rs1445724832

---

Species

Homo sapiens

Symbol

rs1445724832

Category

Variant

Variant type

SNP

Overlaps

DUSP12

Location

1:161751718

Nucleotide Change

A>C

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• NC_000001.11:g.161751718A>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000367943.5:c.395A>C
• ENSEMBL:ENST00000464004.2:n.430A>C

Show All 5

HGVS.p name

• ENSP00000356920:p.Lys132Thr

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences