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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

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.

rs397863049

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:20673377-20673380 (GRCh38.p14) 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
delTT / dupTTT
Variation Type
Indel Insertion and Deletion
Frequency
delTT=0.00000 (0/11862, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
KIF17 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 11862 TTTT=1.00000 TT=0.00000 1.0 0.0 0.0 N/A
European Sub 7618 TTTT=1.0000 TT=0.0000 1.0 0.0 0.0 N/A
African Sub 2816 TTTT=1.0000 TT=0.0000 1.0 0.0 0.0 N/A
African Others Sub 108 TTTT=1.000 TT=0.000 1.0 0.0 0.0 N/A
African American Sub 2708 TTTT=1.0000 TT=0.0000 1.0 0.0 0.0 N/A
Asian Sub 108 TTTT=1.000 TT=0.000 1.0 0.0 0.0 N/A
East Asian Sub 84 TTTT=1.00 TT=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 24 TTTT=1.00 TT=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 TTTT=1.000 TT=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 TTTT=1.000 TT=0.000 1.0 0.0 0.0 N/A
South Asian Sub 94 TTTT=1.00 TT=0.00 1.0 0.0 0.0 N/A
Other Sub 470 TTTT=1.000 TT=0.000 1.0 0.0 0.0 N/A


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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
Allele Frequency Aggregator Total Global 11862 (T)4=1.00000 delTT=0.00000
Allele Frequency Aggregator European Sub 7618 (T)4=1.0000 delTT=0.0000
Allele Frequency Aggregator African Sub 2816 (T)4=1.0000 delTT=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 (T)4=1.000 delTT=0.000
Allele Frequency Aggregator Other Sub 470 (T)4=1.000 delTT=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 (T)4=1.000 delTT=0.000
Allele Frequency Aggregator Asian Sub 108 (T)4=1.000 delTT=0.000
Allele Frequency Aggregator South Asian Sub 94 (T)4=1.00 delTT=0.00
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.p14 chr 1 NC_000001.11:g.20673379_20673380del
GRCh38.p14 chr 1 NC_000001.11:g.20673378_20673380dup
GRCh37.p13 chr 1 NC_000001.10:g.20999872_20999873del
GRCh37.p13 chr 1 NC_000001.10:g.20999871_20999873dup
Gene: KIF17, kinesin family member 17 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
KIF17 transcript variant 2 NM_001122819.3:c.2464-118…

NM_001122819.3:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant 3 NM_001287212.2:c.2164-118…

NM_001287212.2:c.2164-1182_2164-1181del

N/A Intron Variant
KIF17 transcript variant 1 NM_020816.4:c.2464-1182_2…

NM_020816.4:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X1 XM_047426146.1:c.2464-118…

XM_047426146.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X2 XM_047426147.1:c.2464-118…

XM_047426147.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X3 XM_047426148.1:c.2464-118…

XM_047426148.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X5 XM_047426149.1:c.2464-118…

XM_047426149.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X6 XM_047426150.1:c.2464-118…

XM_047426150.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X7 XM_047426151.1:c.2464-118…

XM_047426151.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X8 XM_047426152.1:c.2464-118…

XM_047426152.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X9 XM_047426153.1:c.2464-118…

XM_047426153.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X10 XM_047426154.1:c.2464-118…

XM_047426154.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X11 XM_047426155.1:c.2464-118…

XM_047426155.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X12 XM_047426156.1:c.2464-118…

XM_047426156.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X13 XM_047426157.1:c.2464-118…

XM_047426157.1:c.2464-1182_2464-1181del

N/A Intron Variant
KIF17 transcript variant X14 XM_047426158.1:c.2164-118…

XM_047426158.1:c.2164-1182_2164-1181del

N/A Intron Variant
KIF17 transcript variant X16 XM_047426160.1:c.1042-118…

XM_047426160.1:c.1042-1182_1042-1181del

N/A Intron Variant
KIF17 transcript variant X15 XM_047426159.1:c. N/A Genic Downstream Transcript Variant
KIF17 transcript variant X17 XM_047426161.1:c. N/A Genic Downstream Transcript Variant
KIF17 transcript variant X4 XR_007062426.1:n. N/A Intron 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.

Not Reported in ClinVar
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 (T)4= delTT dupTTT
GRCh38.p14 chr 1 NC_000001.11:g.20673377_20673380= NC_000001.11:g.20673379_20673380del NC_000001.11:g.20673378_20673380dup
GRCh37.p13 chr 1 NC_000001.10:g.20999870_20999873= NC_000001.10:g.20999872_20999873del NC_000001.10:g.20999871_20999873dup
KIF17 transcript variant 2 NM_001122819.1:c.2464-1181= NM_001122819.1:c.2464-1182_2464-1181del NM_001122819.1:c.2464-1183_2464-1181dup
KIF17 transcript variant 2 NM_001122819.3:c.2464-1181= NM_001122819.3:c.2464-1182_2464-1181del NM_001122819.3:c.2464-1183_2464-1181dup
KIF17 transcript variant 3 NM_001287212.2:c.2164-1181= NM_001287212.2:c.2164-1182_2164-1181del NM_001287212.2:c.2164-1183_2164-1181dup
KIF17 transcript variant 1 NM_020816.2:c.2464-1181= NM_020816.2:c.2464-1182_2464-1181del NM_020816.2:c.2464-1183_2464-1181dup
KIF17 transcript variant 1 NM_020816.4:c.2464-1181= NM_020816.4:c.2464-1182_2464-1181del NM_020816.4:c.2464-1183_2464-1181dup
KIF17 transcript variant X1 XM_005245950.1:c.2464-1181= XM_005245950.1:c.2464-1182_2464-1181del XM_005245950.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X2 XM_005245951.1:c.2464-1181= XM_005245951.1:c.2464-1182_2464-1181del XM_005245951.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X1 XM_047426146.1:c.2464-1181= XM_047426146.1:c.2464-1182_2464-1181del XM_047426146.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X2 XM_047426147.1:c.2464-1181= XM_047426147.1:c.2464-1182_2464-1181del XM_047426147.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X3 XM_047426148.1:c.2464-1181= XM_047426148.1:c.2464-1182_2464-1181del XM_047426148.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X5 XM_047426149.1:c.2464-1181= XM_047426149.1:c.2464-1182_2464-1181del XM_047426149.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X6 XM_047426150.1:c.2464-1181= XM_047426150.1:c.2464-1182_2464-1181del XM_047426150.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X7 XM_047426151.1:c.2464-1181= XM_047426151.1:c.2464-1182_2464-1181del XM_047426151.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X8 XM_047426152.1:c.2464-1181= XM_047426152.1:c.2464-1182_2464-1181del XM_047426152.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X9 XM_047426153.1:c.2464-1181= XM_047426153.1:c.2464-1182_2464-1181del XM_047426153.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X10 XM_047426154.1:c.2464-1181= XM_047426154.1:c.2464-1182_2464-1181del XM_047426154.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X11 XM_047426155.1:c.2464-1181= XM_047426155.1:c.2464-1182_2464-1181del XM_047426155.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X12 XM_047426156.1:c.2464-1181= XM_047426156.1:c.2464-1182_2464-1181del XM_047426156.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X13 XM_047426157.1:c.2464-1181= XM_047426157.1:c.2464-1182_2464-1181del XM_047426157.1:c.2464-1183_2464-1181dup
KIF17 transcript variant X14 XM_047426158.1:c.2164-1181= XM_047426158.1:c.2164-1182_2164-1181del XM_047426158.1:c.2164-1183_2164-1181dup
KIF17 transcript variant X16 XM_047426160.1:c.1042-1181= XM_047426160.1:c.1042-1182_1042-1181del XM_047426160.1:c.1042-1183_1042-1181dup
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#.

2 SubSNP, 1 Frequency submissions
No Submitter Submission ID Date (Build)
1 ABI ss41266355 Dec 03, 2013 (138)
2 BUSHMAN ss193090902 Oct 11, 2018 (152)
3 ALFA NC_000001.11 - 20673377 Apr 27, 2021 (155)
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
5098849729 NC_000001.11:20673376:TTTT:TT NC_000001.11:20673376:TTTT:TT (self)
ss41266355, ss193090902 NT_004610.19:7679961:G:TTTG NC_000001.11:20673376:TTTT:TTTTTTT (self)
Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss3070422663 NC_000001.11:20673376:TT: NC_000001.11:20673376:TTTT:TT
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 rs397863049

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

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: 2.0.1.post820+afb47a3d