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dbSNP Short Genetic Variations

Reference SNP (rs) Report

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This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs863225279

Current Build 151

Released July 17, 2018

Organism
Homo sapiens
Position
chr11:17394354-17394357 (GRCh38.p7) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
delCT
Variation Type
Indel Insertion and Deletion
Frequency
None
Clinical Significance
Reported in ClinVar
Gene : Consequence
ABCC8 : Frameshift
Publications
0 citations
Genomic View
See rs on genome
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p7 chr 11 NC_000011.10:g.17394354_17394355[1]
GRCh37.p13 chr 11 NC_000011.9:g.17415901_17415902[1]
ABCC8 RefSeqGene NG_008867.1:g.87546_87547[1]
Gene: ABCC8, ATP binding cassette subfamily C member 8 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ABCC8 transcript variant 2 NM_000352.4:c.445...

NM_000352.4:c.4454_4455[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform 2 NP_000343.2:p.Arg...

NP_000343.2:p.Arg1486fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant 1 NM_001287174.1:c....

NM_001287174.1:c.4457_4458[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform 1 NP_001274103.1:p....

NP_001274103.1:p.Arg1487fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X10 XM_017018203.1:c. N/A Genic Downstream Transcript Variant
ABCC8 transcript variant X1 XM_017018197.1:c....

XM_017018197.1:c.4523_4524[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X1 XP_016873686.1:p....

XP_016873686.1:p.Arg1509fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X2 XM_017018198.1:c....

XM_017018198.1:c.4520_4521[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X2 XP_016873687.1:p....

XP_016873687.1:p.Arg1508fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X2 XM_017018199.1:c....

XM_017018199.1:c.4520_4521[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X2 XP_016873688.1:p....

XP_016873688.1:p.Arg1508fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X4 XM_011520331.2:c....

XM_011520331.2:c.4454_4455[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X4 XP_011518633.1:p....

XP_011518633.1:p.Arg1486fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X5 XM_017018200.1:c....

XM_017018200.1:c.4451_4452[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X5 XP_016873689.1:p....

XP_016873689.1:p.Arg1485fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X7 XM_017018201.1:c....

XM_017018201.1:c.4419_4420[1]

E [GAG]> G [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X3 XP_016873690.1:p....

XP_016873690.1:p.Glu1474fs

E [Glu]> G [Gly] Frameshift
ABCC8 transcript variant X6 XM_017018202.1:c....

XM_017018202.1:c.3020_3021[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X4 XP_016873691.1:p....

XP_016873691.1:p.Arg1008fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X9 XM_017018204.1:c....

XM_017018204.1:c.2411_2412[1]

R [AGG]> A [G] Coding Sequence Variant
ATP-binding cassette sub-family C member 8 isoform X6 XP_016873693.1:p....

XP_016873693.1:p.Arg805fs

R [Arg]> A [Ala] Frameshift
ABCC8 transcript variant X6 XR_001747945.1:n....

XR_001747945.1:n.4482_4483[1]

AGAG>AG Non Coding Transcript Variant
ABCC8 transcript variant X8 XR_001747946.1:n....

XR_001747946.1:n.4413_4414[1]

AGAG>AG Non Coding Transcript Variant
ABCC8 transcript variant X11 XR_001747947.1:n. N/A Genic Downstream Transcript Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Allele: delCT (allele ID: 214501 )
ClinVar Accession Disease Names Clinical Significance
RCV000201891.1 not provided Pathogenic
Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

None
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement CTCT= delCT Note
GRCh38.p7 chr 11 NC_000011.10:g.17394354...

NC_000011.10:g.17394354_17394357CTCT=

NC_000011.10:g.17394354...

NC_000011.10:g.17394354_17394355[1]

GRCh37.p13 chr 11 NC_000011.9:g.17415901_...

NC_000011.9:g.17415901_17415904CTCT=

NC_000011.9:g.17415901_...

NC_000011.9:g.17415901_17415902[1]

ABCC8 RefSeqGene NG_008867.1:g.87546_875...

NG_008867.1:g.87546_87549AGAG=

NG_008867.1:g.87546_875...

NG_008867.1:g.87546_87547[1]

ABCC8 transcript variant 2 NM_000352.4:c.4454_4457...

NM_000352.4:c.4454_4457AGAG=

NM_000352.4:c.4454_4455[1]
ABCC8 transcript NM_000352.3:c.4454_4457...

NM_000352.3:c.4454_4457AGAG=

NM_000352.3:c.4454_4455[1]
ABCC8 transcript variant 1 NM_001287174.1:c.4457_4...

NM_001287174.1:c.4457_4460AGAG=

NM_001287174.1:c.4457_4...

NM_001287174.1:c.4457_4458[1]

ABCC8 transcript variant X4 XM_011520331.2:c.4454_4...

XM_011520331.2:c.4454_4457AGAG=

XM_011520331.2:c.4454_4...

XM_011520331.2:c.4454_4455[1]

ABCC8 transcript variant X2 XM_017018199.1:c.4520_4...

XM_017018199.1:c.4520_4523AGAG=

XM_017018199.1:c.4520_4...

XM_017018199.1:c.4520_4521[1]

ABCC8 transcript variant X1 XM_017018197.1:c.4523_4...

XM_017018197.1:c.4523_4526AGAG=

XM_017018197.1:c.4523_4...

XM_017018197.1:c.4523_4524[1]

ABCC8 transcript variant X2 XM_017018198.1:c.4520_4...

XM_017018198.1:c.4520_4523AGAG=

XM_017018198.1:c.4520_4...

XM_017018198.1:c.4520_4521[1]

ABCC8 transcript variant X5 XM_017018200.1:c.4451_4...

XM_017018200.1:c.4451_4454AGAG=

XM_017018200.1:c.4451_4...

XM_017018200.1:c.4451_4452[1]

ABCC8 transcript variant X6 XR_001747945.1:n.4482_4...

XR_001747945.1:n.4482_4485AGAG=

XR_001747945.1:n.4482_4...

XR_001747945.1:n.4482_4483[1]

ABCC8 transcript variant X8 XR_001747946.1:n.4413_4...

XR_001747946.1:n.4413_4416AGAG=

XR_001747946.1:n.4413_4...

XR_001747946.1:n.4413_4414[1]

ABCC8 transcript variant X6 XM_017018202.1:c.3020_3...

XM_017018202.1:c.3020_3023AGAG=

XM_017018202.1:c.3020_3...

XM_017018202.1:c.3020_3021[1]

ABCC8 transcript variant X7 XM_017018201.1:c.4419_4...

XM_017018201.1:c.4419_4422AGAG=

XM_017018201.1:c.4419_4...

XM_017018201.1:c.4419_4420[1]

ABCC8 transcript variant X9 XM_017018204.1:c.2411_2...

XM_017018204.1:c.2411_2414AGAG=

XM_017018204.1:c.2411_2...

XM_017018204.1:c.2411_2412[1]

ATP-binding cassette sub-family C member 8 isoform 2 NP_000343.2:p.Gln1485_A...

NP_000343.2:p.Gln1485_Arg1486=

NP_000343.2:p.Arg1486fs
ATP-binding cassette sub-family C member 8 isoform 1 NP_001274103.1:p.Gln148...

NP_001274103.1:p.Gln1486_Arg1487=

NP_001274103.1:p.Arg1487fs
ATP-binding cassette sub-family C member 8 isoform X4 XP_011518633.1:p.Gln148...

XP_011518633.1:p.Gln1485_Arg1486=

XP_011518633.1:p.Arg1486fs
ATP-binding cassette sub-family C member 8 isoform X2 XP_016873688.1:p.Gln150...

XP_016873688.1:p.Gln1507_Arg1508=

XP_016873688.1:p.Arg1508fs
ATP-binding cassette sub-family C member 8 isoform X1 XP_016873686.1:p.Gln150...

XP_016873686.1:p.Gln1508_Arg1509=

XP_016873686.1:p.Arg1509fs
ATP-binding cassette sub-family C member 8 isoform X2 XP_016873687.1:p.Gln150...

XP_016873687.1:p.Gln1507_Arg1508=

XP_016873687.1:p.Arg1508fs
ATP-binding cassette sub-family C member 8 isoform X5 XP_016873689.1:p.Gln148...

XP_016873689.1:p.Gln1484_Arg1485=

XP_016873689.1:p.Arg1485fs
ATP-binding cassette sub-family C member 8 isoform X4 XP_016873691.1:p.Gln100...

XP_016873691.1:p.Gln1007_Arg1008=

XP_016873691.1:p.Arg1008fs
ATP-binding cassette sub-family C member 8 isoform X3 XP_016873690.1:p.Thr147...

XP_016873690.1:p.Thr1473_Glu1474=

XP_016873690.1:p.Glu1474fs
ATP-binding cassette sub-family C member 8 isoform X6 XP_016873693.1:p.Gln804...

XP_016873693.1:p.Gln804_Arg805=

XP_016873693.1:p.Arg805fs
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

1 ClinVar, 1 SubSNP submissions
No Submitter Submission ID Date (Build)
1 CLINVAR ss1960974889 Dec 03, 2015 (146)
2 ClinVar RCV000201891.1 Jul 20, 2018 (151)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission ids Observation SPDI Canonical SPDI Source RSIDs
RCV000201891.1, ss1960974889 NC_000011.10:17394353:delCT NC_000011.10:17394353:delCT (self)
Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs863225279

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 0.1.4.post828+704a9a6