Variant #0000561440 (NC_000017.10:g.39969496C>G, NM_021939.3:c.210C>G (FKBP10))

Chromosome 17
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.39969496C>G
DNA change (hg38) g.41813244C>G
Published as FKBP10(NM_021939.4):c.210C>G (p.N70K)
ISCN -
DB-ID FKBP10_000074
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
LEPREL4 NM_006455.2 ?/. - c.-1329G>C r.(?) p.(=)
FKBP10 NM_021939.3 ?/. - c.210C>G r.(?) p.(Asn70Lys)


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