Variant #0000912709 (NC_000007.13:g.154461112A>G, NM_130797.3:c.723A>G (DPP6))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.154461112A>G
DNA change (hg38) -
Published as DPP6(NM_001039350.3):c.531A>G (p.K177=), DPP6(NM_130797.4):c.723A>G (p.K241=)
ISCN -
DB-ID DPP6_000001 See all 5 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) 0.86952 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +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     
DPP6 NM_130797.3 -/. - c.723A>G r.(?) p.(=)


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