Variant #0000255767 (NC_000018.9:g.55253784A>C, NC_000018.9(NM_000140.3):c.67+2T>G (FECH))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.55253784A>C
DNA change (hg38) g.57586552A>C
Published as FECH(NM_000140.4):c.67+2T>G
ISCN -
DB-ID FECH_000020
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FECH NM_000140.3 +/. - c.67+2T>G r.spl? p.?
FECH NM_001012515.2 +/. - c.67+2T>G r.spl? p.?


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