rs754830275

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Species

Homo sapiens

Symbol

rs754830275

Category

Variant

Variant type

SNP

Overlaps

TMEFF1

Location

9:100473554

Nucleotide Change

G>A

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• (GRCh38)9:100473554G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000374879.5:c.10G>A
• ENSEMBL:ENST00000502978.1:c.80-25211G>A

Show All 4

HGVS.p name

• ENSP00000364013:p.Ala4Thr
• NP_003683:p.Ala4Thr

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences