rs198766711

---

Species

Rattus norvegicus

Symbol

rs198766711

Category

Variant

Variant type

SNP

Overlaps

Reg4

Location

2:185821647

Nucleotide Change

C>T

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_051337.1:g.185821647C>T

Show All 5

HGVS.c name

• ENSEMBL:ENSRNOT00000025821.3:c.67+371C>T
• RefSeq:NM_001004096.2:c.67+371C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences