Variant #0000922920 (NC_000001.10:g.116243953A>G, NM_001232.3:c.1109T>C (CASQ2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.116243953A>G
DNA change (hg38) -
Published as CASQ2(NM_001232.4):c.1109T>C (p.I370T)
ISCN -
DB-ID CASQ2_000146
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASQ2 NM_001232.3 ?/. - c.1109T>C r.(?) p.(Ile370Thr)
VANGL1 NM_138959.2 ?/. - c.*9953A>G r.(=) p.(=)


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