Variant #0000553869 (NC_000015.9:g.31197995C>T, NM_014967.4:c.1129C>T (FAN1))

Chromosome 15
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.31197995C>T
DNA change (hg38) g.30905792C>T
Published as FAN1(NM_001146094.1):c.1129C>T (p.(Arg377Trp)), FAN1(NM_014967.5):c.1129C>T (p.R377W)
ISCN -
DB-ID FAN1_000008 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) 0.00428 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAN1 NM_014967.4 ?/. - c.1129C>T r.(?) p.(Arg377Trp)
MTMR10 NM_017762.2 ?/. - c.*35678G>A r.(=) p.(=)


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