Allele/Variant

rs37239875

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

8:83105088

Nucleotide Change

G>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000074.7:g.83105088G>A

HGVS.c name

ENSEMBL:ENSMUST00000034148.1:c.-88+1035C>T
ENSEMBL:ENSMUST00000209363.1:c.-88+1035C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr8:83058261...83129851 (71.59 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:ENSMUST00000034148	protein_coding		Intron 2/7	intron variant
	ENSEMBL:ENSMUST00000209363	protein_coding		Intron 2/7	intron variant
	ENSEMBL:ENSMUST00000209573	protein_coding		Intron 2/7	intron variant
	ENSEMBL:ENSMUST00000210094	protein_coding		Intron 2/4	intron variant
	ENSEMBL:ENSMUST00000210885	transcript		Intron 2/2	intron variant
	ENSEMBL:ENSMUST00000211282	transcript		Intron 1/1	intron variant
	RefSeq:NM_001254747.2	protein_coding		Intron 2/7	intron variant
	RefSeq:NM_008357.3	protein_coding		Intron 2/7	intron variant
	RefSeq:XM_006530705.5	protein_coding		Intron 2/7	intron variant
	RefSeq:XM_006530706.5	protein_coding		Intron 4/9	intron variant

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