Variant #0000930064 (NC_000012.11:g.2558176C>T, NM_000719.6:c.512C>T (CACNA1C))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2558176C>T
DNA change (hg38) -
Published as CACNA1C(NM_199460.4):c.512C>T (p.T171M)
ISCN -
DB-ID CACNA1C_000328
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1C NM_000719.6 ?/. - c.512C>T r.(?) p.(Thr171Met)
DCP1B NM_152640.3 ?/. - c.-444579G>A r.(?) p.(=)
CACNA1C NM_199460.2 ?/. - c.512C>T r.(?) p.(Thr171Met)


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