Variant #0000718339 (NC_000002.11:g.186656460T>A, NM_173651.2:c.4864T>A (FSIP2))

Chromosome 2
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.186656460T>A
DNA change (hg38) -
Published as FSIP2(NM_173651.2):c.4864T>A (p.(Ser1622Thr)), FSIP2(NM_173651.3):c.4597T>A (p.S1533T)
ISCN -
DB-ID FSIP2_000004 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) 0.00035 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FSIP2 NM_173651.2 -?/. - c.4864T>A r.(?) p.(Ser1622Thr)


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