Variant #0000847028 (NC_000001.10:g.26126722A>G, NM_020451.2:c.1A>G (SEPN1))

Chromosome 1
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.26126722A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID SEPN1_000002 See all 21 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121908184
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-04-22 18:57:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEPN1 NM_020451.2 +/. - c.1A>G r.(?) p.(Met1?)


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