rs1765784710

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Species

Homo sapiens

Symbol

rs1765784710

Category

Variant

Variant type

SNP

Overlaps

B3GALT4

Location

6:33278035

Nucleotide Change

C>A

Most Severe Consequence

• missense variant

See all consequences

HGVS.g name

• (GRCh38)6:33278035C>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000451237.3:c.616C>A
• RefSeq:NM_003782.4:c.616C>A

HGVS.p name

• ENSP00000390784:p.Gln206Lys
• NP_003773:p.Gln206Lys

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences