rs106312444

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Species

Rattus norvegicus

Symbol

rs106312444

Category

Variant

Variant type

SNP

Overlaps

Nol8

Location

17:15002312

Nucleotide Change

C>T

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_051352.1:g.15002312C>T

Show All 5

HGVS.c name

• ENSEMBL:ENSRNOT00000073035.2:c.2665+401G>A
• ENSEMBL:ENSRNOT00000093381.2:c.2683+401G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences