Variant #0001039372 (NC_000012.11:g.56713797G>A, NM_001127460.2:c.2809C>T (PAN2))

Chromosome 12
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.56713797G>A
DNA change (hg38) -
Published as PAN2(NM_014871.5):c.2797C>T (p.(Pro933Ser))
ISCN -
DB-ID CNPY2_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) 0.00011 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
PAN2 NM_001127460.2 ?/. - c.2809C>T r.(?) p.(Pro937Ser)
CNPY2 NM_014255.5 ?/. - c.-4218C>T r.(?) p.(=)


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