Variant #0000967006 (NC_000012.11:g.56720687C>T, NM_001127460.2:c.976G>A (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.56720687C>T
DNA change (hg38) -
Published as PAN2(NM_001127460.4):c.976G>A (p.V326M)
ISCN -
DB-ID CNPY2_000001
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) 0.00033 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
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.976G>A r.(?) p.(Val326Met)
CNPY2 NM_014255.5 ?/. - c.-11108G>A r.(?) p.(=)


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