Allele/Variant

rs235563240

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:166229079

Nucleotide Change

C>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000067.7:g.166229079C>A

HGVS.c name

ENSEMBL:ENSMUST00000128861.1:c.358+356G>T
ENSEMBL:ENSMUST00000131487.1:c.358+356G>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:166221179...166237402 (16.22 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:ENSMUST00000128861	protein_coding		Intron 5/5	intron variant
	ENSEMBL:ENSMUST00000131487	protein_coding		Intron 4/4	intron variant
	ENSEMBL:ENSMUST00000135673	protein_coding		Intron 4/5	intron variant
	ENSEMBL:ENSMUST00000148243	protein_coding		Intron 2/3	intron variant
	RefSeq:NM_001142948.4	protein_coding		Intron 4/4	intron variant
	RefSeq:NM_001405162.3	protein_coding		Intron 3/3	intron variant
	RefSeq:NM_001405163.3	protein_coding		Intron 4/4	intron variant
	RefSeq:NM_001405164.1	protein_coding		Intron 2/2	intron variant
	RefSeq:NM_001405165.1	protein_coding		Intron 3/3	intron variant
	RefSeq:NM_175170.7	protein_coding		Intron 5/5	intron variant

Showing 1 - 10 of 10 rows

per page

1