Variant #0000536317 (NC_000009.11:g.130578006G>A, NM_000118.3:c.*190C>T (ENG))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.130578006G>A
DNA change (hg38) g.127815727G>A
Published as ENG(NM_001114753.2):c.1932C>T (p.I644=), ENG(NM_001114753.3):c.1932C>T (p.I644=)
ISCN -
DB-ID FPGS_000001 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) 0.02821 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENG NM_000118.3 ?/. - c.*190C>T r.(=) p.(=)
FPGS NM_001018078.1 ?/. - c.*2123G>A r.(=) p.(=)


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