Variant #0000888135 (NC_000008.10:g.11666240_11666257dup, NC_000008.10(NM_004462.3):c.100-63_100-46dup (FDFT1))

Chromosome 8
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.11666240_11666257dup
DNA change (hg38) -
Published as FDFT1(NM_001287750.2):c.214_231dupCACTCCCACTCCCACTCC (p.H72_S77dup)
ISCN -
DB-ID FDFT1_000002
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FDFT1 NM_004462.3 -/. - c.100-63_100-46dup r.(=) p.(=)


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