Variant #0001040755 (NC_000016.9:g.1245018A>T, NM_021098.2:c.346A>T (CACNA1H))

Chromosome 16
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.1245018A>T
DNA change (hg38) -
Published as CACNA1H(NM_021098.3):c.346A>T (p.(Thr116Ser))
ISCN -
DB-ID TPSG1_000178
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPSG1 NM_012467.3 ?/. - c.*26770T>A r.(=) p.(=)
CACNA1H NM_021098.2 ?/. - c.346A>T r.(?) p.(Thr116Ser)


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