Allele/Variant

rs263407622

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:164146907

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000067.7:g.164146907C>T

HGVS.c name

ENSEMBL:ENSMUST00000086028.1:c.60+6400C>T
ENSEMBL:ENSMUST00000191947.1:c.60+6400C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:164135091...164264870 (129.78 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:ENSMUST00000086028	protein_coding		Intron 1/7	intron variant
	ENSEMBL:ENSMUST00000191947	protein_coding		Intron 2/12	intron variant
	ENSEMBL:ENSMUST00000193683	protein_coding		Intron 3/13	intron variant
	ENSEMBL:ENSMUST00000193808	protein_coding		Intron 4/15	intron variant
	ENSEMBL:ENSMUST00000195474	transcript		Intron 2/8	intron variant
	RefSeq:NM_001293313.1	protein_coding		Intron 3/13	intron variant
	RefSeq:NM_138314.4	protein_coding		Intron 3/13	intron variant
	RefSeq:NM_178071.6	protein_coding		Intron 3/9	intron variant
	RefSeq:XM_006496692.4	protein_coding		Intron 2/12	intron variant
	RefSeq:XM_006496693.5	protein_coding		Intron 1/11	intron variant

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