rs965813960

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Species

Homo sapiens

Symbol

rs965813960

Category

Variant

Variant type

SNP

Overlaps

PFN3

Location

5:177400537

Nucleotide Change

C>G

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)5:177400537C>G

Show All 5

HGVS.c name

• ENSEMBL:ENST00000358571.3:c.40G>C
• RefSeq:NM_001029886.3:c.40G>C

HGVS.p name

• ENSP00000351379:p.Asp14His
• NP_001025057:p.Asp14His

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences