Allele/Variant

rs46414026

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:188711296

Nucleotide Change

G>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)1:188711296G>T

HGVS.c name

ENSEMBL:ENSMUST00000085678.1:c.1313-447C>A
ENSEMBL:ENSMUST00000193143.1:c.1313-447C>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:188703292...188740038 (36.75 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:ENSMUST00000085678	protein_coding		Intron 13/17	intron variant
	ENSEMBL:ENSMUST00000193143	protein_coding		Intron 13/17	intron variant
	RefSeq:NM_001359576.1	protein_coding		Intron 13/17	intron variant
	RefSeq:NM_001359577.1	protein_coding		Intron 11/15	intron variant
	RefSeq:NM_001359578.1	protein_coding		Intron 12/16	intron variant
	RefSeq:NM_172650.2	protein_coding		Intron 13/17	intron variant
	RefSeq:NR_153196.1	transcript		Intron 13/17	intron variant
	RefSeq:XM_017320175.1	protein_coding		Intron 8/12	intron variant
	RefSeq:XM_017320182.1	protein_coding		Intron 8/12	intron variant
	RefSeq:XM_030253563.2	protein_coding		Intron 12/16	intron variant

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