Variant #0000297446 (NC_000007.13:g.56087399G>A, NM_004577.3:c.169C>T (PSPH))

Chromosome 7
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.56087399G>A
DNA change (hg38) g.56019706G>A
Published as PSPH(NM_004577.3):c.169C>T (p.(Pro57Ser)), PSPH(NM_004577.4):c.169C>T (p.P57S)
ISCN -
DB-ID PSPH_000015 See all 2 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSPH NM_004577.3 -/. - c.169C>T r.(?) p.(Pro57Ser)


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