Variant #0000556579 (NC_000016.9:g.1270426C>G, NM_021098.2:c.6494C>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.1270426C>G
DNA change (hg38) g.1220426C>G
Published as CACNA1H(NM_021098.2):c.6494C>G (p.P2165R)
ISCN -
DB-ID TPSG1_000047
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPSG1 NM_012467.3 -?/. - c.*1362G>C r.(=) p.(=)
CACNA1H NM_021098.2 -?/. - c.6494C>G r.(?) p.(Pro2165Arg)


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