Allele/Variant

rs260224757

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

2:33110467

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)2:33110467C>T

HGVS.c name

ENSEMBL:ENSMUST00000004208.1:c.-42+4002C>T
ENSEMBL:ENSMUST00000042615.1:c.559+40023G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr2:33106081...33137729 (31.65 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:ENSMUST00000004208	protein_coding		Intron 1/4	intron variant
	ENSEMBL:ENSMUST00000042615	protein_coding		Intron 7/16	intron variant
	ENSEMBL:ENSMUST00000091039	protein_coding		Intron 8/19	intron variant
	ENSEMBL:ENSMUST00000113165	protein_coding		Intron 8/18	intron variant
	ENSEMBL:ENSMUST00000131298	protein_coding		Intron 8/17	intron variant
	ENSEMBL:ENSMUST00000193373	protein_coding		Intron 1/2	intron variant
	RefSeq:NM_001290570.1	protein_coding		Intron 7/16	intron variant
	RefSeq:NM_001290572.1	protein_coding		Intron 8/17	intron variant
	RefSeq:NM_011923.4	protein_coding		Intron 1/4	intron variant
	RefSeq:NM_175211.5	protein_coding		Intron 8/19	intron variant

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