rs145872059

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Species

Homo sapiens

Symbol

rs145872059

Category

Variant

Variant type

SNP

Overlaps

TPRKB

Location

2:73732282

Nucleotide Change

C>T

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)2:73732282C>T

Show All 5

HGVS.c name

• ENSEMBL:ENST00000272424.11:c.145G>A
• ENSEMBL:ENST00000462166.1:n.150G>A

Show All 8

HGVS.p name

• ENSP00000272424:p.Val49Ile
• NP_001317317:p.Val49Ile

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences