Variant #0000864292 (NC_000016.9:g.1278674G>A, NM_021098.2:c.*7680G>A (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.1278674G>A
DNA change (hg38) -
Published as TPSB2(NM_024164.5):c.804C>T (p.H268=)
ISCN -
DB-ID TPSB2_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.-3422C>T r.(?) p.(=)
CACNA1H NM_021098.2 -?/. - c.*7680G>A r.(=) p.(=)
TPSB2 NM_024164.5 -?/. - c.804C>T r.(?) p.(His268=)


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