Allele/Variant

rs239487164

Species

Mus musculus

Symbol

Category

Variant

Variant type

SNP

Overlaps

Location

1:192343301

Nucleotide Change

C>T

Most Severe Consequence

intron variant

See all consequences

HGVS.g name

(GRCm39)1:192343301C>T

HGVS.c name

ENSEMBL:ENSMUST00000044190.1:c.1061+463G>A
ENSEMBL:ENSMUST00000123721.1:n.247+463G>A

HGVS.p name

Not Available

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr1:192195133...192453546 (258.41 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:ENSMUST00000044190	protein_coding		Intron 9/11	intron variant
	ENSEMBL:ENSMUST00000123721	transcript		Intron 3/3	intron variant
	ENSEMBL:ENSMUST00000128619	protein_coding		Intron 9/11	intron variant
	ENSEMBL:ENSMUST00000154755	transcript		Intron 4/4	intron variant
	ENSEMBL:ENSMUST00000192585	protein_coding		Intron 9/11	intron variant
	RefSeq:NM_144881.5	protein_coding		Intron 9/11	intron variant
	RefSeq:XM_011238934.4	protein_coding		Intron 6/8	intron variant
	RefSeq:XM_017320220.3	protein_coding		Intron 6/8	intron variant
	RefSeq:XM_017320221.3	protein_coding		Intron 4/6	intron variant

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