Allele/Variant

rs243952470

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

14:105533554

Nucleotide Change

A>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)14:105533554A>T

HGVS.c name

ENSEMBL:ENSMUST00000138283.1:c.721+1228A>T
ENSEMBL:ENSMUST00000149358.1:n.239+1228A>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr14:105496008...105546732 (50.72 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:ENSMUST00000138283	protein_coding		Intron 4/7	intron variant
	ENSEMBL:ENSMUST00000149358	transcript		Intron 2/5	intron variant
	ENSEMBL:ENSMUST00000181969	protein_coding		Intron 4/7	intron variant
	ENSEMBL:ENSMUST00000249907	protein_coding		Intron 4/7	intron variant
	ENSEMBL:ENSMUST00000249908	protein_coding		Intron 3/6	intron variant
	ENSEMBL:ENSMUST00000249909	protein_coding		Intron 4/6	intron variant
	RefSeq:NM_001190989.2	protein_coding		Intron 4/7	intron variant
	RefSeq:NM_029561.5	protein_coding		Intron 4/7	intron variant
	RefSeq:XR_001781167.3	transcript		Intron 4/5	intron variant

Showing 1 - 9 of 9 rows

per page

1