Variant #0000537644 (NC_000009.11:g.140772613C>G, NM_000718.3:c.228C>G (CACNA1B))

Chromosome 9
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.140772613C>G
DNA change (hg38) g.137878161C>G
Published as CACNA1B(NM_000718.3):c.228C>G (p.F76L), CACNA1B(NM_000718.4):c.228C>G (p.F76L)
ISCN -
DB-ID CACNA1B_000043 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) Retrieve
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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1B NM_000718.3 ?/. - c.228C>G r.(?) p.(Phe76Leu)


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