Allele/Variant

rs47250862

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

16:26422253

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)16:26422253C>T

HGVS.c name

ENSEMBL:ENSMUST00000023156.1:c.-1-20652C>T
ENSEMBL:ENSMUST00000096129.1:c.-1-20652C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr16:26400454...26548867 (148.41 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:ENSMUST00000023156	protein_coding		Intron 1/10	intron variant
	ENSEMBL:ENSMUST00000096129	protein_coding		Intron 1/10	intron variant
	ENSEMBL:ENSMUST00000166294	protein_coding		Intron 1/11	intron variant
	ENSEMBL:ENSMUST00000174202	protein_coding		Intron 1/7	intron variant
	RefSeq:NM_001159317.1	protein_coding		Intron 1/11	intron variant
	RefSeq:NM_001159318.1	protein_coding		Intron 1/10	intron variant
	RefSeq:NM_008364.2	protein_coding		Intron 1/10	intron variant
	RefSeq:NM_134103.2	protein_coding		Intron 1/7	intron variant
	RefSeq:NR_152416.1	transcript		Intron 1/12	intron variant
	RefSeq:XM_036159791.1	protein_coding		Intron 1/11	intron variant

Showing 1 - 10 of 11 rows

per page

1
2
>