Annotation
Position
chr12 : 2800255
Genotype
T/G
Gene
HGVS DNA code
HGVS=CACNA1C:NM_001129831:exon48:c.6391G>T:p.A2131S,CACNA1C:NM_000719:exon47:c.6307G>T:p.A2103S,CACNA1C:NM_001129842:exon47:c.6307G>T:p.A2103S,CACNA1C:NM_001129835:exon47:c.6364G>T:p.A2122S,CACNA1C:NM_001129830:exon48:c.6412G>T:p.A2138S,CACNA1C:NM_0011298
HGVS protein code
Author:
GeneTalk
dbSNP Flags:
- SNP is Clinical (LSDB,OMIM,TPA,Diagnostic)
- SNP is Precious (Clinical,Pubmed Cited)
- Weight=1. (Weight on NCBI reference assembly.)
- RS Cluster has none TGP Submission(set VCF OTHERKG).
- Submitted from a locus-specific database.
- Single base polymorphism SNP
- SNP is Precious (Clinical,Pubmed Cited)
- Weight=1. (Weight on NCBI reference assembly.)
- RS Cluster has none TGP Submission(set VCF OTHERKG).
- Submitted from a locus-specific database.
- Single base polymorphism SNP
Created at March 09, 2013 16:33, Last update March 09, 2013 16:33
Voting
Clinical significance
Pathogenic
Votes
| Stars | Clinical significance |
|---|---|
| 5 | 3 votes |
| 4 | 0 votes |
| 3 | 0 votes |
| 2 | 0 votes |
| 1 | 0 votes |
Comments
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