rs78795891

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Species

Homo sapiens

Symbol

rs78795891

Category

Variant

Variant type

SNP

Overlaps

PERP

Location

6:138107216

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)6:138107216C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000421351.4:c.125G>T
• RefSeq:NM_022121.5:c.125G>T

HGVS.p name

• ENSP00000397157:p.Gly42Val
• NP_071404:p.Gly42Val

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences