View genomic variant #0000015600

Variant on transcripts

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Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.

Affects function: The variant's effect on the protein's function, in the format 'R/C' where R is the value reported by the source and C is the value concluded by the curator; '+' indicating the variant affects function, '+?' probably affects function, '+*' affects function, not associated with individual's disease phenotype, '#' affects function, not associated with any known disease phenotype, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect not classified.

Location: Location of variant at DNA level; note that the variant location can also be derived from the variant description.
All options:

• 5' gene flanking
• 5' UTR
• Exon
• Intron
• 3' UTR
• 3' gene flanking

Exon: Number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = exons 3 to 7, 8i_9 = border intron 8/exon 9.

DNA change (cDNA): Description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup.

Protein: Description of variant at protein level (following HGVS recommendations).

• p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
• p.Arg345Pro = change derived from RNA analysis
• p.? = unknown effect
• p.0? = probably no protein produced

PolyPhen: Effect of variant, predicted by PolyPhen.
All options:

• benign = Benign
• possiblyDamaging = Possibly damaging
• probablyDamaging = Probably damaging
• noPrediction = No prediction

GVS function: The functional annotation of this position from the Genome Variation Server.
All options:

• intergenic
• near-gene-5
• utr-5
• coding
• coding-near-splice
• coding-synonymous
• coding-synonymous-near-splice
• codingComplex
• codingComplex-near-splice
• frameshift
• frameshift-near-splice
• missense
• missense-near-splice
• splice-5
• intron
• splice-3
• stop-gained
• stop-gained-near-splice
• stop-lost
• stop-lost-near-splice
• utr-3
• near-gene-3

Splice distance: The distance to the nearest splice site.

SIFT: SIFT Annotation

4 entries on 1 page. Showing entries 1 - 4.

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Gene	Transcript ID	Transcript	Variant ID	Affects function	Location	Exon	DNA change (cDNA)	Protein	PolyPhen	GVS function	Splice distance	SIFT
NDUFS2	00000209	NM_001166159.1	0000015600	./.	-	-	c.*328_*329insTGTGTG	p.(=)	-	-	-	-
NDUFS2	00000208	NM_004550.4	0000015600	./.	-	-	c.*76_*77insTGTGTG	p.(=)	-	-	-	-
NDUFS2	00000207	XM_005245208.1	0000015600	./.	-	-	c.*76_*77insTGTGTG	p.(=)	-	-	-	-
NDUFS2	00000210	XM_005245209.1	0000015600	./.	-	-	c.*76_*77insTGTGTG	p.(=)	-	-	-	-

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ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV001662962;
Chromosome	1:161184059..161184060
ClinVar Allele ID	1243345
Disease database name and identifier	MedGen:C3661900
ClinVar preferred disease name	not provided
HGVS variant names	NC 000001.10:g.161184061GT[17]
ClinVar review status	criteria provided, single submitter
Clinical Significance	Benign
Variant type	Microsatellite
Sequence Ontology for variant type	SO:0000289
Gene symbol:Gene id.	NDUFS2:4720
Molecular consequence	SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin	germline
dbSNP ID	10629771
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000317766; RCV001711871;
Chromosome	1:161184059..161184060
ClinVar Allele ID	277891
Disease database name and identifier	MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MedGen:CN517202
ClinVar preferred disease name	Mitochondrial complex I deficiency|not provided
HGVS variant names	NC 000001.10:g.161184061GT[18]
ClinVar review status	criteria provided, conflicting interpretations
Clinical Significance	Conflicting interpretations of pathogenicity
Conflicting clinical significance	Uncertain significance(1)|Benign(1)
Variant type	Microsatellite
Sequence Ontology for variant type	SO:0000289
Variant clinical sources reported	ClinGen:CA10608518
Gene symbol:Gene id.	NDUFS2:4720
Molecular consequence	SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin	germline
dbSNP ID	10629771
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV001696297;
Chromosome	1:161184059..161184060
ClinVar Allele ID	1272012
Disease database name and identifier	MedGen:C3661900
ClinVar preferred disease name	not provided
HGVS variant names	NC 000001.10:g.161184061GT[19]
ClinVar review status	criteria provided, single submitter
Clinical Significance	Benign
Variant type	Microsatellite
Sequence Ontology for variant type	SO:0000289
Gene symbol:Gene id.	NDUFS2:4720
Molecular consequence	SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin	germline
dbSNP ID	10629771
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV001589362;
Chromosome	1:161184059..161184060
ClinVar Allele ID	1202119
Disease database name and identifier	MedGen:C3661900
ClinVar preferred disease name	not provided
HGVS variant names	NC 000001.10:g.161184061GT[20]
ClinVar review status	criteria provided, single submitter
Clinical Significance	Likely benign
Variant type	Microsatellite
Sequence Ontology for variant type	SO:0000289
Gene symbol:Gene id.	NDUFS2:4720
Molecular consequence	SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin	germline
dbSNP ID	10629771
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV001583406;
Chromosome	1:161184059..161184060
ClinVar Allele ID	1201594
Disease database name and identifier	MedGen:C3661900
ClinVar preferred disease name	not provided
HGVS variant names	NC 000001.10:g.161184061GT[21]
ClinVar review status	criteria provided, single submitter
Clinical Significance	Likely benign
Variant type	Microsatellite
Sequence Ontology for variant type	SO:0000289
Gene symbol:Gene id.	NDUFS2:4720
Molecular consequence	SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin	germline
dbSNP ID	10629771
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR
RCVaccession	RCV000378510;
Chromosome	1:161184060..161184061
ClinVar Allele ID	277994
Disease database name and identifier	MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name	Mitochondrial complex I deficiency
HGVS variant names	NC 000001.10:g.161184061GT[14]
ClinVar review status	criteria provided, single submitter
Clinical Significance	Uncertain significance
Variant type	Microsatellite
Sequence Ontology for variant type	SO:0000289
Variant clinical sources reported	ClinGen:CA10608554
Gene symbol:Gene id.	NDUFS2:4720
Molecular consequence	SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin	germline
dbSNP ID	10629771
Variant Flags	:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None