rs1379916593

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Species

Homo sapiens

Symbol

rs1379916593

Category

Variant

Variant type

SNP

Overlaps

ARHGEF33

Location

2:38929821

Nucleotide Change

T>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)2:38929821T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000398800.8:c.353T>C
• ENSEMBL:ENST00000488692.1:n.405T>C

HGVS.p name

• ENSP00000381780:p.Val118Ala

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences