Allele/Variant

rs218577070

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

17:14068163

Nucleotide Change

T>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000083.7:g.14068163T>A

HGVS.c name

ENSEMBL:ENSMUST00000137495.1:n.2290-1207T>A
ENSEMBL:ENSMUST00000137708.1:c.2038-1207T>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr17:13980735...14126059 (145.32 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:ENSMUST00000137495	transcript		Intron 14/18	intron variant
	ENSEMBL:ENSMUST00000137708	protein_coding		Intron 15/30	intron variant
	ENSEMBL:ENSMUST00000137784	protein_coding		Intron 15/33	intron variant
	ENSEMBL:ENSMUST00000139666	protein_coding		Intron 15/32	intron variant
	ENSEMBL:ENSMUST00000150848	protein_coding		Intron 14/31	intron variant
	ENSEMBL:ENSMUST00000170827	protein_coding		Intron 14/32	intron variant
	RefSeq:NM_010806.1	protein_coding		Intron 15/32	intron variant
	RefSeq:NR_151731.1	transcript		Intron 15/33	intron variant
	RefSeq:XM_006523752.4	protein_coding		Intron 15/34	intron variant
	RefSeq:XM_006523753.4	protein_coding		Intron 15/34	intron variant

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