rs749790121

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Species

Homo sapiens

Symbol

rs749790121

Category

Variant

Variant type

SNP

Overlaps

FUCA1

Location

1:23854412

Nucleotide Change

T>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)1:23854412T>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000374479.4:c.917A>T
• RefSeq:NM_000147.5:c.917A>T

HGVS.p name

• ENSP00000363603:p.Tyr306Phe
• NP_000138:p.Tyr306Phe

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences