Allele/Variant

rs258105721

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

3:94943871

Nucleotide Change

A>G

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)3:94943871A>G

HGVS.c name

ENSEMBL:ENSMUST00000071664.1:c.167+45T>C
ENSEMBL:ENSMUST00000107237.1:c.167+45T>C

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr3:94939999...94949880 (9.88 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:ENSMUST00000071664	protein_coding		Intron 2/9	intron variant
	ENSEMBL:ENSMUST00000107237	protein_coding		Intron 2/9	intron variant
	ENSEMBL:ENSMUST00000117355	protein_coding		Intron 2/8	intron variant
	ENSEMBL:ENSMUST00000143688	transcript		Intron 2/2	intron variant
	RefSeq:NM_001282017.2	protein_coding		Intron 2/9	intron variant
	RefSeq:NM_001410538.1	protein_coding		Intron 2/9	intron variant
	RefSeq:NM_001410539.1	protein_coding		Intron 1/8	intron variant
	RefSeq:NM_001410540.1	protein_coding		Intron 1/8	intron variant
	RefSeq:NM_001410541.1	protein_coding		Intron 2/8	intron variant
	RefSeq:NM_001410542.1	protein_coding		Intron 2/8	intron variant

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