rs755864702

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Species

Homo sapiens

Symbol

rs755864702

Category

Variant

Variant type

SNP

Overlaps

SCD5

Location

4:82636609

Nucleotide Change

C>T

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• NC_000004.12:g.82636609C>T

Show All 5

HGVS.c name

• ENSEMBL:ENST00000319540.9:c.784G>A
• RefSeq:NM_001037582.3:c.784G>A

HGVS.p name

• ENSP00000316329:p.Val262Ile
• NP_001032671:p.Val262Ile

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences