Variant #0000708489 (NC_000011.9:g.57365113C>A, NM_000062.2:c.-105C>A (SERPING1))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57365113C>A
DNA change (hg38) g.57597640C>A
Published as -
ISCN -
DB-ID SERPING1_000815
Variant remarks -
Reference -
ClinVar ID ClinVar-000305010
dbSNP ID rs886048397
Origin CLASSIFICATION record
Segregation -
Frequency 0.00006 (TOPMed)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Christian Drouet
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Christian Drouet
Date created 2020-12-04 15:55:23 +01:00 (CET)
Date last edited 2025-03-21 17:41:40 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPING1 NM_000062.2 ?/? 1 c.-105C>A r.(=) p.(=)


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