Variant #0000001792 (NC_000009.12:g.74649312T>A, NC_000009.12(NM_006914.3):c.637+6497T>A (RORB))

Individual ID 00000383
Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.74649312T>A
Published as -
Reference Batoul Sadat Haerian et al. (2015), dbSNP
DB-ID RORB_000004 See all 9 reported entries
dbSNP ID rs3903529
Frequency 43/228
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 2021-01-27 10:35:25 +08:00 (CST)
Date last edited 2021-09-06 17:31:58 +08:00 (CST)
Options




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.637+6497T>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000397 DNA SEQ;SBE RORB 8 Nuur Athirah Binti Mohd Daud