Variant #0001055025 (NC_000015.9:g.31218058G>A, NM_014967.4:c.2404G>A (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.31218058G>A
DNA change (hg38) -
Published as FAN1(NM_014967.5):c.2404G>A (p.(Gly802Arg))
ISCN -
DB-ID FAN1_000073
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) 1.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAN1 NM_014967.4 ?/. - c.2404G>A r.(?) p.(Gly802Arg)
MTMR10 NM_017762.2 ?/. - c.*15615C>T r.(=) p.(=)


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