Allele/Variant

rs220738352

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

2:90995844

Nucleotide Change

T>C

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)2:90995844T>C

HGVS.c name

ENSEMBL:ENSMUST00000066420.1:c.2549-32A>G
ENSEMBL:ENSMUST00000066473.1:c.2549-32A>G

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr2:90967705...91013404 (45.70 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:ENSMUST00000066420	protein_coding		Intron 14/19	intron variant
	ENSEMBL:ENSMUST00000066473	protein_coding		Intron 14/35	intron variant
	ENSEMBL:ENSMUST00000075269	protein_coding		Intron 14/31	intron variant
	ENSEMBL:ENSMUST00000077941	protein_coding		Intron 14/34	intron variant
	ENSEMBL:ENSMUST00000099723	protein_coding		Intron 14/34	intron variant
	ENSEMBL:ENSMUST00000099725	protein_coding		Intron 13/34	intron variant
	ENSEMBL:ENSMUST00000111369	protein_coding		Intron 13/30	intron variant
	ENSEMBL:ENSMUST00000111370	protein_coding		Intron 14/33	intron variant
	ENSEMBL:ENSMUST00000111371	protein_coding		Intron 14/32	intron variant
	ENSEMBL:ENSMUST00000111372	protein_coding		Intron 14/31	intron variant

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