Variant #0000553868 (NC_000015.9:g.31197710dup, NM_014967.4:c.844dup (FAN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31197710dup
DNA change (hg38) g.30905507dup
Published as FAN1(NM_014967.4):c.844dupA (p.S282Kfs*13)
ISCN -
DB-ID FAN1_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 2020-07-06 09:41:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAN1 NM_014967.4 +?/. - c.844dup r.(?) p.(Ser282LysfsTer13)
MTMR10 NM_017762.2 +?/. - c.*35963dup r.(?) p.(=)


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