Variant #0000539784 (NC_000010.10:g.27012981G>C, NM_014317.3:c.760G>C (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.27012981G>C
DNA change (hg38) g.26724052G>C
Published as PDSS1(NM_001321979.1):c.250G>C (p.E84Q)
ISCN -
DB-ID ABI1_000003
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) 0.00014 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.*24518C>G r.(=) p.(=)
PDSS1 NM_014317.3 ?/. - c.760G>C r.(?) p.(Glu254Gln)


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