Variant #0000302048 (NC_000011.9:g.57365723T>C, NM_000062.2:c.-21T>C (SERPING1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method ACMG
Clinical classification likely 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 Journal: Duponchel 2006 Journal: Ponard 2019
ClinVar ID ClinVar-SCV000372547.3
dbSNP ID rs28362944
Origin CLASSIFICATION record
Segregation no
Frequency 0.029081 (GnomAD_exome); 0.030270 (TOPMed)
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.02893 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 2023-07-07 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.-21T>C r.(?) p.(=)


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