Variant #0000265893 (NC_000009.11:g.130580633G>A, NM_000118.3:c.1452C>T (ENG))

Chromosome 9
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.130580633G>A
DNA change (hg38) g.127818354G>A
Published as ENG(NM_000118.3):c.1452C>T (p.S484=), ENG(NM_001114753.3):c.1452C>T (p.(Ser484=))
ISCN -
DB-ID ENG_000094 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00107 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENG NM_000118.3 -/. - c.1452C>T r.(?) p.(Ser484=)
FPGS NM_001018078.1 -/. - c.*4750G>A r.(=) p.(=)


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