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SNPs and other variants for my gene

Variation Table

Find short variants for a gene from dbSNP, COSMIC, and other sources in the Gene Variation table.

Variants are grouped into consequence types.

Click on 'Show' to reveal a table of variant IDs for a specific consequence type.

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Gene sequence

View variants within the nucleotide sequence in the Gene Sequence view.

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In all views, click on any Variant to find population frequencies, alleles, and more in the variation tab.

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Variants along the genome

View variants along the genome in the Location tab. Choose different types and sources, for example 1000 Genomes populations, ClinVar (clinically associated), OMIM and HGMD (public set).

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You can also browse SNPs throughout the genome - find out how in this video: