Variant #0000692313 (NC_000017.10:g.33520642C>T, NM_173167.2:c.*7064C>T (UNC45B))

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.33520642C>T
DNA change (hg38) -
Published as SLC35G3(NM_152462.2):c.685G>A (p.V229M)
ISCN -
DB-ID UNC45B_000031
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) 0.00033 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC35G3 NM_152462.2 ?/. - c.685G>A r.(?) p.(Val229Met)
UNC45B NM_173167.2 ?/. - c.*7064C>T r.(=) p.(=)


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