |||||||
| chr22:38267435 | C | CT | 10 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0015g0313 others(7): Show |
13 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.-59+5448dupA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267435 | |||||||
| chr22:38267435 | CT | C | 8 | a0001c0001t0001g0127 a0001c0001t0001g0159 a0001c0001t0001g0173 others(5): Show |
8 | HG01167.hp2 HG01433.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-59+5448delA | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267435 | |||||||
| chr22:38267456 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-59+5428T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267456 | |||||||
| chr22:38267734 | T | C | 1 | a0001c0009t0002g0212 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-59+5150A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267734 | |||||||
| chr22:38267739 | G | A | 1 | a0001c0005t0001g0179 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-59+5145C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267739 | |||||||
| chr22:38267766 | TA | T | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+5117delT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267766 | |||||||
| chr22:38267813 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(164): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-59+5071T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267813 | |||||||
| chr22:38267850 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(52): Show |
59 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.-59+5034C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38267850 | |||||||
| chr22:38268000 | G | A | 5 | a0001c0001t0006g0081 a0001c0001t0006g0082 a0001c0001t0006g0218 others(2): Show |
5 | HG02559.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-59+4884C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268000 | |||||||
| chr22:38268065 | A | G | 176 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(173): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-59+4819T>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268065 | |||||||
| chr22:38268083 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-59+4801C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268083 | |||||||
| chr22:38268263 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-59+4621G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268263 | |||||||
| chr22:38268271 | C | T | 7 | a0001c0001t0002g0007 a0001c0001t0002g0086 a0001c0001t0002g0087 others(4): Show |
8 | HG00544.hp1 HG00639.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.-59+4613G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268271 | |||||||
| chr22:38268374 | C | CA | 11 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0180 others(8): Show |
12 | HG01934.hp2 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-59+4509dupT | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268374 | |||||||
| chr22:38268374 | C | CAA | 152 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(149): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-59+4508_-59+4509d others(4): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268374 | |||||||
| chr22:38268374 | C | CAAA | 7 | a0001c0001t0001g0035 a0001c0001t0001g0263 a0001c0001t0001g0297 others(4): Show |
7 | HG02155.hp1 HG02615.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-59+4507_-59+4509d others(5): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268374 | |||||||
| chr22:38268439 | T | C | 8 | a0001c0001t0001g0188 a0001c0001t0002g0185 a0001c0001t0003g0018 others(5): Show |
9 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-59+4445A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268439 | |||||||
| chr22:38268528 | G | A | 1 | a0001c0004t0017g0026 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-59+4356C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268528 | |||||||
| chr22:38268533 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(143): Show |
175 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.-59+4351G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268533 | |||||||
| chr22:38268556 | G | A | 3 | a0001c0001t0002g0007 a0001c0001t0002g0086 a0001c0001t0002g0087 |
4 | HG00544.hp1 HG02165.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.-59+4328C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268556 | |||||||
| chr22:38268557 | T | A | 1 | a0001c0004t0011g0190 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-59+4327A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268557 | |||||||
| chr22:38268783 | G | A | 166 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0020 others(163): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-59+4101C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268783 | |||||||
| chr22:38268808 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-59+4076C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268808 | |||||||
| chr22:38268847 | T | C | 6 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(3): Show |
9 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-59+4037A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268847 | |||||||
| chr22:38268863 | C | T | 1 | a0001c0002t0003g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-59+4021G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38268863 | |||||||
| chr22:38269137 | T | C | 2 | a0001c0007t0001g0311 a0001c0007t0001g0312 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+3747A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38269137 | |||||||
| chr22:38269298 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-59+3586C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38269298 | |||||||
| chr22:38269313 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0002g0029 a0001c0001t0002g0031 others(5): Show |
8 | HG02071.hp2 HG02155.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-59+3571G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38269313 | |||||||
| chr22:38269454 | G | A | 1 | a0001c0001t0012g0019 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-59+3430C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38269454 | |||||||
| chr22:38269680 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-59+3204C>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38269680 | |||||||
| chr22:38269770 | G | A | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+3114C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38269770 | |||||||
| chr22:38269809 | A | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(47): Show |
54 | HG00280.hp1 HG00597.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.-59+3075T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38269809 | |||||||
| chr22:38270107 | G | A | 4 | a0001c0001t0002g0216 a0001c0002t0003g0215 a0001c0002t0003g0217 others(1): Show |
4 | HG03710.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-59+2777C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270107 | |||||||
| chr22:38270180 | C | G | 37 | a0001c0001t0001g0278 a0001c0001t0001g0283 a0001c0001t0001g0296 others(34): Show |
39 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-59+2704G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270180 | |||||||
| chr22:38270214 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-59+2670G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270214 | |||||||
| chr22:38270232 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-59+2652G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270232 | |||||||
| chr22:38270367 | G | A | 36 | a0001c0001t0001g0278 a0001c0001t0001g0283 a0001c0001t0001g0296 others(33): Show |
38 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-59+2517C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270367 | |||||||
| chr22:38270510 | T | C | 3 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0220 |
3 | HG02896.hp2 HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-59+2374A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270510 | |||||||
| chr22:38270666 | C | T | 1 | a0001c0002t0003g0222 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-59+2218G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270666 | |||||||
| chr22:38270922 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-59+1962C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270922 | |||||||
| chr22:38270998 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0010g0299 |
2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-59+1886C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38270998 | |||||||
| chr22:38271063 | G | A | 1 | a0001c0001t0002g0300 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-59+1821C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271063 | |||||||
| chr22:38271130 | G | T | 2 | a0001c0001t0006g0081 a0001c0001t0006g0082 |
2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-59+1754C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271130 | |||||||
| chr22:38271162 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-59+1722G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271162 | |||||||
| chr22:38271381 | A | C | 1 | a0001c0001t0002g0027 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-59+1503T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271381 | |||||||
| chr22:38271417 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-59+1467C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271417 | |||||||
| chr22:38271614 | CCTT | C | 95 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(92): Show |
104 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.-59+1267_-59+1269d others(5): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271614 | |||||||
| chr22:38271874 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-59+1010G>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271874 | |||||||
| chr22:38271947 | G | T | 5 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(2): Show |
8 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-59+937C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38271947 | |||||||
| chr22:38272024 | T | A | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG00673.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.-59+860A>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272024 | |||||||
| chr22:38272058 | A | AGGTATCA others(24): Show |
1 | a0001c0001t0001g0078 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-59+795_-59+825dup others(31): Show |
TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272058 | |||||||
| chr22:38272110 | G | A | 1 | a0001c0001t0024g0303 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-59+774C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272110 | |||||||
| chr22:38272218 | G | A | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+666C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272218 | |||||||
| chr22:38272255 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-59+629C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272255 | |||||||
| chr22:38272286 | G | A | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+598C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272286 | |||||||
| chr22:38272306 | A | C | 1 | a0001c0002t0003g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-59+578T>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272306 | |||||||
| chr22:38272342 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-59+542A>G | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272342 | |||||||
| chr22:38272345 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-59+539T>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272345 | |||||||
| chr22:38272362 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0002g0306 |
2 | HG01516.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-59+522C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272362 | |||||||
| chr22:38272427 | C | G | 6 | a0001c0003t0005g0002 a0001c0003t0005g0070 a0001c0003t0005g0071 others(3): Show |
9 | HG01109.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-59+457G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272427 | |||||||
| chr22:38272550 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-59+334C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272550 | |||||||
| chr22:38272654 | C | A | 2 | a0001c0001t0001g0309 a0001c0002t0003g0308 |
2 | NA19007.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-59+230G>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272654 | |||||||
| chr22:38272767 | C | G | 1 | a0001c0001t0002g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-59+117G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272767 | |||||||
| chr22:38272815 | C | G | 43 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(40): Show |
44 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-59+69G>C | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272815 | |||||||
| chr22:38272850 | G | T | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+34C>A | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272850 | |||||||
| chr22:38272861 | G | A | 3 | a0001c0001t0001g0310 a0001c0007t0001g0311 a0001c0007t0001g0312 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-59+23C>T | TMEM184B | ENSG00000198792.13 | transcript | ENST00000361906.8 | protein_coding | 1/8 | chr22 | 38272861 |