Allele/Variant

rs222713600

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:186960237

Nucleotide Change

C>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)1:186960237C>A

HGVS.c name

ENSEMBL:ENSMUST00000044812.1:c.770+1821C>A
ENSEMBL:ENSMUST00000065573.1:c.770+1821C>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:186947705...187083901 (136.20 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:ENSMUST00000044812	protein_coding		Intron 2/5	intron variant
	ENSEMBL:ENSMUST00000065573	protein_coding		Intron 2/9	intron variant
	ENSEMBL:ENSMUST00000097443	transcript		Intron 2/5	intron variant
	ENSEMBL:ENSMUST00000110943	protein_coding		Intron 2/7	intron variant
	ENSEMBL:ENSMUST00000159748	protein_coding		Intron 2/5	intron variant
	ENSEMBL:ENSMUST00000160471	protein_coding		Intron 2/9	intron variant
	ENSEMBL:ENSMUST00000160481	protein_coding		Intron 2/10	intron variant
	ENSEMBL:ENSMUST00000160570	protein_coding		Intron 1/8	intron variant
	RefSeq:NM_001357645.1	protein_coding		Intron 2/9	intron variant
	RefSeq:NM_001357646.1	protein_coding		Intron 2/7	intron variant

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