Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27092 |
| ensemblid | ENSG00000075461.6 |
| hgncid | 1408 |
| symbol | CACNG4 |
| name | calcium voltage-gated channel auxiliary subunit gamma 4 |
| refseq_nuc | NM_014405.4 |
| refseq_prot | NP_055220.1 |
| ensembl_nuc | ENST00000262138.4 |
| ensembl_prot | ENSP00000262138.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 66964707 |
| end | 67033398 |
| strand | + |
| ver | v1.2 |
| region | chr17:66964707-67033398 |
| region5000 | chr17:66959707-67038398 |
| regionname0 | CACNG4_chr17_66964707_67033398 |
| regionname5000 | CACNG4_chr17_66959707_67038398 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 327 | 349 | 91 | 74 | 136 | 8 | 38 | 96 | CACNG4_chr17_66959707_67038398 | CACNG4 | MVRCD others(322): Show |
chr17 | 66959707 | 67038398 |
| a0002 | 0/0 | 327 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | MVRCD others(322): Show |
chr17 | 66959707 | 67038398 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 981 | 305 | 87 | 60 | 117 | 7 | 32 | CACNG4_chr17_66959707_67038398 | CACNG4 | ATGGT others(976): Show |
chr17 | 66959707 | 67038398 | ||
| a0001c0002 | 0/0 | 981 | 32 | 1 | 12 | 17 | 1 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | ATGGT others(976): Show |
chr17 | 66959707 | 67038398 | ||
| a0001c0003 | 0/0 | 981 | 9 | 0 | 2 | 2 | 0 | 5 | CACNG4_chr17_66959707_67038398 | CACNG4 | ATGGT others(976): Show |
chr17 | 66959707 | 67038398 | ||
| a0001c0005 | 0/0 | 981 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ATGGT others(976): Show |
chr17 | 66959707 | 67038398 | ||
| a0002c0004 | 0/0 | 981 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ATGGT others(976): Show |
chr17 | 66959707 | 67038398 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3583 | 101 | 3 | 14 | 70 | 3 | 10 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0002 | 1/0 | 3583 | 55 | 24 | 17 | 2 | 0 | 11 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0003 | 0/0 | 3583 | 55 | 13 | 13 | 22 | 3 | 4 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0004 | 0/0 | 3583 | 18 | 2 | 2 | 12 | 0 | 2 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0005 | 0/0 | 3583 | 12 | 11 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0006 | 0/0 | 3583 | 8 | 7 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0007 | 0/0 | 3583 | 5 | 0 | 0 | 5 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0008 | 0/0 | 3583 | 6 | 3 | 3 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0009 | 0/0 | 3583 | 3 | 0 | 2 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0010 | 0/0 | 3583 | 3 | 0 | 0 | 3 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0011 | 0/0 | 3583 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0012 | 0/0 | 3583 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0013 | 0/0 | 3583 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0014 | 0/0 | 3583 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0015 | 0/0 | 3583 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0016 | 0/0 | 3583 | 2 | 0 | 0 | 0 | 0 | 2 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0017 | 0/0 | 3583 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0019 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0020 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0021 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0023 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0024 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0025 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0026 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0027 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0028 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0029 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0030 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0031 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0032 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0033 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0034 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0035 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0037 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0038 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0039 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0040 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0041 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0042 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0001t0043 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0002t0002 | 0/0 | 3583 | 29 | 1 | 11 | 15 | 1 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0002t0007 | 0/0 | 3583 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0002t0022 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0002t0036 | 0/0 | 3583 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0003t0001 | 0/0 | 3583 | 2 | 0 | 0 | 1 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0003t0002 | 0/0 | 3583 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0003t0003 | 0/0 | 3583 | 4 | 0 | 0 | 1 | 0 | 3 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0003t0018 | 0/0 | 3583 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0005t0002 | 0/0 | 3583 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0001c0005t0005 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0002c0004t0001 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0002c0004t0002 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| a0002c0004t0003 | 0/0 | 3583 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | ACTCG others(3578): Show |
chr17 | 66959707 | 67038398 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0005g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0008g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0008g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0009g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0010g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0011g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0011g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0012g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0013g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0013g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0014g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0015g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0015g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0016g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0016g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0017g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0020g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0021g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0023g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0024g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0025g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0026g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0027g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0028g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0029g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0030g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0031g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0032g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0033g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0034g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0035g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0037g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0038g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0039g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0040g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0041g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0042g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0001t0043g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0022g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0002t0036g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0003t0018g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0005t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0005t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0001c0005t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0002c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0002c0004t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| a0002c0004t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | GBR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0336 | EUR | GBR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0260 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0261 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00609 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0048 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00741 | hp1 | a0001 | c0001 | t0015 | g0290 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0320 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01069 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01099 | hp1 | a0001 | c0001 | t0039 | g0066 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01099 | hp2 | a0001 | c0001 | t0013 | g0244 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01106 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0312 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0231 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0247 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01168 | hp2 | a0001 | c0001 | t0015 | g0299 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0248 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01243 | hp2 | a0001 | c0001 | t0037 | g0329 | AMR | PUR | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01258 | hp2 | a0001 | c0003 | t0002 | g0006 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0192 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0317 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0223 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01361 | hp2 | a0001 | c0001 | t0030 | g0106 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01496 | hp2 | a0001 | c0001 | t0013 | g0255 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01517 | hp1 | a0001 | c0001 | t0031 | g0291 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01891 | hp2 | a0001 | c0001 | t0023 | g0251 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0311 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0313 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0315 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01978 | hp2 | a0001 | c0002 | t0007 | g0258 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0309 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0153 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02027 | hp1 | a0001 | c0001 | t0009 | g0245 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02055 | hp1 | a0002 | c0004 | t0003 | g0323 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02129 | hp1 | a0001 | c0001 | t0007 | g0257 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02165 | hp1 | a0001 | c0003 | t0003 | g0226 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0039 | EAS | CDX | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0324 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0254 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0242 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0151 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0285 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0284 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0090 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0232 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0094 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02602 | hp2 | a0001 | c0003 | t0003 | g0028 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02622 | hp1 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0096 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0012 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02647 | hp1 | a0001 | c0001 | t0040 | g0263 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0095 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02683 | hp2 | a0001 | c0001 | t0016 | g0297 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0338 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02723 | hp1 | a0001 | c0001 | t0011 | g0107 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02723 | hp2 | a0001 | c0001 | t0033 | g0041 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02735 | hp1 | a0001 | c0001 | t0027 | g0052 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02809 | hp1 | a0001 | c0001 | t0021 | g0233 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0330 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0306 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0253 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02922 | hp2 | a0001 | c0005 | t0002 | g0148 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02965 | hp1 | a0001 | c0001 | t0011 | g0194 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02970 | hp1 | a0001 | c0001 | t0035 | g0114 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0337 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03139 | hp1 | a0001 | c0001 | t0020 | g0236 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03139 | hp2 | a0001 | c0001 | t0042 | g0093 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0092 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03225 | hp1 | a0001 | c0001 | t0026 | g0201 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0283 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0279 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | ESN | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03540 | hp2 | a0001 | c0001 | t0038 | g0115 | AFR | GWD | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0105 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03654 | hp1 | a0001 | c0001 | t0024 | g0206 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03654 | hp2 | a0001 | c0003 | t0018 | g0262 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0276 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03688 | hp1 | a0001 | c0001 | t0016 | g0044 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0132 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0275 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0046 | SAS | PJL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03834 | hp2 | a0001 | c0001 | t0025 | g0218 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | BEB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0045 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0237 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18522 | hp2 | a0001 | c0001 | t0032 | g0304 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | CHB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18959 | hp1 | a0001 | c0001 | t0010 | g0267 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18965 | hp2 | a0001 | c0002 | t0036 | g0282 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18966 | hp1 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18982 | hp2 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0051 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0325 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19055 | hp2 | a0001 | c0002 | t0022 | g0026 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19067 | hp1 | a0001 | c0001 | t0010 | g0147 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19074 | hp2 | a0001 | c0001 | t0028 | g0099 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19086 | hp1 | a0001 | c0001 | t0029 | g0059 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA19240 | hp2 | a0001 | c0005 | t0005 | g0149 | AFR | YRI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ASW | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ASW | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0098 | EUR | TSI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02486 | hp2 | a0001 | c0001 | t0034 | g0117 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02559 | hp1 | a0001 | c0001 | t0041 | g0091 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG02559 | hp2 | a0002 | c0004 | t0002 | g0331 | AFR | ACB | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | MSL | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0123 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA20300 | hp2 | a0001 | c0005 | t0002 | g0150 | AFR | USA | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA21309 | hp1 | a0001 | c0001 | t0043 | g0121 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0013 | REF | REF | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0300 | REF | REF | CACNG4_chr17_66959707_67038398 | CACNG4 | chr17 | 66959707 | 67038398 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:67024880 | G | A | 1 | a0002 | 3 | HG02055.hp1 HG02257.hp2 HG02559.hp2 |
missense_variant | MODERATE | c.325G>A | p.Val109Ile | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/4 | 530/3583 | 325/984 | 109/327 | chr17 | 67024880 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:67018244 | C | T | 1 | a0001c0003 | 9 | HG00408.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
synonymous_variant | LOW | c.276C>T | p.Tyr92Tyr | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/4 | 481/3583 | 276/984 | 92/327 | chr17 | 67018244 | |||
| chr17:67024909 | C | T | 1 | a0001c0005 | 3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.354C>T | p.Leu118Leu | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/4 | 559/3583 | 354/984 | 118/327 | chr17 | 67024909 | |||
| chr17:67030770 | C | T | 1 | a0001c0002 | 32 | HG00140.hp2 HG00609.hp1 HG00738.hp2 others(29): Show |
synonymous_variant | LOW | c.750C>T | p.Thr250Thr | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 955/3583 | 750/984 | 250/327 | chr17 | 67030770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:66964745 | C | G | 1 | a0001c0001t0043 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-167C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 167 | chr17 | 66964745 | ||||||
| chr17:66964771 | G | A | 5 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0013 others(2): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-141G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 141 | chr17 | 66964771 | ||||||
| chr17:66964774 | G | C | 5 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0019 others(2): Show |
13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-138G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 138 | chr17 | 66964774 | ||||||
| chr17:66964783 | C | T | 4 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0041 others(1): Show |
7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-129C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/4 | 129 | chr17 | 66964783 | ||||||
| chr17:67031018 | T | A | 1 | a0001c0002t0022 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 14 | chr17 | 67031018 | ||||||
| chr17:67031025 | G | A | 1 | a0001c0001t0023 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 21 | chr17 | 67031025 | ||||||
| chr17:67031177 | G | A | 1 | a0001c0001t0024 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 173 | chr17 | 67031177 | ||||||
| chr17:67031226 | A | T | 2 | a0001c0001t0011 a0001c0001t0040 |
4 | HG02647.hp1 HG02717.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*222A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 222 | chr17 | 67031226 | ||||||
| chr17:67031266 | C | T | 2 | a0001c0001t0017 a0001c0001t0039 |
3 | HG01099.hp1 HG02451.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*262C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 262 | chr17 | 67031266 | ||||||
| chr17:67031392 | T | C | 1 | a0001c0001t0025 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 388 | chr17 | 67031392 | ||||||
| chr17:67031424 | C | T | 2 | a0001c0001t0021 a0001c0001t0038 |
2 | HG02809.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*420C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 420 | chr17 | 67031424 | ||||||
| chr17:67031425 | G | A | 1 | a0001c0001t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 421 | chr17 | 67031425 | ||||||
| chr17:67031440 | G | A | 1 | a0001c0001t0015 | 2 | HG00741.hp1 HG01168.hp2 |
3_prime_UTR_variant | MODIFIER | c.*436G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 436 | chr17 | 67031440 | ||||||
| chr17:67031488 | G | A | 2 | a0001c0001t0017 a0001c0001t0039 |
3 | HG01099.hp1 HG02451.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*484G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 484 | chr17 | 67031488 | ||||||
| chr17:67031510 | C | G | 9 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0020 others(6): Show |
22 | HG01243.hp2 HG01346.hp2 HG01884.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*506C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 506 | chr17 | 67031510 | ||||||
| chr17:67031624 | G | C | 12 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(9): Show |
119 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*620G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 620 | chr17 | 67031624 | ||||||
| chr17:67031652 | C | T | 1 | a0001c0001t0040 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 648 | chr17 | 67031652 | ||||||
| chr17:67031821 | C | A | 1 | a0001c0001t0030 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*817C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 817 | chr17 | 67031821 | ||||||
| chr17:67031879 | G | A | 1 | a0001c0001t0010 | 3 | NA18959.hp1 NA18990.hp2 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*875G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 875 | chr17 | 67031879 | ||||||
| chr17:67031969 | C | T | 1 | a0001c0001t0043 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 965 | chr17 | 67031969 | ||||||
| chr17:67032172 | C | T | 1 | a0001c0002t0036 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1168C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1168 | chr17 | 67032172 | ||||||
| chr17:67032178 | G | A | 2 | a0001c0001t0008 a0001c0001t0014 |
8 | HG01069.hp2 HG01071.hp2 HG01106.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1174G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1174 | chr17 | 67032178 | ||||||
| chr17:67032534 | C | T | 2 | a0001c0001t0012 a0001c0001t0035 |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1530C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1530 | chr17 | 67032534 | ||||||
| chr17:67032624 | G | A | 1 | a0001c0001t0031 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1620G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1620 | chr17 | 67032624 | ||||||
| chr17:67032649 | G | A | 1 | a0001c0001t0027 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1645G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1645 | chr17 | 67032649 | ||||||
| chr17:67032683 | C | T | 1 | a0001c0001t0029 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1679 | chr17 | 67032683 | ||||||
| chr17:67032783 | C | T | 1 | a0001c0001t0034 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1779C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1779 | chr17 | 67032783 | ||||||
| chr17:67032936 | C | T | 7 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0019 others(4): Show |
65 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1932C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1932 | chr17 | 67032936 | ||||||
| chr17:67032948 | C | T | 1 | a0001c0001t0016 | 2 | HG02683.hp2 HG03688.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1944C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 1944 | chr17 | 67032948 | ||||||
| chr17:67033062 | C | G | 1 | a0001c0001t0033 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2058C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2058 | chr17 | 67033062 | ||||||
| chr17:67033123 | C | T | 1 | a0001c0001t0032 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2119C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2119 | chr17 | 67033123 | ||||||
| chr17:67033148 | C | T | 2 | a0001c0001t0004 a0001c0001t0009 |
21 | HG00609.hp2 HG01069.hp1 HG01106.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2144C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2144 | chr17 | 67033148 | ||||||
| chr17:67033336 | C | G | 1 | a0001c0001t0028 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2332C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 4/4 | 2332 | chr17 | 67033336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:66965157 | GCC | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0191 a0001c0001t0001g0198 others(40): Show |
45 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.220+29_220+30delCC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965157 | ||||||
| chr17:66965158 | C | CCA | 31 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0134 others(28): Show |
31 | HG00558.hp1 HG01074.hp1 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | ||||||
| chr17:66965158 | C | CCACA | 13 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0162 others(10): Show |
14 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | ||||||
| chr17:66965158 | C | CCACACA | 10 | a0001c0001t0001g0155 a0001c0001t0002g0015 a0001c0001t0002g0016 others(7): Show |
10 | HG00609.hp2 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | ||||||
| chr17:66965158 | C | CCACACAC others(1): Show |
69 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0029 others(66): Show |
72 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | ||||||
| chr17:66965158 | C | CCACACAC others(3): Show |
17 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01433.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.220+28_220+29insAC others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | ||||||
| chr17:66965158 | C | CCACACAC others(5): Show |
2 | a0001c0001t0003g0027 a0001c0001t0012g0095 |
2 | HG02647.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.220+28_220+29insAC others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | ||||||
| chr17:66965158 | CCCCACAC others(3): Show |
C | 5 | a0001c0001t0003g0011 a0001c0001t0003g0330 a0001c0001t0003g0332 others(2): Show |
6 | HG01243.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+29_220+38delCC others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965158 | ||||||
| chr17:66965160 | C | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(175): Show |
185 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(182): Show |
intron_variant | MODIFIER | c.220+29C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965160 | |||||||
| chr17:66965160 | C | CCA | 17 | a0001c0001t0001g0249 a0001c0001t0002g0246 a0001c0001t0003g0250 others(14): Show |
17 | HG00438.hp1 HG00597.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.220+54_220+55dupCA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965160 | ||||||
| chr17:66965160 | C | CCACA | 6 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(3): Show |
6 | HG01099.hp2 HG02027.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+52_220+55dupCA others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965160 | ||||||
| chr17:66965160 | C | CCACACA | 12 | a0001c0001t0002g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+50_220+55dupCA others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965160 | ||||||
| chr17:66965162 | A | C | 2 | a0001c0001t0005g0337 a0001c0001t0011g0338 |
2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+31A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965162 | |||||||
| chr17:66965176 | ACACACAC others(29): Show |
A | 1 | a0001c0001t0003g0014 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.220+56_220+91delTA others(34): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965176 | ||||||
| chr17:66965177 | CACACACA others(5): Show |
C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0003g0163 |
3 | NA19004.hp2 NA19011.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.220+53_220+64delAC others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965177 | ||||||
| chr17:66965180 | ACACACAT others(25): Show |
A | 1 | a0001c0001t0003g0158 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.220+56_220+87delTA others(30): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965180 | ||||||
| chr17:66965184 | ACATATAC others(21): Show |
A | 1 | a0001c0001t0004g0184 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.220+56_220+83delTA others(26): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965184 | ||||||
| chr17:66965185 | C | CACAT | 5 | a0001c0001t0001g0113 a0001c0001t0002g0111 a0001c0001t0002g0112 others(2): Show |
5 | HG02486.hp1 HG02486.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+55_220+56insCA others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965185 | ||||||
| chr17:66965187 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0124 others(118): Show |
126 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.220+56T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965187 | |||||||
| chr17:66965189 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(156): Show |
168 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.220+58T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965189 | |||||||
| chr17:66965191 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.220+60C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965191 | |||||||
| chr17:66965194 | ACG | A | 6 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+81_220+82delGC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965194 | ||||||
| chr17:66965194 | ACGCGCGC others(11): Show |
A | 1 | a0001c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.220+65_220+82delGC others(16): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965194 | ||||||
| chr17:66965196 | G | A | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 |
3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+65G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965196 | |||||||
| chr17:66965197 | C | T | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 |
3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+66C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965197 | |||||||
| chr17:66965198 | G | A | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 |
3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+67G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965198 | |||||||
| chr17:66965200 | G | A | 3 | a0001c0001t0002g0186 a0001c0001t0002g0187 a0001c0001t0002g0188 |
3 | HG00639.hp1 HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.220+69G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965200 | |||||||
| chr17:66965202 | G | A | 4 | a0001c0001t0002g0065 a0001c0001t0002g0186 a0001c0001t0002g0187 others(1): Show |
4 | HG00639.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+71G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965202 | |||||||
| chr17:66965204 | G | A | 4 | a0001c0001t0002g0065 a0001c0001t0002g0186 a0001c0001t0002g0187 others(1): Show |
4 | HG00639.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+73G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965204 | |||||||
| chr17:66965210 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0002g0108 a0001c0001t0002g0111 others(3): Show |
6 | HG02486.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+79G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965210 | |||||||
| chr17:66965212 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0002g0108 a0001c0001t0002g0109 others(5): Show |
8 | HG00609.hp2 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220+81G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965212 | |||||||
| chr17:66965212 | G | GCA | 41 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(38): Show |
42 | HG00544.hp2 HG00621.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.220+93_220+94dupAC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965212 | ||||||
| chr17:66965212 | G | GCGCA | 23 | a0001c0001t0001g0131 a0001c0001t0001g0140 a0001c0001t0001g0145 others(20): Show |
24 | HG00741.hp2 HG01256.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.220+82_220+83insGC others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965212 | ||||||
| chr17:66965212 | G | GCGCGCA | 5 | a0001c0001t0001g0002 a0001c0001t0001g0161 a0001c0001t0001g0224 others(2): Show |
7 | HG02040.hp2 HG03209.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+82_220+83insGC others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66965212 | ||||||
| chr17:66965217 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.220+86C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965217 | |||||||
| chr17:66965222 | A | G | 1 | a0001c0001t0004g0184 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.220+91A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965222 | |||||||
| chr17:66965224 | A | G | 1 | a0001c0001t0004g0184 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.220+93A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965224 | |||||||
| chr17:66965549 | G | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 |
3 | HG02109.hp1 HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.220+418G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965549 | |||||||
| chr17:66965554 | G | T | 2 | a0001c0001t0001g0182 a0001c0001t0003g0183 |
2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.220+423G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965554 | |||||||
| chr17:66965595 | T | C | 5 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+464T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965595 | |||||||
| chr17:66965791 | C | T | 9 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(6): Show |
9 | HG00438.hp1 HG00597.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+660C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965791 | |||||||
| chr17:66965846 | G | T | 1 | a0001c0001t0004g0181 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.220+715G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965846 | |||||||
| chr17:66965850 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.220+719T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66965850 | |||||||
| chr17:66966002 | T | A | 98 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(95): Show |
103 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.220+871T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966002 | |||||||
| chr17:66966066 | T | G | 1 | a0001c0001t0001g0018 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220+935T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966066 | |||||||
| chr17:66966102 | C | G | 1 | a0001c0001t0004g0180 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.220+971C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966102 | |||||||
| chr17:66966108 | C | G | 12 | a0001c0001t0006g0229 a0001c0001t0006g0230 a0001c0001t0006g0231 others(9): Show |
13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+977C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966108 | |||||||
| chr17:66966295 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.220+1164G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966295 | |||||||
| chr17:66966409 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.220+1278T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966409 | |||||||
| chr17:66966414 | G | T | 1 | a0001c0001t0002g0227 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.220+1283G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966414 | |||||||
| chr17:66966438 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.220+1307C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966438 | |||||||
| chr17:66966476 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(66): Show |
73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.220+1345C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966476 | |||||||
| chr17:66966857 | T | A | 2 | a0001c0001t0003g0190 a0001c0002t0002g0189 |
2 | NA18952.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.220+1726T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966857 | |||||||
| chr17:66966876 | T | C | 4 | a0001c0001t0003g0104 a0001c0001t0005g0105 a0001c0001t0011g0107 others(1): Show |
4 | HG01361.hp2 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+1745T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66966876 | |||||||
| chr17:66967046 | C | T | 1 | a0001c0001t0043g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.220+1915C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967046 | |||||||
| chr17:66967311 | A | G | 3 | a0001c0001t0001g0334 a0001c0001t0002g0335 a0001c0002t0002g0336 |
3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+2180A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967311 | |||||||
| chr17:66967342 | T | G | 4 | a0001c0001t0003g0104 a0001c0001t0005g0105 a0001c0001t0011g0107 others(1): Show |
4 | HG01361.hp2 HG02723.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+2211T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967342 | |||||||
| chr17:66967347 | G | A | 14 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0127 others(11): Show |
15 | HG00741.hp2 HG01074.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.220+2216G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967347 | |||||||
| chr17:66967435 | C | T | 69 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(66): Show |
73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.220+2304C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967435 | |||||||
| chr17:66967573 | G | A | 1 | a0001c0001t0001g0008 | 2 | NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.220+2442G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967573 | |||||||
| chr17:66967582 | G | T | 1 | a0001c0001t0003g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.220+2451G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967582 | |||||||
| chr17:66967653 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.220+2522C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967653 | |||||||
| chr17:66967817 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220+2686G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66967817 | |||||||
| chr17:66968007 | C | A | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.220+2876C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968007 | |||||||
| chr17:66968165 | G | A | 12 | a0001c0001t0006g0229 a0001c0001t0006g0230 a0001c0001t0006g0231 others(9): Show |
13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+3034G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968165 | |||||||
| chr17:66968358 | C | T | 1 | a0001c0001t0006g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220+3227C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968358 | |||||||
| chr17:66968359 | G | A | 3 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 |
3 | HG01099.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.220+3228G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968359 | |||||||
| chr17:66968500 | C | G | 4 | a0001c0001t0001g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 others(1): Show |
4 | NA18971.hp1 NA18979.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+3369C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968500 | |||||||
| chr17:66968514 | A | C | 4 | a0001c0001t0001g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 others(1): Show |
4 | NA18971.hp1 NA18979.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+3383A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968514 | |||||||
| chr17:66968517 | C | T | 2 | a0001c0001t0005g0337 a0001c0001t0011g0338 |
2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+3386C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968517 | |||||||
| chr17:66968518 | T | C | 1 | a0001c0001t0003g0122 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.220+3387T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968518 | |||||||
| chr17:66968519 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.220+3388C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968519 | |||||||
| chr17:66968527 | G | C | 4 | a0001c0001t0001g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 others(1): Show |
4 | NA18971.hp1 NA18979.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+3396G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968527 | |||||||
| chr17:66968527 | G | GCCTCCTC others(101): Show |
6 | a0001c0001t0002g0246 a0001c0001t0003g0250 a0001c0001t0003g0252 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+3437_220+3544d others(110): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968527 | ||||||
| chr17:66968527 | GCCTCCTC others(47): Show |
G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG03490.hp1 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.220+3437_220+3490d others(56): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968527 | ||||||
| chr17:66968527 | GCCTCCTC others(74): Show |
G | 1 | a0001c0001t0005g0266 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.220+3437_220+3517d others(83): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968527 | ||||||
| chr17:66968541 | CCCCTCCT others(20): Show |
C | 3 | a0001c0001t0001g0021 a0001c0001t0002g0020 a0001c0001t0013g0255 |
3 | HG01496.hp2 HG02523.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.220+3437_220+3463d others(29): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968541 | ||||||
| chr17:66968550 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220+3419C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968550 | |||||||
| chr17:66968564 | C | T | 1 | a0001c0001t0003g0122 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.220+3433C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968564 | |||||||
| chr17:66968567 | T | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0122 |
2 | HG01257.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.220+3436T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968567 | |||||||
| chr17:66968568 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(163): Show |
176 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.220+3437T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968568 | |||||||
| chr17:66968568 | T | TCCCTCCT others(20): Show |
1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.220+3542_220+3568d others(29): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968568 | ||||||
| chr17:66968568 | TCCCTCCT others(20): Show |
T | 1 | a0001c0001t0003g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.220+3542_220+3568d others(29): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968568 | ||||||
| chr17:66968568 | TCCCTCCT others(47): Show |
T | 1 | a0001c0001t0004g0308 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.220+3515_220+3568d others(56): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968568 | ||||||
| chr17:66968577 | C | T | 1 | a0001c0001t0003g0190 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.220+3446C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968577 | |||||||
| chr17:66968578 | T | C | 1 | a0001c0001t0003g0190 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.220+3447T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968578 | |||||||
| chr17:66968623 | CCCTCCTC others(23): Show |
C | 12 | a0001c0001t0006g0229 a0001c0001t0006g0230 a0001c0001t0006g0231 others(9): Show |
13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+3500_220+3529d others(32): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968623 | ||||||
| chr17:66968650 | CCCT | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(65): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.220+3527_220+3529d others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968650 | ||||||
| chr17:66968808 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.220+3677C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968808 | |||||||
| chr17:66968814 | CCTCTTT | C | 6 | a0001c0001t0002g0246 a0001c0001t0003g0250 a0001c0001t0003g0252 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+3691_220+3696d others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66968814 | ||||||
| chr17:66968910 | T | C | 1 | a0001c0001t0002g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220+3779T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66968910 | |||||||
| chr17:66969338 | C | T | 2 | a0001c0001t0005g0119 a0001c0001t0005g0120 |
2 | HG02976.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.220+4207C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969338 | |||||||
| chr17:66969541 | G | T | 1 | a0001c0001t0004g0333 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.220+4410G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969541 | |||||||
| chr17:66969720 | A | T | 1 | a0001c0001t0003g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.220+4589A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969720 | |||||||
| chr17:66969768 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(231): Show |
244 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(241): Show |
intron_variant | MODIFIER | c.220+4637A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969768 | |||||||
| chr17:66969831 | T | A | 1 | a0001c0002t0002g0135 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.220+4700T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969831 | |||||||
| chr17:66969876 | T | C | 1 | a0001c0001t0011g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.220+4745T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969876 | |||||||
| chr17:66969957 | G | T | 15 | a0001c0001t0003g0104 a0001c0001t0005g0105 a0001c0001t0006g0229 others(12): Show |
16 | HG01109.hp2 HG01361.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.220+4826G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969957 | |||||||
| chr17:66969982 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0005g0118 |
2 | HG03098.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.220+4851C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969982 | |||||||
| chr17:66969985 | G | A | 2 | a0001c0001t0005g0337 a0001c0001t0011g0338 |
2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+4854G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969985 | |||||||
| chr17:66969998 | G | A | 1 | a0001c0001t0011g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.220+4867G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66969998 | |||||||
| chr17:66970088 | C | T | 7 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(4): Show |
7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+4957C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970088 | |||||||
| chr17:66970169 | G | A | 12 | a0001c0001t0006g0229 a0001c0001t0006g0230 a0001c0001t0006g0231 others(9): Show |
13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+5038G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970169 | |||||||
| chr17:66970193 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.220+5062C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970193 | |||||||
| chr17:66970328 | G | A | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | NA18947.hp2 NA18959.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+5197G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970328 | |||||||
| chr17:66970342 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.220+5211T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970342 | |||||||
| chr17:66970416 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG02074.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.220+5285C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970416 | |||||||
| chr17:66970811 | C | T | 1 | a0001c0001t0003g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.220+5680C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970811 | |||||||
| chr17:66970839 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.220+5708T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66970839 | |||||||
| chr17:66971010 | C | A | 1 | a0001c0002t0002g0273 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.220+5879C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971010 | |||||||
| chr17:66971012 | G | C | 12 | a0001c0001t0006g0229 a0001c0001t0006g0230 a0001c0001t0006g0231 others(9): Show |
13 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.220+5881G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971012 | |||||||
| chr17:66971072 | C | A | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG00558.hp1 HG00621.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+5941C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971072 | |||||||
| chr17:66971114 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0274 a0001c0001t0010g0267 |
3 | NA18959.hp1 NA18970.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.220+5983G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971114 | |||||||
| chr17:66971127 | C | T | 1 | a0001c0001t0034g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220+5996C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971127 | |||||||
| chr17:66971160 | C | T | 6 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+6029C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971160 | |||||||
| chr17:66971176 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(84): Show |
92 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.220+6045A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971176 | |||||||
| chr17:66971178 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(84): Show |
92 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.220+6047A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971178 | |||||||
| chr17:66971192 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(72): Show |
80 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.220+6061C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971192 | |||||||
| chr17:66971228 | GGAGGAGG others(22): Show |
G | 12 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
12 | HG00735.hp1 HG02109.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+6157_220+6185d others(31): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66971228 | ||||||
| chr17:66971371 | C | T | 2 | a0001c0001t0005g0105 a0001c0001t0030g0106 |
2 | HG01361.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.220+6240C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971371 | |||||||
| chr17:66971479 | C | G | 12 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+6348C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971479 | |||||||
| chr17:66971906 | T | G | 4 | a0001c0001t0002g0228 a0001c0001t0003g0104 a0001c0001t0005g0105 others(1): Show |
4 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+6775T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971906 | |||||||
| chr17:66971932 | T | C | 30 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(27): Show |
30 | HG00735.hp1 HG01891.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.220+6801T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66971932 | |||||||
| chr17:66972020 | C | G | 4 | a0001c0001t0002g0228 a0001c0001t0003g0104 a0001c0001t0005g0105 others(1): Show |
4 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+6889C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972020 | |||||||
| chr17:66972097 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+6966G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972097 | |||||||
| chr17:66972116 | G | A | 4 | a0001c0001t0002g0228 a0001c0001t0003g0104 a0001c0001t0005g0105 others(1): Show |
4 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+6985G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972116 | |||||||
| chr17:66972194 | G | T | 38 | a0001c0001t0001g0191 a0001c0001t0001g0198 a0001c0001t0001g0200 others(35): Show |
38 | HG00438.hp2 HG00621.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.220+7063G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972194 | |||||||
| chr17:66972226 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.220+7095C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972226 | |||||||
| chr17:66972358 | C | G | 1 | a0001c0001t0002g0221 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.220+7227C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972358 | |||||||
| chr17:66972359 | G | A | 5 | a0001c0001t0002g0278 a0001c0001t0003g0277 a0001c0001t0004g0275 others(2): Show |
5 | HG02602.hp1 HG03490.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+7228G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972359 | |||||||
| chr17:66972517 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.220+7386A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972517 | |||||||
| chr17:66972661 | C | CA | 247 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(244): Show |
257 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(254): Show |
intron_variant | MODIFIER | c.220+7531dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66972661 | ||||||
| chr17:66972734 | T | C | 18 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(15): Show |
18 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.220+7603T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972734 | |||||||
| chr17:66972754 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0124 others(99): Show |
107 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.220+7623C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972754 | |||||||
| chr17:66972831 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(63): Show |
70 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.220+7700C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972831 | |||||||
| chr17:66972885 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0124 others(151): Show |
160 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.220+7754C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972885 | |||||||
| chr17:66972924 | TCAAAAA | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(68): Show |
76 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.220+7810_220+7815d others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66972924 | ||||||
| chr17:66972951 | C | A | 1 | a0001c0001t0003g0101 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.220+7820C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972951 | |||||||
| chr17:66972985 | C | T | 22 | a0001c0001t0001g0018 a0001c0001t0001g0079 a0001c0001t0001g0080 others(19): Show |
22 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+7854C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66972985 | |||||||
| chr17:66973187 | C | T | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG01891.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.220+8056C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973187 | |||||||
| chr17:66973188 | T | G | 155 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(152): Show |
160 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.220+8057T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973188 | |||||||
| chr17:66973197 | G | A | 2 | a0001c0001t0003g0280 a0001c0002t0002g0281 |
2 | NA18970.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.220+8066G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973197 | |||||||
| chr17:66973237 | T | TA | 74 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0126 others(71): Show |
79 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.220+8121dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66973237 | ||||||
| chr17:66973237 | T | TAA | 8 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0003g0014 others(5): Show |
8 | HG01361.hp2 HG02145.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+8120_220+8121d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66973237 | ||||||
| chr17:66973237 | TA | T | 135 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(132): Show |
140 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.220+8121delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66973237 | ||||||
| chr17:66973276 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.220+8145G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973276 | |||||||
| chr17:66973472 | G | A | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+8341G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973472 | |||||||
| chr17:66973514 | G | T | 2 | a0001c0001t0005g0337 a0001c0001t0011g0338 |
2 | HG02717.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.220+8383G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973514 | |||||||
| chr17:66973592 | G | A | 36 | a0001c0001t0001g0191 a0001c0001t0001g0198 a0001c0001t0001g0200 others(33): Show |
36 | HG00438.hp2 HG00621.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.220+8461G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973592 | |||||||
| chr17:66973620 | C | T | 7 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(4): Show |
7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+8489C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973620 | |||||||
| chr17:66973699 | G | A | 167 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(164): Show |
172 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.220+8568G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973699 | |||||||
| chr17:66973749 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.220+8618G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973749 | |||||||
| chr17:66973886 | A | G | 120 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(117): Show |
125 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.220+8755A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973886 | |||||||
| chr17:66973909 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.220+8778C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973909 | |||||||
| chr17:66973993 | A | C | 1 | a0001c0001t0002g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.220+8862A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66973993 | |||||||
| chr17:66974406 | G | A | 1 | a0001c0001t0006g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.220+9275G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974406 | |||||||
| chr17:66974416 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0136 a0001c0001t0001g0137 others(56): Show |
63 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.220+9285G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974416 | |||||||
| chr17:66974595 | G | A | 7 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(4): Show |
7 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+9464G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974595 | |||||||
| chr17:66974707 | C | T | 9 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0240 others(6): Show |
9 | HG01891.hp1 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+9576C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974707 | |||||||
| chr17:66974749 | A | G | 1 | a0001c0001t0043g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.220+9618A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974749 | |||||||
| chr17:66974820 | T | C | 10 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(7): Show |
10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+9689T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66974820 | |||||||
| chr17:66975033 | C | T | 1 | a0001c0003t0003g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.220+9902C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975033 | |||||||
| chr17:66975133 | G | A | 128 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(125): Show |
133 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.220+10002G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975133 | |||||||
| chr17:66975177 | G | T | 11 | a0001c0001t0006g0230 a0001c0001t0006g0231 a0001c0001t0006g0232 others(8): Show |
12 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+10046G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975177 | |||||||
| chr17:66975510 | G | C | 1 | a0001c0001t0028g0099 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.220+10379G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975510 | |||||||
| chr17:66975634 | T | C | 7 | a0001c0001t0003g0011 a0001c0001t0003g0330 a0001c0001t0003g0332 others(4): Show |
8 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+10503T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975634 | |||||||
| chr17:66975766 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220+10635G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975766 | |||||||
| chr17:66975773 | G | C | 4 | a0001c0001t0001g0272 a0001c0001t0003g0285 a0001c0001t0003g0286 others(1): Show |
4 | HG02056.hp1 HG02293.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+10642G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66975773 | |||||||
| chr17:66976038 | T | C | 2 | a0001c0001t0002g0116 a0001c0001t0038g0115 |
2 | HG00735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.220+10907T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976038 | |||||||
| chr17:66976082 | G | A | 12 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+10951G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976082 | |||||||
| chr17:66976116 | C | T | 12 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+10985C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976116 | |||||||
| chr17:66976218 | C | T | 1 | a0001c0001t0003g0014 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.220+11087C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976218 | |||||||
| chr17:66976326 | C | T | 22 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(19): Show |
22 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+11195C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976326 | |||||||
| chr17:66976332 | C | T | 1 | a0001c0001t0008g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.220+11201C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976332 | |||||||
| chr17:66976471 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.220+11340C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976471 | |||||||
| chr17:66976525 | C | T | 3 | a0001c0001t0001g0334 a0001c0001t0002g0335 a0001c0002t0002g0336 |
3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+11394C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976525 | |||||||
| chr17:66976577 | TC | T | 31 | a0001c0001t0002g0108 a0001c0001t0002g0109 a0001c0001t0002g0240 others(28): Show |
31 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.220+11447delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976577 | |||||||
| chr17:66976728 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.220+11597G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976728 | |||||||
| chr17:66976731 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.220+11600G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976731 | |||||||
| chr17:66976843 | T | C | 101 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(98): Show |
106 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.220+11712T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976843 | |||||||
| chr17:66976890 | G | T | 9 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(6): Show |
9 | HG00438.hp1 HG00597.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+11759G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976890 | |||||||
| chr17:66976953 | A | G | 103 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(100): Show |
108 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.220+11822A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66976953 | |||||||
| chr17:66977062 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0136 others(90): Show |
98 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.220+11931C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977062 | |||||||
| chr17:66977256 | C | T | 10 | a0001c0001t0003g0011 a0001c0001t0003g0332 a0001c0001t0012g0094 others(7): Show |
11 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+12125C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977256 | |||||||
| chr17:66977260 | C | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0137 a0001c0001t0001g0138 others(52): Show |
58 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.220+12129C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977260 | |||||||
| chr17:66977439 | G | C | 1 | a0001c0001t0005g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+12308G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977439 | |||||||
| chr17:66977450 | G | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0137 others(88): Show |
96 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.220+12319G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977450 | |||||||
| chr17:66977797 | C | T | 1 | a0001c0001t0011g0338 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220+12666C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977797 | |||||||
| chr17:66977824 | G | A | 12 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+12693G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977824 | |||||||
| chr17:66977861 | T | C | 12 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+12730T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977861 | |||||||
| chr17:66977950 | C | T | 11 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(8): Show |
11 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+12819C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977950 | |||||||
| chr17:66977970 | C | T | 1 | a0001c0001t0002g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220+12839C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66977970 | |||||||
| chr17:66978284 | G | A | 6 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+13153G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978284 | |||||||
| chr17:66978352 | A | G | 1 | a0001c0001t0007g0261 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.220+13221A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978352 | |||||||
| chr17:66978397 | G | A | 3 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0253 |
3 | HG02055.hp2 HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.220+13266G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978397 | |||||||
| chr17:66978415 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0004g0110 |
2 | NA18947.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.220+13284G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978415 | |||||||
| chr17:66978437 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.220+13306G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978437 | |||||||
| chr17:66978636 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0089 others(7): Show |
10 | HG01433.hp2 HG01981.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.220+13505G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978636 | |||||||
| chr17:66978711 | G | A | 4 | a0001c0001t0003g0152 a0001c0002t0002g0151 a0001c0002t0002g0153 others(1): Show |
4 | HG01361.hp1 HG02004.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+13580G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978711 | |||||||
| chr17:66978749 | G | A | 10 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(7): Show |
10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+13618G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978749 | |||||||
| chr17:66978857 | C | T | 11 | a0001c0001t0002g0228 a0001c0001t0002g0326 a0001c0001t0003g0104 others(8): Show |
11 | HG01361.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+13726C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978857 | |||||||
| chr17:66978957 | C | T | 1 | a0001c0001t0011g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.220+13826C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66978957 | |||||||
| chr17:66979010 | C | T | 1 | a0001c0001t0004g0333 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.220+13879C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979010 | |||||||
| chr17:66979050 | G | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0137 others(87): Show |
95 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.220+13919G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979050 | |||||||
| chr17:66979069 | G | GTCT | 120 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0137 others(117): Show |
125 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.220+13943_220+1394 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979069 | ||||||
| chr17:66979167 | C | T | 11 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(8): Show |
11 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+14036C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979167 | |||||||
| chr17:66979227 | C | G | 12 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+14096C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979227 | |||||||
| chr17:66979281 | T | A | 4 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(1): Show |
4 | HG02258.hp2 HG02717.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+14150T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979281 | |||||||
| chr17:66979376 | ACT | A | 87 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(84): Show |
92 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.220+14248_220+1424 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979376 | ||||||
| chr17:66979599 | TCTC | T | 31 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0216 others(28): Show |
31 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.220+14471_220+1447 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979599 | ||||||
| chr17:66979609 | C | T | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(197): Show |
209 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(206): Show |
intron_variant | MODIFIER | c.220+14478C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979609 | |||||||
| chr17:66979613 | C | T | 11 | a0001c0001t0006g0230 a0001c0001t0006g0231 a0001c0001t0006g0232 others(8): Show |
12 | HG01109.hp2 HG01884.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.220+14482C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979613 | |||||||
| chr17:66979632 | G | C | 1 | a0001c0001t0003g0195 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.220+14501G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979632 | |||||||
| chr17:66979745 | C | CT | 110 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(107): Show |
115 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.220+14636dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | ||||||
| chr17:66979745 | C | CTT | 64 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0137 others(61): Show |
67 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.220+14635_220+1463 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | ||||||
| chr17:66979745 | C | CTTT | 6 | a0001c0001t0003g0007 a0001c0001t0003g0177 a0001c0001t0004g0184 others(3): Show |
7 | HG01361.hp1 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+14634_220+1463 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | ||||||
| chr17:66979745 | CT | C | 24 | a0001c0001t0001g0288 a0001c0001t0002g0197 a0001c0001t0002g0221 others(21): Show |
25 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.220+14636delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979745 | ||||||
| chr17:66979749 | TTTTTTTT others(864): Show |
T | 1 | a0001c0002t0002g0281 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.220+14637_220+1550 others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66979749 | ||||||
| chr17:66979829 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.220+14698A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979829 | |||||||
| chr17:66979882 | A | G | 31 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0216 others(28): Show |
31 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.220+14751A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979882 | |||||||
| chr17:66979883 | G | A | 12 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(9): Show |
12 | HG00438.hp1 HG00597.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+14752G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979883 | |||||||
| chr17:66979912 | T | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0111 |
2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.220+14781T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979912 | |||||||
| chr17:66979943 | A | T | 10 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(7): Show |
10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+14812A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66979943 | |||||||
| chr17:66980005 | C | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(74): Show |
81 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.220+14874C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980005 | |||||||
| chr17:66980037 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220+14906A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980037 | |||||||
| chr17:66980110 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.220+14979G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980110 | |||||||
| chr17:66980234 | G | T | 3 | a0001c0001t0002g0228 a0001c0001t0003g0104 a0001c0001t0030g0106 |
3 | HG01361.hp2 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.220+15103G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980234 | |||||||
| chr17:66980285 | C | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0100 a0001c0001t0003g0101 others(4): Show |
7 | HG02083.hp2 HG02165.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+15154C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980285 | |||||||
| chr17:66980415 | T | C | 118 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0137 others(115): Show |
123 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.220+15284T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980415 | |||||||
| chr17:66980416 | G | C | 3 | a0001c0001t0002g0241 a0001c0001t0002g0243 a0001c0001t0008g0242 |
3 | HG02258.hp2 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.220+15285G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980416 | |||||||
| chr17:66980458 | G | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(225): Show |
238 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.220+15327G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980458 | |||||||
| chr17:66980526 | C | A | 1 | a0001c0001t0003g0289 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.220+15395C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980526 | |||||||
| chr17:66980620 | C | CT | 9 | a0001c0001t0001g0134 a0001c0001t0002g0019 a0001c0001t0002g0278 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+15509dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | ||||||
| chr17:66980620 | C | CTTTTT | 18 | a0001c0001t0006g0229 a0001c0001t0007g0256 a0001c0001t0007g0259 others(15): Show |
18 | HG00597.hp2 HG01099.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.220+15505_220+1550 others(9): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | ||||||
| chr17:66980620 | C | CTTTTTT | 17 | a0001c0001t0001g0161 a0001c0001t0001g0175 a0001c0001t0002g0228 others(14): Show |
17 | HG00438.hp1 HG01361.hp2 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.220+15504_220+1550 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | ||||||
| chr17:66980620 | C | CTTTTTTT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(56): Show |
63 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.220+15503_220+1550 others(11): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | ||||||
| chr17:66980620 | C | CTTTTTTT others(1): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0137 others(18): Show |
21 | HG00544.hp2 HG02040.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+15502_220+1550 others(12): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | ||||||
| chr17:66980620 | CT | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(84): Show |
92 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.220+15509delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | ||||||
| chr17:66980620 | CTT | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0185 a0001c0001t0002g0088 others(6): Show |
9 | HG01070.hp1 HG01256.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+15508_220+1550 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66980620 | ||||||
| chr17:66980793 | A | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0137 a0001c0001t0001g0138 others(64): Show |
72 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.220+15662A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980793 | |||||||
| chr17:66980834 | G | T | 1 | a0001c0001t0004g0040 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.220+15703G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980834 | |||||||
| chr17:66980909 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.220+15778G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66980909 | |||||||
| chr17:66981320 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.220+16189T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981320 | |||||||
| chr17:66981717 | C | G | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+16586C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981717 | |||||||
| chr17:66981784 | A | G | 3 | a0001c0001t0002g0228 a0001c0001t0003g0104 a0001c0001t0030g0106 |
3 | HG01361.hp2 HG02145.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.220+16653A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981784 | |||||||
| chr17:66981808 | T | C | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+16677T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981808 | |||||||
| chr17:66981841 | T | A | 1 | a0001c0001t0006g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.220+16710T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981841 | |||||||
| chr17:66981855 | A | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(52): Show |
59 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.220+16724A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981855 | |||||||
| chr17:66981869 | G | C | 1 | a0001c0001t0017g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.220+16738G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981869 | |||||||
| chr17:66981915 | C | G | 7 | a0001c0001t0001g0191 a0001c0001t0001g0209 a0001c0001t0001g0210 others(4): Show |
7 | HG00621.hp2 HG02056.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+16784C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981915 | |||||||
| chr17:66981930 | C | G | 1 | a0001c0002t0002g0317 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.220+16799C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981930 | |||||||
| chr17:66981945 | A | T | 3 | a0001c0001t0001g0087 a0001c0002t0002g0085 a0001c0002t0002g0086 |
3 | HG00544.hp1 NA18945.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.220+16814A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981945 | |||||||
| chr17:66981962 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.220+16831C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66981962 | |||||||
| chr17:66982042 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.220+16911C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982042 | |||||||
| chr17:66982063 | G | A | 43 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0002g0015 others(40): Show |
43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+16932G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982063 | |||||||
| chr17:66982084 | T | C | 1 | a0001c0001t0008g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.220+16953T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982084 | |||||||
| chr17:66982108 | G | A | 1 | a0001c0001t0033g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220+16977G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982108 | |||||||
| chr17:66982109 | G | A | 3 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0003g0289 |
3 | NA18942.hp1 NA19012.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.220+16978G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982109 | |||||||
| chr17:66982119 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(70): Show |
78 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.220+16988G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982119 | |||||||
| chr17:66982146 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.220+17015G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982146 | |||||||
| chr17:66982187 | C | T | 1 | a0001c0001t0006g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.220+17056C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982187 | |||||||
| chr17:66982204 | C | T | 43 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0002g0015 others(40): Show |
43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+17073C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982204 | |||||||
| chr17:66982240 | G | A | 16 | a0001c0001t0001g0032 a0001c0001t0001g0082 a0001c0001t0001g0191 others(13): Show |
16 | HG00621.hp2 HG01255.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.220+17109G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982240 | |||||||
| chr17:66982249 | CTGCTGAT others(17): Show |
C | 6 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+17132_220+1715 others(28): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66982249 | ||||||
| chr17:66982273 | A | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(107): Show |
115 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.220+17142A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982273 | |||||||
| chr17:66982287 | A | C | 2 | a0001c0001t0009g0247 a0001c0001t0009g0248 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.220+17156A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982287 | |||||||
| chr17:66982309 | G | A | 90 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(87): Show |
95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.220+17178G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982309 | |||||||
| chr17:66982339 | C | A | 8 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+17208C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982339 | |||||||
| chr17:66982403 | T | C | 90 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(87): Show |
95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.220+17272T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982403 | |||||||
| chr17:66982409 | A | C | 43 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0002g0015 others(40): Show |
43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+17278A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982409 | |||||||
| chr17:66982422 | G | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0079 others(5): Show |
8 | HG02015.hp2 HG02040.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.220+17291G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982422 | |||||||
| chr17:66982481 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+17350A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982481 | |||||||
| chr17:66982508 | GT | G | 90 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(87): Show |
95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.220+17381delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66982508 | ||||||
| chr17:66982599 | G | A | 43 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0002g0015 others(40): Show |
43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+17468G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982599 | |||||||
| chr17:66982793 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(87): Show |
95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.220+17662C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982793 | |||||||
| chr17:66982817 | A | G | 1 | a0001c0002t0002g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.220+17686A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66982817 | |||||||
| chr17:66983340 | A | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
47 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.220+18209A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983340 | |||||||
| chr17:66983368 | G | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(203): Show |
216 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.220+18237G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983368 | |||||||
| chr17:66983382 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.220+18251A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983382 | |||||||
| chr17:66983702 | G | T | 1 | a0001c0001t0001g0307 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.220+18571G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66983702 | |||||||
| chr17:66984018 | G | A | 1 | a0001c0001t0003g0158 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.220+18887G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984018 | |||||||
| chr17:66984021 | T | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0318 a0001c0001t0003g0122 others(3): Show |
7 | HG01257.hp1 HG01258.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+18890T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984021 | |||||||
| chr17:66984022 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0130 others(4): Show |
7 | HG00741.hp2 HG01074.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+18891G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984022 | |||||||
| chr17:66984162 | A | C | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+19031A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984162 | |||||||
| chr17:66984167 | C | T | 10 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(7): Show |
10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+19036C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984167 | |||||||
| chr17:66984183 | A | AG | 43 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0002g0015 others(40): Show |
43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+19053dupG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66984183 | ||||||
| chr17:66984185 | T | C | 43 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0002g0015 others(40): Show |
43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+19054T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984185 | |||||||
| chr17:66984185 | T | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(161): Show |
174 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.220+19054T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984185 | |||||||
| chr17:66984186 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(161): Show |
174 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.220+19055T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984186 | |||||||
| chr17:66984187 | T | G | 43 | a0001c0001t0001g0113 a0001c0001t0001g0215 a0001c0001t0002g0015 others(40): Show |
43 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.220+19056T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984187 | |||||||
| chr17:66984259 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+19128T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984259 | |||||||
| chr17:66984398 | G | T | 1 | a0001c0001t0016g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.220+19267G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984398 | |||||||
| chr17:66984462 | C | G | 6 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0119 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+19331C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984462 | |||||||
| chr17:66984482 | C | T | 1 | a0001c0001t0005g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.220+19351C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984482 | |||||||
| chr17:66984562 | T | G | 1 | a0001c0001t0002g0335 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.220+19431T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984562 | |||||||
| chr17:66984841 | C | T | 1 | a0001c0002t0002g0004 | 2 | HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.220+19710C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984841 | |||||||
| chr17:66984842 | G | T | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+19711G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984842 | |||||||
| chr17:66984917 | T | C | 1 | a0001c0002t0002g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.220+19786T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984917 | |||||||
| chr17:66984927 | G | A | 2 | a0001c0003t0003g0045 a0001c0003t0003g0046 |
2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.220+19796G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66984927 | |||||||
| chr17:66985069 | G | A | 1 | a0001c0001t0015g0290 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.220+19938G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985069 | |||||||
| chr17:66985099 | C | T | 1 | a0001c0001t0003g0321 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.220+19968C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985099 | |||||||
| chr17:66985231 | T | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0089 others(15): Show |
18 | HG01433.hp2 HG01981.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.220+20100T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985231 | |||||||
| chr17:66985249 | C | G | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+20118C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985249 | |||||||
| chr17:66985256 | C | T | 10 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(7): Show |
10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+20125C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985256 | |||||||
| chr17:66985374 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+20243A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985374 | |||||||
| chr17:66985400 | A | G | 11 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0186 others(8): Show |
13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.220+20269A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985400 | |||||||
| chr17:66985580 | T | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(204): Show |
217 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.220+20449T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985580 | |||||||
| chr17:66985607 | T | C | 5 | a0001c0001t0002g0160 a0001c0001t0003g0007 a0001c0001t0003g0159 others(2): Show |
6 | HG01515.hp2 HG01517.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+20476T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985607 | |||||||
| chr17:66985610 | A | G | 12 | a0001c0001t0001g0307 a0001c0001t0001g0327 a0001c0001t0001g0328 others(9): Show |
12 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.220+20479A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985610 | |||||||
| chr17:66985642 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220+20511A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985642 | |||||||
| chr17:66985672 | C | T | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+20541C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985672 | |||||||
| chr17:66985739 | G | A | 1 | a0001c0001t0004g0275 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.220+20608G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985739 | |||||||
| chr17:66985863 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.220+20732G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985863 | |||||||
| chr17:66985943 | GA | G | 44 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
47 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.220+20822delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66985943 | ||||||
| chr17:66985951 | AAAG | A | 10 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(7): Show |
10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+20842_220+2084 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66985951 | ||||||
| chr17:66985974 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(205): Show |
218 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.220+20843A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985974 | |||||||
| chr17:66985994 | G | A | 1 | a0001c0001t0002g0020 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.220+20863G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66985994 | |||||||
| chr17:66986021 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+20890T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986021 | |||||||
| chr17:66986022 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+20891C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986022 | |||||||
| chr17:66986024 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+20893G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986024 | |||||||
| chr17:66986506 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.220+21375G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986506 | |||||||
| chr17:66986614 | C | A | 2 | a0001c0001t0002g0116 a0001c0001t0038g0115 |
2 | HG00735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.220+21483C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986614 | |||||||
| chr17:66986976 | C | A | 11 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(8): Show |
11 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+21845C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66986976 | |||||||
| chr17:66987157 | A | G | 10 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(7): Show |
10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+22026A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987157 | |||||||
| chr17:66987278 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+22147C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987278 | |||||||
| chr17:66987294 | A | G | 3 | a0001c0001t0001g0334 a0001c0001t0002g0335 a0001c0002t0002g0336 |
3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+22163A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987294 | |||||||
| chr17:66987417 | C | A | 35 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(32): Show |
36 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.220+22286C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987417 | |||||||
| chr17:66987524 | G | C | 3 | a0001c0001t0001g0319 a0001c0001t0004g0320 a0001c0001t0005g0118 |
3 | HG01069.hp1 HG01167.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.220+22393G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987524 | |||||||
| chr17:66987541 | A | G | 1 | a0001c0001t0039g0066 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.220+22410A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987541 | |||||||
| chr17:66987692 | A | G | 16 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+22561A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987692 | |||||||
| chr17:66987814 | G | A | 5 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+22683G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987814 | |||||||
| chr17:66987906 | G | A | 1 | a0001c0001t0010g0147 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.220+22775G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66987906 | |||||||
| chr17:66988029 | T | A | 5 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0011g0107 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+22898T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988029 | |||||||
| chr17:66988033 | TTTTG | T | 9 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0017g0090 others(6): Show |
9 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+22904_220+2290 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988033 | ||||||
| chr17:66988035 | T | G | 2 | a0001c0001t0002g0219 a0001c0001t0008g0001 |
3 | HG01069.hp2 HG01071.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.220+22904T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988035 | |||||||
| chr17:66988035 | T | TTG | 5 | a0001c0001t0001g0078 a0001c0001t0002g0077 a0001c0001t0003g0195 others(2): Show |
5 | HG01123.hp2 HG01515.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+22922_220+2292 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988035 | ||||||
| chr17:66988051 | GTGTA | G | 25 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(22): Show |
26 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.220+22922_220+2292 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988051 | ||||||
| chr17:66988055 | A | G | 277 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(274): Show |
287 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(284): Show |
intron_variant | MODIFIER | c.220+22924A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988055 | |||||||
| chr17:66988066 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220+22935T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988066 | |||||||
| chr17:66988066 | T | G | 2 | a0001c0001t0006g0229 a0001c0001t0011g0338 |
2 | HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.220+22935T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988066 | |||||||
| chr17:66988125 | A | G | 21 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(18): Show |
21 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+22994A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988125 | |||||||
| chr17:66988331 | T | C | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+23200T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988331 | |||||||
| chr17:66988361 | C | T | 5 | a0001c0001t0003g0330 a0001c0001t0005g0105 a0001c0001t0005g0337 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+23230C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988361 | |||||||
| chr17:66988365 | G | A | 21 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(18): Show |
21 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+23234G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988365 | |||||||
| chr17:66988399 | G | A | 11 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(8): Show |
11 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+23268G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988399 | |||||||
| chr17:66988417 | A | T | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+23286A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988417 | |||||||
| chr17:66988497 | C | T | 4 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+23366C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988497 | |||||||
| chr17:66988561 | G | A | 4 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+23430G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988561 | |||||||
| chr17:66988583 | G | A | 21 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(18): Show |
21 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.220+23452G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988583 | |||||||
| chr17:66988752 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(107): Show |
115 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.220+23621C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988752 | |||||||
| chr17:66988760 | G | A | 1 | a0001c0001t0001g0307 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.220+23629G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988760 | |||||||
| chr17:66988785 | G | A | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+23654G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988785 | |||||||
| chr17:66988819 | G | A | 1 | a0001c0001t0031g0291 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.220+23688G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66988819 | |||||||
| chr17:66988904 | CAAAA | C | 4 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+23777_220+2378 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66988904 | ||||||
| chr17:66989011 | AGATCATG others(936): Show |
A | 16 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+23883_220+2482 others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989011 | ||||||
| chr17:66989016 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(91): Show |
99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.220+23885A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989016 | |||||||
| chr17:66989044 | G | A | 10 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(7): Show |
10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+23913G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989044 | |||||||
| chr17:66989053 | T | A | 1 | a0001c0002t0002g0004 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.220+23922T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989053 | |||||||
| chr17:66989060 | C | CA | 119 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0018 others(116): Show |
123 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.220+23950dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989060 | ||||||
| chr17:66989060 | C | CAA | 25 | a0001c0001t0001g0005 a0001c0001t0003g0102 a0001c0001t0006g0230 others(22): Show |
26 | HG00438.hp1 HG01099.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.220+23949_220+2395 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989060 | ||||||
| chr17:66989060 | CA | C | 7 | a0001c0001t0001g0169 a0001c0001t0001g0307 a0001c0001t0003g0321 others(4): Show |
7 | HG01517.hp1 HG02818.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+23950delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66989060 | ||||||
| chr17:66989084 | C | T | 1 | a0001c0001t0005g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+23953C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989084 | |||||||
| chr17:66989186 | A | G | 8 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0240 others(5): Show |
8 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.220+24055A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989186 | |||||||
| chr17:66989209 | C | G | 11 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(8): Show |
11 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.220+24078C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989209 | |||||||
| chr17:66989318 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(91): Show |
99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.220+24187T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989318 | |||||||
| chr17:66989453 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(91): Show |
99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.220+24322A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989453 | |||||||
| chr17:66989526 | G | A | 46 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(43): Show |
49 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.220+24395G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989526 | |||||||
| chr17:66989617 | G | A | 14 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(11): Show |
15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+24486G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989617 | |||||||
| chr17:66989647 | C | T | 14 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(11): Show |
15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+24516C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989647 | |||||||
| chr17:66989660 | C | A | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+24529C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989660 | |||||||
| chr17:66989771 | G | A | 7 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0001g0078 others(4): Show |
7 | HG01123.hp2 HG01515.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+24640G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989771 | |||||||
| chr17:66989792 | C | A | 3 | a0001c0001t0017g0090 a0001c0001t0017g0092 a0001c0001t0041g0091 |
3 | HG02451.hp1 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.220+24661C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989792 | |||||||
| chr17:66989793 | G | A | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+24662G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989793 | |||||||
| chr17:66989815 | G | A | 1 | a0001c0001t0011g0338 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220+24684G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989815 | |||||||
| chr17:66989891 | T | C | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+24760T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989891 | |||||||
| chr17:66989958 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220+24827C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66989958 | |||||||
| chr17:66990129 | T | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(107): Show |
115 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.220+24998T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990129 | |||||||
| chr17:66990199 | G | T | 6 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+25068G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990199 | |||||||
| chr17:66990313 | C | T | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25182C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990313 | |||||||
| chr17:66990425 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.220+25294C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990425 | |||||||
| chr17:66990449 | T | G | 18 | a0001c0001t0001g0032 a0001c0001t0001g0080 a0001c0001t0001g0081 others(15): Show |
18 | HG00408.hp1 HG00621.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.220+25318T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990449 | |||||||
| chr17:66990460 | A | G | 3 | a0001c0001t0001g0334 a0001c0001t0002g0335 a0001c0002t0002g0336 |
3 | HG00140.hp2 HG01175.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.220+25329A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990460 | |||||||
| chr17:66990546 | C | T | 1 | a0001c0002t0002g0063 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.220+25415C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990546 | |||||||
| chr17:66990639 | TAA | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(3): Show |
6 | HG00741.hp2 HG01074.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+25509_220+2551 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990639 | |||||||
| chr17:66990647 | C | CTTATT | 20 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0097 others(17): Show |
20 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.220+25553_220+2555 others(9): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | ||||||
| chr17:66990647 | C | CTTATTTT others(3): Show |
35 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(32): Show |
37 | HG00621.hp1 HG00733.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.220+25548_220+2555 others(14): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | ||||||
| chr17:66990647 | C | CTTATTTT others(8): Show |
8 | a0001c0001t0001g0161 a0001c0001t0002g0160 a0001c0001t0002g0227 others(5): Show |
9 | HG01069.hp1 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+25543_220+2555 others(19): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | ||||||
| chr17:66990647 | CTTATT | C | 13 | a0001c0001t0001g0198 a0001c0001t0001g0215 a0001c0001t0002g0047 others(10): Show |
14 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.220+25553_220+2555 others(9): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | ||||||
| chr17:66990647 | CTTATTTT others(3): Show |
C | 1 | a0001c0001t0002g0293 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.220+25548_220+2555 others(14): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990647 | ||||||
| chr17:66990660 | ATTTTATT others(14): Show |
A | 6 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+25533_220+2555 others(25): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990660 | ||||||
| chr17:66990665 | ATTTTATT others(9): Show |
A | 10 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(7): Show |
10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.220+25538_220+2555 others(20): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990665 | ||||||
| chr17:66990675 | ATTTTAT | A | 4 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+25548_220+2555 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990675 | ||||||
| chr17:66990681 | T | TTTTA | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25562_220+2556 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990681 | ||||||
| chr17:66990685 | A | ATTTTATT others(4): Show |
5 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+25557_220+2555 others(15): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66990685 | ||||||
| chr17:66990704 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0003g0195 |
2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.220+25573G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990704 | |||||||
| chr17:66990810 | A | G | 14 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(11): Show |
15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+25679A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990810 | |||||||
| chr17:66990839 | C | A | 6 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+25708C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990839 | |||||||
| chr17:66990870 | C | T | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25739C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990870 | |||||||
| chr17:66990896 | G | C | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.220+25765G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66990896 | |||||||
| chr17:66991076 | T | A | 2 | a0001c0001t0001g0182 a0001c0001t0003g0183 |
2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.220+25945T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991076 | |||||||
| chr17:66991078 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0003g0183 |
2 | NA18967.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.220+25947G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991078 | |||||||
| chr17:66991337 | C | A | 1 | a0001c0001t0001g0018 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220+26206C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991337 | |||||||
| chr17:66991337 | C | CA | 54 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(51): Show |
58 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.220+26215dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66991337 | ||||||
| chr17:66991344 | A | C | 1 | a0001c0001t0001g0062 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.220+26213A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991344 | |||||||
| chr17:66991353 | C | T | 8 | a0001c0001t0003g0011 a0001c0001t0003g0330 a0001c0001t0003g0332 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.220+26222C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991353 | |||||||
| chr17:66991445 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.220+26314A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991445 | |||||||
| chr17:66991465 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0011g0107 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+26334G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991465 | |||||||
| chr17:66991553 | G | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(54): Show |
61 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.220+26422G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991553 | |||||||
| chr17:66991592 | A | G | 16 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.220+26461A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991592 | |||||||
| chr17:66991608 | G | T | 1 | a0001c0001t0011g0338 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220+26477G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991608 | |||||||
| chr17:66991716 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.221-26473A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991716 | |||||||
| chr17:66991946 | T | A | 14 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(11): Show |
15 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.221-26243T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991946 | |||||||
| chr17:66991946 | T | C | 1 | a0001c0001t0003g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.221-26243T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66991946 | |||||||
| chr17:66992086 | C | T | 6 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-26103C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992086 | |||||||
| chr17:66992160 | T | TG | 22 | a0001c0001t0001g0072 a0001c0001t0001g0126 a0001c0001t0001g0127 others(19): Show |
23 | HG00597.hp1 HG00741.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.221-26017dupG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66992160 | ||||||
| chr17:66992160 | TG | T | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(180): Show |
193 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.221-26017delG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66992160 | ||||||
| chr17:66992160 | TGG | T | 18 | a0001c0001t0001g0021 a0001c0001t0001g0113 a0001c0001t0002g0015 others(15): Show |
18 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.221-26018_221-2601 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66992160 | ||||||
| chr17:66992164 | G | T | 1 | a0001c0001t0008g0306 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.221-26025G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992164 | |||||||
| chr17:66992166 | G | C | 14 | a0001c0001t0002g0047 a0001c0001t0002g0111 a0001c0001t0006g0229 others(11): Show |
14 | HG02451.hp1 HG02486.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-26023G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992166 | |||||||
| chr17:66992166 | G | T | 9 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0240 others(6): Show |
9 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-26023G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992166 | |||||||
| chr17:66992167 | G | T | 12 | a0001c0001t0001g0215 a0001c0001t0002g0015 a0001c0001t0002g0016 others(9): Show |
12 | HG02109.hp1 HG02258.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-26022G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992167 | |||||||
| chr17:66992265 | A | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(259): Show |
272 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.221-25924A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992265 | |||||||
| chr17:66992282 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0003g0220 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.221-25907C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992282 | |||||||
| chr17:66992302 | G | A | 3 | a0001c0005t0002g0148 a0001c0005t0002g0150 a0001c0005t0005g0149 |
3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.221-25887G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992302 | |||||||
| chr17:66992392 | C | A | 1 | a0001c0001t0001g0008 | 2 | NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.221-25797C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992392 | |||||||
| chr17:66992590 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(207): Show |
220 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(217): Show |
intron_variant | MODIFIER | c.221-25599T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992590 | |||||||
| chr17:66992794 | T | A | 8 | a0001c0001t0003g0011 a0001c0001t0003g0330 a0001c0001t0003g0332 others(5): Show |
9 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-25395T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992794 | |||||||
| chr17:66992806 | C | T | 16 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(13): Show |
17 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.221-25383C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992806 | |||||||
| chr17:66992819 | G | A | 5 | a0001c0001t0001g0185 a0001c0001t0001g0269 a0001c0001t0004g0110 others(2): Show |
5 | NA18944.hp2 NA18947.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-25370G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992819 | |||||||
| chr17:66992894 | G | C | 2 | a0001c0001t0001g0043 a0001c0001t0003g0178 |
2 | HG02300.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.221-25295G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992894 | |||||||
| chr17:66992919 | G | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(108): Show |
116 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.221-25270G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992919 | |||||||
| chr17:66992944 | T | C | 1 | a0001c0001t0004g0295 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.221-25245T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992944 | |||||||
| chr17:66992960 | C | A | 10 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(7): Show |
10 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-25229C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66992960 | |||||||
| chr17:66993019 | T | C | 1 | a0001c0002t0002g0284 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.221-25170T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993019 | |||||||
| chr17:66993089 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(108): Show |
116 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.221-25100T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993089 | |||||||
| chr17:66993111 | GC | G | 12 | a0001c0001t0001g0215 a0001c0001t0002g0108 a0001c0001t0002g0228 others(9): Show |
12 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.221-25077delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993111 | |||||||
| chr17:66993213 | G | T | 6 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-24976G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993213 | |||||||
| chr17:66993256 | G | A | 6 | a0001c0001t0002g0326 a0001c0001t0003g0325 a0001c0001t0005g0266 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-24933G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993256 | |||||||
| chr17:66993436 | A | G | 16 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(13): Show |
16 | HG00735.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-24753A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993436 | |||||||
| chr17:66993534 | C | G | 5 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0011g0107 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-24655C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993534 | |||||||
| chr17:66993535 | C | G | 1 | a0001c0001t0011g0338 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.221-24654C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993535 | |||||||
| chr17:66993560 | G | A | 2 | a0001c0001t0001g0032 a0001c0002t0022g0026 |
2 | HG02132.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.221-24629G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993560 | |||||||
| chr17:66993567 | AC | A | 3 | a0001c0001t0001g0272 a0001c0001t0003g0285 a0001c0001t0003g0286 |
3 | HG02056.hp1 HG02293.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.221-24619delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66993567 | ||||||
| chr17:66993583 | G | C | 1 | a0001c0001t0002g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-24606G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993583 | |||||||
| chr17:66993669 | G | T | 2 | a0001c0001t0001g0029 a0001c0003t0003g0028 |
2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.221-24520G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993669 | |||||||
| chr17:66993706 | A | G | 10 | a0001c0001t0006g0230 a0001c0001t0006g0232 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-24483A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993706 | |||||||
| chr17:66993854 | C | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(3): Show |
7 | HG00639.hp2 HG00733.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-24335C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993854 | |||||||
| chr17:66993967 | T | A | 6 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-24222T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66993967 | |||||||
| chr17:66994020 | TA | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0030 others(16): Show |
21 | HG01109.hp1 HG01433.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.221-24156delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994020 | ||||||
| chr17:66994020 | TAA | T | 106 | a0001c0001t0001g0113 a0001c0001t0001g0138 a0001c0001t0001g0139 others(103): Show |
109 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.221-24157_221-2415 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994020 | ||||||
| chr17:66994031 | A | C | 4 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-24158A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994031 | |||||||
| chr17:66994049 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(92): Show |
99 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.221-24140C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994049 | |||||||
| chr17:66994059 | G | A | 7 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(4): Show |
7 | HG00438.hp1 HG00597.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-24130G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994059 | |||||||
| chr17:66994091 | G | C | 1 | a0001c0001t0003g0102 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.221-24098G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994091 | |||||||
| chr17:66994103 | A | G | 4 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-24086A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994103 | |||||||
| chr17:66994327 | C | A | 1 | a0001c0001t0003g0214 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.221-23862C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994327 | |||||||
| chr17:66994327 | C | CA | 96 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(93): Show |
101 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.221-23844dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994327 | ||||||
| chr17:66994327 | C | CAA | 18 | a0001c0001t0001g0182 a0001c0001t0001g0213 a0001c0001t0002g0022 others(15): Show |
18 | HG00438.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.221-23845_221-2384 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66994327 | ||||||
| chr17:66994339 | A | AC | 14 | a0001c0001t0002g0228 a0001c0001t0003g0104 a0001c0001t0003g0163 others(11): Show |
14 | HG01361.hp2 HG02145.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-23850_221-2384 others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994339 | |||||||
| chr17:66994339 | A | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(88): Show |
96 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.221-23850A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994339 | |||||||
| chr17:66994795 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0011g0107 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-23394G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994795 | |||||||
| chr17:66994808 | G | C | 1 | a0001c0001t0006g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.221-23381G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994808 | |||||||
| chr17:66994834 | G | C | 1 | a0001c0001t0006g0232 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.221-23355G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994834 | |||||||
| chr17:66994874 | G | C | 3 | a0001c0001t0001g0274 a0001c0001t0004g0296 a0001c0001t0004g0308 |
3 | NA19012.hp1 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.221-23315G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994874 | |||||||
| chr17:66994945 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(195): Show |
207 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.221-23244T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994945 | |||||||
| chr17:66994960 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.221-23229G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994960 | |||||||
| chr17:66994962 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.221-23227G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66994962 | |||||||
| chr17:66995006 | G | A | 1 | a0001c0002t0002g0063 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.221-23183G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995006 | |||||||
| chr17:66995038 | G | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(49): Show |
56 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.221-23151G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995038 | |||||||
| chr17:66995112 | A | C | 1 | a0001c0001t0011g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.221-23077A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995112 | |||||||
| chr17:66995143 | G | A | 1 | a0001c0001t0011g0338 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.221-23046G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995143 | |||||||
| chr17:66995146 | C | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(113): Show |
121 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.221-23043C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995146 | |||||||
| chr17:66995421 | T | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(114): Show |
122 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.221-22768T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995421 | |||||||
| chr17:66995456 | C | A | 12 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(9): Show |
13 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-22733C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995456 | |||||||
| chr17:66995493 | G | A | 8 | a0001c0001t0002g0228 a0001c0001t0002g0240 a0001c0001t0002g0241 others(5): Show |
8 | HG01361.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-22696G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995493 | |||||||
| chr17:66995586 | T | C | 1 | a0001c0001t0010g0267 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.221-22603T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995586 | |||||||
| chr17:66995618 | A | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(195): Show |
208 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.221-22571A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995618 | |||||||
| chr17:66995669 | G | A | 2 | a0001c0001t0003g0314 a0001c0002t0002g0309 |
2 | HG01981.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.221-22520G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995669 | |||||||
| chr17:66995850 | G | GA | 57 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(54): Show |
58 | HG00735.hp1 HG01099.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.221-22330dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66995850 | ||||||
| chr17:66995871 | G | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(112): Show |
120 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-22318G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66995871 | |||||||
| chr17:66996087 | G | C | 12 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(9): Show |
13 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-22102G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996087 | |||||||
| chr17:66996172 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.221-22017C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996172 | |||||||
| chr17:66996253 | A | AT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(112): Show |
120 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-21927dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996253 | ||||||
| chr17:66996275 | C | T | 10 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(7): Show |
10 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-21914C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996275 | |||||||
| chr17:66996327 | T | C | 1 | a0001c0001t0002g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-21862T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996327 | |||||||
| chr17:66996379 | C | CT | 14 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0089 others(11): Show |
14 | HG00597.hp2 HG01433.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-21791dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | ||||||
| chr17:66996379 | CT | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0076 a0001c0001t0001g0078 others(6): Show |
9 | HG01123.hp2 HG01515.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-21791delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | ||||||
| chr17:66996379 | CTTT | C | 20 | a0001c0001t0002g0227 a0001c0001t0003g0330 a0001c0001t0003g0332 others(17): Show |
21 | HG01099.hp2 HG01167.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.221-21793_221-2179 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | ||||||
| chr17:66996379 | CTTTT | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(92): Show |
99 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.221-21794_221-2179 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66996379 | ||||||
| chr17:66996398 | T | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(45): Show |
51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-21791T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996398 | |||||||
| chr17:66996411 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(70): Show |
77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.221-21778G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996411 | |||||||
| chr17:66996536 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG02083.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.221-21653C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996536 | |||||||
| chr17:66996587 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.221-21602G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996587 | |||||||
| chr17:66996835 | A | G | 117 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(114): Show |
122 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.221-21354A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996835 | |||||||
| chr17:66996896 | C | T | 1 | a0001c0001t0006g0239 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-21293C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996896 | |||||||
| chr17:66996943 | A | G | 1 | a0001c0001t0006g0238 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.221-21246A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996943 | |||||||
| chr17:66996953 | C | T | 3 | a0001c0001t0001g0087 a0001c0002t0002g0085 a0001c0002t0002g0086 |
3 | HG00544.hp1 NA18945.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.221-21236C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66996953 | |||||||
| chr17:66997245 | AG | A | 6 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(3): Show |
6 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-20940delG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66997245 | ||||||
| chr17:66997339 | C | A | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-20850C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997339 | |||||||
| chr17:66997390 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(116): Show |
125 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.221-20799T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997390 | |||||||
| chr17:66997471 | A | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0221 |
2 | HG01346.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.221-20718A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997471 | |||||||
| chr17:66997474 | T | A | 9 | a0001c0001t0009g0247 a0001c0001t0009g0248 a0001c0001t0013g0244 others(6): Show |
10 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-20715T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997474 | |||||||
| chr17:66997583 | G | A | 1 | a0001c0001t0027g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.221-20606G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997583 | |||||||
| chr17:66997646 | A | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(106): Show |
114 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.221-20543A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997646 | |||||||
| chr17:66997807 | G | T | 7 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0130 others(4): Show |
7 | HG00741.hp2 HG01074.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-20382G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66997807 | |||||||
| chr17:66997817 | AAAAC | A | 11 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0186 others(8): Show |
13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-20352_221-2034 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66997817 | ||||||
| chr17:66998023 | G | A | 13 | a0001c0001t0002g0227 a0001c0001t0003g0330 a0001c0001t0005g0118 others(10): Show |
14 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-20166G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998023 | |||||||
| chr17:66998079 | A | G | 2 | a0001c0001t0007g0260 a0001c0001t0007g0261 |
2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.221-20110A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998079 | |||||||
| chr17:66998248 | A | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(67): Show |
73 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.221-19941A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998248 | |||||||
| chr17:66998258 | T | C | 11 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(8): Show |
11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-19931T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998258 | |||||||
| chr17:66998316 | G | A | 10 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(7): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-19873G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998316 | |||||||
| chr17:66998482 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.221-19707C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998482 | |||||||
| chr17:66998483 | G | A | 13 | a0001c0001t0002g0227 a0001c0001t0003g0330 a0001c0001t0005g0118 others(10): Show |
14 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-19706G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998483 | |||||||
| chr17:66998607 | G | A | 1 | a0001c0001t0005g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-19582G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66998607 | |||||||
| chr17:66999043 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.221-19146G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999043 | |||||||
| chr17:66999092 | G | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(66): Show |
72 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.221-19097G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999092 | |||||||
| chr17:66999183 | T | A | 13 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0089 others(10): Show |
13 | HG01433.hp1 HG01433.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-19006T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999183 | |||||||
| chr17:66999273 | A | AGTT | 11 | a0001c0001t0002g0025 a0001c0001t0002g0065 a0001c0001t0002g0186 others(8): Show |
13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-18914_221-1891 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66999273 | ||||||
| chr17:66999275 | T | TTGG | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(148): Show |
159 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.221-18891_221-1888 others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66999275 | ||||||
| chr17:66999275 | T | TTGGTGG | 21 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-18894_221-1888 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 66999275 | ||||||
| chr17:66999278 | G | T | 1 | a0001c0001t0038g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.221-18911G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999278 | |||||||
| chr17:66999281 | G | T | 1 | a0001c0001t0038g0115 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.221-18908G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999281 | |||||||
| chr17:66999339 | A | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(47): Show |
53 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.221-18850A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999339 | |||||||
| chr17:66999346 | C | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(96): Show |
104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18843C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999346 | |||||||
| chr17:66999368 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(96): Show |
104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18821G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999368 | |||||||
| chr17:66999454 | G | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(47): Show |
53 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.221-18735G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999454 | |||||||
| chr17:66999476 | T | G | 1 | a0001c0001t0005g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-18713T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999476 | |||||||
| chr17:66999519 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(115): Show |
124 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.221-18670A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999519 | |||||||
| chr17:66999653 | G | A | 99 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(96): Show |
104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18536G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999653 | |||||||
| chr17:66999726 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(96): Show |
104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18463C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999726 | |||||||
| chr17:66999753 | AC | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0265 a0001c0001t0001g0303 others(9): Show |
12 | HG00738.hp1 HG01346.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.221-18435delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999753 | |||||||
| chr17:66999784 | G | A | 10 | a0001c0001t0002g0246 a0001c0001t0003g0250 a0001c0001t0003g0252 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-18405G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999784 | |||||||
| chr17:66999805 | A | G | 1 | a0001c0003t0003g0028 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.221-18384A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999805 | |||||||
| chr17:66999891 | G | A | 1 | a0001c0001t0002g0326 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.221-18298G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999891 | |||||||
| chr17:66999933 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.221-18256G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999933 | |||||||
| chr17:66999943 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(46): Show |
52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-18246C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 66999943 | |||||||
| chr17:67000040 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0003g0178 |
2 | HG02300.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.221-18149G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000040 | |||||||
| chr17:67000105 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(96): Show |
104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-18084A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000105 | |||||||
| chr17:67000172 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.221-18017C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000172 | |||||||
| chr17:67000414 | GT | G | 7 | a0001c0001t0001g0210 a0001c0001t0002g0033 a0001c0001t0002g0240 others(4): Show |
7 | HG02071.hp1 HG02258.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-17763delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67000414 | ||||||
| chr17:67000415 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.221-17774T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000415 | |||||||
| chr17:67000416 | T | TG | 94 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(91): Show |
99 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.221-17773_221-1777 others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000416 | |||||||
| chr17:67000417 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.221-17772T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000417 | |||||||
| chr17:67000544 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.221-17645G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000544 | |||||||
| chr17:67000546 | G | A | 1 | a0001c0001t0005g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.221-17643G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000546 | |||||||
| chr17:67000591 | G | A | 1 | a0001c0001t0007g0256 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.221-17598G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000591 | |||||||
| chr17:67000592 | A | C | 1 | a0001c0001t0007g0256 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.221-17597A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000592 | |||||||
| chr17:67000598 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.221-17591C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000598 | |||||||
| chr17:67000599 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(46): Show |
52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-17590G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000599 | |||||||
| chr17:67000883 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0024 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.221-17306C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000883 | |||||||
| chr17:67000903 | A | G | 10 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(7): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-17286A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67000903 | |||||||
| chr17:67001105 | C | T | 4 | a0001c0001t0002g0227 a0001c0001t0011g0107 a0001c0001t0011g0338 others(1): Show |
4 | HG01358.hp2 HG02717.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-17084C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001105 | |||||||
| chr17:67001122 | T | C | 21 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-17067T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001122 | |||||||
| chr17:67001161 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.221-17028C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001161 | |||||||
| chr17:67001289 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0126 |
2 | HG01358.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.221-16900A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001289 | |||||||
| chr17:67001308 | A | G | 70 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(67): Show |
75 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.221-16881A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001308 | |||||||
| chr17:67001373 | C | G | 2 | a0001c0001t0003g0285 a0001c0001t0003g0286 |
2 | HG02293.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.221-16816C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001373 | |||||||
| chr17:67001420 | G | A | 1 | a0001c0002t0002g0172 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.221-16769G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001420 | |||||||
| chr17:67001703 | C | T | 1 | a0001c0002t0002g0336 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.221-16486C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001703 | |||||||
| chr17:67001708 | A | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0034 others(2): Show |
6 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-16481A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001708 | |||||||
| chr17:67001757 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.221-16432G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001757 | |||||||
| chr17:67001844 | G | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(111): Show |
120 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-16345G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001844 | |||||||
| chr17:67001959 | G | A | 1 | a0001c0001t0005g0266 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.221-16230G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001959 | |||||||
| chr17:67001977 | C | T | 21 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-16212C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67001977 | |||||||
| chr17:67002030 | G | GGTATGAA | 15 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(12): Show |
16 | HG00438.hp1 HG00597.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-16159_221-1615 others(11): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002030 | |||||||
| chr17:67002031 | A | T | 15 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(12): Show |
16 | HG00438.hp1 HG00597.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-16158A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002031 | |||||||
| chr17:67002032 | C | A | 15 | a0001c0001t0007g0256 a0001c0001t0007g0257 a0001c0001t0007g0259 others(12): Show |
16 | HG00438.hp1 HG00597.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.221-16157C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002032 | |||||||
| chr17:67002137 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0005g0192 |
2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.221-16052C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002137 | |||||||
| chr17:67002143 | T | C | 2 | a0001c0001t0002g0193 a0001c0001t0005g0192 |
2 | HG01257.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.221-16046T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002143 | |||||||
| chr17:67002198 | C | T | 1 | a0001c0005t0002g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.221-15991C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002198 | |||||||
| chr17:67002212 | A | T | 1 | a0001c0001t0007g0256 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.221-15977A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002212 | |||||||
| chr17:67002264 | C | G | 10 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(7): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-15925C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002264 | |||||||
| chr17:67002384 | C | T | 18 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(15): Show |
19 | HG01243.hp2 HG01891.hp2 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.221-15805C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002384 | |||||||
| chr17:67002393 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(96): Show |
104 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.221-15796A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002393 | |||||||
| chr17:67002567 | C | A | 1 | a0001c0001t0002g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.221-15622C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002567 | |||||||
| chr17:67002618 | T | TTC | 18 | a0001c0001t0001g0171 a0001c0001t0002g0015 a0001c0001t0002g0016 others(15): Show |
19 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.221-15544_221-1554 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTC | 62 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(59): Show |
64 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.221-15546_221-1554 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTCTC | 12 | a0001c0001t0001g0185 a0001c0001t0001g0208 a0001c0001t0001g0288 others(9): Show |
13 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.221-15548_221-1554 others(10): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTCTCT others(7): Show |
3 | a0001c0002t0002g0053 a0001c0003t0003g0045 a0001c0003t0003g0046 |
3 | HG03710.hp2 HG04204.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.221-15556_221-1554 others(18): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTCTCT others(9): Show |
3 | a0001c0001t0007g0257 a0001c0002t0007g0258 a0001c0003t0002g0006 |
4 | HG01256.hp1 HG01258.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-15558_221-1554 others(20): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTCTCT others(11): Show |
3 | a0001c0001t0007g0259 a0001c0001t0007g0260 a0001c0003t0001g0132 |
3 | HG00438.hp1 HG03704.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.221-15560_221-1554 others(22): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTCTCT others(13): Show |
2 | a0001c0001t0007g0256 a0001c0003t0003g0028 |
2 | HG02602.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.221-15562_221-1554 others(24): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTCTCT others(15): Show |
3 | a0001c0001t0009g0245 a0001c0002t0002g0063 a0001c0003t0018g0262 |
3 | HG02027.hp1 HG03654.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.221-15564_221-1554 others(26): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | T | TTCTCTCT others(17): Show |
1 | a0001c0001t0007g0261 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.221-15566_221-1554 others(28): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | TTC | T | 22 | a0001c0001t0001g0113 a0001c0001t0001g0138 a0001c0001t0001g0211 others(19): Show |
23 | HG00621.hp1 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.221-15544_221-1554 others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002618 | TTCTC | T | 5 | a0001c0001t0002g0241 a0001c0001t0002g0243 a0001c0001t0008g0242 others(2): Show |
5 | HG01099.hp2 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-15546_221-1554 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002618 | ||||||
| chr17:67002638 | C | CTCTG | 3 | a0001c0001t0008g0001 a0001c0001t0010g0051 a0001c0001t0039g0066 |
5 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-15548_221-1554 others(8): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67002638 | ||||||
| chr17:67002869 | C | A | 10 | a0001c0001t0002g0227 a0001c0001t0002g0228 a0001c0001t0002g0240 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-15320C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002869 | |||||||
| chr17:67002887 | T | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(94): Show |
102 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.221-15302T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67002887 | |||||||
| chr17:67003002 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(46): Show |
52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-15187G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003002 | |||||||
| chr17:67003011 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(46): Show |
52 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-15178G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003011 | |||||||
| chr17:67003085 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0003g0277 a0001c0001t0004g0275 |
3 | HG02602.hp1 HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.221-15104G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003085 | |||||||
| chr17:67003149 | C | A | 11 | a0001c0001t0003g0330 a0001c0001t0005g0118 a0001c0001t0006g0230 others(8): Show |
12 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.221-15040C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003149 | |||||||
| chr17:67003410 | G | C | 1 | a0001c0001t0004g0070 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.221-14779G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003410 | |||||||
| chr17:67003582 | A | AT | 5 | a0001c0001t0002g0160 a0001c0001t0003g0159 a0001c0001t0003g0325 others(2): Show |
5 | HG02109.hp2 HG02809.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-14604dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67003582 | ||||||
| chr17:67003745 | T | C | 5 | a0001c0003t0001g0132 a0001c0003t0002g0006 a0001c0003t0003g0028 others(2): Show |
6 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-14444T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003745 | |||||||
| chr17:67003754 | C | A | 1 | a0001c0001t0001g0146 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.221-14435C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67003754 | |||||||
| chr17:67004058 | G | A | 2 | a0001c0001t0004g0295 a0001c0001t0016g0297 |
2 | HG02683.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.221-14131G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004058 | |||||||
| chr17:67004103 | C | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(109): Show |
117 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.221-14086C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004103 | |||||||
| chr17:67004277 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(109): Show |
117 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.221-13912G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004277 | |||||||
| chr17:67004280 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.221-13909G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004280 | |||||||
| chr17:67004347 | C | T | 1 | a0001c0003t0003g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.221-13842C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004347 | |||||||
| chr17:67004358 | A | G | 8 | a0001c0001t0006g0229 a0001c0001t0012g0094 a0001c0001t0012g0095 others(5): Show |
8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-13831A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004358 | |||||||
| chr17:67004490 | G | A | 1 | a0001c0001t0008g0306 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.221-13699G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004490 | |||||||
| chr17:67004550 | C | T | 8 | a0001c0001t0006g0229 a0001c0001t0012g0094 a0001c0001t0012g0095 others(5): Show |
8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-13639C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004550 | |||||||
| chr17:67004699 | C | T | 5 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-13490C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004699 | |||||||
| chr17:67004773 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.221-13416G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004773 | |||||||
| chr17:67004812 | T | C | 21 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(18): Show |
21 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-13377T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67004812 | |||||||
| chr17:67005151 | A | G | 9 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0119 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-13038A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005151 | |||||||
| chr17:67005169 | A | G | 71 | a0001c0001t0001g0113 a0001c0001t0002g0015 a0001c0001t0002g0016 others(68): Show |
74 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-13020A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005169 | |||||||
| chr17:67005466 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(43): Show |
48 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.221-12723C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005466 | |||||||
| chr17:67005543 | C | G | 1 | a0001c0001t0030g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.221-12646C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005543 | |||||||
| chr17:67005685 | G | A | 6 | a0001c0001t0003g0011 a0001c0001t0003g0332 a0001c0001t0005g0105 others(3): Show |
7 | HG01243.hp2 HG01891.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-12504G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005685 | |||||||
| chr17:67005795 | G | A | 1 | a0001c0001t0006g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.221-12394G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005795 | |||||||
| chr17:67005887 | C | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0146 a0001c0002t0022g0026 |
3 | HG02132.hp2 NA18994.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.221-12302C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005887 | |||||||
| chr17:67005917 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.221-12272A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005917 | |||||||
| chr17:67005991 | T | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(81): Show |
89 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.221-12198T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67005991 | |||||||
| chr17:67006104 | G | C | 1 | a0001c0001t0003g0027 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.221-12085G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006104 | |||||||
| chr17:67006133 | A | G | 11 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(8): Show |
11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-12056A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006133 | |||||||
| chr17:67006250 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0002g0287 |
2 | HG01167.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.221-11939C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006250 | |||||||
| chr17:67006312 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.221-11877C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006312 | |||||||
| chr17:67006316 | G | A | 11 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(8): Show |
11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-11873G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006316 | |||||||
| chr17:67006533 | C | T | 6 | a0001c0003t0001g0132 a0001c0003t0002g0006 a0001c0003t0003g0028 others(3): Show |
7 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-11656C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006533 | |||||||
| chr17:67006690 | C | T | 2 | a0001c0001t0002g0227 a0001c0001t0011g0107 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.221-11499C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006690 | |||||||
| chr17:67006843 | G | T | 10 | a0001c0001t0005g0118 a0001c0001t0006g0230 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-11346G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006843 | |||||||
| chr17:67006844 | C | T | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-11345C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67006844 | |||||||
| chr17:67007090 | G | A | 2 | a0001c0001t0001g0298 a0001c0001t0003g0321 |
2 | HG02015.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.221-11099G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007090 | |||||||
| chr17:67007119 | G | A | 3 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | NA18970.hp1 NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.221-11070G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007119 | |||||||
| chr17:67007179 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.221-11010C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007179 | |||||||
| chr17:67007202 | A | T | 4 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0002g0075 others(1): Show |
4 | HG01123.hp2 HG01515.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-10987A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007202 | |||||||
| chr17:67007284 | G | T | 11 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(8): Show |
11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-10905G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007284 | |||||||
| chr17:67007407 | G | C | 9 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0119 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-10782G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007407 | |||||||
| chr17:67007497 | T | C | 1 | a0001c0002t0002g0083 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.221-10692T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007497 | |||||||
| chr17:67007885 | T | C | 1 | a0001c0001t0007g0257 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.221-10304T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007885 | |||||||
| chr17:67007967 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(190): Show |
204 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.221-10222T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67007967 | |||||||
| chr17:67008166 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(70): Show |
77 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.221-10023C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008166 | |||||||
| chr17:67008194 | C | G | 1 | a0001c0001t0001g0288 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.221-9995C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008194 | |||||||
| chr17:67008271 | C | T | 1 | a0001c0001t0003g0314 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.221-9918C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008271 | |||||||
| chr17:67008285 | T | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(79): Show |
88 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.221-9904T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008285 | |||||||
| chr17:67008399 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(67): Show |
74 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-9790G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008399 | |||||||
| chr17:67008547 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0003g0178 |
2 | HG02300.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.221-9642C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008547 | |||||||
| chr17:67008590 | C | T | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-9599C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008590 | |||||||
| chr17:67008617 | A | G | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.221-9572A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008617 | |||||||
| chr17:67008821 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.221-9368T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008821 | |||||||
| chr17:67008822 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.221-9367G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008822 | |||||||
| chr17:67008823 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.221-9366C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008823 | |||||||
| chr17:67008890 | A | C | 2 | a0001c0001t0008g0001 a0001c0001t0039g0066 |
4 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-9299A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008890 | |||||||
| chr17:67008904 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(69): Show |
76 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.221-9285G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008904 | |||||||
| chr17:67008904 | G | C | 80 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(77): Show |
86 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.221-9285G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008904 | |||||||
| chr17:67008912 | T | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(69): Show |
76 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.221-9277T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008912 | |||||||
| chr17:67008941 | CCT | C | 9 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0119 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-9247_221-9246d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67008941 | |||||||
| chr17:67009042 | A | T | 1 | a0001c0001t0003g0285 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.221-9147A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009042 | |||||||
| chr17:67009058 | A | T | 5 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-9131A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009058 | |||||||
| chr17:67009200 | T | C | 5 | a0001c0003t0001g0132 a0001c0003t0002g0006 a0001c0003t0003g0028 others(2): Show |
6 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-8989T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009200 | |||||||
| chr17:67009365 | CCT | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(67): Show |
74 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.221-8821_221-8820d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67009365 | ||||||
| chr17:67009388 | G | T | 10 | a0001c0001t0005g0118 a0001c0001t0006g0230 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-8801G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009388 | |||||||
| chr17:67009500 | A | AGCT | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8688_221-8687i others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67009500 | ||||||
| chr17:67009503 | G | GCC | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8686_221-8685i others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009503 | |||||||
| chr17:67009505 | A | T | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8684A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009505 | |||||||
| chr17:67009508 | T | A | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8681T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009508 | |||||||
| chr17:67009509 | C | A | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-8680C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009509 | |||||||
| chr17:67009580 | G | A | 1 | a0001c0001t0005g0119 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221-8609G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009580 | |||||||
| chr17:67009643 | T | G | 2 | a0001c0001t0002g0112 a0001c0001t0034g0117 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.221-8546T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009643 | |||||||
| chr17:67009719 | T | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(92): Show |
102 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.221-8470T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009719 | |||||||
| chr17:67009730 | C | T | 6 | a0001c0003t0001g0132 a0001c0003t0002g0006 a0001c0003t0003g0028 others(3): Show |
7 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.221-8459C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009730 | |||||||
| chr17:67009853 | C | CA | 9 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0119 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-8335dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67009853 | ||||||
| chr17:67009922 | C | T | 6 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(3): Show |
6 | HG01099.hp1 HG02258.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-8267C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009922 | |||||||
| chr17:67009923 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(58): Show |
64 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.221-8266G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67009923 | |||||||
| chr17:67010104 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.221-8085G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010104 | |||||||
| chr17:67010202 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.221-7987G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010202 | |||||||
| chr17:67010339 | A | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0191 |
3 | HG02083.hp1 HG02155.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.221-7850A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010339 | |||||||
| chr17:67010452 | T | C | 9 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0119 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-7737T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010452 | |||||||
| chr17:67010549 | A | C | 4 | a0001c0001t0001g0318 a0001c0001t0003g0152 a0001c0002t0002g0151 others(1): Show |
4 | HG01361.hp1 HG01952.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-7640A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010549 | |||||||
| chr17:67010623 | CT | C | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0004g0296 others(1): Show |
4 | HG00597.hp1 NA19067.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-7563delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67010623 | ||||||
| chr17:67010852 | G | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(74): Show |
82 | HG00438.hp2 HG00609.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.221-7337G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010852 | |||||||
| chr17:67010939 | C | T | 1 | a0001c0001t0007g0261 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.221-7250C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010939 | |||||||
| chr17:67010972 | G | A | 10 | a0001c0001t0005g0118 a0001c0001t0006g0230 a0001c0001t0006g0234 others(7): Show |
11 | HG01884.hp2 HG02622.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-7217G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010972 | |||||||
| chr17:67010985 | C | G | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-7204C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67010985 | |||||||
| chr17:67011311 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0015g0290 a0001c0001t0015g0299 |
3 | HG00741.hp1 HG01168.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.221-6878T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011311 | |||||||
| chr17:67011468 | A | C | 1 | a0001c0001t0002g0061 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.221-6721A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011468 | |||||||
| chr17:67011509 | C | T | 14 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(11): Show |
14 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-6680C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011509 | |||||||
| chr17:67011624 | G | GGAAT | 8 | a0001c0001t0001g0036 a0001c0001t0002g0056 a0001c0001t0002g0057 others(5): Show |
8 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-6538_221-6535d others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67011624 | ||||||
| chr17:67011624 | GGAAT | G | 4 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0002c0004t0001g0324 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-6538_221-6535d others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67011624 | ||||||
| chr17:67011651 | ATGAG | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(77): Show |
86 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.221-6533_221-6530d others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67011651 | ||||||
| chr17:67011655 | G | A | 17 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0119 others(14): Show |
17 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.221-6534G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011655 | |||||||
| chr17:67011687 | G | A | 4 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-6502G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011687 | |||||||
| chr17:67011818 | T | C | 1 | a0001c0001t0003g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.221-6371T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011818 | |||||||
| chr17:67011856 | T | C | 4 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-6333T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67011856 | |||||||
| chr17:67012107 | T | C | 5 | a0001c0001t0013g0255 a0001c0001t0016g0044 a0001c0002t0002g0004 others(2): Show |
6 | HG01496.hp2 HG01934.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-6082T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67012107 | |||||||
| chr17:67012544 | A | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(190): Show |
204 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.221-5645A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67012544 | |||||||
| chr17:67012932 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.221-5257C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67012932 | |||||||
| chr17:67013219 | T | C | 8 | a0001c0001t0006g0229 a0001c0001t0012g0094 a0001c0001t0012g0095 others(5): Show |
8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4970T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013219 | |||||||
| chr17:67013245 | G | A | 8 | a0001c0001t0006g0229 a0001c0001t0012g0094 a0001c0001t0012g0095 others(5): Show |
8 | HG02451.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-4944G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013245 | |||||||
| chr17:67013326 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.221-4863C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013326 | |||||||
| chr17:67013433 | A | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0100 a0001c0001t0001g0136 others(6): Show |
9 | HG00558.hp1 HG02083.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.221-4756A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013433 | |||||||
| chr17:67013435 | T | G | 70 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(67): Show |
74 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.221-4754T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013435 | |||||||
| chr17:67013669 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0034g0117 |
3 | HG02486.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.221-4520G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013669 | |||||||
| chr17:67013769 | C | T | 7 | a0001c0001t0002g0228 a0001c0001t0002g0240 a0001c0001t0002g0241 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-4420C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013769 | |||||||
| chr17:67013803 | C | CA | 130 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(127): Show |
137 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.221-4374dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67013803 | ||||||
| chr17:67013881 | C | T | 14 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(11): Show |
15 | HG00735.hp1 HG01256.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.221-4308C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013881 | |||||||
| chr17:67013883 | A | G | 13 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0118 others(10): Show |
14 | HG01884.hp2 HG02055.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-4306A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013883 | |||||||
| chr17:67013964 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.221-4225T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013964 | |||||||
| chr17:67013976 | G | A | 2 | a0001c0001t0002g0228 a0001c0001t0006g0232 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.221-4213G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013976 | |||||||
| chr17:67013999 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.221-4190G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67013999 | |||||||
| chr17:67014281 | C | A | 3 | a0001c0001t0002g0326 a0001c0001t0005g0266 a0001c0001t0005g0322 |
3 | HG01884.hp1 HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.221-3908C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014281 | |||||||
| chr17:67014327 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0113 a0001c0001t0001g0138 others(116): Show |
127 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.221-3862G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014327 | |||||||
| chr17:67014328 | C | T | 1 | a0001c0001t0005g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.221-3861C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014328 | |||||||
| chr17:67014571 | T | C | 27 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(24): Show |
29 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.221-3618T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014571 | |||||||
| chr17:67014631 | T | A | 1 | a0001c0001t0001g0029 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.221-3558T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014631 | |||||||
| chr17:67014643 | T | TA | 27 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(24): Show |
29 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.221-3539dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014643 | ||||||
| chr17:67014701 | C | T | 1 | a0001c0001t0011g0194 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.221-3488C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014701 | |||||||
| chr17:67014915 | C | T | 9 | a0001c0001t0002g0227 a0001c0001t0005g0119 a0001c0001t0005g0120 others(6): Show |
9 | HG02258.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-3274C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014915 | |||||||
| chr17:67014943 | C | CA | 40 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(37): Show |
43 | HG00639.hp1 HG00735.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.221-3230dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014943 | ||||||
| chr17:67014943 | C | CAA | 26 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(23): Show |
28 | HG00408.hp2 HG01243.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.221-3231_221-3230d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014943 | ||||||
| chr17:67014956 | A | AAG | 6 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0254 others(3): Show |
6 | HG02258.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-3232_221-3231i others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67014956 | ||||||
| chr17:67014956 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(45): Show |
51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-3233A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67014956 | |||||||
| chr17:67015092 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(45): Show |
51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-3097C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015092 | |||||||
| chr17:67015358 | C | G | 3 | a0001c0001t0002g0227 a0001c0001t0011g0107 a0001c0001t0011g0338 |
3 | HG02717.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.221-2831C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015358 | |||||||
| chr17:67015378 | G | A | 5 | a0001c0001t0002g0108 a0001c0001t0003g0330 a0001c0001t0008g0283 others(2): Show |
5 | HG02723.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-2811G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015378 | |||||||
| chr17:67015382 | A | G | 3 | a0001c0001t0002g0227 a0001c0001t0011g0107 a0001c0001t0011g0338 |
3 | HG02717.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.221-2807A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015382 | |||||||
| chr17:67015628 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.221-2561C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015628 | |||||||
| chr17:67015658 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(54): Show |
60 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.221-2531A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015658 | |||||||
| chr17:67015717 | G | C | 3 | a0001c0005t0002g0148 a0001c0005t0002g0150 a0001c0005t0005g0149 |
3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.221-2472G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015717 | |||||||
| chr17:67015992 | C | T | 1 | a0001c0001t0005g0253 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.221-2197C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67015992 | |||||||
| chr17:67016009 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(98): Show |
105 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.221-2180T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016009 | |||||||
| chr17:67016065 | C | T | 6 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0254 others(3): Show |
6 | HG02258.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-2124C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016065 | |||||||
| chr17:67016066 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(192): Show |
206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.221-2123A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016066 | |||||||
| chr17:67016121 | T | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(90): Show |
99 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.221-2068T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016121 | |||||||
| chr17:67016238 | A | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(46): Show |
52 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.221-1951A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016238 | |||||||
| chr17:67016328 | C | T | 1 | a0001c0002t0002g0048 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.221-1861C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016328 | |||||||
| chr17:67016339 | C | T | 14 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0254 others(11): Show |
14 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.221-1850C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016339 | |||||||
| chr17:67016384 | G | A | 1 | a0001c0001t0011g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.221-1805G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016384 | |||||||
| chr17:67016457 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(36): Show |
41 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.221-1732G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016457 | |||||||
| chr17:67016587 | T | C | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-1602T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016587 | |||||||
| chr17:67016646 | G | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(183): Show |
196 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.221-1543G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016646 | |||||||
| chr17:67016654 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0029g0059 |
3 | NA19004.hp1 NA19080.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.221-1535T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016654 | |||||||
| chr17:67016882 | G | A | 11 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(8): Show |
11 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-1307G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016882 | |||||||
| chr17:67016936 | G | T | 15 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0254 others(12): Show |
15 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.221-1253G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67016936 | |||||||
| chr17:67017088 | T | G | 9 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(6): Show |
9 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.221-1101T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017088 | |||||||
| chr17:67017091 | TTTTGAGA others(435): Show |
T | 1 | a0001c0001t0003g0178 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.221-1087_221-646de others(1): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017091 | ||||||
| chr17:67017139 | T | C | 3 | a0001c0001t0002g0326 a0001c0001t0005g0266 a0001c0001t0005g0322 |
3 | HG01884.hp1 HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.221-1050T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017139 | |||||||
| chr17:67017170 | A | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(210): Show |
224 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.221-1019A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017170 | |||||||
| chr17:67017296 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-893C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017296 | |||||||
| chr17:67017329 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(192): Show |
206 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.221-860A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017329 | |||||||
| chr17:67017498 | C | A | 5 | a0001c0001t0001g0058 a0001c0001t0002g0056 a0001c0001t0002g0057 others(2): Show |
5 | HG00140.hp1 HG00738.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-691C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017498 | |||||||
| chr17:67017498 | C | CGTT | 93 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(90): Show |
99 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.221-666_221-664dup others(3): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017498 | ||||||
| chr17:67017498 | C | CGTTGTT | 4 | a0001c0001t0001g0141 a0001c0003t0001g0055 a0001c0003t0003g0226 others(1): Show |
4 | HG00408.hp2 HG02015.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-669_221-664dup others(6): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017498 | ||||||
| chr17:67017527 | GTTGTTGT | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(46): Show |
52 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.221-658_221-652del others(7): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017527 | ||||||
| chr17:67017549 | T | C | 21 | a0001c0001t0002g0227 a0001c0001t0005g0119 a0001c0001t0005g0120 others(18): Show |
21 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-640T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017549 | |||||||
| chr17:67017565 | TG | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(45): Show |
51 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.221-622delG | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr17 | 67017565 | ||||||
| chr17:67017566 | G | A | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-623G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017566 | |||||||
| chr17:67017567 | G | A | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-622G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017567 | |||||||
| chr17:67017578 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-611C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017578 | |||||||
| chr17:67017580 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-609C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017580 | |||||||
| chr17:67017586 | T | C | 9 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0003g0011 others(6): Show |
10 | HG01243.hp2 HG01891.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-603T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017586 | |||||||
| chr17:67017611 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(76): Show |
83 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.221-578G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017611 | |||||||
| chr17:67017728 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.221-461G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017728 | |||||||
| chr17:67017768 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0146 |
2 | HG02132.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.221-421G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017768 | |||||||
| chr17:67017782 | C | T | 1 | a0001c0002t0002g0053 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.221-407C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017782 | |||||||
| chr17:67017869 | G | A | 145 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(142): Show |
153 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.221-320G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67017869 | |||||||
| chr17:67018085 | A | G | 1 | a0001c0001t0002g0088 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.221-104A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018085 | |||||||
| chr17:67018089 | C | A | 1 | a0001c0001t0033g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.221-100C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018089 | |||||||
| chr17:67018107 | C | G | 1 | a0001c0001t0010g0051 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.221-82C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018107 | |||||||
| chr17:67018138 | G | T | 3 | a0001c0001t0001g0113 a0001c0001t0002g0112 a0001c0001t0034g0117 |
3 | HG02486.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.221-51G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 1/3 | chr17 | 67018138 | |||||||
| chr17:67018333 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0003g0332 |
3 | HG03516.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.304+61G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018333 | |||||||
| chr17:67018399 | T | C | 11 | a0001c0001t0002g0065 a0001c0001t0002g0186 a0001c0001t0002g0187 others(8): Show |
13 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.304+127T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018399 | |||||||
| chr17:67018476 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.304+204G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018476 | |||||||
| chr17:67018725 | A | C | 5 | a0001c0001t0002g0240 a0001c0001t0002g0241 a0001c0001t0002g0243 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+453A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018725 | |||||||
| chr17:67018817 | T | C | 3 | a0001c0005t0002g0148 a0001c0005t0002g0150 a0001c0005t0005g0149 |
3 | HG02922.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.304+545T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018817 | |||||||
| chr17:67018821 | G | T | 12 | a0001c0001t0003g0250 a0001c0001t0003g0252 a0001c0001t0005g0118 others(9): Show |
13 | HG01884.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.304+549G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018821 | |||||||
| chr17:67018853 | A | G | 45 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
48 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.304+581A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018853 | |||||||
| chr17:67018853 | A | T | 1 | a0001c0001t0032g0304 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.304+581A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018853 | |||||||
| chr17:67018857 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.304+585G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018857 | |||||||
| chr17:67018890 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0124 |
3 | HG01981.hp2 NA18971.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.304+618A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67018890 | |||||||
| chr17:67019199 | G | A | 3 | a0001c0001t0002g0326 a0001c0001t0005g0266 a0001c0001t0005g0322 |
3 | HG01884.hp1 HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.304+927G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019199 | |||||||
| chr17:67019234 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0007g0259 |
2 | NA18966.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.304+962A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019234 | |||||||
| chr17:67019272 | C | G | 5 | a0001c0001t0001g0029 a0001c0001t0002g0019 a0001c0001t0002g0022 others(2): Show |
5 | HG03490.hp1 HG03492.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+1000C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019272 | |||||||
| chr17:67019465 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0138 a0001c0001t0001g0139 others(39): Show |
44 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.304+1193C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019465 | |||||||
| chr17:67019878 | C | G | 1 | a0001c0003t0003g0046 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.304+1606C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67019878 | |||||||
| chr17:67020017 | G | A | 6 | a0001c0003t0001g0132 a0001c0003t0002g0006 a0001c0003t0003g0028 others(3): Show |
7 | HG01256.hp1 HG01258.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+1745G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020017 | |||||||
| chr17:67020123 | G | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0137 a0001c0001t0001g0294 others(4): Show |
7 | HG00408.hp2 HG00609.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+1851G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020123 | |||||||
| chr17:67020143 | C | CAATGCCA others(6): Show |
1 | a0001c0001t0001g0062 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.304+1872_304+1884d others(15): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67020143 | ||||||
| chr17:67020153 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.304+1881C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020153 | |||||||
| chr17:67020160 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.304+1888C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020160 | |||||||
| chr17:67020192 | C | A | 9 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(6): Show |
9 | HG00735.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.304+1920C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020192 | |||||||
| chr17:67020429 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.304+2157C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020429 | |||||||
| chr17:67020498 | C | T | 9 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0254 others(6): Show |
9 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.304+2226C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020498 | |||||||
| chr17:67020564 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.304+2292C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020564 | |||||||
| chr17:67020567 | A | G | 92 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0021 others(89): Show |
98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.304+2295A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020567 | |||||||
| chr17:67020729 | A | G | 11 | a0001c0001t0002g0025 a0001c0001t0002g0047 a0001c0001t0002g0216 others(8): Show |
11 | HG02145.hp2 HG02258.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.304+2457A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67020729 | |||||||
| chr17:67021052 | T | C | 4 | a0001c0001t0001g0097 a0001c0001t0009g0247 a0001c0001t0009g0248 others(1): Show |
4 | HG01099.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2780T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021052 | |||||||
| chr17:67021124 | C | T | 1 | a0001c0001t0012g0095 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.304+2852C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021124 | |||||||
| chr17:67021156 | G | A | 2 | a0001c0001t0002g0112 a0001c0001t0034g0117 |
2 | HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.304+2884G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021156 | |||||||
| chr17:67021160 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.304+2888C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021160 | |||||||
| chr17:67021191 | A | T | 1 | a0001c0003t0003g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.304+2919A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021191 | |||||||
| chr17:67021200 | T | TA | 9 | a0001c0001t0003g0129 a0001c0001t0003g0310 a0001c0001t0003g0311 others(6): Show |
9 | HG00558.hp2 HG01934.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.304+2943dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67021200 | ||||||
| chr17:67021200 | TA | T | 28 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0078 others(25): Show |
29 | HG01069.hp1 HG01070.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.304+2943delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67021200 | ||||||
| chr17:67021301 | G | A | 5 | a0001c0001t0003g0011 a0001c0001t0003g0332 a0001c0001t0005g0105 others(2): Show |
6 | HG01243.hp2 HG03130.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+3029G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021301 | |||||||
| chr17:67021339 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.304+3067T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021339 | |||||||
| chr17:67021367 | T | C | 10 | a0001c0001t0001g0030 a0001c0001t0001g0089 a0001c0001t0002g0022 others(7): Show |
10 | HG01433.hp1 HG01433.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.304+3095T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021367 | |||||||
| chr17:67021385 | G | A | 1 | a0001c0001t0005g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.304+3113G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021385 | |||||||
| chr17:67021391 | G | A | 9 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(6): Show |
9 | HG01257.hp1 HG01258.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.304+3119G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021391 | |||||||
| chr17:67021468 | C | G | 3 | a0002c0004t0001g0324 a0002c0004t0002g0331 a0002c0004t0003g0323 |
3 | HG02055.hp1 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.304+3196C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021468 | |||||||
| chr17:67021500 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.304+3228G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021500 | |||||||
| chr17:67021517 | T | C | 12 | a0001c0001t0002g0246 a0001c0001t0003g0250 a0001c0001t0003g0252 others(9): Show |
13 | HG01884.hp2 HG02055.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.304+3245T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021517 | |||||||
| chr17:67021811 | C | G | 19 | a0001c0001t0002g0112 a0001c0001t0002g0241 a0001c0001t0002g0243 others(16): Show |
20 | HG02258.hp2 HG02451.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.305-3049C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021811 | |||||||
| chr17:67021916 | G | A | 1 | a0001c0001t0002g0219 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305-2944G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021916 | |||||||
| chr17:67021933 | G | A | 2 | a0001c0001t0003g0321 a0001c0001t0004g0060 |
2 | NA18959.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.305-2927G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021933 | |||||||
| chr17:67021957 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.305-2903A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67021957 | |||||||
| chr17:67022076 | C | CT | 41 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0002g0047 others(38): Show |
42 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.305-2767dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67022076 | ||||||
| chr17:67022076 | C | CTT | 80 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0021 others(77): Show |
84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.305-2768_305-2767d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67022076 | ||||||
| chr17:67022099 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.305-2761G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022099 | |||||||
| chr17:67022137 | G | A | 21 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0001g0155 others(18): Show |
21 | HG00544.hp2 HG01891.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.305-2723G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022137 | |||||||
| chr17:67022168 | G | A | 8 | a0001c0001t0002g0228 a0001c0001t0005g0143 a0001c0001t0005g0144 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-2692G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022168 | |||||||
| chr17:67022279 | T | C | 6 | a0001c0001t0005g0120 a0001c0001t0011g0338 a0001c0001t0035g0114 others(3): Show |
6 | HG02717.hp2 HG02922.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-2581T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022279 | |||||||
| chr17:67022327 | G | A | 1 | a0001c0001t0002g0278 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.305-2533G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022327 | |||||||
| chr17:67022598 | A | T | 3 | a0002c0004t0001g0324 a0002c0004t0002g0331 a0002c0004t0003g0323 |
3 | HG02055.hp1 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.305-2262A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022598 | |||||||
| chr17:67022652 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0216 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.305-2208C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022652 | |||||||
| chr17:67022691 | C | T | 2 | a0001c0001t0003g0011 a0001c0001t0003g0332 |
3 | HG03516.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.305-2169C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022691 | |||||||
| chr17:67022747 | C | T | 1 | a0001c0001t0034g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.305-2113C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022747 | |||||||
| chr17:67022810 | T | C | 146 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0021 others(143): Show |
151 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.305-2050T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022810 | |||||||
| chr17:67022825 | C | T | 84 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0021 others(81): Show |
88 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.305-2035C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67022825 | |||||||
| chr17:67023007 | G | A | 2 | a0001c0003t0003g0028 a0001c0003t0018g0262 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.305-1853G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023007 | |||||||
| chr17:67023099 | C | T | 8 | a0001c0001t0002g0228 a0001c0001t0005g0143 a0001c0001t0005g0144 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-1761C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023099 | |||||||
| chr17:67023143 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0003g0142 a0001c0001t0003g0316 others(2): Show |
5 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-1717C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023143 | |||||||
| chr17:67023188 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.305-1672C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023188 | |||||||
| chr17:67023207 | C | T | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.305-1653C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023207 | |||||||
| chr17:67023270 | C | CT | 185 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(182): Show |
192 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.305-1567dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023270 | ||||||
| chr17:67023270 | C | CTT | 15 | a0001c0001t0001g0030 a0001c0001t0001g0089 a0001c0001t0001g0146 others(12): Show |
15 | HG00621.hp2 HG01123.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.305-1568_305-1567d others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023270 | ||||||
| chr17:67023270 | CT | C | 19 | a0001c0001t0001g0161 a0001c0001t0002g0111 a0001c0001t0002g0219 others(16): Show |
21 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.305-1567delT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023270 | ||||||
| chr17:67023339 | G | A | 265 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(262): Show |
275 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.305-1521G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023339 | |||||||
| chr17:67023359 | T | C | 4 | a0001c0001t0001g0318 a0001c0001t0003g0152 a0001c0002t0002g0151 others(1): Show |
4 | HG01361.hp1 HG01952.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.305-1501T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023359 | |||||||
| chr17:67023377 | G | C | 8 | a0001c0001t0002g0228 a0001c0001t0005g0143 a0001c0001t0005g0144 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-1483G>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023377 | |||||||
| chr17:67023433 | G | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0029 others(28): Show |
34 | HG00597.hp1 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.305-1427G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023433 | |||||||
| chr17:67023574 | CCTT | C | 21 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0001g0155 others(18): Show |
21 | HG00544.hp2 HG01891.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.305-1285_305-1283d others(5): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023574 | |||||||
| chr17:67023575 | C | CT | 199 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(196): Show |
206 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.305-1272dupT | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr17 | 67023575 | ||||||
| chr17:67023629 | T | C | 11 | a0001c0001t0002g0246 a0001c0001t0003g0250 a0001c0001t0003g0252 others(8): Show |
12 | HG02055.hp2 HG02622.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-1231T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023629 | |||||||
| chr17:67023832 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.305-1028C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023832 | |||||||
| chr17:67023834 | C | T | 9 | a0001c0001t0001g0200 a0001c0001t0002g0108 a0001c0001t0003g0330 others(6): Show |
11 | HG01069.hp2 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.305-1026C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023834 | |||||||
| chr17:67023845 | G | A | 2 | a0001c0001t0003g0330 a0001c0001t0008g0306 |
2 | HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.305-1015G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023845 | |||||||
| chr17:67023940 | G | A | 1 | a0001c0001t0010g0147 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.305-920G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67023940 | |||||||
| chr17:67024040 | A | G | 222 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0018 others(219): Show |
229 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.305-820A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024040 | |||||||
| chr17:67024082 | T | C | 1 | a0001c0001t0008g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.305-778T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024082 | |||||||
| chr17:67024096 | T | G | 98 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0038 others(95): Show |
100 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.305-764T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024096 | |||||||
| chr17:67024263 | T | C | 2 | a0001c0001t0003g0325 a0001c0001t0030g0106 |
2 | HG01361.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.305-597T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024263 | |||||||
| chr17:67024399 | C | T | 2 | a0001c0003t0003g0028 a0001c0003t0018g0262 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.305-461C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024399 | |||||||
| chr17:67024412 | C | G | 8 | a0001c0001t0002g0228 a0001c0001t0005g0143 a0001c0001t0005g0144 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-448C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024412 | |||||||
| chr17:67024430 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.305-430C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024430 | |||||||
| chr17:67024547 | G | A | 2 | a0001c0003t0003g0028 a0001c0003t0018g0262 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.305-313G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024547 | |||||||
| chr17:67024561 | C | G | 9 | a0001c0001t0001g0067 a0001c0001t0002g0009 a0001c0001t0002g0293 others(6): Show |
10 | HG00735.hp2 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.305-299C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024561 | |||||||
| chr17:67024615 | A | G | 84 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0021 others(81): Show |
88 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.305-245A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024615 | |||||||
| chr17:67024657 | C | T | 1 | a0001c0001t0005g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.305-203C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024657 | |||||||
| chr17:67024711 | C | T | 10 | a0001c0001t0001g0030 a0001c0001t0001g0089 a0001c0001t0002g0022 others(7): Show |
10 | HG01433.hp1 HG01433.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.305-149C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024711 | |||||||
| chr17:67024717 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.305-143C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024717 | |||||||
| chr17:67024796 | C | T | 8 | a0001c0001t0002g0228 a0001c0001t0005g0143 a0001c0001t0005g0144 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.305-64C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024796 | |||||||
| chr17:67024804 | G | A | 1 | a0001c0001t0034g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.305-56G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024804 | |||||||
| chr17:67024806 | G | A | 1 | a0001c0001t0005g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.305-54G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024806 | |||||||
| chr17:67024845 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.305-15C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 2/3 | chr17 | 67024845 | |||||||
| chr17:67025143 | T | G | 1 | a0001c0002t0022g0026 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.445+143T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025143 | |||||||
| chr17:67025276 | C | T | 1 | a0001c0002t0002g0050 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.445+276C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025276 | |||||||
| chr17:67025343 | A | T | 5 | a0001c0001t0002g0065 a0001c0001t0002g0187 a0001c0001t0002g0188 others(2): Show |
5 | HG00639.hp1 HG01109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+343A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025343 | |||||||
| chr17:67025407 | G | A | 4 | a0001c0001t0001g0078 a0001c0001t0001g0265 a0001c0001t0001g0303 others(1): Show |
4 | HG01123.hp2 HG01515.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+407G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025407 | |||||||
| chr17:67025423 | A | C | 5 | a0001c0001t0002g0047 a0001c0001t0002g0186 a0001c0001t0003g0252 others(2): Show |
5 | HG02922.hp1 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+423A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025423 | |||||||
| chr17:67025444 | G | A | 1 | a0001c0001t0002g0197 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.445+444G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025444 | |||||||
| chr17:67025456 | C | T | 1 | a0001c0001t0003g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.445+456C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025456 | |||||||
| chr17:67025488 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.445+488C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025488 | |||||||
| chr17:67025515 | A | G | 3 | a0001c0001t0002g0109 a0001c0001t0002g0160 a0001c0001t0019g0237 |
3 | HG01891.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.445+515A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025515 | |||||||
| chr17:67025566 | GC | G | 4 | a0001c0001t0006g0229 a0001c0001t0021g0233 a0001c0001t0038g0115 others(1): Show |
4 | HG02257.hp2 HG02809.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+567delC | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025566 | |||||||
| chr17:67025568 | G | A | 5 | a0001c0001t0002g0103 a0001c0001t0003g0035 a0001c0001t0003g0312 others(2): Show |
5 | HG00140.hp2 HG01070.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+568G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025568 | |||||||
| chr17:67025630 | G | A | 1 | a0001c0001t0002g0020 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.445+630G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025630 | |||||||
| chr17:67025647 | C | T | 3 | a0001c0001t0002g0116 a0001c0001t0003g0122 a0001c0001t0003g0125 |
3 | HG00735.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.445+647C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025647 | |||||||
| chr17:67025648 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.445+648G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025648 | |||||||
| chr17:67025711 | A | C | 4 | a0001c0001t0002g0112 a0001c0001t0003g0159 a0001c0001t0011g0107 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.445+711A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025711 | |||||||
| chr17:67025795 | T | C | 5 | a0001c0001t0001g0155 a0001c0001t0003g0190 a0001c0001t0003g0280 others(2): Show |
5 | HG02683.hp2 NA18960.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+795T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025795 | |||||||
| chr17:67025882 | T | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(295): Show |
307 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.445+882T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67025882 | |||||||
| chr17:67026043 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(247): Show |
258 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.445+1043T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026043 | |||||||
| chr17:67026054 | G | A | 1 | a0001c0001t0034g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.445+1054G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026054 | |||||||
| chr17:67026459 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG03490.hp1 HG03492.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.445+1459G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026459 | |||||||
| chr17:67026485 | CTGTATTT others(47): Show |
C | 52 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(49): Show |
52 | HG00597.hp1 HG00609.hp2 HG01106.hp2 others(49): Show |
intron_variant | MODIFIER | c.445+1498_445+1551d others(56): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67026485 | ||||||
| chr17:67026517 | A | G | 2 | a0001c0001t0005g0120 a0001c0001t0037g0329 |
2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.445+1517A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026517 | |||||||
| chr17:67026654 | C | A | 40 | a0001c0001t0001g0164 a0001c0001t0001g0171 a0001c0001t0002g0278 others(37): Show |
41 | HG00558.hp2 HG00733.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.445+1654C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026654 | |||||||
| chr17:67026679 | G | GTGTGTGT others(57): Show |
1 | a0001c0001t0001g0185 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.445+1701_445+1764d others(66): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67026679 | ||||||
| chr17:67026875 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.445+1875C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026875 | |||||||
| chr17:67026928 | G | T | 5 | a0001c0001t0001g0087 a0001c0001t0001g0328 a0001c0002t0002g0085 others(2): Show |
5 | HG00544.hp1 NA18945.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.445+1928G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026928 | |||||||
| chr17:67026959 | A | C | 9 | a0001c0001t0017g0090 a0001c0001t0017g0092 a0001c0001t0021g0233 others(6): Show |
9 | HG01099.hp1 HG01361.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.445+1959A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026959 | |||||||
| chr17:67026971 | C | T | 3 | a0001c0001t0002g0243 a0001c0001t0005g0120 a0001c0001t0037g0329 |
3 | HG01243.hp2 HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.445+1971C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67026971 | |||||||
| chr17:67027026 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0141 |
2 | HG02015.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.445+2026C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027026 | |||||||
| chr17:67027079 | G | A | 1 | a0001c0001t0005g0120 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.445+2079G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027079 | |||||||
| chr17:67027131 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.445+2131C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027131 | |||||||
| chr17:67027221 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0024g0206 |
2 | HG02698.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.445+2221G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027221 | |||||||
| chr17:67027275 | C | T | 5 | a0001c0001t0021g0233 a0001c0001t0026g0201 a0001c0001t0030g0106 others(2): Show |
5 | HG01361.hp2 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.445+2275C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027275 | |||||||
| chr17:67027301 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(289): Show |
300 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.445+2301A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027301 | |||||||
| chr17:67027360 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.445+2360C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027360 | |||||||
| chr17:67027511 | G | T | 2 | a0001c0001t0002g0278 a0001c0001t0003g0277 |
2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.445+2511G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027511 | |||||||
| chr17:67027514 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.445+2514T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027514 | |||||||
| chr17:67027661 | A | C | 1 | a0001c0001t0024g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.445+2661A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027661 | |||||||
| chr17:67027661 | A | G | 26 | a0001c0001t0001g0087 a0001c0001t0001g0328 a0001c0001t0021g0233 others(23): Show |
27 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.445+2661A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027661 | |||||||
| chr17:67027785 | G | A | 1 | a0001c0001t0024g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-2681G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027785 | |||||||
| chr17:67027968 | T | A | 1 | a0001c0001t0035g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.446-2498T>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027968 | |||||||
| chr17:67027998 | C | T | 1 | a0001c0002t0002g0153 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.446-2468C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027998 | |||||||
| chr17:67027999 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.446-2467G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67027999 | |||||||
| chr17:67028024 | A | T | 1 | a0001c0001t0005g0253 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.446-2442A>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028024 | |||||||
| chr17:67028072 | T | C | 23 | a0001c0001t0001g0087 a0001c0001t0001g0328 a0001c0002t0002g0004 others(20): Show |
24 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.446-2394T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028072 | |||||||
| chr17:67028225 | C | T | 2 | a0001c0001t0021g0233 a0001c0001t0038g0115 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.446-2241C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028225 | |||||||
| chr17:67028276 | G | A | 11 | a0001c0001t0002g0112 a0001c0001t0005g0119 a0001c0001t0005g0143 others(8): Show |
11 | HG01346.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.446-2190G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028276 | |||||||
| chr17:67028281 | C | T | 4 | a0001c0001t0017g0090 a0001c0001t0017g0092 a0001c0001t0024g0206 others(1): Show |
4 | HG01099.hp1 HG02451.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-2185C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028281 | |||||||
| chr17:67028329 | G | A | 3 | a0001c0001t0003g0250 a0001c0001t0003g0330 a0002c0004t0003g0323 |
3 | HG02055.hp1 HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.446-2137G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028329 | |||||||
| chr17:67028349 | C | T | 2 | a0001c0005t0002g0148 a0001c0005t0002g0150 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.446-2117C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028349 | |||||||
| chr17:67028358 | T | C | 2 | a0001c0005t0002g0148 a0001c0005t0002g0150 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.446-2108T>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028358 | |||||||
| chr17:67028446 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.446-2020A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028446 | |||||||
| chr17:67028477 | C | T | 1 | a0001c0001t0010g0051 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.446-1989C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028477 | |||||||
| chr17:67028519 | C | G | 1 | a0001c0001t0003g0311 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.446-1947C>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028519 | |||||||
| chr17:67028547 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0080 others(10): Show |
14 | HG00438.hp2 HG02071.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.446-1919C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028547 | |||||||
| chr17:67028552 | C | CA | 14 | a0001c0001t0001g0146 a0001c0001t0003g0011 a0001c0001t0003g0064 others(11): Show |
15 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.446-1908dupA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67028552 | ||||||
| chr17:67028559 | G | A | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(261): Show |
271 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.446-1907G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028559 | |||||||
| chr17:67028565 | C | A | 8 | a0001c0001t0002g0065 a0001c0001t0002g0187 a0001c0001t0002g0188 others(5): Show |
8 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.446-1901C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028565 | |||||||
| chr17:67028607 | G | A | 1 | a0001c0002t0002g0336 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.446-1859G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028607 | |||||||
| chr17:67028613 | C | A | 1 | a0001c0001t0033g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-1853C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028613 | |||||||
| chr17:67028613 | C | T | 1 | a0001c0001t0024g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-1853C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028613 | |||||||
| chr17:67028668 | C | A | 1 | a0001c0001t0002g0112 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.446-1798C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028668 | |||||||
| chr17:67028733 | A | G | 1 | a0001c0001t0003g0220 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.446-1733A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028733 | |||||||
| chr17:67028870 | C | T | 1 | a0001c0001t0004g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.446-1596C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67028870 | |||||||
| chr17:67029059 | G | A | 2 | a0001c0001t0021g0233 a0001c0001t0038g0115 |
2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.446-1407G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029059 | |||||||
| chr17:67029163 | C | A | 1 | a0001c0001t0024g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-1303C>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029163 | |||||||
| chr17:67029272 | C | T | 1 | a0001c0001t0026g0201 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.446-1194C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029272 | |||||||
| chr17:67029280 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.446-1186G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029280 | |||||||
| chr17:67029287 | G | A | 1 | a0001c0001t0011g0107 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.446-1179G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029287 | |||||||
| chr17:67029395 | G | A | 56 | a0001c0001t0001g0062 a0001c0001t0001g0138 a0001c0001t0001g0139 others(53): Show |
57 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.446-1071G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029395 | |||||||
| chr17:67029444 | A | C | 44 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(41): Show |
44 | HG00597.hp1 HG00609.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.446-1022A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029444 | |||||||
| chr17:67029475 | CA | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(263): Show |
273 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.446-982delA | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67029475 | ||||||
| chr17:67029502 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.446-964C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029502 | |||||||
| chr17:67029558 | C | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(184): Show |
194 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.446-908C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029558 | |||||||
| chr17:67029570 | G | T | 1 | a0001c0001t0033g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-896G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029570 | |||||||
| chr17:67029580 | G | T | 1 | a0001c0001t0006g0229 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.446-886G>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029580 | |||||||
| chr17:67029582 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.446-884C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029582 | |||||||
| chr17:67029637 | A | AAAAC | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(186): Show |
196 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.446-809_446-806dup others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67029637 | ||||||
| chr17:67029716 | C | T | 1 | a0001c0001t0033g0041 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.446-750C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029716 | |||||||
| chr17:67029733 | A | C | 1 | a0001c0001t0031g0291 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.446-733A>C | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029733 | |||||||
| chr17:67029828 | C | T | 3 | a0001c0001t0011g0107 a0001c0001t0011g0338 a0001c0001t0040g0263 |
3 | HG02647.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.446-638C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029828 | |||||||
| chr17:67029895 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(293): Show |
307 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(304): Show |
intron_variant | MODIFIER | c.446-571G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029895 | |||||||
| chr17:67029973 | C | T | 1 | a0001c0001t0024g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446-493C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029973 | |||||||
| chr17:67029988 | C | T | 2 | a0001c0001t0005g0119 a0001c0001t0005g0254 |
2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.446-478C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67029988 | |||||||
| chr17:67030152 | GGT | G | 69 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(66): Show |
70 | HG00597.hp1 HG00609.hp2 HG01099.hp1 others(67): Show |
intron_variant | MODIFIER | c.446-294_446-293del others(2): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67030152 | ||||||
| chr17:67030152 | GGTGT | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(222): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.446-296_446-293del others(4): Show |
CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr17 | 67030152 | ||||||
| chr17:67030156 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.446-310T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030156 | |||||||
| chr17:67030158 | T | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(165): Show |
174 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.446-308T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030158 | |||||||
| chr17:67030160 | T | G | 2 | a0001c0001t0001g0113 a0002c0004t0001g0324 |
2 | HG02257.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.446-306T>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030160 | |||||||
| chr17:67030215 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.446-251C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030215 | |||||||
| chr17:67030399 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(171): Show |
183 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.446-67A>G | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030399 | |||||||
| chr17:67030400 | C | T | 4 | a0001c0001t0012g0094 a0001c0001t0012g0095 a0001c0001t0012g0096 others(1): Show |
4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.446-66C>T | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030400 | |||||||
| chr17:67030439 | G | A | 1 | a0001c0003t0018g0262 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.446-27G>A | CACNG4 | ENSG00000075461.6 | transcript | ENST00000262138.4 | protein_coding | 3/3 | chr17 | 67030439 |