Unique variants in the HBB gene

Information The variants shown are described using the NM_000518.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Splice distance     

GVS function     

Protein     

PolyPhen prediction     

Position     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

Owner     
./. 30 - c.9T>C r.(?) - coding-synonymous p.(=) - 9 g.5248243A>G - HBB_000003 - - LOVD
./. 28 - c.315+16G>C r.(=) 16 intron p.(=) - 315 g.5247791C>G - HBB_000002 - - LOVD
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