rs780401976

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Species

Homo sapiens

Symbol

rs780401976

Category

Variant

Variant type

SNP

Overlaps

E2F8

Location

11:19225514

Nucleotide Change

C>T

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• NC_000011.10:g.19225514C>T

Show All 5

HGVS.c name

• ENSEMBL:ENST00000250024.9:c.2128G>A
• ENSEMBL:ENST00000527884.5:c.2128G>A

Show All 10

HGVS.p name

• ENSP00000250024:p.Val710Ile
• ENSP00000434199:p.Val710Ile

Show All 4

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences