Variant #0000994839 (NC_000005.9:g.156723747G>A, NM_001037332.2:c.352G>A (CYFIP2))

Chromosome 5
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.156723747G>A
DNA change (hg38) -
Published as CYFIP2(NM_001037333.1):c.352G>A (p.(Ala118Thr))
ISCN -
DB-ID CYFIP2_000048
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FNDC9 NM_001001343.3 ?/. - c.*46123C>T r.(=) p.(=)
CYFIP2 NM_001037332.2 ?/. - c.352G>A r.(?) p.(Glu118Lys)


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