Variant #0000571080 (NC_000021.8:g.47574206C>G, NM_006657.2:c.95G>C (FTCD))

Chromosome 21
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.47574206C>G
DNA change (hg38) g.46154292C>G
Published as FTCD(NM_006657.2):c.95G>C (p.G32A), FTCD(NM_206965.1):c.95G>C (p.(Gly32Ala))
ISCN -
DB-ID FTCD_000021 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) 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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTCD NM_006657.2 ?/. - c.95G>C r.(?) p.(Gly32Ala)


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