Variant #0000565121 (NC_000018.9:g.55247336C>A, NM_000140.3:c.163G>T (FECH))

Chromosome 18
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.55247336C>A
DNA change (hg38) g.57580104C>A
Published as FECH(NM_000140.4):c.163G>T (p.G55C), FECH(NM_001012515.4):c.163G>T (p.G55C)
ISCN -
DB-ID FECH_000018 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) 0.02216 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
FECH NM_000140.3 -?/. - c.163G>T r.(?) p.(Gly55Cys)
FECH NM_001012515.2 -?/. - c.163G>T r.(?) p.(Gly55Cys)


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