rs1386499550

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Species

Homo sapiens

Symbol

rs1386499550

Category

Variant

Variant type

SNP

Overlaps

ENPP4

Location

6:46140152

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000006.12:g.46140152C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000321037.5:c.569C>A
• RefSeq:NM_014936.5:c.569C>A

HGVS.p name

• ENSP00000318066:p.Ala190Glu
• NP_055751:p.Ala190Glu

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences