Variant #0000306524 (NC_000010.10:g.104173584G>C, NM_001270965.1:c.1495C>G (PSD))

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.104173584G>C
DNA change (hg38) g.102413827G>C
Published as PSD(NM_002779.5):c.1495C>G (p.P499A)
ISCN -
DB-ID PSD_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) 1.0E-5 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 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     
PSD NM_001270965.1 ?/. - c.1495C>G r.(?) p.(Pro499Ala)
FBXL15 NM_024326.3 ?/. - c.-7303G>C r.(?) p.(=)


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