Variant #0001007098 (NC_000009.11:g.8733779C>G, NC_000009.11(NM_002839.3):c.64+1G>C (PTPRD))

Chromosome 9
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.8733779C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID PTPRD_000009
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2154434733
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-09-05 13:50:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPRD NM_002839.3 ?/. - c.64+1G>C r.(?) p.(?)


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