Variant #0000293645 (NC_000010.10:g.26986729G>T, NM_014317.3:c.89G>T (PDSS1))

Chromosome 10
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.26986729G>T
DNA change (hg38) g.26697800G>T
Published as PDSS1(NM_014317.5):c.89G>T (p.G30V)
ISCN -
DB-ID PDSS1_000004 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) 0.00244 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABI1 NM_005470.3 -?/. - c.*50770C>A r.(=) p.(=)
PDSS1 NM_014317.3 -?/. - c.89G>T r.(?) p.(Gly30Val)


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