Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84071 |
| ensemblid | ENSG00000118690.13 |
| hgncid | 23045 |
| symbol | ARMC2 |
| name | armadillo repeat containing 2 |
| refseq_nuc | NM_032131.6 |
| refseq_prot | NP_115507.4 |
| ensembl_nuc | ENST00000392644.9 |
| ensembl_prot | ENSP00000376417.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 108848422 |
| end | 108974476 |
| strand | + |
| ver | v1.2 |
| region | chr6:108848422-108974476 |
| region5000 | chr6:108843422-108979476 |
| regionname0 | ARMC2_chr6_108848422_108974476 |
| regionname5000 | ARMC2_chr6_108843422_108979476 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 867 | 255 | 68 | 53 | 85 | 14 | 33 | 52 | ARMC2_chr6_108843422_108979476 | ARMC2 | MLSPN others(862): Show |
chr6 | 108843422 | 108979476 |
| a0002 | 0/0 | 867 | 24 | 1 | 5 | 17 | 0 | 1 | 14 | ARMC2_chr6_108843422_108979476 | ARMC2 | MLSPN others(862): Show |
chr6 | 108843422 | 108979476 |
| a0003 | 0/0 | 867 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | MLSPN others(862): Show |
chr6 | 108843422 | 108979476 |
| a0004 | 0/0 | 867 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | MLSPN others(862): Show |
chr6 | 108843422 | 108979476 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2601 | 248 | 65 | 53 | 85 | 12 | 31 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 | ||
| a0001c0004 | 0/0 | 2601 | 3 | 0 | 0 | 0 | 1 | 2 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 | ||
| a0001c0006 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 | ||
| a0001c0007 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 | ||
| a0001c0008 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 | ||
| a0002c0002 | 0/0 | 2601 | 24 | 1 | 5 | 17 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 | ||
| a0003c0003 | 0/0 | 2601 | 8 | 8 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 | ||
| a0004c0005 | 0/0 | 2601 | 3 | 1 | 2 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | ATGCT others(2596): Show |
chr6 | 108843422 | 108979476 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3734 | 189 | 43 | 44 | 71 | 9 | 20 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0002 | 0/0 | 3734 | 24 | 11 | 4 | 5 | 0 | 4 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0003 | 0/0 | 3734 | 22 | 7 | 3 | 7 | 1 | 4 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0004 | 0/0 | 3734 | 6 | 0 | 1 | 0 | 2 | 3 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0005 | 0/0 | 3734 | 2 | 2 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0006 | 0/0 | 3734 | 2 | 0 | 0 | 2 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0007 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0009 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0001t0010 | 0/0 | 3734 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0004t0001 | 0/0 | 3734 | 3 | 0 | 0 | 0 | 1 | 2 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0006t0001 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0006t0002 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0007t0008 | 0/0 | 3734 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0001c0008t0001 | 0/0 | 3734 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0002c0002t0001 | 0/0 | 3734 | 23 | 1 | 5 | 16 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0002c0002t0002 | 0/0 | 3734 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0003c0003t0001 | 0/0 | 3734 | 3 | 3 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0003c0003t0002 | 0/0 | 3734 | 5 | 5 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| a0004c0005t0001 | 0/0 | 3734 | 3 | 1 | 2 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | AGTGG others(3729): Show |
chr6 | 108843422 | 108979476 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0004t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0006t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0007t0008g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0001c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0003c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0004c0005t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0004c0005t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| a0004c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0045 | EUR | GBR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0169 | EUR | FIN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0071 | EUR | FIN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0149 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01106 | hp1 | a0004 | c0005 | t0001 | g0040 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0047 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0273 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01884 | hp1 | a0004 | c0005 | t0001 | g0129 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01891 | hp2 | a0001 | c0008 | t0001 | g0123 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0276 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG01981 | hp2 | a0004 | c0005 | t0001 | g0052 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0274 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0266 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CDX | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0065 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0039 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02723 | hp2 | a0001 | c0006 | t0001 | g0058 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0181 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0116 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02886 | hp2 | a0003 | c0003 | t0002 | g0193 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03195 | hp2 | a0003 | c0003 | t0002 | g0092 | AFR | ESN | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03239 | hp1 | a0001 | c0004 | t0001 | g0184 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0183 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0249 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0046 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0219 | SAS | BEB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | BEB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0288 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0090 | AFR | YRI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | YRI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0269 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0282 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0272 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19240 | hp1 | a0003 | c0003 | t0002 | g0125 | AFR | YRI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA19240 | hp2 | a0001 | c0006 | t0002 | g0057 | AFR | YRI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ASW | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0070 | AFR | ASW | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20752 | hp2 | a0001 | c0004 | t0001 | g0185 | EUR | TSI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20805 | hp1 | a0001 | c0007 | t0008 | g0262 | EUR | TSI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02486 | hp1 | a0003 | c0003 | t0002 | g0187 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | USA | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | USA | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | USA | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | USA | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0016 | REF | REF | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0100 | REF | REF | ARMC2_chr6_108843422_108979476 | ARMC2 | chr6 | 108843422 | 108979476 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108876176 | T | C | 1 | a0002 | 24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
missense_variant | MODERATE | c.497T>C | p.Met166Thr | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/18 | 665/3734 | 497/2604 | 166/867 | chr6 | 108876176 | |||
| chr6:108953073 | C | T | 1 | a0004 | 3 | HG01106.hp1 HG01884.hp1 HG01981.hp2 |
missense_variant | MODERATE | c.1637C>T | p.Thr546Met | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/18 | 1805/3734 | 1637/2604 | 546/867 | chr6 | 108953073 | |||
| chr6:108953324 | A | G | 1 | a0003 | 8 | HG02486.hp1 HG02615.hp2 HG02809.hp1 others(5): Show |
missense_variant | MODERATE | c.1888A>G | p.Ile630Val | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/18 | 2056/3734 | 1888/2604 | 630/867 | chr6 | 108953324 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108868829 | G | A | 1 | a0001c0006 | 2 | HG02723.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.297G>A | p.Pro99Pro | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/18 | 465/3734 | 297/2604 | 99/867 | chr6 | 108868829 | |||
| chr6:108912522 | T | C | 1 | a0002c0002 | 24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
synonymous_variant | LOW | c.1314T>C | p.Gly438Gly | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/18 | 1482/3734 | 1314/2604 | 438/867 | chr6 | 108912522 | |||
| chr6:108953215 | G | A | 1 | a0001c0004 | 3 | HG03239.hp1 HG03492.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.1779G>A | p.Ala593Ala | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/18 | 1947/3734 | 1779/2604 | 593/867 | chr6 | 108953215 | |||
| chr6:108953311 | C | T | 1 | a0001c0008 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1875C>T | p.Ala625Ala | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/18 | 2043/3734 | 1875/2604 | 625/867 | chr6 | 108953311 | |||
| chr6:108953320 | G | A | 1 | a0001c0007 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1884G>A | p.Pro628Pro | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/18 | 2052/3734 | 1884/2604 | 628/867 | chr6 | 108953320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108848451 | C | G | 1 | a0001c0001t0010 | 1 | HG01257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-139C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/18 | 5817 | chr6 | 108848451 | ||||||
| chr6:108848452 | G | T | 1 | a0001c0001t0009 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-138G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/18 | 5816 | chr6 | 108848452 | ||||||
| chr6:108854238 | T | C | 2 | a0001c0001t0005 a0001c0001t0007 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-30T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/18 | 30 | chr6 | 108854238 | ||||||
| chr6:108973533 | T | G | 1 | a0001c0001t0006 | 2 | NA18944.hp2 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 19 | chr6 | 108973533 | ||||||
| chr6:108973549 | C | T | 3 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 |
29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*35C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 35 | chr6 | 108973549 | ||||||
| chr6:108973644 | A | T | 1 | a0001c0001t0006 | 2 | NA18944.hp2 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*130A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 130 | chr6 | 108973644 | ||||||
| chr6:108973814 | A | G | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*300A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 300 | chr6 | 108973814 | ||||||
| chr6:108973837 | T | C | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*323T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 323 | chr6 | 108973837 | ||||||
| chr6:108973917 | A | G | 2 | a0001c0001t0004 a0001c0001t0010 |
7 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*403A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 403 | chr6 | 108973917 | ||||||
| chr6:108974047 | T | C | 1 | a0001c0007t0008 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*533T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 533 | chr6 | 108974047 | ||||||
| chr6:108974090 | T | C | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(5): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*576T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 18/18 | 576 | chr6 | 108974090 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:108848859 | G | T | 1 | a0001c0001t0003g0290 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-44+313G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108848859 | |||||||
| chr6:108848871 | C | T | 25 | a0001c0001t0001g0289 a0002c0002t0001g0265 a0002c0002t0001g0267 others(22): Show |
25 | HG00423.hp2 HG00738.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.-44+325C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108848871 | |||||||
| chr6:108848964 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-44+418A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108848964 | |||||||
| chr6:108849053 | G | A | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-44+507G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108849053 | |||||||
| chr6:108849401 | A | G | 107 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0001g0189 others(104): Show |
107 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-44+855A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108849401 | |||||||
| chr6:108849726 | C | T | 61 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0209 others(58): Show |
61 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.-44+1180C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108849726 | |||||||
| chr6:108849803 | A | G | 45 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(42): Show |
45 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.-44+1257A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108849803 | |||||||
| chr6:108850058 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-44+1512G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108850058 | |||||||
| chr6:108850080 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-44+1534A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108850080 | |||||||
| chr6:108850668 | T | C | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+2122T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108850668 | |||||||
| chr6:108850685 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-44+2139A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108850685 | |||||||
| chr6:108850742 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+2196C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108850742 | |||||||
| chr6:108850783 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44+2237T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108850783 | |||||||
| chr6:108850823 | T | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-44+2277T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108850823 | |||||||
| chr6:108851047 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0002g0203 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-44+2501C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851047 | |||||||
| chr6:108851123 | T | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-44+2577T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851123 | |||||||
| chr6:108851138 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-44+2592A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851138 | |||||||
| chr6:108851330 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-44+2784G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851330 | |||||||
| chr6:108851343 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+2797A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851343 | |||||||
| chr6:108851455 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-43-2770A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851455 | |||||||
| chr6:108851719 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-43-2506T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851719 | |||||||
| chr6:108851842 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-43-2383G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851842 | |||||||
| chr6:108851940 | C | T | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-2285C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108851940 | |||||||
| chr6:108852102 | A | G | 23 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-2123A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852102 | |||||||
| chr6:108852212 | C | T | 2 | a0001c0001t0001g0128 a0004c0005t0001g0129 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-43-2013C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852212 | |||||||
| chr6:108852305 | C | T | 11 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(8): Show |
11 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-1920C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852305 | |||||||
| chr6:108852766 | C | CTG | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-1457_-43-1456d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 108852766 | ||||||
| chr6:108852768 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-43-1457G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852768 | |||||||
| chr6:108852805 | A | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-1420A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852805 | |||||||
| chr6:108852858 | T | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-1367T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852858 | |||||||
| chr6:108852876 | C | T | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-1349C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852876 | |||||||
| chr6:108852942 | A | G | 1 | a0001c0001t0004g0071 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-43-1283A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852942 | |||||||
| chr6:108852964 | A | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-1261A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108852964 | |||||||
| chr6:108853493 | A | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-732A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108853493 | |||||||
| chr6:108853682 | T | G | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-43-543T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108853682 | |||||||
| chr6:108853880 | CT | C | 17 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(14): Show |
17 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-43-344delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108853880 | |||||||
| chr6:108853938 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG01361.hp2 HG01975.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-287T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108853938 | |||||||
| chr6:108854065 | A | G | 6 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-160A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108854065 | |||||||
| chr6:108854169 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-43-56G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108854169 | |||||||
| chr6:108854196 | A | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-29A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 1/17 | chr6 | 108854196 | |||||||
| chr6:108854541 | T | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.218+56T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108854541 | |||||||
| chr6:108854562 | T | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.218+77T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108854562 | |||||||
| chr6:108854964 | A | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+479A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108854964 | |||||||
| chr6:108855197 | A | T | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+712A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855197 | |||||||
| chr6:108855222 | G | A | 1 | a0002c0002t0001g0265 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.218+737G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855222 | |||||||
| chr6:108855248 | T | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+763T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855248 | |||||||
| chr6:108855250 | C | CTT | 9 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(6): Show |
9 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+780_218+781dup others(2): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 108855250 | ||||||
| chr6:108855441 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.218+956C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855441 | |||||||
| chr6:108855531 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.218+1046G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855531 | |||||||
| chr6:108855561 | C | G | 1 | a0002c0002t0001g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.218+1076C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855561 | |||||||
| chr6:108855592 | G | T | 37 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.218+1107G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855592 | |||||||
| chr6:108855614 | C | T | 10 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(7): Show |
10 | HG02109.hp2 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+1129C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855614 | |||||||
| chr6:108855878 | G | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.218+1393G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855878 | |||||||
| chr6:108855926 | GAATT | G | 8 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(5): Show |
8 | HG00597.hp2 HG01175.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+1443_218+1446d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 108855926 | ||||||
| chr6:108855935 | A | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.218+1450A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108855935 | |||||||
| chr6:108856058 | G | T | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.218+1573G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108856058 | |||||||
| chr6:108856124 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.218+1639G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108856124 | |||||||
| chr6:108856652 | A | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-1547A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108856652 | |||||||
| chr6:108856907 | A | G | 4 | a0001c0001t0001g0067 a0001c0001t0002g0066 a0001c0001t0003g0064 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-1292A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108856907 | |||||||
| chr6:108856952 | A | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-1247A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108856952 | |||||||
| chr6:108857017 | GTTC | G | 28 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0209 others(25): Show |
28 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.219-1176_219-1174d others(5): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 108857017 | ||||||
| chr6:108857047 | T | C | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0245 |
3 | NA19007.hp1 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.219-1152T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857047 | |||||||
| chr6:108857067 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.219-1132A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857067 | |||||||
| chr6:108857068 | T | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-1131T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857068 | |||||||
| chr6:108857128 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG00423.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.219-1071G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857128 | |||||||
| chr6:108857207 | C | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-992C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857207 | |||||||
| chr6:108857474 | C | T | 1 | a0003c0003t0002g0125 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.219-725C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857474 | |||||||
| chr6:108857519 | A | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-680A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857519 | |||||||
| chr6:108857533 | T | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-666T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857533 | |||||||
| chr6:108857602 | C | CTCTT | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-596_219-593dup others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 108857602 | ||||||
| chr6:108857662 | T | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-537T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857662 | |||||||
| chr6:108857671 | C | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-528C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857671 | |||||||
| chr6:108857766 | A | C | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.219-433A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857766 | |||||||
| chr6:108857770 | ATCT | A | 35 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(32): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.219-424_219-422del others(3): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 108857770 | ||||||
| chr6:108857873 | CAT | C | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.219-325_219-324del others(2): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108857873 | |||||||
| chr6:108858021 | GT | G | 6 | a0002c0002t0001g0282 a0002c0002t0001g0283 a0002c0002t0001g0284 others(3): Show |
6 | NA18940.hp1 NA18952.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-177delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108858021 | |||||||
| chr6:108858030 | A | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.219-169A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108858030 | |||||||
| chr6:108858074 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.219-125G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108858074 | |||||||
| chr6:108858148 | T | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-51T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108858148 | |||||||
| chr6:108858195 | C | T | 1 | a0001c0001t0003g0002 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.219-4C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 2/17 | chr6 | 108858195 | |||||||
| chr6:108858667 | GTCTC | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+400_291+403del others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108858667 | ||||||
| chr6:108858741 | A | G | 2 | a0002c0002t0001g0279 a0002c0002t0001g0280 |
2 | NA19001.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.291+470A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108858741 | |||||||
| chr6:108858821 | A | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(114): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.291+550A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108858821 | |||||||
| chr6:108858991 | A | T | 1 | a0001c0007t0008g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.291+720A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108858991 | |||||||
| chr6:108859032 | A | G | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0245 |
3 | NA19007.hp1 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.291+761A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859032 | |||||||
| chr6:108859165 | T | C | 1 | a0001c0007t0008g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.291+894T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859165 | |||||||
| chr6:108859246 | C | T | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291+975C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859246 | |||||||
| chr6:108859323 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.291+1052C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859323 | |||||||
| chr6:108859331 | C | CCTT | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+1061_291+1063d others(5): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108859331 | ||||||
| chr6:108859335 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.291+1064G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859335 | |||||||
| chr6:108859349 | G | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+1078G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859349 | |||||||
| chr6:108859630 | T | A | 1 | a0002c0002t0002g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.291+1359T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859630 | |||||||
| chr6:108859765 | C | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+1494C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859765 | |||||||
| chr6:108859795 | C | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+1524C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859795 | |||||||
| chr6:108859796 | G | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | NA18962.hp2 NA18971.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+1525G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859796 | |||||||
| chr6:108859907 | G | C | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.291+1636G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108859907 | |||||||
| chr6:108860003 | TTAA | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+1733_291+1735d others(5): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860003 | |||||||
| chr6:108860004 | TA | T | 108 | a0001c0001t0001g0013 a0001c0001t0001g0076 a0001c0001t0001g0083 others(105): Show |
108 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.291+1751delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108860004 | ||||||
| chr6:108860007 | A | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+1736A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860007 | |||||||
| chr6:108860195 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291+1924A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860195 | |||||||
| chr6:108860389 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.291+2118G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860389 | |||||||
| chr6:108860471 | C | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+2200C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860471 | |||||||
| chr6:108860520 | A | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+2249A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860520 | |||||||
| chr6:108860551 | A | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.291+2280A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860551 | |||||||
| chr6:108860602 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.291+2331C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860602 | |||||||
| chr6:108860603 | A | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.291+2332A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860603 | |||||||
| chr6:108860622 | A | C | 37 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.291+2351A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860622 | |||||||
| chr6:108860641 | G | A | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG03098.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.291+2370G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860641 | |||||||
| chr6:108860661 | C | CA | 67 | a0001c0001t0001g0024 a0001c0001t0001g0096 a0001c0001t0001g0205 others(64): Show |
67 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.291+2410dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108860661 | ||||||
| chr6:108860661 | CA | C | 13 | a0001c0001t0001g0017 a0001c0001t0001g0082 a0001c0001t0001g0120 others(10): Show |
13 | HG00738.hp2 HG01081.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.291+2410delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108860661 | ||||||
| chr6:108860704 | G | A | 1 | a0001c0001t0004g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.291+2433G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860704 | |||||||
| chr6:108860727 | C | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.291+2456C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108860727 | |||||||
| chr6:108861020 | A | G | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291+2749A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861020 | |||||||
| chr6:108861043 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.291+2772C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861043 | |||||||
| chr6:108861299 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.291+3028C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861299 | |||||||
| chr6:108861301 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.291+3030C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861301 | |||||||
| chr6:108861468 | A | G | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.291+3197A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861468 | |||||||
| chr6:108861519 | A | G | 2 | a0001c0001t0005g0089 a0001c0001t0005g0090 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.291+3248A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861519 | |||||||
| chr6:108861635 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.291+3364A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861635 | |||||||
| chr6:108861687 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.291+3416A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861687 | |||||||
| chr6:108861741 | C | T | 118 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0085 others(115): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.291+3470C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108861741 | |||||||
| chr6:108862167 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.291+3896A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862167 | |||||||
| chr6:108862325 | T | C | 1 | a0001c0001t0003g0243 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.291+4054T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862325 | |||||||
| chr6:108862342 | C | CA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0026 others(12): Show |
15 | HG00642.hp2 HG01175.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.291+4087dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108862342 | ||||||
| chr6:108862342 | C | CAA | 16 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(13): Show |
16 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.291+4086_291+4087d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108862342 | ||||||
| chr6:108862346 | AAAAAAAA others(6): Show |
A | 2 | a0001c0001t0001g0182 a0001c0001t0003g0290 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.291+4084_291+4096d others(15): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108862346 | ||||||
| chr6:108862357 | A | C | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.291+4086A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862357 | |||||||
| chr6:108862358 | AC | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(133): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.291+4088delC | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862358 | |||||||
| chr6:108862359 | C | A | 94 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(91): Show |
94 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.291+4088C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862359 | |||||||
| chr6:108862363 | A | C | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.291+4092A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862363 | |||||||
| chr6:108862368 | C | A | 3 | a0001c0001t0001g0202 a0001c0001t0002g0203 a0003c0003t0002g0193 |
3 | HG02572.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.291+4097C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862368 | |||||||
| chr6:108862537 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0002g0203 a0003c0003t0002g0193 |
3 | HG02572.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.291+4266T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108862537 | |||||||
| chr6:108863044 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG01099.hp2 HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.291+4773C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863044 | |||||||
| chr6:108863176 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.291+4905G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863176 | |||||||
| chr6:108863181 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.291+4910G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863181 | |||||||
| chr6:108863311 | A | G | 284 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.291+5040A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863311 | |||||||
| chr6:108863410 | A | C | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.291+5139A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863410 | |||||||
| chr6:108863435 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0083 |
2 | HG02155.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.291+5164G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863435 | |||||||
| chr6:108863460 | A | G | 1 | a0002c0002t0001g0277 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.291+5189A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863460 | |||||||
| chr6:108863556 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02965.hp2 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.292-5268C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863556 | |||||||
| chr6:108863826 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.292-4998A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863826 | |||||||
| chr6:108863912 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.292-4912C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863912 | |||||||
| chr6:108863924 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.292-4900C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863924 | |||||||
| chr6:108863975 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.292-4849A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108863975 | |||||||
| chr6:108864253 | C | CT | 229 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(226): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.292-4557dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108864253 | ||||||
| chr6:108864329 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.292-4495A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864329 | |||||||
| chr6:108864330 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.292-4494C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864330 | |||||||
| chr6:108864352 | G | A | 1 | a0002c0002t0001g0282 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.292-4472G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864352 | |||||||
| chr6:108864580 | T | A | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.292-4244T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864580 | |||||||
| chr6:108864584 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.292-4240A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864584 | |||||||
| chr6:108864708 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.292-4116G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864708 | |||||||
| chr6:108864827 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.292-3997C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864827 | |||||||
| chr6:108864946 | A | G | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.292-3878A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108864946 | |||||||
| chr6:108864997 | A | AT | 152 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(149): Show |
152 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.292-3808dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108864997 | ||||||
| chr6:108864997 | A | ATT | 8 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG01081.hp2 HG01109.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.292-3809_292-3808d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108864997 | ||||||
| chr6:108864997 | AT | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0122 others(3): Show |
6 | HG01169.hp2 HG01891.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.292-3808delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108864997 | ||||||
| chr6:108865087 | A | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.292-3737A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108865087 | |||||||
| chr6:108865674 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.292-3150G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108865674 | |||||||
| chr6:108866016 | T | TA | 19 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0075 others(16): Show |
19 | HG00423.hp2 HG00621.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.292-2786dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108866016 | ||||||
| chr6:108866016 | TAA | T | 24 | a0001c0001t0001g0083 a0002c0002t0001g0265 a0002c0002t0001g0267 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.292-2787_292-2786d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr6 | 108866016 | ||||||
| chr6:108866703 | C | T | 1 | a0001c0001t0002g0260 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.292-2121C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108866703 | |||||||
| chr6:108866707 | G | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.292-2117G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108866707 | |||||||
| chr6:108866729 | T | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-2095T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108866729 | |||||||
| chr6:108866744 | A | G | 3 | a0002c0002t0001g0267 a0002c0002t0001g0273 a0002c0002t0001g0278 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.292-2080A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108866744 | |||||||
| chr6:108866800 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.292-2024A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108866800 | |||||||
| chr6:108866963 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0002g0203 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.292-1861A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108866963 | |||||||
| chr6:108866983 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292-1841G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108866983 | |||||||
| chr6:108867099 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG01099.hp2 HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.292-1725G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867099 | |||||||
| chr6:108867101 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.292-1723T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867101 | |||||||
| chr6:108867126 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.292-1698A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867126 | |||||||
| chr6:108867188 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.292-1636A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867188 | |||||||
| chr6:108867191 | T | C | 5 | a0002c0002t0001g0282 a0002c0002t0001g0283 a0002c0002t0001g0284 others(2): Show |
5 | NA18940.hp1 NA18952.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.292-1633T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867191 | |||||||
| chr6:108867211 | G | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.292-1613G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867211 | |||||||
| chr6:108867285 | G | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.292-1539G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867285 | |||||||
| chr6:108867331 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01361.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.292-1493T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867331 | |||||||
| chr6:108867406 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.292-1418C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867406 | |||||||
| chr6:108867407 | G | A | 1 | a0002c0002t0001g0275 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.292-1417G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867407 | |||||||
| chr6:108867565 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.292-1259G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867565 | |||||||
| chr6:108867566 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.292-1258C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867566 | |||||||
| chr6:108867627 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.292-1197C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867627 | |||||||
| chr6:108867721 | A | C | 1 | a0001c0001t0007g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.292-1103A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867721 | |||||||
| chr6:108867818 | C | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(216): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.292-1006C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867818 | |||||||
| chr6:108867840 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.292-984C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867840 | |||||||
| chr6:108867866 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.292-958G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867866 | |||||||
| chr6:108867952 | C | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.292-872C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108867952 | |||||||
| chr6:108868125 | A | G | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292-699A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108868125 | |||||||
| chr6:108868210 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.292-614T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108868210 | |||||||
| chr6:108868356 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.292-468A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108868356 | |||||||
| chr6:108868461 | C | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(191): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.292-363C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108868461 | |||||||
| chr6:108868784 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.292-40C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 3/17 | chr6 | 108868784 | |||||||
| chr6:108869064 | A | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.463+69A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108869064 | |||||||
| chr6:108869102 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.463+107A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108869102 | |||||||
| chr6:108869189 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0180 |
2 | NA19060.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.463+194A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108869189 | |||||||
| chr6:108869653 | A | G | 23 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.463+658A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108869653 | |||||||
| chr6:108869690 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.463+695G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108869690 | |||||||
| chr6:108869807 | T | C | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.463+812T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108869807 | |||||||
| chr6:108870196 | C | A | 1 | a0001c0001t0002g0068 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.463+1201C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108870196 | |||||||
| chr6:108870301 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.463+1306T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108870301 | |||||||
| chr6:108870509 | AAGAG | A | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.463+1520_463+1523d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 108870509 | ||||||
| chr6:108870553 | AAGAGAGG others(5): Show |
A | 23 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.463+1573_463+1584d others(14): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 108870553 | ||||||
| chr6:108870604 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.463+1609G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108870604 | |||||||
| chr6:108870707 | A | G | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.463+1712A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108870707 | |||||||
| chr6:108870897 | ATAAG | A | 60 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0209 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.463+1907_463+1910d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 108870897 | ||||||
| chr6:108871045 | C | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.463+2050C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871045 | |||||||
| chr6:108871283 | G | T | 1 | a0001c0001t0003g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.463+2288G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871283 | |||||||
| chr6:108871452 | G | C | 60 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0209 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.463+2457G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871452 | |||||||
| chr6:108871616 | T | C | 227 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(224): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.463+2621T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871616 | |||||||
| chr6:108871647 | A | G | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.463+2652A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871647 | |||||||
| chr6:108871695 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0002g0203 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.463+2700C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871695 | |||||||
| chr6:108871726 | C | T | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.463+2731C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871726 | |||||||
| chr6:108871733 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.463+2738C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871733 | |||||||
| chr6:108871860 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.463+2865T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871860 | |||||||
| chr6:108871939 | A | G | 224 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(221): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.463+2944A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871939 | |||||||
| chr6:108871970 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.463+2975G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108871970 | |||||||
| chr6:108872182 | G | A | 5 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG03041.hp1 HG03098.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.463+3187G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108872182 | |||||||
| chr6:108872281 | G | A | 144 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0085 others(141): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.463+3286G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108872281 | |||||||
| chr6:108872436 | G | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(76): Show |
79 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.463+3441G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108872436 | |||||||
| chr6:108872459 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.463+3464C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108872459 | |||||||
| chr6:108872790 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(217): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.464-3353C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108872790 | |||||||
| chr6:108872859 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.464-3284G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108872859 | |||||||
| chr6:108873101 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.464-3042C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873101 | |||||||
| chr6:108873336 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.464-2807C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873336 | |||||||
| chr6:108873388 | G | A | 1 | a0001c0001t0003g0001 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.464-2755G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873388 | |||||||
| chr6:108873468 | C | T | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.464-2675C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873468 | |||||||
| chr6:108873482 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0174 |
2 | HG01069.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.464-2661C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873482 | |||||||
| chr6:108873593 | T | TA | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG00639.hp1 HG01358.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-2548dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 108873593 | ||||||
| chr6:108873737 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.464-2406C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873737 | |||||||
| chr6:108873804 | C | T | 4 | a0002c0002t0001g0265 a0002c0002t0001g0270 a0002c0002t0001g0271 others(1): Show |
4 | NA18957.hp2 NA18964.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-2339C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873804 | |||||||
| chr6:108873839 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.464-2304C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873839 | |||||||
| chr6:108873925 | G | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.464-2218G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108873925 | |||||||
| chr6:108874012 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.464-2131G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874012 | |||||||
| chr6:108874051 | T | C | 1 | a0001c0001t0003g0001 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.464-2092T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874051 | |||||||
| chr6:108874055 | T | A | 1 | a0001c0001t0003g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.464-2088T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874055 | |||||||
| chr6:108874190 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.464-1953C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874190 | |||||||
| chr6:108874243 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.464-1900A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874243 | |||||||
| chr6:108874350 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(216): Show |
219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.464-1793C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874350 | |||||||
| chr6:108874429 | A | G | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.464-1714A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874429 | |||||||
| chr6:108874618 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.464-1525A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108874618 | |||||||
| chr6:108874835 | TA | T | 8 | a0001c0001t0001g0069 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | HG00323.hp2 HG01081.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-1294delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr6 | 108874835 | ||||||
| chr6:108875066 | C | A | 1 | a0001c0004t0001g0184 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.464-1077C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875066 | |||||||
| chr6:108875212 | A | G | 2 | a0001c0006t0001g0058 a0001c0006t0002g0057 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.464-931A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875212 | |||||||
| chr6:108875223 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.464-920G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875223 | |||||||
| chr6:108875594 | C | G | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-549C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875594 | |||||||
| chr6:108875637 | A | T | 1 | a0001c0001t0003g0219 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.464-506A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875637 | |||||||
| chr6:108875643 | T | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.464-500T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875643 | |||||||
| chr6:108875682 | T | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.464-461T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875682 | |||||||
| chr6:108875874 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.464-269C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 4/17 | chr6 | 108875874 | |||||||
| chr6:108876400 | A | C | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.671+50A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108876400 | |||||||
| chr6:108876505 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 |
3 | HG01346.hp2 HG01975.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.671+155G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108876505 | |||||||
| chr6:108876886 | T | C | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+536T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108876886 | |||||||
| chr6:108876928 | C | G | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(1): Show |
4 | HG02886.hp1 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+578C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108876928 | |||||||
| chr6:108877321 | C | A | 2 | a0002c0002t0001g0277 a0002c0002t0002g0266 |
2 | HG02129.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.671+971C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108877321 | |||||||
| chr6:108878010 | T | C | 39 | a0001c0001t0001g0069 a0001c0001t0001g0122 a0001c0001t0001g0150 others(36): Show |
39 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.671+1660T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108878010 | |||||||
| chr6:108878566 | A | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+2216A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108878566 | |||||||
| chr6:108879038 | TACTCATC others(1): Show |
T | 3 | a0001c0001t0001g0202 a0001c0001t0002g0203 a0003c0003t0002g0193 |
3 | HG02572.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.671+2696_671+2703d others(10): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108879038 | ||||||
| chr6:108879040 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0160 |
2 | HG00140.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.671+2690C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879040 | |||||||
| chr6:108879066 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.671+2716C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879066 | |||||||
| chr6:108879089 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(1): Show |
4 | HG01346.hp2 HG01975.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+2739C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879089 | |||||||
| chr6:108879230 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2880C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879230 | |||||||
| chr6:108879298 | A | G | 4 | a0002c0002t0001g0265 a0002c0002t0001g0270 a0002c0002t0001g0271 others(1): Show |
4 | NA18957.hp2 NA18964.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+2948A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879298 | |||||||
| chr6:108879345 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.671+2995C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879345 | |||||||
| chr6:108879365 | A | G | 2 | a0001c0001t0006g0021 a0001c0001t0006g0054 |
2 | NA18944.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.671+3015A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879365 | |||||||
| chr6:108879575 | T | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.671+3225T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879575 | |||||||
| chr6:108879691 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01361.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.671+3341G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879691 | |||||||
| chr6:108879926 | A | C | 37 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.671+3576A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108879926 | |||||||
| chr6:108880114 | T | C | 3 | a0001c0001t0001g0225 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG01099.hp2 HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.671+3764T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108880114 | |||||||
| chr6:108880537 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.671+4187G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108880537 | |||||||
| chr6:108880578 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG00423.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.671+4228A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108880578 | |||||||
| chr6:108880746 | T | A | 25 | a0001c0001t0001g0020 a0002c0002t0001g0265 a0002c0002t0001g0267 others(22): Show |
25 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(22): Show |
intron_variant | MODIFIER | c.671+4396T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108880746 | |||||||
| chr6:108880777 | C | CTCCT | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.671+4440_671+4443d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108880777 | ||||||
| chr6:108880942 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.671+4592G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108880942 | |||||||
| chr6:108880982 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.671+4632T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108880982 | |||||||
| chr6:108881275 | TCCCTC | T | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.671+4945_671+4949d others(7): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881275 | ||||||
| chr6:108881296 | C | CCCTCCCC others(42): Show |
2 | a0001c0001t0005g0090 a0001c0001t0007g0088 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.671+4949_671+4950i others(51): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTCCCC others(46): Show |
1 | a0001c0001t0005g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.671+4949_671+4950i others(55): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(9): Show |
24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.671+4952_671+4967d others(18): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(13): Show |
3 | a0001c0001t0001g0159 a0001c0001t0002g0055 a0002c0002t0001g0280 |
3 | HG02083.hp2 HG03471.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.671+4948_671+4967d others(22): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(17): Show |
104 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0022 others(101): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.671+4967_671+4968i others(26): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(21): Show |
30 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0030 others(27): Show |
30 | HG00558.hp1 HG01081.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.671+4967_671+4968i others(30): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(25): Show |
18 | a0001c0001t0001g0186 a0001c0001t0001g0197 a0001c0001t0001g0229 others(15): Show |
18 | HG00597.hp2 HG01106.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.671+4967_671+4968i others(34): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(29): Show |
22 | a0001c0001t0001g0201 a0001c0001t0001g0205 a0001c0001t0001g0220 others(19): Show |
22 | HG01099.hp2 HG01109.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.671+4967_671+4968i others(38): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(33): Show |
17 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(14): Show |
17 | HG00408.hp1 HG02040.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.671+4967_671+4968i others(42): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CCCTTCCT others(37): Show |
4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0002g0218 others(1): Show |
4 | HG00438.hp1 HG01069.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+4967_671+4968i others(46): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881296 | ||||||
| chr6:108881296 | C | CTTCCTTC others(19): Show |
1 | a0001c0001t0001g0191 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.671+4946_671+4947i others(28): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108881296 | |||||||
| chr6:108881318 | A | C | 5 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0005g0089 others(2): Show |
5 | HG01069.hp1 HG01255.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+4968A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108881318 | |||||||
| chr6:108881568 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.671+5218C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108881568 | |||||||
| chr6:108881585 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.671+5235G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108881585 | |||||||
| chr6:108881700 | T | TTG | 5 | a0001c0001t0001g0084 a0001c0001t0001g0205 a0001c0001t0002g0204 others(2): Show |
5 | HG02027.hp1 HG03471.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+5354_671+5355d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108881700 | ||||||
| chr6:108881706 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(233): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.671+5356A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108881706 | |||||||
| chr6:108881801 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.671+5451A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108881801 | |||||||
| chr6:108881905 | C | T | 2 | a0001c0006t0001g0058 a0001c0006t0002g0057 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.671+5555C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108881905 | |||||||
| chr6:108882049 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.671+5699A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108882049 | |||||||
| chr6:108882136 | TA | T | 28 | a0001c0001t0001g0053 a0001c0001t0001g0094 a0001c0001t0001g0198 others(25): Show |
28 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.671+5798delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108882136 | ||||||
| chr6:108882438 | CA | C | 232 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(229): Show |
232 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.671+6103delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108882438 | ||||||
| chr6:108882493 | G | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.671+6143G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108882493 | |||||||
| chr6:108882645 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.671+6295A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108882645 | |||||||
| chr6:108882768 | C | T | 1 | a0002c0002t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.671+6418C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108882768 | |||||||
| chr6:108882788 | TCAGA | T | 35 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(32): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.671+6441_671+6444d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108882788 | ||||||
| chr6:108882813 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(132): Show |
135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.671+6463G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108882813 | |||||||
| chr6:108883331 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.671+6981A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108883331 | |||||||
| chr6:108883586 | C | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(233): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.671+7236C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108883586 | |||||||
| chr6:108883670 | A | T | 5 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
5 | HG00280.hp2 HG00642.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+7320A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108883670 | |||||||
| chr6:108883713 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.671+7363A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108883713 | |||||||
| chr6:108884519 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.671+8169G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108884519 | |||||||
| chr6:108884572 | T | G | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.671+8222T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108884572 | |||||||
| chr6:108884614 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.671+8264C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108884614 | |||||||
| chr6:108884621 | G | C | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.671+8271G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108884621 | |||||||
| chr6:108885211 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(233): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.671+8861A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885211 | |||||||
| chr6:108885221 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.671+8871C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885221 | |||||||
| chr6:108885227 | G | GGTGT | 23 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0101 others(20): Show |
23 | HG00423.hp2 HG00597.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.671+8898_671+8901d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108885227 | ||||||
| chr6:108885227 | G | GGTGTGT | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.671+8896_671+8901d others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108885227 | ||||||
| chr6:108885227 | GGT | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(214): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.671+8900_671+8901d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108885227 | ||||||
| chr6:108885258 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.671+8908T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885258 | |||||||
| chr6:108885275 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.671+8925G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885275 | |||||||
| chr6:108885434 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.672-9033C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885434 | |||||||
| chr6:108885473 | G | T | 1 | a0002c0002t0001g0287 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.672-8994G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885473 | |||||||
| chr6:108885576 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.672-8891G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885576 | |||||||
| chr6:108885588 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.672-8879C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885588 | |||||||
| chr6:108885672 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.672-8795G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885672 | |||||||
| chr6:108885673 | C | CA | 8 | a0001c0001t0001g0008 a0002c0002t0001g0282 a0002c0002t0001g0283 others(5): Show |
8 | HG01346.hp2 HG04204.hp2 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-8783dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108885673 | ||||||
| chr6:108885673 | C | CAA | 15 | a0002c0002t0001g0267 a0002c0002t0001g0268 a0002c0002t0001g0269 others(12): Show |
15 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.672-8784_672-8783d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108885673 | ||||||
| chr6:108885678 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.672-8789A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885678 | |||||||
| chr6:108885765 | G | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-8702G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885765 | |||||||
| chr6:108885826 | G | T | 4 | a0001c0001t0001g0067 a0001c0001t0002g0066 a0001c0001t0003g0064 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-8641G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885826 | |||||||
| chr6:108885944 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.672-8523G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885944 | |||||||
| chr6:108885979 | A | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.672-8488A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108885979 | |||||||
| chr6:108886113 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0002g0203 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.672-8354T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886113 | |||||||
| chr6:108886284 | C | T | 3 | a0002c0002t0001g0275 a0002c0002t0001g0276 a0002c0002t0001g0281 |
3 | HG01928.hp1 HG02040.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.672-8183C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886284 | |||||||
| chr6:108886295 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.672-8172C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886295 | |||||||
| chr6:108886333 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.672-8134G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886333 | |||||||
| chr6:108886377 | G | A | 1 | a0002c0002t0001g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.672-8090G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886377 | |||||||
| chr6:108886476 | G | C | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.672-7991G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886476 | |||||||
| chr6:108886585 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.672-7882A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886585 | |||||||
| chr6:108886761 | CA | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.672-7703delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108886761 | ||||||
| chr6:108886883 | GT | G | 36 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(33): Show |
36 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.672-7574delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108886883 | ||||||
| chr6:108886890 | T | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG00099.hp2 HG00140.hp1 HG00597.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-7577T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886890 | |||||||
| chr6:108886897 | T | G | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.672-7570T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108886897 | |||||||
| chr6:108886907 | G | GT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.672-7549dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108886907 | ||||||
| chr6:108887007 | A | C | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.672-7460A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887007 | |||||||
| chr6:108887030 | C | T | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-7437C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887030 | |||||||
| chr6:108887032 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.672-7435C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887032 | |||||||
| chr6:108887493 | A | G | 1 | a0001c0001t0003g0064 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.672-6974A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887493 | |||||||
| chr6:108887539 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672-6928G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887539 | |||||||
| chr6:108887705 | A | G | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.672-6762A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887705 | |||||||
| chr6:108887767 | G | A | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-6700G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887767 | |||||||
| chr6:108887855 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.672-6612G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887855 | |||||||
| chr6:108887904 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.672-6563G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108887904 | |||||||
| chr6:108888045 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.672-6422G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108888045 | |||||||
| chr6:108888064 | C | G | 1 | a0001c0008t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.672-6403C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108888064 | |||||||
| chr6:108888420 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.672-6047G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108888420 | |||||||
| chr6:108888498 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.672-5969G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108888498 | |||||||
| chr6:108888626 | G | A | 1 | a0001c0001t0006g0021 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.672-5841G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108888626 | |||||||
| chr6:108888922 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.672-5545T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108888922 | |||||||
| chr6:108888929 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.672-5538C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108888929 | |||||||
| chr6:108889078 | T | C | 1 | a0003c0003t0002g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.672-5389T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108889078 | |||||||
| chr6:108889111 | G | A | 1 | a0001c0001t0003g0001 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.672-5356G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108889111 | |||||||
| chr6:108889365 | C | T | 2 | a0001c0001t0002g0066 a0001c0001t0009g0065 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.672-5102C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108889365 | |||||||
| chr6:108889397 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.672-5070C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108889397 | |||||||
| chr6:108889508 | A | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.672-4959A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108889508 | |||||||
| chr6:108889583 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.672-4884G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108889583 | |||||||
| chr6:108889669 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0118 |
2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.672-4798G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108889669 | |||||||
| chr6:108890189 | C | CA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0015 others(3): Show |
6 | HG01346.hp2 HG01975.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-4238dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
7 | HG00140.hp1 HG01169.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.672-4243_672-4238d others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAAA | 8 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0225 others(5): Show |
8 | HG01099.hp2 HG01175.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-4244_672-4238d others(9): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0217 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.672-4247_672-4238d others(12): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0002g0222 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.672-4248_672-4238d others(13): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAAA others(5): Show |
6 | a0001c0001t0001g0237 a0001c0001t0002g0206 a0001c0001t0002g0216 others(3): Show |
6 | HG02809.hp2 HG03239.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-4249_672-4238d others(14): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.672-4250_672-4238d others(15): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0205 a0001c0001t0001g0234 |
2 | HG03453.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.672-4252_672-4238d others(17): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.672-4256_672-4238d others(21): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CA | C | 12 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0106 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.672-4238delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAA | C | 16 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0115 others(13): Show |
16 | HG01069.hp1 HG01106.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.672-4239_672-4238d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAA | C | 12 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0215 others(9): Show |
12 | HG01516.hp1 HG02004.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.672-4240_672-4238d others(5): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0204 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.672-4247_672-4238d others(12): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG06807.hp1 NA18952.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-4250_672-4238d others(15): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(7): Show |
C | 22 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0022 others(19): Show |
22 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.672-4251_672-4238d others(16): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(8): Show |
C | 67 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.672-4252_672-4238d others(17): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(9): Show |
C | 42 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0084 others(39): Show |
42 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.672-4253_672-4238d others(18): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0001g0148 a0001c0001t0003g0257 a0003c0003t0002g0193 |
3 | HG02886.hp2 NA18951.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.672-4254_672-4238d others(19): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(12): Show |
C | 1 | a0001c0001t0005g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.672-4256_672-4238d others(21): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890189 | CAAAAAAA others(13): Show |
C | 5 | a0001c0001t0001g0232 a0001c0001t0003g0001 a0001c0001t0003g0002 others(2): Show |
5 | HG02615.hp1 HG03225.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-4257_672-4238d others(22): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890189 | ||||||
| chr6:108890205 | A | C | 22 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(19): Show |
22 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.672-4262A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890205 | |||||||
| chr6:108890206 | A | C | 2 | a0002c0002t0001g0280 a0002c0002t0001g0288 |
2 | HG04204.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.672-4261A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890206 | |||||||
| chr6:108890207 | A | C | 1 | a0001c0007t0008g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.672-4260A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890207 | |||||||
| chr6:108890214 | A | AAAACAAA others(5): Show |
22 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(19): Show |
22 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.672-4250_672-4249i others(14): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890214 | ||||||
| chr6:108890217 | A | AACAAACA others(7): Show |
2 | a0002c0002t0001g0280 a0002c0002t0001g0288 |
2 | HG04204.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.672-4249_672-4248i others(16): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890217 | ||||||
| chr6:108890217 | A | C | 7 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0172 others(4): Show |
7 | HG00140.hp2 HG00323.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-4250A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890217 | |||||||
| chr6:108890218 | A | C | 50 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(47): Show |
50 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.672-4249A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890218 | |||||||
| chr6:108890219 | A | C | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.672-4248A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890219 | |||||||
| chr6:108890257 | AT | A | 61 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(58): Show |
61 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.672-4206delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108890257 | ||||||
| chr6:108890328 | A | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.672-4139A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890328 | |||||||
| chr6:108890337 | T | G | 1 | a0001c0006t0002g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.672-4130T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890337 | |||||||
| chr6:108890388 | T | A | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.672-4079T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890388 | |||||||
| chr6:108890867 | T | C | 67 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(64): Show |
67 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.672-3600T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890867 | |||||||
| chr6:108890917 | C | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG00408.hp2 HG02132.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.672-3550C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890917 | |||||||
| chr6:108890920 | G | A | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-3547G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108890920 | |||||||
| chr6:108891076 | C | T | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-3391C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108891076 | |||||||
| chr6:108891098 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.672-3369C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108891098 | |||||||
| chr6:108891278 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.672-3189C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108891278 | |||||||
| chr6:108891595 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.672-2872A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108891595 | |||||||
| chr6:108891685 | A | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(64): Show |
67 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.672-2782A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108891685 | |||||||
| chr6:108891690 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.672-2777G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108891690 | |||||||
| chr6:108891902 | C | CCATCTT | 3 | a0001c0001t0001g0225 a0001c0001t0002g0223 a0001c0001t0002g0224 |
3 | HG01099.hp2 HG03490.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.672-2564_672-2559d others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108891902 | ||||||
| chr6:108892067 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.672-2400A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892067 | |||||||
| chr6:108892451 | A | G | 11 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(8): Show |
11 | HG01074.hp2 HG01081.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-2016A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892451 | |||||||
| chr6:108892494 | T | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.672-1973T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892494 | |||||||
| chr6:108892525 | C | T | 37 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.672-1942C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892525 | |||||||
| chr6:108892527 | A | G | 1 | a0004c0005t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.672-1940A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892527 | |||||||
| chr6:108892631 | C | A | 1 | a0001c0001t0001g0005 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.672-1836C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892631 | |||||||
| chr6:108892631 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.672-1836C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892631 | |||||||
| chr6:108892636 | G | A | 2 | a0001c0001t0001g0122 a0001c0008t0001g0123 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.672-1831G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892636 | |||||||
| chr6:108892652 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.672-1815G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892652 | |||||||
| chr6:108892759 | C | CA | 8 | a0001c0001t0001g0007 a0001c0001t0001g0155 a0001c0001t0001g0225 others(5): Show |
8 | HG01099.hp2 HG01358.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-1690dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108892759 | ||||||
| chr6:108892759 | CAAAAA | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.672-1694_672-1690d others(7): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr6 | 108892759 | ||||||
| chr6:108892959 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.672-1508C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108892959 | |||||||
| chr6:108893320 | T | A | 1 | a0001c0001t0001g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.672-1147T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108893320 | |||||||
| chr6:108893464 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.672-1003G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108893464 | |||||||
| chr6:108893790 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.672-677G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108893790 | |||||||
| chr6:108893797 | G | A | 8 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-670G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108893797 | |||||||
| chr6:108894077 | C | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-390C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108894077 | |||||||
| chr6:108894086 | G | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0225 a0001c0001t0002g0223 others(1): Show |
4 | HG01069.hp2 HG01099.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-381G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108894086 | |||||||
| chr6:108894363 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0002g0133 a0001c0001t0002g0136 |
3 | HG03579.hp1 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.672-104A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108894363 | |||||||
| chr6:108894439 | C | T | 1 | a0002c0002t0001g0287 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.672-28C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 5/17 | chr6 | 108894439 | |||||||
| chr6:108894640 | A | T | 1 | a0001c0001t0003g0161 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.748+97A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108894640 | |||||||
| chr6:108894760 | C | CT | 17 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0050 others(14): Show |
17 | HG00408.hp2 HG01168.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.748+241dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 108894760 | ||||||
| chr6:108894767 | T | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.748+224T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108894767 | |||||||
| chr6:108894887 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.748+344C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108894887 | |||||||
| chr6:108894999 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.748+456C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108894999 | |||||||
| chr6:108895023 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.748+480T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108895023 | |||||||
| chr6:108895226 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.748+683A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108895226 | |||||||
| chr6:108895236 | G | A | 3 | a0003c0003t0001g0039 a0004c0005t0001g0040 a0004c0005t0001g0052 |
3 | HG01106.hp1 HG01981.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.748+693G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108895236 | |||||||
| chr6:108895307 | A | T | 1 | a0002c0002t0001g0284 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.748+764A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108895307 | |||||||
| chr6:108895482 | C | CA | 194 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(191): Show |
194 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.748+958dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 108895482 | ||||||
| chr6:108895482 | C | CAA | 13 | a0001c0001t0001g0017 a0001c0001t0001g0059 a0001c0001t0001g0062 others(10): Show |
13 | HG00438.hp1 HG02109.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.748+957_748+958dup others(2): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 108895482 | ||||||
| chr6:108895501 | A | AAG | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.748+958_748+959ins others(2): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108895501 | |||||||
| chr6:108895547 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.748+1004G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108895547 | |||||||
| chr6:108895588 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.748+1045T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108895588 | |||||||
| chr6:108896075 | T | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.748+1532T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108896075 | |||||||
| chr6:108896371 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.748+1828A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108896371 | |||||||
| chr6:108896482 | T | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.748+1939T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108896482 | |||||||
| chr6:108896510 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.748+1967C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108896510 | |||||||
| chr6:108896732 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.748+2189A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108896732 | |||||||
| chr6:108896933 | A | G | 223 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(220): Show |
223 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.748+2390A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108896933 | |||||||
| chr6:108897055 | A | G | 23 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.748+2512A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108897055 | |||||||
| chr6:108897446 | C | T | 5 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(2): Show |
5 | HG01243.hp2 HG01891.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.749-2248C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108897446 | |||||||
| chr6:108897452 | A | G | 7 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
7 | HG02809.hp1 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.749-2242A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108897452 | |||||||
| chr6:108897627 | G | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.749-2067G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108897627 | |||||||
| chr6:108898011 | G | A | 2 | a0001c0001t0006g0021 a0001c0001t0006g0054 |
2 | NA18944.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.749-1683G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898011 | |||||||
| chr6:108898026 | A | G | 1 | a0001c0001t0004g0181 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.749-1668A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898026 | |||||||
| chr6:108898035 | A | T | 1 | a0001c0001t0002g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.749-1659A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898035 | |||||||
| chr6:108898057 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.749-1637A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898057 | |||||||
| chr6:108898063 | A | AC | 4 | a0001c0001t0001g0106 a0001c0001t0001g0213 a0001c0001t0001g0255 others(1): Show |
4 | HG02071.hp1 HG03927.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-1627dupC | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 108898063 | ||||||
| chr6:108898233 | C | T | 61 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(58): Show |
61 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.749-1461C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898233 | |||||||
| chr6:108898241 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.749-1453T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898241 | |||||||
| chr6:108898242 | CCT | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.749-1449_749-1448d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 108898242 | ||||||
| chr6:108898314 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.749-1380G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898314 | |||||||
| chr6:108898518 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.749-1176A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898518 | |||||||
| chr6:108898871 | A | C | 2 | a0001c0001t0005g0089 a0001c0001t0005g0090 |
2 | HG02055.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.749-823A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898871 | |||||||
| chr6:108898957 | G | A | 4 | a0001c0001t0001g0205 a0001c0001t0002g0204 a0001c0001t0002g0206 others(1): Show |
4 | HG02027.hp1 NA18964.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-737G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108898957 | |||||||
| chr6:108899110 | A | G | 1 | a0002c0002t0001g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.749-584A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899110 | |||||||
| chr6:108899182 | G | T | 4 | a0002c0002t0001g0265 a0002c0002t0001g0270 a0002c0002t0001g0271 others(1): Show |
4 | NA18957.hp2 NA18964.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.749-512G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899182 | |||||||
| chr6:108899204 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0147 |
2 | HG00558.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.749-490C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899204 | |||||||
| chr6:108899342 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG00639.hp1 HG01358.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.749-352A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899342 | |||||||
| chr6:108899351 | G | C | 2 | a0001c0001t0002g0061 a0003c0003t0002g0070 |
2 | HG02886.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.749-343G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899351 | |||||||
| chr6:108899409 | T | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.749-285T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899409 | |||||||
| chr6:108899483 | G | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.749-211G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899483 | |||||||
| chr6:108899606 | G | A | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.749-88G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899606 | |||||||
| chr6:108899627 | T | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.749-67T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 6/17 | chr6 | 108899627 | |||||||
| chr6:108899838 | T | A | 1 | a0002c0002t0001g0269 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.847+46T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108899838 | |||||||
| chr6:108899839 | A | T | 43 | a0001c0001t0001g0062 a0001c0001t0001g0148 a0001c0001t0001g0205 others(40): Show |
43 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.847+47A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108899839 | |||||||
| chr6:108900042 | T | C | 38 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(35): Show |
38 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.847+250T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900042 | |||||||
| chr6:108900175 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.847+383T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900175 | |||||||
| chr6:108900262 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.847+470G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900262 | |||||||
| chr6:108900343 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.847+551G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900343 | |||||||
| chr6:108900359 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.847+567G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900359 | |||||||
| chr6:108900559 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.847+767G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900559 | |||||||
| chr6:108900643 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(114): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.847+851G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900643 | |||||||
| chr6:108900746 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0003g0132 |
3 | HG02451.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.847+954C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900746 | |||||||
| chr6:108900800 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
77 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.847+1008C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900800 | |||||||
| chr6:108900814 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(179): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.847+1022G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108900814 | |||||||
| chr6:108901098 | A | AT | 18 | a0001c0001t0001g0029 a0001c0001t0001g0099 a0001c0001t0001g0162 others(15): Show |
18 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.847+1343dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | A | ATT | 28 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.847+1342_847+1343d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | A | ATTT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(19): Show |
22 | HG00099.hp1 HG00408.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.847+1341_847+1343d others(5): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | A | ATTTT | 9 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0072 others(6): Show |
9 | HG01106.hp1 HG01243.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+1340_847+1343d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | A | ATTTTT | 6 | a0001c0001t0001g0060 a0001c0001t0001g0084 a0001c0001t0001g0086 others(3): Show |
6 | HG00558.hp1 HG01081.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.847+1339_847+1343d others(7): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | A | ATTTTTT | 9 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0062 others(6): Show |
9 | HG02071.hp2 NA18747.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+1338_847+1343d others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | AT | A | 54 | a0001c0001t0001g0069 a0001c0001t0001g0091 a0001c0001t0001g0103 others(51): Show |
54 | HG00140.hp2 HG00323.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.847+1343delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATT | A | 32 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0096 others(29): Show |
32 | HG00423.hp2 HG00597.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.847+1342_847+1343d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTT | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0189 others(18): Show |
21 | HG00597.hp2 HG00738.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.847+1341_847+1343d others(5): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTT | A | 7 | a0002c0002t0001g0267 a0002c0002t0001g0268 a0002c0002t0001g0270 others(4): Show |
7 | HG01256.hp2 HG01258.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.847+1340_847+1343d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0202 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.847+1330_847+1343d others(16): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTTTTT others(8): Show |
A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(13): Show |
16 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.847+1329_847+1343d others(17): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTTTTT others(9): Show |
A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.847+1328_847+1343d others(18): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTTTTT others(10): Show |
A | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.847+1327_847+1343d others(19): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTTTTT others(11): Show |
A | 1 | a0001c0001t0001g0229 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.847+1326_847+1343d others(20): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTTTTT others(12): Show |
A | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.847+1325_847+1343d others(21): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901098 | ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0003g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.847+1324_847+1343d others(22): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901098 | ||||||
| chr6:108901101 | T | C | 1 | a0001c0001t0003g0219 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.847+1309T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901101 | |||||||
| chr6:108901163 | G | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.847+1371G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901163 | |||||||
| chr6:108901196 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.847+1404C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901196 | |||||||
| chr6:108901253 | A | G | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.847+1461A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901253 | |||||||
| chr6:108901417 | A | AT | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.847+1636dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108901417 | ||||||
| chr6:108901523 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.847+1731C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901523 | |||||||
| chr6:108901546 | G | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.847+1754G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901546 | |||||||
| chr6:108901562 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.847+1770C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901562 | |||||||
| chr6:108901564 | C | T | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.847+1772C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901564 | |||||||
| chr6:108901691 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.847+1899A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901691 | |||||||
| chr6:108901921 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.847+2129C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901921 | |||||||
| chr6:108901924 | A | C | 1 | a0001c0001t0001g0289 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.847+2132A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901924 | |||||||
| chr6:108901950 | G | C | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.847+2158G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108901950 | |||||||
| chr6:108902027 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.848-2203G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902027 | |||||||
| chr6:108902047 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.848-2183A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902047 | |||||||
| chr6:108902056 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.848-2174C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902056 | |||||||
| chr6:108902118 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.848-2112A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902118 | |||||||
| chr6:108902247 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
77 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.848-1983G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902247 | |||||||
| chr6:108902329 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.848-1901C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902329 | |||||||
| chr6:108902419 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.848-1811C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902419 | |||||||
| chr6:108902574 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0120 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.848-1656A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902574 | |||||||
| chr6:108902698 | G | A | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.848-1532G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902698 | |||||||
| chr6:108902728 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0174 |
2 | HG01069.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.848-1502G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902728 | |||||||
| chr6:108902886 | G | A | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.848-1344G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902886 | |||||||
| chr6:108902927 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.848-1303G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108902927 | |||||||
| chr6:108903255 | C | CT | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.848-968dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 108903255 | ||||||
| chr6:108903535 | A | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG00408.hp2 HG02132.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.848-695A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108903535 | |||||||
| chr6:108903580 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.848-650T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108903580 | |||||||
| chr6:108903863 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.848-367G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108903863 | |||||||
| chr6:108903879 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.848-351C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 7/17 | chr6 | 108903879 | |||||||
| chr6:108904646 | TA | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0130 others(9): Show |
12 | HG00099.hp2 HG01975.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1023+255delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108904646 | ||||||
| chr6:108904646 | TAA | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(192): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1023+254_1023+255d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108904646 | ||||||
| chr6:108904660 | AGAAG | A | 21 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(18): Show |
21 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1023+256_1023+259d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108904660 | |||||||
| chr6:108904664 | G | A | 1 | a0002c0002t0001g0287 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1023+259G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108904664 | |||||||
| chr6:108904689 | A | G | 1 | a0001c0001t0003g0161 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1023+284A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108904689 | |||||||
| chr6:108904795 | G | A | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1023+390G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108904795 | |||||||
| chr6:108904803 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1023+398C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108904803 | |||||||
| chr6:108904826 | C | T | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+421C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108904826 | |||||||
| chr6:108904865 | T | G | 1 | a0001c0001t0001g0259 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1023+460T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108904865 | |||||||
| chr6:108905020 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1023+615T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905020 | |||||||
| chr6:108905084 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0002g0222 |
2 | NA18964.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1023+679T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905084 | |||||||
| chr6:108905113 | C | T | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1023+708C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905113 | |||||||
| chr6:108905232 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1023+827A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905232 | |||||||
| chr6:108905308 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(114): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1023+903A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905308 | |||||||
| chr6:108905379 | T | C | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+974T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905379 | |||||||
| chr6:108905403 | A | G | 10 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(7): Show |
10 | HG02109.hp2 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1023+998A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905403 | |||||||
| chr6:108905443 | G | A | 28 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(25): Show |
28 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1023+1038G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905443 | |||||||
| chr6:108905535 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0194 others(1): Show |
4 | HG01175.hp2 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+1130G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905535 | |||||||
| chr6:108905538 | G | GA | 28 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(25): Show |
28 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1023+1146dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108905538 | ||||||
| chr6:108905633 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0192 |
2 | HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1023+1228G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905633 | |||||||
| chr6:108905779 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1023+1374C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905779 | |||||||
| chr6:108905932 | A | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1023+1527A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905932 | |||||||
| chr6:108905949 | G | C | 1 | a0002c0002t0001g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1023+1544G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905949 | |||||||
| chr6:108905953 | A | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+1548A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108905953 | |||||||
| chr6:108906109 | T | C | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+1704T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108906109 | |||||||
| chr6:108906318 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1023+1913A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108906318 | |||||||
| chr6:108906475 | AT | A | 27 | a0001c0001t0003g0002 a0001c0006t0001g0058 a0001c0006t0002g0057 others(24): Show |
27 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1023+2082delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108906475 | ||||||
| chr6:108906606 | G | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(114): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1023+2201G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108906606 | |||||||
| chr6:108906619 | C | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1023+2214C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108906619 | |||||||
| chr6:108906885 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1023+2480C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108906885 | |||||||
| chr6:108907098 | G | C | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1023+2693G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907098 | |||||||
| chr6:108907101 | A | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
80 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.1023+2696A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907101 | |||||||
| chr6:108907134 | A | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+2729A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907134 | |||||||
| chr6:108907446 | TTTTC | T | 11 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(8): Show |
11 | HG00597.hp2 HG01243.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1023+3053_1023+305 others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108907446 | ||||||
| chr6:108907458 | CT | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1023+3072delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108907458 | ||||||
| chr6:108907458 | CTT | C | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+3071_1023+307 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108907458 | ||||||
| chr6:108907463 | T | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1023+3058T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907463 | |||||||
| chr6:108907477 | T | A | 72 | a0001c0001t0001g0032 a0001c0001t0001g0060 a0001c0001t0001g0069 others(69): Show |
72 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1023+3072T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907477 | |||||||
| chr6:108907477 | T | TA | 117 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(114): Show |
117 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1023+3073dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108907477 | ||||||
| chr6:108907477 | T | TTA | 10 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0028 others(7): Show |
10 | HG00423.hp1 HG02015.hp1 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.1023+3072_1023+307 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907477 | |||||||
| chr6:108907480 | C | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(179): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1023+3075C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907480 | |||||||
| chr6:108907536 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1023+3131G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907536 | |||||||
| chr6:108907544 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1023+3139T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907544 | |||||||
| chr6:108907598 | G | A | 8 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
8 | HG01106.hp2 HG01361.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1023+3193G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907598 | |||||||
| chr6:108907795 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1024-3104C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907795 | |||||||
| chr6:108907821 | CCA | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1024-3077_1024-307 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108907821 | |||||||
| chr6:108908040 | A | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-2859A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908040 | |||||||
| chr6:108908095 | C | T | 1 | a0001c0006t0002g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1024-2804C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908095 | |||||||
| chr6:108908130 | G | A | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1024-2769G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908130 | |||||||
| chr6:108908138 | T | TG | 38 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(35): Show |
38 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1024-2753dupG | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108908138 | ||||||
| chr6:108908138 | TG | T | 61 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(58): Show |
61 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.1024-2753delG | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108908138 | ||||||
| chr6:108908145 | G | T | 3 | a0001c0001t0001g0134 a0001c0001t0002g0133 a0001c0001t0002g0136 |
3 | HG03579.hp1 NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1024-2754G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908145 | |||||||
| chr6:108908253 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0003g0290 |
2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1024-2646A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908253 | |||||||
| chr6:108908346 | G | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1024-2553G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908346 | |||||||
| chr6:108908468 | A | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1024-2431A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908468 | |||||||
| chr6:108908677 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1024-2222G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908677 | |||||||
| chr6:108908764 | A | G | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0241 |
3 | HG02809.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1024-2135A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908764 | |||||||
| chr6:108908889 | G | A | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-2010G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108908889 | |||||||
| chr6:108909244 | A | G | 1 | a0001c0007t0008g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1024-1655A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909244 | |||||||
| chr6:108909245 | C | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1024-1654C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909245 | |||||||
| chr6:108909306 | G | GA | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1024-1592dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108909306 | ||||||
| chr6:108909340 | T | A | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024-1559T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909340 | |||||||
| chr6:108909454 | A | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1024-1445A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909454 | |||||||
| chr6:108909468 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1024-1431T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909468 | |||||||
| chr6:108909613 | G | A | 23 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1024-1286G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909613 | |||||||
| chr6:108909680 | C | T | 1 | a0002c0002t0001g0279 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1024-1219C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909680 | |||||||
| chr6:108909690 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1024-1209C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909690 | |||||||
| chr6:108909755 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1024-1144C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909755 | |||||||
| chr6:108909785 | C | T | 1 | a0004c0005t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1024-1114C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909785 | |||||||
| chr6:108909826 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1024-1073G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909826 | |||||||
| chr6:108909866 | G | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024-1033G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108909866 | |||||||
| chr6:108910039 | G | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1024-860G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910039 | |||||||
| chr6:108910266 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1024-633C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910266 | |||||||
| chr6:108910342 | G | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1024-557G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910342 | |||||||
| chr6:108910373 | T | C | 28 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(25): Show |
28 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1024-526T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910373 | |||||||
| chr6:108910387 | T | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0120 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1024-512T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910387 | |||||||
| chr6:108910653 | A | G | 27 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(24): Show |
27 | HG00738.hp2 HG01081.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.1024-246A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910653 | |||||||
| chr6:108910656 | G | A | 1 | a0001c0001t0003g0257 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1024-243G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910656 | |||||||
| chr6:108910786 | T | TTC | 234 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(231): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1024-112_1024-111i others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108910786 | ||||||
| chr6:108910811 | G | A | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024-88G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | chr6 | 108910811 | |||||||
| chr6:108910826 | A | ATGTT | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1024-70_1024-69ins others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 108910826 | ||||||
| chr6:108911285 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1126+284A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108911285 | |||||||
| chr6:108911318 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1126+317A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108911318 | |||||||
| chr6:108911350 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1126+349G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108911350 | |||||||
| chr6:108911490 | T | C | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1126+489T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108911490 | |||||||
| chr6:108911607 | A | C | 1 | a0001c0001t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1126+606A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108911607 | |||||||
| chr6:108912123 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1127-212C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108912123 | |||||||
| chr6:108912156 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1127-179C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108912156 | |||||||
| chr6:108912236 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1127-99A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108912236 | |||||||
| chr6:108912315 | A | G | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1127-20A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 9/17 | chr6 | 108912315 | |||||||
| chr6:108912766 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1350+208G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108912766 | |||||||
| chr6:108913347 | C | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1350+789C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108913347 | |||||||
| chr6:108913531 | T | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1350+973T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108913531 | |||||||
| chr6:108913745 | G | A | 37 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1350+1187G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108913745 | |||||||
| chr6:108913878 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1350+1320T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108913878 | |||||||
| chr6:108913977 | T | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1350+1419T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108913977 | |||||||
| chr6:108914146 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1350+1588G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108914146 | |||||||
| chr6:108914403 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1350+1845C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108914403 | |||||||
| chr6:108914419 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1350+1861C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108914419 | |||||||
| chr6:108914493 | C | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1350+1935C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108914493 | |||||||
| chr6:108914579 | T | C | 1 | a0001c0001t0007g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1350+2021T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108914579 | |||||||
| chr6:108914950 | A | AT | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1350+2405dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108914950 | ||||||
| chr6:108914950 | AT | A | 67 | a0001c0001t0001g0005 a0001c0001t0001g0067 a0001c0001t0001g0148 others(64): Show |
67 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.1350+2405delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108914950 | ||||||
| chr6:108915141 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0107 |
2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1350+2583A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915141 | |||||||
| chr6:108915166 | T | G | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1350+2608T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915166 | |||||||
| chr6:108915251 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1350+2693T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915251 | |||||||
| chr6:108915398 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1350+2840G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915398 | |||||||
| chr6:108915557 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1350+2999G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915557 | |||||||
| chr6:108915573 | C | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1350+3015C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915573 | |||||||
| chr6:108915577 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1350+3019A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915577 | |||||||
| chr6:108915785 | T | G | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1350+3227T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915785 | |||||||
| chr6:108915814 | G | A | 1 | a0001c0006t0001g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1350+3256G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915814 | |||||||
| chr6:108915923 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(75): Show |
78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1350+3365G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108915923 | |||||||
| chr6:108916039 | G | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1350+3481G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916039 | |||||||
| chr6:108916060 | C | T | 7 | a0001c0001t0001g0059 a0002c0002t0001g0282 a0002c0002t0001g0283 others(4): Show |
7 | HG04184.hp2 NA18940.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1350+3502C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916060 | |||||||
| chr6:108916080 | GA | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+3531delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108916080 | ||||||
| chr6:108916129 | C | T | 9 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(6): Show |
9 | HG00423.hp2 HG00621.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.1350+3571C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916129 | |||||||
| chr6:108916223 | C | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+3665C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916223 | |||||||
| chr6:108916242 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+3684A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916242 | |||||||
| chr6:108916280 | G | A | 61 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(58): Show |
61 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.1350+3722G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916280 | |||||||
| chr6:108916445 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1350+3887G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916445 | |||||||
| chr6:108916448 | G | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1350+3890G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916448 | |||||||
| chr6:108916632 | G | A | 2 | a0002c0002t0001g0279 a0002c0002t0001g0280 |
2 | NA19001.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1350+4074G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916632 | |||||||
| chr6:108916721 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1350+4163G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916721 | |||||||
| chr6:108916865 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1350+4307A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916865 | |||||||
| chr6:108916906 | A | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+4348A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916906 | |||||||
| chr6:108916999 | A | C | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+4441A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108916999 | |||||||
| chr6:108917121 | C | G | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1350+4563C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917121 | |||||||
| chr6:108917126 | T | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1350+4568T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917126 | |||||||
| chr6:108917323 | C | T | 1 | a0001c0001t0004g0025 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1350+4765C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917323 | |||||||
| chr6:108917427 | G | A | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+4869G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917427 | |||||||
| chr6:108917496 | C | T | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+4938C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917496 | |||||||
| chr6:108917740 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+5182T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917740 | |||||||
| chr6:108917869 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(199): Show |
202 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1350+5311T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917869 | |||||||
| chr6:108917911 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0133 others(1): Show |
4 | HG03453.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+5353C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917911 | |||||||
| chr6:108917976 | C | T | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1350+5418C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108917976 | |||||||
| chr6:108918026 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+5468A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918026 | |||||||
| chr6:108918045 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1350+5487T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918045 | |||||||
| chr6:108918068 | G | A | 1 | a0002c0002t0001g0285 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1350+5510G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918068 | |||||||
| chr6:108918311 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0003g0196 |
3 | HG01884.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1350+5753C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918311 | |||||||
| chr6:108918351 | G | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1350+5793G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918351 | |||||||
| chr6:108918362 | C | T | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1350+5804C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918362 | |||||||
| chr6:108918378 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1350+5820G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918378 | |||||||
| chr6:108918482 | A | ATT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1350+5937_1350+593 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108918482 | ||||||
| chr6:108918482 | AT | A | 35 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0130 others(32): Show |
35 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.1350+5938delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108918482 | ||||||
| chr6:108918496 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1350+5938T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918496 | |||||||
| chr6:108918497 | A | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG02965.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1350+5939A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918497 | |||||||
| chr6:108918555 | T | G | 3 | a0001c0001t0001g0202 a0001c0001t0002g0203 a0003c0003t0002g0193 |
3 | HG02572.hp1 HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1350+5997T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918555 | |||||||
| chr6:108918568 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1350+6010G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918568 | |||||||
| chr6:108918681 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+6123G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918681 | |||||||
| chr6:108918725 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1350+6167C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918725 | |||||||
| chr6:108918808 | A | G | 1 | a0001c0006t0001g0058 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1350+6250A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918808 | |||||||
| chr6:108918877 | A | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+6319A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108918877 | |||||||
| chr6:108919022 | A | G | 3 | a0002c0002t0001g0267 a0002c0002t0001g0273 a0002c0002t0001g0278 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1350+6464A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919022 | |||||||
| chr6:108919143 | CA | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+6587delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108919143 | ||||||
| chr6:108919216 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1350+6658C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919216 | |||||||
| chr6:108919217 | G | A | 1 | a0002c0002t0001g0271 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1350+6659G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919217 | |||||||
| chr6:108919262 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+6704T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919262 | |||||||
| chr6:108919359 | A | G | 37 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0151 others(34): Show |
37 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1350+6801A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919359 | |||||||
| chr6:108919416 | A | G | 4 | a0001c0001t0001g0067 a0001c0001t0002g0066 a0001c0001t0003g0064 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1350+6858A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919416 | |||||||
| chr6:108919485 | C | T | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1350+6927C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919485 | |||||||
| chr6:108919517 | A | AT | 60 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.1350+6968dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108919517 | ||||||
| chr6:108919920 | C | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+7362C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919920 | |||||||
| chr6:108919962 | C | T | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1350+7404C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108919962 | |||||||
| chr6:108920075 | A | G | 35 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(32): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1350+7517A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920075 | |||||||
| chr6:108920154 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1350+7596A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920154 | |||||||
| chr6:108920159 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(223): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1350+7601A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920159 | |||||||
| chr6:108920283 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1350+7725G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920283 | |||||||
| chr6:108920448 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG00408.hp2 HG02132.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1351-7640C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920448 | |||||||
| chr6:108920496 | C | T | 13 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(10): Show |
13 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1351-7592C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920496 | |||||||
| chr6:108920772 | T | C | 37 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(34): Show |
37 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1351-7316T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920772 | |||||||
| chr6:108920870 | G | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1351-7218G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108920870 | |||||||
| chr6:108921062 | G | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1351-7026G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108921062 | |||||||
| chr6:108921271 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1351-6817C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108921271 | |||||||
| chr6:108921508 | AC | A | 35 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(32): Show |
35 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.1351-6579delC | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108921508 | |||||||
| chr6:108921674 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1351-6414A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108921674 | |||||||
| chr6:108921883 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1351-6205G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108921883 | |||||||
| chr6:108921930 | A | T | 3 | a0003c0003t0001g0116 a0003c0003t0001g0117 a0003c0003t0002g0125 |
3 | HG02809.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1351-6158A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108921930 | |||||||
| chr6:108921931 | A | T | 3 | a0003c0003t0001g0116 a0003c0003t0001g0117 a0003c0003t0002g0125 |
3 | HG02809.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1351-6157A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108921931 | |||||||
| chr6:108922069 | C | T | 10 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(7): Show |
10 | HG02109.hp2 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1351-6019C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108922069 | |||||||
| chr6:108922227 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0118 |
2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1351-5861G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108922227 | |||||||
| chr6:108922269 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0002g0203 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1351-5819C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108922269 | |||||||
| chr6:108922413 | C | T | 1 | a0001c0001t0007g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1351-5675C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108922413 | |||||||
| chr6:108922433 | C | T | 1 | a0001c0001t0002g0206 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1351-5655C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108922433 | |||||||
| chr6:108922705 | T | C | 1 | a0001c0001t0002g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1351-5383T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108922705 | |||||||
| chr6:108922841 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1351-5247C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108922841 | |||||||
| chr6:108923029 | T | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(65): Show |
68 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1351-5059T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923029 | |||||||
| chr6:108923233 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(196): Show |
199 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1351-4855G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923233 | |||||||
| chr6:108923375 | G | A | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1351-4713G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923375 | |||||||
| chr6:108923383 | A | AGTGG | 27 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(24): Show |
27 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1351-4699_1351-469 others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108923383 | ||||||
| chr6:108923464 | T | A | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1351-4624T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923464 | |||||||
| chr6:108923491 | T | A | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1351-4597T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923491 | |||||||
| chr6:108923491 | TC | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0148 a0001c0001t0001g0202 others(2): Show |
5 | HG01975.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351-4596delC | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923491 | |||||||
| chr6:108923492 | C | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(191): Show |
194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1351-4596C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923492 | |||||||
| chr6:108923589 | T | A | 5 | a0001c0001t0004g0025 a0001c0001t0004g0045 a0001c0001t0004g0046 others(2): Show |
5 | HG00099.hp1 HG00323.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1351-4499T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923589 | |||||||
| chr6:108923616 | C | G | 1 | a0001c0001t0002g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1351-4472C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108923616 | |||||||
| chr6:108923618 | C | CT | 78 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0085 others(75): Show |
78 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1351-4454dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108923618 | ||||||
| chr6:108923618 | C | CTTTT | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1351-4457_1351-445 others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108923618 | ||||||
| chr6:108923618 | CT | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0069 a0001c0001t0001g0150 others(28): Show |
31 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.1351-4454delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108923618 | ||||||
| chr6:108924109 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1351-3979G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924109 | |||||||
| chr6:108924157 | G | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(233): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.1351-3931G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924157 | |||||||
| chr6:108924293 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0077 |
2 | HG01952.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1351-3795G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924293 | |||||||
| chr6:108924351 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1351-3737C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924351 | |||||||
| chr6:108924442 | C | T | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-3646C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924442 | |||||||
| chr6:108924449 | C | T | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1351-3639C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924449 | |||||||
| chr6:108924466 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1351-3622C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924466 | |||||||
| chr6:108924486 | G | A | 2 | a0001c0001t0001g0122 a0001c0008t0001g0123 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1351-3602G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924486 | |||||||
| chr6:108924499 | GA | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1351-3582delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108924499 | ||||||
| chr6:108924682 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1351-3406A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108924682 | |||||||
| chr6:108925016 | A | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0062 |
3 | NA18747.hp1 NA18945.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1351-3072A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925016 | |||||||
| chr6:108925092 | G | T | 1 | a0001c0001t0001g0289 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1351-2996G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925092 | |||||||
| chr6:108925373 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0234 a0001c0001t0002g0203 |
3 | HG02572.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1351-2715G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925373 | |||||||
| chr6:108925487 | C | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1351-2601C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925487 | |||||||
| chr6:108925688 | A | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(231): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1351-2400A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925688 | |||||||
| chr6:108925743 | T | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1351-2345T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925743 | |||||||
| chr6:108925852 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1351-2236G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925852 | |||||||
| chr6:108925931 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1351-2157T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108925931 | |||||||
| chr6:108926010 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1351-2078A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108926010 | |||||||
| chr6:108926104 | T | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(192): Show |
195 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1351-1984T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108926104 | |||||||
| chr6:108926331 | G | A | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(1): Show |
4 | HG02886.hp1 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-1757G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108926331 | |||||||
| chr6:108926596 | G | A | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1351-1492G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108926596 | |||||||
