rs3321624812

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Species

Rattus norvegicus

Symbol

rs3321624812

Category

Variant

Variant type

SNP

Overlaps

Rev1

Location

9:40298534

Nucleotide Change

C>G

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_051344.1:g.40298534C>G

Show All 5

HGVS.c name

• ENSEMBL:ENSRNOT00000067197.3:c.1541+579G>C
• ENSEMBL:ENSRNOT00000109166.1:c.-89-76602G>C

Show All 10

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences