rs762424812

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Species

Homo sapiens

Symbol

rs762424812

Category

Variant

Variant type

SNP

Overlaps

TMEFF1

Location

9:100473630

Nucleotide Change

T>A

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• (GRCh38)9:100473630T>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000374879.5:c.86T>A
• ENSEMBL:ENST00000502978.1:c.80-25135T>A

Show All 4

HGVS.p name

• ENSP00000364013:p.Leu29His
• NP_003683:p.Leu29His

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences