Allele/Variant

rs212427935

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:171978394

Nucleotide Change

G>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)1:171978394G>A

HGVS.c name

ENSEMBL:ENSMUST00000074144.1:c.-20+1506G>A
ENSEMBL:ENSMUST00000191689.1:c.-20+1506G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:171975574...172023959 (48.39 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:ENSMUST00000074144	protein_coding		Intron 1/12	intron variant
	ENSEMBL:ENSMUST00000191689	protein_coding		Intron 2/13	intron variant
	ENSEMBL:ENSMUST00000192704	protein_coding		Intron 2/13	intron variant
	ENSEMBL:ENSMUST00000193638	protein_coding		Intron 2/13	intron variant
	RefSeq:NM_001357204.2	protein_coding		Intron 2/13	intron variant
	RefSeq:NM_001421210.1	protein_coding		Intron 2/13	intron variant
	RefSeq:NM_001421211.1	protein_coding		Intron 1/12	intron variant
	RefSeq:NM_001421212.1	protein_coding		Intron 2/12	intron variant
	RefSeq:NM_001421213.1	protein_coding		Intron 2/12	intron variant
	RefSeq:NM_001421214.1	protein_coding		Intron 2/12	intron variant

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