Allele/Variant

rs254963555

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

3:145531907

Nucleotide Change

C>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)3:145531907C>A

HGVS.c name

ENSEMBL:ENSMUST00000029845.1:c.304-19553C>A
ENSEMBL:ENSMUST00000120310.1:c.-6-19553C>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr3:145464447...145600032 (135.59 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:ENSMUST00000029845	protein_coding		Intron 1/5	intron variant
	ENSEMBL:ENSMUST00000120310	protein_coding		Intron 1/5	intron variant
	ENSEMBL:ENSMUST00000127193	transcript		Intron 1/4	intron variant
	RefSeq:NM_026993.3	protein_coding		Intron 1/5	intron variant
	RefSeq:XM_011240221.4	protein_coding		Intron 1/5	intron variant
	RefSeq:XM_030252803.1	protein_coding		Intron 1/5	intron variant

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