Variant #0000556591 (NC_000016.9:g.1278919G>C, NM_021098.2:c.*7925G>C (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.1278919G>C
DNA change (hg38) g.1228919G>C
Published as TPSB2(NM_024164.5):c.645C>G (p.(His215Gln))
ISCN -
DB-ID TPSB2_000006
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) 0.0755 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPSG1 NM_012467.3 -?/. - c.-3667C>G r.(?) p.(=)
CACNA1H NM_021098.2 -?/. - c.*7925G>C r.(=) p.(=)
TPSB2 NM_024164.5 -?/. - c.644C>G r.(?) p.(Thr215Ser)


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