Variant #0000339493 (NC_000005.9:g.156899869T>C, NM_001037332.2:c.*79861T>C (CYFIP2))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.156899869T>C
DNA change (hg38) g.157472861T>C
Published as NIPAL4(NM_001099287.2):c.1116T>C (p.V372=)
ISCN -
DB-ID ADAM19_000001 See all 2 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) 0.97827 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CYFIP2 NM_001037332.2 -/. - c.*79861T>C r.(=) p.(=)
NIPAL4 NM_001099287.1 -/. - c.1302T>C r.(?) p.(Val434=)
ADAM19 NM_033274.3 -/. - c.*8088A>G r.(=) p.(=)


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