Name: rs1491301918
Published: September 21, 2022
License: Open Access

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.

rs1491301918

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:75999282-75999283 (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: insA / insATA / insATATA / ins(AT)…
insA / insATA / insATATA / ins(AT)₃A / ins(AT)₄A / ins(AT)₉A / ins(AT)₁₀A / ins(AT)₁₁A / insG(TA)₄
Variation Type: Insertion
Frequency: insA=0.00000 (0/11860, ALFA)
insATA=0.00000 (0/11860, ALFA)
insATATA=0.00000 (0/11860, ALFA) (+ 1 more)
insG(TA)₄=0.00000 (0/11860, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IFT43 : 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	HWEP
Total	Global	11860	=1.00000	A=0.00000, ATA=0.00000, ATATA=0.00000, GTATATATA=0.00000	1.0	N/A
European	Sub	7618	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, GTATATATA=0.0000	1.0	N/A
African	Sub	2816	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, GTATATATA=0.0000	1.0	N/A
African Others	Sub	108	=1.000	A=0.000, ATA=0.000, ATATA=0.000, GTATATATA=0.000	1.0	N/A
African American	Sub	2708	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, GTATATATA=0.0000	1.0	N/A
Asian	Sub	108	=1.000	A=0.000, ATA=0.000, ATATA=0.000, GTATATATA=0.000	1.0	N/A
East Asian	Sub	84	=1.00	A=0.00, ATA=0.00, ATATA=0.00, GTATATATA=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	A=0.00, ATA=0.00, ATATA=0.00, GTATATATA=0.00	1.0	N/A
Latin American 1	Sub	144	=1.000	A=0.000, ATA=0.000, ATATA=0.000, GTATATATA=0.000	1.0	N/A
Latin American 2	Sub	610	=1.000	A=0.000, ATA=0.000, ATATA=0.000, GTATATATA=0.000	1.0	N/A
South Asian	Sub	94	=1.00	A=0.00, ATA=0.00, ATATA=0.00, GTATATATA=0.00	1.0	N/A
Other	Sub	470	=1.000	A=0.000, ATA=0.000, ATATA=0.000, GTATATATA=0.000	1.0	N/A

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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11860	- No frequency provided	insA=0.00000, insATA=0.00000, insATATA=0.00000, insG(TA)₄=0.00000
Allele Frequency Aggregator	European	Sub	7618	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, insG(TA)₄=0.0000
Allele Frequency Aggregator	African	Sub	2816	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, insG(TA)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, insG(TA)₄=0.000
Allele Frequency Aggregator	Other	Sub	470	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, insG(TA)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, insG(TA)₄=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, insG(TA)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insA=0.00, insATA=0.00, insATATA=0.00, insG(TA)₄=0.00

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 14	NC_000014.9:g.75999282_75999283insA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insATA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insATATA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insATATATA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insATATATATA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insATATATATATATATATATA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insATATATATATATATATATATA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insATATATATATATATATATATATA
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283insGTATATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insATATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insATATATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insATATATATATATATATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insATATATATATATATATATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insATATATATATATATATATATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626insGTATATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insATATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insATATATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insATATATATATATATATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insATATATATATATATATATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insATATATATATATATATATATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531insGTATATATA

Gene: IFT43, intraflagellar transport 43 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IFT43 transcript variant 2	NM_001102564.3:c.147+1030… NM_001102564.3:c.147+10305_147+10306insA	N/A	Intron Variant
IFT43 transcript variant 3	NM_001255995.3:c.147+1030… NM_001255995.3:c.147+10305_147+10306insA	N/A	Intron Variant
IFT43 transcript variant 1	NM_052873.3:c.147+10305_1… NM_052873.3:c.147+10305_147+10306insA	N/A	Intron Variant
IFT43 transcript variant 4	NR_045664.2:n.	N/A	Intron Variant
IFT43 transcript variant 5	NR_045665.2:n.	N/A	Intron Variant

