Variant #0000539783 (NC_000010.10:g.26986676C>T, NM_014317.3:c.36C>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.26986676C>T
DNA change (hg38) g.26697747C>T
Published as PDSS1(NM_014317.4):c.36C>T (p.C12=)
ISCN -
DB-ID ABI1_000002
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-26 13:59:46 +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.*50823G>A r.(=) p.(=)
PDSS1 NM_014317.3 -?/. - c.36C>T r.(?) p.(Cys12=)


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