rs748006465

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Species

Homo sapiens

Symbol

rs748006465

Category

Variant

Variant type

SNP

Overlaps

CIBAR2

Location

16:85110359

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000016.10:g.85110359C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000539556.6:c.122G>T
• ENSEMBL:ENST00000629253.1:c.122G>T

HGVS.p name

• ENSP00000443411:p.Arg41Leu
• ENSP00000487117:p.Arg41Leu

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences