Variant #0000547766 (NC_000012.11:g.2800220A>G, NM_000719.6:c.6272A>G (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.2800220A>G
DNA change (hg38) g.2691054A>G
Published as CACNA1C(NM_000719.6):c.6272A>G (p.(Asn2091Ser)), CACNA1C(NM_001167623.2):c.6272A>G (p.N2091S), CACNA1C(NM_199460.3):c.6521A>G (p.N2174S), CACNA1C...)
ISCN -
DB-ID CACNA1C_000219 See all 7 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) 0.00049 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.6272A>G r.(?) p.(Asn2091Ser)
DCP1B NM_152640.3 -?/. - c.-686623T>C r.(?) p.(=)
CACNA1C NM_199460.2 -?/. - c.6521A>G r.(?) p.(Asn2174Ser)
CACNA1C-AS1 NR_045725.1 -?/. - n.89+15T>C r.(?) -


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