Variant #0000569724 (NC_000020.10:g.428553T>C, NM_144628.2:c.236A>G (TBC1D20))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.428553T>C
DNA change (hg38) g.447909T>C
Published as TBC1D20(NM_144628.2):c.236A>G (p.(Asn79Ser)), TBC1D20(NM_144628.3):c.236A>G (p.N79S)
ISCN -
DB-ID TBC1D20_000010 See all 2 reported entries
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) 0.04981 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D20 NM_144628.2 -/. - c.236A>G r.(?) p.(Asn79Ser)


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