rs754240894

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Species

Homo sapiens

Symbol

rs754240894

Category

Variant

Variant type

SNP

Overlaps

GALNT10

Location

5:154412971

Nucleotide Change

G>C

Most Severe Consequence

• intron variant&non coding transcript variant

See all consequences

HGVS.g name

• NC_000005.10:g.154412971G>C

Show All 5

HGVS.c name

• ENSEMBL:ENST00000297107.11:c.1469G>C
• ENSEMBL:ENST00000377661.2:c.1283G>C

Show All 11

HGVS.p name

• ENSP00000297107:p.Arg490Pro
• ENSP00000366889:p.Arg428Pro

Show All 3

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences