rs773271544

---

Species

Homo sapiens

Symbol

rs773271544

Category

Variant

Variant type

SNP

Overlaps

PRKCE

Location

2:46086289

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000002.12:g.46086289C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000306156.8:c.1519C>A
• ENSEMBL:ENST00000469753.5:n.606C>A

Show All 12

HGVS.p name

• ENSP00000306124:p.Pro507Thr
• NP_005391:p.Ala564Asp

Show All 10

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences