Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 59284 |
| ensemblid | ENSG00000105605.8 |
| hgncid | 13626 |
| symbol | CACNG7 |
| name | calcium voltage-gated channel auxiliary subunit gamma 7 |
| refseq_nuc | NM_031896.5 |
| refseq_prot | NP_114102.2 |
| ensembl_nuc | ENST00000391767.6 |
| ensembl_prot | ENSP00000375647.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 53909278 |
| end | 53943950 |
| strand | + |
| ver | v1.2 |
| region | chr19:53909278-53943950 |
| region5000 | chr19:53904278-53948950 |
| regionname0 | CACNG7_chr19_53909278_53943950 |
| regionname5000 | CACNG7_chr19_53904278_53948950 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 825 | 363 | 93 | 70 | 142 | 18 | 40 | CACNG7_chr19_53904278_53948950 | CACNG7 | ATGAG others(820): Show |
chr19 | 53904278 | 53948950 | ||
| a0001c0002 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | ATGAG others(820): Show |
chr19 | 53904278 | 53948950 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2753 | 289 | 56 | 57 | 128 | 15 | 33 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0002 | 0/0 | 2754 | 29 | 4 | 10 | 8 | 2 | 5 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0003 | 0/0 | 2753 | 8 | 8 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0004 | 0/0 | 2753 | 8 | 8 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0005 | 0/0 | 2754 | 6 | 2 | 1 | 2 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0006 | 0/0 | 2754 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0007 | 0/0 | 2753 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0008 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0009 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0010 | 0/0 | 2753 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0011 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0012 | 0/0 | 2755 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2750): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0013 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0014 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0015 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0016 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0017 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0018 | 0/0 | 2753 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0019 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0020 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0021 | 0/0 | 2753 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0022 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0023 | 0/0 | 2753 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0024 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0001t0025 | 0/0 | 2753 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2748): Show |
chr19 | 53904278 | 53948950 |
| a0001c0002t0002 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | AGTAG others(2749): Show |
chr19 | 53904278 | 53948950 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0010g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0011g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0012g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0013g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0014g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0016g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0017g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0018g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0020g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0021g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0022g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0023g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0024g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0001t0025g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0324 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | GBR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0163 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0301 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0336 | EUR | FIN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00621 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0333 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01106 | hp2 | a0001 | c0001 | t0023 | g0213 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01261 | hp1 | a0001 | c0001 | t0018 | g0271 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0323 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0286 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0064 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0340 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0341 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0346 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02630 | hp2 | a0001 | c0001 | t0017 | g0071 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0310 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0066 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0343 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03453 | hp1 | a0001 | c0001 | t0021 | g0076 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0207 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | ESN | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0345 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03669 | hp2 | a0001 | c0001 | t0010 | g0233 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04115 | hp2 | a0001 | c0001 | t0005 | g0107 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0060 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18939 | hp1 | a0001 | c0001 | t0025 | g0106 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18989 | hp1 | a0001 | c0001 | t0022 | g0264 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19010 | hp2 | a0001 | c0001 | t0024 | g0018 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19077 | hp2 | a0001 | c0001 | t0012 | g0219 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ASW | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | GIH | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | GIH | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02109 | hp1 | a0001 | c0001 | t0019 | g0277 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0013 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | USA | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0041 | AFR | LWK | CACNG7_chr19_53904278_53948950 | CACNG7 | chr19 | 53904278 | 53948950 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53942218 | C | T | 1 | a0001c0002 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.753C>T | p.Ser251Ser | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1022/2754 | 753/828 | 251/275 | chr19 | 53942218 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53909285 | A | C | 1 | a0001c0001t0025 | 1 | NA18939.hp1 | 5_prime_UTR_variant | MODIFIER | c.-262A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3547 | chr19 | 53909285 | ||||||
| chr19:53909318 | G | A | 2 | a0001c0001t0003 a0001c0001t0008 |
9 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-229G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3514 | chr19 | 53909318 | ||||||
| chr19:53909365 | G | C | 1 | a0001c0001t0009 | 1 | HG00280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3467 | chr19 | 53909365 | ||||||
| chr19:53909395 | C | G | 1 | a0001c0001t0024 | 1 | NA19010.hp2 | 5_prime_UTR_variant | MODIFIER | c.-152C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3437 | chr19 | 53909395 | ||||||
| chr19:53909450 | G | A | 1 | a0001c0001t0010 | 1 | HG03669.hp2 | 5_prime_UTR_variant | MODIFIER | c.-97G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/6 | 3382 | chr19 | 53909450 | ||||||
| chr19:53942340 | AG | A | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*53delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 53 | INFO_REALIGN_3_PRIME | chr19 | 53942340 | |||||
| chr19:53942366 | C | T | 1 | a0001c0001t0023 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*73C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 73 | chr19 | 53942366 | ||||||
| chr19:53942398 | C | T | 1 | a0001c0001t0004 | 8 | HG02055.hp2 HG02615.hp1 HG03139.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*105C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 105 | chr19 | 53942398 | ||||||
| chr19:53942460 | C | A | 1 | a0001c0001t0006 | 3 | HG02615.hp2 HG02647.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*167C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 167 | chr19 | 53942460 | ||||||
| chr19:53942519 | C | T | 1 | a0001c0001t0022 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*226C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 226 | chr19 | 53942519 | ||||||
| chr19:53942551 | C | T | 2 | a0001c0001t0008 a0001c0001t0021 |
2 | HG02145.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*258C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 258 | chr19 | 53942551 | ||||||
| chr19:53942644 | G | C | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 351 | chr19 | 53942644 | ||||||
| chr19:53942645 | C | T | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 352 | chr19 | 53942645 | ||||||
| chr19:53942656 | A | G | 1 | a0001c0001t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 363 | chr19 | 53942656 | ||||||
| chr19:53942672 | G | A | 1 | a0001c0001t0015 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*379G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 379 | chr19 | 53942672 | ||||||
| chr19:53942720 | T | C | 1 | a0001c0001t0007 | 2 | HG02451.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*427T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 427 | chr19 | 53942720 | ||||||
| chr19:53942906 | C | A | 1 | a0001c0001t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*613C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 613 | chr19 | 53942906 | ||||||
| chr19:53943025 | C | T | 1 | a0001c0001t0013 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 732 | chr19 | 53943025 | ||||||
| chr19:53943186 | T | A | 2 | a0001c0001t0008 a0001c0001t0021 |
2 | HG02145.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*893T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 893 | chr19 | 53943186 | ||||||
| chr19:53943275 | T | C | 2 | a0001c0001t0004 a0001c0001t0017 |
9 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*982T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 982 | chr19 | 53943275 | ||||||
| chr19:53943441 | G | A | 1 | a0001c0001t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1148G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1148 | chr19 | 53943441 | ||||||
| chr19:53943547 | A | G | 1 | a0001c0001t0012 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1254A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1254 | chr19 | 53943547 | ||||||
| chr19:53943600 | T | TG | 2 | a0001c0001t0005 a0001c0001t0012 |
7 | HG00621.hp1 HG01099.hp1 HG02027.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1313dupG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1314 | INFO_REALIGN_3_PRIME | chr19 | 53943600 | |||||
| chr19:53943681 | A | T | 1 | a0001c0001t0020 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1388A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1388 | chr19 | 53943681 | ||||||
| chr19:53943748 | T | A | 1 | a0001c0001t0018 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1455T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1455 | chr19 | 53943748 | ||||||
| chr19:53943808 | G | A | 2 | a0001c0001t0011 a0001c0001t0019 |
2 | HG02109.hp1 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1515G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 6/6 | 1515 | chr19 | 53943808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:53909612 | A | T | 2 | a0001c0001t0001g0347 a0001c0001t0004g0346 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-30+95A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909612 | |||||||
| chr19:53909695 | G | A | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-30+178G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909695 | |||||||
| chr19:53909778 | A | G | 1 | a0001c0001t0002g0345 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-30+261A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909778 | |||||||
| chr19:53909837 | AGAGCAGG others(4): Show |
A | 1 | a0001c0001t0001g0344 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-30+322_-30+332del others(11): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53909837 | ||||||
| chr19:53909851 | G | A | 1 | a0001c0001t0013g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-30+334G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53909851 | |||||||
| chr19:53910003 | T | C | 92 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(89): Show |
94 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-30+486T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910003 | |||||||
| chr19:53910061 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30+544C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910061 | |||||||
| chr19:53910075 | G | T | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(248): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-30+558G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910075 | |||||||
| chr19:53910085 | T | C | 1 | a0001c0001t0013g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-30+568T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910085 | |||||||
| chr19:53910250 | G | T | 1 | a0001c0001t0006g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-30+733G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910250 | |||||||
| chr19:53910255 | G | A | 49 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(46): Show |
49 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-30+738G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910255 | |||||||
| chr19:53910279 | C | T | 44 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0058 others(41): Show |
45 | HG00741.hp2 HG01109.hp2 HG02055.hp2 others(42): Show |
intron_variant | MODIFIER | c.-30+762C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910279 | |||||||
| chr19:53910324 | C | A | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG02896.hp1 HG02897.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+807C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910324 | |||||||
| chr19:53910385 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+868G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910385 | |||||||
| chr19:53910386 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+869G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910386 | |||||||
| chr19:53910387 | A | T | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+870A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910387 | |||||||
| chr19:53910388 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+871G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910388 | |||||||
| chr19:53910389 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+872G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910389 | |||||||
| chr19:53910392 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+875G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910392 | |||||||
| chr19:53910393 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+876G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910393 | |||||||
| chr19:53910394 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+877G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910394 | |||||||
| chr19:53910396 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+879G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910396 | |||||||
| chr19:53910397 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+880T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910397 | |||||||
| chr19:53910398 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+881G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910398 | |||||||
| chr19:53910404 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+887T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910404 | |||||||
| chr19:53910412 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+895G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910412 | |||||||
| chr19:53910413 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+896G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910413 | |||||||
| chr19:53910415 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+898G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910415 | |||||||
| chr19:53910419 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+902T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910419 | |||||||
| chr19:53910423 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+906G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910423 | |||||||
| chr19:53910424 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+907G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910424 | |||||||
| chr19:53910425 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+908T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910425 | |||||||
| chr19:53910427 | G | C | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+910G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910427 | |||||||
| chr19:53910433 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+916G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910433 | |||||||
| chr19:53910436 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+919T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910436 | |||||||
| chr19:53910437 | C | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+920C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910437 | |||||||
| chr19:53910439 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+922A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910439 | |||||||
| chr19:53910451 | C | G | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+934C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910451 | |||||||
| chr19:53910455 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+938T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910455 | |||||||
| chr19:53910459 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+942G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910459 | |||||||
| chr19:53910460 | C | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+943C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910460 | |||||||
| chr19:53910466 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+949T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910466 | |||||||
| chr19:53910468 | C | A | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+951C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910468 | |||||||
| chr19:53910469 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+952A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910469 | |||||||
| chr19:53910471 | G | T | 1 | a0001c0001t0001g0342 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-30+954G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910471 | |||||||
| chr19:53910513 | TGATTAGT others(8): Show |
T | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-30+999_-30+1013de others(16): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53910513 | ||||||
| chr19:53910625 | T | A | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-30+1108T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910625 | |||||||
| chr19:53910650 | G | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0042 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-30+1133G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910650 | |||||||
| chr19:53910689 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0002g0038 a0001c0001t0002g0039 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-30+1172C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910689 | |||||||
| chr19:53910725 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-30+1208T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910725 | |||||||
| chr19:53910783 | G | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0042 others(57): Show |
62 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-30+1266G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910783 | |||||||
| chr19:53910988 | G | A | 6 | a0001c0001t0001g0067 a0001c0001t0004g0062 a0001c0001t0004g0063 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1471G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53910988 | |||||||
| chr19:53911001 | A | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(106): Show |
111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-30+1484A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911001 | |||||||
| chr19:53911040 | T | TTGGTGGT others(2): Show |
93 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(90): Show |
94 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.-30+1530_-30+1538d others(11): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53911040 | ||||||
| chr19:53911073 | A | ATT | 95 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(92): Show |
97 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-30+1566_-30+1567d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53911073 | ||||||
| chr19:53911073 | A | ATTT | 14 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0204 others(11): Show |
14 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30+1565_-30+1567d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr19 | 53911073 | ||||||
| chr19:53911093 | G | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(95): Show |
100 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.-30+1576G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911093 | |||||||
| chr19:53911136 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-30+1619G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911136 | |||||||
| chr19:53911196 | T | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(106): Show |
111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1607T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911196 | |||||||
| chr19:53911211 | G | A | 109 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(106): Show |
111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1592G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911211 | |||||||
| chr19:53911226 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
12 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-29-1577C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911226 | |||||||
| chr19:53911383 | T | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(106): Show |
111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1420T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911383 | |||||||
| chr19:53911396 | G | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(96): Show |
101 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.-29-1407G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911396 | |||||||
| chr19:53911411 | G | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
9 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-1392G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911411 | |||||||
| chr19:53911469 | G | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(79): Show |
84 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.-29-1334G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911469 | |||||||
| chr19:53911527 | A | C | 11 | a0001c0001t0001g0040 a0001c0001t0002g0038 a0001c0001t0002g0039 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29-1276A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911527 | |||||||
| chr19:53911570 | G | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0020 others(79): Show |
84 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.-29-1233G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911570 | |||||||
| chr19:53911626 | G | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-1177G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911626 | |||||||
| chr19:53911638 | C | T | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-1165C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911638 | |||||||
| chr19:53911646 | G | A | 109 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(106): Show |
111 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-29-1157G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911646 | |||||||
| chr19:53911742 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-29-1061C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53911742 | |||||||
| chr19:53912018 | A | G | 44 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
45 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.-29-785A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912018 | |||||||
| chr19:53912085 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-29-718G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912085 | |||||||
| chr19:53912147 | A | G | 44 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(41): Show |
45 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.-29-656A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912147 | |||||||
| chr19:53912238 | G | A | 1 | a0001c0001t0020g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-29-565G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912238 | |||||||
| chr19:53912470 | C | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-333C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912470 | |||||||
| chr19:53912491 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03688.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-29-312C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912491 | |||||||
| chr19:53912653 | G | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-29-150G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912653 | |||||||
| chr19:53912731 | C | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-72C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 1/5 | chr19 | 53912731 | |||||||
| chr19:53913047 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.196+20T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913047 | |||||||
| chr19:53913102 | T | A | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.196+75T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913102 | |||||||
| chr19:53913434 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.196+407C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913434 | |||||||
| chr19:53913555 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196+528G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913555 | |||||||
| chr19:53913589 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.196+562C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913589 | |||||||
| chr19:53913603 | A | G | 2 | a0001c0001t0001g0347 a0001c0001t0004g0346 |
2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.196+576A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913603 | |||||||
| chr19:53913658 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
8 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.196+631C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913658 | |||||||
| chr19:53913716 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0347 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.196+689C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913716 | |||||||
| chr19:53913772 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0187 a0001c0001t0001g0337 |
4 | HG01106.hp1 HG01123.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-728A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913772 | |||||||
| chr19:53913785 | T | TA | 54 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
55 | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.197-692dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | ||||||
| chr19:53913785 | T | TAA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(38): Show |
44 | HG00140.hp2 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.197-693_197-692dup others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | ||||||
| chr19:53913785 | T | TAAA | 6 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG01106.hp2 HG02300.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.197-694_197-692dup others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | ||||||
| chr19:53913785 | TA | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0021 others(22): Show |
26 | HG00323.hp2 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.197-692delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53913785 | ||||||
| chr19:53913799 | A | G | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
12 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-701A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913799 | |||||||
| chr19:53913802 | A | AG | 12 | a0001c0001t0001g0040 a0001c0001t0001g0208 a0001c0001t0002g0038 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.197-698_197-697ins others(1): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913802 | |||||||
| chr19:53913803 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.197-697A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913803 | |||||||
| chr19:53913809 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.197-691G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913809 | |||||||
| chr19:53913817 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.197-683A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913817 | |||||||
| chr19:53913827 | G | A | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-673G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913827 | |||||||
| chr19:53913879 | C | T | 11 | a0001c0001t0001g0040 a0001c0001t0002g0038 a0001c0001t0002g0039 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.197-621C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913879 | |||||||
| chr19:53913925 | A | G | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(19): Show |
22 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-575A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913925 | |||||||
| chr19:53913929 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
12 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.197-571C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53913929 | |||||||
| chr19:53914048 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.197-452G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914048 | |||||||
| chr19:53914064 | A | T | 6 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(3): Show |
6 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.197-436A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914064 | |||||||
| chr19:53914102 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0332 a0001c0001t0002g0179 |
4 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.197-398C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914102 | |||||||
| chr19:53914110 | C | A | 7 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
8 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.197-390C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914110 | |||||||
| chr19:53914205 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.197-295T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914205 | |||||||
| chr19:53914273 | C | CAAAAAA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0043 others(21): Show |
25 | HG00423.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.197-218_197-213dup others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914273 | ||||||
| chr19:53914273 | C | CAAAAAAA | 62 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0016 others(59): Show |
63 | HG00544.hp2 HG00609.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.197-219_197-213dup others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914273 | ||||||
| chr19:53914284 | AAAAG | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0101 others(39): Show |
45 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-212_197-209del others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914284 | ||||||
| chr19:53914288 | G | A | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(19): Show |
22 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.197-212G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914288 | |||||||
| chr19:53914290 | A | AAAAG | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.197-207_197-206ins others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914290 | ||||||
| chr19:53914290 | A | AAGAAAAA others(1): Show |
11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
11 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.197-209_197-208ins others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr19 | 53914290 | ||||||
| chr19:53914290 | A | G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0101 others(39): Show |
45 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.197-210A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914290 | |||||||
| chr19:53914296 | G | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02630.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.197-204G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914296 | |||||||
| chr19:53914341 | G | A | 17 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(14): Show |
18 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.197-159G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 2/5 | chr19 | 53914341 | |||||||
| chr19:53914604 | C | T | 1 | a0001c0001t0002g0306 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.283+18C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914604 | |||||||
| chr19:53914692 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.283+106G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914692 | |||||||
| chr19:53914801 | A | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(51): Show |
57 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.283+215A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914801 | |||||||
| chr19:53914802 | A | G | 64 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(61): Show |
67 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.283+216A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914802 | |||||||
| chr19:53914995 | G | C | 7 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0003g0029 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-370G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53914995 | |||||||
| chr19:53915005 | C | CA | 13 | a0001c0001t0001g0067 a0001c0001t0001g0123 a0001c0001t0001g0204 others(10): Show |
13 | HG01346.hp2 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-349dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 53915005 | ||||||
| chr19:53915005 | C | CAAA | 9 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0003g0032 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-351_284-349dup others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 53915005 | ||||||
| chr19:53915013 | A | T | 7 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0095 others(4): Show |
7 | HG01109.hp2 HG02258.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-352A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915013 | |||||||
| chr19:53915015 | AAT | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(42): Show |
47 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.284-348_284-347del others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr19 | 53915015 | ||||||
| chr19:53915016 | AT | A | 5 | a0001c0001t0001g0222 a0001c0001t0001g0235 a0001c0001t0001g0347 others(2): Show |
5 | HG02615.hp1 HG02738.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-348delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915016 | |||||||
| chr19:53915017 | T | A | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-348T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915017 | |||||||
| chr19:53915021 | T | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(58): Show |
64 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.284-344T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915021 | |||||||
| chr19:53915031 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(58): Show |
64 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.284-334G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915031 | |||||||
| chr19:53915091 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0307 a0001c0001t0001g0332 others(2): Show |
6 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-274G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915091 | |||||||
| chr19:53915295 | G | C | 2 | a0001c0001t0001g0270 a0001c0001t0018g0271 |
2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.284-70G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 3/5 | chr19 | 53915295 | |||||||
| chr19:53915534 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.424+29G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915534 | |||||||
| chr19:53915716 | T | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0101 others(44): Show |
50 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.424+211T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915716 | |||||||
| chr19:53915846 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.424+341A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915846 | |||||||
| chr19:53915868 | A | G | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.424+363A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53915868 | |||||||
| chr19:53916084 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.424+579G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916084 | |||||||
| chr19:53916139 | T | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0249 |
3 | HG02809.hp1 HG02818.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.424+634T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916139 | |||||||
| chr19:53916285 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(16): Show |
19 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+780C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916285 | |||||||
| chr19:53916342 | GGTACCAA others(31): Show |
G | 129 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(126): Show |
133 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.424+873_424+910del others(38): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916342 | ||||||
| chr19:53916487 | C | CT | 123 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+1002dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | ||||||
| chr19:53916487 | C | CTT | 31 | a0001c0001t0001g0020 a0001c0001t0001g0058 a0001c0001t0001g0059 others(28): Show |
31 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+1001_424+1002d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | ||||||
| chr19:53916487 | C | CTTT | 8 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0061 others(5): Show |
9 | HG02965.hp1 HG03041.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+1000_424+1002d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | ||||||
| chr19:53916487 | C | CTTTT | 7 | a0001c0001t0001g0206 a0001c0001t0003g0029 a0001c0001t0003g0030 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+999_424+1002du others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916487 | ||||||
| chr19:53916489 | T | TTC | 43 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0101 others(40): Show |
46 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.424+985_424+986ins others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916489 | ||||||
| chr19:53916552 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0007g0072 a0001c0001t0017g0071 |
3 | HG01891.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.424+1047G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916552 | |||||||
| chr19:53916662 | A | AT | 12 | a0001c0001t0001g0214 a0001c0001t0001g0320 a0001c0001t0002g0038 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+1174dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916662 | ||||||
| chr19:53916662 | AT | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0001g0057 others(22): Show |
26 | HG00639.hp2 HG01069.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.424+1174delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916662 | ||||||
| chr19:53916662 | ATT | A | 7 | a0001c0001t0001g0206 a0001c0001t0003g0029 a0001c0001t0003g0030 others(4): Show |
7 | HG02280.hp1 HG02572.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+1173_424+1174d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916662 | ||||||
| chr19:53916706 | G | A | 1 | a0001c0001t0012g0219 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.424+1201G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916706 | |||||||
| chr19:53916731 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0007g0072 a0001c0001t0017g0071 |
3 | HG01891.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.424+1226C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916731 | |||||||
| chr19:53916792 | G | A | 10 | a0001c0001t0001g0040 a0001c0001t0002g0038 a0001c0001t0002g0039 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+1287G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916792 | |||||||
| chr19:53916798 | C | CT | 24 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0067 others(21): Show |
25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+1310dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916798 | ||||||
| chr19:53916798 | CT | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0127 others(15): Show |
18 | HG00597.hp1 HG01069.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+1310delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53916798 | ||||||
| chr19:53916866 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.424+1361C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916866 | |||||||
| chr19:53916867 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0332 |
3 | HG01256.hp1 HG01258.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.424+1362G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916867 | |||||||
| chr19:53916921 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.424+1416C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53916921 | |||||||
| chr19:53917023 | C | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.424+1518C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917023 | |||||||
| chr19:53917058 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0202 |
2 | HG02080.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.424+1553G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917058 | |||||||
| chr19:53917265 | T | A | 66 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0067 others(63): Show |
69 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.424+1760T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917265 | |||||||
| chr19:53917357 | G | T | 57 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(54): Show |
58 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.424+1852G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917357 | |||||||
| chr19:53917416 | C | A | 8 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0095 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+1911C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917416 | |||||||
| chr19:53917669 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0113 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2164G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917669 | |||||||
| chr19:53917705 | A | G | 35 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
35 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.424+2200A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917705 | |||||||
| chr19:53917809 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.424+2304T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917809 | |||||||
| chr19:53917815 | CAG | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
11 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+2313_424+2314d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53917815 | ||||||
| chr19:53917824 | G | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+2319G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917824 | |||||||
| chr19:53917887 | A | T | 1 | a0001c0001t0007g0072 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.424+2382A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917887 | |||||||
| chr19:53917929 | C | CAAGGTCA others(20): Show |
1 | a0001c0001t0001g0095 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.424+2431_424+2432i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53917929 | ||||||
| chr19:53917937 | T | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(157): Show |
165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.424+2432T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917937 | |||||||
| chr19:53917952 | G | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | NA18939.hp1 NA18971.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+2447G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53917952 | |||||||
| chr19:53918031 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.424+2526C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918031 | |||||||
| chr19:53918066 | C | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+2561C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918066 | |||||||
| chr19:53918165 | T | A | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+2660T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918165 | |||||||
| chr19:53918182 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0002g0181 |
6 | HG00735.hp1 HG01255.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+2677G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918182 | |||||||
| chr19:53918307 | G | A | 9 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(6): Show |
9 | HG01257.hp2 HG01258.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2802G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918307 | |||||||
| chr19:53918510 | T | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+3005T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918510 | |||||||
| chr19:53918575 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+3070T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918575 | |||||||
| chr19:53918597 | C | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(107): Show |
114 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.424+3092C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918597 | |||||||
| chr19:53918669 | TGATAGTA others(52): Show |
T | 1 | a0001c0001t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+3167_424+3225d others(61): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53918669 | ||||||
| chr19:53918670 | G | A | 49 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(46): Show |
50 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.424+3165G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918670 | |||||||
| chr19:53918698 | G | C | 10 | a0001c0001t0001g0040 a0001c0001t0002g0038 a0001c0001t0002g0039 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+3193G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918698 | |||||||
| chr19:53918701 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+3196C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918701 | |||||||
| chr19:53918807 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+3302C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918807 | |||||||
| chr19:53918922 | G | C | 129 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(126): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.424+3417G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53918922 | |||||||
| chr19:53919064 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+3559G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919064 | |||||||
| chr19:53919085 | T | A | 1 | a0001c0001t0002g0311 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.424+3580T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919085 | |||||||
| chr19:53919091 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.424+3586T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919091 | |||||||
| chr19:53919140 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+3635C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919140 | |||||||
| chr19:53919195 | A | C | 32 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(29): Show |
33 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+3690A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919195 | |||||||
| chr19:53919323 | A | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
17 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+3818A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919323 | |||||||
| chr19:53919376 | G | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(110): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+3871G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919376 | |||||||
| chr19:53919421 | CTTGCCCC others(19): Show |
C | 1 | a0001c0001t0001g0222 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.424+3942_424+3967d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919421 | ||||||
| chr19:53919450 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.424+3945G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919450 | |||||||
| chr19:53919483 | GT | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+3979delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919483 | |||||||
| chr19:53919510 | G | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4005G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919510 | |||||||
| chr19:53919533 | T | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+4028T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919533 | |||||||
| chr19:53919538 | TCTGGTCA others(519): Show |
T | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+4075_424+4600d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919538 | ||||||
| chr19:53919554 | GTTGCCCC others(19): Show |
G | 3 | a0001c0001t0001g0067 a0001c0001t0011g0341 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+4075_424+4100d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919554 | ||||||
| chr19:53919560 | C | G | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+4055C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919560 | |||||||
| chr19:53919566 | T | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0101 others(46): Show |
52 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.424+4061T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919566 | |||||||
| chr19:53919580 | C | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(113): Show |
120 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.424+4075C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919580 | |||||||
| chr19:53919590 | G | GC | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+4086dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919590 | ||||||
| chr19:53919606 | G | C | 1 | a0001c0001t0001g0011 | 2 | HG01123.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.424+4101G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919606 | |||||||
| chr19:53919615 | GGCTGGTC others(280): Show |
G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4112_424+4398d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919615 | ||||||
| chr19:53919616 | G | GT | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4111_424+4112i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919616 | |||||||
| chr19:53919632 | C | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4127C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919632 | |||||||
| chr19:53919635 | G | GT | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4130_424+4131i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919635 | |||||||
| chr19:53919642 | G | GT | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4137_424+4138i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919642 | |||||||
| chr19:53919647 | TCATTGGT others(256): Show |
T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4143_424+4405d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919647 | |||||||
| chr19:53919665 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG00609.hp1 NA18969.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4160C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919665 | |||||||
| chr19:53919675 | TATTGGTG others(20): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.424+4191_424+4217d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919675 | ||||||
| chr19:53919696 | TCTGGTCA others(19): Show |
T | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.424+4214_424+4239d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919696 | ||||||
| chr19:53919700 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0001g0307 a0001c0001t0001g0332 others(3): Show |
7 | HG01256.hp1 HG01258.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+4195G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919700 | |||||||
| chr19:53919702 | C | A | 1 | a0001c0001t0001g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424+4197C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919702 | |||||||
| chr19:53919742 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.424+4237C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919742 | |||||||
| chr19:53919782 | T | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(111): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.424+4277T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919782 | |||||||
| chr19:53919836 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.424+4331G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919836 | |||||||
| chr19:53919851 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.424+4346G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919851 | |||||||
| chr19:53919868 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.424+4363C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919868 | |||||||
| chr19:53919886 | T | C | 1 | a0001c0001t0001g0012 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.424+4381T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919886 | |||||||
| chr19:53919904 | G | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4399G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919904 | |||||||
| chr19:53919922 | T | C | 1 | a0001c0001t0005g0064 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.424+4417T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919922 | |||||||
| chr19:53919931 | GCCTGGTA others(20): Show |
G | 1 | a0001c0001t0001g0090 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.424+4428_424+4454d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919931 | ||||||
| chr19:53919932 | C | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+4427C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919932 | |||||||
| chr19:53919937 | TATTGGTG others(312): Show |
T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4446_424+4764d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919937 | ||||||
| chr19:53919950 | G | GT | 7 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4445_424+4446i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919950 | |||||||
| chr19:53919958 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4453T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919958 | |||||||
| chr19:53919963 | TC | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4459delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919963 | |||||||
| chr19:53919978 | TCCCCAGG others(20): Show |
T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4477_424+4503d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919978 | ||||||
| chr19:53919978 | TCCCCAGG others(47): Show |
T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4477_424+4530d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53919978 | ||||||
| chr19:53919986 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+4481C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919986 | |||||||
| chr19:53919991 | T | TC | 7 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0074 others(4): Show |
7 | HG01109.hp1 HG02145.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4486_424+4487i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53919991 | |||||||
| chr19:53920005 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4500C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920005 | |||||||
| chr19:53920022 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+4517G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920022 | |||||||
| chr19:53920028 | C | CTTGCCCC others(45): Show |
1 | a0001c0001t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.424+4548_424+4549i others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920028 | ||||||
| chr19:53920028 | C | G | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0042 others(9): Show |
12 | HG00597.hp2 HG01109.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+4523C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920028 | |||||||
| chr19:53920031 | G | GT | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4526_424+4527i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920031 | |||||||
| chr19:53920032 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4527C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920032 | |||||||
| chr19:53920034 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+4529C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920034 | |||||||
| chr19:53920038 | G | GT | 8 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0042 others(5): Show |
8 | HG01243.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+4533_424+4534i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920038 | |||||||
| chr19:53920038 | GCTGGTCA others(72): Show |
G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4560_424+4638d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920038 | ||||||
| chr19:53920048 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4543G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920048 | |||||||
| chr19:53920054 | C | G | 15 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0040 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+4549C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920054 | |||||||
| chr19:53920054 | CTTGCCCC others(19): Show |
C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0285 |
2 | HG02559.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.424+4587_424+4612d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920054 | ||||||
| chr19:53920058 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4553C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920058 | |||||||
| chr19:53920060 | C | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+4555C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920060 | |||||||
| chr19:53920064 | G | GT | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4559_424+4560i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920064 | |||||||
| chr19:53920080 | G | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4575G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920080 | |||||||
| chr19:53920084 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4579C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920084 | |||||||
| chr19:53920090 | G | GCTGGTCA others(20): Show |
1 | a0001c0001t0002g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.424+4600_424+4601i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920090 | ||||||
| chr19:53920090 | G | GT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4585_424+4586i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920090 | |||||||
| chr19:53920101 | G | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0234 |
2 | HG00733.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.424+4596G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920101 | |||||||
| chr19:53920104 | G | C | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4599G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920104 | |||||||
| chr19:53920106 | G | C | 32 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(29): Show |
33 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+4601G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920106 | |||||||
| chr19:53920110 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4605C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920110 | |||||||
| chr19:53920117 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0090 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+4612C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920117 | |||||||
| chr19:53920131 | G | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4626G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920131 | |||||||
| chr19:53920133 | C | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+4628C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920133 | |||||||
| chr19:53920137 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4632C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920137 | |||||||
| chr19:53920144 | T | C | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4639T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920144 | |||||||
| chr19:53920144 | TCTGGTCA others(99): Show |
T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0276 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+4720_424+4825d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920144 | ||||||
| chr19:53920164 | TC | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4663delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920164 | ||||||
| chr19:53920172 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0006g0027 |
3 | HG02647.hp1 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4667C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920172 | |||||||
| chr19:53920172 | CCTGGTAT others(71): Show |
C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0024 |
2 | HG01243.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.424+4673_424+4750d others(80): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920172 | ||||||
| chr19:53920172 | CCTGGTAT others(340): Show |
C | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+4673_424+5019d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920172 | ||||||
| chr19:53920173 | C | G | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+4668C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920173 | |||||||
| chr19:53920177 | T | TC | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0011g0341 |
3 | HG02572.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4672_424+4673i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920177 | |||||||
| chr19:53920185 | G | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4680G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920185 | |||||||
| chr19:53920187 | G | C | 1 | a0001c0001t0011g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+4682G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920187 | |||||||
| chr19:53920203 | TCATTGGT others(234): Show |
T | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+4699_424+4939d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920203 | |||||||
| chr19:53920204 | CATTGGTG others(900): Show |
C | 1 | a0001c0001t0011g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+4720_424+5626d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920204 | ||||||
| chr19:53920218 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4713C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920218 | |||||||
| chr19:53920225 | CTGGTCAT others(18): Show |
C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+4721_424+4745d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920225 | |||||||
| chr19:53920283 | T | TC | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
6 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+4778_424+4779i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920283 | |||||||
| chr19:53920296 | GCCCCAGG others(155): Show |
G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4845_424+5006d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920296 | ||||||
| chr19:53920297 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4792C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920297 | |||||||
| chr19:53920303 | GT | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4799delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920303 | |||||||
| chr19:53920310 | CATTGGTG others(900): Show |
C | 11 | a0001c0001t0001g0206 a0001c0001t0001g0267 a0001c0001t0002g0038 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+4845_424+5751d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920310 | ||||||
| chr19:53920323 | G | T | 5 | a0001c0001t0001g0265 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG01123.hp2 HG01346.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+4818G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920323 | |||||||
| chr19:53920323 | GCCCCAGG others(20): Show |
G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0210 others(13): Show |
17 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.424+4845_424+4871d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920323 | ||||||
| chr19:53920324 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4819C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920324 | |||||||
| chr19:53920326 | CCAGGTCT others(954): Show |
C | 1 | a0001c0001t0001g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.424+4842_424+5802d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920326 | ||||||
| chr19:53920331 | T | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4826T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920331 | |||||||
| chr19:53920347 | GTTTCCCC others(820): Show |
G | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+4845_424+5671d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920347 | ||||||
| chr19:53920350 | T | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(88): Show |
94 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.424+4845T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920350 | |||||||
| chr19:53920351 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4846C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920351 | |||||||
| chr19:53920353 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4848C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920353 | |||||||
| chr19:53920374 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4869G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920374 | |||||||
| chr19:53920377 | G | GT | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4872_424+4873i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920377 | |||||||
| chr19:53920378 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4873C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920378 | |||||||
| chr19:53920380 | T | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+4875T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920380 | |||||||
| chr19:53920399 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4894G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920399 | |||||||
| chr19:53920401 | C | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+4896C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920401 | |||||||
| chr19:53920405 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4900C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920405 | |||||||
| chr19:53920411 | GT | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4907delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920411 | |||||||
| chr19:53920411 | GTCTGGTC others(155): Show |
G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4907_424+5068d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920411 | |||||||
| chr19:53920423 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+4918G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920423 | |||||||
| chr19:53920428 | C | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0028 others(3): Show |
6 | HG02615.hp1 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+4923C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920428 | |||||||
| chr19:53920430 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4925T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920430 | |||||||
| chr19:53920431 | G | GT | 4 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 others(1): Show |
4 | HG02615.hp1 HG03209.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+4926_424+4927i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920431 | |||||||
| chr19:53920432 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4927C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920432 | |||||||
| chr19:53920438 | G | GT | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+4933_424+4934i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920438 | |||||||
| chr19:53920440 | C | CT | 3 | a0001c0001t0001g0021 a0001c0001t0001g0347 a0001c0001t0015g0041 |
3 | HG03209.hp1 HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+4935_424+4936i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920440 | |||||||
| chr19:53920440 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(97): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.424+4935C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920440 | |||||||
| chr19:53920442 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0004g0346 |
2 | HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.424+4937G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920442 | |||||||
| chr19:53920456 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0028 others(7): Show |
10 | HG00438.hp2 HG00544.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+4951C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920456 | |||||||
| chr19:53920457 | GT | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0090 others(2): Show |
5 | HG02615.hp1 HG03209.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+4953delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920457 | |||||||
| chr19:53920466 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0347 a0001c0001t0006g0027 |
3 | HG02647.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+4961T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920466 | |||||||
| chr19:53920482 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.424+4977G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920482 | |||||||
| chr19:53920486 | C | T | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+4981C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920486 | |||||||
| chr19:53920513 | C | T | 2 | a0001c0001t0006g0027 a0001c0001t0015g0041 |
2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5008C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920513 | |||||||
| chr19:53920539 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+5034C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920539 | |||||||
| chr19:53920545 | G | GT | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.424+5040_424+5041i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920545 | |||||||
| chr19:53920550 | TC | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(319): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.424+5046delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920550 | |||||||
| chr19:53920556 | G | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(318): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.424+5051G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920556 | |||||||
| chr19:53920561 | GTTGTCCC others(499): Show |
G | 1 | a0001c0001t0001g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5060_424+5565d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920561 | ||||||
| chr19:53920562 | T | A | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5057T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920562 | |||||||
| chr19:53920564 | GT | G | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5060delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920564 | |||||||
| chr19:53920565 | TCCCCAGG others(46): Show |
T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0347 |
2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.424+5068_424+5120d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920565 | ||||||
| chr19:53920573 | C | A | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5068C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920573 | |||||||
| chr19:53920573 | C | T | 2 | a0001c0001t0006g0027 a0001c0001t0015g0041 |
2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5068C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920573 | |||||||
| chr19:53920584 | G | C | 28 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
29 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+5079G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920584 | |||||||
| chr19:53920587 | G | C | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5082G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920587 | |||||||
| chr19:53920593 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5088C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920593 | |||||||
| chr19:53920600 | T | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5095T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920600 | |||||||
| chr19:53920605 | T | TC | 9 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(6): Show |
9 | HG01109.hp1 HG01891.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+5100_424+5101i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920605 | |||||||
| chr19:53920618 | G | GT | 3 | a0001c0001t0002g0019 a0001c0001t0006g0026 a0001c0002t0002g0025 |
3 | HG01109.hp1 HG02145.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.424+5113_424+5114i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920618 | |||||||
| chr19:53920619 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5114C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920619 | |||||||
| chr19:53920624 | G | A | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5119G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920624 | |||||||
| chr19:53920626 | T | C | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5121T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920626 | |||||||
| chr19:53920640 | G | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5135G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920640 | |||||||
| chr19:53920646 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0347 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5141C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920646 | |||||||
| chr19:53920651 | GGCTGGTC others(72): Show |
G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5148_424+5226d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920651 | ||||||
| chr19:53920652 | G | GT | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5147_424+5148i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920652 | |||||||
| chr19:53920672 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5167C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920672 | |||||||
| chr19:53920678 | GT | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+5174delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920678 | |||||||
| chr19:53920679 | T | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5174T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920679 | |||||||
| chr19:53920684 | TC | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0347 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5180delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920684 | |||||||
| chr19:53920695 | C | G | 15 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0069 others(12): Show |
15 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+5190C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920695 | |||||||
| chr19:53920695 | CTTGCTCC others(552): Show |
C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(26): Show |
30 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+5195_424+5753d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920695 | ||||||
| chr19:53920697 | T | C | 3 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0008g0031 |
3 | HG01884.hp2 HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.424+5192T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920697 | |||||||
| chr19:53920698 | G | GT | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5193_424+5194i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920698 | |||||||
| chr19:53920698 | GCTCCAGG others(955): Show |
G | 2 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+5194_424+6155d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920698 | |||||||
| chr19:53920699 | C | T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0347 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5194C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920699 | |||||||
| chr19:53920700 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(77): Show |
83 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.424+5195T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920700 | |||||||
| chr19:53920706 | T | A | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5201T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920706 | |||||||
| chr19:53920706 | TCTGGTCA others(19): Show |
T | 1 | a0001c0001t0001g0302 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.424+5218_424+5243d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920706 | ||||||
| chr19:53920711 | TC | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5207delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920711 | |||||||
| chr19:53920720 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0347 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5215G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920720 | |||||||
| chr19:53920723 | C | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5218C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920723 | |||||||
| chr19:53920723 | C | T | 10 | a0001c0001t0001g0021 a0001c0001t0001g0329 a0001c0001t0001g0347 others(7): Show |
10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+5218C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920723 | |||||||
| chr19:53920726 | T | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0329 a0001c0001t0001g0347 others(5): Show |
8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+5221T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920726 | |||||||
| chr19:53920726 | TCCCAGGC others(18): Show |
T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5225_424+5249d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920726 | ||||||
| chr19:53920728 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0002g0310 |
2 | HG01496.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5223C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920728 | |||||||
| chr19:53920732 | G | GT | 9 | a0001c0001t0001g0021 a0001c0001t0001g0329 a0001c0001t0001g0347 others(6): Show |
9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+5227_424+5228i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920732 | |||||||
| chr19:53920732 | G | GTCTGGTC others(75): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5227_424+5228i others(84): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920732 | |||||||
| chr19:53920732 | G | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG01243.hp2 HG01891.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5227G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920732 | |||||||
| chr19:53920744 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5239T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920744 | |||||||
| chr19:53920748 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5243G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920748 | |||||||
| chr19:53920752 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+5247C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920752 | |||||||
| chr19:53920754 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5249C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920754 | |||||||
| chr19:53920758 | G | T | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5253G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920758 | |||||||
| chr19:53920759 | T | TCTGGTCA others(18): Show |
1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+5267_424+5268i others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920759 | ||||||
| chr19:53920759 | T | TCTGGTCA others(19): Show |
1 | a0001c0001t0001g0234 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.424+5269_424+5270i others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920759 | ||||||
| chr19:53920759 | T | TCTGGTCA others(19): Show |
1 | a0001c0001t0001g0200 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.424+5270_424+5295d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920759 | ||||||
| chr19:53920775 | G | C | 3 | a0001c0001t0001g0191 a0001c0001t0001g0234 a0001c0001t0001g0329 |
3 | HG01243.hp1 HG01496.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.424+5270G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920775 | |||||||
| chr19:53920775 | G | GTTGCCCC others(19): Show |
78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(75): Show |
82 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.424+5296_424+5321d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920775 | ||||||
| chr19:53920778 | G | GT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(13): Show |
16 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+5273_424+5274i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920778 | |||||||
| chr19:53920779 | C | T | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5274C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920779 | |||||||
| chr19:53920785 | G | GC | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5281dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920785 | ||||||
| chr19:53920785 | G | GT | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+5280_424+5281i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920785 | |||||||
| chr19:53920790 | TC | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5286delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920790 | |||||||
| chr19:53920795 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.424+5290G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920795 | |||||||
| chr19:53920801 | C | G | 9 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(6): Show |
9 | HG01496.hp2 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+5296C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920801 | |||||||
| chr19:53920802 | T | TCGTCCCC others(289): Show |
1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5297_424+5298i others(298): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920802 | |||||||
| chr19:53920805 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0329 |
3 | HG01496.hp2 HG02071.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.424+5300C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920805 | |||||||
| chr19:53920808 | C | CA | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5304dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920808 | ||||||
| chr19:53920811 | G | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5306G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920811 | |||||||
| chr19:53920816 | TC | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5312delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920816 | |||||||
| chr19:53920822 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5317G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920822 | |||||||
| chr19:53920827 | G | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(17): Show |
20 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.424+5322G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920827 | |||||||
| chr19:53920828 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5323T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920828 | |||||||
| chr19:53920830 | GT | G | 21 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
21 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+5326delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920830 | |||||||
| chr19:53920831 | TC | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0191 a0001c0001t0006g0027 others(1): Show |
4 | HG02647.hp1 NA18972.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5330delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920831 | ||||||
| chr19:53920838 | GC | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(9): Show |
12 | HG02145.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5335delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920838 | ||||||
| chr19:53920839 | C | T | 2 | a0001c0001t0006g0027 a0001c0001t0015g0041 |
2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5334C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920839 | |||||||
| chr19:53920844 | T | TC | 29 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(26): Show |
29 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+5339_424+5340i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920844 | |||||||
| chr19:53920852 | G | C | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5347G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920852 | |||||||
| chr19:53920854 | G | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5349G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920854 | |||||||
| chr19:53920857 | G | GT | 12 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(9): Show |
12 | HG01496.hp2 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5352_424+5353i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920857 | |||||||
| chr19:53920858 | C | T | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5353C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920858 | |||||||
| chr19:53920865 | T | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0042 others(14): Show |
17 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+5360T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920865 | |||||||
| chr19:53920865 | T | TCTGGTAT others(45): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5365_424+5366i others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920865 | ||||||
| chr19:53920870 | TC | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5366delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920870 | |||||||
| chr19:53920881 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.424+5376G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920881 | |||||||
| chr19:53920885 | T | C | 14 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(11): Show |
14 | HG01496.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5380T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920885 | |||||||
| chr19:53920885 | T | TC | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+5383dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920885 | ||||||
| chr19:53920892 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0008g0031 |
2 | HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.424+5387T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920892 | |||||||
| chr19:53920894 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.424+5389T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920894 | |||||||
| chr19:53920906 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.424+5401G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920906 | |||||||
| chr19:53920910 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5405T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920910 | |||||||
| chr19:53920911 | GT | G | 3 | a0001c0001t0001g0226 a0001c0001t0008g0031 a0001c0001t0015g0041 |
3 | HG02145.hp1 NA19007.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5407delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920911 | |||||||
| chr19:53920912 | TC | T | 11 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5411delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920912 | ||||||
| chr19:53920912 | TCCCCAGG others(392): Show |
T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0024 |
2 | HG01891.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.424+5457_424+5855d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920912 | ||||||
| chr19:53920915 | C | T | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5410C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920915 | |||||||
| chr19:53920920 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5415T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920920 | |||||||
| chr19:53920920 | T | TCTGGTCA others(19): Show |
1 | a0001c0001t0023g0213 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.424+5457_424+5482d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920920 | ||||||
| chr19:53920920 | TCTGGTCA others(19): Show |
T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0002g0336 others(1): Show |
4 | HG00323.hp2 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5457_424+5482d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920920 | ||||||
| chr19:53920920 | TCTGGTCA others(45): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5431_424+5482d others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920920 | ||||||
| chr19:53920936 | C | G | 23 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(20): Show |
23 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+5431C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920936 | |||||||
| chr19:53920939 | G | GT | 11 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(8): Show |
11 | HG02280.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5434_424+5435i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920939 | |||||||
| chr19:53920940 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+5435C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920940 | |||||||
| chr19:53920942 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.424+5437C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920942 | |||||||
| chr19:53920946 | G | GT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(11): Show |
14 | HG02040.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5441_424+5442i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920946 | |||||||
| chr19:53920962 | C | G | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(13): Show |
16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+5457C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920962 | |||||||
| chr19:53920962 | CTTGCCCC others(19): Show |
C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0077 a0001c0001t0001g0080 others(8): Show |
11 | HG00673.hp1 HG01109.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+5521_424+5546d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920962 | ||||||
| chr19:53920963 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5458T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920963 | |||||||
| chr19:53920964 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5459T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920964 | |||||||
| chr19:53920965 | G | GT | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5460_424+5461i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920965 | |||||||
| chr19:53920966 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.424+5461C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920966 | |||||||
| chr19:53920966 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0002g0310 others(1): Show |
4 | HG02451.hp2 HG02818.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5461C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920966 | |||||||
| chr19:53920972 | G | GC | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5468dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920972 | ||||||
| chr19:53920972 | G | GCTGGTCA others(48): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5483_424+5484i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920972 | ||||||
| chr19:53920972 | G | GT | 3 | a0001c0001t0001g0042 a0001c0001t0001g0329 a0001c0001t0015g0041 |
3 | HG01496.hp2 HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.424+5467_424+5468i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920972 | |||||||
| chr19:53920973 | CTGGTCAT others(258): Show |
C | 1 | a0001c0001t0006g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.424+5469_424+5733d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920973 | |||||||
| chr19:53920976 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5471G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920976 | |||||||
| chr19:53920986 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5481G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920986 | |||||||
| chr19:53920988 | G | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(119): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.424+5483G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920988 | |||||||
| chr19:53920992 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5487C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920992 | |||||||
| chr19:53920998 | G | GT | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(10): Show |
13 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+5493_424+5494i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53920998 | |||||||
| chr19:53920998 | GCTGGTCA others(73): Show |
G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0180 |
2 | NA18954.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.424+5513_424+5592d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53920998 | ||||||
| chr19:53921002 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5497G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921002 | |||||||
| chr19:53921002 | G | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5497G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921002 | |||||||
| chr19:53921003 | TC | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5499delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921003 | |||||||
| chr19:53921014 | G | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0097 others(2): Show |
5 | HG01109.hp2 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5509G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921014 | |||||||
| chr19:53921017 | G | GT | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5512_424+5513i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921017 | |||||||
| chr19:53921024 | G | GC | 6 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5520dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921024 | ||||||
| chr19:53921024 | G | GT | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.424+5519_424+5520i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921024 | |||||||
| chr19:53921026 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5521T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921026 | |||||||
| chr19:53921028 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5523G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921028 | |||||||
| chr19:53921028 | G | C | 13 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0070 others(10): Show |
13 | HG01109.hp2 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+5523G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921028 | |||||||
| chr19:53921031 | A | G | 6 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5526A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921031 | |||||||
| chr19:53921038 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+5533G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921038 | |||||||
| chr19:53921040 | G | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG02109.hp1 HG02895.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5535G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921040 | |||||||
| chr19:53921043 | G | GT | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG01496.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+5538_424+5539i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921043 | |||||||
| chr19:53921043 | GCCCCAGG others(989): Show |
G | 1 | a0001c0001t0002g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.424+5552_424+6547d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921043 | ||||||
| chr19:53921044 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5539C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921044 | |||||||
| chr19:53921051 | C | T | 19 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(16): Show |
19 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.424+5546C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921051 | |||||||
| chr19:53921056 | TC | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+5552delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921056 | |||||||
| chr19:53921058 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0097 |
3 | HG01109.hp2 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+5553A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921058 | |||||||
| chr19:53921062 | G | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5557G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921062 | |||||||
| chr19:53921065 | G | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5560G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921065 | |||||||
| chr19:53921067 | C | G | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(18): Show |
21 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+5562C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921067 | |||||||
| chr19:53921070 | G | GT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(13): Show |
16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+5565_424+5566i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921070 | |||||||
| chr19:53921078 | T | C | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.424+5573T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921078 | |||||||
| chr19:53921083 | TC | T | 11 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0073 others(8): Show |
11 | HG02080.hp1 HG02109.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+5579delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921083 | |||||||
| chr19:53921089 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5584G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921089 | |||||||
| chr19:53921091 | G | A | 1 | a0001c0001t0021g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.424+5586G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921091 | |||||||
| chr19:53921092 | G | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5587G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921092 | |||||||
| chr19:53921092 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5587G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921092 | |||||||
| chr19:53921094 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5589G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921094 | |||||||
| chr19:53921097 | G | GCCCCAGG others(69): Show |
1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5592_424+5593i others(78): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921097 | |||||||
| chr19:53921097 | GT | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(11): Show |
14 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5593delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921097 | |||||||
| chr19:53921098 | T | G | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5593T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921098 | |||||||
| chr19:53921098 | TCCCCAGG others(125): Show |
T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5601_424+5732d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921098 | ||||||
| chr19:53921106 | C | CCTGGTAT others(19): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG00609.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.424+5607_424+5632d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921106 | ||||||
| chr19:53921106 | C | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+5601C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921106 | |||||||
| chr19:53921108 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5603T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921108 | |||||||
| chr19:53921111 | T | TATTGGTG others(20): Show |
3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0097 |
3 | HG01109.hp2 HG02258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+5627_424+5653d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921111 | ||||||
| chr19:53921111 | T | TC | 10 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0095 others(7): Show |
10 | HG01496.hp2 HG01891.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+5606_424+5607i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921111 | |||||||
| chr19:53921122 | T | G | 1 | a0001c0001t0001g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.424+5617T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921122 | |||||||
| chr19:53921123 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5618T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921123 | |||||||
| chr19:53921125 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5620C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921125 | |||||||
| chr19:53921132 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5627T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921132 | |||||||
| chr19:53921132 | T | TCTGGTCA others(19): Show |
1 | a0001c0001t0001g0126 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.424+5643_424+5668d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921132 | ||||||
| chr19:53921138 | CATTGGTG others(72): Show |
C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0113 others(1): Show |
4 | HG01243.hp2 HG02717.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5654_424+5732d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921138 | ||||||
| chr19:53921146 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5641G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921146 | |||||||
| chr19:53921148 | GTTGCCCC others(19): Show |
G | 2 | a0001c0001t0001g0012 a0001c0001t0004g0346 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5669_424+5694d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921148 | ||||||
| chr19:53921152 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+5647C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921152 | |||||||
| chr19:53921158 | G | GT | 4 | a0001c0001t0001g0028 a0001c0001t0001g0042 a0001c0001t0001g0254 others(1): Show |
4 | HG01891.hp1 HG02080.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5653_424+5654i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921158 | |||||||
| chr19:53921158 | GCTGGTCA others(73): Show |
G | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+5669_424+5748d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921158 | ||||||
| chr19:53921159 | CTGGTCAT others(18): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5655_424+5679d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921159 | |||||||
| chr19:53921174 | C | G | 10 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0042 others(7): Show |
10 | HG00642.hp1 HG01109.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+5669C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921174 | |||||||
| chr19:53921178 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5673C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921178 | |||||||
| chr19:53921184 | G | GT | 5 | a0001c0001t0001g0021 a0001c0001t0001g0329 a0001c0001t0002g0019 others(2): Show |
5 | HG01109.hp1 HG01496.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+5679_424+5680i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921184 | |||||||
| chr19:53921190 | CATTGGTG others(20): Show |
C | 1 | a0001c0001t0001g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5699_424+5725d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921190 | ||||||
| chr19:53921200 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5695G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921200 | |||||||
| chr19:53921200 | G | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5695G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921200 | |||||||
| chr19:53921202 | T | C | 4 | a0001c0001t0001g0021 a0001c0001t0002g0019 a0001c0001t0006g0026 others(1): Show |
4 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5697T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921202 | |||||||
| chr19:53921203 | GT | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0208 a0001c0001t0002g0281 others(1): Show |
4 | HG00642.hp1 HG01891.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5699delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921203 | |||||||
| chr19:53921204 | TCCCCAGG others(100): Show |
T | 4 | a0001c0001t0001g0021 a0001c0001t0002g0019 a0001c0001t0006g0026 others(1): Show |
4 | HG01109.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5707_424+5813d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921204 | ||||||
| chr19:53921212 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0208 a0001c0001t0001g0329 others(1): Show |
4 | HG00642.hp1 HG01496.hp2 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5707C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921212 | |||||||
| chr19:53921213 | C | G | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5708C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921213 | |||||||
| chr19:53921217 | T | TATTGGTG others(20): Show |
166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(163): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.424+5755_424+5781d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921217 | ||||||
| chr19:53921217 | T | TC | 6 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0001g0329 others(3): Show |
6 | HG00642.hp1 HG01496.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5712_424+5713i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921217 | |||||||
| chr19:53921222 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+5717G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921222 | |||||||
| chr19:53921230 | G | GT | 3 | a0001c0001t0001g0042 a0001c0001t0001g0208 a0001c0001t0008g0031 |
3 | HG01891.hp1 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+5725_424+5726i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921230 | |||||||
| chr19:53921231 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0329 a0001c0001t0002g0310 |
3 | HG01496.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5726C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921231 | |||||||
| chr19:53921237 | GT | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0329 |
3 | HG01243.hp2 HG01496.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.424+5733delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921237 | |||||||
| chr19:53921238 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0208 a0001c0001t0008g0031 |
3 | HG01891.hp1 HG02145.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+5733T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921238 | |||||||
| chr19:53921254 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424+5749G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921254 | |||||||
| chr19:53921257 | G | GT | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5752_424+5753i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921257 | |||||||
| chr19:53921258 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0074 a0001c0001t0002g0310 |
3 | HG01891.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5753C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921258 | |||||||
| chr19:53921265 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5760T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921265 | |||||||
| chr19:53921283 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0347 |
3 | HG01243.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+5778T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921283 | |||||||
| chr19:53921284 | G | GT | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0006g0027 others(2): Show |
5 | HG02145.hp1 HG02451.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5779_424+5780i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921284 | |||||||
| chr19:53921284 | GCCTCAGG others(19): Show |
G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0347 |
3 | HG01243.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+5780_424+5805d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921284 | |||||||
| chr19:53921285 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5780C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921285 | |||||||
| chr19:53921287 | T | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0042 others(23): Show |
26 | HG00280.hp2 HG01109.hp2 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.424+5782T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921287 | |||||||
| chr19:53921292 | T | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 others(1): Show |
4 | HG02145.hp1 HG02451.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5787T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921292 | |||||||
| chr19:53921298 | C | A | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+5793C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921298 | |||||||
| chr19:53921301 | T | TGGTGCAG others(101): Show |
1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5800_424+5801i others(110): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921301 | ||||||
| chr19:53921304 | T | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(27): Show |
31 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+5799T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921304 | |||||||
| chr19:53921308 | C | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0042 others(15): Show |
18 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+5803C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921308 | |||||||
| chr19:53921311 | G | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0347 |
3 | HG01243.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+5806G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921311 | |||||||
| chr19:53921312 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5807C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921312 | |||||||
| chr19:53921314 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0209 others(3): Show |
6 | HG00280.hp2 HG01993.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5809C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921314 | |||||||
| chr19:53921319 | T | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0074 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5814T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921319 | |||||||
| chr19:53921335 | C | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
17 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.424+5830C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921335 | |||||||
| chr19:53921335 | CTTGCCCC others(47): Show |
C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5841_424+5894d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921335 | ||||||
| chr19:53921339 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5834C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921339 | |||||||
| chr19:53921343 | A | T | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5838A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921343 | |||||||
| chr19:53921345 | G | GT | 7 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0209 others(4): Show |
7 | HG00280.hp2 HG01496.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+5840_424+5841i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921345 | |||||||
| chr19:53921361 | G | C | 5 | a0001c0001t0001g0067 a0001c0001t0001g0209 a0001c0001t0001g0301 others(2): Show |
5 | HG00280.hp2 HG01993.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+5856G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921361 | |||||||
| chr19:53921362 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.424+5857T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921362 | |||||||
| chr19:53921363 | C | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(11): Show |
14 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+5858C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921363 | |||||||
| chr19:53921364 | GT | G | 12 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(9): Show |
12 | HG00280.hp2 HG01891.hp1 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5860delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921364 | |||||||
| chr19:53921372 | GT | G | 4 | a0001c0001t0001g0209 a0001c0001t0001g0301 a0001c0001t0001g0304 others(1): Show |
4 | HG00280.hp2 HG01993.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+5868delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921372 | |||||||
| chr19:53921373 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0006g0027 |
3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+5868T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921373 | |||||||
| chr19:53921389 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5884G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921389 | |||||||
| chr19:53921390 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+5885T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921390 | |||||||
| chr19:53921391 | T | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0301 a0001c0001t0001g0304 |
3 | HG00280.hp2 HG01993.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.424+5886T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921391 | |||||||
| chr19:53921392 | G | GT | 7 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0208 others(4): Show |
7 | HG00280.hp2 HG01993.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5887_424+5888i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921392 | |||||||
| chr19:53921393 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0329 a0001c0001t0002g0310 |
3 | HG01496.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5888C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921393 | |||||||
| chr19:53921395 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(89): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.424+5890C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921395 | |||||||
| chr19:53921399 | GT | G | 3 | a0001c0001t0001g0067 a0001c0001t0008g0031 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5895delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921399 | |||||||
| chr19:53921400 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5895T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921400 | |||||||
| chr19:53921400 | TCTGGTCA others(19): Show |
T | 1 | a0001c0001t0001g0006 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.424+5922_424+5947d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921400 | ||||||
| chr19:53921414 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5909G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921414 | |||||||
| chr19:53921416 | G | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5911G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921416 | |||||||
| chr19:53921418 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5913T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921418 | |||||||
| chr19:53921419 | G | GT | 3 | a0001c0001t0001g0067 a0001c0001t0001g0208 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5914_424+5915i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921419 | |||||||
| chr19:53921420 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+5915C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921420 | |||||||
| chr19:53921426 | G | GT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
20 | HG00280.hp2 HG01109.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.424+5921_424+5922i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921426 | |||||||
| chr19:53921428 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0006g0027 |
3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+5923T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921428 | |||||||
| chr19:53921442 | G | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+5937G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921442 | |||||||
| chr19:53921445 | GCCCCAGG others(20): Show |
G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+5948_424+5974d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921445 | ||||||
| chr19:53921446 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0002g0310 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.424+5941C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921446 | |||||||
| chr19:53921448 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+5943C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921448 | |||||||
| chr19:53921451 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+5946G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921451 | |||||||
| chr19:53921452 | GT | G | 3 | a0001c0001t0001g0209 a0001c0001t0001g0301 a0001c0001t0001g0304 |
3 | HG00280.hp2 HG01993.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.424+5948delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921452 | |||||||
| chr19:53921453 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+5948T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921453 | |||||||
| chr19:53921453 | TCTGGTAT others(99): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+5954_424+6059d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921453 | ||||||
| chr19:53921458 | T | TC | 11 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(8): Show |
11 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+5953_424+5954i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921458 | |||||||
| chr19:53921458 | TATTGCTG others(21): Show |
T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+5958_424+5985d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921458 | ||||||
| chr19:53921458 | TATTGCTG others(46): Show |
T | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+5954_424+6006d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921458 | |||||||
| chr19:53921463 | C | G | 12 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(9): Show |
12 | HG00280.hp2 HG01496.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+5958C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921463 | |||||||
| chr19:53921466 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+5961G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921466 | |||||||
| chr19:53921471 | GT | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0209 others(3): Show |
6 | HG00280.hp2 HG01891.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+5967delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921471 | |||||||
| chr19:53921480 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0329 |
3 | HG01496.hp2 HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+5975C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921480 | |||||||
| chr19:53921494 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0280 others(1): Show |
4 | HG01891.hp2 HG02647.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+5989G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921494 | |||||||
| chr19:53921494 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+5989G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921494 | |||||||
| chr19:53921500 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0002g0310 |
3 | HG01891.hp1 HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+5995C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921500 | |||||||
| chr19:53921507 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0208 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+6002T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921507 | |||||||
| chr19:53921512 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6007T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921512 | |||||||
| chr19:53921512 | T | TATTGGTG others(20): Show |
2 | a0001c0001t0001g0047 a0001c0001t0002g0168 |
2 | HG01168.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.424+6028_424+6054d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921512 | ||||||
| chr19:53921512 | T | TC | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0208 others(3): Show |
6 | HG01496.hp2 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6007_424+6008i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921512 | |||||||
| chr19:53921515 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6010T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921515 | |||||||
| chr19:53921517 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+6012G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921517 | |||||||
| chr19:53921524 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0006g0027 |
3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6019T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921524 | |||||||
| chr19:53921525 | G | GT | 4 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0208 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6020_424+6021i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921525 | |||||||
| chr19:53921526 | C | A | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6021C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921526 | |||||||
| chr19:53921526 | C | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6021C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921526 | |||||||
| chr19:53921528 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6023C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921528 | |||||||
| chr19:53921532 | GT | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0301 a0001c0001t0001g0304 others(2): Show |
5 | HG00280.hp2 HG01496.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6028delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921532 | |||||||
| chr19:53921533 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0019g0277 |
3 | HG01891.hp1 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+6028T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921533 | |||||||
| chr19:53921533 | T | TCTGGTCA others(19): Show |
7 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+6055_424+6080d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921533 | ||||||
| chr19:53921549 | G | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6044G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921549 | |||||||
| chr19:53921550 | T | TC | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6045_424+6046i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921550 | |||||||
| chr19:53921551 | T | G | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6046T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921551 | |||||||
| chr19:53921552 | GCCCCAGG others(128): Show |
G | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6048_424+6182d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921552 | |||||||
| chr19:53921553 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG01891.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6048C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921553 | |||||||
| chr19:53921553 | CCCCAGGC others(156): Show |
C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6087_424+6249d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921553 | ||||||
| chr19:53921559 | G | GCTGGTCA others(20): Show |
4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0296 others(1): Show |
4 | HG00408.hp1 NA18957.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6072_424+6098d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921559 | ||||||
| chr19:53921559 | G | GT | 7 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0209 others(4): Show |
7 | HG00280.hp2 HG01993.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+6054_424+6055i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921559 | |||||||
| chr19:53921559 | GCTGGTCA others(20): Show |
G | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6072_424+6098d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921559 | ||||||
| chr19:53921575 | G | GTCGGCCC others(49): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
8 | HG00597.hp1 HG02083.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6071_424+6072i others(58): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921575 | ||||||
| chr19:53921575 | GTTGCCCC others(76): Show |
G | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6097_424+6179d others(85): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921575 | ||||||
| chr19:53921576 | T | TC | 12 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
13 | HG02055.hp1 HG02056.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6071_424+6072i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921576 | |||||||
| chr19:53921577 | T | G | 12 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
13 | HG02055.hp1 HG02056.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6072T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921577 | |||||||
| chr19:53921579 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0310 |
2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6074C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921579 | |||||||
| chr19:53921585 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
8 | HG00597.hp1 HG02083.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6080G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921585 | |||||||
| chr19:53921586 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6081T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921586 | |||||||
| chr19:53921604 | C | T | 20 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(17): Show |
20 | HG00597.hp1 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+6099C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921604 | |||||||
| chr19:53921605 | GT | G | 7 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0274 others(4): Show |
7 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6101delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921605 | |||||||
| chr19:53921606 | T | G | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6101T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921606 | |||||||
| chr19:53921606 | T | TCCCCAGG others(20): Show |
10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6124_424+6125i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921606 | ||||||
| chr19:53921606 | TCCCCAGG others(48): Show |
T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(91): Show |
98 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.424+6125_424+6179d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921606 | ||||||
| chr19:53921606 | TCCCCAGG others(183): Show |
T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+6105_424+6294d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921606 | ||||||
| chr19:53921620 | C | CATTGGTG others(73): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6124_424+6125i others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921620 | ||||||
| chr19:53921620 | C | CATTGGTG others(234): Show |
1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+6124_424+6125i others(243): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921620 | ||||||
| chr19:53921620 | C | CATTGGTG others(207): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6124_424+6125i others(216): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921620 | ||||||
| chr19:53921628 | G | C | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.424+6123G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921628 | |||||||
| chr19:53921630 | G | C | 11 | a0001c0001t0001g0040 a0001c0001t0001g0209 a0001c0001t0001g0246 others(8): Show |
11 | HG00280.hp2 HG01070.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6125G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921630 | |||||||
| chr19:53921632 | C | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(41): Show |
45 | HG00280.hp2 HG00597.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+6127C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921632 | |||||||
| chr19:53921633 | GT | G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0040 others(15): Show |
18 | HG00280.hp2 HG01070.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6129delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921633 | |||||||
| chr19:53921634 | T | TCCCAGGC others(341): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6132_424+6133i others(350): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921634 | ||||||
| chr19:53921634 | T | TCCCCAGG others(182): Show |
1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6142_424+6143i others(191): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921634 | ||||||
| chr19:53921634 | T | TCCCCAGG others(20): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0093 |
2 | NA18961.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.424+6180_424+6206d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921634 | ||||||
| chr19:53921641 | GT | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0006g0027 |
3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6137delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921641 | |||||||
| chr19:53921642 | T | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6137T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921642 | |||||||
| chr19:53921642 | TCTGGTCA others(207): Show |
T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 others(5): Show |
8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6153_424+6366d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921642 | ||||||
| chr19:53921656 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424+6151G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921656 | |||||||
| chr19:53921658 | C | G | 15 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0067 others(12): Show |
15 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6153C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921658 | |||||||
| chr19:53921660 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0067 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6155T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921660 | |||||||
| chr19:53921661 | G | GT | 5 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0067 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6156_424+6157i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921661 | |||||||
| chr19:53921661 | G | T | 2 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6156G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921661 | |||||||
| chr19:53921662 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6157C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921662 | |||||||
| chr19:53921668 | G | A | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6163G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921668 | |||||||
| chr19:53921669 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0010g0233 |
2 | HG03139.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.424+6164T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921669 | |||||||
| chr19:53921683 | G | C | 5 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0080 others(2): Show |
5 | HG01109.hp2 HG02451.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6178G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921683 | |||||||
| chr19:53921685 | C | G | 23 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0069 others(20): Show |
23 | HG01109.hp2 HG01891.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.424+6180C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921685 | |||||||
| chr19:53921688 | G | GT | 15 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0080 others(12): Show |
15 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6183_424+6184i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921688 | |||||||
| chr19:53921688 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6183G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921688 | |||||||
| chr19:53921689 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0002g0310 |
2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.424+6184C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921689 | |||||||
| chr19:53921691 | C | T | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6186C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921691 | |||||||
| chr19:53921696 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0074 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6191T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921696 | |||||||
| chr19:53921696 | T | TCTGGTCA others(48): Show |
2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6207_424+6208i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921696 | ||||||
| chr19:53921702 | CATTGGTG others(45): Show |
C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0006g0027 |
3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6208_424+6259d others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921702 | ||||||
| chr19:53921710 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6205G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921710 | |||||||
| chr19:53921712 | G | C | 11 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
12 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6207G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921712 | |||||||
| chr19:53921713 | C | G | 1 | a0001c0001t0005g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424+6208C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921713 | |||||||
| chr19:53921713 | C | T | 32 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(29): Show |
33 | HG01109.hp2 HG01496.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+6208C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921713 | |||||||
| chr19:53921716 | T | C | 12 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
13 | HG01496.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6211T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921716 | |||||||
| chr19:53921716 | T | TC | 14 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0080 others(11): Show |
14 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+6214dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921716 | ||||||
| chr19:53921722 | G | GC | 4 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0080 others(1): Show |
4 | HG01109.hp2 HG02559.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6218dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921722 | ||||||
| chr19:53921722 | G | GT | 21 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(18): Show |
22 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+6217_424+6218i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921722 | |||||||
| chr19:53921722 | GCTGGTCA others(290): Show |
G | 33 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0206 others(30): Show |
34 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.424+6237_424+6533d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921722 | ||||||
| chr19:53921728 | CATTGGTG others(343): Show |
C | 5 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0002g0227 others(2): Show |
5 | HG02074.hp1 NA18944.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6237_424+6586d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921728 | ||||||
| chr19:53921738 | G | C | 12 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(9): Show |
12 | HG01496.hp2 HG01934.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6233G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921738 | |||||||
| chr19:53921739 | T | C | 11 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6234T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921739 | |||||||
| chr19:53921741 | G | GT | 46 | a0001c0001t0001g0008 a0001c0001t0001g0067 a0001c0001t0001g0070 others(43): Show |
47 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.424+6236_424+6237i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921741 | |||||||
| chr19:53921741 | GCCCCAGG others(181): Show |
G | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6250_424+6437d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921741 | ||||||
| chr19:53921741 | GCCCCAGG others(316): Show |
G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0028 others(14): Show |
19 | HG01175.hp1 HG02083.hp2 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6237_424+6559d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921741 | |||||||
| chr19:53921742 | C | T | 11 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+6237C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921742 | |||||||
| chr19:53921748 | GT | G | 12 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(9): Show |
13 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6244delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921748 | |||||||
| chr19:53921749 | T | C | 47 | a0001c0001t0001g0008 a0001c0001t0001g0067 a0001c0001t0001g0070 others(44): Show |
48 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.424+6244T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921749 | |||||||
| chr19:53921753 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0222 |
2 | HG02738.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+6248G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921753 | |||||||
| chr19:53921754 | T | TATTGGTG others(20): Show |
1 | a0001c0001t0001g0006 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.424+6267_424+6293d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921754 | ||||||
| chr19:53921754 | T | TC | 30 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(27): Show |
31 | HG01109.hp2 HG01496.hp2 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6249_424+6250i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921754 | |||||||
| chr19:53921754 | TATTGGTG others(20): Show |
T | 2 | a0001c0001t0001g0120 a0001c0001t0019g0277 |
2 | HG02109.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.424+6267_424+6293d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921754 | ||||||
| chr19:53921760 | T | A | 1 | a0001c0001t0001g0020 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.424+6255T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921760 | |||||||
| chr19:53921764 | G | C | 11 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(8): Show |
11 | HG01496.hp2 HG01934.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6259G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921764 | |||||||
| chr19:53921766 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6261T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921766 | |||||||
| chr19:53921768 | T | C | 25 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0056 others(22): Show |
26 | HG01496.hp2 HG01891.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.424+6263T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921768 | |||||||
| chr19:53921768 | T | TC | 11 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0095 others(8): Show |
11 | HG01884.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6266dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | ||||||
| chr19:53921768 | T | TCCCAGGT others(21): Show |
2 | a0001c0001t0001g0274 a0001c0001t0001g0276 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.424+6290_424+6317d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | ||||||
| chr19:53921768 | T | TCCCCAGG others(427): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6266_424+6267i others(436): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | ||||||
| chr19:53921768 | TCCCAGGT others(181): Show |
T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0210 others(28): Show |
32 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+6267_424+6454d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | ||||||
| chr19:53921768 | TCCCAGGT others(208): Show |
T | 1 | a0001c0001t0011g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+6267_424+6481d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | ||||||
| chr19:53921768 | TCCCAGGT others(344): Show |
T | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+6267_424+6617d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921768 | ||||||
| chr19:53921775 | T | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0095 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6270T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921775 | |||||||
| chr19:53921780 | TC | T | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6276delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921780 | |||||||
| chr19:53921790 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.424+6285A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921790 | |||||||
| chr19:53921791 | G | C | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6286G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921791 | |||||||
| chr19:53921794 | GT | G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0070 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6290delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921794 | |||||||
| chr19:53921795 | T | TCCCCAGG others(20): Show |
2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.424+6318_424+6344d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921795 | ||||||
| chr19:53921795 | TC | T | 17 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(14): Show |
18 | HG01109.hp2 HG02055.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6294delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921795 | ||||||
| chr19:53921795 | TCCCCAGG others(21): Show |
T | 1 | a0001c0001t0001g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.424+6294_424+6321d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921795 | ||||||
| chr19:53921803 | T | C | 9 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0070 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6298T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921803 | |||||||
| chr19:53921817 | G | C | 2 | a0001c0001t0001g0208 a0001c0001t0002g0310 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.424+6312G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921817 | |||||||
| chr19:53921820 | T | C | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6315T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921820 | |||||||
| chr19:53921822 | G | GT | 14 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(11): Show |
15 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6317_424+6318i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921822 | |||||||
| chr19:53921822 | GCCCCAGG others(73): Show |
G | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6331_424+6410d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921822 | ||||||
| chr19:53921823 | C | T | 21 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0073 others(18): Show |
21 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(18): Show |
intron_variant | MODIFIER | c.424+6318C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921823 | |||||||
| chr19:53921829 | GT | G | 14 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0191 others(11): Show |
14 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+6325delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921829 | |||||||
| chr19:53921829 | GTCTGGTC others(319): Show |
G | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02258.hp2 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6325_424+6650d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921829 | |||||||
| chr19:53921830 | T | TCTGGTCA others(48): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6347_424+6348i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921830 | ||||||
| chr19:53921830 | TCTGGTCA others(19): Show |
T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(4): Show |
7 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6375_424+6400d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921830 | ||||||
| chr19:53921835 | TC | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0006g0027 |
3 | HG01891.hp2 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.424+6331delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921835 | |||||||
| chr19:53921850 | T | C | 25 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(22): Show |
26 | HG01496.hp2 HG01934.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.424+6345T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921850 | |||||||
| chr19:53921856 | G | GT | 30 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0056 others(27): Show |
31 | HG01109.hp2 HG01891.hp2 HG01934.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6351_424+6352i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921856 | |||||||
| chr19:53921861 | T | A | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6356T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921861 | |||||||
| chr19:53921861 | TC | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(8): Show |
11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6357delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921861 | |||||||
| chr19:53921862 | CATTGGTG others(46): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.424+6375_424+6427d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921862 | ||||||
| chr19:53921867 | G | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6362G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921867 | |||||||
| chr19:53921872 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6367G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921872 | |||||||
| chr19:53921873 | T | C | 8 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 others(5): Show |
8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6368T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921873 | |||||||
| chr19:53921876 | T | C | 8 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0042 others(5): Show |
8 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6371T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921876 | |||||||
| chr19:53921882 | G | GT | 16 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(13): Show |
16 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+6377_424+6378i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921882 | |||||||
| chr19:53921887 | T | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 |
3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6382T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921887 | |||||||
| chr19:53921888 | CATTGGTG others(400): Show |
C | 1 | a0001c0001t0019g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.424+6411_424+6817d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921888 | ||||||
| chr19:53921896 | G | C | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6391G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921896 | |||||||
| chr19:53921901 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.424+6396G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921901 | |||||||
| chr19:53921901 | GT | G | 13 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0070 others(10): Show |
13 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+6397delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921901 | |||||||
| chr19:53921902 | TC | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6401delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921902 | ||||||
| chr19:53921910 | T | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 others(6): Show |
9 | HG01070.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+6405T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921910 | |||||||
| chr19:53921915 | T | TC | 20 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(17): Show |
20 | HG01109.hp2 HG01891.hp1 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+6410_424+6411i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921915 | |||||||
| chr19:53921923 | G | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6418G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921923 | |||||||
| chr19:53921928 | GT | G | 18 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(15): Show |
18 | HG01496.hp2 HG01891.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6424delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921928 | |||||||
| chr19:53921929 | T | TCCCAGGT others(73): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6427_424+6428i others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921929 | ||||||
| chr19:53921929 | TC | T | 6 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0077 others(3): Show |
6 | HG01109.hp2 HG01891.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6428delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921929 | ||||||
| chr19:53921930 | C | A | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6425C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921930 | |||||||
| chr19:53921932 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6427C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921932 | |||||||
| chr19:53921937 | T | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0103 a0001c0001t0001g0246 others(6): Show |
9 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6432T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921937 | |||||||
| chr19:53921937 | T | TCTGGTCA others(20): Show |
3 | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 |
3 | NA18950.hp2 NA18982.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.424+6479_424+6505d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921937 | ||||||
| chr19:53921951 | G | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0211 |
3 | HG01109.hp2 HG03579.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.424+6446G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921951 | |||||||
| chr19:53921956 | G | GT | 16 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0024 others(13): Show |
16 | HG01106.hp1 HG01123.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+6451_424+6452i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921956 | |||||||
| chr19:53921956 | GCCCCAGG others(129): Show |
G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(3): Show |
6 | HG01109.hp1 HG01243.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+6538_424+6673d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921956 | ||||||
| chr19:53921956 | GCCCCAGG others(155): Show |
G | 1 | a0001c0001t0001g0011 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.424+6452_424+6613d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921956 | |||||||
| chr19:53921956 | GCCCCAGG others(346): Show |
G | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.424+6459_424+6811d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921956 | ||||||
| chr19:53921957 | C | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 |
3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6452C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921957 | |||||||
| chr19:53921959 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 |
3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6454C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921959 | |||||||
| chr19:53921963 | GC | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+6460delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921963 | ||||||
| chr19:53921964 | C | T | 32 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0022 others(29): Show |
32 | HG01106.hp1 HG01109.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+6459C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921964 | |||||||
| chr19:53921978 | G | C | 2 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6473G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921978 | |||||||
| chr19:53921980 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6475G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921980 | |||||||
| chr19:53921983 | G | GT | 11 | a0001c0001t0001g0040 a0001c0001t0001g0208 a0001c0001t0001g0246 others(8): Show |
11 | HG01070.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6478_424+6479i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921983 | |||||||
| chr19:53921984 | C | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0191 others(10): Show |
13 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6479C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921984 | |||||||
| chr19:53921985 | C | G | 1 | a0001c0001t0005g0300 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.424+6480C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921985 | |||||||
| chr19:53921990 | GC | G | 11 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(8): Show |
11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6487delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921990 | ||||||
| chr19:53921991 | C | CCTGGTCA others(21): Show |
1 | a0001c0001t0001g0002 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.424+6514_424+6541d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921991 | ||||||
| chr19:53921991 | C | T | 19 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0040 others(16): Show |
19 | HG01070.hp2 HG01496.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6486C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921991 | |||||||
| chr19:53921992 | C | A | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6487C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53921992 | |||||||
| chr19:53921997 | CATTGGTG others(209): Show |
C | 1 | a0001c0001t0001g0312 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.424+6542_424+6757d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53921997 | ||||||
| chr19:53922005 | G | C | 2 | a0001c0001t0003g0036 a0001c0001t0003g0037 |
2 | HG01884.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6500G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922005 | |||||||
| chr19:53922007 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6502G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922007 | |||||||
| chr19:53922009 | T | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6504T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922009 | |||||||
| chr19:53922010 | G | GCCTCAGG others(100): Show |
1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6505_424+6506i others(109): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922010 | |||||||
| chr19:53922010 | GT | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 others(2): Show |
5 | HG01891.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6506delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922010 | |||||||
| chr19:53922011 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6506T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922011 | |||||||
| chr19:53922011 | TC | T | 22 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0040 others(19): Show |
22 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+6510delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922011 | ||||||
| chr19:53922011 | TCCCCAGG others(182): Show |
T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0187 others(8): Show |
11 | HG01106.hp1 HG01123.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6520_424+6708d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922011 | ||||||
| chr19:53922018 | GT | G | 22 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0040 others(19): Show |
22 | HG01070.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+6514delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922018 | |||||||
| chr19:53922019 | T | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0115 others(1): Show |
4 | HG01109.hp2 HG03579.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6514T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922019 | |||||||
| chr19:53922020 | C | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 |
3 | HG01891.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6515C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922020 | |||||||
| chr19:53922024 | TC | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0007g0075 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6520delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922024 | |||||||
| chr19:53922035 | G | C | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6530G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922035 | |||||||
| chr19:53922036 | T | C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(26): Show |
30 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+6531T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922036 | |||||||
| chr19:53922039 | TC | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0208 others(2): Show |
5 | HG01109.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6538delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922039 | ||||||
| chr19:53922039 | TCCCCAGG others(47): Show |
T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 others(5): Show |
8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6538_424+6591d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922039 | ||||||
| chr19:53922039 | TCCCCAGG others(102): Show |
T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0210 others(29): Show |
33 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.424+6538_424+6646d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922039 | ||||||
| chr19:53922046 | GC | G | 6 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0208 others(3): Show |
6 | HG01109.hp2 HG01496.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6543delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922046 | ||||||
| chr19:53922047 | C | T | 22 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0042 others(19): Show |
22 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+6542C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922047 | |||||||
| chr19:53922047 | CCTGGTAT others(19): Show |
C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0212 others(27): Show |
31 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6561_424+6586d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922047 | ||||||
| chr19:53922052 | T | TC | 8 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0208 others(5): Show |
8 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6547_424+6548i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922052 | |||||||
| chr19:53922052 | T | TCATTGGT others(20): Show |
1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.424+6547_424+6548i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922052 | |||||||
| chr19:53922062 | G | GT | 3 | a0001c0001t0001g0070 a0001c0001t0001g0105 a0001c0001t0010g0233 |
3 | HG02630.hp1 HG03669.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.424+6559dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922062 | ||||||
| chr19:53922065 | G | GT | 24 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0042 others(21): Show |
24 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+6560_424+6561i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922065 | |||||||
| chr19:53922065 | G | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0028 others(16): Show |
21 | HG01175.hp1 HG02083.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.424+6560G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922065 | |||||||
| chr19:53922065 | GCCCCAGG others(46): Show |
G | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6561_424+6613d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922065 | |||||||
| chr19:53922066 | C | T | 2 | a0001c0001t0002g0311 a0001c0001t0002g0336 |
2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.424+6561C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922066 | |||||||
| chr19:53922073 | T | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0028 others(21): Show |
26 | HG01175.hp1 HG01884.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.424+6568T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922073 | |||||||
| chr19:53922078 | T | TC | 20 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0077 others(17): Show |
20 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.424+6573_424+6574i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922078 | |||||||
| chr19:53922078 | TATTGGTG others(21): Show |
T | 1 | a0001c0001t0001g0098 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.424+6587_424+6614d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922078 | ||||||
| chr19:53922083 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6578G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922083 | |||||||
| chr19:53922091 | GT | G | 19 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0077 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6587delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922091 | |||||||
| chr19:53922092 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.424+6587T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922092 | |||||||
| chr19:53922092 | TC | T | 4 | a0001c0001t0001g0002 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
4 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6591delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922092 | ||||||
| chr19:53922099 | GC | G | 8 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 others(5): Show |
8 | HG01070.hp2 HG01884.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6596delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922099 | ||||||
| chr19:53922100 | C | CCTGGTCA others(20): Show |
1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6614_424+6615i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922100 | ||||||
| chr19:53922100 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0080 others(3): Show |
6 | HG01109.hp2 HG01952.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6595C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922100 | |||||||
| chr19:53922105 | TCATTGGT others(101): Show |
T | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+6601_424+6708d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922105 | |||||||
| chr19:53922107 | A | T | 1 | a0001c0001t0002g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.424+6602A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922107 | |||||||
| chr19:53922119 | G | GT | 6 | a0001c0001t0001g0115 a0001c0001t0001g0206 a0001c0001t0002g0310 others(3): Show |
6 | HG02818.hp1 HG03195.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6614_424+6615i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922119 | |||||||
| chr19:53922119 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG03516.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.424+6614G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922119 | |||||||
| chr19:53922120 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+6615C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922120 | |||||||
| chr19:53922123 | C | CAGGTCTG others(234): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6621_424+6622i others(243): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922123 | ||||||
| chr19:53922127 | C | T | 24 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0042 others(21): Show |
24 | HG01070.hp2 HG01109.hp2 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+6622C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922127 | |||||||
| chr19:53922127 | CCTGGTCA others(1019): Show |
C | 1 | a0001c0001t0001g0141 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.424+6646_424+7671d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922127 | ||||||
| chr19:53922132 | TC | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 others(6): Show |
9 | HG01070.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+6628delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922132 | |||||||
| chr19:53922141 | GAGTTGTC others(509): Show |
G | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+6646_424+7161d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922141 | ||||||
| chr19:53922143 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6638G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922143 | |||||||
| chr19:53922146 | GT | G | 4 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0002g0310 others(1): Show |
4 | HG01496.hp2 HG02818.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+6642delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922146 | |||||||
| chr19:53922147 | TC | T | 15 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(12): Show |
15 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6646delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922147 | ||||||
| chr19:53922153 | G | GGCCTGGT others(19): Show |
1 | a0001c0001t0001g0006 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.424+6649_424+6650i others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922153 | ||||||
| chr19:53922154 | GT | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0069 others(34): Show |
38 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.424+6650delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922154 | |||||||
| chr19:53922155 | T | C | 3 | a0001c0001t0001g0328 a0001c0001t0002g0310 a0001c0001t0010g0233 |
3 | HG02818.hp1 HG03669.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.424+6650T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922155 | |||||||
| chr19:53922155 | T | G | 1 | a0001c0001t0001g0006 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.424+6650T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922155 | |||||||
| chr19:53922169 | GAGTTGTC others(101): Show |
G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 |
3 | HG01993.hp2 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.424+6670_424+6777d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922169 | ||||||
| chr19:53922171 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6666G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922171 | |||||||
| chr19:53922174 | GTCCCAGG others(46): Show |
G | 3 | a0001c0001t0003g0033 a0001c0001t0003g0034 a0001c0001t0003g0035 |
3 | HG01884.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+6670_424+6722d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922174 | |||||||
| chr19:53922174 | GTCCCAGG others(74): Show |
G | 1 | a0001c0001t0002g0038 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.424+6670_424+6750d others(83): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922174 | |||||||
| chr19:53922175 | T | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0273 a0001c0001t0001g0329 others(2): Show |
5 | HG01496.hp2 HG02647.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6670T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922175 | |||||||
| chr19:53922175 | T | TC | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6673dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922175 | ||||||
| chr19:53922175 | T | TCCCCAGG others(49): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6673_424+6674i others(58): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922175 | ||||||
| chr19:53922175 | TCCCAGGC others(18): Show |
T | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+6674_424+6698d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922175 | ||||||
| chr19:53922181 | G | GC | 11 | a0001c0001t0001g0011 a0001c0001t0001g0191 a0001c0001t0001g0195 others(8): Show |
11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6677dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922181 | ||||||
| chr19:53922181 | G | GT | 3 | a0001c0001t0001g0273 a0001c0001t0002g0310 a0001c0001t0003g0032 |
3 | HG02647.hp2 HG02818.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.424+6676_424+6677i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922181 | |||||||
| chr19:53922181 | GCTGGTCA others(20): Show |
G | 1 | a0001c0001t0001g0016 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.424+6682_424+6708d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922181 | ||||||
| chr19:53922186 | TC | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(8): Show |
11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6682delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922186 | |||||||
| chr19:53922187 | C | CATTGGTG others(19): Show |
21 | a0001c0001t0001g0102 a0001c0001t0001g0112 a0001c0001t0001g0114 others(18): Show |
21 | HG00438.hp1 HG00597.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.424+6696_424+6721d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922187 | ||||||
| chr19:53922195 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6690G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922195 | |||||||
| chr19:53922197 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6692G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922197 | |||||||
| chr19:53922201 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0002g0099 a0001c0001t0007g0075 others(1): Show |
4 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+6696C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922201 | |||||||
| chr19:53922207 | GT | G | 3 | a0001c0001t0001g0073 a0001c0001t0007g0075 a0001c0001t0008g0031 |
3 | HG02145.hp1 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6703delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922207 | |||||||
| chr19:53922207 | GTCTGGTA others(103): Show |
G | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6703_424+6812d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922207 | |||||||
| chr19:53922207 | GTCTGGTA others(294): Show |
G | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.424+6703_424+7003d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922207 | |||||||
| chr19:53922213 | T | TATTGGTG others(21): Show |
1 | a0001c0001t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.424+6744_424+6771d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922213 | ||||||
| chr19:53922213 | T | TC | 13 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(10): Show |
13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6708_424+6709i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | |||||||
| chr19:53922213 | T | TCATTGGT others(47): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6708_424+6709i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | |||||||
| chr19:53922213 | T | TCATTGGT others(101): Show |
1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+6708_424+6709i others(110): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | |||||||
| chr19:53922213 | T | TCATTGGT others(505): Show |
1 | a0001c0001t0001g0329 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.424+6708_424+6709i others(514): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922213 | |||||||
| chr19:53922213 | TATTGGTG others(21): Show |
T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0335 |
2 | NA18953.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.424+6744_424+6771d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922213 | ||||||
| chr19:53922221 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6716G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922221 | |||||||
| chr19:53922226 | GT | G | 9 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0080 others(6): Show |
9 | HG01109.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6722delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922226 | |||||||
| chr19:53922227 | T | G | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6722T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922227 | |||||||
| chr19:53922227 | TC | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6726delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922227 | ||||||
| chr19:53922228 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6723C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922228 | |||||||
| chr19:53922235 | T | C | 12 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0191 others(9): Show |
12 | HG01109.hp2 HG01934.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+6730T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922235 | |||||||
| chr19:53922240 | TC | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0180 others(5): Show |
8 | HG02145.hp1 HG03669.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6736delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922240 | |||||||
| chr19:53922249 | G | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0074 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+6744G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922249 | |||||||
| chr19:53922249 | G | T | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6744G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922249 | |||||||
| chr19:53922254 | GT | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0069 others(55): Show |
61 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.424+6750delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922254 | |||||||
| chr19:53922254 | GTCCCCAG others(48): Show |
G | 42 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0028 others(39): Show |
43 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.424+6750_424+6804d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922254 | |||||||
| chr19:53922254 | GTCCCCAG others(132): Show |
G | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6750_424+6888d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922254 | |||||||
| chr19:53922255 | TC | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0208 a0001c0001t0001g0329 others(3): Show |
6 | HG01496.hp2 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6754delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922255 | ||||||
| chr19:53922263 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6758T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922263 | |||||||
| chr19:53922263 | T | TCTGGTAT others(126): Show |
1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+6763_424+6764i others(135): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922263 | ||||||
| chr19:53922269 | CATTGGTG others(19): Show |
C | 3 | a0001c0001t0001g0206 a0001c0001t0006g0343 a0001c0001t0014g0207 |
3 | HG03195.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.424+6772_424+6797d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922269 | ||||||
| chr19:53922277 | C | G | 16 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0077 others(13): Show |
16 | HG01109.hp2 HG01496.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+6772C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922277 | |||||||
| chr19:53922277 | CAGTTGCC others(19): Show |
C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0173 others(45): Show |
51 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.424+6778_424+6803d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922277 | ||||||
| chr19:53922277 | CAGTTGCC others(75): Show |
C | 1 | a0001c0001t0004g0346 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.424+6778_424+6859d others(84): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922277 | ||||||
| chr19:53922282 | G | GT | 13 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0113 others(10): Show |
13 | HG01070.hp2 HG01109.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6777_424+6778i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922282 | |||||||
| chr19:53922282 | GCCCCAGG others(20): Show |
G | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6791_424+6817d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922282 | ||||||
| chr19:53922283 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0208 |
3 | HG02559.hp2 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6778C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922283 | |||||||
| chr19:53922290 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0003g0032 |
3 | HG02559.hp2 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6785T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922290 | |||||||
| chr19:53922292 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.424+6787T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922292 | |||||||
| chr19:53922295 | T | TC | 29 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(26): Show |
29 | HG00597.hp1 HG01070.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.424+6790_424+6791i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922295 | |||||||
| chr19:53922295 | T | TCATTGGT others(155): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6790_424+6791i others(164): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922295 | |||||||
| chr19:53922295 | TATTGGTG others(21): Show |
T | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6812_424+6839d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922295 | ||||||
| chr19:53922303 | G | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(16): Show |
19 | HG00597.hp1 HG01993.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.424+6798G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922303 | |||||||
| chr19:53922308 | GT | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+6804delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922308 | |||||||
| chr19:53922309 | T | TCCCAGGC others(99): Show |
1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+6807_424+6808i others(108): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922309 | ||||||
| chr19:53922309 | TCCCCAGG others(1367): Show |
T | 1 | a0001c0001t0001g0250 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.424+6808_424+8181d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922309 | ||||||
| chr19:53922317 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0002g0038 others(3): Show |
6 | HG01070.hp2 HG01884.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+6812T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922317 | |||||||
| chr19:53922317 | T | TCTGGTCA others(21): Show |
1 | a0001c0001t0002g0319 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.424+6892_424+6919d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922317 | ||||||
| chr19:53922317 | TCTGGTCA others(21): Show |
T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(27): Show |
31 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.424+6892_424+6919d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922317 | ||||||
| chr19:53922321 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6816G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922321 | |||||||
| chr19:53922322 | TC | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
17 | HG00323.hp1 HG00597.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.424+6818delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922322 | |||||||
| chr19:53922331 | G | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0028 others(40): Show |
44 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.424+6826G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922331 | |||||||
| chr19:53922331 | G | GAGTTGCC others(20): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+6831_424+6832i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922331 | ||||||
| chr19:53922333 | G | A | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+6828G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922333 | |||||||
| chr19:53922333 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6828G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922333 | |||||||
| chr19:53922336 | GT | G | 3 | a0001c0001t0001g0232 a0001c0001t0015g0041 a0001c0001t0019g0277 |
3 | HG02109.hp1 NA20905.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+6832delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922336 | |||||||
| chr19:53922337 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6832T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922337 | |||||||
| chr19:53922337 | TC | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6836delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922337 | ||||||
| chr19:53922340 | C | CAGGTCTG others(46): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6835_424+6836i others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922340 | |||||||
| chr19:53922345 | C | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0028 others(53): Show |
57 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.424+6840C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922345 | |||||||
| chr19:53922350 | TC | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0010g0233 |
3 | HG01109.hp2 HG03579.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.424+6846delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922350 | |||||||
| chr19:53922359 | G | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG02109.hp1 HG02258.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+6854G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922359 | |||||||
| chr19:53922361 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6856G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922361 | |||||||
| chr19:53922364 | G | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+6859G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922364 | |||||||
| chr19:53922364 | GT | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0115 others(2): Show |
5 | HG02559.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6860delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922364 | |||||||
| chr19:53922365 | TC | T | 5 | a0001c0001t0001g0328 a0001c0001t0002g0038 a0001c0001t0003g0033 others(2): Show |
5 | HG01070.hp2 HG01884.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+6864delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922365 | ||||||
| chr19:53922373 | C | T | 13 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0077 others(10): Show |
13 | HG01070.hp2 HG01109.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+6868C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922373 | |||||||
| chr19:53922373 | CCTGGTCA others(154): Show |
C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0180 |
3 | NA18954.hp2 NA19085.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.424+6888_424+7048d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922373 | ||||||
| chr19:53922378 | TC | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0115 |
3 | HG01109.hp2 HG03579.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.424+6874delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922378 | |||||||
| chr19:53922387 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+6882G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922387 | |||||||
| chr19:53922387 | GAGTTGTC others(263): Show |
G | 3 | a0001c0001t0001g0042 a0001c0001t0003g0036 a0001c0001t0003g0037 |
3 | HG01884.hp2 HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.424+6892_424+7161d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922387 | ||||||
| chr19:53922389 | G | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(24): Show |
28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+6884G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922389 | |||||||
| chr19:53922392 | GT | G | 3 | a0001c0001t0003g0033 a0001c0001t0003g0034 a0001c0001t0003g0035 |
3 | HG01884.hp1 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+6888delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922392 | |||||||
| chr19:53922393 | TC | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0069 others(29): Show |
34 | HG01070.hp2 HG01071.hp1 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+6892delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922393 | ||||||
| chr19:53922400 | GC | G | 5 | a0001c0001t0001g0073 a0001c0001t0001g0208 a0001c0001t0001g0328 others(2): Show |
5 | HG01070.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+6897delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922400 | ||||||
| chr19:53922401 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0069 others(27): Show |
32 | HG01071.hp1 HG01884.hp1 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+6896C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922401 | |||||||
| chr19:53922406 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0212 a0001c0001t0001g0215 others(13): Show |
18 | HG02074.hp1 HG02083.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+6901T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922406 | |||||||
| chr19:53922417 | G | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0074 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+6912G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922417 | |||||||
| chr19:53922421 | T | C | 9 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+6916T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922421 | |||||||
| chr19:53922421 | T | TC | 16 | a0001c0001t0001g0115 a0001c0001t0001g0191 a0001c0001t0001g0195 others(13): Show |
16 | HG01934.hp1 HG01978.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+6919dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922421 | ||||||
| chr19:53922427 | GT | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0206 others(23): Show |
28 | HG00323.hp1 HG01071.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+6923delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922427 | |||||||
| chr19:53922428 | T | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0209 a0001c0001t0002g0169 others(4): Show |
7 | HG01993.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+6923T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922428 | |||||||
| chr19:53922433 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | NA18747.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.424+6928T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922433 | |||||||
| chr19:53922448 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0212 others(20): Show |
25 | HG01993.hp2 HG02074.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.424+6943T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922448 | |||||||
| chr19:53922448 | TCCCAGGC others(19): Show |
T | 1 | a0001c0001t0001g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.424+6950_424+6975d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922448 | ||||||
| chr19:53922454 | G | GCTGGTCA others(690): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+6964_424+6965i others(699): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922454 | ||||||
| chr19:53922454 | G | GT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0073 others(25): Show |
30 | HG01071.hp1 HG01993.hp2 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+6949_424+6950i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922454 | |||||||
| chr19:53922454 | GCTGGTCA others(20): Show |
G | 1 | a0001c0001t0001g0108 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.424+6969_424+6995d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922454 | ||||||
| chr19:53922454 | GCTGGTCA others(47): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.424+6969_424+7022d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922454 | ||||||
| chr19:53922470 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+6965G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922470 | |||||||
| chr19:53922470 | G | T | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+6965G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922470 | |||||||
| chr19:53922474 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0209 others(23): Show |
28 | HG01071.hp1 HG01993.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.424+6969C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922474 | |||||||
| chr19:53922479 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+6974G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922479 | |||||||
| chr19:53922480 | GT | G | 6 | a0001c0001t0001g0209 a0001c0001t0001g0328 a0001c0001t0002g0039 others(3): Show |
6 | HG01071.hp1 HG01993.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+6976delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922480 | |||||||
| chr19:53922481 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+6976T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922481 | |||||||
| chr19:53922481 | TCTGGTCA others(422): Show |
T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.424+7023_424+7451d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922481 | ||||||
| chr19:53922486 | T | G | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6981T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922486 | |||||||
| chr19:53922486 | TC | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(8): Show |
11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+6982delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922486 | |||||||
| chr19:53922487 | C | T | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6982C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922487 | |||||||
| chr19:53922497 | G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+6992G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922497 | |||||||
| chr19:53922501 | T | C | 11 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0232 others(8): Show |
11 | HG01071.hp1 HG01109.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+6996T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922501 | |||||||
| chr19:53922501 | T | TC | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+6999dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922501 | ||||||
| chr19:53922501 | TCCCAGGT others(46): Show |
T | 4 | a0001c0001t0002g0038 a0001c0001t0003g0033 a0001c0001t0003g0034 others(1): Show |
4 | HG01070.hp2 HG01884.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+7030_424+7082d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922501 | ||||||
| chr19:53922501 | TCCCAGGT others(287): Show |
T | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7000_424+7293d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922501 | ||||||
| chr19:53922507 | GT | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0073 others(19): Show |
24 | HG01993.hp2 HG02074.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+7003delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922507 | |||||||
| chr19:53922508 | TCTGGTCA others(19): Show |
T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0090 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.424+7023_424+7048d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922508 | ||||||
| chr19:53922522 | G | C | 2 | a0001c0001t0001g0069 a0001c0001t0001g0074 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+7017G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922522 | |||||||
| chr19:53922524 | G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7019G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922524 | |||||||
| chr19:53922528 | T | C | 28 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0069 others(25): Show |
30 | HG01993.hp2 HG02074.hp1 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.424+7023T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922528 | |||||||
| chr19:53922528 | T | TC | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7026dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922528 | ||||||
| chr19:53922532 | A | G | 1 | a0001c0001t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+7027A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922532 | |||||||
| chr19:53922534 | G | GT | 44 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0069 others(41): Show |
46 | HG01071.hp1 HG01175.hp1 HG01934.hp1 others(43): Show |
intron_variant | MODIFIER | c.424+7029_424+7030i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922534 | |||||||
| chr19:53922534 | GCTGGTCA others(396): Show |
G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+7103_424+7505d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922534 | ||||||
| chr19:53922548 | G | C | 13 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(10): Show |
13 | HG01071.hp1 HG01934.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+7043G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922548 | |||||||
| chr19:53922554 | C | T | 31 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0073 others(28): Show |
33 | HG00438.hp2 HG01175.hp1 HG01993.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+7049C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922554 | |||||||
| chr19:53922556 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0074 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+7051C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922556 | |||||||
| chr19:53922560 | GT | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0108 others(2): Show |
5 | HG00438.hp2 HG01993.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+7056delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922560 | |||||||
| chr19:53922562 | CTGGTCAT others(397): Show |
C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+7058_424+7461d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922562 | |||||||
| chr19:53922575 | G | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0073 others(40): Show |
45 | HG01070.hp2 HG01175.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.424+7070G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922575 | |||||||
| chr19:53922575 | G | T | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7070G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922575 | |||||||
| chr19:53922575 | GAGTTGTC others(20): Show |
G | 1 | a0001c0001t0002g0039 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.424+7083_424+7109d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922575 | ||||||
| chr19:53922579 | T | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7074T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922579 | |||||||
| chr19:53922581 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0069 others(40): Show |
45 | HG01070.hp2 HG01175.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.424+7076T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922581 | |||||||
| chr19:53922581 | T | TCCCAGAT others(20): Show |
1 | a0001c0001t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.424+7081_424+7082i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922581 | ||||||
| chr19:53922581 | T | TCCCCAGG others(102): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7079_424+7080i others(111): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922581 | ||||||
| chr19:53922582 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7077C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922582 | |||||||
| chr19:53922588 | A | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0140 others(3): Show |
6 | HG01358.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7083A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922588 | |||||||
| chr19:53922588 | A | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(115): Show |
122 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.424+7083A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922588 | |||||||
| chr19:53922588 | ACTGGTCA others(20): Show |
A | 1 | a0001c0001t0001g0161 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.424+7107_424+7133d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922588 | ||||||
| chr19:53922593 | TC | T | 10 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7089delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922593 | |||||||
| chr19:53922602 | C | CAGTTGCC others(20): Show |
36 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(33): Show |
37 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+7102_424+7103i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922602 | ||||||
| chr19:53922602 | C | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0040 a0001c0001t0001g0067 others(48): Show |
53 | HG00323.hp1 HG01070.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.424+7097C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922602 | |||||||
| chr19:53922608 | T | C | 57 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(54): Show |
59 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.424+7103T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922608 | |||||||
| chr19:53922608 | T | TC | 12 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(9): Show |
12 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+7106dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922608 | ||||||
| chr19:53922608 | T | TCCCAGGC others(21): Show |
1 | a0001c0001t0001g0261 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.424+7134_424+7161d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922608 | ||||||
| chr19:53922608 | TCCCAGGC others(21): Show |
T | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.424+7134_424+7161d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922608 | ||||||
| chr19:53922610 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+7105C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922610 | |||||||
| chr19:53922614 | GC | G | 4 | a0001c0001t0001g0073 a0001c0001t0001g0208 a0001c0001t0001g0252 others(1): Show |
4 | HG00323.hp1 HG02451.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7111delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922614 | ||||||
| chr19:53922614 | GCCTGGTC others(343): Show |
G | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+7111_424+7460d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922614 | ||||||
| chr19:53922615 | C | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
5 | HG02071.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7110C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922615 | |||||||
| chr19:53922615 | C | T | 40 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0069 others(37): Show |
41 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.424+7110C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922615 | |||||||
| chr19:53922629 | C | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(118): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+7124C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922629 | |||||||
| chr19:53922629 | CAGTTGTC others(47): Show |
C | 1 | a0001c0001t0001g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.424+7130_424+7183d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922629 | ||||||
| chr19:53922634 | GT | G | 6 | a0001c0001t0001g0073 a0001c0001t0001g0208 a0001c0001t0001g0252 others(3): Show |
6 | HG00323.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7130delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922634 | |||||||
| chr19:53922635 | TC | T | 53 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(50): Show |
55 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.424+7134delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922635 | ||||||
| chr19:53922639 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7134C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922639 | |||||||
| chr19:53922643 | C | T | 7 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0208 others(4): Show |
7 | HG00323.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7138C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922643 | |||||||
| chr19:53922648 | TCATTGGT others(47): Show |
T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0074 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.424+7144_424+7197d others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922648 | |||||||
| chr19:53922652 | T | C | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+7147T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922652 | |||||||
| chr19:53922657 | C | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(118): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+7152C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922657 | |||||||
| chr19:53922659 | G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7154G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922659 | |||||||
| chr19:53922663 | T | A | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7158T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922663 | |||||||
| chr19:53922663 | T | C | 6 | a0001c0001t0001g0073 a0001c0001t0001g0209 a0001c0001t0001g0328 others(3): Show |
6 | HG01993.hp1 HG02451.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7158T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922663 | |||||||
| chr19:53922663 | T | TC | 51 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
53 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+7161dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922663 | ||||||
| chr19:53922664 | CCCAGGCT others(152): Show |
C | 9 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0198 others(6): Show |
9 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+7162_424+7320d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922664 | ||||||
| chr19:53922665 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7160C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922665 | |||||||
| chr19:53922669 | G | GC | 51 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
53 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+7165dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922669 | ||||||
| chr19:53922669 | G | GT | 7 | a0001c0001t0001g0073 a0001c0001t0001g0208 a0001c0001t0001g0252 others(4): Show |
7 | HG00323.hp1 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7164_424+7165i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922669 | |||||||
| chr19:53922670 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7165C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922670 | |||||||
| chr19:53922671 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7166T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922671 | |||||||
| chr19:53922681 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.424+7176T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922681 | |||||||
| chr19:53922683 | G | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0208 a0001c0001t0001g0252 |
3 | HG00323.hp1 HG00438.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.424+7178G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922683 | |||||||
| chr19:53922689 | C | T | 51 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(48): Show |
53 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.424+7184C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922689 | |||||||
| chr19:53922695 | GT | G | 50 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(47): Show |
52 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.424+7191delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922695 | |||||||
| chr19:53922696 | T | C | 2 | a0001c0001t0003g0032 a0001c0001t0010g0233 |
2 | HG02647.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.424+7191T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922696 | |||||||
| chr19:53922701 | TC | T | 3 | a0001c0001t0001g0073 a0001c0001t0002g0310 a0001c0001t0007g0075 |
3 | HG02451.hp2 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+7197delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922701 | |||||||
| chr19:53922705 | T | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0241 others(24): Show |
28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7200T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922705 | |||||||
| chr19:53922712 | G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7207G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922712 | |||||||
| chr19:53922715 | G | GT | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7210_424+7211i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922715 | |||||||
| chr19:53922716 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0130 a0001c0001t0001g0191 others(5): Show |
8 | HG00323.hp1 HG01891.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+7211C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922716 | |||||||
| chr19:53922718 | C | G | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7213C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922718 | |||||||
| chr19:53922720 | AGGTCTGG others(155): Show |
A | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+7217_424+7378d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922720 | ||||||
| chr19:53922723 | T | C | 3 | a0001c0001t0001g0208 a0001c0001t0001g0232 a0001c0001t0001g0252 |
3 | HG00323.hp1 HG02886.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.424+7218T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922723 | |||||||
| chr19:53922723 | TCTGGTCA others(153): Show |
T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7238_424+7397d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922723 | ||||||
| chr19:53922726 | GGTCATTG others(46): Show |
G | 29 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0242 others(26): Show |
30 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+7238_424+7290d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922726 | ||||||
| chr19:53922728 | TC | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7224delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922728 | |||||||
| chr19:53922739 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+7234G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922739 | |||||||
| chr19:53922743 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0070 a0001c0001t0001g0211 others(1): Show |
4 | HG01891.hp1 HG02630.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7238T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922743 | |||||||
| chr19:53922743 | T | TC | 8 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
8 | HG00323.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7241dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922743 | ||||||
| chr19:53922743 | T | TCCCCAGG others(48): Show |
1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7241_424+7242i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922743 | ||||||
| chr19:53922750 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
7 | HG00323.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7245T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922750 | |||||||
| chr19:53922753 | GGTCATTG others(19): Show |
G | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7260_424+7285d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922753 | ||||||
| chr19:53922764 | G | C | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7259G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922764 | |||||||
| chr19:53922765 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0021 others(83): Show |
89 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.424+7260G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922765 | |||||||
| chr19:53922770 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7265T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922770 | |||||||
| chr19:53922770 | T | TC | 7 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7268dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922770 | ||||||
| chr19:53922770 | TCCCAGGC others(289): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7273_424+7568d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922770 | ||||||
| chr19:53922776 | G | GC | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7272dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922776 | ||||||
| chr19:53922776 | G | GT | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(69): Show |
75 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.424+7271_424+7272i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922776 | |||||||
| chr19:53922779 | C | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(82): Show |
88 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.424+7274C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922779 | |||||||
| chr19:53922790 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7285G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922790 | |||||||
| chr19:53922796 | C | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(66): Show |
72 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.424+7291C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922796 | |||||||
| chr19:53922802 | GT | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(65): Show |
71 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.424+7298delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922802 | |||||||
| chr19:53922803 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7298T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922803 | |||||||
| chr19:53922813 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+7308G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922813 | |||||||
| chr19:53922817 | G | C | 1 | a0001c0001t0001g0344 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.424+7312G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922817 | |||||||
| chr19:53922819 | G | A | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7314G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922819 | |||||||
| chr19:53922823 | T | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(72): Show |
78 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.424+7318T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922823 | |||||||
| chr19:53922823 | T | TC | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7321dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922823 | ||||||
| chr19:53922825 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7320C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922825 | |||||||
| chr19:53922829 | GT | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0211 others(1): Show |
4 | HG01109.hp2 HG02647.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7325delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922829 | |||||||
| chr19:53922830 | T | C | 10 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0198 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7325T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922830 | |||||||
| chr19:53922844 | C | G | 52 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0073 others(49): Show |
53 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+7339C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922844 | |||||||
| chr19:53922849 | G | GT | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7344_424+7345i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922849 | |||||||
| chr19:53922850 | C | A | 1 | a0001c0001t0001g0344 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.424+7345C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922850 | |||||||
| chr19:53922850 | C | T | 43 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0195 others(40): Show |
44 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.424+7345C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922850 | |||||||
| chr19:53922852 | C | T | 1 | a0001c0001t0001g0344 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.424+7347C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922852 | |||||||
| chr19:53922853 | C | G | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7348C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922853 | |||||||
| chr19:53922857 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
7 | HG01109.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7352T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922857 | |||||||
| chr19:53922857 | T | TCTGGTAT others(1547): Show |
1 | a0001c0001t0001g0211 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.424+7357_424+7358i others(1556): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922857 | ||||||
| chr19:53922857 | T | TCTGGTAT others(597): Show |
1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7357_424+7358i others(606): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922857 | ||||||
| chr19:53922857 | TCTGGTCA others(19): Show |
T | 2 | a0001c0001t0001g0209 a0001c0001t0005g0107 |
2 | HG01993.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.424+7372_424+7397d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922857 | ||||||
| chr19:53922862 | TC | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7358delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922862 | |||||||
| chr19:53922871 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.424+7366G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922871 | |||||||
| chr19:53922871 | GAGTTGAC others(154): Show |
G | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+7372_424+7532d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922871 | ||||||
| chr19:53922873 | G | C | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7368G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922873 | |||||||
| chr19:53922877 | A | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(7): Show |
10 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+7372A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922877 | |||||||
| chr19:53922877 | A | T | 42 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0195 others(39): Show |
43 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.424+7372A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922877 | |||||||
| chr19:53922879 | T | C | 51 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0073 others(48): Show |
52 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.424+7374T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922879 | |||||||
| chr19:53922879 | TCAGGCTG others(46): Show |
T | 1 | a0001c0001t0001g0130 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.424+7379_424+7431d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922879 | ||||||
| chr19:53922880 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.424+7375C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922880 | |||||||
| chr19:53922883 | G | GC | 15 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0265 others(12): Show |
15 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.424+7379dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922883 | ||||||
| chr19:53922883 | G | GT | 10 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
10 | HG00323.hp1 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+7378_424+7379i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922883 | |||||||
| chr19:53922888 | TC | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7384delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922888 | |||||||
| chr19:53922898 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7393A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922898 | |||||||
| chr19:53922902 | G | GT | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7397_424+7398i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922902 | |||||||
| chr19:53922903 | C | T | 4 | a0001c0001t0001g0208 a0001c0001t0001g0211 a0001c0001t0001g0232 others(1): Show |
4 | HG00323.hp1 HG02886.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+7398C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922903 | |||||||
| chr19:53922909 | GC | G | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0232 others(1): Show |
4 | HG00323.hp1 HG01993.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7406delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922909 | ||||||
| chr19:53922910 | C | T | 47 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0080 others(44): Show |
48 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.424+7405C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922910 | |||||||
| chr19:53922915 | T | C | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+7410T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922915 | |||||||
| chr19:53922924 | G | C | 1 | a0001c0001t0003g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7419G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922924 | |||||||
| chr19:53922930 | T | C | 82 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(79): Show |
85 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.424+7425T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922930 | |||||||
| chr19:53922930 | TCCCAGGT others(20): Show |
T | 1 | a0001c0001t0001g0140 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.424+7452_424+7478d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922930 | ||||||
| chr19:53922936 | GT | G | 3 | a0001c0001t0001g0211 a0001c0001t0003g0032 a0001c0001t0010g0233 |
3 | HG02647.hp2 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+7432delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922936 | |||||||
| chr19:53922937 | T | C | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7432T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922937 | |||||||
| chr19:53922937 | T | TCTGGTCA others(19): Show |
11 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(8): Show |
12 | HG02055.hp1 HG02257.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+7451_424+7452i others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922937 | ||||||
| chr19:53922944 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.424+7439A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922944 | |||||||
| chr19:53922951 | G | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7446G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922951 | |||||||
| chr19:53922952 | AGTTGCCC others(236): Show |
A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7452_424+7694d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922952 | ||||||
| chr19:53922956 | G | GT | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(75): Show |
81 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.424+7451_424+7452i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922956 | |||||||
| chr19:53922957 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7452C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922957 | |||||||
| chr19:53922957 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7452C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922957 | |||||||
| chr19:53922959 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7454C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922959 | |||||||
| chr19:53922969 | TC | T | 66 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(63): Show |
69 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.424+7465delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922969 | |||||||
| chr19:53922978 | G | A | 1 | a0001c0001t0010g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.424+7473G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922978 | |||||||
| chr19:53922984 | T | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7479T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922984 | |||||||
| chr19:53922984 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0003g0030 |
2 | HG03041.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.424+7479T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922984 | |||||||
| chr19:53922984 | T | TC | 71 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(68): Show |
74 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.424+7482dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922984 | ||||||
| chr19:53922984 | TCCCAGGA others(19): Show |
T | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7483_424+7508d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922984 | ||||||
| chr19:53922984 | TCCCAGGA others(368): Show |
T | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+7483_424+7857d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53922984 | ||||||
| chr19:53922985 | C | G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+7480C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922985 | |||||||
| chr19:53922986 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7481C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922986 | |||||||
| chr19:53922990 | GA | G | 37 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0073 others(34): Show |
38 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.424+7486delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922990 | |||||||
| chr19:53922991 | A | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0003g0030 |
3 | HG01109.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7486A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922991 | |||||||
| chr19:53922991 | A | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(83): Show |
89 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.424+7486A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922991 | |||||||
| chr19:53922996 | TC | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(66): Show |
72 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.424+7492delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53922996 | |||||||
| chr19:53923005 | C | G | 111 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(108): Show |
115 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.424+7500C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923005 | |||||||
| chr19:53923007 | G | GT | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0101 others(50): Show |
56 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.424+7504dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923007 | ||||||
| chr19:53923010 | G | GT | 18 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0077 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.424+7505_424+7506i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923010 | |||||||
| chr19:53923010 | G | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0101 others(50): Show |
56 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.424+7505G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923010 | |||||||
| chr19:53923011 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0005g0107 |
2 | HG04115.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.424+7506C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923011 | |||||||
| chr19:53923018 | C | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0285 |
2 | NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.424+7513C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923018 | |||||||
| chr19:53923018 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(89): Show |
95 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.424+7513C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923018 | |||||||
| chr19:53923023 | TC | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(70): Show |
76 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(73): Show |
intron_variant | MODIFIER | c.424+7519delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923023 | |||||||
| chr19:53923026 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+7521T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923026 | |||||||
| chr19:53923032 | C | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(123): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.424+7527C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923032 | |||||||
| chr19:53923037 | G | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7532G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923037 | |||||||
| chr19:53923038 | T | C | 33 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0080 others(30): Show |
34 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+7533T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923038 | |||||||
| chr19:53923038 | T | TC | 78 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(75): Show |
81 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.424+7536dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923038 | ||||||
| chr19:53923041 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0003g0032 |
2 | HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+7536C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923041 | |||||||
| chr19:53923045 | C | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0073 others(42): Show |
46 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.424+7540C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923045 | |||||||
| chr19:53923050 | TC | T | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+7546delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923050 | |||||||
| chr19:53923059 | C | G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(122): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.424+7554C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923059 | |||||||
| chr19:53923064 | GT | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0241 a0001c0001t0001g0329 |
3 | HG01496.hp2 HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7560delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923064 | |||||||
| chr19:53923065 | TC | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(60): Show |
66 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.424+7564delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923065 | ||||||
| chr19:53923073 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(100): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.424+7568C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923073 | |||||||
| chr19:53923073 | CCTGGTCA others(19): Show |
C | 1 | a0001c0001t0001g0261 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.424+7588_424+7613d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923073 | ||||||
| chr19:53923078 | T | C | 6 | a0001c0001t0001g0079 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG02155.hp2 NA18961.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7573T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923078 | |||||||
| chr19:53923078 | TC | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(29): Show |
33 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.424+7574delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923078 | |||||||
| chr19:53923087 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.424+7582G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923087 | |||||||
| chr19:53923092 | G | T | 1 | a0001c0001t0003g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.424+7587G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923092 | |||||||
| chr19:53923093 | T | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7588T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923093 | |||||||
| chr19:53923093 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7588T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923093 | |||||||
| chr19:53923093 | T | TC | 33 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0173 others(30): Show |
34 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+7591dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923093 | ||||||
| chr19:53923095 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7590C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923095 | |||||||
| chr19:53923099 | G | GCTGGTCA others(20): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+7602_424+7603i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923099 | ||||||
| chr19:53923099 | G | GT | 42 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0077 others(39): Show |
43 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.424+7594_424+7595i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923099 | |||||||
| chr19:53923099 | GCTGGTCA others(20): Show |
G | 12 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0196 others(9): Show |
12 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+7641_424+7667d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923099 | ||||||
| chr19:53923102 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7597G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923102 | |||||||
| chr19:53923104 | TC | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(29): Show |
33 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.424+7600delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923104 | |||||||
| chr19:53923113 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7608G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923113 | |||||||
| chr19:53923113 | GAGTTGCC others(530): Show |
G | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+7641_424+8177d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923113 | ||||||
| chr19:53923115 | G | GT | 31 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7612dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923115 | ||||||
| chr19:53923118 | G | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7613G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923118 | |||||||
| chr19:53923119 | C | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(4): Show |
7 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7614C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923119 | |||||||
| chr19:53923125 | GT | G | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+7621delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923125 | |||||||
| chr19:53923126 | T | C | 4 | a0001c0001t0001g0042 a0001c0001t0001g0241 a0001c0001t0001g0329 others(1): Show |
4 | HG01496.hp2 HG01891.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+7621T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923126 | |||||||
| chr19:53923131 | TC | T | 36 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0069 others(33): Show |
37 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+7627delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923131 | |||||||
| chr19:53923145 | G | GT | 35 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0073 others(32): Show |
36 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.424+7640_424+7641i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923145 | |||||||
| chr19:53923146 | C | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0022 others(13): Show |
16 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+7641C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923146 | |||||||
| chr19:53923149 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7644C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923149 | |||||||
| chr19:53923153 | T | C | 33 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0080 others(30): Show |
34 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.424+7648T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923153 | |||||||
| chr19:53923168 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+7663A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923168 | |||||||
| chr19:53923172 | G | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7667G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923172 | |||||||
| chr19:53923173 | T | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0095 others(61): Show |
65 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.424+7668T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923173 | |||||||
| chr19:53923173 | T | TC | 9 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(6): Show |
9 | HG01109.hp2 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+7671dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923173 | ||||||
| chr19:53923173 | TCCCAGGT others(46): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7690_424+7742d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923173 | ||||||
| chr19:53923175 | C | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0043 a0001c0001t0001g0044 others(23): Show |
27 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.424+7670C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923175 | |||||||
| chr19:53923179 | GTCTGGTC others(290): Show |
G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0212 a0001c0001t0001g0230 others(2): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7675_424+7971d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923179 | |||||||
| chr19:53923180 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0077 a0001c0001t0001g0080 |
3 | HG01109.hp2 HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7675T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923180 | |||||||
| chr19:53923183 | GGTCATTG others(19): Show |
G | 1 | a0001c0001t0002g0319 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.424+7690_424+7715d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923183 | ||||||
| chr19:53923185 | TC | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7681delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923185 | |||||||
| chr19:53923185 | TCATTGGT others(154): Show |
T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7681_424+7841d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923185 | |||||||
| chr19:53923195 | G | A | 119 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(116): Show |
121 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.424+7690G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923195 | |||||||
| chr19:53923200 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0003g0032 |
2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+7695T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923200 | |||||||
| chr19:53923206 | G | GT | 8 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
8 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7701_424+7702i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923206 | |||||||
| chr19:53923209 | C | G | 116 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(113): Show |
118 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.424+7704C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923209 | |||||||
| chr19:53923220 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7715G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923220 | |||||||
| chr19:53923226 | C | T | 3 | a0001c0001t0001g0211 a0001c0001t0010g0233 a0001c0001t0015g0041 |
3 | HG03669.hp2 HG03834.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+7721C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923226 | |||||||
| chr19:53923232 | GTCTGGTC others(210): Show |
G | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7728_424+7944d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923232 | |||||||
| chr19:53923233 | TCTGGTCA others(262): Show |
T | 1 | a0001c0001t0001g0328 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.424+7748_424+8016d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923233 | ||||||
| chr19:53923238 | TC | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7734delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923238 | |||||||
| chr19:53923243 | G | A | 44 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0193 others(41): Show |
45 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+7738G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923243 | |||||||
| chr19:53923247 | G | C | 2 | a0001c0001t0001g0021 a0001c0001t0003g0032 |
2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.424+7742G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923247 | |||||||
| chr19:53923252 | GTCCCAGG others(182): Show |
G | 1 | a0001c0001t0002g0278 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.424+7748_424+7936d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923252 | |||||||
| chr19:53923253 | T | C | 34 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0173 others(31): Show |
35 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.424+7748T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923253 | |||||||
| chr19:53923253 | T | TC | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7751dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923253 | ||||||
| chr19:53923260 | T | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7755T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923260 | |||||||
| chr19:53923274 | C | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0042 others(36): Show |
40 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.424+7769C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923274 | |||||||
| chr19:53923274 | CAGTTGCC others(315): Show |
C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7802_424+8123d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923274 | ||||||
| chr19:53923279 | G | GT | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7774_424+7775i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923279 | |||||||
| chr19:53923280 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+7775C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923280 | |||||||
| chr19:53923280 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0242 others(24): Show |
28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7775C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923280 | |||||||
| chr19:53923280 | CCCCAGGT others(262): Show |
C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0101 others(54): Show |
58 | HG00140.hp2 HG00639.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.424+7802_424+8070d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923280 | ||||||
| chr19:53923282 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0003g0032 |
2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.424+7777C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923282 | |||||||
| chr19:53923287 | T | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7782T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923287 | |||||||
| chr19:53923294 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7789A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923294 | |||||||
| chr19:53923301 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7796G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923301 | |||||||
| chr19:53923306 | G | GT | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+7801_424+7802i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923306 | |||||||
| chr19:53923306 | GACTCAGG others(101): Show |
G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7802_424+7909d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923306 | |||||||
| chr19:53923307 | A | C | 9 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0069 others(6): Show |
9 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+7802A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923307 | |||||||
| chr19:53923307 | A | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0208 others(28): Show |
32 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+7802A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923307 | |||||||
| chr19:53923309 | T | C | 40 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0042 others(37): Show |
41 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.424+7804T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923309 | |||||||
| chr19:53923310 | C | T | 1 | a0001c0001t0020g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.424+7805C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923310 | |||||||
| chr19:53923313 | G | GC | 7 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+7809dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923313 | ||||||
| chr19:53923313 | G | GTCTGGTC others(47): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7808_424+7809i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923313 | |||||||
| chr19:53923320 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7815A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923320 | |||||||
| chr19:53923332 | GCCCCAGG others(102): Show |
G | 1 | a0001c0001t0001g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.424+7855_424+7963d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923332 | ||||||
| chr19:53923333 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+7828C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923333 | |||||||
| chr19:53923338 | GGCCTGGT others(155): Show |
G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0232 a0001c0001t0001g0252 |
3 | HG00323.hp1 HG02886.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.424+7835_424+7996d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923338 | ||||||
| chr19:53923340 | C | T | 32 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0069 others(29): Show |
33 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.424+7835C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923340 | |||||||
| chr19:53923360 | C | T | 43 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0073 others(40): Show |
44 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.424+7855C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923360 | |||||||
| chr19:53923366 | GT | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7862delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923366 | |||||||
| chr19:53923366 | GTCTGGTC others(290): Show |
G | 1 | a0001c0001t0020g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.424+7862_424+8158d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923366 | |||||||
| chr19:53923367 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.424+7862T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923367 | |||||||
| chr19:53923370 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+7865G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923370 | |||||||
| chr19:53923372 | TC | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0241 others(2): Show |
5 | HG01496.hp2 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+7868delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923372 | |||||||
| chr19:53923373 | C | CATTGGTG others(20): Show |
10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+7917_424+7943d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923373 | ||||||
| chr19:53923386 | G | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+7881G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923386 | |||||||
| chr19:53923386 | GT | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+7882delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923386 | |||||||
| chr19:53923387 | TC | T | 28 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0191 others(25): Show |
29 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+7886delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923387 | ||||||
| chr19:53923387 | TCCCCAGG others(48): Show |
T | 10 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7886_424+7940d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923387 | ||||||
| chr19:53923400 | T | TC | 43 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0022 others(40): Show |
44 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.424+7895_424+7896i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923400 | |||||||
| chr19:53923408 | G | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0242 others(24): Show |
28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7903G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923408 | |||||||
| chr19:53923413 | G | GTCCCCAG others(20): Show |
3 | a0001c0001t0001g0211 a0001c0001t0002g0310 a0001c0001t0010g0233 |
3 | HG02818.hp1 HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+7934_424+7935i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923413 | ||||||
| chr19:53923413 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0019g0277 |
3 | HG01891.hp1 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+7908G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923413 | |||||||
| chr19:53923413 | GT | G | 28 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0191 others(25): Show |
29 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+7909delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923413 | |||||||
| chr19:53923415 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+7910C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923415 | |||||||
| chr19:53923416 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7911C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923416 | |||||||
| chr19:53923422 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
8 | HG00597.hp1 HG01496.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+7917T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923422 | |||||||
| chr19:53923427 | T | TC | 40 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
41 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.424+7922_424+7923i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923427 | |||||||
| chr19:53923434 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+7929G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923434 | |||||||
| chr19:53923438 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+7933T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923438 | |||||||
| chr19:53923440 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+7935G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923440 | |||||||
| chr19:53923441 | TC | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0173 others(28): Show |
32 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.424+7940delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923441 | ||||||
| chr19:53923445 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0242 others(24): Show |
28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+7940C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923445 | |||||||
| chr19:53923448 | GC | G | 10 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7945delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923448 | ||||||
| chr19:53923449 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+7944C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923449 | |||||||
| chr19:53923449 | C | CCTGGTAT others(20): Show |
1 | a0001c0001t0005g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.424+7949_424+7950i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923449 | ||||||
| chr19:53923449 | C | T | 16 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0022 others(13): Show |
16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+7944C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923449 | |||||||
| chr19:53923454 | TC | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
13 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+7950delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923454 | |||||||
| chr19:53923454 | TCATTGGT others(451): Show |
T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+7950_424+8407d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923454 | |||||||
| chr19:53923456 | A | G | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+7951A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923456 | |||||||
| chr19:53923463 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0191 |
2 | HG01891.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.424+7958G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923463 | |||||||
| chr19:53923469 | T | C | 17 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(14): Show |
17 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+7964T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923469 | |||||||
| chr19:53923469 | T | TC | 44 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
45 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+7967dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923469 | ||||||
| chr19:53923469 | TCCCAGGT others(45): Show |
T | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+7968_424+8019d others(54): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923469 | ||||||
| chr19:53923474 | G | C | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+7969G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923474 | |||||||
| chr19:53923476 | T | C | 44 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(41): Show |
45 | HG00099.hp1 HG00597.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.424+7971T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923476 | |||||||
| chr19:53923492 | G | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0123 others(3): Show |
7 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+7987G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923492 | |||||||
| chr19:53923493 | T | C | 10 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7988T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923493 | |||||||
| chr19:53923496 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0073 others(12): Show |
16 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+7991T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923496 | |||||||
| chr19:53923502 | G | GA | 10 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+7997_424+7998i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923502 | |||||||
| chr19:53923502 | G | GCCTGGTC others(77): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+7998_424+7999i others(86): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923502 | ||||||
| chr19:53923502 | G | GCTGGTCA others(20): Show |
2 | a0001c0001t0001g0211 a0001c0001t0010g0233 |
2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+8017_424+8043d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923502 | ||||||
| chr19:53923502 | G | GT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(13): Show |
16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.424+7997_424+7998i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923502 | |||||||
| chr19:53923502 | G | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0232 a0001c0001t0001g0252 |
3 | HG00323.hp1 HG02886.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.424+7997G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923502 | |||||||
| chr19:53923512 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0212 a0001c0001t0001g0230 others(4): Show |
9 | HG00323.hp1 HG02486.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8007G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923512 | |||||||
| chr19:53923516 | G | C | 11 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+8011G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923516 | |||||||
| chr19:53923518 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8013G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923518 | |||||||
| chr19:53923520 | T | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0123 others(3): Show |
7 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.424+8015T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923520 | |||||||
| chr19:53923521 | G | GT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0111 others(6): Show |
10 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+8016_424+8017i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923521 | |||||||
| chr19:53923522 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(18): Show |
23 | HG00323.hp1 HG01109.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.424+8017C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923522 | |||||||
| chr19:53923528 | GT | G | 8 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(5): Show |
8 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8024delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923528 | |||||||
| chr19:53923529 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0191 a0001c0001t0001g0347 |
3 | HG01891.hp1 HG03209.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.424+8024T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923529 | |||||||
| chr19:53923529 | TCTGGTCA others(154): Show |
T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(3): Show |
6 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8071_424+8231d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923529 | ||||||
| chr19:53923536 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8031A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923536 | |||||||
| chr19:53923543 | G | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0208 a0001c0001t0001g0212 others(5): Show |
10 | HG00323.hp1 HG02486.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+8038G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923543 | |||||||
| chr19:53923546 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.424+8041T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923546 | |||||||
| chr19:53923549 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0020 others(24): Show |
30 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.424+8044T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923549 | |||||||
| chr19:53923552 | C | T | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+8047C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923552 | |||||||
| chr19:53923555 | GT | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8051delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923555 | |||||||
| chr19:53923556 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.424+8051T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923556 | |||||||
| chr19:53923556 | T | C | 13 | a0001c0001t0001g0042 a0001c0001t0001g0191 a0001c0001t0001g0195 others(10): Show |
13 | HG01891.hp1 HG01934.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.424+8051T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923556 | |||||||
| chr19:53923561 | T | G | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8056T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923561 | |||||||
| chr19:53923562 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8057C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923562 | |||||||
| chr19:53923563 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8058A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923563 | |||||||
| chr19:53923564 | T | C | 9 | a0001c0001t0001g0040 a0001c0001t0002g0038 a0001c0001t0002g0039 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8059T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923564 | |||||||
| chr19:53923569 | G | A | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+8064G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923569 | |||||||
| chr19:53923570 | G | C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0241 a0001c0001t0001g0328 others(2): Show |
5 | HG01496.hp2 HG02135.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8065G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923570 | |||||||
| chr19:53923570 | G | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8065G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923570 | |||||||
| chr19:53923572 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8067G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923572 | |||||||
| chr19:53923576 | T | C | 13 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0123 others(10): Show |
14 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.424+8071T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923576 | |||||||
| chr19:53923576 | T | TC | 11 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(8): Show |
11 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+8074dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923576 | ||||||
| chr19:53923576 | TCCCAGGC others(18): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.424+8075_424+8099d others(27): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923576 | ||||||
| chr19:53923576 | TCCCAGGC others(154): Show |
T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0173 a0001c0001t0001g0242 others(24): Show |
28 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.424+8078_424+8238d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923576 | ||||||
| chr19:53923579 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(62): Show |
68 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.424+8074C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923579 | |||||||
| chr19:53923582 | G | GC | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(73): Show |
79 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.424+8078dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923582 | ||||||
| chr19:53923582 | G | GT | 21 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(18): Show |
21 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.424+8077_424+8078i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923582 | |||||||
| chr19:53923582 | G | GTCTGGTC others(76): Show |
1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8077_424+8078i others(85): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923582 | |||||||
| chr19:53923582 | G | GTCTGGTC others(47): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+8077_424+8078i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923582 | |||||||
| chr19:53923596 | G | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0080 a0001c0001t0001g0135 |
3 | HG01109.hp2 HG03579.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8091G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923596 | |||||||
| chr19:53923598 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8093G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923598 | |||||||
| chr19:53923601 | G | GT | 83 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(80): Show |
86 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.424+8096_424+8097i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923601 | |||||||
| chr19:53923602 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0001g0199 others(6): Show |
9 | HG01496.hp2 HG01891.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8097C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923602 | |||||||
| chr19:53923605 | C | T | 4 | a0001c0001t0001g0241 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG01496.hp2 HG02280.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8100C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923605 | |||||||
| chr19:53923608 | GT | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0015g0041 |
3 | HG01891.hp1 NA18950.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+8104delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923608 | |||||||
| chr19:53923609 | T | C | 89 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(86): Show |
92 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.424+8104T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923609 | |||||||
| chr19:53923614 | TC | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8110delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923614 | |||||||
| chr19:53923615 | CATTGGTG others(73): Show |
C | 1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+8111_424+8190d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923615 | |||||||
| chr19:53923619 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0010g0233 |
2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+8114G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923619 | |||||||
| chr19:53923623 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8118G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923623 | |||||||
| chr19:53923629 | T | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(16): Show |
19 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.424+8124T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923629 | |||||||
| chr19:53923629 | T | TC | 5 | a0001c0001t0001g0199 a0001c0001t0001g0241 a0001c0001t0001g0328 others(2): Show |
5 | HG01496.hp2 HG02135.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8127dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923629 | ||||||
| chr19:53923632 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8127C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923632 | |||||||
| chr19:53923635 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8130G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923635 | |||||||
| chr19:53923635 | GT | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(62): Show |
68 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.424+8131delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923635 | |||||||
| chr19:53923635 | GTCTGGTC others(21): Show |
G | 10 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01934.hp1 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+8131_424+8158d others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923635 | |||||||
| chr19:53923636 | T | C | 10 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(7): Show |
10 | HG01496.hp2 HG02135.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8131T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923636 | |||||||
| chr19:53923650 | C | CAGTTGCC others(101): Show |
2 | a0001c0001t0001g0211 a0001c0001t0010g0233 |
2 | HG03669.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.424+8180_424+8181i others(110): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923650 | ||||||
| chr19:53923650 | C | G | 94 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(91): Show |
97 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.424+8145C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923650 | |||||||
| chr19:53923650 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8145C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923650 | |||||||
| chr19:53923652 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8147G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923652 | |||||||
| chr19:53923655 | G | GT | 7 | a0001c0001t0001g0042 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8150_424+8151i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923655 | |||||||
| chr19:53923656 | C | T | 7 | a0001c0001t0001g0241 a0001c0001t0001g0328 a0001c0001t0001g0329 others(4): Show |
7 | HG01496.hp2 HG02280.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8151C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923656 | |||||||
| chr19:53923657 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8152C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923657 | |||||||
| chr19:53923662 | GT | G | 4 | a0001c0001t0001g0241 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG01496.hp2 HG02280.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8158delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923662 | |||||||
| chr19:53923663 | T | C | 7 | a0001c0001t0001g0045 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG00609.hp1 HG02135.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8158T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923663 | |||||||
| chr19:53923676 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8171G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923676 | |||||||
| chr19:53923677 | G | C | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8172G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923677 | |||||||
| chr19:53923683 | T | C | 22 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(19): Show |
22 | HG01109.hp2 HG01496.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.424+8178T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923683 | |||||||
| chr19:53923683 | T | TCCTAGGC others(74): Show |
1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424+8180_424+8181i others(83): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923683 | ||||||
| chr19:53923686 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8181C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923686 | |||||||
| chr19:53923689 | GC | G | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG02135.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8186delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923689 | ||||||
| chr19:53923690 | C | CCTGGTCA others(47): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0080 |
2 | HG01109.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.424+8200_424+8201i others(56): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923690 | ||||||
| chr19:53923690 | C | CCTGGTCA others(102): Show |
2 | a0001c0001t0001g0058 a0001c0001t0016g0060 |
2 | HG02896.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.424+8208_424+8209i others(111): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923690 | ||||||
| chr19:53923690 | C | T | 100 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0020 others(97): Show |
103 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.424+8185C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923690 | |||||||
| chr19:53923695 | TCATTGGT others(48): Show |
T | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+8191_424+8245d others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923695 | |||||||
| chr19:53923705 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8200A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923705 | |||||||
| chr19:53923706 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8201G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923706 | |||||||
| chr19:53923710 | T | C | 13 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(10): Show |
13 | HG01891.hp1 HG02135.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.424+8205T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923710 | |||||||
| chr19:53923710 | T | TCCCCAGG others(75): Show |
8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0059 others(5): Show |
9 | HG02055.hp1 HG02257.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8208_424+8209i others(84): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923710 | ||||||
| chr19:53923717 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0250 a0001c0001t0019g0277 |
3 | HG01952.hp2 HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8212T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923717 | |||||||
| chr19:53923720 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8215G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923720 | |||||||
| chr19:53923733 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8228G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923733 | |||||||
| chr19:53923735 | T | TG | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8231dupG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923735 | ||||||
| chr19:53923737 | C | T | 36 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(33): Show |
37 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+8232C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923737 | |||||||
| chr19:53923743 | GT | G | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
11 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.424+8239delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923743 | |||||||
| chr19:53923754 | G | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0006g0343 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8249G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923754 | |||||||
| chr19:53923758 | G | C | 2 | a0001c0001t0015g0041 a0001c0001t0020g0066 |
2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424+8253G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923758 | |||||||
| chr19:53923764 | C | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+8259C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923764 | |||||||
| chr19:53923771 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8266T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923771 | |||||||
| chr19:53923779 | T | C | 3 | a0001c0001t0004g0062 a0001c0001t0004g0063 a0001c0001t0005g0064 |
3 | HG02055.hp2 HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.424+8274T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923779 | |||||||
| chr19:53923785 | C | G | 49 | a0001c0001t0001g0010 a0001c0001t0001g0042 a0001c0001t0001g0056 others(46): Show |
51 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.424+8280C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923785 | |||||||
| chr19:53923787 | G | C | 3 | a0001c0001t0001g0067 a0001c0001t0003g0032 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8282G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923787 | |||||||
| chr19:53923791 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8286C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923791 | |||||||
| chr19:53923793 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8288C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923793 | |||||||
| chr19:53923812 | G | C | 43 | a0001c0001t0001g0010 a0001c0001t0001g0056 a0001c0001t0001g0057 others(40): Show |
45 | HG00099.hp1 HG00621.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.424+8307G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923812 | |||||||
| chr19:53923817 | G | GT | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8312_424+8313i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923817 | |||||||
| chr19:53923818 | C | A | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8313C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923818 | |||||||
| chr19:53923818 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0347 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8313C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923818 | |||||||
| chr19:53923820 | C | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(73): Show |
79 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.424+8315C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923820 | |||||||
| chr19:53923824 | GT | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0040 others(73): Show |
79 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.424+8320delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923824 | |||||||
| chr19:53923825 | T | C | 29 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(26): Show |
29 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.424+8320T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923825 | |||||||
| chr19:53923825 | T | TCTGGTCA others(20): Show |
8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0059 others(5): Show |
9 | HG02055.hp1 HG02257.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8374_424+8400d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923825 | ||||||
| chr19:53923825 | TCTGGTCA others(20): Show |
T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0136 |
2 | NA18982.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.424+8374_424+8400d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53923825 | ||||||
| chr19:53923839 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8334G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923839 | |||||||
| chr19:53923841 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8336G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923841 | |||||||
| chr19:53923844 | G | GT | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8339_424+8340i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923844 | |||||||
| chr19:53923845 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+8340C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923845 | |||||||
| chr19:53923852 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8347C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923852 | |||||||
| chr19:53923853 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8348C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923853 | |||||||
| chr19:53923866 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8361G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923866 | |||||||
| chr19:53923872 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0347 |
2 | HG03209.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8367C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923872 | |||||||
| chr19:53923874 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8369C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923874 | |||||||
| chr19:53923878 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8373G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923878 | |||||||
| chr19:53923879 | C | T | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
12 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.424+8374C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923879 | |||||||
| chr19:53923893 | G | C | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8388G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923893 | |||||||
| chr19:53923895 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8390G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923895 | |||||||
| chr19:53923899 | C | T | 2 | a0001c0001t0001g0347 a0001c0001t0003g0032 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8394C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923899 | |||||||
| chr19:53923901 | C | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8396C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923901 | |||||||
| chr19:53923906 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8401T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923906 | |||||||
| chr19:53923920 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0347 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8415G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923920 | |||||||
| chr19:53923925 | GT | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0347 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+8421delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923925 | |||||||
| chr19:53923925 | GTCCCCAG others(131): Show |
G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+8421_424+8558d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923925 | |||||||
| chr19:53923930 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8425C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923930 | |||||||
| chr19:53923934 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8429T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923934 | |||||||
| chr19:53923934 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+8429T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923934 | |||||||
| chr19:53923939 | T | TC | 12 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0042 others(9): Show |
12 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+8434_424+8435i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923939 | |||||||
| chr19:53923947 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8442G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923947 | |||||||
| chr19:53923949 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8444G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923949 | |||||||
| chr19:53923961 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8456T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923961 | |||||||
| chr19:53923965 | G | A | 10 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
11 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.424+8460G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923965 | |||||||
| chr19:53923966 | T | TC | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8461_424+8462i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923966 | |||||||
| chr19:53923974 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8469G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923974 | |||||||
| chr19:53923979 | GT | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8475delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923979 | |||||||
| chr19:53923980 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8475T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923980 | |||||||
| chr19:53923981 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8476C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923981 | |||||||
| chr19:53923988 | C | T | 8 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8483C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923988 | |||||||
| chr19:53923993 | TC | T | 3 | a0001c0001t0001g0067 a0001c0001t0003g0032 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8489delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53923993 | |||||||
| chr19:53924002 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8497G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924002 | |||||||
| chr19:53924008 | TC | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8507delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924008 | ||||||
| chr19:53924009 | C | CCGAGGTC others(225): Show |
1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8505_424+8506i others(234): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924009 | ||||||
| chr19:53924012 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8507C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924012 | |||||||
| chr19:53924016 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8511C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924016 | |||||||
| chr19:53924016 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8511C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924016 | |||||||
| chr19:53924030 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0347 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.424+8525G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924030 | |||||||
| chr19:53924032 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8527G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924032 | |||||||
| chr19:53924036 | C | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8531C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924036 | |||||||
| chr19:53924039 | C | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8534C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924039 | |||||||
| chr19:53924043 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8538C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924043 | |||||||
| chr19:53924048 | TC | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8544delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924048 | |||||||
| chr19:53924062 | GT | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0135 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8558delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924062 | |||||||
| chr19:53924071 | T | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8566T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924071 | |||||||
| chr19:53924077 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8572C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924077 | |||||||
| chr19:53924085 | G | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8580G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924085 | |||||||
| chr19:53924087 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0003g0032 |
2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+8582G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924087 | |||||||
| chr19:53924090 | GT | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(14): Show |
17 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+8586delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924090 | |||||||
| chr19:53924099 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8594T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924099 | |||||||
| chr19:53924101 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+8596T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924101 | |||||||
| chr19:53924101 | TG | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8599delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924101 | ||||||
| chr19:53924104 | G | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+8599G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924104 | |||||||
| chr19:53924105 | T | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG01109.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.424+8600T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924105 | |||||||
| chr19:53924113 | G | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8608G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924113 | |||||||
| chr19:53924115 | C | G | 9 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+8610C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924115 | |||||||
| chr19:53924118 | GCCCCAGG others(19): Show |
G | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8614_424+8639d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924118 | |||||||
| chr19:53924118 | GCCCCAGG others(156): Show |
G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02071.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.424+8627_424+8789d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924118 | ||||||
| chr19:53924119 | C | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8614C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924119 | |||||||
| chr19:53924122 | C | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8617C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924122 | |||||||
| chr19:53924126 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8621T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924126 | |||||||
| chr19:53924128 | T | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+8623T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924128 | |||||||
| chr19:53924130 | GT | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8627delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924130 | ||||||
| chr19:53924132 | T | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(122): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.424+8627T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924132 | |||||||
| chr19:53924141 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8636A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924141 | |||||||
| chr19:53924142 | C | G | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8637C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924142 | |||||||
| chr19:53924143 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8638T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924143 | |||||||
| chr19:53924146 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0135 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG03098.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8641C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924146 | |||||||
| chr19:53924148 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8643C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924148 | |||||||
| chr19:53924152 | GT | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+8648delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924152 | |||||||
| chr19:53924156 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8651G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924156 | |||||||
| chr19:53924167 | G | T | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8662G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924167 | |||||||
| chr19:53924171 | TG | T | 4 | a0001c0001t0001g0067 a0001c0001t0001g0135 a0001c0001t0003g0032 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+8668delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924171 | ||||||
| chr19:53924172 | GGT | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8668_424+8669d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924172 | |||||||
| chr19:53924173 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8668G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924173 | |||||||
| chr19:53924174 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0135 |
2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8669T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924174 | |||||||
| chr19:53924180 | GT | G | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8676delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924180 | |||||||
| chr19:53924187 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8682C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924187 | |||||||
| chr19:53924195 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8690G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924195 | |||||||
| chr19:53924195 | G | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(109): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.424+8690G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924195 | |||||||
| chr19:53924196 | A | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8691A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924196 | |||||||
| chr19:53924197 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8692G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924197 | |||||||
| chr19:53924201 | T | C | 6 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG02109.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8696T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924201 | |||||||
| chr19:53924204 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8699C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924204 | |||||||
| chr19:53924207 | GT | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8703delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924207 | |||||||
| chr19:53924208 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8703T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924208 | |||||||
| chr19:53924211 | G | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0122 a0001c0001t0001g0174 |
3 | HG02074.hp2 HG04184.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.424+8706G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924211 | |||||||
| chr19:53924222 | C | G | 8 | a0001c0001t0001g0042 a0001c0001t0001g0067 a0001c0001t0001g0069 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8717C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924222 | |||||||
| chr19:53924228 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8723C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924228 | |||||||
| chr19:53924231 | C | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8726C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924231 | |||||||
| chr19:53924240 | TC | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8736delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924240 | |||||||
| chr19:53924249 | G | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(4): Show |
7 | HG00597.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+8744G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924249 | |||||||
| chr19:53924251 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8746G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924251 | |||||||
| chr19:53924255 | C | A | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8750C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924255 | |||||||
| chr19:53924255 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8750C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924255 | |||||||
| chr19:53924257 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8752C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924257 | |||||||
| chr19:53924261 | G | T | 6 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(3): Show |
6 | HG02451.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8756G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924261 | |||||||
| chr19:53924267 | TC | T | 5 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8763delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924267 | |||||||
| chr19:53924278 | C | G | 20 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(17): Show |
20 | HG00597.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.424+8773C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924278 | |||||||
| chr19:53924281 | T | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(134): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.424+8776T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924281 | |||||||
| chr19:53924282 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8777C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924282 | |||||||
| chr19:53924284 | C | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02071.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.424+8779C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924284 | |||||||
| chr19:53924285 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8780C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924285 | |||||||
| chr19:53924288 | G | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8783G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924288 | |||||||
| chr19:53924289 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0135 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG03098.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8784T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924289 | |||||||
| chr19:53924294 | TC | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8790delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924294 | |||||||
| chr19:53924305 | G | C | 3 | a0001c0001t0001g0067 a0001c0001t0003g0032 a0001c0001t0019g0277 |
3 | HG02109.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.424+8800G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924305 | |||||||
| chr19:53924305 | G | GTTGCCCC others(20): Show |
6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG02258.hp2 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+8806_424+8832d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924305 | ||||||
| chr19:53924312 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8807C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924312 | |||||||
| chr19:53924316 | C | G | 2 | a0001c0001t0001g0320 a0001c0001t0003g0032 |
2 | HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.424+8811C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924316 | |||||||
| chr19:53924316 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.424+8811C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924316 | |||||||
| chr19:53924322 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8817C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924322 | |||||||
| chr19:53924332 | C | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0135 |
2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8827C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924332 | |||||||
| chr19:53924337 | CG | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8833delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924337 | |||||||
| chr19:53924338 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0032 |
3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+8833G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924338 | |||||||
| chr19:53924339 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8834C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924339 | |||||||
| chr19:53924343 | T | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8838T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924343 | |||||||
| chr19:53924359 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8854G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924359 | |||||||
| chr19:53924362 | GTC | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8858_424+8859d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924362 | |||||||
| chr19:53924363 | TCCCCAGG others(680): Show |
T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0136 |
2 | NA18982.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.424+8886_424+9572d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924363 | ||||||
| chr19:53924367 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+8862C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924367 | |||||||
| chr19:53924367 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8862C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924367 | |||||||
| chr19:53924371 | T | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8866T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924371 | |||||||
| chr19:53924387 | G | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8882G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924387 | |||||||
| chr19:53924390 | GT | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8886delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924390 | |||||||
| chr19:53924399 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8894C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924399 | |||||||
| chr19:53924411 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+8906T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924411 | |||||||
| chr19:53924413 | G | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8908G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924413 | |||||||
| chr19:53924415 | G | C | 3 | a0001c0001t0003g0032 a0001c0001t0003g0034 a0001c0001t0003g0035 |
3 | HG02647.hp2 HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8910G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924415 | |||||||
| chr19:53924419 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8914C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924419 | |||||||
| chr19:53924442 | G | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8937G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924442 | |||||||
| chr19:53924443 | T | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8938T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924443 | |||||||
| chr19:53924446 | T | C | 8 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(5): Show |
8 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+8941T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924446 | |||||||
| chr19:53924446 | T | TCCCAGGC others(153): Show |
1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8947_424+8948i others(162): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924446 | ||||||
| chr19:53924452 | GT | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8948delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924452 | |||||||
| chr19:53924467 | G | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8962G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924467 | |||||||
| chr19:53924469 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8964G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924469 | |||||||
| chr19:53924473 | T | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+8968T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924473 | |||||||
| chr19:53924473 | TCCGAGGT others(150): Show |
T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+8971_424+9127d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924473 | ||||||
| chr19:53924476 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.424+8971G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924476 | |||||||
| chr19:53924476 | G | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8971G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924476 | |||||||
| chr19:53924480 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+8975T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924480 | |||||||
| chr19:53924485 | T | TC | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+8980_424+8981i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924485 | |||||||
| chr19:53924498 | GT | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+8994delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924498 | |||||||
| chr19:53924507 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9002C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924507 | |||||||
| chr19:53924513 | T | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9008T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924513 | |||||||
| chr19:53924523 | G | C | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+9018G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924523 | |||||||
| chr19:53924527 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9022C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924527 | |||||||
| chr19:53924533 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9028G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924533 | |||||||
| chr19:53924533 | GT | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9029delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924533 | |||||||
| chr19:53924539 | T | TG | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9034_424+9035i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924539 | |||||||
| chr19:53924548 | A | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9043A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924548 | |||||||
| chr19:53924553 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0032 |
3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9048T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924553 | |||||||
| chr19:53924556 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0032 |
3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9051G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924556 | |||||||
| chr19:53924565 | T | TCATTGGT others(46): Show |
1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9060_424+9061i others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924565 | |||||||
| chr19:53924573 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9068G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924573 | |||||||
| chr19:53924585 | G | GT | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+9080_424+9081i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924585 | |||||||
| chr19:53924590 | TC | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9086delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924590 | |||||||
| chr19:53924601 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9096G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924601 | |||||||
| chr19:53924604 | G | GTCCCAGG others(152): Show |
1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+9099_424+9100i others(161): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924604 | |||||||
| chr19:53924607 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9102C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924607 | |||||||
| chr19:53924608 | A | AG | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9105dupG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924608 | ||||||
| chr19:53924610 | G | GT | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0032 |
3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9105_424+9106i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924610 | |||||||
| chr19:53924616 | C | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9111C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924616 | |||||||
| chr19:53924626 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9121C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924626 | |||||||
| chr19:53924636 | GCTGGTCA others(71): Show |
G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9132_424+9209d others(80): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924636 | |||||||
| chr19:53924639 | G | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+9134G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924639 | |||||||
| chr19:53924642 | C | G | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9137C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924642 | |||||||
| chr19:53924650 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9145G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924650 | |||||||
| chr19:53924651 | A | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9146A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924651 | |||||||
| chr19:53924652 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0003g0032 |
2 | HG01891.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.424+9147G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924652 | |||||||
| chr19:53924656 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0032 |
3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9151T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924656 | |||||||
| chr19:53924659 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0032 |
3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9154G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924659 | |||||||
| chr19:53924668 | T | TC | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0032 |
3 | HG01891.hp1 HG02647.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9163_424+9164i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924668 | |||||||
| chr19:53924674 | T | G | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.424+9169T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924674 | |||||||
| chr19:53924682 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9177C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924682 | |||||||
| chr19:53924703 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9198A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924703 | |||||||
| chr19:53924708 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9203C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924708 | |||||||
| chr19:53924711 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9206C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924711 | |||||||
| chr19:53924714 | T | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0001g0157 others(2): Show |
5 | HG01891.hp1 HG02922.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+9209T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924714 | |||||||
| chr19:53924720 | T | TC | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9215_424+9216i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924720 | |||||||
| chr19:53924741 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9236T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924741 | |||||||
| chr19:53924742 | C | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9237C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924742 | |||||||
| chr19:53924757 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9252C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924757 | |||||||
| chr19:53924763 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9258T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924763 | |||||||
| chr19:53924766 | GGCTGGTC others(19): Show |
G | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9284_424+9309d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924766 | ||||||
| chr19:53924767 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9262G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924767 | |||||||
| chr19:53924783 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9278C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924783 | |||||||
| chr19:53924789 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0135 |
2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9284T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924789 | |||||||
| chr19:53924792 | T | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(127): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.424+9287T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924792 | |||||||
| chr19:53924793 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9288G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924793 | |||||||
| chr19:53924793 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9288G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924793 | |||||||
| chr19:53924800 | A | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9295A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924800 | |||||||
| chr19:53924809 | C | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(3): Show |
6 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9304C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924809 | |||||||
| chr19:53924833 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+9328G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924833 | |||||||
| chr19:53924836 | G | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0042 others(47): Show |
53 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.424+9331G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924836 | |||||||
| chr19:53924843 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9338C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924843 | |||||||
| chr19:53924847 | T | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9342T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924847 | |||||||
| chr19:53924852 | T | G | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9347T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924852 | |||||||
| chr19:53924853 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9348C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924853 | |||||||
| chr19:53924863 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0070 others(51): Show |
57 | HG00140.hp2 HG00323.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.424+9358C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924863 | |||||||
| chr19:53924869 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9364C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924869 | |||||||
| chr19:53924870 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9365C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924870 | |||||||
| chr19:53924871 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9366A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924871 | |||||||
| chr19:53924879 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9374C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924879 | |||||||
| chr19:53924885 | T | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9380T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924885 | |||||||
| chr19:53924887 | T | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0003g0034 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+9382T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924887 | |||||||
| chr19:53924889 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9384C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924889 | |||||||
| chr19:53924917 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(110): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9412T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924917 | |||||||
| chr19:53924920 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9415C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924920 | |||||||
| chr19:53924943 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9438G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924943 | |||||||
| chr19:53924944 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9439T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924944 | |||||||
| chr19:53924947 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0268 |
2 | HG01891.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.424+9442T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924947 | |||||||
| chr19:53924947 | TCCCAGGC others(283): Show |
T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9449_424+9738d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53924947 | ||||||
| chr19:53924959 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0001g0268 |
3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9454G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924959 | |||||||
| chr19:53924961 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.424+9456T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924961 | |||||||
| chr19:53924963 | G | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9458G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924963 | |||||||
| chr19:53924966 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+9461G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924966 | |||||||
| chr19:53924967 | G | C | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9462G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924967 | |||||||
| chr19:53924967 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9462G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924967 | |||||||
| chr19:53924968 | T | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0001g0268 |
3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9463T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924968 | |||||||
| chr19:53924969 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9464G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924969 | |||||||
| chr19:53924973 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0135 |
2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9468T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924973 | |||||||
| chr19:53924976 | G | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9471G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924976 | |||||||
| chr19:53924976 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0001g0268 |
3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9471G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924976 | |||||||
| chr19:53924988 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+9483T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924988 | |||||||
| chr19:53924994 | A | T | 1 | a0001c0001t0001g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9489A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924994 | |||||||
| chr19:53924999 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9494C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53924999 | |||||||
| chr19:53925002 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9497C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925002 | |||||||
| chr19:53925011 | T | TCATTGGT others(48): Show |
1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9506_424+9507i others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925011 | |||||||
| chr19:53925011 | TATTGGTG others(19): Show |
T | 1 | a0001c0001t0001g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.424+9522_424+9547d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925011 | ||||||
| chr19:53925011 | TATTGGTG others(46): Show |
T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(118): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+9516_424+9568d others(55): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925011 | ||||||
| chr19:53925011 | TATTGGTG others(73): Show |
T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9548_424+9627d others(82): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925011 | ||||||
| chr19:53925021 | C | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0218 |
2 | HG00639.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.424+9516C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925021 | |||||||
| chr19:53925025 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9520C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925025 | |||||||
| chr19:53925025 | CCTAGGGC others(72): Show |
C | 1 | a0001c0001t0001g0218 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+9522_424+9600d others(81): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925025 | ||||||
| chr19:53925027 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0135 |
2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9522T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925027 | |||||||
| chr19:53925028 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9523A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925028 | |||||||
| chr19:53925029 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9524G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925029 | |||||||
| chr19:53925031 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.424+9526G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925031 | |||||||
| chr19:53925037 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9532C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925037 | |||||||
| chr19:53925046 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9541A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925046 | |||||||
| chr19:53925047 | C | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0135 a0001c0001t0001g0268 |
3 | HG01891.hp1 HG04204.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.424+9542C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925047 | |||||||
| chr19:53925051 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9546C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925051 | |||||||
| chr19:53925054 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.424+9549C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925054 | |||||||
| chr19:53925085 | TCTGGTCA others(19): Show |
T | 6 | a0001c0001t0001g0132 a0001c0001t0001g0172 a0001c0001t0001g0275 others(3): Show |
6 | HG01168.hp2 HG01261.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.424+9628_424+9653d others(28): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925085 | ||||||
| chr19:53925090 | TC | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(110): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9586delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925090 | |||||||
| chr19:53925101 | C | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(109): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.424+9596C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925101 | |||||||
| chr19:53925104 | G | GC | 112 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(109): Show |
116 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.424+9601dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925104 | ||||||
| chr19:53925107 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(110): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9602T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925107 | |||||||
| chr19:53925111 | G | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(110): Show |
117 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.424+9606G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925111 | |||||||
| chr19:53925153 | CTTGCCCC others(20): Show |
C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9673_424+9699d others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925153 | ||||||
| chr19:53925167 | G | GGTCATTG others(23): Show |
1 | a0001c0001t0001g0091 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.424+9663_424+9692d others(32): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925167 | ||||||
| chr19:53925178 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(143): Show |
151 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.424+9673A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925178 | |||||||
| chr19:53925181 | T | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9676T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925181 | |||||||
| chr19:53925217 | G | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+9712G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925217 | |||||||
| chr19:53925229 | C | T | 4 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0005g0340 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9724C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925229 | |||||||
| chr19:53925230 | G | A | 28 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
29 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(26): Show |
intron_variant | MODIFIER | c.424+9725G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925230 | |||||||
| chr19:53925256 | TG | T | 4 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0036 others(1): Show |
4 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+9753delG | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925256 | ||||||
| chr19:53925271 | T | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9766T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925271 | |||||||
| chr19:53925275 | G | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+9770G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925275 | |||||||
| chr19:53925291 | T | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9786T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925291 | |||||||
| chr19:53925326 | C | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9821C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925326 | |||||||
| chr19:53925336 | G | A | 1 | a0001c0001t0013g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+9831G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925336 | |||||||
| chr19:53925372 | C | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9867C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925372 | |||||||
| chr19:53925394 | G | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9889G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925394 | |||||||
| chr19:53925400 | C | A | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9895C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925400 | |||||||
| chr19:53925406 | C | A | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9901C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925406 | |||||||
| chr19:53925410 | T | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+9905T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925410 | |||||||
| chr19:53925425 | T | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9920T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925425 | |||||||
| chr19:53925451 | C | A | 1 | a0001c0001t0013g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+9946C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925451 | |||||||
| chr19:53925453 | A | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9948A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925453 | |||||||
| chr19:53925454 | C | G | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.424+9949C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925454 | |||||||
| chr19:53925459 | A | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9954A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925459 | |||||||
| chr19:53925463 | C | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9958C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925463 | |||||||
| chr19:53925474 | G | C | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9969G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925474 | |||||||
| chr19:53925484 | G | GCTGGTCA others(20): Show |
121 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(118): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.424+10005_424+1000 others(31): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925484 | ||||||
| chr19:53925484 | G | GCTGGTCA others(20): Show |
4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0006g0343 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+9994_424+9995i others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925484 | ||||||
| chr19:53925500 | C | G | 4 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0003g0034 others(1): Show |
4 | HG02080.hp2 HG02135.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+9995C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925500 | |||||||
| chr19:53925502 | T | TGCCCCAG others(20): Show |
1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+10005_424+1000 others(31): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925502 | ||||||
| chr19:53925504 | C | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0035 |
2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.424+9999C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925504 | |||||||
| chr19:53925526 | G | C | 4 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0003g0034 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+10021G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925526 | |||||||
| chr19:53925530 | T | C | 4 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0003g0034 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+10025T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925530 | |||||||
| chr19:53925536 | G | GCTGGTCA others(46): Show |
2 | a0001c0001t0001g0214 a0001c0001t0001g0231 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.424+10046_424+1004 others(57): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925536 | ||||||
| chr19:53925562 | GT | G | 4 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0003g0034 others(1): Show |
4 | HG02622.hp1 HG02723.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+10058delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925562 | |||||||
| chr19:53925563 | T | TCTGGTCA others(19): Show |
153 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(150): Show |
158 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.424+10070_424+1009 others(30): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925563 | ||||||
| chr19:53925583 | C | CCCCAGGC others(18): Show |
1 | a0001c0001t0001g0191 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.424+10095_424+1009 others(29): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53925583 | ||||||
| chr19:53925599 | G | C | 1 | a0001c0001t0001g0180 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.424+10094G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925599 | |||||||
| chr19:53925614 | G | A | 5 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
5 | HG02027.hp1 HG02083.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+10109G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925614 | |||||||
| chr19:53925616 | T | C | 1 | a0001c0001t0005g0340 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.424+10111T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925616 | |||||||
| chr19:53925666 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+10161C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925666 | |||||||
| chr19:53925678 | G | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+10173G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925678 | |||||||
| chr19:53925726 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.424+10221G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925726 | |||||||
| chr19:53925732 | G | T | 1 | a0001c0001t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.424+10227G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925732 | |||||||
| chr19:53925747 | G | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0329 |
2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.424+10242G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925747 | |||||||
| chr19:53925749 | C | G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+10244C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925749 | |||||||
| chr19:53925791 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.424+10286C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925791 | |||||||
| chr19:53925795 | A | C | 1 | a0001c0001t0002g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.424+10290A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925795 | |||||||
| chr19:53925892 | A | G | 1 | a0001c0001t0001g0047 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.424+10387A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925892 | |||||||
| chr19:53925930 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.424+10425C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925930 | |||||||
| chr19:53925944 | G | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(112): Show |
119 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.424+10439G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925944 | |||||||
| chr19:53925993 | C | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+10488C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53925993 | |||||||
| chr19:53926036 | A | G | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0006g0343 others(1): Show |
4 | HG02886.hp1 HG03195.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+10531A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926036 | |||||||
| chr19:53926151 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0004g0346 |
3 | HG02615.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.424+10646A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926151 | |||||||
| chr19:53926163 | C | G | 1 | a0001c0001t0015g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.424+10658C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926163 | |||||||
| chr19:53926196 | A | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(127): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.424+10691A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926196 | |||||||
| chr19:53926206 | T | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(15): Show |
18 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.424+10701T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926206 | |||||||
| chr19:53926237 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0069 a0001c0001t0001g0073 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+10732G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926237 | |||||||
| chr19:53926276 | A | G | 1 | a0001c0001t0023g0213 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.424+10771A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926276 | |||||||
| chr19:53926401 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0004g0216 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.424+10896C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926401 | |||||||
| chr19:53926435 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0004g0216 |
2 | HG03516.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.424+10930G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926435 | |||||||
| chr19:53926545 | T | G | 15 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0187 others(12): Show |
16 | HG00323.hp2 HG01106.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.424+11040T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926545 | |||||||
| chr19:53926640 | C | T | 1 | a0001c0001t0002g0336 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.424+11135C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926640 | |||||||
| chr19:53926710 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0094 |
2 | NA19064.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.424+11205C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926710 | |||||||
| chr19:53926723 | G | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG00438.hp1 HG02040.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.424+11218G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926723 | |||||||
| chr19:53926750 | T | TA | 10 | a0001c0001t0001g0040 a0001c0001t0002g0038 a0001c0001t0002g0039 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+11250dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53926750 | ||||||
| chr19:53926905 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0004g0346 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.424+11400T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926905 | |||||||
| chr19:53926932 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0004g0346 |
2 | HG02615.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.424+11427G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53926932 | |||||||
| chr19:53927003 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0223 others(6): Show |
10 | HG00140.hp2 HG00323.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.424+11498C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927003 | |||||||
| chr19:53927022 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0098 |
3 | HG02155.hp2 NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.424+11517G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927022 | |||||||
| chr19:53927085 | A | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01243.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.424+11580A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927085 | |||||||
| chr19:53927187 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.424+11682C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927187 | |||||||
| chr19:53927192 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.424+11687T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927192 | |||||||
| chr19:53927200 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(130): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.424+11695G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927200 | |||||||
| chr19:53927215 | G | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(96): Show |
103 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.424+11710G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927215 | |||||||
| chr19:53927275 | T | C | 1 | a0001c0001t0011g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+11770T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927275 | |||||||
| chr19:53927414 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.424+11909C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927414 | |||||||
| chr19:53927425 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(105): Show |
113 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.424+11920C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927425 | |||||||
| chr19:53927510 | A | G | 36 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(33): Show |
37 | HG00597.hp1 HG01256.hp1 HG01258.hp2 others(34): Show |
intron_variant | MODIFIER | c.424+12005A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927510 | |||||||
| chr19:53927575 | C | T | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(102): Show |
110 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.424+12070C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927575 | |||||||
| chr19:53927602 | C | T | 8 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
9 | HG02055.hp1 HG02257.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+12097C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927602 | |||||||
| chr19:53927717 | A | C | 21 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(18): Show |
22 | HG00597.hp1 HG01256.hp1 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.424+12212A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927717 | |||||||
| chr19:53927762 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(126): Show |
133 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.424+12257C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927762 | |||||||
| chr19:53927792 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(101): Show |
108 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.424+12287C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927792 | |||||||
| chr19:53927795 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.424+12290A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927795 | |||||||
| chr19:53927799 | T | C | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.424+12294T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927799 | |||||||
| chr19:53927811 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(77): Show |
82 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.424+12306T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927811 | |||||||
| chr19:53927817 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0040 others(47): Show |
53 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.424+12312A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927817 | |||||||
| chr19:53927838 | C | CA | 88 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0043 others(85): Show |
90 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.424+12348dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927838 | ||||||
| chr19:53927838 | C | CAA | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+12347_424+1234 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927838 | ||||||
| chr19:53927838 | CAAAAAAA others(7): Show |
C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0080 a0001c0001t0001g0095 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+12335_424+1234 others(18): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927838 | ||||||
| chr19:53927840 | A | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+12335A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927840 | |||||||
| chr19:53927841 | A | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+12336A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927841 | |||||||
| chr19:53927845 | A | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.424+12340A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927845 | |||||||
| chr19:53927854 | G | A | 1 | a0001c0001t0013g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.424+12349G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927854 | |||||||
| chr19:53927859 | G | GA | 9 | a0001c0001t0001g0040 a0001c0001t0001g0080 a0001c0001t0001g0095 others(6): Show |
9 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.424+12361dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53927859 | ||||||
| chr19:53927968 | T | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00597.hp1 HG01934.hp1 HG01978.hp1 others(21): Show |
intron_variant | MODIFIER | c.424+12463T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53927968 | |||||||
| chr19:53928007 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0014 others(38): Show |
44 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.424+12502T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928007 | |||||||
| chr19:53928033 | A | G | 97 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(94): Show |
99 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.424+12528A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928033 | |||||||
| chr19:53928039 | G | T | 3 | a0001c0001t0001g0073 a0001c0001t0003g0036 a0001c0001t0007g0075 |
3 | HG01884.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+12534G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928039 | |||||||
| chr19:53928043 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0003g0036 a0001c0001t0007g0075 |
3 | HG01884.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.424+12538G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928043 | |||||||
| chr19:53928062 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(138): Show |
145 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.424+12557A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928062 | |||||||
| chr19:53928073 | GGA | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0015 others(84): Show |
89 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.424+12571_424+1257 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928073 | ||||||
| chr19:53928074 | GA | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(62): Show |
67 | HG00733.hp1 HG00741.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.424+12570delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928074 | |||||||
| chr19:53928077 | A | G | 65 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(62): Show |
67 | HG00733.hp1 HG00741.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.424+12572A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928077 | |||||||
| chr19:53928202 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.424+12697G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928202 | |||||||
| chr19:53928261 | GTATT | G | 17 | a0001c0001t0001g0069 a0001c0001t0001g0197 a0001c0001t0001g0198 others(14): Show |
17 | HG01934.hp1 HG01978.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+12775_424+1277 others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928261 | ||||||
| chr19:53928263 | AT | A | 7 | a0001c0001t0001g0040 a0001c0001t0001g0080 a0001c0001t0001g0095 others(4): Show |
7 | HG01109.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+12761delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928263 | ||||||
| chr19:53928264 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(108): Show |
116 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.424+12759T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928264 | |||||||
| chr19:53928361 | T | TC | 4 | a0001c0001t0001g0080 a0001c0001t0004g0062 a0001c0001t0004g0063 others(1): Show |
4 | HG01109.hp2 HG02055.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.424+12857dupC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928361 | ||||||
| chr19:53928366 | G | A | 1 | a0001c0001t0016g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.424+12861G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928366 | |||||||
| chr19:53928485 | G | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0013g0013 |
3 | HG01070.hp2 HG01071.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.424+12980G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928485 | |||||||
| chr19:53928495 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-12975G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928495 | |||||||
| chr19:53928567 | A | C | 39 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0057 others(36): Show |
39 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.425-12903A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928567 | |||||||
| chr19:53928674 | G | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(157): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.425-12796G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928674 | |||||||
| chr19:53928818 | TA | T | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0021g0076 |
3 | HG01070.hp2 HG01071.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.425-12650delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53928818 | ||||||
| chr19:53928876 | T | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.425-12594T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928876 | |||||||
| chr19:53928877 | G | A | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.425-12593G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928877 | |||||||
| chr19:53928977 | C | T | 2 | a0001c0001t0004g0192 a0001c0001t0011g0341 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-12493C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53928977 | |||||||
| chr19:53929057 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.425-12413T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929057 | |||||||
| chr19:53929058 | G | A | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-12412G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929058 | |||||||
| chr19:53929065 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.425-12405C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929065 | |||||||
| chr19:53929111 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.425-12348_425-1233 others(18): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929111 | ||||||
| chr19:53929117 | AAAAAC | A | 15 | a0001c0001t0001g0092 a0001c0001t0001g0130 a0001c0001t0001g0131 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-12348_425-1234 others(9): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929117 | ||||||
| chr19:53929118 | AAAAC | A | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.425-12348_425-1234 others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929118 | ||||||
| chr19:53929120 | AAC | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0198 a0001c0001t0001g0199 others(9): Show |
12 | HG00621.hp1 HG01934.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-12348_425-1234 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929120 | ||||||
| chr19:53929121 | AC | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0197 a0001c0001t0001g0203 others(1): Show |
4 | HG01978.hp1 HG02109.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-12348delC | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929121 | |||||||
| chr19:53929122 | C | CA | 17 | a0001c0001t0001g0042 a0001c0001t0001g0105 a0001c0001t0001g0146 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.425-12332dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929122 | ||||||
| chr19:53929122 | C | CAAA | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-12334_425-1233 others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929122 | ||||||
| chr19:53929160 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0110 |
2 | NA19000.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.425-12310G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929160 | |||||||
| chr19:53929263 | TGAGAGAG others(7): Show |
T | 35 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(32): Show |
36 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.425-12192_425-1217 others(18): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53929263 | ||||||
| chr19:53929352 | T | C | 35 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(32): Show |
36 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.425-12118T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929352 | |||||||
| chr19:53929467 | A | T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(21): Show |
24 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.425-12003A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929467 | |||||||
| chr19:53929633 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
4 | HG01243.hp2 HG02717.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-11837T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929633 | |||||||
| chr19:53929686 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.425-11784G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929686 | |||||||
| chr19:53929813 | G | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0220 a0001c0001t0008g0031 |
3 | HG02145.hp1 HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.425-11657G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929813 | |||||||
| chr19:53929955 | A | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(216): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.425-11515A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53929955 | |||||||
| chr19:53930074 | C | CA | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(162): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.425-11377dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930074 | ||||||
| chr19:53930074 | C | CAA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(36): Show |
42 | HG00438.hp1 HG00735.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.425-11378_425-1137 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930074 | ||||||
| chr19:53930074 | C | CAAA | 10 | a0001c0001t0001g0012 a0001c0001t0001g0084 a0001c0001t0001g0162 others(7): Show |
10 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.425-11379_425-1137 others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930074 | ||||||
| chr19:53930179 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.425-11291C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930179 | |||||||
| chr19:53930208 | CCA | C | 9 | a0001c0001t0001g0042 a0001c0001t0001g0206 a0001c0001t0001g0214 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-11261_425-1126 others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930208 | |||||||
| chr19:53930210 | A | AT | 20 | a0001c0001t0001g0012 a0001c0001t0001g0024 a0001c0001t0001g0040 others(17): Show |
20 | HG01168.hp2 HG01261.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.425-11247dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930210 | ||||||
| chr19:53930210 | AT | A | 37 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(34): Show |
38 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.425-11247delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930210 | ||||||
| chr19:53930212 | T | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0206 a0001c0001t0001g0214 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-11258T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930212 | |||||||
| chr19:53930249 | C | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-11221C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930249 | |||||||
| chr19:53930312 | A | G | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(26): Show |
30 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.425-11158A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930312 | |||||||
| chr19:53930333 | C | T | 28 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(25): Show |
29 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.425-11137C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930333 | |||||||
| chr19:53930384 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-11086T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930384 | |||||||
| chr19:53930395 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.425-11075C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930395 | |||||||
| chr19:53930467 | GGTACACA others(25): Show |
G | 1 | a0001c0001t0018g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.425-10999_425-1096 others(36): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930467 | ||||||
| chr19:53930497 | C | T | 1 | a0001c0001t0004g0346 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-10973C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930497 | |||||||
| chr19:53930532 | T | C | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(27): Show |
31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-10938T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930532 | |||||||
| chr19:53930662 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.425-10808C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930662 | |||||||
| chr19:53930752 | C | CCCT | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(27): Show |
31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-10716_425-1071 others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53930752 | ||||||
| chr19:53930872 | T | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(232): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.425-10598T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930872 | |||||||
| chr19:53930961 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
8 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-10509C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53930961 | |||||||
| chr19:53931001 | G | C | 1 | a0001c0001t0001g0347 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.425-10469G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931001 | |||||||
| chr19:53931008 | C | A | 2 | a0001c0001t0004g0192 a0001c0001t0011g0341 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-10462C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931008 | |||||||
| chr19:53931234 | A | G | 1 | a0001c0001t0004g0346 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-10236A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931234 | |||||||
| chr19:53931266 | G | A | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(27): Show |
31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-10204G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931266 | |||||||
| chr19:53931398 | C | G | 1 | a0001c0001t0001g0298 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.425-10072C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931398 | |||||||
| chr19:53931453 | G | A | 1 | a0001c0002t0002g0025 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.425-10017G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931453 | |||||||
| chr19:53931462 | A | G | 2 | a0001c0001t0004g0192 a0001c0001t0011g0341 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-10008A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931462 | |||||||
| chr19:53931465 | C | T | 2 | a0001c0001t0004g0192 a0001c0001t0011g0341 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-10005C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931465 | |||||||
| chr19:53931547 | G | T | 1 | a0001c0001t0001g0299 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-9923G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931547 | |||||||
| chr19:53931615 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0018g0271 |
2 | HG00639.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.425-9855G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931615 | |||||||
| chr19:53931684 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.425-9786C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931684 | |||||||
| chr19:53931685 | T | TA | 84 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0021 others(81): Show |
84 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.425-9762dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | ||||||
| chr19:53931685 | T | TAA | 15 | a0001c0001t0001g0020 a0001c0001t0001g0042 a0001c0001t0001g0102 others(12): Show |
15 | HG00639.hp1 HG00673.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.425-9763_425-9762d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | ||||||
| chr19:53931685 | T | TAAA | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(6): Show |
9 | HG00733.hp2 HG01070.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-9764_425-9762d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | ||||||
| chr19:53931685 | TAAAAAAA others(1): Show |
T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-9769_425-9762d others(10): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931685 | ||||||
| chr19:53931710 | A | G | 1 | a0001c0001t0020g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.425-9760A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931710 | |||||||
| chr19:53931723 | C | T | 2 | a0001c0001t0004g0192 a0001c0001t0011g0341 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-9747C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931723 | |||||||
| chr19:53931731 | CACT | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(5): Show |
9 | HG01109.hp2 HG02055.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-9734_425-9732d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931731 | ||||||
| chr19:53931759 | C | CT | 56 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0024 others(53): Show |
57 | HG00639.hp2 HG01123.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.425-9691dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931759 | ||||||
| chr19:53931759 | CT | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
8 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.425-9691delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53931759 | ||||||
| chr19:53931784 | T | C | 2 | a0001c0001t0004g0192 a0001c0001t0011g0341 |
2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.425-9686T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931784 | |||||||
| chr19:53931855 | A | G | 30 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(27): Show |
31 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.425-9615A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931855 | |||||||
| chr19:53931906 | C | T | 1 | a0001c0001t0004g0346 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.425-9564C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931906 | |||||||
| chr19:53931919 | G | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(9): Show |
13 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-9551G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931919 | |||||||
| chr19:53931969 | G | C | 1 | a0001c0001t0021g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425-9501G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53931969 | |||||||
| chr19:53932018 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-9452T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932018 | |||||||
| chr19:53932036 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-9434C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932036 | |||||||
| chr19:53932056 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-9414C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932056 | |||||||
| chr19:53932168 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.425-9302G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932168 | |||||||
| chr19:53932224 | A | G | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
22 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.425-9246A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932224 | |||||||
| chr19:53932252 | T | TA | 14 | a0001c0001t0001g0093 a0001c0001t0001g0108 a0001c0001t0001g0120 others(11): Show |
14 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.425-9198dupA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932252 | ||||||
| chr19:53932252 | TA | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0058 others(10): Show |
13 | HG00323.hp1 HG01099.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-9198delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932252 | ||||||
| chr19:53932252 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0205 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.425-9207_425-9198d others(12): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932252 | ||||||
| chr19:53932260 | A | AG | 4 | a0001c0001t0001g0074 a0001c0001t0001g0212 a0001c0001t0007g0072 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-9210_425-9209i others(3): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932260 | |||||||
| chr19:53932331 | C | T | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(19): Show |
23 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.425-9139C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932331 | |||||||
| chr19:53932466 | C | CTGAGT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
21 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.425-9002_425-8998d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932466 | ||||||
| chr19:53932576 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0236 others(3): Show |
8 | HG00099.hp1 HG02486.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-8894C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932576 | |||||||
| chr19:53932581 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.425-8889T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932581 | |||||||
| chr19:53932636 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8834C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932636 | |||||||
| chr19:53932774 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.425-8696A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932774 | |||||||
| chr19:53932792 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.425-8678G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932792 | |||||||
| chr19:53932830 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8640T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932830 | |||||||
| chr19:53932831 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0068 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-8639C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932831 | |||||||
| chr19:53932834 | C | CT | 16 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0198 others(13): Show |
16 | HG00621.hp1 HG01934.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-8619dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932834 | ||||||
| chr19:53932834 | CT | C | 11 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(8): Show |
12 | HG01109.hp2 HG01168.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.425-8619delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932834 | ||||||
| chr19:53932834 | CTTT | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02145.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-8621_425-8619d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53932834 | ||||||
| chr19:53932865 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.425-8605G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932865 | |||||||
| chr19:53932954 | T | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8516T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932954 | |||||||
| chr19:53932966 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8504C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932966 | |||||||
| chr19:53932968 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0013g0013 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.425-8502C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53932968 | |||||||
| chr19:53933048 | C | T | 1 | a0001c0001t0023g0213 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.425-8422C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933048 | |||||||
| chr19:53933089 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.425-8381T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933089 | |||||||
| chr19:53933110 | A | G | 23 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(20): Show |
24 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.425-8360A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933110 | |||||||
| chr19:53933182 | ACTGCAAC others(16): Show |
A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.425-8263_425-8241d others(25): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933182 | ||||||
| chr19:53933297 | A | AT | 30 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0049 others(27): Show |
30 | HG00544.hp1 HG00673.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.425-8152dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933297 | ||||||
| chr19:53933297 | AT | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0135 a0001c0001t0001g0282 others(3): Show |
6 | HG01099.hp2 HG01261.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-8152delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933297 | ||||||
| chr19:53933297 | ATTT | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-8154_425-8152d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933297 | ||||||
| chr19:53933424 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.425-8046T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933424 | |||||||
| chr19:53933655 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.425-7815G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933655 | |||||||
| chr19:53933661 | A | AT | 10 | a0001c0001t0001g0028 a0001c0001t0001g0197 a0001c0001t0001g0244 others(7): Show |
10 | HG01168.hp1 HG01978.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.425-7794dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933661 | ||||||
| chr19:53933661 | AT | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
10 | HG01243.hp2 HG01516.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-7794delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53933661 | ||||||
| chr19:53933896 | T | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-7574T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53933896 | |||||||
| chr19:53934058 | C | T | 15 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.425-7412C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934058 | |||||||
| chr19:53934196 | T | C | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(19): Show |
23 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.425-7274T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934196 | |||||||
| chr19:53934591 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.425-6879A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934591 | |||||||
| chr19:53934608 | TA | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
13 | HG01099.hp1 HG01243.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-6847delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53934608 | ||||||
| chr19:53934827 | GA | G | 12 | a0001c0001t0001g0016 a0001c0001t0001g0091 a0001c0001t0001g0093 others(9): Show |
12 | HG03669.hp2 HG03831.hp2 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.425-6632delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53934827 | ||||||
| chr19:53934848 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-6622G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934848 | |||||||
| chr19:53934864 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-6606A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53934864 | |||||||
| chr19:53935071 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0002g0039 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.425-6399C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935071 | |||||||
| chr19:53935082 | C | CAT | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.425-6382_425-6381d others(4): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935082 | ||||||
| chr19:53935174 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.425-6296T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935174 | |||||||
| chr19:53935323 | C | CT | 7 | a0001c0001t0001g0050 a0001c0001t0001g0170 a0001c0001t0001g0327 others(4): Show |
7 | HG00544.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-6132dupT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935323 | ||||||
| chr19:53935323 | CT | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0089 a0001c0001t0001g0293 others(3): Show |
6 | HG01099.hp1 HG02015.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-6132delT | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935323 | ||||||
| chr19:53935490 | T | G | 1 | a0001c0001t0001g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.425-5980T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935490 | |||||||
| chr19:53935588 | ACTGGGAT others(311): Show |
A | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.425-5863_425-5546d others(2): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935588 | ||||||
| chr19:53935613 | G | A | 4 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0004g0192 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-5857G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935613 | |||||||
| chr19:53935634 | C | CTTT | 13 | a0001c0001t0001g0045 a0001c0001t0001g0073 a0001c0001t0001g0135 others(10): Show |
13 | HG00609.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.425-5815_425-5813d others(5): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | ||||||
| chr19:53935634 | C | CTTTT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(191): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.425-5816_425-5813d others(6): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | ||||||
| chr19:53935634 | C | CTTTTT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
89 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.425-5817_425-5813d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | ||||||
| chr19:53935634 | C | CTTTTTT | 8 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0070 others(5): Show |
8 | HG01192.hp2 HG01515.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-5818_425-5813d others(8): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53935634 | ||||||
| chr19:53935764 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.425-5706C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935764 | |||||||
| chr19:53935800 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0003g0036 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.425-5670C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935800 | |||||||
| chr19:53935850 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.425-5620A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935850 | |||||||
| chr19:53935962 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.425-5508A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935962 | |||||||
| chr19:53935980 | A | G | 9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(6): Show |
9 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-5490A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935980 | |||||||
| chr19:53935996 | C | T | 2 | a0001c0001t0014g0207 a0001c0001t0019g0277 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.425-5474C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53935996 | |||||||
| chr19:53936031 | C | T | 10 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(7): Show |
11 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.425-5439C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936031 | |||||||
| chr19:53936148 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.425-5322G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936148 | |||||||
| chr19:53936205 | G | C | 1 | a0001c0001t0002g0181 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.425-5265G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936205 | |||||||
| chr19:53936278 | A | G | 7 | a0001c0001t0001g0070 a0001c0001t0001g0220 a0001c0001t0002g0038 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-5192A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936278 | |||||||
| chr19:53936279 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.425-5191G>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936279 | |||||||
| chr19:53936280 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0220 a0001c0001t0002g0038 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-5190G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936280 | |||||||
| chr19:53936429 | C | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0014 others(55): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.425-5041C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936429 | |||||||
| chr19:53936660 | T | G | 5 | a0001c0001t0001g0070 a0001c0001t0001g0220 a0001c0001t0004g0192 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-4810T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936660 | |||||||
| chr19:53936701 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0180 |
2 | NA18954.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.425-4769T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936701 | |||||||
| chr19:53936845 | G | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0080 others(9): Show |
13 | HG01070.hp2 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.425-4625G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936845 | |||||||
| chr19:53936879 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0299 |
2 | HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.425-4591G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936879 | |||||||
| chr19:53936905 | A | C | 1 | a0001c0001t0002g0308 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.425-4565A>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936905 | |||||||
| chr19:53936969 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.425-4501G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53936969 | |||||||
| chr19:53937090 | A | G | 1 | a0001c0001t0025g0106 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425-4380A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937090 | |||||||
| chr19:53937156 | C | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-4314C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937156 | |||||||
| chr19:53937161 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0299 |
2 | HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.425-4309A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937161 | |||||||
| chr19:53937193 | A | G | 1 | a0001c0001t0014g0207 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.425-4277A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937193 | |||||||
| chr19:53937220 | C | T | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.425-4250C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937220 | |||||||
| chr19:53937397 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-4073A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937397 | |||||||
| chr19:53937406 | T | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0220 a0001c0001t0004g0192 others(2): Show |
5 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-4064T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937406 | |||||||
| chr19:53937568 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.425-3902C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937568 | |||||||
| chr19:53937569 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0005g0064 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.425-3901C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937569 | |||||||
| chr19:53937576 | TCCCTC | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.425-3867_425-3863d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53937576 | ||||||
| chr19:53937605 | T | A | 4 | a0001c0001t0002g0118 a0001c0001t0002g0281 a0001c0001t0002g0311 others(1): Show |
4 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-3865T>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937605 | |||||||
| chr19:53937654 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0014g0207 |
2 | HG01109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.425-3816G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937654 | |||||||
| chr19:53937682 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0068 others(2): Show |
5 | HG02055.hp1 HG02257.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.425-3788C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937682 | |||||||
| chr19:53937727 | G | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.425-3743G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937727 | |||||||
| chr19:53937746 | G | A | 1 | a0001c0001t0019g0277 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.425-3724G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937746 | |||||||
| chr19:53937883 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.425-3587G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937883 | |||||||
| chr19:53937946 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.425-3524T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53937946 | |||||||
| chr19:53938074 | T | G | 1 | a0001c0001t0001g0070 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.425-3396T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938074 | |||||||
| chr19:53938145 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.425-3325G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938145 | |||||||
| chr19:53938209 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0237 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.425-3261A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938209 | |||||||
| chr19:53938246 | T | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(314): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.425-3224T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938246 | |||||||
| chr19:53938397 | G | T | 30 | a0001c0001t0001g0042 a0001c0001t0001g0050 a0001c0001t0001g0067 others(27): Show |
30 | HG00621.hp1 HG00673.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.425-3073G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938397 | |||||||
| chr19:53938427 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-3043G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938427 | |||||||
| chr19:53938481 | G | A | 1 | a0001c0001t0021g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.425-2989G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938481 | |||||||
| chr19:53938536 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-2934G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938536 | |||||||
| chr19:53938565 | A | T | 1 | a0001c0001t0009g0163 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.425-2905A>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938565 | |||||||
| chr19:53938804 | C | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0021g0076 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2666C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938804 | |||||||
| chr19:53938847 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.425-2623C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53938847 | |||||||
| chr19:53938947 | TCAAAA | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.425-2502_425-2498d others(7): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53938947 | ||||||
| chr19:53939149 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.425-2321G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939149 | |||||||
| chr19:53939198 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.425-2272C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939198 | |||||||
| chr19:53939408 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.425-2062C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939408 | |||||||
| chr19:53939693 | C | G | 1 | a0001c0001t0003g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.425-1777C>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939693 | |||||||
| chr19:53939717 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0013g0013 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.425-1753G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939717 | |||||||
| chr19:53939779 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0013g0013 |
2 | HG01109.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.425-1691T>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939779 | |||||||
| chr19:53939797 | G | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.425-1673G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53939797 | |||||||
| chr19:53940040 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.425-1430C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940040 | |||||||
| chr19:53940162 | A | G | 2 | a0001c0001t0003g0029 a0001c0001t0005g0340 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.425-1308A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940162 | |||||||
| chr19:53940611 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.425-859A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940611 | |||||||
| chr19:53940612 | T | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.425-858T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940612 | |||||||
| chr19:53940627 | C | T | 1 | a0001c0001t0002g0164 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.425-843C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940627 | |||||||
| chr19:53940642 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.425-828T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940642 | |||||||
| chr19:53940777 | G | A | 1 | a0001c0001t0008g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.425-693G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940777 | |||||||
| chr19:53940781 | G | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0288 a0001c0001t0002g0019 others(1): Show |
4 | HG01109.hp1 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-689G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940781 | |||||||
| chr19:53940857 | C | A | 1 | a0001c0001t0002g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.425-613C>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940857 | |||||||
| chr19:53940863 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG01891.hp2 HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.425-607T>C | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940863 | |||||||
| chr19:53940900 | TA | T | 11 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0133 others(8): Show |
11 | HG01257.hp2 HG01258.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.425-559delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53940900 | ||||||
| chr19:53940918 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.425-552G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940918 | |||||||
| chr19:53940929 | C | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0102 a0001c0001t0001g0122 others(4): Show |
7 | HG00140.hp1 HG01099.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.425-541C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940929 | |||||||
| chr19:53940933 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.425-537C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940933 | |||||||
| chr19:53940934 | G | A | 2 | a0001c0001t0007g0072 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.425-536G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53940934 | |||||||
| chr19:53941017 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0206 a0001c0001t0001g0214 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-453G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | chr19 | 53941017 | |||||||
| chr19:53941061 | CA | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(312): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.425-396delA | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | 53941061 | ||||||
| chr19:53941670 | G | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+55G>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941670 | |||||||
| chr19:53941671 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.570+56C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941671 | |||||||
| chr19:53941691 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0334 |
2 | NA18957.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.570+76G>A | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941691 | |||||||
| chr19:53941712 | A | G | 1 | a0001c0001t0007g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.570+97A>G | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941712 | |||||||
| chr19:53941882 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.571-154C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53941882 | |||||||
| chr19:53942026 | C | T | 2 | a0001c0001t0007g0072 a0001c0001t0007g0075 |
2 | HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.571-10C>T | CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 5/5 | chr19 | 53942026 |