Variant #0000892504 (NC_000016.9:g.1244986T>G, NM_021098.2:c.314T>G (CACNA1H))

Chromosome 16
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.1244986T>G
DNA change (hg38) -
Published as CACNA1H(NM_021098.3):c.314T>G (p.(Val105Gly), p.V105G)
ISCN -
DB-ID TPSG1_000090 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) 0.00017 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPSG1 NM_012467.3 -?/. - c.*26802A>C r.(=) p.(=)
CACNA1H NM_021098.2 -?/. - c.314T>G r.(?) p.(Val105Gly)


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