chr11:2160887:G>C Detail (hg38) (INS, INS-IGF2)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr11:2,182,117-2,182,117 View the variant detail on this assembly version.
hg38	chr11:2,160,887-2,160,887

HGVS

INS
INS-IGF2

Type	Transcript	Protein
RefSeq	NM_000207.2:c.85C>G	NP_000198.1:p.His29Asp
	NM_001185097.1:c.85C>G	NP_001172026.1:p.His29Asp
	NM_001185098.1:c.85C>G	NP_001172027.1:p.His29Asp
	NM_001291897.1:c.85C>G	NP_001278826.1:p.His29Asp
Ensemble	ENST00000250971.7:c.85C>G	ENST00000250971.7:p.His29Asp
	ENST00000381330.5:c.85C>G	ENST00000381330.5:p.His29Asp
	ENST00000397262.5:c.85C>G	ENST00000397262.5:p.His29Asp
	ENST00000512523.1:c.85C>G	ENST00000512523.1:p.His29Asp

Type	Transcript	Protein
RefSeq	NM_001042376.2:c.85C>G	NP_001035835.1:p.His29Asp
Ensemble	ENST00000397270.1:c.85C>G	ENST00000397270.1:p.His29Asp

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Uncertain significance
Review star
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Links

INS
INS-IGF2

Type	Database	ID	Link
Gene	MIM	176730	OMIM
	HGNC	6081	HGNC
	Ensembl	ENSG00000254647	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Type	Database	ID	Link
Gene	MIM
	HGNC	33527	HGNC
	Ensembl	ENSG00000129965	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
not provided		no assertion provided	permanent neonatal diabetes mellitus	not provided	Detail
Uncertain significance		criteria provided, single submitter	Diabetes mellitus, permanent neonatal 4	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.568	DIABETES MELLITUS, PERMANENT NEONATAL	Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS...	UNIPROT	18162506	Detail

Annotation

Annotations

Descrption	Source	Links
NM_000207.3(INS):c.85C>G (p.His29Asp) AND Permanent neonatal diabetes mellitus	ClinVar	Detail
NM_000207.3(INS):c.85C>G (p.His29Asp) AND Diabetes mellitus, permanent neonatal 4	ClinVar	Detail
Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common c...	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs121908272 dbSNP
Genome: hg38
Position: chr11:2,160,887-2,160,887
Variant Type: snv
Reference Allele: G
Alternative Allele: C

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