rs1438811085

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Species

Homo sapiens

Symbol

rs1438811085

Category

Variant

Variant type

SNP

Overlaps

TPRKB

Location

2:73734564

Nucleotide Change

C>G

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)2:73734564C>G

Show All 5

HGVS.c name

• ENSEMBL:ENST00000272424.11:c.6G>C
• ENSEMBL:ENST00000462166.1:n.110G>C

Show All 8

HGVS.p name

• ENSP00000272424:p.Gln2His
• NP_001317317:p.Gln2His

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences