Variant #0000502598 (NC_000001.10:g.116245571G>A, NM_001232.3:c.985C>T (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.116245571G>A
DNA change (hg38) g.115702950G>A
Published as CASQ2(NM_001232.3):c.985C>T (p.P329S), CASQ2(NM_001232.4):c.985C>T (p.P329S)
ISCN -
DB-ID CASQ2_000052 See all 3 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) 0.00022 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASQ2 NM_001232.3 ?/. - c.985C>T r.(?) p.(Pro329Ser)
VANGL1 NM_138959.2 ?/. - c.*11571G>A r.(=) p.(=)


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