Allele/Variant

rs257232422

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

5:138267263

Nucleotide Change

C>A

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

NC_000071.7:g.138267263C>A

HGVS.c name

ENSEMBL:ENSMUST00000100530.1:c.429+1767G>T
ENSEMBL:ENSMUST00000159067.1:c.*4108+1767G>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr5:138263183...138271102 (7.92 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:ENSMUST00000100530	protein_coding		Intron 2/2	intron variant
	ENSEMBL:ENSMUST00000159067	protein_coding		Intron 10/10	intron variant
	ENSEMBL:ENSMUST00000161279	protein_coding		Intron 3/3	intron variant
	ENSEMBL:ENSMUST00000161647	protein_coding		Intron 3/3	intron variant
	ENSEMBL:ENSMUST00000162557	transcript		Intron 2/2	intron variant
	RefSeq:NM_001347507.1	protein_coding		Intron 3/3	intron variant
	RefSeq:NM_001361283.1	protein_coding		Intron 3/3	intron variant
	RefSeq:XM_006504579.5	protein_coding		Intron 3/3	intron variant
	RefSeq:XM_006504582.4	protein_coding		Intron 3/3	intron variant
	RefSeq:XM_006504583.5	protein_coding		Intron 1/1	intron variant

Showing 1 - 10 of 13 rows

per page

1
2
>