Variant #0001001876 (NC_000016.9:g.1268246T>C, NM_021098.2:c.5482T>C (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.1268246T>C
DNA change (hg38) -
Published as CACNA1H(NM_021098.2):c.5482T>C (p.(Cys1828Arg))
ISCN -
DB-ID TPSG1_000169
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 2024-08-28 13:16:32 +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.*3542A>G r.(=) p.(=)
CACNA1H NM_021098.2 ?/. - c.5482T>C r.(?) p.(Cys1828Arg)


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