rs886059161

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Species

Homo sapiens

Symbol

rs886059161

Category

Variant

Variant type

SNP

Overlaps

LRAT

Location

4:154744229

Nucleotide Change

A>C

Most Severe Consequence

• splice region variant&intron variant

See all consequences

HGVS.g name

• (GRCh38)4:154744229A>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000336356.4:c.-2+7A>C
• ENSEMBL:ENST00000499392.1:n.472-3960A>C

Show All 8

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences