rs35777875

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Species

Homo sapiens

Symbol

rs35777875

Category

Variant

Variant type

SNP

Overlaps

PRKCE

Location

2:46159645

Nucleotide Change

G>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000002.12:g.46159645G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000306156.8:c.1960G>A
• ENSEMBL:ENST00000494472.1:n.168G>A

Show All 21

HGVS.p name

• ENSP00000306124:p.Ala654Thr
• NP_005391:p.Ala654Thr

Show All 19

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences