rs758390323

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Species

Homo sapiens

Symbol

rs758390323

Category

Variant

Variant type

SNP

Overlaps

CGNL1

Location

15:57439469

Nucleotide Change

G>C

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)15:57439469G>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000281282.6:c.1470G>C
• RefSeq:XM_017022686.2:c.1470G>C

Show All 8

HGVS.p name

• ENSP00000281282:p.Gln490His
• XP_016878175:p.Gln490His

Show All 8

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences