Allele/Variant

rs263855605

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

2:71304016

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)2:71304016C>T

HGVS.c name

ENSEMBL:ENSMUST00000037210.1:c.40+20274C>T
ENSEMBL:ENSMUST00000123858.1:n.66+20274C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr2:71283625...71355538 (71.91 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:ENSMUST00000037210	protein_coding		Intron 1/9	intron variant
	ENSEMBL:ENSMUST00000123858	transcript		Intron 1/5	intron variant
	ENSEMBL:ENSMUST00000124875	transcript		Intron 1/8	intron variant
	ENSEMBL:ENSMUST00000139045	transcript		Intron 1/8	intron variant
	RefSeq:NM_001418521.1	protein_coding		Intron 1/10	intron variant
	RefSeq:NM_001418522.1	protein_coding		Intron 1/9	intron variant
	RefSeq:NM_001418523.1	protein_coding		Intron 1/5	intron variant
	RefSeq:NM_001418524.1	protein_coding		Intron 1/5	intron variant
	RefSeq:NM_001418525.1	protein_coding		Intron 1/5	intron variant
	RefSeq:NM_001418526.1	protein_coding		Intron 1/5	intron variant

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