Variant #0001065508 (NC_000011.9:g.65402737G>A, NM_006747.3:c.-3008G>A (SIPA1))

Chromosome 11
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.65402737G>A
DNA change (hg38) -
Published as PCNX3(NM_032223.4):c.5002G>A (p.(Asp1668Asn))
ISCN -
DB-ID PCNXL3_000007
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIPA1 NM_006747.3 ?/. - c.-3008G>A r.(?) p.(=)
PCNXL3 NM_032223.2 ?/. - c.5002G>A r.(?) p.(Asp1668Asn)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.