Variant #0000532284 (NC_000007.13:g.56087365A>G, NM_004577.3:c.203T>C (PSPH))

Chromosome 7
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.56087365A>G
DNA change (hg38) g.56019672A>G
Published as PSPH(NM_004577.3):c.203T>C (p.(Leu68Pro)), PSPH(NM_004577.4):c.203T>C (p.L68P)
ISCN -
DB-ID PSPH_000011 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.203T>C r.(?) p.(Leu68Pro)


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