rs759496728

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Species

Homo sapiens

Symbol

rs759496728

Category

Variant

Variant type

SNP

Overlaps

PERP

Location

6:138092233

Nucleotide Change

C>T

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)6:138092233C>T

Show All 5

HGVS.c name

• ENSEMBL:ENST00000421351.4:c.391G>A
• RefSeq:NM_022121.5:c.391G>A

HGVS.p name

• ENSP00000397157:p.Val131Met
• NP_071404:p.Val131Met

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences