Variant #0000263916 (NC_000012.11:g.2602441C>T, NM_000719.6:c.1002C>T (CACNA1C))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2602441C>T
DNA change (hg38) g.2493275C>T
Published as CACNA1C(NM_001167623.2):c.1002C>T (p.P334=), CACNA1C(NM_199460.4):c.1002C>T (p.P334=)
ISCN -
DB-ID CACNA1C_000041 See all 2 reported entries
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) 0.00023 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1C NM_000719.6 -/. - c.1002C>T r.(?) p.(Pro334=)
DCP1B NM_152640.3 -/. - c.-488844G>A r.(?) p.(=)
CACNA1C NM_199460.2 -/. - c.1002C>T r.(?) p.(Pro334=)


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