Variant #0000305032 (NC_000001.10:g.8030994G>A, PARK7(NM_007262.4):c.293G>A)

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8030994G>A
DNA change (hg38) g.7970934G>A
Published as PARK7(NM_001123377.1):c.293G>A (p.R98Q), PARK7(NM_001123377.2):c.293G>A (p.R98Q), PARK7(NM_007262.5):c.293G>A (p.R98Q)
ISCN -
DB-ID PARK7_000011 See all 6 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) 0.00795 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PARK7 NM_007262.4 -?/. - c.293G>A r.(?) p.(Arg98Gln)