Variant #0001001246 (NC_000015.9:g.23006301_23006303dup, NM_014608.2:c.*3261_*3263dup (CYFIP1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.23006301_23006303dup
DNA change (hg38) -
Published as NIPA2(NM_030922.6):c.1002_1004dupTGA (p.(Asn334_Glu335insAsp))
ISCN -
DB-ID NIPA2_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NIPA2 NM_001184889.1 -?/. - c.1002_1004dup r.(?) p.(Asn334_Glu335insAsp)
CYFIP1 NM_014608.2 -?/. - c.*3261_*3263dup r.(=) p.(=)
NIPA2 NM_030922.6 -?/. - c.1002_1004dup r.(?) p.(Asn334_Glu335insAsp)


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