Variant #0000979000 (NC_000010.10:g.27024223G>A, NM_014317.3:c.886G>A (PDSS1))

Chromosome 10
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.27024223G>A
DNA change (hg38) -
Published as PDSS1(NM_014317.5):c.886G>A (p.(Gly296Arg))
ISCN -
DB-ID PDSS1_000021 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
ABI1 NM_005470.3 ?/. - c.*13276C>T r.(=) p.(=)
PDSS1 NM_014317.3 ?/. - c.886G>A r.(?) p.(Gly296Arg)


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