Variant #0000615695 (NC_000016.9:g.1270554G>A, NM_021098.2:c.6622G>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.1270554G>A
DNA change (hg38) g.1220554G>A
Published as CACNA1H(NM_001005407.1):c.6604G>A (p.(Ala2202Thr)), CACNA1H(NM_021098.2):c.6622G>A (p.A2208T)
ISCN -
DB-ID TPSG1_000049 See all 2 reported entries
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) 0.00061 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPSG1 NM_012467.3 -?/. - c.*1234C>T r.(=) p.(=)
CACNA1H NM_021098.2 -?/. - c.6622G>A r.(?) p.(Ala2208Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.