rs144828075

---

Species

Homo sapiens

Symbol

rs144828075

Category

Variant

Variant type

SNP

Overlaps

ENPP4

Location

6:46140022

Nucleotide Change

A>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)6:46140022A>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000321037.5:c.439A>C
• RefSeq:NM_014936.5:c.439A>C

HGVS.p name

• ENSP00000318066:p.Ile147Leu
• NP_055751:p.Ile147Leu

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences