| Submitters from clinical diagnostic labs use tranSNP.cgi to enter HGVS names |
| for variations. Software behind tranSNP.cgi will use HGVS names to map to |
| NCBI reference contigs and get flanking sequences for the variations and |
| submit all information to dbSNP. Submitter may provided submitter web link, |
| pubmed id, OMIM id and/or MeSH term which will be reported on snp_ss.cgi on |
| dbSNP website and on Variation viewer. Please see those links for more details. |