Allele/Variant

rs239777531

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

3:107847613

Nucleotide Change

G>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)3:107847613G>T

HGVS.c name

ENSEMBL:ENSMUST00000106683.1:c.282+696C>A
ENSEMBL:ENSMUST00000106684.1:c.609+696C>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr3:107846163...107851065 (4.90 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:ENSMUST00000106683	protein_coding		Intron 4/4	intron variant
	ENSEMBL:ENSMUST00000106684	protein_coding		Intron 7/7	intron variant
	ENSEMBL:ENSMUST00000106685	protein_coding		Intron 7/7	intron variant
	ENSEMBL:ENSMUST00000155926	protein_coding		Intron 5/5	intron variant
	RefSeq:NM_001379504.1	protein_coding		Intron 9/9	intron variant
	RefSeq:NM_001379505.1	protein_coding		Intron 7/7	intron variant
	RefSeq:NM_001379506.1	protein_coding		Intron 7/7	intron variant
	RefSeq:NM_001379507.1	protein_coding		Intron 8/8	intron variant
	RefSeq:NM_001379508.1	protein_coding		Intron 6/6	intron variant
	RefSeq:NM_001379509.1	protein_coding		Intron 5/5	intron variant

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