Allele/Variant

rs37363055

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:135389079

Nucleotide Change

T>C

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)1:135389079T>C

HGVS.c name

ENSEMBL:ENSMUST00000067414.1:c.3316-567A>G
ENSEMBL:ENSMUST00000189252.1:c.336-567A>G

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:135362318...135615843 (253.53 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:ENSMUST00000067414	protein_coding		Intron 13/29	intron variant
	ENSEMBL:ENSMUST00000189252	protein_coding		Intron 4/7	intron variant
	ENSEMBL:ENSMUST00000190130	transcript		Intron 11/13	intron variant
	ENSEMBL:ENSMUST00000190298	protein_coding		Intron 15/30	intron variant
	RefSeq:NM_001427516.1	protein_coding		Intron 16/32	intron variant
	RefSeq:NM_173437.2	protein_coding		Intron 13/29	intron variant
	RefSeq:XM_006529369.4	protein_coding		Intron 19/35	intron variant
	RefSeq:XM_006529370.4	protein_coding		Intron 18/34	intron variant
	RefSeq:XM_006529371.4	protein_coding		Intron 19/34	intron variant
	RefSeq:XM_006529372.4	protein_coding		Intron 18/34	intron variant

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