Variant #0000246468 (NC_000006.11:g.107780483A>G, NM_020381.3:c.7T>C (PDSS2))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.107780483A>G
DNA change (hg38) g.107459279A>G
Published as PDSS2(NM_020381.3):c.7T>C (p.(Phe3Leu)), PDSS2(NM_020381.4):c.7T>C (p.F3L)
ISCN -
DB-ID PDSS2_000003 See all 3 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) 0.01548 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     
PDSS2 NM_020381.3 -/. - c.7T>C r.(?) p.(Phe3Leu)


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