rs139937578

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Species

Homo sapiens

Symbol

rs139937578

Category

Variant

Variant type

SNP

Overlaps

CD96

Location

3:111593841

Nucleotide Change

G>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)3:111593841G>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000283285.10:c.856-4279G>C
• ENSEMBL:ENST00000317012.5:c.361C>G

Show All 8

HGVS.p name

• ENSP00000321370:p.Arg121Gly
• NP_078784:p.Arg121Gly

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences