Variant #0000000362 (NC_000011.10:g.5225923G>A, NC_000011.10(NM_000518.4):c.316-197C>T (HBB))

Individual ID 00000068
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.5225923G>A
Published as IVS II-654 C>T
Reference Lai Kuan Teh et al. (2014), dbSNP, (OMIM 0368), ClinVar
DB-ID HBB_000015 See all 29 reported entries
dbSNP ID rs34451549
Frequency 3/504
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 2020-10-20 09:47:27 +08:00 (CST)
Date last edited 2021-08-19 10:55:34 +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     
HBB NM_000518.4 +/. 2i c.316-197C>T IVS II-654 C>T r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000081 DNA PCRm HBB 14 Nuur Athirah Binti Mohd Daud