rs376957775

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Species

Homo sapiens

Symbol

rs376957775

Category

Variant

Variant type

SNP

Overlaps

PERP

Location

6:138107131

Nucleotide Change

C>G

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000006.12:g.138107131C>G

Show All 5

HGVS.c name

• ENSEMBL:ENST00000421351.4:c.210G>C
• RefSeq:NM_022121.5:c.210G>C

HGVS.p name

• ENSP00000397157:p.Glu70Asp
• NP_071404:p.Glu70Asp

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences