Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79632 |
| ensemblid | ENSG00000111879.20 |
| hgncid | 20991 |
| symbol | FAM184A |
| name | family with sequence similarity 184 member A |
| refseq_nuc | NM_024581.6 |
| refseq_prot | NP_078857.5 |
| ensembl_nuc | ENST00000338891.12 |
| ensembl_prot | ENSP00000342604.7 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 118959763 |
| end | 119078664 |
| strand | - |
| ver | v1.2 |
| region | chr6:118959763-119078664 |
| region5000 | chr6:118954763-119083664 |
| regionname0 | FAM184A_chr6_118959763_119078664 |
| regionname5000 | FAM184A_chr6_118954763_119083664 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1140 | 259 | 80 | 56 | 94 | 7 | 20 | 72 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| a0002 | 0/0 | 1140 | 17 | 3 | 5 | 4 | 1 | 4 | 2 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| a0003 | 0/0 | 1140 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| a0004 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| a0005 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| a0006 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| a0007 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| a0008 | 0/0 | 1140 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | MATPG others(1135): Show |
chr6 | 118954763 | 119083664 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3420 | 250 | 72 | 55 | 94 | 7 | 20 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0001c0003 | 0/0 | 3420 | 8 | 7 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0001c0006 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0002c0002 | 0/0 | 3420 | 17 | 3 | 5 | 4 | 1 | 4 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0003c0004 | 0/0 | 3420 | 5 | 0 | 5 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0004c0010 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0005c0008 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0006c0009 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0007c0007 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 | ||
| a0008c0005 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | ATGGC others(3415): Show |
chr6 | 118954763 | 119083664 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4131 | 206 | 51 | 46 | 83 | 7 | 18 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0002 | 1/0 | 4128 | 10 | 6 | 2 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4123): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0003 | 0/0 | 4131 | 13 | 0 | 6 | 7 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0004 | 0/0 | 4131 | 8 | 8 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0005 | 0/0 | 4131 | 5 | 5 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0006 | 0/0 | 4131 | 2 | 1 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0007 | 0/0 | 4131 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0008 | 0/0 | 4131 | 2 | 0 | 0 | 2 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0009 | 0/0 | 4131 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0001t0010 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0003t0001 | 0/0 | 4131 | 7 | 6 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0003t0005 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0001c0006t0005 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0002c0002t0001 | 0/0 | 4131 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0002c0002t0002 | 0/0 | 4128 | 16 | 3 | 5 | 3 | 1 | 4 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4123): Show |
chr6 | 118954763 | 119083664 |
| a0003c0004t0001 | 0/0 | 4131 | 5 | 0 | 5 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0004c0010t0004 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0005c0008t0001 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0006c0009t0004 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0007c0007t0001 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| a0008c0005t0001 | 0/0 | 4131 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | AGCCT others(4126): Show |
chr6 | 118954763 | 119083664 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0009g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0001t0010g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0001c0006t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0004c0010t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0005c0008t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0006c0009t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0007c0007t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| a0008c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | GBR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0133 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0228 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00738 | hp2 | a0003 | c0004 | t0001 | g0095 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0185 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0035 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0230 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0227 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01433 | hp1 | a0003 | c0004 | t0001 | g0094 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01496 | hp1 | a0003 | c0004 | t0001 | g0141 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | IBS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01884 | hp1 | a0001 | c0006 | t0005 | g0030 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01891 | hp1 | a0004 | c0010 | t0004 | g0006 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01891 | hp2 | a0005 | c0008 | t0001 | g0064 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02004 | hp1 | a0003 | c0004 | t0001 | g0093 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CDX | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02273 | hp2 | a0003 | c0004 | t0001 | g0103 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0139 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02572 | hp2 | a0006 | c0009 | t0004 | g0007 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0282 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0003 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0260 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03195 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0207 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0208 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | ESN | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03540 | hp2 | a0007 | c0007 | t0001 | g0240 | AFR | GWD | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0218 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0214 | SAS | BEB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18612 | hp2 | a0001 | c0001 | t0008 | g0283 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | YRI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18986 | hp1 | a0001 | c0001 | t0007 | g0281 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0284 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0129 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0032 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19055 | hp2 | a0001 | c0001 | t0007 | g0280 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | ASW | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ASW | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0143 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | GIH | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | ACB | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA20300 | hp2 | a0008 | c0005 | t0001 | g0036 | AFR | USA | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | LWK | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0057 | REF | REF | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0051 | REF | REF | FAM184A_chr6_118954763_119083664 | FAM184A | chr6 | 118954763 | 119083664 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:118974486 | C | A | 1 | a0005 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2857G>T | p.Ala953Ser | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/18 | 3222/4128 | 2857/3423 | 953/1140 | chr6 | 118974486 | |||
| chr6:118975978 | T | A | 1 | a0003 | 5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
missense_variant | MODERATE | c.2522A>T | p.His841Leu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/18 | 2887/4128 | 2522/3423 | 841/1140 | chr6 | 118975978 | |||
| chr6:119002985 | T | C | 1 | a0006 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.2002A>G | p.Met668Val | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/18 | 2367/4128 | 2002/3423 | 668/1140 | chr6 | 119002985 | |||
| chr6:119006467 | C | T | 1 | a0002 | 17 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(14): Show |
missense_variant | MODERATE | c.1795G>A | p.Asp599Asn | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/18 | 2160/4128 | 1795/3423 | 599/1140 | chr6 | 119006467 | |||
| chr6:119006589 | A | G | 1 | a0007 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1673T>C | p.Met558Thr | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/18 | 2038/4128 | 1673/3423 | 558/1140 | chr6 | 119006589 | |||
| chr6:119016749 | T | C | 1 | a0004 | 1 | HG01891.hp1 | missense_variant&splice_region_variant | MODERATE | c.1528A>G | p.Met510Val | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/18 | 1893/4128 | 1528/3423 | 510/1140 | chr6 | 119016749 | |||
| chr6:119078220 | G | T | 1 | a0008 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.80C>A | p.Ala27Glu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 445/4128 | 80/3423 | 27/1140 | chr6 | 119078220 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:119024243 | G | A | 1 | a0001c0003 | 8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
synonymous_variant | LOW | c.730C>T | p.Leu244Leu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/18 | 1095/4128 | 730/3423 | 244/1140 | chr6 | 119024243 | |||
| chr6:119024373 | C | T | 1 | a0001c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.600G>A | p.Glu200Glu | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/18 | 965/4128 | 600/3423 | 200/1140 | chr6 | 119024373 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:118959824 | G | GCAT | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*276_*278dupATG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 18/18 | 278 | chr6 | 118959824 | ||||||
| chr6:119078324 | C | T | 1 | a0001c0001t0006 | 2 | HG01243.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-25G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 25 | chr6 | 119078324 | ||||||
| chr6:119078343 | A | T | 3 | a0001c0001t0005 a0001c0003t0005 a0001c0006t0005 |
7 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-44T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 44 | chr6 | 119078343 | ||||||
| chr6:119078432 | G | A | 1 | a0001c0001t0007 | 2 | NA18986.hp1 NA19055.hp2 |
5_prime_UTR_variant | MODIFIER | c.-133C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 133 | chr6 | 119078432 | ||||||
| chr6:119078454 | C | T | 1 | a0001c0001t0003 | 13 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-155G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 155 | chr6 | 119078454 | ||||||
| chr6:119078496 | C | T | 3 | a0001c0001t0004 a0004c0010t0004 a0006c0009t0004 |
10 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-197G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 197 | chr6 | 119078496 | ||||||
| chr6:119078556 | G | A | 1 | a0001c0001t0010 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-257C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 257 | chr6 | 119078556 | ||||||
| chr6:119078570 | T | C | 1 | a0001c0001t0008 | 2 | NA18612.hp2 NA19002.hp1 |
5_prime_UTR_variant | MODIFIER | c.-271A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 271 | chr6 | 119078570 | ||||||
| chr6:119078614 | C | T | 1 | a0001c0001t0009 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-315G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/18 | 315 | chr6 | 119078614 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:118960257 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.3342-73T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960257 | |||||||
| chr6:118960534 | C | G | 1 | a0002c0002t0002g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3342-350G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960534 | |||||||
| chr6:118960552 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3342-368C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960552 | |||||||
| chr6:118960673 | A | G | 1 | a0001c0001t0008g0284 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3342-489T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118960673 | |||||||
| chr6:118961324 | C | CAT | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(1): Show |
4 | HG01106.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.3341+435_3341+436d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961324 | |||||||
| chr6:118961333 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3341+428T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961333 | |||||||
| chr6:118961637 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3341+124C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961637 | |||||||
| chr6:118961667 | GGTT | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3341+91_3341+93del others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961667 | |||||||
| chr6:118961753 | G | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG03491.hp2 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.3341+8C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 17/17 | chr6 | 118961753 | |||||||
| chr6:118962131 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3139-168C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118962131 | |||||||
| chr6:118962557 | T | C | 1 | a0002c0002t0002g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3139-594A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118962557 | |||||||
| chr6:118962903 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3139-940T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118962903 | |||||||
| chr6:118963263 | A | G | 4 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0131 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3139-1300T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963263 | |||||||
| chr6:118963361 | T | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3138+1306A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963361 | |||||||
| chr6:118963414 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3138+1253T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963414 | |||||||
| chr6:118963719 | A | G | 93 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0052 others(90): Show |
94 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.3138+948T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963719 | |||||||
| chr6:118963735 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0130 others(7): Show |
11 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.3138+932T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963735 | |||||||
| chr6:118963776 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00408.hp1 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.3138+891C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118963776 | |||||||
| chr6:118964166 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3138+501T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964166 | |||||||
| chr6:118964279 | G | C | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3138+388C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964279 | |||||||
| chr6:118964307 | G | A | 1 | a0002c0002t0002g0228 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3138+360C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964307 | |||||||
| chr6:118964356 | G | A | 1 | a0002c0002t0002g0217 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3138+311C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964356 | |||||||
| chr6:118964416 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(253): Show |
258 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.3138+251G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964416 | |||||||
| chr6:118964514 | T | C | 5 | a0003c0004t0001g0093 a0003c0004t0001g0094 a0003c0004t0001g0095 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.3138+153A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964514 | |||||||
| chr6:118964526 | A | G | 53 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0085 others(50): Show |
53 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.3138+141T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964526 | |||||||
| chr6:118964526 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3138+141T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964526 | |||||||
| chr6:118964529 | AGTTT | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.3138+134_3138+137d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964529 | |||||||
| chr6:118964623 | A | C | 1 | a0002c0002t0002g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3138+44T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964623 | |||||||
| chr6:118964637 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3138+30A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 16/17 | chr6 | 118964637 | |||||||
| chr6:118965057 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3034-286C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965057 | |||||||
| chr6:118965086 | G | T | 1 | a0001c0001t0004g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3034-315C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965086 | |||||||
| chr6:118965155 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3034-384A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965155 | |||||||
| chr6:118965205 | G | GT | 245 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0043 others(242): Show |
247 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.3034-435dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965205 | |||||||
| chr6:118965205 | G | GTT | 10 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0077 others(7): Show |
10 | HG00735.hp1 HG01192.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.3034-436_3034-435d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965205 | |||||||
| chr6:118965205 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3034-434C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965205 | |||||||
| chr6:118965208 | T | TG | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3034-438_3034-437i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965208 | |||||||
| chr6:118965211 | T | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.3034-440A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965211 | |||||||
| chr6:118965212 | T | G | 7 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0109 others(4): Show |
7 | HG01106.hp2 HG01515.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.3034-441A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965212 | |||||||
| chr6:118965580 | C | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0131 others(1): Show |
4 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3034-809G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965580 | |||||||
| chr6:118965866 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3033+969G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118965866 | |||||||
| chr6:118966012 | C | G | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3033+823G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966012 | |||||||
| chr6:118966444 | C | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(249): Show |
254 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.3033+391G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966444 | |||||||
| chr6:118966634 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3033+201C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966634 | |||||||
| chr6:118966694 | T | A | 1 | a0001c0001t0001g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3033+141A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966694 | |||||||
| chr6:118966750 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3033+85G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 15/17 | chr6 | 118966750 | |||||||
| chr6:118967428 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2916-476G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967428 | |||||||
| chr6:118967444 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2916-492A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967444 | |||||||
| chr6:118967500 | AT | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2916-549delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967500 | |||||||
| chr6:118967635 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0167 |
2 | NA18939.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2916-683G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967635 | |||||||
| chr6:118967816 | CAT | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-866_2916-865d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118967816 | |||||||
| chr6:118968113 | G | A | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-1161C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968113 | |||||||
| chr6:118968174 | G | T | 1 | a0002c0002t0002g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2916-1222C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968174 | |||||||
| chr6:118968370 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2916-1418C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968370 | |||||||
| chr6:118968463 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2916-1511A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968463 | |||||||
| chr6:118968545 | A | G | 5 | a0001c0001t0001g0229 a0001c0001t0001g0277 a0001c0001t0001g0278 others(2): Show |
5 | HG01934.hp1 HG02273.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-1593T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968545 | |||||||
| chr6:118968670 | C | A | 229 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(226): Show |
230 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.2916-1718G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968670 | |||||||
| chr6:118968836 | AAT | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(249): Show |
254 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.2916-1886_2916-188 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118968836 | |||||||
| chr6:118969300 | G | A | 10 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
10 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.2916-2348C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969300 | |||||||
| chr6:118969708 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2916-2756G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969708 | |||||||
| chr6:118969798 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2916-2846C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969798 | |||||||
| chr6:118969804 | C | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-2852G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969804 | |||||||
| chr6:118969805 | A | AC | 90 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0001g0053 others(87): Show |
91 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2916-2854dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969805 | |||||||
| chr6:118969810 | G | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.2916-2858C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969810 | |||||||
| chr6:118969827 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2916-2875C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969827 | |||||||
| chr6:118969861 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2916-2909A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969861 | |||||||
| chr6:118969992 | T | TATAA | 140 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(137): Show |
140 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.2916-3041_2916-304 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969992 | |||||||
| chr6:118969992 | T | TATATAA | 3 | a0001c0001t0001g0186 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00408.hp1 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.2916-3041_2916-304 others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969992 | |||||||
| chr6:118969992 | TA | T | 3 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0012 |
3 | HG02109.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2916-3041delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969992 | |||||||
| chr6:118969993 | A | ATAAAATA others(1): Show |
7 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(4): Show |
7 | HG00639.hp1 HG02559.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(5): Show |
7 | a0001c0001t0001g0063 a0001c0001t0001g0076 a0001c0001t0001g0087 others(4): Show |
7 | HG00642.hp2 HG01123.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(7): Show |
2 | a0001c0001t0001g0229 a0001c0001t0003g0025 |
2 | HG02293.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(9): Show |
14 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(11): Show |
14 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(11): Show |
1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(22): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(15): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0162 |
3 | HG02109.hp2 NA18747.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(26): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(17): Show |
1 | a0001c0001t0006g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(28): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(19): Show |
5 | a0001c0001t0001g0085 a0001c0001t0001g0171 a0001c0001t0001g0279 others(2): Show |
5 | HG02135.hp2 HG02683.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(30): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(57): Show |
1 | a0005c0008t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(68): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(21): Show |
1 | a0001c0001t0006g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(32): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(28): Show |
1 | a0001c0003t0001g0139 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(23): Show |
1 | a0001c0001t0001g0160 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(34): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(48): Show |
1 | a0001c0001t0001g0158 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(59): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(25): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0109 a0001c0001t0001g0253 |
3 | HG02280.hp1 HG02280.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(36): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(62): Show |
1 | a0006c0009t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(73): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(44): Show |
1 | a0001c0001t0001g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(55): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(68): Show |
1 | a0001c0001t0003g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(79): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(27): Show |
2 | a0001c0001t0001g0105 a0001c0001t0005g0031 |
2 | HG01515.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(38): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(29): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0117 |
2 | HG01346.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(31): Show |
11 | a0001c0001t0001g0052 a0001c0001t0001g0106 a0001c0001t0001g0111 others(8): Show |
11 | HG00733.hp1 HG01106.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(42): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(33): Show |
7 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0116 others(4): Show |
7 | HG01081.hp1 HG02135.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(35): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(37): Show |
4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0110 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(39): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0003g0014 |
3 | NA18947.hp1 NA18968.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(41): Show |
5 | a0001c0001t0001g0108 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | HG01978.hp1 HG02155.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(52): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(43): Show |
4 | a0001c0001t0001g0239 a0001c0001t0001g0244 a0001c0001t0003g0017 others(1): Show |
4 | HG01243.hp2 NA18943.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(54): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(49): Show |
1 | a0001c0001t0001g0219 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(60): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAAAATA others(33): Show |
1 | a0001c0001t0001g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATAATATA others(35): Show |
1 | a0001c0001t0001g0172 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2916-3042_2916-304 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATACAATA others(3): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02055.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATATAAAA others(15): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(26): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969993 | A | ATATAAAA others(17): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2916-3042_2916-304 others(28): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969993 | |||||||
| chr6:118969995 | T | A | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(4): Show |
7 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2916-3043A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118969995 | |||||||
| chr6:118970006 | A | T | 19 | a0001c0001t0001g0045 a0001c0001t0001g0085 a0001c0001t0001g0160 others(16): Show |
19 | HG01081.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2916-3054T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970006 | |||||||
| chr6:118970008 | A | ATATATAA others(46): Show |
1 | a0001c0001t0001g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(57): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(46): Show |
2 | a0001c0001t0004g0005 a0004c0010t0004g0006 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(57): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(47): Show |
1 | a0002c0002t0001g0235 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(58): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(57): Show |
1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(68): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(66): Show |
1 | a0001c0001t0001g0215 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(77): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(82): Show |
1 | a0001c0001t0001g0252 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(93): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(86): Show |
1 | a0001c0001t0001g0272 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(97): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(49): Show |
1 | a0001c0001t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(60): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(44): Show |
1 | a0001c0001t0001g0203 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(55): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(41): Show |
1 | a0001c0001t0001g0038 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(52): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(43): Show |
1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(54): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(44): Show |
1 | a0001c0001t0001g0247 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(55): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(41): Show |
1 | a0001c0001t0008g0283 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(52): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(36): Show |
2 | a0001c0001t0001g0191 a0001c0001t0001g0268 |
2 | NA18961.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(47): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(37): Show |
3 | a0001c0001t0001g0190 a0001c0001t0001g0245 a0001c0001t0001g0259 |
3 | HG02080.hp2 HG03017.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(39): Show |
1 | a0001c0001t0001g0277 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(48): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0271 |
2 | HG00597.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(59): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(45): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0234 a0001c0001t0003g0022 |
2 | HG01167.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(36): Show |
2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(47): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(38): Show |
1 | a0001c0001t0001g0248 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(49): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(39): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0278 |
2 | HG02273.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(45): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(35): Show |
1 | a0001c0001t0001g0241 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(36): Show |
1 | a0007c0007t0001g0240 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(47): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(37): Show |
3 | a0001c0001t0001g0192 a0001c0001t0001g0226 a0001c0001t0001g0269 |
3 | HG02071.hp1 HG02698.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(38): Show |
2 | a0001c0001t0004g0004 a0001c0001t0005g0027 |
2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(49): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(42): Show |
1 | a0001c0001t0002g0121 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(53): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0186 a0001c0001t0003g0016 |
2 | HG00408.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0194 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(48): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(39): Show |
1 | a0001c0001t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(50): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(28): Show |
2 | a0001c0001t0001g0113 a0001c0001t0003g0019 |
2 | HG01361.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(29): Show |
1 | a0001c0001t0003g0026 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0233 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(31): Show |
3 | a0001c0001t0001g0222 a0001c0001t0001g0243 a0001c0001t0001g0249 |
3 | HG01496.hp2 NA18747.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(42): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(33): Show |
5 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0238 others(2): Show |
5 | HG01358.hp1 HG02083.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0037 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(45): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(29): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0149 |
2 | HG01074.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(33): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0212 |
2 | NA19012.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(38): Show |
1 | a0001c0001t0002g0199 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(49): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(36): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(37): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0242 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(38): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0264 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0273 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(42): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0168 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0225 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(44): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(32): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(24): Show |
3 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0102 |
3 | HG01168.hp1 HG01192.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(26): Show |
1 | a0003c0004t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(37): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0224 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0166 a0001c0001t0001g0170 |
2 | NA18975.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(31): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(22): Show |
1 | a0003c0004t0001g0094 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0263 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(36): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(29): Show |
1 | a0001c0001t0004g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(40): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(30): Show |
1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(35): Show |
1 | a0001c0001t0004g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(46): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(18): Show |
4 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0001g0173 others(1): Show |
4 | HG02083.hp2 HG02523.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(29): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(32): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(22): Show |
8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0124 others(5): Show |
8 | HG00738.hp2 HG01981.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(24): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0258 |
2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(26): Show |
1 | a0001c0001t0001g0084 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(37): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0081 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(32): Show |
1 | a0001c0001t0001g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(43): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(16): Show |
5 | a0001c0001t0001g0144 a0001c0001t0001g0177 a0001c0001t0001g0181 others(2): Show |
5 | HG00408.hp2 HG01071.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(27): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(20): Show |
9 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0060 others(6): Show |
9 | HG00140.hp2 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(31): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(22): Show |
5 | a0001c0001t0001g0078 a0001c0001t0001g0138 a0001c0001t0005g0028 others(2): Show |
5 | HG00733.hp2 HG02451.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(34): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(14): Show |
12 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0145 others(9): Show |
12 | HG01192.hp2 HG03195.hp2 HG03225.hp2 others(9): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(25): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0146 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(26): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0175 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(27): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(30): Show |
1 | a0001c0001t0001g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(41): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(14): Show |
8 | a0001c0001t0001g0096 a0001c0001t0001g0151 a0001c0001t0001g0152 others(5): Show |
8 | HG00609.hp2 HG02080.hp1 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.2916-3057_2916-305 others(25): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(39): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0097 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2916-3057_2916-305 others(25): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATTT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0105 others(24): Show |
28 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.2916-3059_2916-305 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0002g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2916-3067_2916-305 others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970008 | A | T | 33 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0070 others(30): Show |
33 | HG00423.hp2 HG00609.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.2916-3056T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970008 | |||||||
| chr6:118970009 | T | TA | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.2916-3058_2916-305 others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970009 | |||||||
| chr6:118970010 | T | A | 13 | a0001c0001t0001g0071 a0001c0001t0001g0132 a0001c0001t0004g0011 others(10): Show |
13 | HG00639.hp1 HG01358.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.2916-3058A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970010 | |||||||
| chr6:118970011 | T | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02055.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2916-3059A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970011 | |||||||
| chr6:118970012 | T | A | 8 | a0001c0001t0004g0011 a0001c0003t0001g0048 a0001c0003t0001g0133 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2916-3060A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970012 | |||||||
| chr6:118970017 | T | A | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3065A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970017 | |||||||
| chr6:118970036 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(255): Show |
259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.2916-3084A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970036 | |||||||
| chr6:118970106 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2916-3154G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970106 | |||||||
| chr6:118970246 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2916-3294G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970246 | |||||||
| chr6:118970247 | G | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0001g0130 others(7): Show |
11 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2916-3295C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970247 | |||||||
| chr6:118970255 | C | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(118): Show |
122 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.2916-3303G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970255 | |||||||
| chr6:118970259 | C | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2916-3307G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970259 | |||||||
| chr6:118970580 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2916-3628C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970580 | |||||||
| chr6:118970764 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2915+3664G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970764 | |||||||
| chr6:118970782 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2915+3646T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970782 | |||||||
| chr6:118970853 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2915+3575C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118970853 | |||||||
| chr6:118971451 | AT | A | 17 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(14): Show |
17 | HG00639.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.2915+2976delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971451 | |||||||
| chr6:118971548 | T | TA | 100 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(97): Show |
101 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.2915+2879dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971548 | |||||||
| chr6:118971720 | A | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2915+2708T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971720 | |||||||
| chr6:118971860 | C | A | 1 | a0001c0001t0003g0022 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2915+2568G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971860 | |||||||
| chr6:118971860 | C | CAGA | 187 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0043 others(184): Show |
188 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.2915+2565_2915+256 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971860 | |||||||
| chr6:118971863 | A | AAGC | 5 | a0001c0001t0001g0083 a0001c0001t0001g0202 a0001c0001t0001g0241 others(2): Show |
5 | HG01074.hp2 HG01109.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2915+2562_2915+256 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118971863 | |||||||
| chr6:118972269 | T | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(252): Show |
257 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.2915+2159A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972269 | |||||||
| chr6:118972300 | G | A | 2 | a0002c0002t0002g0207 a0002c0002t0002g0208 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2915+2128C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972300 | |||||||
| chr6:118972637 | G | C | 1 | a0001c0001t0001g0250 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2915+1791C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972637 | |||||||
| chr6:118972864 | C | T | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2915+1564G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118972864 | |||||||
| chr6:118973049 | A | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0187 a0001c0001t0003g0016 |
3 | NA18954.hp2 NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2915+1379T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973049 | |||||||
| chr6:118973058 | A | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2915+1370T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973058 | |||||||
| chr6:118973078 | A | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2915+1350T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973078 | |||||||
| chr6:118973412 | C | T | 91 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(88): Show |
91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2915+1016G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973412 | |||||||
| chr6:118973502 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2915+926C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118973502 | |||||||
| chr6:118974125 | T | G | 1 | a0001c0001t0001g0149 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2915+303A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118974125 | |||||||
| chr6:118974252 | C | A | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2915+176G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 14/17 | chr6 | 118974252 | |||||||
| chr6:118974640 | T | C | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-66A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 13/17 | chr6 | 118974640 | |||||||
| chr6:118974642 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2769-68G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 13/17 | chr6 | 118974642 | |||||||
| chr6:118974706 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2769-132C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 13/17 | chr6 | 118974706 | |||||||
| chr6:118975213 | T | TA | 54 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(51): Show |
56 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(53): Show |
splice_region_variant&intron_variant | LOW | c.2584-6dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975213 | |||||||
| chr6:118975378 | C | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2584-170G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975378 | |||||||
| chr6:118975572 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2583+345A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975572 | |||||||
| chr6:118975607 | G | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2583+310C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975607 | |||||||
| chr6:118975751 | C | A | 14 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(11): Show |
14 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.2583+166G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975751 | |||||||
| chr6:118975857 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2583+60T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 12/17 | chr6 | 118975857 | |||||||
| chr6:118976220 | C | T | 43 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(40): Show |
43 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.2456-176G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976220 | |||||||
| chr6:118976390 | C | T | 9 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2456-346G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976390 | |||||||
| chr6:118976577 | T | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2456-533A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976577 | |||||||
| chr6:118976663 | CAAAA | C | 35 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(32): Show |
35 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.2456-623_2456-620d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976663 | |||||||
| chr6:118976952 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2456-908T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118976952 | |||||||
| chr6:118977145 | C | T | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2456-1101G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977145 | |||||||
| chr6:118977266 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2456-1222T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977266 | |||||||
| chr6:118977504 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0249 |
2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2456-1460G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977504 | |||||||
| chr6:118977609 | GATTTC | G | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2456-1570_2456-156 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977609 | |||||||
| chr6:118977665 | G | A | 1 | a0002c0002t0002g0217 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2456-1621C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977665 | |||||||
| chr6:118977672 | G | T | 91 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(88): Show |
91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2456-1628C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977672 | |||||||
| chr6:118977701 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2456-1657A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977701 | |||||||
| chr6:118977986 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(42): Show |
46 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.2455+1379T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118977986 | |||||||
| chr6:118978121 | G | A | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2455+1244C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978121 | |||||||
| chr6:118978191 | G | A | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2455+1174C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978191 | |||||||
| chr6:118978278 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(145): Show |
149 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.2455+1087C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978278 | |||||||
| chr6:118978418 | C | G | 148 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(145): Show |
149 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.2455+947G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978418 | |||||||
| chr6:118978430 | T | G | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2455+935A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978430 | |||||||
| chr6:118978582 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2455+783T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978582 | |||||||
| chr6:118978593 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2455+772C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978593 | |||||||
| chr6:118978921 | A | C | 1 | a0002c0002t0002g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2455+444T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118978921 | |||||||
| chr6:118979263 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG01934.hp1 HG02273.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2455+102C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118979263 | |||||||
| chr6:118979312 | A | G | 95 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(92): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2455+53T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 11/17 | chr6 | 118979312 | |||||||
| chr6:118979788 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2302-270T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118979788 | |||||||
| chr6:118979879 | C | CA | 95 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0063 others(92): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2301+258dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118979879 | |||||||
| chr6:118979910 | C | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0210 a0001c0001t0001g0268 others(1): Show |
4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.2301+228G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118979910 | |||||||
| chr6:118980066 | T | A | 1 | a0001c0001t0001g0254 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2301+72A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 10/17 | chr6 | 118980066 | |||||||
| chr6:118980499 | T | TA | 6 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0100 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2089-150dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118980499 | |||||||
| chr6:118980588 | A | G | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089-238T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118980588 | |||||||
| chr6:118980682 | A | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-332T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118980682 | |||||||
| chr6:118981161 | CTTAAAA | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-817_2089-812d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981161 | |||||||
| chr6:118981192 | A | T | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2089-842T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981192 | |||||||
| chr6:118981430 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2089-1080C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981430 | |||||||
| chr6:118981896 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(31): Show |
36 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2089-1546T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118981896 | |||||||
| chr6:118982170 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(44): Show |
49 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.2089-1820G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982170 | |||||||
| chr6:118982171 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(44): Show |
49 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.2089-1821C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982171 | |||||||
| chr6:118982185 | G | A | 35 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(32): Show |
35 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.2089-1835C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982185 | |||||||
| chr6:118982216 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2089-1866A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982216 | |||||||
| chr6:118982317 | C | G | 35 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(32): Show |
35 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.2089-1967G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982317 | |||||||
| chr6:118982324 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2089-1974A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982324 | |||||||
| chr6:118982397 | T | C | 16 | a0002c0002t0002g0123 a0002c0002t0002g0129 a0002c0002t0002g0143 others(13): Show |
16 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2089-2047A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982397 | |||||||
| chr6:118982624 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0249 |
2 | NA18964.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2089-2274T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982624 | |||||||
| chr6:118982723 | G | A | 1 | a0005c0008t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2089-2373C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982723 | |||||||
| chr6:118982753 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-2403G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118982753 | |||||||
| chr6:118983034 | G | C | 1 | a0001c0003t0001g0048 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2089-2684C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983034 | |||||||
| chr6:118983166 | G | C | 24 | a0001c0001t0002g0001 a0001c0001t0002g0062 a0001c0001t0002g0074 others(21): Show |
25 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.2089-2816C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983166 | |||||||
| chr6:118983244 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-2894A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983244 | |||||||
| chr6:118983388 | C | A | 2 | a0001c0001t0002g0001 a0001c0001t0002g0122 |
3 | HG02818.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2089-3038G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983388 | |||||||
| chr6:118983433 | A | G | 5 | a0001c0001t0001g0190 a0001c0001t0001g0205 a0001c0001t0001g0222 others(2): Show |
5 | HG00423.hp1 NA18747.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-3083T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983433 | |||||||
| chr6:118983460 | T | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2089-3110A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983460 | |||||||
| chr6:118983563 | A | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3213T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983563 | |||||||
| chr6:118983718 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2089-3368C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983718 | |||||||
| chr6:118983834 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2089-3484T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983834 | |||||||
| chr6:118983870 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2089-3520G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983870 | |||||||
| chr6:118983953 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3603C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983953 | |||||||
| chr6:118983994 | C | CA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3645dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118983994 | |||||||
| chr6:118984018 | C | T | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-3668G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984018 | |||||||
| chr6:118984022 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2089-3672G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984022 | |||||||
| chr6:118984023 | G | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-3673C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984023 | |||||||
| chr6:118984149 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2089-3799A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984149 | |||||||
| chr6:118984149 | T | TAA | 91 | a0001c0001t0001g0038 a0001c0001t0001g0083 a0001c0001t0001g0119 others(88): Show |
92 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.2089-3801_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984149 | |||||||
| chr6:118984149 | TAA | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-3801_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984149 | |||||||
| chr6:118984150 | A | T | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2089-3800T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984150 | |||||||
| chr6:118984156 | A | T | 16 | a0001c0001t0001g0063 a0001c0001t0001g0076 a0001c0001t0001g0078 others(13): Show |
16 | HG00733.hp2 HG00738.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.2089-3806T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984156 | |||||||
| chr6:118984158 | A | AAAT | 7 | a0001c0001t0001g0050 a0001c0001t0001g0186 a0001c0001t0001g0188 others(4): Show |
7 | HG00408.hp1 HG01255.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3809_2089-380 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | |||||||
| chr6:118984158 | A | AAT | 21 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0069 others(18): Show |
21 | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.2089-3810_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | |||||||
| chr6:118984158 | A | ATAT | 4 | a0001c0001t0001g0047 a0001c0001t0001g0106 a0001c0001t0001g0132 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-3809_2089-380 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | |||||||
| chr6:118984158 | A | T | 43 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0055 others(40): Show |
44 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.2089-3808T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | |||||||
| chr6:118984158 | AAT | A | 7 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(4): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3810_2089-380 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984158 | |||||||
| chr6:118984159 | AT | A | 18 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(15): Show |
18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089-3810delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984159 | |||||||
| chr6:118984159 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2089-3820_2089-381 others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984159 | |||||||
| chr6:118984160 | T | A | 33 | a0001c0001t0001g0070 a0001c0001t0001g0119 a0001c0001t0001g0170 others(30): Show |
33 | HG00597.hp1 HG00735.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.2089-3810A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984160 | |||||||
| chr6:118984162 | T | A | 24 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(21): Show |
24 | HG00639.hp1 HG00733.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-3812A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984162 | |||||||
| chr6:118984177 | A | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2089-3827T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984177 | |||||||
| chr6:118984179 | T | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0259 others(1): Show |
4 | HG02145.hp1 HG02965.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-3829A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984179 | |||||||
| chr6:118984179 | T | TTA | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(2): Show |
5 | HG01884.hp2 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089-3831_2089-383 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984179 | |||||||
| chr6:118984191 | TTATATTT others(3): Show |
T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-3851_2089-384 others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984191 | |||||||
| chr6:118984247 | T | TTA | 5 | a0001c0001t0001g0138 a0001c0001t0001g0258 a0001c0001t0005g0028 others(2): Show |
5 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089-3899_2089-389 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984247 | |||||||
| chr6:118984376 | C | G | 22 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(19): Show |
22 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2089-4026G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984376 | |||||||
| chr6:118984429 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4079G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984429 | |||||||
| chr6:118984519 | TA | T | 91 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(88): Show |
91 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.2089-4170delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984519 | |||||||
| chr6:118984520 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4170T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984520 | |||||||
| chr6:118984713 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-4363T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984713 | |||||||
| chr6:118984779 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2089-4429A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984779 | |||||||
| chr6:118984998 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4648G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118984998 | |||||||
| chr6:118985034 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-4684T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985034 | |||||||
| chr6:118985095 | G | A | 7 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(4): Show |
7 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-4745C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985095 | |||||||
| chr6:118985128 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(227): Show |
232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.2089-4778A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985128 | |||||||
| chr6:118985247 | T | C | 94 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(91): Show |
94 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2089-4897A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985247 | |||||||
| chr6:118985426 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2089-5076C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985426 | |||||||
| chr6:118985467 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2089-5117C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985467 | |||||||
| chr6:118985593 | G | GTC | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-5245_2089-524 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985593 | |||||||
| chr6:118985603 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-5253A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985603 | |||||||
| chr6:118985618 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-5268G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985618 | |||||||
| chr6:118985817 | G | T | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-5467C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985817 | |||||||
| chr6:118985873 | A | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2089-5523T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985873 | |||||||
| chr6:118985894 | C | T | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2089-5544G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985894 | |||||||
| chr6:118985939 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0050 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2089-5589A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118985939 | |||||||
| chr6:118986109 | C | T | 2 | a0001c0001t0004g0004 a0007c0007t0001g0240 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2089-5759G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986109 | |||||||
| chr6:118986322 | C | T | 1 | a0001c0001t0005g0027 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2089-5972G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986322 | |||||||
| chr6:118986608 | T | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-6258A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986608 | |||||||
| chr6:118986644 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(146): Show |
151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-6294A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986644 | |||||||
| chr6:118986933 | T | C | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-6583A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986933 | |||||||
| chr6:118986958 | ATGC | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-6611_2089-660 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118986958 | |||||||
| chr6:118987008 | G | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2089-6658C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987008 | |||||||
| chr6:118987027 | G | GT | 6 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0100 others(3): Show |
6 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2089-6678dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987027 | |||||||
| chr6:118987032 | A | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2089-6682T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987032 | |||||||
| chr6:118987049 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2089-6699A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987049 | |||||||
| chr6:118987127 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2089-6777G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987127 | |||||||
| chr6:118987566 | A | G | 2 | a0001c0003t0001g0048 a0001c0003t0001g0260 |
2 | HG02717.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2089-7216T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987566 | |||||||
| chr6:118987574 | T | G | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2089-7224A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987574 | |||||||
| chr6:118987972 | A | C | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089-7622T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118987972 | |||||||
| chr6:118988099 | A | G | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2089-7749T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988099 | |||||||
| chr6:118988420 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2089-8070T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988420 | |||||||
| chr6:118988512 | G | A | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089-8162C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988512 | |||||||
| chr6:118988597 | G | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-8247C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988597 | |||||||
| chr6:118988698 | C | T | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-8348G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988698 | |||||||
| chr6:118988725 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2089-8375A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988725 | |||||||
| chr6:118988859 | A | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(226): Show |
231 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2089-8509T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988859 | |||||||
| chr6:118988917 | GA | G | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-8568delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988917 | |||||||
| chr6:118988954 | A | AT | 115 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0042 others(112): Show |
115 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2089-8605dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988954 | |||||||
| chr6:118988954 | A | ATT | 42 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0040 others(39): Show |
44 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.2089-8606_2089-860 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118988954 | |||||||
| chr6:118989119 | G | A | 5 | a0003c0004t0001g0093 a0003c0004t0001g0094 a0003c0004t0001g0095 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-8769C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989119 | |||||||
| chr6:118989197 | G | A | 4 | a0001c0001t0002g0001 a0001c0001t0002g0062 a0001c0001t0002g0074 others(1): Show |
5 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2089-8847C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989197 | |||||||
| chr6:118989227 | CT | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(146): Show |
151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-8878delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989227 | |||||||
| chr6:118989253 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0211 |
2 | HG04115.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2089-8903G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989253 | |||||||
| chr6:118989428 | A | G | 5 | a0001c0001t0001g0203 a0001c0001t0001g0210 a0001c0001t0001g0268 others(2): Show |
5 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-9078T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989428 | |||||||
| chr6:118989498 | A | AGTGACAC others(54): Show |
18 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(15): Show |
18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089-9209_2089-914 others(65): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989498 | |||||||
| chr6:118989525 | T | C | 1 | a0001c0001t0004g0005 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2089-9175A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989525 | |||||||
| chr6:118989650 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-9300A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989650 | |||||||
| chr6:118989787 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-9437A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989787 | |||||||
| chr6:118989801 | C | CATTT | 79 | a0001c0001t0001g0038 a0001c0001t0001g0052 a0001c0001t0001g0065 others(76): Show |
79 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.2089-9455_2089-945 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | |||||||
| chr6:118989801 | C | CATTTATT others(1): Show |
24 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(21): Show |
24 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-9459_2089-945 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | |||||||
| chr6:118989801 | C | CATTTATT others(5): Show |
2 | a0001c0001t0004g0010 a0001c0001t0004g0012 |
2 | NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2089-9463_2089-945 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | |||||||
| chr6:118989801 | CATTT | C | 24 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(21): Show |
24 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-9455_2089-945 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | |||||||
| chr6:118989801 | CATTTATT others(1): Show |
C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0113 others(27): Show |
32 | HG00735.hp2 HG00741.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.2089-9459_2089-945 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | |||||||
| chr6:118989801 | CATTTATT others(9): Show |
C | 1 | a0001c0001t0002g0197 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2089-9467_2089-945 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989801 | |||||||
| chr6:118989953 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2089-9603G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989953 | |||||||
| chr6:118989982 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-9632G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989982 | |||||||
| chr6:118989985 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(226): Show |
231 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2089-9635A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118989985 | |||||||
| chr6:118990197 | T | C | 5 | a0001c0001t0001g0155 a0001c0001t0001g0160 a0001c0001t0001g0166 others(2): Show |
5 | NA18954.hp1 NA18975.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.2089-9847A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990197 | |||||||
| chr6:118990245 | G | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0050 |
2 | HG01884.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2089-9895C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990245 | |||||||
| chr6:118990400 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2089-10050G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990400 | |||||||
| chr6:118990491 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-10141C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990491 | |||||||
| chr6:118990507 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0232 |
2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2089-10157A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990507 | |||||||
| chr6:118990589 | C | CCAG | 149 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(146): Show |
151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-10240_2089-10 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990589 | |||||||
| chr6:118990590 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(146): Show |
151 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.2089-10240T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990590 | |||||||
| chr6:118990664 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2089-10314C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990664 | |||||||
| chr6:118990686 | C | T | 1 | a0001c0001t0004g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2089-10336G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990686 | |||||||
| chr6:118990720 | C | CA | 24 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(21): Show |
24 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2089-10371dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990720 | |||||||
| chr6:118990924 | T | C | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2089-10574A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990924 | |||||||
| chr6:118990924 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2089-10574A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118990924 | |||||||
| chr6:118991159 | T | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2089-10809A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991159 | |||||||
| chr6:118991163 | AT | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0105 others(4): Show |
7 | HG01169.hp1 HG01515.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2089-10814delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991163 | |||||||
| chr6:118991225 | C | T | 16 | a0002c0002t0002g0123 a0002c0002t0002g0129 a0002c0002t0002g0143 others(13): Show |
16 | HG00597.hp1 HG00735.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.2089-10875G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991225 | |||||||
| chr6:118991426 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2089-11076C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991426 | |||||||
| chr6:118991441 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-11091C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991441 | |||||||
| chr6:118991445 | G | T | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2089-11095C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991445 | |||||||
| chr6:118991484 | T | C | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2089-11134A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991484 | |||||||
| chr6:118991711 | G | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(226): Show |
231 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2088+11188C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991711 | |||||||
| chr6:118991751 | C | CT | 16 | a0001c0001t0001g0085 a0001c0001t0001g0146 a0001c0001t0001g0158 others(13): Show |
16 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2088+11147dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | |||||||
| chr6:118991751 | C | CTTT | 6 | a0001c0001t0002g0001 a0001c0001t0002g0062 a0001c0001t0002g0121 others(3): Show |
7 | HG02258.hp1 HG02486.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+11145_2088+11 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | |||||||
| chr6:118991751 | C | CTTTT | 12 | a0001c0001t0001g0269 a0001c0001t0002g0074 a0001c0001t0002g0198 others(9): Show |
12 | HG00642.hp2 HG00741.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.2088+11144_2088+11 others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | |||||||
| chr6:118991751 | CT | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(43): Show |
47 | HG00140.hp2 HG00423.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.2088+11147delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | |||||||
| chr6:118991751 | CTT | C | 132 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(129): Show |
132 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.2088+11146_2088+11 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | |||||||
| chr6:118991751 | CTTT | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0102 others(3): Show |
6 | HG00741.hp2 HG01168.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.2088+11145_2088+11 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | |||||||
| chr6:118991751 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2088+11134_2088+11 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991751 | |||||||
| chr6:118991780 | T | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+11119A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991780 | |||||||
| chr6:118991908 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+10991C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991908 | |||||||
| chr6:118991948 | T | A | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2088+10951A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118991948 | |||||||
| chr6:118992120 | T | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.2088+10779A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992120 | |||||||
| chr6:118992140 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2088+10759T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992140 | |||||||
| chr6:118992258 | T | C | 229 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(226): Show |
231 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2088+10641A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992258 | |||||||
| chr6:118992352 | A | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(143): Show |
147 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2088+10547T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992352 | |||||||
| chr6:118992410 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2088+10489A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992410 | |||||||
| chr6:118992468 | A | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(144): Show |
148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+10431T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992468 | |||||||
| chr6:118992496 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+10403T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118992496 | |||||||
| chr6:118993020 | C | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+9879G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993020 | |||||||
| chr6:118993034 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2088+9865T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993034 | |||||||
| chr6:118993227 | G | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+9672C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993227 | |||||||
| chr6:118993429 | A | G | 1 | a0001c0001t0004g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2088+9470T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993429 | |||||||
| chr6:118993513 | CT | C | 22 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(19): Show |
22 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2088+9385delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993513 | |||||||
| chr6:118993517 | T | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(144): Show |
148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+9382A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993517 | |||||||
| chr6:118993610 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(144): Show |
148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+9289A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993610 | |||||||
| chr6:118993668 | C | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+9231G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993668 | |||||||
| chr6:118993728 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2088+9171C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993728 | |||||||
| chr6:118993780 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2088+9119A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993780 | |||||||
| chr6:118993959 | T | G | 147 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(144): Show |
148 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.2088+8940A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993959 | |||||||
| chr6:118993981 | C | A | 13 | a0001c0001t0001g0063 a0001c0001t0001g0112 a0001c0001t0004g0005 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2088+8918G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118993981 | |||||||
| chr6:118994330 | A | AAAAT | 94 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(91): Show |
94 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2088+8565_2088+856 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994330 | |||||||
| chr6:118994368 | G | C | 5 | a0001c0001t0001g0106 a0001c0001t0004g0009 a0001c0001t0004g0010 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2088+8531C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994368 | |||||||
| chr6:118994540 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2088+8359C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994540 | |||||||
| chr6:118994557 | G | A | 20 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0052 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2088+8342C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994557 | |||||||
| chr6:118994596 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2088+8303C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994596 | |||||||
| chr6:118994685 | C | CAAAA | 16 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0098 others(13): Show |
16 | HG00609.hp2 HG01243.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2088+8213_2088+821 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | |||||||
| chr6:118994685 | C | CAAAATAA others(1): Show |
5 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0168 others(2): Show |
5 | HG03041.hp2 HG03490.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.2088+8213_2088+821 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | |||||||
| chr6:118994685 | CTAAA | C | 67 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(64): Show |
67 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.2088+8210_2088+821 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | |||||||
| chr6:118994685 | CTAAATAA others(1): Show |
C | 81 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(78): Show |
81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2088+8206_2088+821 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | |||||||
| chr6:118994685 | CTAAATAA others(5): Show |
C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0132 others(5): Show |
9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2088+8202_2088+821 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | |||||||
| chr6:118994685 | CTAAATAA others(9): Show |
C | 12 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2088+8198_2088+821 others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994685 | |||||||
| chr6:118994686 | T | A | 93 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0052 others(90): Show |
94 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.2088+8213A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994686 | |||||||
| chr6:118994690 | T | A | 66 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(63): Show |
66 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.2088+8209A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994690 | |||||||
| chr6:118994694 | T | A | 81 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(78): Show |
81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2088+8205A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994694 | |||||||
| chr6:118994698 | T | A | 8 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0132 others(5): Show |
9 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2088+8201A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994698 | |||||||
| chr6:118994702 | T | A | 12 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2088+8197A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994702 | |||||||
| chr6:118994726 | TAAATAAA others(5): Show |
T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0108 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2088+8161_2088+817 others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994726 | |||||||
| chr6:118994730 | TAAATAAA others(1): Show |
T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(5): Show |
8 | HG00733.hp1 HG01106.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994730 | |||||||
| chr6:118994732 | A | G | 1 | a0001c0003t0001g0048 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2088+8167T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994732 | |||||||
| chr6:118994733 | A | C | 1 | a0001c0003t0001g0048 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2088+8166T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994733 | |||||||
| chr6:118994734 | TAAAA | T | 8 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
8 | HG01069.hp2 HG01071.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994734 | |||||||
| chr6:118994736 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(139): Show |
144 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2088+8163T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994736 | |||||||
| chr6:118994737 | A | ATAAATAG others(1): Show |
3 | a0001c0001t0002g0122 a0002c0002t0002g0206 a0007c0007t0001g0240 |
3 | HG00597.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994737 | |||||||
| chr6:118994737 | A | ATAGC | 4 | a0001c0001t0001g0042 a0001c0003t0001g0142 a0001c0003t0001g0260 others(1): Show |
4 | HG02559.hp2 HG02717.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+8161_2088+816 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994737 | |||||||
| chr6:118994737 | A | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(139): Show |
144 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.2088+8162T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118994737 | |||||||
| chr6:118995005 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0004g0013 |
2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2088+7894T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995005 | |||||||
| chr6:118995215 | G | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+7684C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995215 | |||||||
| chr6:118995555 | C | T | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+7344G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995555 | |||||||
| chr6:118995681 | T | C | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+7218A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995681 | |||||||
| chr6:118995825 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2088+7074A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995825 | |||||||
| chr6:118995976 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0178 |
2 | HG02135.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2088+6923T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118995976 | |||||||
| chr6:118996257 | T | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2088+6642A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996257 | |||||||
| chr6:118996413 | T | C | 2 | a0001c0001t0002g0001 a0001c0001t0002g0122 |
3 | HG02818.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2088+6486A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996413 | |||||||
| chr6:118996678 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+6221A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996678 | |||||||
| chr6:118996684 | A | G | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+6215T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996684 | |||||||
| chr6:118996776 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2088+6123C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996776 | |||||||
| chr6:118996881 | A | AT | 13 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0090 others(10): Show |
13 | HG01069.hp1 HG02622.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2088+6017dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996881 | |||||||
| chr6:118996881 | A | ATT | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+6016_2088+601 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118996881 | |||||||
| chr6:118997003 | C | T | 1 | a0001c0001t0005g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2088+5896G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997003 | |||||||
| chr6:118997008 | G | GAAGAC | 101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0046 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5890_2088+589 others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997008 | |||||||
| chr6:118997010 | C | CTGTGGGA others(1): Show |
101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0046 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5888_2088+588 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997010 | |||||||
| chr6:118997011 | A | T | 101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0046 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5888T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997011 | |||||||
| chr6:118997012 | C | A | 101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0046 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2088+5887G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997012 | |||||||
| chr6:118997217 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+5682C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997217 | |||||||
| chr6:118997245 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(195): Show |
200 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.2088+5654A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997245 | |||||||
| chr6:118997282 | C | G | 1 | a0001c0006t0005g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2088+5617G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997282 | |||||||
| chr6:118997304 | G | A | 1 | a0005c0008t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2088+5595C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997304 | |||||||
| chr6:118997324 | CA | C | 179 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(176): Show |
180 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.2088+5574delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997324 | |||||||
| chr6:118997356 | A | T | 2 | a0001c0001t0004g0004 a0007c0007t0001g0240 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2088+5543T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997356 | |||||||
| chr6:118997368 | G | A | 18 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(15): Show |
18 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.2088+5531C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997368 | |||||||
| chr6:118997455 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2088+5444G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997455 | |||||||
| chr6:118997611 | C | T | 1 | a0001c0001t0005g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2088+5288G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997611 | |||||||
| chr6:118997634 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2088+5265A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997634 | |||||||
| chr6:118997843 | C | T | 1 | a0001c0001t0003g0017 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2088+5056G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997843 | |||||||
| chr6:118997887 | C | G | 89 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(86): Show |
89 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2088+5012G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997887 | |||||||
| chr6:118997920 | G | T | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2088+4979C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118997920 | |||||||
| chr6:118998028 | T | C | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2088+4871A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998028 | |||||||
| chr6:118998047 | CTA | C | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+4850_2088+485 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998047 | |||||||
| chr6:118998216 | C | A | 1 | a0001c0001t0008g0283 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2088+4683G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998216 | |||||||
| chr6:118998359 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2088+4540T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998359 | |||||||
| chr6:118998518 | CA | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+4380delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998518 | |||||||
| chr6:118998676 | G | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2088+4223C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998676 | |||||||
| chr6:118998707 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2088+4192C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998707 | |||||||
| chr6:118998829 | C | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+4070G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998829 | |||||||
| chr6:118998841 | G | C | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+4058C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118998841 | |||||||
| chr6:118999109 | T | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2088+3790A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999109 | |||||||
| chr6:118999146 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2088+3753C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999146 | |||||||
| chr6:118999148 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+3751T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999148 | |||||||
| chr6:118999578 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2088+3321A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999578 | |||||||
| chr6:118999617 | A | G | 29 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(26): Show |
30 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2088+3282T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999617 | |||||||
| chr6:118999669 | A | T | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2088+3230T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999669 | |||||||
| chr6:118999815 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2088+3084G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 118999815 | |||||||
| chr6:119000040 | C | T | 1 | a0004c0010t0004g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2088+2859G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000040 | |||||||
| chr6:119000166 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2088+2733C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000166 | |||||||
| chr6:119000305 | A | G | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+2594T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000305 | |||||||
| chr6:119000314 | G | A | 25 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(22): Show |
26 | HG00597.hp1 HG00735.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.2088+2585C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000314 | |||||||
| chr6:119000386 | T | C | 94 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(91): Show |
94 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.2088+2513A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000386 | |||||||
| chr6:119000529 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG00741.hp2 NA18995.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+2370A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000529 | |||||||
| chr6:119000575 | G | A | 1 | a0001c0001t0002g0001 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2088+2324C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000575 | |||||||
| chr6:119000608 | T | C | 1 | a0002c0002t0002g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2088+2291A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000608 | |||||||
| chr6:119000720 | G | A | 1 | a0001c0003t0001g0140 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2088+2179C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000720 | |||||||
| chr6:119000928 | G | T | 2 | a0002c0002t0001g0235 a0002c0002t0002g0189 |
2 | HG02071.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.2088+1971C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119000928 | |||||||
| chr6:119001257 | G | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+1642C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001257 | |||||||
| chr6:119001303 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.2088+1596A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001303 | |||||||
| chr6:119001391 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2088+1508G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001391 | |||||||
| chr6:119001536 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2088+1363T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001536 | |||||||
| chr6:119001548 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2088+1351A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001548 | |||||||
| chr6:119001661 | C | T | 29 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(26): Show |
30 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.2088+1238G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001661 | |||||||
| chr6:119001719 | T | G | 35 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(32): Show |
35 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.2088+1180A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001719 | |||||||
| chr6:119001827 | C | T | 88 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(85): Show |
88 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2088+1072G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001827 | |||||||
| chr6:119001895 | G | T | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2088+1004C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119001895 | |||||||
| chr6:119002271 | G | T | 1 | a0001c0001t0005g0029 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2088+628C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002271 | |||||||
| chr6:119002384 | A | G | 1 | a0001c0001t0003g0015 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2088+515T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002384 | |||||||
| chr6:119002665 | TA | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2088+233delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002665 | |||||||
| chr6:119002822 | A | T | 90 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(87): Show |
90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2088+77T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 9/17 | chr6 | 119002822 | |||||||
| chr6:119003343 | C | T | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1937+158G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 8/17 | chr6 | 119003343 | |||||||
| chr6:119003348 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1937+153C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 8/17 | chr6 | 119003348 | |||||||
| chr6:119003438 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1937+63A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 8/17 | chr6 | 119003438 | |||||||
| chr6:119003658 | T | G | 13 | a0001c0001t0001g0063 a0001c0001t0001g0112 a0001c0001t0004g0005 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1816-36A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003658 | |||||||
| chr6:119003711 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-89G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003711 | |||||||
| chr6:119003798 | A | G | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-176T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003798 | |||||||
| chr6:119003822 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0102 |
2 | HG01168.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1816-200A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003822 | |||||||
| chr6:119003870 | A | G | 13 | a0001c0001t0001g0063 a0001c0001t0001g0112 a0001c0001t0004g0005 others(10): Show |
13 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1816-248T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119003870 | |||||||
| chr6:119004128 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1816-506A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004128 | |||||||
| chr6:119004255 | A | G | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1816-633T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004255 | |||||||
| chr6:119004536 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-914A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004536 | |||||||
| chr6:119004567 | G | C | 1 | a0002c0002t0002g0228 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1816-945C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004567 | |||||||
| chr6:119004753 | G | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1816-1131C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004753 | |||||||
| chr6:119004947 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1816-1325G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119004947 | |||||||
| chr6:119005020 | C | A | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-1398G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005020 | |||||||
| chr6:119005171 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1815+1276G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005171 | |||||||
| chr6:119005210 | T | C | 27 | a0001c0001t0001g0269 a0001c0001t0002g0001 a0001c0001t0002g0062 others(24): Show |
28 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1815+1237A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005210 | |||||||
| chr6:119005273 | T | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1815+1174A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005273 | |||||||
| chr6:119005408 | G | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+1039C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005408 | |||||||
| chr6:119005521 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1815+926G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005521 | |||||||
| chr6:119005845 | CAG | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0113 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+600_1815+601d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005845 | |||||||
| chr6:119005931 | C | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0130 a0001c0001t0001g0201 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+516G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005931 | |||||||
| chr6:119005947 | G | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1815+500C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119005947 | |||||||
| chr6:119006192 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1815+255T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119006192 | |||||||
| chr6:119006366 | G | C | 1 | a0001c0001t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1815+81C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 7/17 | chr6 | 119006366 | |||||||
| chr6:119006627 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0004g0005 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-19G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119006627 | |||||||
| chr6:119006635 | A | G | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-27T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119006635 | |||||||
| chr6:119006743 | G | A | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1654-135C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119006743 | |||||||
| chr6:119007313 | T | C | 1 | a0001c0003t0005g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1654-705A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007313 | |||||||
| chr6:119007352 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1654-744C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007352 | |||||||
| chr6:119007400 | C | T | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1654-792G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007400 | |||||||
| chr6:119007434 | G | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1654-826C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007434 | |||||||
| chr6:119007460 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1654-852C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007460 | |||||||
| chr6:119007667 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1654-1059C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007667 | |||||||
| chr6:119007668 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1654-1060G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007668 | |||||||
| chr6:119007770 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1654-1162C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007770 | |||||||
| chr6:119007802 | G | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG00639.hp2 HG01168.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-1194C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007802 | |||||||
| chr6:119007813 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-1205G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007813 | |||||||
| chr6:119007866 | G | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-1258C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007866 | |||||||
| chr6:119007889 | G | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1654-1281C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007889 | |||||||
| chr6:119007941 | G | GA | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(6): Show |
9 | HG00741.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1654-1334dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119007941 | |||||||
| chr6:119008222 | G | A | 90 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(87): Show |
90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1654-1614C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008222 | |||||||
| chr6:119008243 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-1635G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008243 | |||||||
| chr6:119008295 | G | T | 17 | a0001c0001t0001g0150 a0001c0001t0001g0229 a0001c0001t0001g0277 others(14): Show |
17 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1654-1687C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008295 | |||||||
| chr6:119008336 | G | A | 1 | a0003c0004t0001g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1654-1728C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008336 | |||||||
| chr6:119008344 | G | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0270 |
2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1654-1736C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008344 | |||||||
| chr6:119008393 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(155): Show |
160 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1654-1785G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008393 | |||||||
| chr6:119008474 | A | G | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1654-1866T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008474 | |||||||
| chr6:119008604 | G | A | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1654-1996C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008604 | |||||||
| chr6:119008779 | A | G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1654-2171T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008779 | |||||||
| chr6:119008800 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1654-2192T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008800 | |||||||
| chr6:119008837 | T | C | 150 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(147): Show |
152 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1654-2229A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119008837 | |||||||
| chr6:119009014 | T | C | 15 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(12): Show |
15 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.1653+2295A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009014 | |||||||
| chr6:119009077 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1653+2232G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009077 | |||||||
| chr6:119009103 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+2206A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009103 | |||||||
| chr6:119009139 | G | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0120 others(31): Show |
36 | HG00597.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.1653+2170C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009139 | |||||||
| chr6:119009258 | G | C | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1653+2051C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009258 | |||||||
| chr6:119009643 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1653+1666A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009643 | |||||||
| chr6:119009813 | C | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0131 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1653+1496G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009813 | |||||||
| chr6:119009905 | T | G | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1653+1404A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009905 | |||||||
| chr6:119009949 | A | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(227): Show |
232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1653+1360T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119009949 | |||||||
| chr6:119010025 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1653+1284T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010025 | |||||||
| chr6:119010219 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0063 |
3 | HG01168.hp2 HG01169.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1653+1090G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010219 | |||||||
| chr6:119010236 | G | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1653+1073C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010236 | |||||||
| chr6:119010402 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1653+907T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010402 | |||||||
| chr6:119010723 | T | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(101): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1653+586A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010723 | |||||||
| chr6:119010939 | T | A | 93 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(90): Show |
93 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1653+370A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010939 | |||||||
| chr6:119010995 | G | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1653+314C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119010995 | |||||||
| chr6:119011292 | G | T | 4 | a0001c0001t0001g0203 a0001c0001t0001g0210 a0001c0001t0001g0268 others(1): Show |
4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1653+17C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 6/17 | chr6 | 119011292 | |||||||
| chr6:119011452 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1531-21T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011452 | |||||||
| chr6:119011484 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1531-53A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011484 | |||||||
| chr6:119011553 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1531-122G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011553 | |||||||
| chr6:119011608 | A | C | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-177T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011608 | |||||||
| chr6:119011765 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1531-334A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011765 | |||||||
| chr6:119011791 | G | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(227): Show |
232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1531-360C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119011791 | |||||||
| chr6:119012035 | C | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1531-604G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012035 | |||||||
| chr6:119012109 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0272 |
2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1531-678G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012109 | |||||||
| chr6:119012260 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1531-829C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012260 | |||||||
| chr6:119012273 | A | T | 104 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1531-842T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012273 | |||||||
| chr6:119012332 | G | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1531-901C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012332 | |||||||
| chr6:119012356 | G | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1531-925C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012356 | |||||||
| chr6:119012406 | G | T | 1 | a0002c0002t0002g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1531-975C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012406 | |||||||
| chr6:119012539 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1531-1108G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012539 | |||||||
| chr6:119012607 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1531-1176G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012607 | |||||||
| chr6:119012643 | A | G | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1531-1212T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012643 | |||||||
| chr6:119012693 | T | G | 1 | a0001c0001t0003g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1531-1262A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012693 | |||||||
| chr6:119012964 | G | A | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1531-1533C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119012964 | |||||||
| chr6:119013107 | TA | T | 230 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(227): Show |
232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1531-1677delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013107 | |||||||
| chr6:119013193 | G | A | 3 | a0001c0003t0001g0133 a0001c0003t0001g0136 a0001c0003t0001g0142 |
3 | HG00639.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1531-1762C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013193 | |||||||
| chr6:119013261 | A | T | 1 | a0005c0008t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1531-1830T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013261 | |||||||
| chr6:119013360 | G | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-1929C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013360 | |||||||
| chr6:119013716 | T | C | 1 | a0001c0001t0001g0037 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1531-2285A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013716 | |||||||
| chr6:119013767 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1531-2336A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119013767 | |||||||
| chr6:119014079 | T | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1531-2648A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014079 | |||||||
| chr6:119014117 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530+2630T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014117 | |||||||
| chr6:119014237 | C | G | 1 | a0001c0006t0005g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1530+2510G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014237 | |||||||
| chr6:119014670 | A | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(227): Show |
232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1530+2077T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014670 | |||||||
| chr6:119014684 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1530+2063T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014684 | |||||||
| chr6:119014700 | A | G | 104 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1530+2047T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014700 | |||||||
| chr6:119014724 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1530+2023T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014724 | |||||||
| chr6:119014786 | C | T | 104 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1530+1961G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014786 | |||||||
| chr6:119014853 | G | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1530+1894C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119014853 | |||||||
| chr6:119015063 | C | CA | 21 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(18): Show |
21 | HG00639.hp1 HG02257.hp2 HG02293.hp2 others(18): Show |
intron_variant | MODIFIER | c.1530+1683dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015063 | |||||||
| chr6:119015156 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1530+1591A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015156 | |||||||
| chr6:119015194 | G | A | 5 | a0001c0001t0001g0037 a0001c0001t0002g0001 a0001c0001t0002g0062 others(2): Show |
6 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1530+1553C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015194 | |||||||
| chr6:119015258 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1530+1489C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015258 | |||||||
| chr6:119015294 | C | T | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1530+1453G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015294 | |||||||
| chr6:119015295 | G | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1530+1452C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015295 | |||||||
| chr6:119015301 | C | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(96): Show |
100 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1530+1446G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015301 | |||||||
| chr6:119015355 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1530+1392G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015355 | |||||||
| chr6:119015356 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1530+1391C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015356 | |||||||
| chr6:119015369 | G | A | 5 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0131 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+1378C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015369 | |||||||
| chr6:119015480 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1530+1267G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015480 | |||||||
| chr6:119015688 | C | T | 108 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(105): Show |
109 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1530+1059G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015688 | |||||||
| chr6:119015692 | C | T | 5 | a0003c0004t0001g0093 a0003c0004t0001g0094 a0003c0004t0001g0095 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+1055G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015692 | |||||||
| chr6:119015753 | G | A | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1530+994C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015753 | |||||||
| chr6:119015816 | T | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0100 others(3): Show |
6 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1530+931A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015816 | |||||||
| chr6:119015894 | C | A | 1 | a0001c0001t0003g0024 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1530+853G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015894 | |||||||
| chr6:119015895 | A | T | 1 | a0001c0001t0003g0024 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1530+852T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015895 | |||||||
| chr6:119015962 | C | G | 104 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1530+785G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015962 | |||||||
| chr6:119015967 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1530+780T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119015967 | |||||||
| chr6:119016050 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(96): Show |
100 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1530+697A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016050 | |||||||
| chr6:119016093 | C | T | 9 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0192 others(6): Show |
9 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.1530+654G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016093 | |||||||
| chr6:119016108 | T | C | 1 | a0001c0001t0006g0035 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1530+639A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016108 | |||||||
| chr6:119016148 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1530+599T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016148 | |||||||
| chr6:119016160 | G | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1530+587C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016160 | |||||||
| chr6:119016219 | C | T | 11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0068 others(8): Show |
11 | HG00735.hp1 HG00741.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1530+528G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016219 | |||||||
| chr6:119016233 | G | A | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1530+514C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016233 | |||||||
| chr6:119016331 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1530+416G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016331 | |||||||
| chr6:119016333 | A | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1530+414T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016333 | |||||||
| chr6:119016443 | C | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0258 a0001c0001t0005g0028 others(2): Show |
5 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530+304G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016443 | |||||||
| chr6:119016445 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(115): Show |
120 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1530+302C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016445 | |||||||
| chr6:119016459 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0159 |
2 | HG01192.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1530+288T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016459 | |||||||
| chr6:119016467 | C | T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0131 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+280G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016467 | |||||||
| chr6:119016567 | C | T | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0060 others(1): Show |
4 | HG00140.hp2 HG00642.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1530+180G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 5/17 | chr6 | 119016567 | |||||||
| chr6:119017007 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1333-63A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017007 | |||||||
| chr6:119017019 | A | G | 1 | a0001c0006t0005g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1333-75T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017019 | |||||||
| chr6:119017358 | C | T | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1333-414G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017358 | |||||||
| chr6:119017420 | A | C | 120 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(117): Show |
121 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.1333-476T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017420 | |||||||
| chr6:119017429 | CAG | C | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1333-487_1333-486d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017429 | |||||||
| chr6:119017497 | CA | C | 16 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(13): Show |
16 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1333-554delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017497 | |||||||
| chr6:119017546 | A | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1333-602T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017546 | |||||||
| chr6:119017582 | T | A | 1 | a0004c0010t0004g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1333-638A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017582 | |||||||
| chr6:119017670 | T | C | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1333-726A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017670 | |||||||
| chr6:119017672 | G | C | 1 | a0001c0001t0003g0022 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1333-728C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017672 | |||||||
| chr6:119017899 | C | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG00733.hp1 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1333-955G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017899 | |||||||
| chr6:119017900 | A | T | 1 | a0002c0002t0002g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1333-956T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017900 | |||||||
| chr6:119017917 | C | T | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1333-973G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119017917 | |||||||
| chr6:119018131 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1333-1187G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018131 | |||||||
| chr6:119018340 | A | G | 1 | a0005c0008t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1333-1396T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018340 | |||||||
| chr6:119018472 | G | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1332+1506C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018472 | |||||||
| chr6:119018510 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1332+1468T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018510 | |||||||
| chr6:119018516 | G | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0001g0126 |
3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1332+1462C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018516 | |||||||
| chr6:119018570 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0087 |
2 | HG01123.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1332+1408A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018570 | |||||||
| chr6:119018643 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1332+1335A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018643 | |||||||
| chr6:119018741 | C | T | 5 | a0001c0001t0001g0155 a0001c0001t0001g0160 a0001c0001t0001g0166 others(2): Show |
5 | NA18954.hp1 NA18975.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332+1237G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018741 | |||||||
| chr6:119018893 | TAGAC | T | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1332+1081_1332+108 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018893 | |||||||
| chr6:119018949 | A | G | 114 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(111): Show |
115 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1332+1029T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018949 | |||||||
| chr6:119018980 | T | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332+998A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119018980 | |||||||
| chr6:119019002 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1332+976T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019002 | |||||||
| chr6:119019098 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1332+880C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019098 | |||||||
| chr6:119019145 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1332+833G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019145 | |||||||
| chr6:119019254 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1332+724A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019254 | |||||||
| chr6:119019423 | T | C | 226 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1332+555A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019423 | |||||||
| chr6:119019716 | T | C | 120 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(117): Show |
121 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.1332+262A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019716 | |||||||
| chr6:119019751 | A | G | 12 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(9): Show |
12 | HG00639.hp1 HG01433.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332+227T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019751 | |||||||
| chr6:119019773 | T | C | 49 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(46): Show |
49 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1332+205A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019773 | |||||||
| chr6:119019783 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0201 |
3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1332+195T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 4/17 | chr6 | 119019783 | |||||||
| chr6:119020169 | A | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-10T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020169 | |||||||
| chr6:119020343 | G | A | 10 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(7): Show |
11 | HG00741.hp1 HG01099.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1151-184C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020343 | |||||||
| chr6:119020419 | G | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(223): Show |
228 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1151-260C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020419 | |||||||
| chr6:119020630 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1151-471C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020630 | |||||||
| chr6:119020735 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0100 a0001c0001t0001g0257 |
3 | HG02559.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1151-576C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020735 | |||||||
| chr6:119020835 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1151-676C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020835 | |||||||
| chr6:119020840 | C | G | 97 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(94): Show |
97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1151-681G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119020840 | |||||||
| chr6:119021012 | G | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | NA18949.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.1151-853C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021012 | |||||||
| chr6:119021069 | C | T | 104 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1151-910G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021069 | |||||||
| chr6:119021239 | CTGA | C | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0004g0008 |
3 | HG02145.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1151-1083_1151-108 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021239 | |||||||
| chr6:119021325 | T | C | 1 | a0002c0002t0002g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1151-1166A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021325 | |||||||
| chr6:119021342 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-1183G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021342 | |||||||
| chr6:119021679 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1150+1266G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021679 | |||||||
| chr6:119021805 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+1140C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021805 | |||||||
| chr6:119021934 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1150+1011G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119021934 | |||||||
| chr6:119022050 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1150+895A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022050 | |||||||
| chr6:119022053 | C | CT | 19 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0071 others(16): Show |
19 | HG00639.hp2 HG00735.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.1150+891dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022053 | |||||||
| chr6:119022053 | CT | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(117): Show |
122 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1150+891delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022053 | |||||||
| chr6:119022053 | CTT | C | 9 | a0001c0001t0001g0041 a0001c0001t0001g0119 a0001c0001t0001g0120 others(6): Show |
9 | HG01099.hp2 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150+890_1150+891d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022053 | |||||||
| chr6:119022261 | G | A | 5 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0131 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+684C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022261 | |||||||
| chr6:119022374 | G | A | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+571C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022374 | |||||||
| chr6:119022382 | T | C | 3 | a0001c0001t0001g0132 a0001c0001t0001g0267 a0001c0001t0001g0269 |
3 | HG02004.hp2 HG02698.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1150+563A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022382 | |||||||
| chr6:119022507 | G | A | 2 | a0005c0008t0001g0064 a0008c0005t0001g0036 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1150+438C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022507 | |||||||
| chr6:119022693 | G | A | 1 | a0001c0003t0005g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1150+252C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022693 | |||||||
| chr6:119022825 | C | T | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1150+120G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022825 | |||||||
| chr6:119022855 | C | T | 47 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(44): Show |
47 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1150+90G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022855 | |||||||
| chr6:119022899 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1150+46C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 3/17 | chr6 | 119022899 | |||||||
| chr6:119023091 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1015-11A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023091 | |||||||
| chr6:119023292 | C | A | 1 | a0001c0001t0004g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1015-212G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023292 | |||||||
| chr6:119023343 | A | G | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1015-263T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023343 | |||||||
| chr6:119023364 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(121): Show |
126 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1015-284G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023364 | |||||||
| chr6:119023381 | A | C | 92 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0083 others(89): Show |
92 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1015-301T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023381 | |||||||
| chr6:119023552 | T | TC | 3 | a0001c0001t0001g0047 a0002c0002t0002g0129 a0004c0010t0004g0006 |
3 | HG01891.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1014+406dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023552 | |||||||
| chr6:119023553 | CCG | C | 76 | a0001c0001t0001g0037 a0001c0001t0001g0052 a0001c0001t0001g0053 others(73): Show |
76 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1014+404_1014+405d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023553 | |||||||
| chr6:119023554 | CG | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(107): Show |
111 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.1014+404delC | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023554 | |||||||
| chr6:119023555 | G | C | 44 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0047 others(41): Show |
45 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1014+404C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023555 | |||||||
| chr6:119023555 | G | GC | 14 | a0001c0001t0001g0085 a0001c0001t0001g0154 a0001c0001t0001g0156 others(11): Show |
14 | HG01069.hp1 HG01192.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1014+403dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023555 | |||||||
| chr6:119023562 | C | G | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(12): Show |
15 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1014+397G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023562 | |||||||
| chr6:119023563 | C | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0131 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014+396G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023563 | |||||||
| chr6:119023564 | C | G | 52 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(49): Show |
52 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.1014+395G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023564 | |||||||
| chr6:119023565 | C | G | 1 | a0005c0008t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1014+394G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023565 | |||||||
| chr6:119023672 | G | A | 2 | a0002c0002t0002g0123 a0002c0002t0002g0129 |
2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1014+287C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023672 | |||||||
| chr6:119023822 | T | TA | 7 | a0001c0001t0001g0128 a0001c0001t0001g0145 a0001c0001t0001g0250 others(4): Show |
8 | HG02615.hp2 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1014+136dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023822 | |||||||
| chr6:119023822 | TA | T | 80 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0055 others(77): Show |
80 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.1014+136delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023822 | |||||||
| chr6:119023822 | TAA | T | 10 | a0001c0001t0001g0046 a0001c0001t0001g0058 a0001c0001t0001g0132 others(7): Show |
10 | HG02293.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1014+135_1014+136d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023822 | |||||||
| chr6:119023823 | A | T | 1 | a0001c0001t0004g0005 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1014+136T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 2/17 | chr6 | 119023823 | |||||||
| chr6:119024820 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.160-7C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024820 | |||||||
| chr6:119024839 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-26C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024839 | |||||||
| chr6:119024845 | T | C | 107 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(104): Show |
107 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.160-32A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024845 | |||||||
| chr6:119024963 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-150A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119024963 | |||||||
| chr6:119025030 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-217T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025030 | |||||||
| chr6:119025134 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.160-321T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025134 | |||||||
| chr6:119025283 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0238 |
2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.160-470A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025283 | |||||||
| chr6:119025553 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-740G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025553 | |||||||
| chr6:119025554 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-741G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025554 | |||||||
| chr6:119025652 | G | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-839C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025652 | |||||||
| chr6:119025681 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160-868G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025681 | |||||||
| chr6:119025741 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.160-928C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025741 | |||||||
| chr6:119025747 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(109): Show |
113 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.160-934C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025747 | |||||||
| chr6:119025921 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0241 |
2 | HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.160-1108T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025921 | |||||||
| chr6:119025925 | A | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(1): Show |
4 | HG02145.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-1112T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119025925 | |||||||
| chr6:119026186 | T | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0084 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.160-1373A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026186 | |||||||
| chr6:119026288 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.160-1475T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026288 | |||||||
| chr6:119026366 | C | G | 1 | a0001c0001t0001g0212 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.160-1553G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026366 | |||||||
| chr6:119026412 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(4): Show |
7 | HG01258.hp2 HG01358.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1599G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026412 | |||||||
| chr6:119026498 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160-1685C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026498 | |||||||
| chr6:119026508 | AC | A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1696delG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026508 | |||||||
| chr6:119026574 | G | A | 3 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0012 |
3 | HG02109.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.160-1761C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026574 | |||||||
| chr6:119026636 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.160-1823C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026636 | |||||||
| chr6:119026646 | C | T | 1 | a0001c0001t0004g0008 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.160-1833G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026646 | |||||||
| chr6:119026648 | C | A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-1835G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026648 | |||||||
| chr6:119026691 | CA | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-1879delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119026691 | |||||||
| chr6:119027102 | C | A | 103 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.160-2289G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027102 | |||||||
| chr6:119027419 | T | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-2606A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027419 | |||||||
| chr6:119027436 | T | C | 112 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(109): Show |
112 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.160-2623A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027436 | |||||||
| chr6:119027437 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-2624T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027437 | |||||||
| chr6:119027551 | A | G | 23 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0154 others(20): Show |
23 | HG00408.hp2 HG01192.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-2738T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027551 | |||||||
| chr6:119027560 | C | T | 23 | a0001c0001t0001g0144 a0001c0001t0001g0146 a0001c0001t0001g0154 others(20): Show |
23 | HG00408.hp2 HG01192.hp2 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-2747G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027560 | |||||||
| chr6:119027634 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0001g0126 |
3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-2821T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027634 | |||||||
| chr6:119027690 | A | G | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-2877T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027690 | |||||||
| chr6:119027951 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160-3138C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119027951 | |||||||
| chr6:119028255 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-3442A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028255 | |||||||
| chr6:119028273 | T | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-3460A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028273 | |||||||
| chr6:119028295 | T | C | 1 | a0001c0001t0003g0024 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.160-3482A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028295 | |||||||
| chr6:119028371 | G | A | 86 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(83): Show |
86 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.160-3558C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028371 | |||||||
| chr6:119028407 | T | C | 1 | a0002c0002t0002g0189 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.160-3594A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028407 | |||||||
| chr6:119028575 | G | A | 3 | a0001c0001t0001g0137 a0001c0001t0004g0013 a0001c0003t0001g0136 |
3 | HG02723.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.160-3762C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028575 | |||||||
| chr6:119028649 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.160-3836T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028649 | |||||||
| chr6:119028662 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-3849G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028662 | |||||||
| chr6:119028685 | C | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0270 |
2 | HG00140.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.160-3872G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028685 | |||||||
| chr6:119028860 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-4047A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028860 | |||||||
| chr6:119028871 | G | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160-4058C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119028871 | |||||||
| chr6:119029017 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-4204G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029017 | |||||||
| chr6:119029031 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0272 |
2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.160-4218A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029031 | |||||||
| chr6:119029350 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-4537T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029350 | |||||||
| chr6:119029386 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0001g0126 |
3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-4573C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029386 | |||||||
| chr6:119029472 | A | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-4659T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029472 | |||||||
| chr6:119029529 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.160-4716T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029529 | |||||||
| chr6:119029584 | C | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(216): Show |
220 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.160-4771G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029584 | |||||||
| chr6:119029614 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-4801G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029614 | |||||||
| chr6:119029623 | T | C | 6 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-4810A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029623 | |||||||
| chr6:119029769 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.160-4956C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029769 | |||||||
| chr6:119029788 | C | G | 53 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(50): Show |
53 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.160-4975G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119029788 | |||||||
| chr6:119030289 | T | G | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-5476A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030289 | |||||||
| chr6:119030554 | A | G | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-5741T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030554 | |||||||
| chr6:119030555 | C | T | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.160-5742G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030555 | |||||||
| chr6:119030644 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.160-5831G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030644 | |||||||
| chr6:119030828 | A | G | 223 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(220): Show |
224 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.160-6015T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030828 | |||||||
| chr6:119030894 | A | AATTTCAT others(24): Show |
1 | a0001c0001t0001g0278 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.160-6112_160-6082d others(33): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119030894 | |||||||
| chr6:119031143 | C | G | 1 | a0002c0002t0002g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.160-6330G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031143 | |||||||
| chr6:119031225 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.160-6412A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031225 | |||||||
| chr6:119031417 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-6604A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031417 | |||||||
| chr6:119031549 | C | T | 103 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.160-6736G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031549 | |||||||
| chr6:119031597 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(1): Show |
4 | HG02145.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-6784A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031597 | |||||||
| chr6:119031600 | A | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-6787T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031600 | |||||||
| chr6:119031705 | T | C | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-6892A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031705 | |||||||
| chr6:119031801 | T | C | 1 | a0002c0002t0002g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160-6988A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031801 | |||||||
| chr6:119031853 | A | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(92): Show |
96 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.160-7040T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031853 | |||||||
| chr6:119031861 | G | A | 1 | a0004c0010t0004g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.160-7048C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031861 | |||||||
| chr6:119031879 | G | A | 1 | a0002c0002t0002g0266 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.160-7066C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119031879 | |||||||
| chr6:119032047 | G | A | 103 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(100): Show |
103 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.160-7234C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032047 | |||||||
| chr6:119032092 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.160-7279G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032092 | |||||||
| chr6:119032096 | A | T | 14 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.160-7283T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032096 | |||||||
| chr6:119032143 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160-7330C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032143 | |||||||
| chr6:119032352 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(113): Show |
117 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.160-7539T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032352 | |||||||
| chr6:119032466 | C | A | 1 | a0001c0001t0005g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160-7653G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032466 | |||||||
| chr6:119032523 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.160-7710C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032523 | |||||||
| chr6:119032524 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.160-7711T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032524 | |||||||
| chr6:119032524 | AAGAGGG | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0100 others(3): Show |
6 | HG02559.hp1 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-7717_160-7712d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032524 | |||||||
| chr6:119032567 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-7754T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032567 | |||||||
| chr6:119032574 | G | C | 4 | a0001c0001t0002g0001 a0001c0001t0002g0062 a0001c0001t0002g0074 others(1): Show |
5 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-7761C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032574 | |||||||
| chr6:119032723 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.160-7910T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032723 | |||||||
| chr6:119032885 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160-8072C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032885 | |||||||
| chr6:119032930 | T | C | 1 | a0002c0002t0002g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.160-8117A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119032930 | |||||||
| chr6:119033028 | A | G | 1 | a0001c0006t0005g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160-8215T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033028 | |||||||
| chr6:119033093 | T | A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-8280A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033093 | |||||||
| chr6:119033184 | C | T | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-8371G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033184 | |||||||
| chr6:119033262 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | NA18951.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.160-8449A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033262 | |||||||
| chr6:119033269 | A | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0269 |
2 | HG02004.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.160-8456T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033269 | |||||||
| chr6:119033292 | T | A | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-8479A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033292 | |||||||
| chr6:119033525 | C | T | 11 | a0001c0001t0002g0001 a0001c0001t0002g0062 a0001c0001t0002g0074 others(8): Show |
12 | HG00642.hp2 HG00741.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.160-8712G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033525 | |||||||
| chr6:119033571 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-8758G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033571 | |||||||
| chr6:119033586 | A | G | 41 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0186 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.160-8773T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033586 | |||||||
| chr6:119033664 | C | CA | 20 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(17): Show |
20 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-8852dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033664 | |||||||
| chr6:119033664 | C | CAA | 21 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0099 others(18): Show |
21 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-8853_160-8852d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033664 | |||||||
| chr6:119033677 | AAG | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-8866_160-8865d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033677 | |||||||
| chr6:119033690 | A | T | 1 | a0001c0001t0003g0026 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.160-8877T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033690 | |||||||
| chr6:119033703 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160-8890G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033703 | |||||||
| chr6:119033720 | G | A | 7 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0112 others(4): Show |
7 | HG00408.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-8907C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033720 | |||||||
| chr6:119033864 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-9051G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033864 | |||||||
| chr6:119033905 | T | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9092A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033905 | |||||||
| chr6:119033939 | C | T | 1 | a0001c0003t0001g0260 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.160-9126G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033939 | |||||||
| chr6:119033990 | CA | C | 19 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0172 others(16): Show |
19 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.160-9178delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | |||||||
| chr6:119033990 | CAAAAAAA | C | 7 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(4): Show |
7 | HG00423.hp2 HG00741.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-9184_160-9178d others(9): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | |||||||
| chr6:119033990 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0002g0001 a0001c0001t0002g0074 a0001c0001t0002g0122 |
4 | HG00741.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9187_160-9178d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | |||||||
| chr6:119033990 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0045 a0001c0001t0002g0062 |
2 | HG02723.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160-9188_160-9178d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119033990 | |||||||
| chr6:119034009 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-9208_160-9197d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034009 | |||||||
| chr6:119034010 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-9208_160-9198d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034010 | |||||||
| chr6:119034010 | AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0100 a0001c0001t0001g0135 others(1): Show |
4 | HG02559.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9210_160-9198d others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034010 | |||||||
| chr6:119034011 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0105 |
2 | HG01515.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.160-9210_160-9199d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034011 | |||||||
| chr6:119034012 | AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0072 |
3 | HG00735.hp1 HG01978.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.160-9210_160-9200d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034012 | |||||||
| chr6:119034013 | AAAAAAAA others(3): Show |
A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0256 |
2 | NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.160-9210_160-9201d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034013 | |||||||
| chr6:119034013 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160-9212_160-9201d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034013 | |||||||
| chr6:119034014 | AAAAAAAT others(4): Show |
A | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0111 others(2): Show |
5 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-9212_160-9202d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034014 | |||||||
| chr6:119034015 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160-9203_160-9202i others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034015 | |||||||
| chr6:119034015 | AAAAAAT | A | 6 | a0001c0001t0001g0113 a0001c0001t0001g0132 a0001c0003t0001g0048 others(3): Show |
6 | HG02055.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-9208_160-9203d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034015 | |||||||
| chr6:119034015 | AAAAAATA others(3): Show |
A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0003t0001g0136 |
3 | HG02723.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.160-9212_160-9203d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034015 | |||||||
| chr6:119034016 | AAAAATAT others(4): Show |
A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0001g0126 |
3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-9214_160-9204d others(13): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034016 | |||||||
| chr6:119034017 | A | T | 2 | a0001c0001t0001g0046 a0001c0001t0002g0001 |
3 | HG02965.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.160-9204T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034017 | |||||||
| chr6:119034018 | AAAT | A | 11 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0119 others(8): Show |
11 | HG01099.hp2 HG01433.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-9208_160-9206d others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034018 | |||||||
| chr6:119034018 | AAATAT | A | 21 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0075 others(18): Show |
21 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-9210_160-9206d others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034018 | |||||||
| chr6:119034019 | A | AT | 3 | a0001c0001t0002g0199 a0001c0001t0006g0034 a0001c0001t0006g0035 |
3 | HG01243.hp1 HG03486.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.160-9207_160-9206i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034019 | |||||||
| chr6:119034019 | A | T | 25 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0102 others(22): Show |
26 | HG00140.hp1 HG00741.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.160-9206T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034019 | |||||||
| chr6:119034019 | AAT | A | 11 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0001g0175 others(8): Show |
11 | HG00408.hp2 HG01192.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.160-9208_160-9207d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034019 | |||||||
| chr6:119034020 | AT | A | 20 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0086 others(17): Show |
20 | HG00609.hp2 HG02080.hp1 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.160-9208delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034020 | |||||||
| chr6:119034020 | ATAT | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0130 a0001c0001t0001g0201 |
3 | HG01934.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.160-9210_160-9208d others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034020 | |||||||
| chr6:119034021 | T | A | 28 | a0001c0001t0001g0002 a0001c0001t0001g0085 a0001c0001t0001g0090 others(25): Show |
28 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.160-9208A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034021 | |||||||
| chr6:119034023 | T | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0098 |
3 | HG02622.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.160-9210A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034023 | |||||||
| chr6:119034025 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160-9212A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034025 | |||||||
| chr6:119034035 | T | A | 1 | a0001c0001t0001g0041 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.160-9222A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034035 | |||||||
| chr6:119034035 | TATATATA others(3): Show |
T | 1 | a0001c0001t0004g0009 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160-9232_160-9223d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034035 | |||||||
| chr6:119034035 | TATATATA others(11): Show |
T | 2 | a0001c0001t0001g0102 a0001c0001t0005g0028 |
2 | HG01168.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.160-9240_160-9223d others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034035 | |||||||
| chr6:119034037 | T | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 |
3 | HG01167.hp1 HG01169.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.160-9224A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | |||||||
| chr6:119034037 | T | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0168 a0001c0001t0001g0176 |
3 | NA18959.hp2 NA19002.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.160-9224A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | |||||||
| chr6:119034037 | TATATAG | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0251 a0001c0001t0001g0271 |
3 | HG00597.hp2 HG02109.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.160-9230_160-9225d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | |||||||
| chr6:119034037 | TATATAGA others(3): Show |
T | 2 | a0001c0001t0004g0008 a0001c0001t0004g0010 |
2 | HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160-9234_160-9225d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | |||||||
| chr6:119034037 | TATATAGA others(9): Show |
T | 1 | a0001c0001t0001g0125 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160-9240_160-9225d others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034037 | |||||||
| chr6:119034039 | T | G | 18 | a0001c0001t0001g0119 a0001c0001t0001g0128 a0001c0001t0001g0144 others(15): Show |
18 | HG01099.hp2 HG02523.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.160-9226A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | |||||||
| chr6:119034039 | TATAGAGA others(1): Show |
T | 9 | a0001c0001t0001g0149 a0001c0001t0001g0212 a0001c0001t0001g0245 others(6): Show |
9 | HG00735.hp2 HG01361.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.160-9234_160-9227d others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | |||||||
| chr6:119034039 | TATAGAGA others(5): Show |
T | 4 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0096 others(1): Show |
4 | HG02622.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9238_160-9227d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | |||||||
| chr6:119034039 | TATAGAGA others(9): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.160-9242_160-9227d others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034039 | |||||||
| chr6:119034041 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.160-9228A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | T | G | 45 | a0001c0001t0001g0070 a0001c0001t0001g0119 a0001c0001t0001g0128 others(42): Show |
46 | HG00408.hp2 HG00609.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-9228A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | T | TAGAGAGA others(5): Show |
1 | a0006c0009t0004g0007 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.160-9240_160-9229d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAG | T | 23 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(20): Show |
23 | HG00423.hp2 HG00741.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-9232_160-9229d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAGAG | T | 38 | a0001c0001t0001g0038 a0001c0001t0001g0107 a0001c0001t0001g0109 others(35): Show |
38 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.160-9234_160-9229d others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAGAGA others(1): Show |
T | 62 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0040 others(59): Show |
62 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.160-9236_160-9229d others(10): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAGAGA others(3): Show |
T | 11 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
11 | HG00733.hp2 HG01258.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-9238_160-9229d others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAGAGA others(5): Show |
T | 23 | a0001c0001t0001g0055 a0001c0001t0001g0059 a0001c0001t0001g0075 others(20): Show |
23 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.160-9240_160-9229d others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAGAGA others(7): Show |
T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0003c0004t0001g0094 |
3 | HG01433.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.160-9242_160-9229d others(16): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAGAGA others(9): Show |
T | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160-9244_160-9229d others(18): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034041 | TAGAGAGA others(11): Show |
T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG01074.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-9246_160-9229d others(20): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034041 | |||||||
| chr6:119034043 | G | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0050 others(26): Show |
29 | HG00642.hp2 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.160-9230C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034043 | |||||||
| chr6:119034045 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160-9232C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034045 | |||||||
| chr6:119034047 | G | T | 11 | a0001c0001t0001g0065 a0001c0001t0001g0068 a0001c0001t0001g0073 others(8): Show |
11 | HG02071.hp1 HG02083.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-9234C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034047 | |||||||
| chr6:119034049 | G | T | 33 | a0001c0001t0001g0038 a0001c0001t0001g0187 a0001c0001t0001g0188 others(30): Show |
33 | HG00597.hp1 HG00609.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.160-9236C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034049 | |||||||
| chr6:119034051 | G | T | 61 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(58): Show |
61 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.160-9238C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034051 | |||||||
| chr6:119034053 | G | T | 18 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.160-9240C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034053 | |||||||
| chr6:119034055 | G | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9242C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034055 | |||||||
| chr6:119034059 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160-9246C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034059 | |||||||
| chr6:119034212 | G | A | 40 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(37): Show |
40 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.160-9399C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034212 | |||||||
| chr6:119034384 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.160-9571A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034384 | |||||||
| chr6:119034533 | AGTC | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9723_160-9721d others(5): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034533 | |||||||
| chr6:119034566 | G | GT | 14 | a0001c0001t0001g0137 a0001c0001t0002g0001 a0001c0001t0002g0062 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.160-9754dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034566 | |||||||
| chr6:119034568 | T | TG | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-9756_160-9755i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034568 | |||||||
| chr6:119034578 | T | A | 32 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(29): Show |
32 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.160-9765A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034578 | |||||||
| chr6:119034579 | T | A | 47 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(44): Show |
47 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.160-9766A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034579 | |||||||
| chr6:119034579 | T | TA | 22 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0060 others(19): Show |
22 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.160-9767_160-9766i others(3): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034579 | |||||||
| chr6:119034580 | T | A | 128 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(125): Show |
128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.160-9767A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034580 | |||||||
| chr6:119034580 | T | TA | 135 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(132): Show |
136 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.160-9768dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034580 | |||||||
| chr6:119034581 | A | T | 3 | a0001c0001t0001g0137 a0001c0001t0002g0074 a0001c0001t0004g0013 |
3 | HG00741.hp1 HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.160-9768T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034581 | |||||||
| chr6:119034727 | C | T | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-9914G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034727 | |||||||
| chr6:119034732 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160-9919A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119034732 | |||||||
| chr6:119035036 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(104): Show |
108 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.160-10223A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035036 | |||||||
| chr6:119035080 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-10267G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035080 | |||||||
| chr6:119035170 | A | T | 121 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(118): Show |
123 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.160-10357T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035170 | |||||||
| chr6:119035181 | A | G | 165 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(162): Show |
167 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.160-10368T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035181 | |||||||
| chr6:119035222 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.160-10409G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035222 | |||||||
| chr6:119035230 | CTTGGCCA others(6): Show |
C | 4 | a0001c0001t0001g0137 a0001c0001t0004g0004 a0001c0001t0004g0013 others(1): Show |
4 | HG02258.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-10430_160-1041 others(17): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035230 | |||||||
| chr6:119035246 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160-10433G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035246 | |||||||
| chr6:119035266 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.160-10453A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035266 | |||||||
| chr6:119035396 | G | A | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-10583C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035396 | |||||||
| chr6:119035668 | A | G | 47 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(44): Show |
47 | HG00423.hp2 HG00639.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.160-10855T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035668 | |||||||
| chr6:119035686 | C | G | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.160-10873G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035686 | |||||||
| chr6:119035726 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.160-10913C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035726 | |||||||
| chr6:119035891 | T | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-11078A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035891 | |||||||
| chr6:119035909 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-11096G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119035909 | |||||||
| chr6:119036020 | C | A | 1 | a0001c0006t0005g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160-11207G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036020 | |||||||
| chr6:119036161 | A | ATAGTTCA others(3): Show |
1 | a0001c0001t0001g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160-11349_160-1134 others(14): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036161 | |||||||
| chr6:119036205 | C | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(224): Show |
229 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.160-11392G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036205 | |||||||
| chr6:119036216 | C | CT | 234 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(231): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.160-11404dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036216 | |||||||
| chr6:119036540 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.160-11727C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036540 | |||||||
| chr6:119036686 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.160-11873A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036686 | |||||||
| chr6:119036702 | T | G | 1 | a0001c0001t0001g0239 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160-11889A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119036702 | |||||||
| chr6:119037033 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-12220T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037033 | |||||||
| chr6:119037051 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.160-12238T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037051 | |||||||
| chr6:119037320 | G | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-12507C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037320 | |||||||
| chr6:119037334 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-12521A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037334 | |||||||
| chr6:119037354 | C | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0215 |
2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.160-12541G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037354 | |||||||
| chr6:119037372 | C | A | 1 | a0001c0001t0001g0205 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.160-12559G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037372 | |||||||
| chr6:119037402 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0279 |
2 | HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.160-12589T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037402 | |||||||
| chr6:119037457 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-12644G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037457 | |||||||
| chr6:119037628 | A | T | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-12815T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037628 | |||||||
| chr6:119037986 | CAAG | C | 7 | a0001c0001t0002g0001 a0001c0001t0002g0062 a0001c0001t0002g0074 others(4): Show |
8 | HG00741.hp1 HG02615.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-13176_160-1317 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119037986 | |||||||
| chr6:119038089 | G | A | 39 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(36): Show |
39 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.160-13276C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038089 | |||||||
| chr6:119038261 | G | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-13448C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038261 | |||||||
| chr6:119038389 | A | G | 1 | a0001c0001t0003g0018 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.160-13576T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038389 | |||||||
| chr6:119038392 | T | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0210 a0001c0001t0001g0268 others(1): Show |
4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-13579A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038392 | |||||||
| chr6:119038533 | G | A | 2 | a0002c0002t0001g0235 a0002c0002t0002g0189 |
2 | HG02071.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.160-13720C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038533 | |||||||
| chr6:119038624 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-13811C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038624 | |||||||
| chr6:119038668 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.160-13855G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038668 | |||||||
| chr6:119038753 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-13940C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038753 | |||||||
| chr6:119038783 | G | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-13970C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038783 | |||||||
| chr6:119038799 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0001g0126 |
3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160-13986C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038799 | |||||||
| chr6:119038808 | G | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0274 |
3 | HG01069.hp1 HG01071.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.160-13995C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038808 | |||||||
| chr6:119038861 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-14048C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119038861 | |||||||
| chr6:119039102 | T | C | 1 | a0001c0001t0008g0284 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.160-14289A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039102 | |||||||
| chr6:119039413 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160-14600C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039413 | |||||||
| chr6:119039473 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-14660T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039473 | |||||||
| chr6:119039540 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-14727T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039540 | |||||||
| chr6:119039815 | A | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-15002T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039815 | |||||||
| chr6:119039817 | G | A | 39 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(36): Show |
39 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.160-15004C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039817 | |||||||
| chr6:119039838 | G | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0087 |
2 | HG01123.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.160-15025C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039838 | |||||||
| chr6:119039964 | C | G | 6 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0196 others(3): Show |
6 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-15151G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119039964 | |||||||
| chr6:119040092 | G | A | 33 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(30): Show |
33 | HG00423.hp2 HG00733.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.160-15279C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040092 | |||||||
| chr6:119040169 | CTGTT | C | 20 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(17): Show |
20 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-15360_160-1535 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040169 | |||||||
| chr6:119040445 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-15632T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040445 | |||||||
| chr6:119040486 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.160-15673A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040486 | |||||||
| chr6:119040578 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.160-15765G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040578 | |||||||
| chr6:119040731 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0127 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.160-15918G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040731 | |||||||
| chr6:119040832 | T | A | 8 | a0001c0003t0001g0048 a0001c0003t0001g0133 a0001c0003t0001g0136 others(5): Show |
8 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.160-16019A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040832 | |||||||
| chr6:119040888 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-16075C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040888 | |||||||
| chr6:119040894 | G | A | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-16081C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040894 | |||||||
| chr6:119040990 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-16177G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119040990 | |||||||
| chr6:119041096 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-16283G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041096 | |||||||
| chr6:119041290 | G | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-16477C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041290 | |||||||
| chr6:119041477 | G | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(6): Show |
9 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.160-16664C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041477 | |||||||
| chr6:119041685 | G | A | 9 | a0001c0001t0001g0134 a0001c0003t0001g0048 a0001c0003t0001g0133 others(6): Show |
9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-16872C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041685 | |||||||
| chr6:119041804 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160-16991G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041804 | |||||||
| chr6:119041908 | G | A | 40 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(37): Show |
40 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.160-17095C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041908 | |||||||
| chr6:119041998 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.160-17185G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119041998 | |||||||
| chr6:119042160 | C | G | 1 | a0001c0001t0001g0259 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.160-17347G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042160 | |||||||
| chr6:119042236 | G | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.160-17423C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042236 | |||||||
| chr6:119042348 | G | A | 4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0060 others(1): Show |
4 | HG00140.hp2 HG00642.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-17535C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042348 | |||||||
| chr6:119042411 | T | C | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.160-17598A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042411 | |||||||
| chr6:119042470 | C | CT | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-17658dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042470 | |||||||
| chr6:119042478 | T | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-17665A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042478 | |||||||
| chr6:119042535 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-17722C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042535 | |||||||
| chr6:119042752 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-17939A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042752 | |||||||
| chr6:119042811 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-17998G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042811 | |||||||
| chr6:119042862 | CT | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-18050delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119042862 | |||||||
| chr6:119043076 | T | TA | 9 | a0001c0001t0001g0134 a0001c0003t0001g0048 a0001c0003t0001g0133 others(6): Show |
9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-18264dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043076 | |||||||
| chr6:119043082 | T | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-18269A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043082 | |||||||
| chr6:119043125 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.160-18312A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043125 | |||||||
| chr6:119043191 | T | C | 9 | a0001c0001t0001g0134 a0001c0003t0001g0048 a0001c0003t0001g0133 others(6): Show |
9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-18378A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119043191 | |||||||
| chr6:119044278 | C | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-19465G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044278 | |||||||
| chr6:119044364 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-19551G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044364 | |||||||
| chr6:119044459 | T | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0088 others(3): Show |
6 | HG01106.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-19646A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044459 | |||||||
| chr6:119044496 | T | C | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-19683A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044496 | |||||||
| chr6:119044538 | T | C | 1 | a0001c0001t0003g0014 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.160-19725A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044538 | |||||||
| chr6:119044591 | TA | T | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-19779delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044591 | |||||||
| chr6:119044651 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-19838A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044651 | |||||||
| chr6:119044731 | T | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-19918A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044731 | |||||||
| chr6:119044872 | T | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-20059A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044872 | |||||||
| chr6:119044986 | A | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.160-20173T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119044986 | |||||||
| chr6:119045037 | C | T | 59 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0130 others(56): Show |
59 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.160-20224G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045037 | |||||||
| chr6:119045038 | G | A | 4 | a0001c0001t0001g0203 a0001c0001t0001g0210 a0001c0001t0001g0268 others(1): Show |
4 | NA18612.hp2 NA18947.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-20225C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045038 | |||||||
| chr6:119045228 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.160-20415A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045228 | |||||||
| chr6:119045291 | A | AT | 21 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(18): Show |
21 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.160-20479dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045291 | |||||||
| chr6:119045291 | A | ATT | 220 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.160-20480_160-2047 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045291 | |||||||
| chr6:119045291 | A | ATTT | 20 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0049 others(17): Show |
20 | HG01884.hp2 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.160-20481_160-2047 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045291 | |||||||
| chr6:119045475 | C | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0092 others(2): Show |
5 | HG00639.hp2 HG01168.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-20662G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045475 | |||||||
| chr6:119045521 | C | G | 1 | a0001c0001t0009g0003 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.160-20708G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045521 | |||||||
| chr6:119045548 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-20735A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045548 | |||||||
| chr6:119045630 | C | T | 9 | a0001c0001t0001g0134 a0001c0003t0001g0048 a0001c0003t0001g0133 others(6): Show |
9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-20817G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045630 | |||||||
| chr6:119045644 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.160-20831G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045644 | |||||||
| chr6:119045703 | G | T | 1 | a0002c0002t0002g0214 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160-20890C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045703 | |||||||
| chr6:119045805 | AT | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-20993delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045805 | |||||||
| chr6:119045806 | T | A | 1 | a0001c0006t0005g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160-20993A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119045806 | |||||||
| chr6:119046226 | CT | C | 34 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(31): Show |
34 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.160-21414delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046226 | |||||||
| chr6:119046316 | T | G | 3 | a0001c0001t0001g0188 a0001c0001t0001g0239 a0001c0001t0001g0271 |
3 | HG00597.hp2 HG01255.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.160-21503A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046316 | |||||||
| chr6:119046423 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-21610G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046423 | |||||||
| chr6:119046453 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(240): Show |
245 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.160-21640T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046453 | |||||||
| chr6:119046495 | T | A | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-21682A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046495 | |||||||
| chr6:119046564 | T | TA | 162 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(159): Show |
164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.160-21752dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046564 | |||||||
| chr6:119046740 | G | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-21927C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046740 | |||||||
| chr6:119046840 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-22027T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046840 | |||||||
| chr6:119046872 | T | C | 2 | a0001c0001t0004g0004 a0007c0007t0001g0240 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.160-22059A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119046872 | |||||||
| chr6:119047052 | T | TA | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-22240dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047052 | |||||||
| chr6:119047065 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.160-22252T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047065 | |||||||
| chr6:119047121 | TA | T | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-22309delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047121 | |||||||
| chr6:119047129 | T | G | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.160-22316A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047129 | |||||||
| chr6:119047156 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-22343T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047156 | |||||||
| chr6:119047248 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-22435A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047248 | |||||||
| chr6:119047300 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.160-22487A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047300 | |||||||
| chr6:119047448 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-22635G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047448 | |||||||
| chr6:119047777 | C | T | 4 | a0001c0001t0004g0005 a0001c0001t0010g0282 a0004c0010t0004g0006 others(1): Show |
4 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.160-22964G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047777 | |||||||
| chr6:119047790 | C | T | 9 | a0001c0001t0001g0134 a0001c0003t0001g0048 a0001c0003t0001g0133 others(6): Show |
9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-22977G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119047790 | |||||||
| chr6:119048055 | G | T | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-23242C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048055 | |||||||
| chr6:119048057 | G | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-23244C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048057 | |||||||
| chr6:119048351 | T | A | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.160-23538A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048351 | |||||||
| chr6:119048353 | C | A | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-23540G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048353 | |||||||
| chr6:119048491 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.160-23678C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048491 | |||||||
| chr6:119048682 | G | A | 9 | a0001c0001t0001g0134 a0001c0003t0001g0048 a0001c0003t0001g0133 others(6): Show |
9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-23869C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048682 | |||||||
| chr6:119048796 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-23983C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048796 | |||||||
| chr6:119048921 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-24108A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048921 | |||||||
| chr6:119048936 | A | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-24123T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119048936 | |||||||
| chr6:119049121 | A | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-24308T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049121 | |||||||
| chr6:119049164 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-24351A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049164 | |||||||
| chr6:119049166 | C | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(240): Show |
245 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.160-24353G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049166 | |||||||
| chr6:119049222 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.160-24409G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049222 | |||||||
| chr6:119049246 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.160-24433C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049246 | |||||||
| chr6:119049810 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.160-24997G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049810 | |||||||
| chr6:119049868 | A | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-25055T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119049868 | |||||||
| chr6:119050203 | A | G | 9 | a0001c0001t0001g0134 a0001c0003t0001g0048 a0001c0003t0001g0133 others(6): Show |
9 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.160-25390T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050203 | |||||||
| chr6:119050378 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.160-25565C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050378 | |||||||
| chr6:119050390 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.160-25577G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050390 | |||||||
| chr6:119050415 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(171): Show |
176 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.160-25602T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050415 | |||||||
| chr6:119050438 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(240): Show |
245 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.160-25625A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050438 | |||||||
| chr6:119050452 | GT | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(237): Show |
242 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.160-25640delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050452 | |||||||
| chr6:119050454 | T | G | 5 | a0001c0001t0001g0083 a0001c0001t0001g0202 a0001c0001t0001g0241 others(2): Show |
5 | HG01074.hp2 HG01109.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.160-25641A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050454 | |||||||
| chr6:119050462 | T | A | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160-25649A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050462 | |||||||
| chr6:119050504 | T | TA | 166 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.160-25692dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050504 | |||||||
| chr6:119050504 | T | TAA | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.160-25693_160-2569 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050504 | |||||||
| chr6:119050515 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.160-25702A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050515 | |||||||
| chr6:119050572 | T | C | 2 | a0002c0002t0002g0123 a0002c0002t0002g0129 |
2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.160-25759A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050572 | |||||||
| chr6:119050663 | G | T | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-25850C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050663 | |||||||
| chr6:119050678 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.160-25865G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050678 | |||||||
| chr6:119050698 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.160-25885C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050698 | |||||||
| chr6:119050740 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0256 |
2 | NA18995.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.160-25927C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050740 | |||||||
| chr6:119050811 | C | CA | 50 | a0001c0001t0001g0049 a0001c0001t0001g0100 a0001c0001t0001g0101 others(47): Show |
50 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.160-25999dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050811 | |||||||
| chr6:119050811 | CA | C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0119 a0001c0001t0001g0203 others(8): Show |
11 | HG01099.hp2 HG01884.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.160-25999delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050811 | |||||||
| chr6:119050899 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(233): Show |
238 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.160-26086T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119050899 | |||||||
| chr6:119051002 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(156): Show |
161 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.160-26189C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051002 | |||||||
| chr6:119051116 | AC | A | 49 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(46): Show |
49 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.160-26304delG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051116 | |||||||
| chr6:119051118 | T | A | 49 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(46): Show |
49 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.160-26305A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051118 | |||||||
| chr6:119051156 | A | AAAAG | 242 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(239): Show |
244 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.160-26347_160-2634 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051156 | |||||||
| chr6:119051156 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160-26343T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051156 | |||||||
| chr6:119051182 | A | G | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.160-26369T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051182 | |||||||
| chr6:119051299 | C | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-26486G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051299 | |||||||
| chr6:119051627 | C | T | 13 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(10): Show |
13 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.159+26514G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051627 | |||||||
| chr6:119051642 | G | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+26499C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051642 | |||||||
| chr6:119051711 | T | C | 7 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0138 others(4): Show |
7 | HG02451.hp2 HG02895.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.159+26430A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051711 | |||||||
| chr6:119051719 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+26422A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051719 | |||||||
| chr6:119051756 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG00609.hp2 HG02080.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.159+26385C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051756 | |||||||
| chr6:119051849 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.159+26292C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051849 | |||||||
| chr6:119051956 | C | G | 1 | a0001c0001t0001g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.159+26185G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119051956 | |||||||
| chr6:119052007 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(161): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.159+26134G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052007 | |||||||
| chr6:119052034 | C | T | 273 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(270): Show |
275 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.159+26107G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052034 | |||||||
| chr6:119052146 | T | C | 3 | a0001c0001t0001g0182 a0001c0001t0007g0280 a0001c0001t0007g0281 |
3 | NA18986.hp1 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.159+25995A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052146 | |||||||
| chr6:119052413 | C | T | 1 | a0001c0001t0004g0004 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159+25728G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052413 | |||||||
| chr6:119052667 | C | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+25474G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052667 | |||||||
| chr6:119052669 | A | T | 2 | a0002c0002t0002g0207 a0002c0002t0002g0208 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.159+25472T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052669 | |||||||
| chr6:119052746 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159+25395G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052746 | |||||||
| chr6:119052747 | T | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(113): Show |
117 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.159+25394A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052747 | |||||||
| chr6:119052998 | A | T | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+25143T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119052998 | |||||||
| chr6:119053493 | A | G | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+24648T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053493 | |||||||
| chr6:119053584 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(102): Show |
106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.159+24557A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053584 | |||||||
| chr6:119053599 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.159+24542A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053599 | |||||||
| chr6:119053676 | C | T | 13 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+24465G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053676 | |||||||
| chr6:119053735 | A | C | 1 | a0001c0001t0003g0017 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.159+24406T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053735 | |||||||
| chr6:119053894 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+24247A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053894 | |||||||
| chr6:119053966 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.159+24175C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053966 | |||||||
| chr6:119053997 | T | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+24144A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119053997 | |||||||
| chr6:119054085 | GA | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(265): Show |
270 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.159+24055delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054085 | |||||||
| chr6:119054241 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.159+23900G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054241 | |||||||
| chr6:119054392 | G | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+23749C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054392 | |||||||
| chr6:119054705 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159+23436G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054705 | |||||||
| chr6:119054866 | A | AT | 272 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(269): Show |
273 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.159+23274dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054866 | |||||||
| chr6:119054933 | C | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(3): Show |
6 | HG02257.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+23208G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119054933 | |||||||
| chr6:119055182 | C | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(155): Show |
159 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.159+22959G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055182 | |||||||
| chr6:119055368 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.159+22773T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055368 | |||||||
| chr6:119055547 | A | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+22594T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055547 | |||||||
| chr6:119055711 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.159+22430A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055711 | |||||||
| chr6:119055736 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0002g0122 |
3 | HG02818.hp2 HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.159+22405G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055736 | |||||||
| chr6:119055931 | T | TC | 20 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(17): Show |
21 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.159+22209dupG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119055931 | |||||||
| chr6:119056038 | C | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG01168.hp1 HG01192.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+22103G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056038 | |||||||
| chr6:119056076 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.159+22065C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056076 | |||||||
| chr6:119056211 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0081 a0001c0001t0001g0084 others(1): Show |
4 | HG02145.hp1 HG02717.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+21930A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056211 | |||||||
| chr6:119056334 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(109): Show |
113 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.159+21807A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056334 | |||||||
| chr6:119056434 | C | T | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.159+21707G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056434 | |||||||
| chr6:119056483 | T | C | 42 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(39): Show |
42 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.159+21658A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056483 | |||||||
| chr6:119056609 | A | AAT | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 |
3 | HG01884.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.159+21530_159+2153 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056609 | |||||||
| chr6:119056904 | G | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(6): Show |
9 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+21237C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056904 | |||||||
| chr6:119056959 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+21182A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119056959 | |||||||
| chr6:119057417 | A | C | 14 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+20724T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057417 | |||||||
| chr6:119057418 | A | G | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+20723T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057418 | |||||||
| chr6:119057521 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(259): Show |
264 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.159+20620G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057521 | |||||||
| chr6:119057692 | G | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.159+20449C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057692 | |||||||
| chr6:119057704 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.159+20437C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057704 | |||||||
| chr6:119057794 | G | A | 4 | a0001c0001t0002g0121 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
4 | HG00642.hp2 HG02258.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+20347C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057794 | |||||||
| chr6:119057843 | GT | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(239): Show |
244 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.159+20297delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057843 | |||||||
| chr6:119057895 | A | G | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.159+20246T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057895 | |||||||
| chr6:119057939 | T | C | 1 | a0001c0001t0003g0026 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.159+20202A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057939 | |||||||
| chr6:119057953 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0187 a0001c0001t0001g0244 others(1): Show |
4 | HG02080.hp2 NA18954.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+20188C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057953 | |||||||
| chr6:119057972 | TA | T | 153 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(150): Show |
154 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.159+20168delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057972 | |||||||
| chr6:119057973 | A | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0110 a0001c0001t0001g0126 |
3 | HG02970.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.159+20168T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119057973 | |||||||
| chr6:119058012 | G | T | 1 | a0002c0002t0002g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.159+20129C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058012 | |||||||
| chr6:119058052 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.159+20089T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058052 | |||||||
| chr6:119058154 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.159+19987T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058154 | |||||||
| chr6:119058175 | C | CT | 30 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(27): Show |
30 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.159+19965dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058175 | |||||||
| chr6:119058175 | CT | C | 73 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(70): Show |
73 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.159+19965delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058175 | |||||||
| chr6:119058349 | C | T | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+19792G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058349 | |||||||
| chr6:119058479 | A | C | 1 | a0001c0001t0001g0082 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.159+19662T>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058479 | |||||||
| chr6:119058594 | C | G | 14 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+19547G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058594 | |||||||
| chr6:119058889 | G | GCTTTATT others(1): Show |
3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+19251_159+1925 others(12): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119058889 | |||||||
| chr6:119059029 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+19112G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059029 | |||||||
| chr6:119059228 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.159+18913G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059228 | |||||||
| chr6:119059249 | G | A | 14 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(11): Show |
15 | HG00642.hp2 HG00741.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+18892C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059249 | |||||||
| chr6:119059571 | G | T | 1 | a0003c0004t0001g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.159+18570C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059571 | |||||||
| chr6:119059597 | T | G | 2 | a0001c0001t0001g0065 a0001c0001t0001g0073 |
2 | NA18980.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.159+18544A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059597 | |||||||
| chr6:119059720 | T | C | 18 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(15): Show |
19 | HG00642.hp2 HG00741.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.159+18421A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059720 | |||||||
| chr6:119059921 | T | C | 3 | a0001c0001t0004g0005 a0004c0010t0004g0006 a0006c0009t0004g0007 |
3 | HG01891.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.159+18220A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059921 | |||||||
| chr6:119059937 | T | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+18204A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119059937 | |||||||
| chr6:119060173 | G | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0002g0001 others(5): Show |
9 | HG00741.hp1 HG01884.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.159+17968C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060173 | |||||||
| chr6:119060297 | T | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00408.hp1 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.159+17844A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060297 | |||||||
| chr6:119060337 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(238): Show |
243 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.159+17804A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060337 | |||||||
| chr6:119060540 | G | A | 1 | a0003c0004t0001g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.159+17601C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060540 | |||||||
| chr6:119060855 | CCT | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+17284_159+1728 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060855 | |||||||
| chr6:119060882 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.159+17259C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060882 | |||||||
| chr6:119060936 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(102): Show |
106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.159+17205A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119060936 | |||||||
| chr6:119061186 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(101): Show |
105 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.159+16955G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061186 | |||||||
| chr6:119061299 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.159+16842A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061299 | |||||||
| chr6:119061335 | G | C | 1 | a0002c0002t0002g0206 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.159+16806C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061335 | |||||||
| chr6:119061337 | G | A | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.159+16804C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061337 | |||||||
| chr6:119061485 | A | G | 1 | a0002c0002t0002g0266 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.159+16656T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061485 | |||||||
| chr6:119061531 | C | CT | 23 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0045 others(20): Show |
24 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.159+16609dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | |||||||
| chr6:119061531 | C | CTT | 58 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0067 others(55): Show |
58 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.159+16608_159+1660 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | |||||||
| chr6:119061531 | C | CTTT | 16 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0066 others(13): Show |
16 | HG00741.hp2 HG01978.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.159+16607_159+1660 others(7): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | |||||||
| chr6:119061531 | CT | C | 41 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(38): Show |
41 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.159+16609delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061531 | |||||||
| chr6:119061532 | T | C | 4 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+16609A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061532 | |||||||
| chr6:119061583 | GC | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+16557delG | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061583 | |||||||
| chr6:119061873 | G | A | 13 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+16268C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061873 | |||||||
| chr6:119061875 | A | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+16266T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061875 | |||||||
| chr6:119061915 | AGAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0038 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.159+16215_159+1622 others(15): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061915 | |||||||
| chr6:119061934 | G | A | 5 | a0003c0004t0001g0093 a0003c0004t0001g0094 a0003c0004t0001g0095 others(2): Show |
5 | HG00738.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+16207C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061934 | |||||||
| chr6:119061989 | G | C | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+16152C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119061989 | |||||||
| chr6:119062025 | T | C | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+16116A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062025 | |||||||
| chr6:119062291 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.159+15850G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062291 | |||||||
| chr6:119062394 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.159+15747A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062394 | |||||||
| chr6:119062552 | G | A | 13 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+15589C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062552 | |||||||
| chr6:119062572 | T | C | 13 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+15569A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062572 | |||||||
| chr6:119062614 | C | T | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+15527G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062614 | |||||||
| chr6:119062655 | A | G | 1 | a0001c0001t0004g0005 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.159+15486T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062655 | |||||||
| chr6:119062710 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159+15431A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062710 | |||||||
| chr6:119062817 | G | C | 101 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0148 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.159+15324C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119062817 | |||||||
| chr6:119063523 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.159+14618A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063523 | |||||||
| chr6:119063543 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.159+14598C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063543 | |||||||
| chr6:119063711 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+14430C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063711 | |||||||
| chr6:119063757 | T | TA | 11 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(8): Show |
11 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.159+14383dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063757 | |||||||
| chr6:119063891 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+14250G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063891 | |||||||
| chr6:119063938 | T | C | 1 | a0001c0001t0005g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.159+14203A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063938 | |||||||
| chr6:119063963 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0272 |
2 | NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.159+14178A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119063963 | |||||||
| chr6:119064013 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159+14128A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064013 | |||||||
| chr6:119064069 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.159+14072A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064069 | |||||||
| chr6:119064303 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA18959.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.159+13838C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064303 | |||||||
| chr6:119064351 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.159+13790A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064351 | |||||||
| chr6:119064421 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.159+13720G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064421 | |||||||
| chr6:119064879 | G | T | 46 | a0001c0001t0001g0049 a0001c0001t0001g0101 a0001c0001t0001g0144 others(43): Show |
46 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.159+13262C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064879 | |||||||
| chr6:119064908 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0131 a0001c0001t0004g0008 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+13233G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119064908 | |||||||
| chr6:119065011 | T | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02055.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+13130A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065011 | |||||||
| chr6:119065019 | C | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(102): Show |
106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.159+13122G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065019 | |||||||
| chr6:119065114 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.159+13027A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065114 | |||||||
| chr6:119065138 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(106): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.159+13003G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065138 | |||||||
| chr6:119065175 | G | A | 13 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+12966C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065175 | |||||||
| chr6:119065345 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.159+12796T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065345 | |||||||
| chr6:119065563 | T | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+12578A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065563 | |||||||
| chr6:119065623 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 |
3 | HG00609.hp2 HG02080.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.159+12518G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065623 | |||||||
| chr6:119065661 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.159+12480G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065661 | |||||||
| chr6:119065703 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.159+12438C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065703 | |||||||
| chr6:119065809 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.159+12332G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065809 | |||||||
| chr6:119065900 | C | T | 2 | a0001c0001t0006g0034 a0001c0001t0006g0035 |
2 | HG01243.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.159+12241G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065900 | |||||||
| chr6:119065991 | C | A | 13 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(10): Show |
13 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+12150G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119065991 | |||||||
| chr6:119066447 | G | C | 54 | a0001c0001t0001g0049 a0001c0001t0001g0063 a0001c0001t0001g0101 others(51): Show |
54 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.159+11694C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066447 | |||||||
| chr6:119066582 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.159+11559C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066582 | |||||||
| chr6:119066626 | C | G | 3 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 |
3 | HG00642.hp2 HG02486.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.159+11515G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066626 | |||||||
| chr6:119066879 | C | A | 1 | a0002c0002t0002g0262 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.159+11262G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119066879 | |||||||
| chr6:119067149 | A | G | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0194 others(5): Show |
8 | HG00738.hp1 HG01358.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+10992T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067149 | |||||||
| chr6:119067304 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159+10837A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067304 | |||||||
| chr6:119067304 | T | C | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG02622.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+10837A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067304 | |||||||
| chr6:119067313 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG03471.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.159+10828C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067313 | |||||||
| chr6:119067326 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.159+10815T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067326 | |||||||
| chr6:119067394 | T | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0177 a0001c0001t0001g0181 others(1): Show |
4 | HG00408.hp2 NA18947.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+10747A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067394 | |||||||
| chr6:119067707 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.159+10434A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067707 | |||||||
| chr6:119067723 | C | T | 17 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0137 others(14): Show |
17 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.159+10418G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067723 | |||||||
| chr6:119067733 | G | C | 1 | a0005c0008t0001g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.159+10408C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067733 | |||||||
| chr6:119067783 | C | T | 5 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0008 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+10358G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067783 | |||||||
| chr6:119067987 | TAAAC | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+10150_159+1015 others(8): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119067987 | |||||||
| chr6:119068030 | TG | T | 3 | a0001c0001t0005g0031 a0001c0003t0005g0032 a0001c0006t0005g0030 |
3 | HG01884.hp1 HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.159+10110delC | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068030 | |||||||
| chr6:119068047 | GT | G | 63 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(60): Show |
63 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.159+10093delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068047 | |||||||
| chr6:119068047 | GTT | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(194): Show |
199 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.159+10092_159+1009 others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068047 | |||||||
| chr6:119068108 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+10033C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068108 | |||||||
| chr6:119068111 | A | G | 45 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(42): Show |
45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+10030T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068111 | |||||||
| chr6:119068181 | G | C | 2 | a0001c0001t0001g0100 a0001c0001t0010g0282 |
2 | HG02615.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.159+9960C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068181 | |||||||
| chr6:119068344 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+9797A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068344 | |||||||
| chr6:119068405 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.159+9736C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068405 | |||||||
| chr6:119068474 | T | C | 1 | a0001c0001t0001g0177 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.159+9667A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068474 | |||||||
| chr6:119068493 | T | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+9648A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068493 | |||||||
| chr6:119068845 | AG | A | 55 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(52): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.159+9295delC | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068845 | |||||||
| chr6:119068895 | C | T | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.159+9246G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068895 | |||||||
| chr6:119068942 | T | C | 10 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(7): Show |
10 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.159+9199A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119068942 | |||||||
| chr6:119069098 | G | C | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.159+9043C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069098 | |||||||
| chr6:119069296 | A | AAC | 15 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0003g0014 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+8843_159+8844d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069296 | |||||||
| chr6:119069486 | G | A | 11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.159+8655C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069486 | |||||||
| chr6:119069550 | C | T | 11 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0130 others(8): Show |
12 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+8591G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119069550 | |||||||
| chr6:119070016 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(274): Show |
279 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.159+8125T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070016 | |||||||
| chr6:119070041 | A | G | 55 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(52): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.159+8100T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070041 | |||||||
| chr6:119070300 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.159+7841G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070300 | |||||||
| chr6:119070558 | T | C | 1 | a0001c0003t0005g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.159+7583A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070558 | |||||||
| chr6:119070605 | TTTTC | T | 45 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(42): Show |
45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+7532_159+7535d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070605 | |||||||
| chr6:119070784 | G | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 |
3 | HG01099.hp2 HG02630.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.159+7357C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070784 | |||||||
| chr6:119070844 | A | G | 1 | a0001c0001t0002g0121 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.159+7297T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070844 | |||||||
| chr6:119070910 | T | TA | 55 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(52): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.159+7230dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070910 | |||||||
| chr6:119070910 | TA | T | 44 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(41): Show |
44 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.159+7230delT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070910 | |||||||
| chr6:119070938 | A | T | 3 | a0001c0001t0001g0063 a0001c0001t0002g0062 a0005c0008t0001g0064 |
3 | HG01891.hp2 HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.159+7203T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119070938 | |||||||
| chr6:119071189 | T | C | 40 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(37): Show |
40 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.159+6952A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071189 | |||||||
| chr6:119071210 | G | A | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159+6931C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071210 | |||||||
| chr6:119071286 | T | C | 45 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(42): Show |
45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+6855A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071286 | |||||||
| chr6:119071296 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.159+6845T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071296 | |||||||
| chr6:119071402 | C | T | 103 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(100): Show |
103 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.159+6739G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071402 | |||||||
| chr6:119071752 | T | C | 5 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0008 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+6389A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071752 | |||||||
| chr6:119071778 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+6363T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071778 | |||||||
| chr6:119071860 | C | CT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(121): Show |
125 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.159+6280dupA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071860 | |||||||
| chr6:119071860 | C | CTT | 10 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
10 | HG00597.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+6279_159+6280d others(4): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071860 | |||||||
| chr6:119071860 | CT | C | 11 | a0001c0001t0001g0050 a0001c0001t0001g0102 a0001c0001t0001g0126 others(8): Show |
11 | HG00408.hp2 HG01168.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.159+6280delA | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071860 | |||||||
| chr6:119071868 | T | C | 1 | a0002c0002t0002g0129 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.159+6273A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071868 | |||||||
| chr6:119071912 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.159+6229G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119071912 | |||||||
| chr6:119072008 | C | T | 40 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(37): Show |
40 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.159+6133G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072008 | |||||||
| chr6:119072012 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG00741.hp1 HG02055.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+6129G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072012 | |||||||
| chr6:119072290 | C | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG02257.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.159+5851G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072290 | |||||||
| chr6:119072300 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.159+5841A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072300 | |||||||
| chr6:119072571 | T | G | 10 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(7): Show |
10 | HG00639.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.159+5570A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072571 | |||||||
| chr6:119072638 | ATGAC | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0275 a0001c0001t0001g0276 |
3 | HG02055.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.159+5499_159+5502d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072638 | |||||||
| chr6:119072672 | G | C | 15 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(12): Show |
15 | HG00639.hp1 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.159+5469C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072672 | |||||||
| chr6:119072883 | A | ATACAATT others(308): Show |
2 | a0001c0003t0001g0139 a0001c0003t0001g0140 |
2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.159+5257_159+5258i others(317): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | |||||||
| chr6:119072883 | A | ATACAATT others(328): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0003t0001g0136 |
3 | HG02723.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.159+5257_159+5258i others(337): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | |||||||
| chr6:119072883 | A | ATACAATT others(329): Show |
4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0003t0001g0133 others(1): Show |
4 | HG00639.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+5257_159+5258i others(338): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | |||||||
| chr6:119072883 | A | ATACAATT others(330): Show |
4 | a0001c0001t0001g0132 a0001c0001t0004g0011 a0001c0001t0004g0012 others(1): Show |
4 | HG02486.hp1 HG02809.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.159+5257_159+5258i others(339): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | |||||||
| chr6:119072883 | A | ATACAATT others(331): Show |
2 | a0001c0001t0004g0009 a0001c0001t0004g0010 |
2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.159+5257_159+5258i others(340): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072883 | |||||||
| chr6:119072892 | C | T | 22 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(19): Show |
22 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.159+5249G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072892 | |||||||
| chr6:119072971 | C | T | 11 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(8): Show |
11 | HG00423.hp2 HG00735.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.159+5170G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119072971 | |||||||
| chr6:119073053 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.159+5088G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073053 | |||||||
| chr6:119073070 | AAAAC | A | 3 | a0001c0001t0001g0182 a0001c0001t0007g0280 a0001c0001t0007g0281 |
3 | NA18986.hp1 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.159+5067_159+5070d others(6): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073070 | |||||||
| chr6:119073448 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.159+4693T>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073448 | |||||||
| chr6:119073619 | G | T | 1 | a0001c0003t0001g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159+4522C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073619 | |||||||
| chr6:119073639 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.159+4502C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073639 | |||||||
| chr6:119073717 | G | A | 15 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(12): Show |
15 | HG00639.hp1 HG02109.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.159+4424C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073717 | |||||||
| chr6:119073802 | G | T | 1 | a0002c0002t0002g0185 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.159+4339C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073802 | |||||||
| chr6:119073831 | T | C | 5 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+4310A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119073831 | |||||||
| chr6:119074043 | T | C | 22 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(19): Show |
22 | HG00639.hp1 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.159+4098A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074043 | |||||||
| chr6:119074447 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.159+3694T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074447 | |||||||
| chr6:119074549 | C | A | 1 | a0003c0004t0001g0141 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.159+3592G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074549 | |||||||
| chr6:119074603 | C | CA | 45 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(42): Show |
45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+3537dupT | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074603 | |||||||
| chr6:119074701 | T | C | 1 | a0001c0003t0001g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.159+3440A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074701 | |||||||
| chr6:119074765 | T | A | 1 | a0002c0002t0002g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.159+3376A>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074765 | |||||||
| chr6:119074769 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.159+3372T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074769 | |||||||
| chr6:119074950 | C | T | 5 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0008 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+3191G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119074950 | |||||||
| chr6:119075034 | A | G | 66 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(63): Show |
66 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.159+3107T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075034 | |||||||
| chr6:119075046 | T | C | 5 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0008 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+3095A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075046 | |||||||
| chr6:119075101 | T | C | 45 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(42): Show |
45 | HG00408.hp2 HG00609.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.159+3040A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075101 | |||||||
| chr6:119075172 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.159+2969C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075172 | |||||||
| chr6:119075277 | C | A | 1 | a0001c0001t0001g0272 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.159+2864G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075277 | |||||||
| chr6:119075344 | T | C | 5 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0008 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+2797A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075344 | |||||||
| chr6:119075417 | A | G | 6 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0058 others(3): Show |
6 | HG00140.hp2 HG00642.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+2724T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075417 | |||||||
| chr6:119075458 | G | T | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+2683C>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075458 | |||||||
| chr6:119075494 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+2647A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075494 | |||||||
| chr6:119075563 | G | A | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.159+2578C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075563 | |||||||
| chr6:119075652 | T | C | 2 | a0001c0001t0008g0283 a0001c0001t0008g0284 |
2 | NA18612.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.159+2489A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075652 | |||||||
| chr6:119075764 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG02257.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.159+2377T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075764 | |||||||
| chr6:119075934 | T | G | 1 | a0001c0001t0001g0183 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.159+2207A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119075934 | |||||||
| chr6:119076052 | C | T | 15 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0003g0014 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+2089G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076052 | |||||||
| chr6:119076080 | T | C | 1 | a0001c0001t0010g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.159+2061A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076080 | |||||||
| chr6:119076183 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.159+1958A>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076183 | |||||||
| chr6:119076210 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.159+1931C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076210 | |||||||
| chr6:119076695 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(91): Show |
95 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.159+1446A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076695 | |||||||
| chr6:119076748 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.159+1393C>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076748 | |||||||
| chr6:119076839 | T | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0037 a0001c0001t0001g0038 others(276): Show |
281 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.159+1302A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119076839 | |||||||
| chr6:119077131 | C | T | 13 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+1010G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077131 | |||||||
| chr6:119077198 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.159+943G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077198 | |||||||
| chr6:119077214 | A | G | 1 | a0008c0005t0001g0036 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.159+927T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077214 | |||||||
| chr6:119077294 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.159+847G>A | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077294 | |||||||
| chr6:119077501 | A | G | 5 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0008 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.159+640T>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077501 | |||||||
| chr6:119077582 | T | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.159+559A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077582 | |||||||
| chr6:119077877 | T | C | 15 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0003g0014 others(12): Show |
15 | HG01081.hp1 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.159+264A>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077877 | |||||||
| chr6:119077905 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.159+236C>G | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077905 | |||||||
| chr6:119077933 | C | A | 7 | a0001c0001t0005g0027 a0001c0001t0005g0028 a0001c0001t0005g0029 others(4): Show |
7 | HG01884.hp1 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.159+208G>T | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119077933 | |||||||
| chr6:119078105 | C | G | 1 | a0001c0001t0001g0037 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.159+36G>C | FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | 119078105 |