Variant #0001001277 (NC_000015.9:g.31235251G>C, NM_014967.4:c.*1486G>C (FAN1))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31235251G>C
DNA change (hg38) -
Published as MTMR10(NM_017762.2):c.1573C>G (p.(Gln525Glu))
ISCN -
DB-ID FAN1_000067
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 2024-08-28 13:16:32 +02:00 (CEST)
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.*1486G>C r.(=) p.(=)
MTMR10 NM_017762.2 -?/. - c.1573C>G r.(?) p.(Gln525Glu)


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