Variant #0000680525 (NC_000016.9:g.30369889G>C, NM_015527.3:c.1803C>G (TBC1D10B))

Chromosome 16
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.30369889G>C
DNA change (hg38) -
Published as TBC1D10B(NM_015527.4):c.1803C>G (p.T601=)
ISCN -
DB-ID CD2BP2_000001
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) 0.00042 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD2BP2 NM_006110.2 -?/. - c.-3383C>G r.(?) p.(=)
TBC1D10B NM_015527.3 -?/. - c.1803C>G r.(?) p.(Thr601=)


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