rs1775596006

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Species

Homo sapiens

Symbol

rs1775596006

Category

Variant

Variant type

SNP

Overlaps

PERP

Location

6:138092158

Nucleotide Change

C>T

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000006.12:g.138092158C>T

Show All 5

HGVS.c name

• ENSEMBL:ENST00000421351.4:c.466G>A
• RefSeq:NM_022121.5:c.466G>A

HGVS.p name

• ENSP00000397157:p.Gly156Arg
• NP_071404:p.Gly156Arg

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences