rs779868381

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Species

Homo sapiens

Symbol

rs779868381

Category

Variant

Variant type

SNP

Overlaps

PFN3

Location

5:177400389

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)5:177400389C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000358571.3:c.188G>T
• RefSeq:NM_001029886.3:c.188G>T

HGVS.p name

• ENSP00000351379:p.Gly63Val
• NP_001025057:p.Gly63Val

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences