rs1470650959

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Species

Homo sapiens

Symbol

rs1470650959

Category

Variant

Variant type

SNP

Overlaps

PRKCE

Location

2:45976482

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000002.12:g.45976482C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000306156.8:c.466C>A
• ENSEMBL:ENST00000476675.5:n.368C>A

Show All 12

HGVS.p name

• ENSP00000306124:p.Arg156=
• NP_005391:p.Ala213Glu

Show All 10

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences