Variant #0000349023 (NC_000005.9:g.156899925C>T, NM_001037332.2:c.*79917C>T (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.156899925C>T
DNA change (hg38) g.157472917C>T
Published as -
ISCN -
DB-ID ADAM19_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) 0.06294 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 2022-11-01 13:01:21 +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.*79917C>T r.(=) p.(=)
NIPAL4 NM_001099287.1 -/. - c.1358C>T r.(?) p.(Ser453Leu)
ADAM19 NM_033274.3 -/. - c.*8032G>A r.(=) p.(=)


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