rs1581036449

---

Species

Homo sapiens

Symbol

rs1581036449

Category

Variant

Variant type

SNP

Overlaps

PURA

Location

5:140114684

Nucleotide Change

T>C

Most Severe Consequence

• non coding transcript exon variant

See all consequences

HGVS.g name

• (GRCh38)5:140114684T>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000331327.5:c.503T>C
• ENSEMBL:ENST00000520928.2:n.32A>G

Show All 4

HGVS.p name

• ENSP00000332706:p.Leu168Pro
• ENSP00000499133:p.Leu168Pro

Show All 3

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences