Allele/Variant

rs262415227

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

3:9034940

Nucleotide Change

T>C

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000069.7:g.9034940T>C

HGVS.c name

ENSEMBL:ENSMUST00000063496.1:c.20-16081A>G
ENSEMBL:ENSMUST00000091355.1:c.20-16081A>G

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr3:8991590...9069824 (78.23 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:ENSMUST00000063496	protein_coding		Intron 1/6	intron variant
	ENSEMBL:ENSMUST00000091355	protein_coding		Intron 1/6	intron variant
	ENSEMBL:ENSMUST00000120143	protein_coding		Intron 1/5	intron variant
	ENSEMBL:ENSMUST00000121038	protein_coding		Intron 1/5	intron variant
	ENSEMBL:ENSMUST00000124956	protein_coding		Intron 1/3	intron variant
	ENSEMBL:ENSMUST00000129736	transcript		Intron 1/3	intron variant
	ENSEMBL:ENSMUST00000134788	protein_coding		Intron 2/6	intron variant
	ENSEMBL:ENSMUST00000155450	protein_coding		Intron 2/3	intron variant
	RefSeq:NM_001025263.2	protein_coding		Intron 1/6	intron variant
	RefSeq:NM_001025264.2	protein_coding		Intron 1/6	intron variant

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