Variant #0000295754 (NC_000011.9:g.57365748C>T, NM_000062.2:c.5C>T (SERPING1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.57365748C>T
DNA change (hg38) g.57598275C>T
Published as SERPING1(NM_000062.2):c.5C>T (p.A2V), SERPING1(NM_000062.3):c.5C>T (p.A2V)
ISCN -
DB-ID SERPING1_000002 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID ClinVar-000305016
dbSNP ID rs185342631
Origin CLASSIFICATION record
Segregation -
Frequency 0.0009841 (gnomAD v3)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00128 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPING1 NM_000062.2 +/. 2 c.5C>T r.(?) p.(Ala2Val)


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