Allele/Variant

rs231669810

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

2:18207197

Nucleotide Change

G>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000068.8:g.18207197G>A

HGVS.c name

ENSEMBL:ENSMUST00000028076.1:c.2070-1215G>A
ENSEMBL:ENSMUST00000114669.1:c.441-1215G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr2:18060048...18217199 (157.15 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:ENSMUST00000028076	protein_coding		Intron 16/22	intron variant
	ENSEMBL:ENSMUST00000114669	protein_coding		Intron 9/15	intron variant
	ENSEMBL:ENSMUST00000114671	protein_coding		Intron 17/23	intron variant
	ENSEMBL:ENSMUST00000114680	protein_coding		Intron 16/22	intron variant
	ENSEMBL:ENSMUST00000148401	protein_coding		Intron 2/2	intron variant
	RefSeq:NM_001252560.1	protein_coding		Intron 16/22	intron variant
	RefSeq:NM_001252561.1	protein_coding		Intron 17/23	intron variant
	RefSeq:NM_010804.4	protein_coding		Intron 16/22	intron variant
	RefSeq:NR_045538.1	transcript		Intron 16/22	intron variant
	RefSeq:NR_045539.1	transcript		Intron 18/24	intron variant

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