rs782790209

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Species

Homo sapiens

Symbol

rs782790209

Category

Variant

Variant type

SNP

Overlaps

GSPT2

Location

X:51744836

Nucleotide Change

T>G

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)X:51744836T>G

Show All 5

HGVS.c name

• ENSEMBL:ENST00000340438.6:c.1210T>G
• RefSeq:NM_018094.5:c.1210T>G

HGVS.p name

• ENSP00000341247:p.Phe404Val
• NP_060564:p.Phe404Val

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences