Variant #0000981145 (NC_000015.9:g.31217363C>G, NM_014967.4:c.2206C>G (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.31217363C>G
DNA change (hg38) -
Published as FAN1(NM_014967.5):c.2206C>G (p.P736A)
ISCN -
DB-ID FAN1_000063
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAN1 NM_014967.4 ?/. - c.2206C>G r.(?) p.(Pro736Ala)
MTMR10 NM_017762.2 ?/. - c.*16310G>C r.(=) p.(=)


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