Variant #0000981567 (NC_000016.9:g.1245529C>A, NM_021098.2:c.509C>A (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.1245529C>A
DNA change (hg38) -
Published as CACNA1H(NM_021098.3):c.509C>A (p.(Thr170Lys))
ISCN -
DB-ID TPSG1_000134
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 2024-04-19 20:27:30 +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.*26259G>T r.(=) p.(=)
CACNA1H NM_021098.2 ?/. - c.509C>A r.(?) p.(Thr170Lys)


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