Allele/Variant

rs227026257

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

3:83902449

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000069.7:g.83902449C>T

HGVS.c name

ENSEMBL:ENSMUST00000052342.1:c.240-26916G>A
ENSEMBL:ENSMUST00000191758.1:c.240-26916G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr3:83804962...83947482 (142.52 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:ENSMUST00000052342	protein_coding		Intron 3/33	intron variant
	ENSEMBL:ENSMUST00000191758	protein_coding		Intron 3/34	intron variant
	ENSEMBL:ENSMUST00000192095	protein_coding		Intron 3/33	intron variant
	RefSeq:NM_001399526.1	protein_coding		Intron 3/34	intron variant
	RefSeq:NM_172681.5	protein_coding		Intron 3/34	intron variant
	RefSeq:XM_006501323.3	protein_coding		Intron 3/34	intron variant
	RefSeq:XM_006501324.3	protein_coding		Intron 3/34	intron variant
	RefSeq:XM_006501325.2	protein_coding		Intron 3/33	intron variant
	RefSeq:XM_006501326.4	protein_coding		Intron 3/33	intron variant
	RefSeq:XM_006501327.3	protein_coding		Intron 3/33	intron variant

Showing 1 - 10 of 12 rows

per page

1
2
>