Variant #0000254071 (NC_000010.10:g.27009268A>G, NM_014317.3:c.589A>G (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.27009268A>G
DNA change (hg38) g.26720339A>G
Published as PDSS1(NM_014317.4):c.589A>G (p.K197E), PDSS1(NM_014317.5):c.589A>G (p.K197E)
ISCN -
DB-ID PDSS1_000011 See all 6 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) 0.00144 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABI1 NM_005470.3 -?/. - c.*28231T>C r.(=) p.(=)
PDSS1 NM_014317.3 -?/. - c.589A>G r.(?) p.(Lys197Glu)


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