rs769700432

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Species

Homo sapiens

Symbol

rs769700432

Category

Variant

Variant type

SNP

Overlaps

MTO1

Location

6:73461959

Nucleotide Change

G>A

Most Severe Consequence

• synonymous variant

See all consequences

HGVS.g name

• (GRCh38)6:73461959G>A

Show All 5

HGVS.c name

• ENSEMBL:ENST00000370300.8:c.105G>A
• ENSEMBL:ENST00000370305.5:c.-6+165G>A

Show All 32

HGVS.p name

• ENSP00000359323:p.Pro35=
• ENSP00000402038:p.Pro35=

Show All 8

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences