Allele/Variant

rs248424701

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

14:79770553

Nucleotide Change

A>G

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)14:79770553A>G

HGVS.c name

ENSEMBL:ENSMUST00000040131.1:c.-228-3010A>G
ENSEMBL:ENSMUST00000110835.1:c.-228-3010A>G

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr14:79718619...79819916 (101.30 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:ENSMUST00000040131	protein_coding		Intron 1/8	intron variant
	ENSEMBL:ENSMUST00000110835	protein_coding		Intron 1/8	intron variant
	ENSEMBL:ENSMUST00000227104	transcript		Intron 1/1	intron variant
	ENSEMBL:ENSMUST00000227192	protein_coding		Intron 1/7	intron variant
	RefSeq:NM_001286411.2	protein_coding		Intron 1/8	intron variant
	RefSeq:NM_001286412.2	protein_coding		Intron 1/7	intron variant
	RefSeq:NM_001422240.1	protein_coding		Intron 1/8	intron variant
	RefSeq:NM_001422244.1	protein_coding		Intron 1/7	intron variant
	RefSeq:NM_007920.5	protein_coding		Intron 1/8	intron variant

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