Variant #0000264003 (NC_000012.11:g.2595423T>C, NM_000719.6:c.911T>C (CACNA1C))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2595423T>C
DNA change (hg38) g.2486257T>C
Published as CACNA1C(NM_001167623.2):c.911T>C (p.I304T)
ISCN -
DB-ID CACNA1C_000037
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) 0.00048 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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1C NM_000719.6 -?/. - c.911T>C r.(?) p.(Ile304Thr)
DCP1B NM_152640.3 -?/. - c.-481826A>G r.(?) p.(=)
CACNA1C NM_199460.2 -?/. - c.911T>C r.(?) p.(Ile304Thr)


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