Allele/Variant

rs31177059

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

3:132795140

Nucleotide Change

G>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)3:132795140G>A

HGVS.c name

ENSEMBL:ENSMUST00000029651.1:c.-22+2201C>T
ENSEMBL:ENSMUST00000080583.1:c.-22+2498C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr3:132687513...132797794 (110.28 kb)

Assembly version

Not Available

Viewer Help

Data currently unavailable; sequence viewer under construction

Variant Molecular Consequences

	Sequence feature	Sequence feature type	Associated gene	Location	Molecular consequence	Codon and amino acid change
	ENSEMBL:ENSMUST00000029651	protein_coding		Intron 1/11	intron variant
	ENSEMBL:ENSMUST00000080583	protein_coding		Intron 1/11	intron variant
	ENSEMBL:ENSMUST00000161577	transcript		Intron 1/9	intron variant
	RefSeq:NM_001356309.1	protein_coding		Intron 1/11	intron variant
	RefSeq:NM_026231.3	protein_coding		Intron 1/11	intron variant
	RefSeq:XR_003954372.2	transcript		Intron 1/12	intron variant

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