Allele/Variant

rs244105673

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

3:19318299

Nucleotide Change

G>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)3:19318299G>T

HGVS.c name

ENSEMBL:ENSMUST00000091314.1:c.60+685C>A
ENSEMBL:ENSMUST00000099195.1:c.139-3843C>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr3:19277272...19365486 (88.21 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:ENSMUST00000091314	protein_coding		Intron 1/12	intron variant
	ENSEMBL:ENSMUST00000099195	protein_coding		Intron 1/12	intron variant
	ENSEMBL:ENSMUST00000121951	protein_coding		Intron 1/3	intron variant
	ENSEMBL:ENSMUST00000143120	transcript		Intron 1/2	intron variant
	ENSEMBL:ENSMUST00000156652	protein_coding		Intron 1/8	intron variant
	RefSeq:NM_001122759.2	protein_coding		Intron 1/12	intron variant
	RefSeq:NM_008802.3	protein_coding		Intron 1/12	intron variant
	RefSeq:XM_006535405.4	protein_coding		Intron 1/12	intron variant
	RefSeq:XM_006535406.5	protein_coding		Intron 1/11	intron variant
	RefSeq:XM_006535408.5	protein_coding		Intron 1/10	intron variant

Showing 1 - 10 of 16 rows

per page

1
2
>