Variant #0000865090 (NC_000017.10:g.1673212G>A, NM_002615.5:c.151G>A (SERPINF1))

Chromosome 17
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.1673212G>A
DNA change (hg38) -
Published as SERPINF1(NM_001329903.1):c.151G>A (p.(Val51Met)), SERPINF1(NM_002615.7):c.151G>A (p.V51M)
ISCN -
DB-ID SERPINF1_000079 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) 0.00152 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.151G>A r.(?) p.(Val51Met)


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