Variant #0000340496 (NC_000010.10:g.86004873T>C, NM_002921.3:c.27T>C (RGR))

Chromosome 10
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.86004873T>C
DNA change (hg38) g.84245117T>C
Published as RGR(NM_002921.4):c.27T>C (p.T9=)
ISCN -
DB-ID RGR_000003 See all 3 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) 0.52493 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
RGR NM_002921.3 -/. - c.27T>C r.(?) p.(Thr9=)
LRIT1 NM_015613.2 -/. - c.-3678A>G r.(?) p.(=)


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