Variant #0000692333 (NC_000017.10:g.39973027T>A, NC_000017.10(NM_021939.3):c.246-283T>A (FKBP10))

Chromosome 17
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.39973027T>A
DNA change (hg38) -
Published as FKBP10(NM_021939.4):c.246-283T>A
ISCN -
DB-ID FKBP10_000087
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 2020-09-15 15:50:26 +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.-4860A>T r.(?) p.(=)
FKBP10 NM_021939.3 -?/. - c.246-283T>A r.(=) p.(=)


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