Hello everyone, I am working on a research project where i need to identify the variants based on NM_ numbers.

In my annotated file i am getting the NM_ numbers for exonic , UTR5´,UTR3´and splice site varaints. Eg. an exonic variant annotated as this .......KIAA2013:NM_138346:exon1:c.96_97insATCATGTG:p.L33Ifs*80.

Now i need to identify the intronic variants also eg in this way.for a variant 675 bp into the intron.( NM_004006.3:c.4375+675C>T).just an example.

The database AAChange.refGene is giving me list of all NM_ numbers for exonic region. Is there any other database which can annotate my intron variants in a similar way. Or is there any other way to get these intron variants identifiers.

Thanks for the help. Regards, Sabeen