Allele/Variant

rs219690801

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

2:134945684

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000068.8:g.134945684C>T

HGVS.c name

ENSEMBL:ENSMUST00000070724.1:c.246+115572C>T
ENSEMBL:ENSMUST00000110116.1:c.246+115572C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr2:134628084...135317178 (689.09 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:ENSMUST00000070724	protein_coding		Intron 3/31	intron variant
	ENSEMBL:ENSMUST00000110116	protein_coding		Intron 3/31	intron variant
	ENSEMBL:ENSMUST00000131552	protein_coding		Intron 3/32	intron variant
	RefSeq:NM_001145830.1	protein_coding		Intron 3/31	intron variant
	RefSeq:NM_019677.2	protein_coding		Intron 3/32	intron variant
	RefSeq:XM_006498930.4	protein_coding		Intron 2/30	intron variant
	RefSeq:XM_036159560.1	protein_coding		Intron 2/30	intron variant

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