Allele/Variant

rs216356498

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

2:49101601

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)2:49101601C>T

HGVS.c name

ENSEMBL:ENSMUST00000112745.1:c.-729-20083C>T
ENSEMBL:ENSMUST00000112754.1:c.-552-33953C>T

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr2:48839511...49209702 (370.19 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:ENSMUST00000112745	protein_coding		Intron 6/10	intron variant
	ENSEMBL:ENSMUST00000112754	protein_coding		Intron 5/14	intron variant
	ENSEMBL:ENSMUST00000147055	transcript		Intron 6/7	intron variant
	RefSeq:NM_029924.2	protein_coding		Intron 6/16	intron variant
	RefSeq:XM_006497604.3	protein_coding		Intron 6/15	intron variant
	RefSeq:XM_017314911.3	protein_coding		Intron 6/17	intron variant
	RefSeq:XM_030246624.1	protein_coding		Intron 6/16	intron variant
	RefSeq:XM_030246625.2	protein_coding		Intron 9/19	intron variant
	RefSeq:XM_030246628.2	protein_coding		Intron 7/17	intron variant
	RefSeq:XM_030246629.2	protein_coding		Intron 5/15	intron variant

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