Variant #0000304171 (NC_000005.9:g.156895764C>A, NM_001037332.2:c.*75756C>A (CYFIP2))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.156895764C>A
DNA change (hg38) g.157468756C>A
Published as NIPAL4(NM_001099287.1):c.555C>A (p.Y185*)
ISCN -
DB-ID NIPAL4_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-18 09:11:22 +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.*75756C>A r.(=) p.(=)
NIPAL4 NM_001099287.1 +/. - c.555C>A r.(?) p.(Tyr185Ter)


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