Variant #0000865728 (NC_000018.9:g.55233702G>A, NM_000140.3:c.575C>T (FECH))

Chromosome 18
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.55233702G>A
DNA change (hg38) -
Published as FECH(NM_001012515.3):c.593C>T (p.P198L)
ISCN -
DB-ID FECH_000032
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FECH NM_000140.3 ?/. - c.575C>T r.(?) p.(Pro192Leu)
FECH NM_001012515.2 ?/. - c.593C>T r.(?) p.(Pro198Leu)


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