rs1300524106

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Species

Homo sapiens

Symbol

rs1300524106

Category

Variant

Variant type

SNP

Overlaps

WARS2

Location

1:119033282

Nucleotide Change

C>T

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)1:119033282C>T

Show All 5

HGVS.c name

• ENSEMBL:ENST00000235521.5:c.712G>A
• ENSEMBL:ENST00000369426.9:c.*78G>A

Show All 3

HGVS.p name

• ENSP00000235521:p.Val238Ile
• XP_005270407:p.Val220Ile

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences