Allele/Variant

rs217702422

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

5:117258478

Nucleotide Change

G>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000071.7:g.117258478G>A

HGVS.c name

ENSEMBL:ENSMUST00000111978.1:c.-177+74G>A
RefSeq:NM_001199685.1:c.-177+74G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr5:117258194...117413284 (155.09 kb)

Assembly version

Not Available

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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:ENSMUST00000111978	protein_coding		Intron 1/20	intron variant
	RefSeq:NM_001199685.1	protein_coding		Intron 1/20	intron variant
	RefSeq:XM_006530385.5	protein_coding		Intron 1/21	intron variant
	RefSeq:XM_011248219.4	protein_coding		Intron 1/20	intron variant
	RefSeq:XM_011248220.4	protein_coding		Intron 1/19	intron variant
	RefSeq:XM_011248221.4	protein_coding		Intron 1/20	intron variant
	RefSeq:XM_030254601.2	protein_coding		Intron 1/21	intron variant

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