rs3321615687

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Species

Rattus norvegicus

Symbol

rs3321615687

Category

Variant

Variant type

SNP

Overlaps

Fhl2

Location

9:45413222

Nucleotide Change

T>C

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_051344.1:g.45413222T>C

Show All 5

HGVS.c name

• ENSEMBL:ENSRNOT00000023014.4:c.156+5182A>G
• ENSEMBL:ENSRNOT00000101412.1:c.156+5182A>G

Show All 6

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences