Information

Variants

Display target variant

MGeND data only All data

Search Word

Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

Search Word

Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Exon

CDS

Exon number	Type	Start	Stop
3	CDS	135,965,175	135,965,183
2	CDS	135,971,058	135,971,110
1	CDS	135,973,597	135,973,675

Other genome

Genome	Chromosome	Start	End	Links
hg19	chrX	135,045,332	135,055,843	Link

CDS sequence

ATGGCGCCGTCGCTGTGGAAGGGGCTGGTGGGCATCGGTCTCTTTGCCCTAGCCCACGCCGCCTTTTCCGCTGCGCAGCATCGTTCTTATATGCGATTAACAGAAAAAGAAGATGAATCACTGCCAATAGATGACATTTGA

Amino sequence

MAPSLWKGLVGIGLFALAHAAFSAAQHRSYMRLTEKEDESLPIDDI*

ENST00000681201.1 MMGT1