Allele/Variant

rs244199860

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

9:15638829

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000075.7:g.15638829C>T

HGVS.c name

ENSEMBL:ENSMUST00000061568.1:c.759+495C>T
ENSEMBL:ENSMUST00000115588.1:c.759+495C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr9:15621034...15653684 (32.65 kb)

Assembly version

Not Available

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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:ENSMUST00000061568	protein_coding		Intron 7/10	intron variant
	ENSEMBL:ENSMUST00000115588	protein_coding		Intron 7/10	intron variant
	ENSEMBL:ENSMUST00000214954	protein_coding		Intron 1/4	intron variant
	RefSeq:NM_001357565.1	protein_coding		Intron 7/10	intron variant
	RefSeq:NM_001357566.1	protein_coding		Intron 7/10	intron variant
	RefSeq:NM_001357567.1	protein_coding		Intron 7/10	intron variant
	RefSeq:NM_172289.5	protein_coding		Intron 7/10	intron variant
	RefSeq:XM_006510170.5	protein_coding		Intron 7/10	intron variant
	RefSeq:XM_030244281.2	protein_coding		Intron 7/10	intron variant

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