rs911623465

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Species

Homo sapiens

Symbol

rs911623465

Category

Variant

Variant type

SNP

Overlaps

ARHGEF33

Location

2:38960502

Nucleotide Change

G>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)2:38960502G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000398800.8:c.2197G>A
• ENSEMBL:ENST00000486958.5:n.289+2304G>A

HGVS.p name

• ENSP00000381780:p.Gly733Ser

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences