rs104939222

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Species

Rattus norvegicus

Symbol

rs104939222

Category

Variant

Variant type

SNP

Overlaps

Snx12

Location

X:66281363

Nucleotide Change

C>A

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_051356.1:g.66281363C>A

Show All 5

HGVS.c name

• ENSEMBL:ENSRNOT00000076635.3:c.466-50051G>T
• RefSeq:NM_001108817.2:c.478-50051G>T

Show All 4

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences