Variant #0000323890 (NC_000015.9:g.23002926_23002928del, NM_014608.2:c.3648_3650del (CYFIP1))

Chromosome 15
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.23002926_23002928del
DNA change (hg38) g.22870145_22870147del
Published as CYFIP1(NM_014608.2):c.3648_3650delTGA (p.(Asp1216del))
ISCN -
DB-ID CYFIP1_000004
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NIPA2 NM_001184889.1 ?/. - c.*3297_*3299del r.(=) p.(=)
CYFIP1 NM_014608.2 ?/. - c.3648_3650del r.(?) p.(Asp1216del)
NIPA2 NM_030922.6 ?/. - c.*3297_*3299del r.(=) p.(=)


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