Allele/Variant

rs587298688

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

6:6004001

Nucleotide Change

A>G

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000072.7:g.6004001A>G

HGVS.c name

ENSEMBL:ENSMUST00000115554.1:c.1450-2269A>G
ENSEMBL:ENSMUST00000115555.1:c.1561-2269A>G

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr6:5725772...6028030 (302.26 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:ENSMUST00000115554	protein_coding		Intron 13/15	intron variant
	ENSEMBL:ENSMUST00000115555	protein_coding		Intron 14/16	intron variant
	ENSEMBL:ENSMUST00000115556	protein_coding		Intron 14/16	intron variant
	ENSEMBL:ENSMUST00000115559	protein_coding		Intron 14/16	intron variant
	RefSeq:NM_001191023.2	protein_coding		Intron 13/15	intron variant
	RefSeq:NM_001191025.2	protein_coding		Intron 13/15	intron variant
	RefSeq:NM_001191026.2	protein_coding		Intron 14/16	intron variant
	RefSeq:NM_001191027.2	protein_coding		Intron 13/15	intron variant
	RefSeq:NM_001409608.1	protein_coding		Intron 14/16	intron variant
	RefSeq:NM_001409609.1	protein_coding		Intron 15/17	intron variant

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