Allele/Variant

rs51576668

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

7:79394672

Nucleotide Change

T>C

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)7:79394672T>C

HGVS.c name

ENSEMBL:ENSMUST00000035622.1:c.-39+1741T>C
RefSeq:NM_001037927.1:c.-39+1741T>C

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr7:79392911...79435698 (42.79 kb)

Assembly version

Not Available

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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:ENSMUST00000035622	protein_coding		Intron 1/17	intron variant
	RefSeq:NM_001037927.1	protein_coding		Intron 1/17	intron variant
	RefSeq:NM_001381990.1	protein_coding		Intron 1/17	intron variant
	RefSeq:NM_001381991.1	protein_coding		Intron 1/16	intron variant
	RefSeq:NM_001381992.1	protein_coding		Intron 1/18	intron variant
	RefSeq:NM_001421522.1	protein_coding		Intron 1/17	intron variant

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