S100A16 S100 calcium binding protein A16

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Variants
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Information

Symbol: S100A16
Type: protein-coding
Description: S100 calcium binding protein A16
Entrez Gene ID: 140576
Genome: hg19
Position: chr1:153,579,362-153,585,613
Genome: hg38
Position: chr1:153,606,886-153,613,137
MIM: 617437 OMIM
HGNC: HGNC:20441 HGNC
Ensembl: ENSG00000188643 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
Uncertain significance	0	16

Ranking

	ClinVar
	0
	0
	0
	18
	0

Frequency

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

EXAC_EAS

EXAC_EAS

HGVD

HGVD

TOMMO

TOMMO

Gene

Position

Disease area statistics

[No Data.]

Locus Zoom

Variants

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Target data	:	MGeND data only
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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

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Target data	:	MGeND data only
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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

Target data	:	MGeND data only
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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

Type	ID
SYNONYM	AAG13
SYNONYM	DT1P1A7
SYNONYM	S100F
MIM	617437 OMIM
HGNC	HGNC:20441 HGNC
Ensembl	ENSG00000188643 Ensembl
AllianceGenome	HGNC:20441

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000368703.6	hg38	chr1	153,606,975	153,608,322	1,348
ENST00000368704.5	hg38	chr1	153,606,886	153,609,337	2,452
ENST00000368705.2	hg38	chr1	153,607,362	153,609,344	1,983
ENST00000368706.9	hg38	chr1	153,606,886	153,613,137	6,252
ENST00000368704.5	hg19	chr1	153,579,362	153,581,813	2,452
ENST00000368706.9	hg19	chr1	153,579,362	153,585,613	6,252
ENST00000368703.6	hg19	chr1	153,579,451	153,580,798	1,348
ENST00000368705.2	hg19	chr1	153,579,838	153,581,820	1,983

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