rs58066621

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Species

Homo sapiens

Symbol

rs58066621

Category

Variant

Variant type

SNP

Overlaps

GSPT2

Location

X:51744049

Nucleotide Change

G>A

Most Severe Consequence

• synonymous variant

See all consequences

HGVS.g name

• (GRCh38)X:51744049G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000340438.6:c.423G>A
• RefSeq:NM_018094.5:c.423G>A

HGVS.p name

• ENSP00000341247:p.Glu141=
• NP_060564:p.Glu141=

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences