Allele/Variant

rs33746319

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

10:30475254

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000076.7:g.30475254C>T

HGVS.c name

ENSEMBL:ENSMUST00000019927.1:c.72+1332G>A
ENSEMBL:ENSMUST00000215595.1:c.72+1332G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr10:30410221...30476745 (66.52 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:ENSMUST00000019927	protein_coding		Intron 1/12	intron variant
	ENSEMBL:ENSMUST00000215595	protein_coding		Intron 1/10	intron variant
	ENSEMBL:ENSMUST00000216705	protein_coding		Intron 1/4	intron variant
	ENSEMBL:ENSMUST00000216790	protein_coding		Intron 1/6	intron variant
	RefSeq:NM_001358806.1	protein_coding		Intron 1/10	intron variant
	RefSeq:NM_028604.3	protein_coding		Intron 1/12	intron variant
	RefSeq:XM_006512877.4	protein_coding		Intron 1/10	intron variant
	RefSeq:XM_006512880.5	protein_coding		Intron 1/11	intron variant
	RefSeq:XM_030245317.2	protein_coding		Intron 1/11	intron variant
	RefSeq:XM_030245319.2	protein_coding		Intron 1/11	intron variant

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