Variant #0000981576 (NC_000016.9:g.1252228_1252239del, NM_021098.2:c.1778_1789del (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.1252228_1252239del
DNA change (hg38) -
Published as CACNA1H(NM_021098.3):c.1778_1789del (p.(His593_Thr597delinsPro))
ISCN -
DB-ID TPSG1_000140
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) 0.00011 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 2024-04-19 20:27:30 +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.*19549_*19560del r.(=) p.(=)
CACNA1H NM_021098.2 -?/. - c.1778_1789del r.(?) p.(His593_Thr597delinsPro)


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