rs197996022

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Species

Rattus norvegicus

Symbol

rs197996022

Category

Variant

Variant type

SNP

Overlaps

Wars2

Location

2:186470286

Nucleotide Change

T>C

Most Severe Consequence

• intron variant

See all consequences

HGVS.g name

• NC_051337.1:g.186470286T>C

Show All 5

HGVS.c name

• ENSEMBL:ENSRNOT00000104876.1:c.90+8525T>C
• ENSEMBL:ENSRNOT00000106687.1:c.90+8525T>C

Show All 5

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Variant Molecular Consequences