rs199121197

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Species

Rattus norvegicus

Symbol

rs199121197

Category

Variant

Variant type

SNP

Overlaps

Gltp

Location

12:41921622

Nucleotide Change

A>C

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_051347.1:g.41921622A>C

Show All 5

HGVS.c name

• ENSEMBL:ENSRNOT00000001581.7:c.162+833A>C
• RefSeq:NM_001134413.1:c.162+833A>C

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences