Variant #0000001773 (NC_000009.12:g.74629537G>A, NC_000009.12(NM_006914.3):c.8-745G>A (RORB))

Individual ID 00000381
Chromosome 9
Allele Both (homozygous)
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), dbSNP
DB-ID RORB_000002 See all 9 reported entries
dbSNP ID rs7022435
Frequency 215/251
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-26 12:48:17 +08:00 (CST)
Date last edited 2021-09-02 13:31:40 +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     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000395 DNA SEQ;SBE RORB 8 Nuur Athirah Binti Mohd Daud