Allele/Variant

rs50851940

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

12:79038618

Nucleotide Change

A>G

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)12:79038618A>G

HGVS.c name

ENSEMBL:ENSMUST00000056660.1:c.-199-13903T>C
ENSEMBL:ENSMUST00000173095.1:n.288-13903T>C

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr12:79008569...79054333 (45.76 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:ENSMUST00000056660	protein_coding		Intron 1/2	intron variant
	ENSEMBL:ENSMUST00000173095	transcript		Intron 1/1	intron variant
	ENSEMBL:ENSMUST00000174697	protein_coding		Intron 1/1	intron variant
	ENSEMBL:ENSMUST00000174721	protein_coding		Intron 1/2	intron variant
	RefSeq:NM_178745.5	protein_coding		Intron 1/2	intron variant
	RefSeq:XM_006515909.3	protein_coding		Intron 1/2	intron variant
	RefSeq:XM_006515913.3	protein_coding		Intron 1/2	intron variant
	RefSeq:XM_006515914.2	protein_coding		Intron 1/2	intron variant
	RefSeq:XM_006515915.5	protein_coding		Intron 1/1	intron variant
	RefSeq:XM_030246736.2	protein_coding		Intron 1/1	intron variant

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