rs201883435

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Species

Homo sapiens

Symbol

rs201883435

Category

Variant

Variant type

SNP

Overlaps

ARHGEF33

Location

2:38929743

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000002.12:g.38929743C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000398800.8:c.275C>A
• ENSEMBL:ENST00000488692.1:n.327C>A

HGVS.p name

• ENSP00000381780:p.Ala92Asp

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences