Variant #0000623624 (NC_000017.10:g.1679865T>A, NM_002615.5:c.826T>A (SERPINF1))

Chromosome 17
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.1679865T>A
DNA change (hg38) g.1776571T>A
Published as SERPINF1(NM_002615.6):c.826T>A (p.F276I)
ISCN -
DB-ID SERPINF1_000084
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) 0.00024 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-05-16 13:02:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINF1 NM_002615.5 ?/. - c.826T>A r.(?) p.(Phe276Ile)
SMYD4 NM_052928.2 ?/. - c.*4715A>T r.(=) p.(=)


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