Variant #0000565114 (NC_000018.9:g.55221717_55221718del, NC_000018.9(NM_000140.3):c.913-62_913-61del (FECH))

Chromosome 18
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.55221717_55221718del
DNA change (hg38) g.57554485_57554486del
Published as FECH(NM_000140.4):c.913-62_913-61delAG
ISCN -
DB-ID FECH_000022
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +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.913-62_913-61del r.(=) p.(=)
FECH NM_001012515.2 -/. - c.931-62_931-61del r.(=) p.(=)


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