Variant #0000924291 (NC_000005.9:g.156895736C>A, NM_001037332.2:c.*75728C>A (CYFIP2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.156895736C>A
DNA change (hg38) -
Published as NIPAL4(NM_001099287.1):c.527C>A (p.A176D), NIPAL4(NM_001099287.2):c.341C>A (p.A114D), NIPAL4(NM_001172292.1):c.470C>A (p.A157D)
ISCN -
DB-ID NIPAL4_000004 See all 5 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) 0.00066 View details
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 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CYFIP2 NM_001037332.2 +?/. - c.*75728C>A r.(=) p.(=)
NIPAL4 NM_001099287.1 +?/. - c.527C>A r.(?) p.(Ala176Asp)


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