Allele/Variant

rs215485028

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:160902163

Nucleotide Change

C>G

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)1:160902163C>G

HGVS.c name

ENSEMBL:ENSMUST00000028035.1:c.-3-164C>G
ENSEMBL:ENSMUST00000111618.1:c.-3-164C>G

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:160898337...160914294 (15.96 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:ENSMUST00000028035	protein_coding		Intron 1/3	intron variant
	ENSEMBL:ENSMUST00000111618	protein_coding		Intron 2/5	intron variant
	ENSEMBL:ENSMUST00000111620	protein_coding		Intron 1/4	intron variant
	ENSEMBL:ENSMUST00000143486	protein_coding		Intron 1/4	intron variant
	ENSEMBL:ENSMUST00000192150	protein_coding		Intron 1/5	intron variant
	ENSEMBL:ENSMUST00000192850	protein_coding		Intron 1/5	intron variant
	ENSEMBL:ENSMUST00000194855	protein_coding		Intron 1/4	intron variant
	ENSEMBL:ENSMUST00000195571	protein_coding		Intron 1/4	intron variant
	RefSeq:NM_001159930.2	protein_coding		Intron 1/4	intron variant
	RefSeq:NR_131028.1	transcript		Intron 1/5	intron variant

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