Variant #0000619654 (NC_000023.10:g.49079179T>G, NM_005183.2:c.2237A>C (CACNA1F))

Chromosome X
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.49079179T>G
DNA change (hg38) g.49222720T>G
Published as CACNA1F(NM_001256789.1):c.2204A>C (p.(Asn735Thr)), CACNA1F(NM_005183.3):c.2237A>C (p.N746T), CACNA1F(NM_005183.4):c.2237A>C (p.N746T)
ISCN -
DB-ID CACNA1F_000061 See all 8 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) 0.00152 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 2019-12-04 15:24:38 +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     
CACNA1F NM_001256789.1 -/. - c.2204A>C r.(?) p.(Asn735Thr)
CACNA1F NM_005183.2 -/. - c.2237A>C r.(?) p.(Asn746Thr)


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