Allele/Variant

rs232565529

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

13:95359836

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000079.7:g.95359836C>T

HGVS.c name

ENSEMBL:ENSMUST00000159598.1:c.-31+26922G>A
ENSEMBL:ENSMUST00000159608.1:c.-74+142G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr13:95160962...95386844 (225.88 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:ENSMUST00000159598	protein_coding		Intron 1/4	intron variant
	ENSEMBL:ENSMUST00000159608	protein_coding		Intron 1/17	intron variant
	ENSEMBL:ENSMUST00000160957	protein_coding		Intron 1/12	intron variant
	ENSEMBL:ENSMUST00000162153	protein_coding		Intron 1/21	intron variant
	ENSEMBL:ENSMUST00000162412	protein_coding		Intron 1/19	intron variant
	RefSeq:NM_001346782.2	protein_coding		Intron 1/21	intron variant
	RefSeq:NM_001374005.1	protein_coding		Intron 1/18	intron variant
	RefSeq:NM_001374006.1	protein_coding		Intron 1/18	intron variant
	RefSeq:NM_001374007.1	protein_coding		Intron 1/21	intron variant
	RefSeq:NM_001404691.1	protein_coding		Intron 1/20	intron variant

Showing 1 - 10 of 22 rows

per page

1
2
3
>