Variant #0000861137 (NC_000008.10:g.145649235C>T, NM_013432.4:c.*5291G>A (TONSL))

Chromosome 8
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.145649235C>T
DNA change (hg38) -
Published as VPS28(NM_016208.3):c.619G>A (p.D207N)
ISCN -
DB-ID TONSL_000043
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TONSL NM_013432.4 ?/. - c.*5291G>A r.(=) p.(=)
VPS28 NM_016208.2 ?/. - c.619G>A r.(?) p.(Asp207Asn)


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