Variant #0000691933 (NC_000016.9:g.1268566C>G, NM_021098.2:c.5802C>G (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.1268566C>G
DNA change (hg38) -
Published as CACNA1H(NM_001005407.1):c.5784C>G (p.(Phe1928Leu))
ISCN -
DB-ID TPSG1_000071
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +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.*3222G>C r.(=) p.(=)
CACNA1H NM_021098.2 ?/. - c.5802C>G r.(?) p.(Phe1934Leu)


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