Variant #0000338430 (NC_000011.9:g.57365723T>C, NM_000062.2:c.-21T>C (SERPING1))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Probably does not affect function
Classification method ACMG
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57365723T>C
DNA change (hg38) g.57598250T>C
Published as SERPING1(NM_000062.2):c.-21T>C
ISCN -
DB-ID SERPING1_000001 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID rs28362944
Origin CLASSIFICATION record
Segregation -
Frequency 0.02908
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02893 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-07 11:54:10 +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.-21T>C r.(?) p.(=)


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