Variant #0000568857 (NC_000019.9:g.7695513G>A, NM_001171155.1:c.82G>A (PET100))

Chromosome 19
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.7695513G>A
DNA change (hg38) g.7630627G>A
Published as PET100(NM_001171155.1):c.82G>A (p.E28K)
ISCN -
DB-ID PET100_000005 See all 2 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) 0.00105 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PET100 NM_001171155.1 -/. - c.82G>A r.(?) p.(Glu28Lys)
XAB2 NM_020196.2 -/. - c.-1100C>T r.(?) p.(=)
PCP2 NM_174895.1 -/. - c.*1062C>T r.(=) p.(=)


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