rs752702804

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Species

Homo sapiens

Symbol

rs752702804

Category

Variant

Variant type

SNP

Overlaps

DYNC2I2

Location

9:128633785

Nucleotide Change

C>T

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)9:128633785C>T

Show All 5

HGVS.c name

• ENSEMBL:ENST00000372715.7:c.1570G>A
• RefSeq:NM_052844.4:c.1570G>A

HGVS.p name

• ENSP00000361800:p.Ala524Thr
• NP_443076:p.Ala524Thr

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences