Variant #0000933906 (NC_000005.9:g.95729049T>C, NM_000439.4:c.1918A>G (PCSK1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.95729049T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID PCSK1_000004 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs139453594
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00132 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-10-09 15:45:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCSK1 NM_000439.4 -?/. - c.1918A>G r.(?) p.(Thr640Ala)


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