Variant #0000313037 (NC_000016.9:g.46696284G>A, VPS35(NM_018206.4):c.1938=)

Chromosome 16
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.46696284G>A
DNA change (hg38) g.46662372G>A
Published as VPS35(NM_018206.5):c.1938C>T (p.H646=), VPS35(NM_018206.6):c.1938C>T (p.H646=)
ISCN -
DB-ID VPS35_000003 See all 3 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) 0.99415 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS35 NM_018206.4 -/. - c.1938= r.(=) p.(His646=)