Variant #0000302050 (NC_000011.9:g.57381989G>A, NM_000062.2:c.1438G>A (SERPING1))

Chromosome 11
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.57381989G>A
DNA change (hg38) g.57614516G>A
Published as SERPING1(NM_000062.2):c.1438G>A (p.V480M), SERPING1(NM_000062.3):c.1438G>A (p.V480M)
ISCN -
DB-ID SERPING1_000007 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID ClinVar-000254786
dbSNP ID rs4926
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.22318 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPING1 NM_000062.2 -/. 8 c.1438G>A r.(?) p.(Val480Met)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.