Variant #0000002052 (NC_000009.12:g.74629537G>A, NC_000009.12(NM_006914.3):c.8-745G>A (RORB))

Individual ID 00000432
Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.74629537G>A
Published as -
Reference Batoul Sadat Haerian et al. (2015)
DB-ID RORB_000002 See all 9 reported entries
dbSNP ID rs7022435
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-02-18 15:36:15 +08:00 (CST)
Date last edited 2021-08-01 12:58:34 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
RORB NM_006914.3 +/. - c.8-745G>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

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Genes screened     

Variants found     

Owner     
0000000467 DNA SBE RORB 4 Nur Aisyah Athirah