| chr6:108926921 | C | CT | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1351-1151dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108926921 | ||||||
| chr6:108926921 | CT | C | 67 | a0001c0001t0001g0069 a0001c0001t0001g0095 a0001c0001t0001g0119 others(64): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1351-1151delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108926921 | ||||||
| chr6:108927037 | T | C | 3 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01081.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1351-1051T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927037 | |||||||
| chr6:108927176 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1351-912T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927176 | |||||||
| chr6:108927381 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1351-707T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927381 | |||||||
| chr6:108927549 | A | AT | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1351-529dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108927549 | ||||||
| chr6:108927604 | G | A | 7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(4): Show |
7 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1351-484G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927604 | |||||||
| chr6:108927651 | C | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG00639.hp1 HG01358.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351-437C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927651 | |||||||
| chr6:108927677 | A | G | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG00639.hp1 HG01358.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351-411A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927677 | |||||||
| chr6:108927709 | T | TA | 126 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(123): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1351-367dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 108927709 | ||||||
| chr6:108927838 | G | T | 4 | a0001c0001t0001g0067 a0001c0001t0002g0066 a0001c0001t0003g0064 others(1): Show |
4 | HG02280.hp2 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-250G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927838 | |||||||
| chr6:108927848 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1351-240A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927848 | |||||||
| chr6:108927871 | A | G | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1351-217A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108927871 | |||||||
| chr6:108928003 | T | G | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351-85T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 10/17 | chr6 | 108928003 | |||||||
| chr6:108928249 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1496+16C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928249 | |||||||
| chr6:108928264 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1496+31C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928264 | |||||||
| chr6:108928277 | G | C | 1 | a0001c0001t0001g0003 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1496+44G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928277 | |||||||
| chr6:108928409 | A | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1496+176A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928409 | |||||||
| chr6:108928412 | C | T | 1 | a0001c0001t0003g0249 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1496+179C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928412 | |||||||
| chr6:108928422 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1496+189A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928422 | |||||||
| chr6:108928492 | G | A | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(1): Show |
4 | HG02886.hp1 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1496+259G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928492 | |||||||
| chr6:108928762 | T | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1496+529T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928762 | |||||||
| chr6:108928811 | C | G | 7 | a0001c0001t0001g0150 a0001c0001t0001g0160 a0001c0001t0001g0172 others(4): Show |
7 | HG00140.hp2 HG00323.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1496+578C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928811 | |||||||
| chr6:108928821 | C | G | 12 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(9): Show |
12 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1496+588C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928821 | |||||||
| chr6:108928892 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1496+659T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108928892 | |||||||
| chr6:108929048 | T | C | 1 | a0003c0003t0002g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1496+815T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929048 | |||||||
| chr6:108929076 | C | G | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0003g0245 |
3 | NA19007.hp1 NA19063.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1496+843C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929076 | |||||||
| chr6:108929078 | T | C | 2 | a0002c0002t0001g0277 a0002c0002t0002g0266 |
2 | HG02129.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1496+845T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929078 | |||||||
| chr6:108929220 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1496+987A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929220 | |||||||
| chr6:108929243 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1496+1010G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929243 | |||||||
| chr6:108929261 | G | A | 52 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1496+1028G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929261 | |||||||
| chr6:108929291 | T | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0003g0132 |
3 | HG02451.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1496+1058T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929291 | |||||||
| chr6:108929505 | C | T | 1 | a0002c0002t0001g0278 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1496+1272C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929505 | |||||||
| chr6:108929519 | G | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1496+1286G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929519 | |||||||
| chr6:108929760 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1496+1527G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929760 | |||||||
| chr6:108929904 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1496+1671C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929904 | |||||||
| chr6:108929964 | C | G | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1496+1731C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108929964 | |||||||
| chr6:108930126 | T | TA | 16 | a0001c0001t0001g0084 a0001c0001t0001g0188 a0001c0001t0001g0189 others(13): Show |
16 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1496+1907dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108930126 | ||||||
| chr6:108930589 | A | C | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1496+2356A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108930589 | |||||||
| chr6:108930592 | C | CT | 7 | a0001c0001t0001g0157 a0001c0001t0002g0203 a0001c0001t0002g0204 others(4): Show |
7 | HG00099.hp1 HG01358.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1496+2381dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108930592 | ||||||
| chr6:108930592 | CT | C | 93 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
93 | HG00099.hp2 HG00423.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1496+2381delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108930592 | ||||||
| chr6:108930620 | G | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1496+2387G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108930620 | |||||||
| chr6:108930724 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1496+2491G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108930724 | |||||||
| chr6:108930742 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1496+2509A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108930742 | |||||||
| chr6:108930806 | A | G | 5 | a0002c0002t0001g0282 a0002c0002t0001g0283 a0002c0002t0001g0284 others(2): Show |
5 | NA18940.hp1 NA18952.hp1 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.1496+2573A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108930806 | |||||||
| chr6:108930846 | TGGCCTCC others(1926): Show |
T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0003g0132 |
3 | HG02451.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1496+2651_1497-408 others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108930846 | ||||||
| chr6:108930903 | CT | C | 9 | a0001c0001t0001g0069 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG01192.hp2 HG01257.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1496+2684delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108930903 | ||||||
| chr6:108930904 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1496+2671T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108930904 | |||||||
| chr6:108931461 | A | C | 1 | a0001c0001t0002g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1496+3228A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108931461 | |||||||
| chr6:108931647 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1496+3414C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108931647 | |||||||
| chr6:108931920 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1496+3687T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108931920 | |||||||
| chr6:108932054 | C | T | 3 | a0003c0003t0001g0116 a0003c0003t0001g0117 a0003c0003t0002g0125 |
3 | HG02809.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1496+3821C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932054 | |||||||
| chr6:108932055 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1496+3822G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932055 | |||||||
| chr6:108932254 | T | G | 1 | a0001c0001t0003g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1496+4021T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932254 | |||||||
| chr6:108932301 | A | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0145 |
2 | HG00558.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1496+4068A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932301 | |||||||
| chr6:108932385 | C | G | 22 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(19): Show |
22 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1496+4152C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932385 | |||||||
| chr6:108932485 | A | T | 9 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0186 others(6): Show |
9 | HG02109.hp1 HG03239.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.1496+4252A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932485 | |||||||
| chr6:108932516 | C | CT | 7 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0226 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1496+4310dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932516 | C | CTT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(3): Show |
6 | HG01346.hp2 HG01975.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496+4309_1496+431 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932516 | C | CTTT | 22 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1496+4308_1496+431 others(7): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932516 | C | CTTTT | 30 | a0001c0001t0001g0007 a0001c0001t0001g0091 a0001c0001t0001g0093 others(27): Show |
30 | HG00597.hp1 HG01358.hp1 HG01952.hp1 others(27): Show |
intron_variant | MODIFIER | c.1496+4307_1496+431 others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932516 | C | CTTTTT | 13 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
13 | HG00423.hp2 HG00621.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1496+4306_1496+431 others(9): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932516 | CTTT | C | 43 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0051 others(40): Show |
43 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1496+4308_1496+431 others(7): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932516 | CTTTT | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(97): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.1496+4307_1496+431 others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932516 | CTTTTT | C | 18 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0152 others(15): Show |
18 | HG00639.hp2 HG01192.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1496+4306_1496+431 others(9): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108932516 | ||||||
| chr6:108932597 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1497-4303C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932597 | |||||||
| chr6:108932614 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1497-4286T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932614 | |||||||
| chr6:108932621 | C | T | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.1497-4279C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932621 | |||||||
| chr6:108932669 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1497-4231T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932669 | |||||||
| chr6:108932770 | T | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1497-4130T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932770 | |||||||
| chr6:108932774 | C | T | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1497-4126C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932774 | |||||||
| chr6:108932780 | G | A | 1 | a0003c0003t0001g0116 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1497-4120G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932780 | |||||||
| chr6:108932783 | C | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1497-4117C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932783 | |||||||
| chr6:108932823 | C | T | 4 | a0001c0001t0001g0186 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG03239.hp1 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497-4077C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932823 | |||||||
| chr6:108932831 | A | G | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1497-4069A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932831 | |||||||
| chr6:108932893 | G | A | 1 | a0002c0002t0001g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1497-4007G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932893 | |||||||
| chr6:108932989 | G | A | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1497-3911G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108932989 | |||||||
| chr6:108933025 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1497-3875A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933025 | |||||||
| chr6:108933027 | A | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0006g0021 others(1): Show |
4 | HG01361.hp2 HG01975.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497-3873A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933027 | |||||||
| chr6:108933078 | G | GT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1497-3811dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108933078 | ||||||
| chr6:108933240 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.1497-3660T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933240 | |||||||
| chr6:108933486 | A | G | 8 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0163 others(5): Show |
8 | HG01192.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497-3414A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933486 | |||||||
| chr6:108933501 | T | C | 1 | a0004c0005t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1497-3399T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933501 | |||||||
| chr6:108933547 | T | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1497-3353T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933547 | |||||||
| chr6:108933758 | A | G | 23 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0247 others(20): Show |
23 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1497-3142A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933758 | |||||||
| chr6:108933900 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0008 |
2 | HG01346.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1497-3000C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108933900 | |||||||
| chr6:108934170 | A | G | 1 | a0001c0001t0004g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1497-2730A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108934170 | |||||||
| chr6:108934926 | G | A | 7 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(4): Show |
7 | HG02809.hp1 HG02897.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1497-1974G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108934926 | |||||||
| chr6:108935041 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0133 others(1): Show |
4 | HG03453.hp1 HG03579.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497-1859C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935041 | |||||||
| chr6:108935107 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1497-1793C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935107 | |||||||
| chr6:108935363 | CTCCTT | C | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1497-1534_1497-153 others(9): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108935363 | ||||||
| chr6:108935380 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1497-1520T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935380 | |||||||
| chr6:108935399 | T | C | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1497-1501T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935399 | |||||||
| chr6:108935465 | A | C | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1497-1435A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935465 | |||||||
| chr6:108935640 | G | A | 28 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(25): Show |
28 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1497-1260G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935640 | |||||||
| chr6:108935858 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1497-1042G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935858 | |||||||
| chr6:108935859 | G | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
88 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1497-1041G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935859 | |||||||
| chr6:108935867 | A | T | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1497-1033A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935867 | |||||||
| chr6:108935904 | T | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1497-996T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935904 | |||||||
| chr6:108935933 | C | G | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1497-967C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108935933 | |||||||
| chr6:108936086 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1497-814G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936086 | |||||||
| chr6:108936109 | A | G | 1 | a0003c0003t0002g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1497-791A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936109 | |||||||
| chr6:108936246 | T | TTTTG | 4 | a0001c0001t0001g0069 a0001c0001t0001g0202 a0001c0001t0002g0068 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497-630_1497-627d others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108936246 | ||||||
| chr6:108936270 | GT | G | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(5): Show |
8 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1497-626delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr6 | 108936270 | ||||||
| chr6:108936381 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1497-519A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936381 | |||||||
| chr6:108936470 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1497-430C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936470 | |||||||
| chr6:108936471 | G | A | 3 | a0001c0001t0005g0089 a0001c0001t0005g0090 a0001c0001t0007g0088 |
3 | HG02055.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1497-429G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936471 | |||||||
| chr6:108936485 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1497-415A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936485 | |||||||
| chr6:108936568 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1497-332T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936568 | |||||||
| chr6:108936660 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1497-240C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936660 | |||||||
| chr6:108936665 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): Show |
89 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1497-235G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936665 | |||||||
| chr6:108936705 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1497-195C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936705 | |||||||
| chr6:108936785 | C | A | 24 | a0002c0002t0001g0265 a0002c0002t0001g0267 a0002c0002t0001g0268 others(21): Show |
24 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.1497-115C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 11/17 | chr6 | 108936785 | |||||||
| chr6:108937081 | T | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1596+82T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937081 | |||||||
| chr6:108937133 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1596+134T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937133 | |||||||
| chr6:108937302 | G | T | 2 | a0001c0001t0001g0202 a0001c0001t0002g0203 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1596+303G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937302 | |||||||
| chr6:108937446 | T | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
94 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.1596+447T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937446 | |||||||
| chr6:108937755 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1596+756C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937755 | |||||||
| chr6:108937808 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0014 others(60): Show |
63 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1596+809C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937808 | |||||||
| chr6:108937819 | C | G | 3 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0003c0003t0002g0193 |
3 | HG02886.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1596+820C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937819 | |||||||
| chr6:108937888 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0002g0068 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1596+889A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937888 | |||||||
| chr6:108937960 | A | G | 98 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0030 others(95): Show |
98 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596+961A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108937960 | |||||||
| chr6:108938086 | A | C | 21 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0001g0247 others(18): Show |
21 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1596+1087A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938086 | |||||||
| chr6:108938122 | G | A | 114 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0095 others(111): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1596+1123G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938122 | |||||||
| chr6:108938172 | G | A | 110 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0095 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1596+1173G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938172 | |||||||
| chr6:108938174 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1596+1175G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938174 | |||||||
| chr6:108938198 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1596+1199G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938198 | |||||||
| chr6:108938211 | G | A | 106 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0095 others(103): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1596+1212G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938211 | |||||||
| chr6:108938262 | C | T | 127 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0085 others(124): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1596+1263C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938262 | |||||||
| chr6:108938357 | A | T | 118 | a0001c0001t0001g0027 a0001c0001t0001g0033 a0001c0001t0001g0060 others(115): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.1596+1358A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938357 | |||||||
| chr6:108938379 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0003g0002 |
2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1596+1380G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938379 | |||||||
| chr6:108938415 | ATT | A | 114 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0095 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.1596+1432_1596+143 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108938415 | ||||||
| chr6:108938497 | G | T | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1596+1498G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938497 | |||||||
| chr6:108938527 | A | G | 94 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0095 others(91): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1596+1528A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938527 | |||||||
| chr6:108938599 | C | CT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596+1618dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108938599 | ||||||
| chr6:108938599 | C | CTT | 10 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(7): Show |
10 | HG00639.hp2 HG01975.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596+1617_1596+161 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108938599 | ||||||
| chr6:108938599 | C | CTTT | 164 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(161): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1596+1616_1596+161 others(7): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108938599 | ||||||
| chr6:108938599 | C | CTTTT | 14 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0130 others(11): Show |
14 | HG01243.hp2 HG01358.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+1615_1596+161 others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108938599 | ||||||
| chr6:108938599 | CT | C | 40 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0086 others(37): Show |
40 | HG00323.hp2 HG00408.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1596+1618delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108938599 | ||||||
| chr6:108938930 | G | C | 1 | a0001c0001t0002g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1596+1931G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108938930 | |||||||
| chr6:108939111 | G | A | 6 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0133 others(3): Show |
6 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+2112G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939111 | |||||||
| chr6:108939183 | G | A | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+2184G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939183 | |||||||
| chr6:108939328 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+2329T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939328 | |||||||
| chr6:108939361 | G | A | 14 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(11): Show |
14 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+2362G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939361 | |||||||
| chr6:108939372 | G | A | 6 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0133 others(3): Show |
6 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+2373G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939372 | |||||||
| chr6:108939403 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1596+2404C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939403 | |||||||
| chr6:108939540 | A | G | 2 | a0001c0006t0001g0058 a0001c0006t0002g0057 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+2541A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939540 | |||||||
| chr6:108939567 | C | T | 1 | a0001c0001t0003g0196 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1596+2568C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939567 | |||||||
| chr6:108939631 | A | G | 1 | a0001c0001t0003g0001 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1596+2632A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939631 | |||||||
| chr6:108939671 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+2672T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939671 | |||||||
| chr6:108939683 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+2684A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108939683 | |||||||
| chr6:108940220 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0003c0003t0002g0187 |
3 | HG02451.hp1 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1596+3221C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940220 | |||||||
| chr6:108940261 | A | G | 14 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(11): Show |
14 | HG00597.hp2 HG01175.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596+3262A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940261 | |||||||
| chr6:108940330 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0033 others(4): Show |
7 | HG00408.hp2 HG02132.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+3331A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940330 | |||||||
| chr6:108940354 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1596+3355C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940354 | |||||||
| chr6:108940354 | C | T | 4 | a0001c0001t0002g0203 a0001c0004t0001g0183 a0001c0004t0001g0184 others(1): Show |
4 | HG02572.hp1 HG03239.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+3355C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940354 | |||||||
| chr6:108940355 | G | A | 2 | a0001c0001t0001g0256 a0001c0001t0001g0259 |
2 | HG01069.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1596+3356G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940355 | |||||||
| chr6:108940485 | G | T | 2 | a0001c0001t0006g0021 a0001c0001t0006g0054 |
2 | NA18944.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1596+3486G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940485 | |||||||
| chr6:108940675 | G | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0003c0003t0002g0187 others(1): Show |
4 | HG02451.hp1 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596+3676G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108940675 | |||||||
| chr6:108941006 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+4007T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941006 | |||||||
| chr6:108941023 | A | G | 30 | a0001c0001t0001g0069 a0001c0001t0001g0091 a0001c0001t0001g0148 others(27): Show |
30 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1596+4024A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941023 | |||||||
| chr6:108941083 | TAGAC | T | 5 | a0001c0001t0001g0041 a0001c0001t0002g0203 a0001c0004t0001g0183 others(2): Show |
5 | HG02486.hp2 HG02572.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+4108_1596+411 others(8): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108941083 | ||||||
| chr6:108941148 | G | A | 2 | a0001c0006t0001g0058 a0001c0006t0002g0057 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1596+4149G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941148 | |||||||
| chr6:108941239 | G | C | 95 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0060 others(92): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1596+4240G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941239 | |||||||
| chr6:108941584 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+4585T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941584 | |||||||
| chr6:108941652 | G | A | 1 | a0001c0006t0002g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1596+4653G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941652 | |||||||
| chr6:108941704 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+4705C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941704 | |||||||
| chr6:108941725 | A | G | 6 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0133 others(3): Show |
6 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596+4726A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941725 | |||||||
| chr6:108941738 | G | A | 67 | a0001c0001t0001g0060 a0001c0001t0001g0096 a0001c0001t0001g0101 others(64): Show |
67 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1596+4739G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941738 | |||||||
| chr6:108941776 | G | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(187): Show |
190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1596+4777G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941776 | |||||||
| chr6:108941819 | CTTTTAAA others(14): Show |
C | 1 | a0001c0001t0001g0142 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1596+4821_1596+484 others(25): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941819 | |||||||
| chr6:108941899 | A | AT | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0098 others(1): Show |
4 | HG02965.hp2 HG03139.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+4907dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108941899 | ||||||
| chr6:108941984 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596+4985C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108941984 | |||||||
| chr6:108942258 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1596+5259C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108942258 | |||||||
| chr6:108942259 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+5260G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108942259 | |||||||
| chr6:108942414 | A | G | 44 | a0001c0001t0001g0069 a0001c0001t0001g0085 a0001c0001t0001g0086 others(41): Show |
44 | HG00408.hp1 HG01081.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.1596+5415A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108942414 | |||||||
| chr6:108942455 | T | C | 2 | a0001c0001t0001g0122 a0001c0008t0001g0123 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1596+5456T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108942455 | |||||||
| chr6:108942486 | G | A | 5 | a0001c0001t0002g0137 a0003c0003t0001g0116 a0003c0003t0001g0117 others(2): Show |
5 | HG02109.hp1 HG02809.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+5487G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108942486 | |||||||
| chr6:108943489 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1596+6490A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943489 | |||||||
| chr6:108943586 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0136 others(2): Show |
5 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+6587C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943586 | |||||||
| chr6:108943675 | C | A | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1596+6676C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943675 | |||||||
| chr6:108943676 | C | A | 1 | a0002c0002t0001g0268 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1596+6677C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943676 | |||||||
| chr6:108943707 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1596+6708G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943707 | |||||||
| chr6:108943769 | G | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596+6770G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943769 | |||||||
| chr6:108943823 | A | C | 1 | a0001c0001t0001g0142 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1596+6824A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943823 | |||||||
| chr6:108943919 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1596+6920T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108943919 | |||||||
| chr6:108944137 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1596+7138A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944137 | |||||||
| chr6:108944404 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1596+7405C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944404 | |||||||
| chr6:108944443 | G | T | 1 | a0001c0001t0002g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596+7444G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944443 | |||||||
| chr6:108944652 | G | C | 1 | a0001c0001t0003g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1596+7653G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944652 | |||||||
| chr6:108944749 | A | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0136 others(2): Show |
5 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+7750A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944749 | |||||||
| chr6:108944790 | TG | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0136 others(2): Show |
5 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596+7792delG | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944790 | |||||||
| chr6:108944943 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1596+7944A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944943 | |||||||
| chr6:108944996 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1596+7997G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108944996 | |||||||
| chr6:108945052 | T | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(56): Show |
59 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1597-7981T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108945052 | |||||||
| chr6:108945193 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0002g0124 a0001c0008t0001g0123 |
3 | HG01891.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1597-7840G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108945193 | |||||||
| chr6:108945322 | T | C | 1 | a0001c0001t0007g0088 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1597-7711T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108945322 | |||||||
| chr6:108946420 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0003c0003t0002g0187 |
3 | HG02451.hp1 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1597-6613C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108946420 | |||||||
| chr6:108946484 | C | T | 6 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0133 others(3): Show |
6 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-6549C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108946484 | |||||||
| chr6:108946554 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1597-6479T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108946554 | |||||||
| chr6:108946570 | T | A | 27 | a0001c0001t0001g0027 a0001c0001t0001g0095 a0001c0001t0001g0107 others(24): Show |
27 | HG00738.hp2 HG01256.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1597-6463T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108946570 | |||||||
| chr6:108946685 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1597-6348G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108946685 | |||||||
| chr6:108946747 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1597-6286G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108946747 | |||||||
| chr6:108946847 | C | T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
61 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.1597-6186C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108946847 | |||||||
| chr6:108947117 | T | C | 5 | a0001c0001t0001g0091 a0001c0001t0003g0001 a0001c0001t0003g0002 others(2): Show |
5 | HG02723.hp2 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-5916T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108947117 | |||||||
| chr6:108947175 | G | A | 6 | a0001c0001t0002g0137 a0003c0003t0001g0116 a0003c0003t0001g0117 others(3): Show |
6 | HG02109.hp1 HG02809.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1597-5858G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108947175 | |||||||
| chr6:108947180 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1597-5853C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108947180 | |||||||
| chr6:108947414 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1597-5619C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108947414 | |||||||
| chr6:108947592 | C | T | 1 | a0003c0003t0002g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1597-5441C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108947592 | |||||||
| chr6:108947643 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1597-5390A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108947643 | |||||||
| chr6:108947829 | G | GA | 10 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0159 others(7): Show |
10 | HG00438.hp2 HG01192.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1597-5191dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108947829 | ||||||
| chr6:108947829 | GA | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(83): Show |
86 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1597-5191delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 108947829 | ||||||
| chr6:108948055 | G | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0003c0003t0002g0187 |
3 | HG02451.hp1 HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1597-4978G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108948055 | |||||||
| chr6:108948310 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1597-4723G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108948310 | |||||||
| chr6:108948412 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1597-4621A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108948412 | |||||||
| chr6:108948587 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1597-4446G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108948587 | |||||||
| chr6:108948619 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1597-4414T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108948619 | |||||||
| chr6:108948717 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0002g0136 others(2): Show |
5 | HG02055.hp1 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-4316C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108948717 | |||||||
| chr6:108948820 | G | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0220 |
3 | NA18945.hp1 NA18961.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1597-4213G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108948820 | |||||||
| chr6:108949131 | T | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-3902T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108949131 | |||||||
| chr6:108949348 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(131): Show |
134 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.1597-3685G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108949348 | |||||||
| chr6:108949453 | G | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1597-3580G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108949453 | |||||||
| chr6:108949761 | A | T | 8 | a0001c0001t0001g0095 a0002c0002t0001g0282 a0002c0002t0001g0283 others(5): Show |
8 | HG04204.hp2 NA18940.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1597-3272A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108949761 | |||||||
| chr6:108949928 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1597-3105G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108949928 | |||||||
| chr6:108949954 | C | T | 2 | a0001c0001t0005g0089 a0001c0001t0007g0088 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1597-3079C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108949954 | |||||||
| chr6:108949998 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.1597-3035G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108949998 | |||||||
| chr6:108950035 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1597-2998G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950035 | |||||||
| chr6:108950162 | C | T | 4 | a0001c0001t0001g0099 a0001c0001t0001g0234 a0001c0001t0002g0066 others(1): Show |
4 | HG02258.hp2 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-2871C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950162 | |||||||
| chr6:108950211 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1597-2822C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950211 | |||||||
| chr6:108950303 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1597-2730A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950303 | |||||||
| chr6:108950371 | C | T | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1597-2662C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950371 | |||||||
| chr6:108950425 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1597-2608A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950425 | |||||||
| chr6:108950532 | C | T | 3 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0115 |
3 | HG00621.hp2 HG02155.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1597-2501C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950532 | |||||||
| chr6:108950571 | G | A | 3 | a0001c0004t0001g0183 a0001c0004t0001g0184 a0001c0004t0001g0185 |
3 | HG03239.hp1 HG03492.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1597-2462G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950571 | |||||||
| chr6:108950728 | C | G | 3 | a0001c0004t0001g0183 a0001c0004t0001g0184 a0001c0004t0001g0185 |
3 | HG03239.hp1 HG03492.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1597-2305C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950728 | |||||||
| chr6:108950735 | A | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0121 |
2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1597-2298A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950735 | |||||||
| chr6:108950762 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1597-2271C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108950762 | |||||||
| chr6:108951039 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1597-1994A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951039 | |||||||
| chr6:108951195 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1597-1838C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951195 | |||||||
| chr6:108951215 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1597-1818C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951215 | |||||||
| chr6:108951536 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0003g0064 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1597-1497T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951536 | |||||||
| chr6:108951702 | C | T | 93 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0060 others(90): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1597-1331C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951702 | |||||||
| chr6:108951703 | G | A | 23 | a0001c0001t0001g0148 a0001c0001t0001g0205 a0001c0001t0001g0208 others(20): Show |
23 | HG00408.hp1 HG01099.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1597-1330G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951703 | |||||||
| chr6:108951723 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1597-1310C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951723 | |||||||
| chr6:108951747 | C | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.1597-1286C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108951747 | |||||||
| chr6:108952007 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1597-1026C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952007 | |||||||
| chr6:108952455 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0160 |
2 | HG00140.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1597-578G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952455 | |||||||
| chr6:108952483 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1597-550T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952483 | |||||||
| chr6:108952495 | A | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(215): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1597-538A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952495 | |||||||
| chr6:108952499 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1597-534G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952499 | |||||||
| chr6:108952558 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1597-475A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952558 | |||||||
| chr6:108952673 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1597-360C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952673 | |||||||
| chr6:108952706 | A | G | 4 | a0001c0001t0004g0025 a0001c0001t0004g0045 a0001c0001t0004g0046 others(1): Show |
4 | HG00099.hp1 HG01257.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-327A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952706 | |||||||
| chr6:108952827 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1597-206G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952827 | |||||||
| chr6:108952852 | T | C | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0091 others(7): Show |
10 | HG01081.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1597-181T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952852 | |||||||
| chr6:108952967 | A | C | 1 | a0001c0001t0001g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1597-66A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 12/17 | chr6 | 108952967 | |||||||
| chr6:108953643 | T | A | 5 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1915+292T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108953643 | |||||||
| chr6:108953825 | T | G | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1915+474T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108953825 | |||||||
| chr6:108953835 | G | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(213): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1915+484G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108953835 | |||||||
| chr6:108954468 | C | T | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0134 others(3): Show |
6 | HG02451.hp1 HG02559.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1915+1117C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108954468 | |||||||
| chr6:108954537 | C | T | 2 | a0001c0001t0006g0021 a0001c0001t0006g0054 |
2 | NA18944.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1915+1186C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108954537 | |||||||
| chr6:108954554 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1915+1203C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108954554 | |||||||
| chr6:108954691 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1915+1340G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108954691 | |||||||
| chr6:108954745 | C | T | 1 | a0001c0008t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1915+1394C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108954745 | |||||||
| chr6:108954923 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1915+1572C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108954923 | |||||||
| chr6:108954990 | A | G | 5 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0002g0055 others(2): Show |
5 | HG01884.hp2 HG02976.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1915+1639A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108954990 | |||||||
| chr6:108955062 | C | T | 1 | a0002c0002t0002g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1915+1711C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955062 | |||||||
| chr6:108955118 | C | T | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1915+1767C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955118 | |||||||
| chr6:108955197 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1915+1846A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955197 | |||||||
| chr6:108955286 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1915+1935A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955286 | |||||||
| chr6:108955320 | G | A | 1 | a0001c0001t0003g0138 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1915+1969G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955320 | |||||||
| chr6:108955343 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0085 a0001c0001t0001g0135 others(2): Show |
5 | HG00558.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1915+1992C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955343 | |||||||
| chr6:108955349 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1915+1998C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955349 | |||||||
| chr6:108955539 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1915+2188C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955539 | |||||||
| chr6:108955562 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1915+2211C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955562 | |||||||
| chr6:108955848 | T | C | 5 | a0001c0001t0001g0041 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG00639.hp2 HG01106.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1915+2497T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955848 | |||||||
| chr6:108955906 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1915+2555A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955906 | |||||||
| chr6:108955957 | T | C | 1 | a0001c0001t0005g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1915+2606T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955957 | |||||||
| chr6:108955962 | A | C | 15 | a0001c0001t0001g0098 a0001c0001t0001g0128 a0001c0001t0001g0130 others(12): Show |
15 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1915+2611A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108955962 | |||||||
| chr6:108956434 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1915+3083C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956434 | |||||||
| chr6:108956496 | G | A | 3 | a0001c0001t0002g0068 a0001c0001t0003g0002 a0001c0001t0007g0088 |
3 | HG02630.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1915+3145G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956496 | |||||||
| chr6:108956534 | T | TAA | 30 | a0001c0001t0001g0094 a0001c0001t0001g0255 a0001c0001t0002g0068 others(27): Show |
30 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.1915+3199_1915+320 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 108956534 | ||||||
| chr6:108956564 | G | C | 2 | a0001c0001t0002g0068 a0001c0001t0007g0088 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1915+3213G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956564 | |||||||
| chr6:108956705 | A | T | 37 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0122 others(34): Show |
37 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1915+3354A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956705 | |||||||
| chr6:108956714 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1915+3363G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956714 | |||||||
| chr6:108956724 | GC | G | 12 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(9): Show |
12 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1915+3374delC | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956724 | |||||||
| chr6:108956970 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1915+3619C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956970 | |||||||
| chr6:108956971 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0119 a0002c0002t0001g0277 |
3 | HG02083.hp1 HG02135.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1915+3620G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108956971 | |||||||
| chr6:108957127 | G | A | 1 | a0001c0001t0003g0290 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1915+3776G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957127 | |||||||
| chr6:108957146 | CTTAGGCA others(3873): Show |
C | 1 | a0002c0002t0001g0288 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1915+3801_1916-541 others(3): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 108957146 | ||||||
| chr6:108957219 | G | T | 2 | a0001c0001t0002g0124 a0003c0003t0002g0193 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1915+3868G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957219 | |||||||
| chr6:108957222 | G | T | 26 | a0001c0001t0001g0255 a0001c0001t0002g0068 a0001c0001t0003g0011 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.1915+3871G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957222 | |||||||
| chr6:108957670 | A | G | 30 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0002g0068 others(27): Show |
30 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1916-3902A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957670 | |||||||
| chr6:108957737 | G | A | 1 | a0001c0001t0004g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1916-3835G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957737 | |||||||
| chr6:108957766 | T | G | 2 | a0001c0001t0009g0065 a0003c0003t0001g0116 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1916-3806T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957766 | |||||||
| chr6:108957902 | A | C | 29 | a0001c0001t0002g0068 a0001c0001t0002g0136 a0001c0001t0002g0137 others(26): Show |
29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1916-3670A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957902 | |||||||
| chr6:108957971 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1916-3601C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108957971 | |||||||
| chr6:108958008 | G | A | 24 | a0001c0001t0002g0068 a0001c0001t0002g0136 a0001c0001t0002g0137 others(21): Show |
24 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.1916-3564G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958008 | |||||||
| chr6:108958009 | A | G | 4 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1916-3563A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958009 | |||||||
| chr6:108958044 | C | G | 2 | a0001c0004t0001g0183 a0001c0004t0001g0185 |
2 | HG03492.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1916-3528C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958044 | |||||||
| chr6:108958178 | C | T | 28 | a0001c0001t0002g0068 a0001c0001t0002g0136 a0001c0001t0002g0137 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1916-3394C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958178 | |||||||
| chr6:108958396 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1916-3176G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958396 | |||||||
| chr6:108958436 | A | G | 5 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0097 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1916-3136A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958436 | |||||||
| chr6:108958547 | C | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1916-3025C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958547 | |||||||
| chr6:108958580 | A | T | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1916-2992A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958580 | |||||||
| chr6:108958751 | C | T | 21 | a0001c0001t0001g0205 a0001c0001t0002g0055 a0001c0001t0002g0056 others(18): Show |
21 | HG01109.hp1 HG02004.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.1916-2821C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958751 | |||||||
| chr6:108958779 | A | G | 1 | a0001c0001t0006g0054 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1916-2793A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958779 | |||||||
| chr6:108958823 | A | G | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0003c0003t0001g0117 |
3 | HG01884.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1916-2749A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958823 | |||||||
| chr6:108958911 | C | T | 2 | a0001c0001t0002g0233 a0003c0003t0002g0092 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1916-2661C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108958911 | |||||||
| chr6:108959208 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1916-2364A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959208 | |||||||
| chr6:108959272 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0003c0003t0002g0187 |
3 | HG02486.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1916-2300T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959272 | |||||||
| chr6:108959491 | C | T | 2 | a0002c0002t0001g0265 a0002c0002t0001g0272 |
2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1916-2081C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959491 | |||||||
| chr6:108959517 | C | G | 1 | a0001c0001t0004g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1916-2055C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959517 | |||||||
| chr6:108959590 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1916-1982C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959590 | |||||||
| chr6:108959594 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1916-1978G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959594 | |||||||
| chr6:108959669 | T | A | 2 | a0001c0001t0001g0103 a0002c0002t0001g0281 |
2 | HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1916-1903T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959669 | |||||||
| chr6:108959729 | G | A | 28 | a0001c0001t0002g0068 a0001c0001t0002g0137 a0001c0001t0003g0011 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1916-1843G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959729 | |||||||
| chr6:108959730 | G | T | 28 | a0001c0001t0002g0068 a0001c0001t0002g0137 a0001c0001t0003g0011 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1916-1842G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959730 | |||||||
| chr6:108959885 | C | T | 5 | a0001c0001t0002g0068 a0001c0001t0002g0137 a0001c0001t0007g0088 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-1687C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959885 | |||||||
| chr6:108959955 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1916-1617G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959955 | |||||||
| chr6:108959993 | T | G | 7 | a0001c0001t0001g0083 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG00408.hp1 HG02040.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1916-1579T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108959993 | |||||||
| chr6:108960208 | G | T | 39 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(36): Show |
39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.1916-1364G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960208 | |||||||
| chr6:108960210 | C | G | 89 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(86): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.1916-1362C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960210 | |||||||
| chr6:108960211 | G | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-1361G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960211 | |||||||
| chr6:108960280 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1916-1292C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960280 | |||||||
| chr6:108960358 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1916-1214C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960358 | |||||||
| chr6:108960417 | C | T | 5 | a0001c0001t0002g0068 a0001c0001t0002g0137 a0001c0001t0007g0088 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-1155C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960417 | |||||||
| chr6:108960440 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1916-1132C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960440 | |||||||
| chr6:108960486 | A | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0056 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1916-1086A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960486 | |||||||
| chr6:108960527 | A | G | 3 | a0001c0001t0002g0066 a0001c0001t0002g0133 a0001c0001t0002g0136 |
3 | HG02559.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1916-1045A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960527 | |||||||
| chr6:108960616 | G | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-956G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960616 | |||||||
| chr6:108960623 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1916-949G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960623 | |||||||
| chr6:108960647 | G | A | 5 | a0001c0001t0002g0068 a0001c0001t0002g0137 a0001c0001t0007g0088 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1916-925G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960647 | |||||||
| chr6:108960790 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1916-782A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108960790 | |||||||
| chr6:108961061 | A | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0168 others(3): Show |
6 | HG00642.hp1 HG01074.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1916-511A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108961061 | |||||||
| chr6:108961199 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1916-373G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108961199 | |||||||
| chr6:108961242 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1916-330G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 13/17 | chr6 | 108961242 | |||||||
| chr6:108961863 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2039-151A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 14/17 | chr6 | 108961863 | |||||||
| chr6:108962227 | G | A | 2 | a0001c0001t0001g0111 a0002c0002t0001g0268 |
2 | NA18940.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2152+100G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108962227 | |||||||
| chr6:108962249 | G | A | 5 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0236 others(2): Show |
5 | HG01891.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2152+122G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108962249 | |||||||
| chr6:108962590 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0136 |
2 | HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2152+463A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108962590 | |||||||
| chr6:108962698 | A | G | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2152+571A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108962698 | |||||||
| chr6:108962774 | G | A | 11 | a0001c0001t0002g0079 a0001c0001t0002g0204 a0001c0001t0002g0206 others(8): Show |
11 | HG01109.hp1 HG02004.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.2152+647G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108962774 | |||||||
| chr6:108963020 | A | G | 32 | a0001c0001t0002g0124 a0001c0001t0002g0133 a0001c0001t0003g0001 others(29): Show |
32 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.2152+893A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108963020 | |||||||
| chr6:108963052 | A | G | 33 | a0001c0001t0002g0124 a0001c0001t0002g0133 a0001c0001t0002g0136 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.2152+925A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108963052 | |||||||
| chr6:108963658 | C | T | 2 | a0001c0001t0002g0203 a0001c0006t0002g0057 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2153-522C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108963658 | |||||||
| chr6:108963684 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2153-496A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108963684 | |||||||
| chr6:108963973 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2153-207G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108963973 | |||||||
| chr6:108963986 | A | G | 61 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0002g0055 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2153-194A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108963986 | |||||||
| chr6:108964000 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2153-180T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108964000 | |||||||
| chr6:108964075 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2153-105C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 15/17 | chr6 | 108964075 | |||||||
| chr6:108964555 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2285+243C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 16/17 | chr6 | 108964555 | |||||||
| chr6:108964634 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2285+322C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 16/17 | chr6 | 108964634 | |||||||
| chr6:108964699 | G | A | 1 | a0001c0001t0001g0003 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2286-281G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 16/17 | chr6 | 108964699 | |||||||
| chr6:108964748 | C | T | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2286-232C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 16/17 | chr6 | 108964748 | |||||||
| chr6:108964749 | G | A | 7 | a0001c0001t0001g0121 a0001c0001t0001g0188 a0001c0001t0001g0192 others(4): Show |
7 | HG01891.hp1 HG02809.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2286-231G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 16/17 | chr6 | 108964749 | |||||||
| chr6:108964859 | T | C | 2 | a0001c0001t0002g0203 a0001c0006t0002g0057 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2286-121T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 16/17 | chr6 | 108964859 | |||||||
| chr6:108965163 | GTC | G | 14 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0036 others(11): Show |
14 | HG01106.hp2 HG01361.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.2446+25_2446+26del others(2): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108965163 | ||||||
| chr6:108965371 | C | CT | 195 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.2446+248dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108965371 | ||||||
| chr6:108965371 | C | CTT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0074 others(13): Show |
16 | HG01109.hp2 HG01175.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.2446+247_2446+248d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108965371 | ||||||
| chr6:108965371 | CT | C | 25 | a0001c0001t0002g0133 a0001c0001t0003g0011 a0001c0001t0003g0044 others(22): Show |
25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2446+248delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108965371 | ||||||
| chr6:108965556 | G | T | 1 | a0004c0005t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2446+416G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108965556 | |||||||
| chr6:108965708 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2446+568G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108965708 | |||||||
| chr6:108965752 | C | T | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0003c0003t0001g0117 |
3 | HG01884.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2446+612C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108965752 | |||||||
| chr6:108965823 | T | A | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(30): Show |
33 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.2446+683T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108965823 | |||||||
| chr6:108965943 | T | G | 1 | a0001c0001t0002g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2446+803T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108965943 | |||||||
| chr6:108965983 | A | T | 2 | a0001c0001t0001g0229 a0001c0006t0001g0058 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2446+843A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108965983 | |||||||
| chr6:108965984 | T | A | 2 | a0001c0001t0001g0229 a0001c0006t0001g0058 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2446+844T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108965984 | |||||||
| chr6:108966006 | T | A | 65 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0122 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2446+866T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966006 | |||||||
| chr6:108966256 | A | G | 31 | a0001c0001t0002g0066 a0001c0001t0002g0133 a0001c0001t0003g0001 others(28): Show |
31 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.2446+1116A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966256 | |||||||
| chr6:108966324 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2446+1184G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966324 | |||||||
| chr6:108966593 | A | T | 1 | a0001c0001t0002g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2446+1453A>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966593 | |||||||
| chr6:108966630 | AT | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2446+1499delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108966630 | ||||||
| chr6:108966707 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2446+1567A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966707 | |||||||
| chr6:108966727 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2446+1587C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966727 | |||||||
| chr6:108966833 | C | G | 25 | a0001c0001t0002g0133 a0001c0001t0003g0011 a0001c0001t0003g0044 others(22): Show |
25 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2446+1693C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966833 | |||||||
| chr6:108966899 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2446+1759C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108966899 | |||||||
| chr6:108967052 | T | C | 3 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0003c0003t0001g0117 |
3 | HG01884.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2446+1912T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967052 | |||||||
| chr6:108967304 | G | A | 1 | a0003c0003t0001g0039 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2446+2164G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967304 | |||||||
| chr6:108967387 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2446+2247G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967387 | |||||||
| chr6:108967519 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2446+2379C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967519 | |||||||
| chr6:108967525 | G | C | 1 | a0001c0001t0002g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2446+2385G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967525 | |||||||
| chr6:108967566 | C | A | 19 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(16): Show |
19 | HG01109.hp1 HG02004.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.2446+2426C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967566 | |||||||
| chr6:108967567 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2446+2427C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967567 | |||||||
| chr6:108967690 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2446+2550G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967690 | |||||||
| chr6:108967738 | T | TTC | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2446+2600_2446+260 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108967738 | ||||||
| chr6:108967776 | C | T | 4 | a0001c0001t0002g0124 a0001c0001t0002g0239 a0001c0001t0002g0240 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2446+2636C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967776 | |||||||
| chr6:108967777 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2446+2637G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967777 | |||||||
| chr6:108967824 | C | G | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2446+2684C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967824 | |||||||
| chr6:108967926 | C | T | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2446+2786C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108967926 | |||||||
| chr6:108968000 | G | A | 64 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.2446+2860G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968000 | |||||||
| chr6:108968021 | C | T | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2446+2881C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968021 | |||||||
| chr6:108968127 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2446+2987T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968127 | |||||||
| chr6:108968337 | T | C | 65 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2446+3197T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968337 | |||||||
| chr6:108968349 | G | A | 1 | a0001c0001t0004g0046 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2446+3209G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968349 | |||||||
| chr6:108968388 | T | C | 9 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | HG01891.hp2 HG02572.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.2446+3248T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968388 | |||||||
| chr6:108968389 | T | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(269): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2446+3249T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968389 | |||||||
| chr6:108968405 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2446+3265G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968405 | |||||||
| chr6:108968406 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2446+3266G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968406 | |||||||
| chr6:108968451 | C | T | 1 | a0002c0002t0001g0280 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2446+3311C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968451 | |||||||
| chr6:108968509 | T | C | 4 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2446+3369T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968509 | |||||||
| chr6:108968678 | A | G | 61 | a0001c0001t0001g0067 a0001c0001t0001g0091 a0001c0001t0001g0130 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2446+3538A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968678 | |||||||
| chr6:108968698 | C | CA | 9 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | HG01891.hp2 HG02572.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.2446+3561dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108968698 | ||||||
| chr6:108968702 | C | A | 9 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | HG01891.hp2 HG02572.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.2446+3562C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968702 | |||||||
| chr6:108968771 | T | A | 1 | a0002c0002t0001g0268 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2446+3631T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108968771 | |||||||
| chr6:108969116 | C | A | 59 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.2446+3976C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969116 | |||||||
| chr6:108969125 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2446+3985G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969125 | |||||||
| chr6:108969154 | A | G | 21 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(18): Show |
21 | HG01109.hp1 HG02004.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.2446+4014A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969154 | |||||||
| chr6:108969235 | C | T | 3 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0004c0005t0001g0052 |
3 | HG01109.hp2 HG01516.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.2446+4095C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969235 | |||||||
| chr6:108969389 | A | G | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2447-3968A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969389 | |||||||
| chr6:108969403 | CAT | C | 60 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2447-3951_2447-395 others(6): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108969403 | ||||||
| chr6:108969446 | C | G | 1 | a0001c0001t0002g0233 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2447-3911C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969446 | |||||||
| chr6:108969532 | A | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02132.hp1 HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2447-3825A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969532 | |||||||
| chr6:108969533 | G | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02132.hp1 HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2447-3824G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969533 | |||||||
| chr6:108969648 | A | C | 2 | a0002c0002t0001g0265 a0002c0002t0001g0272 |
2 | NA18964.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2447-3709A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108969648 | |||||||
| chr6:108970037 | T | TA | 6 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0168 others(3): Show |
6 | HG00642.hp1 HG01074.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.2447-3309dupA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108970037 | ||||||
| chr6:108970147 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2447-3210G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970147 | |||||||
| chr6:108970418 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2447-2939C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970418 | |||||||
| chr6:108970494 | C | CT | 58 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(55): Show |
58 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2447-2842dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108970494 | ||||||
| chr6:108970494 | CT | C | 58 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0230 others(55): Show |
58 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.2447-2842delT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108970494 | ||||||
| chr6:108970498 | T | C | 7 | a0001c0001t0002g0124 a0001c0001t0003g0001 a0001c0001t0003g0002 others(4): Show |
7 | HG02451.hp2 HG02572.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2447-2859T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970498 | |||||||
| chr6:108970499 | T | C | 58 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0114 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.2447-2858T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970499 | |||||||
| chr6:108970538 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0148 |
2 | HG00423.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.2447-2819C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970538 | |||||||
| chr6:108970579 | T | C | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-2778T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970579 | |||||||
| chr6:108970621 | C | A | 60 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2447-2736C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970621 | |||||||
| chr6:108970855 | G | A | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-2502G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970855 | |||||||
| chr6:108970884 | G | A | 1 | a0003c0003t0002g0193 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2447-2473G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970884 | |||||||
| chr6:108970930 | G | C | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-2427G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108970930 | |||||||
| chr6:108971021 | G | A | 19 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0019 others(16): Show |
19 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2447-2336G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971021 | |||||||
| chr6:108971056 | C | G | 2 | a0001c0001t0002g0124 a0003c0003t0002g0193 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2447-2301C>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971056 | |||||||
| chr6:108971383 | G | T | 1 | a0001c0008t0001g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2447-1974G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971383 | |||||||
| chr6:108971482 | G | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG01891.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2447-1875G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971482 | |||||||
| chr6:108971527 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2447-1830C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971527 | |||||||
| chr6:108971533 | T | C | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-1824T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971533 | |||||||
| chr6:108971603 | A | G | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-1754A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971603 | |||||||
| chr6:108971613 | C | A | 65 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.2447-1744C>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971613 | |||||||
| chr6:108971623 | T | A | 60 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2447-1734T>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971623 | |||||||
| chr6:108971633 | G | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0096 |
2 | HG04115.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.2447-1724G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971633 | |||||||
| chr6:108971734 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2447-1623C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971734 | |||||||
| chr6:108971738 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0162 |
2 | HG00438.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.2447-1619A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971738 | |||||||
| chr6:108971878 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2447-1479G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108971878 | |||||||
| chr6:108971920 | CA | C | 26 | a0001c0001t0001g0051 a0001c0001t0001g0177 a0001c0001t0003g0011 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.2447-1419delA | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108971920 | ||||||
| chr6:108972428 | G | A | 1 | a0003c0003t0001g0117 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.2447-929G>A | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972428 | |||||||
| chr6:108972645 | A | G | 6 | a0001c0001t0002g0066 a0001c0001t0002g0068 a0001c0001t0002g0136 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2447-712A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972645 | |||||||
| chr6:108972647 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2447-710A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972647 | |||||||
| chr6:108972695 | T | G | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-662T>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972695 | |||||||
| chr6:108972724 | C | T | 21 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(18): Show |
21 | HG01109.hp1 HG02004.hp2 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.2447-633C>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972724 | |||||||
| chr6:108972770 | T | C | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-587T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972770 | |||||||
| chr6:108972839 | A | AT | 59 | a0001c0001t0001g0122 a0001c0001t0001g0134 a0001c0001t0001g0135 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.2447-503dupT | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108972839 | ||||||
| chr6:108972839 | A | ATT | 6 | a0001c0001t0002g0124 a0001c0001t0002g0214 a0001c0001t0002g0239 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2447-504_2447-503d others(4): Show |
ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 108972839 | ||||||
| chr6:108972929 | A | G | 7 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0102 others(4): Show |
7 | HG00597.hp1 HG00621.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.2447-428A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972929 | |||||||
| chr6:108972961 | A | C | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-396A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108972961 | |||||||
| chr6:108973090 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2447-267G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108973090 | |||||||
| chr6:108973119 | G | T | 60 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(57): Show |
60 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.2447-238G>T | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108973119 | |||||||
| chr6:108973133 | T | C | 61 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0061 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2447-224T>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108973133 | |||||||
| chr6:108973192 | A | G | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2447-165A>G | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108973192 | |||||||
| chr6:108973244 | G | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0132 others(2): Show |
5 | HG02572.hp2 HG03225.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2447-113G>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108973244 | |||||||
| chr6:108973335 | A | C | 1 | a0003c0003t0001g0116 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2447-22A>C | ARMC2 | ENSG00000118690.13 | transcript | ENST00000392644.9 | protein_coding | 17/17 | chr6 | 108973335 |