Allele/Variant

rs32687443

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

4:150536275

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)4:150536275C>T

HGVS.c name

ENSEMBL:ENSMUST00000105682.1:c.522+12350C>T
ENSEMBL:ENSMUST00000131600.1:c.343-16877C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr4:150366103...150706423 (340.32 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:ENSMUST00000105682	protein_coding		Intron 4/22	intron variant
	ENSEMBL:ENSMUST00000131600	protein_coding		Intron 2/3	intron variant
	RefSeq:NM_001085492.1	protein_coding		Intron 4/22	intron variant
	RefSeq:XM_006539136.5	protein_coding		Intron 4/22	intron variant
	RefSeq:XM_006539137.5	protein_coding		Intron 4/22	intron variant
	RefSeq:XM_006539139.4	protein_coding		Intron 4/22	intron variant
	RefSeq:XM_006539143.4	protein_coding		Intron 3/21	intron variant
	RefSeq:XM_030253741.2	protein_coding		Intron 4/22	intron variant
	RefSeq:XM_030253743.2	protein_coding		Intron 4/22	intron variant
	RefSeq:XM_030253744.2	protein_coding		Intron 4/22	intron variant

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