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

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	=	insA	insATA	insATATA	ins(AT)₃A	ins(AT)₄A	ins(AT)₉A	ins(AT)₁₀A	ins(AT)₁₁A	insG(TA)₄
GRCh38.p14 chr 14	NC_000014.9:g.75999282_75999283=	NC_000014.9:g.75999282_75999283insA	NC_000014.9:g.75999282_75999283insATA	NC_000014.9:g.75999282_75999283insATATA	NC_000014.9:g.75999282_75999283insATATATA	NC_000014.9:g.75999282_75999283insATATATATA	NC_000014.9:g.75999282_75999283insATATATATATATATATATA	NC_000014.9:g.75999282_75999283insATATATATATATATATATATA	NC_000014.9:g.75999282_75999283insATATATATATATATATATATATA	NC_000014.9:g.75999282_75999283insGTATATATA
GRCh37.p13 chr 14	NC_000014.8:g.76465625_76465626=	NC_000014.8:g.76465625_76465626insA	NC_000014.8:g.76465625_76465626insATA	NC_000014.8:g.76465625_76465626insATATA	NC_000014.8:g.76465625_76465626insATATATA	NC_000014.8:g.76465625_76465626insATATATATA	NC_000014.8:g.76465625_76465626insATATATATATATATATATA	NC_000014.8:g.76465625_76465626insATATATATATATATATATATA	NC_000014.8:g.76465625_76465626insATATATATATATATATATATATA	NC_000014.8:g.76465625_76465626insGTATATATA
IFT43 RefSeqGene	NG_031957.1:g.18530_18531=	NG_031957.1:g.18530_18531insA	NG_031957.1:g.18530_18531insATA	NG_031957.1:g.18530_18531insATATA	NG_031957.1:g.18530_18531insATATATA	NG_031957.1:g.18530_18531insATATATATA	NG_031957.1:g.18530_18531insATATATATATATATATATA	NG_031957.1:g.18530_18531insATATATATATATATATATATA	NG_031957.1:g.18530_18531insATATATATATATATATATATATA	NG_031957.1:g.18530_18531insGTATATATA
IFT43 transcript variant 2	NM_001102564.1:c.147+10306=	NM_001102564.1:c.147+10305_147+10306insA	NM_001102564.1:c.147+10305_147+10306insATA	NM_001102564.1:c.147+10305_147+10306insATATA	NM_001102564.1:c.147+10305_147+10306insATATATA	NM_001102564.1:c.147+10305_147+10306insATATATATA	NM_001102564.1:c.147+10305_147+10306insATATATATATATATATATA	NM_001102564.1:c.147+10305_147+10306insATATATATATATATATATATA	NM_001102564.1:c.147+10305_147+10306insATATATATATATATATATATATA	NM_001102564.1:c.147+10305_147+10306insGTATATATA
IFT43 transcript variant 2	NM_001102564.3:c.147+10306=	NM_001102564.3:c.147+10305_147+10306insA	NM_001102564.3:c.147+10305_147+10306insATA	NM_001102564.3:c.147+10305_147+10306insATATA	NM_001102564.3:c.147+10305_147+10306insATATATA	NM_001102564.3:c.147+10305_147+10306insATATATATA	NM_001102564.3:c.147+10305_147+10306insATATATATATATATATATA	NM_001102564.3:c.147+10305_147+10306insATATATATATATATATATATA	NM_001102564.3:c.147+10305_147+10306insATATATATATATATATATATATA	NM_001102564.3:c.147+10305_147+10306insGTATATATA
IFT43 transcript variant 3	NM_001255995.1:c.147+10306=	NM_001255995.1:c.147+10305_147+10306insA	NM_001255995.1:c.147+10305_147+10306insATA	NM_001255995.1:c.147+10305_147+10306insATATA	NM_001255995.1:c.147+10305_147+10306insATATATA	NM_001255995.1:c.147+10305_147+10306insATATATATA	NM_001255995.1:c.147+10305_147+10306insATATATATATATATATATA	NM_001255995.1:c.147+10305_147+10306insATATATATATATATATATATA	NM_001255995.1:c.147+10305_147+10306insATATATATATATATATATATATA	NM_001255995.1:c.147+10305_147+10306insGTATATATA
IFT43 transcript variant 3	NM_001255995.3:c.147+10306=	NM_001255995.3:c.147+10305_147+10306insA	NM_001255995.3:c.147+10305_147+10306insATA	NM_001255995.3:c.147+10305_147+10306insATATA	NM_001255995.3:c.147+10305_147+10306insATATATA	NM_001255995.3:c.147+10305_147+10306insATATATATA	NM_001255995.3:c.147+10305_147+10306insATATATATATATATATATA	NM_001255995.3:c.147+10305_147+10306insATATATATATATATATATATA	NM_001255995.3:c.147+10305_147+10306insATATATATATATATATATATATA	NM_001255995.3:c.147+10305_147+10306insGTATATATA
IFT43 transcript variant 1	NM_052873.2:c.147+10306=	NM_052873.2:c.147+10305_147+10306insA	NM_052873.2:c.147+10305_147+10306insATA	NM_052873.2:c.147+10305_147+10306insATATA	NM_052873.2:c.147+10305_147+10306insATATATA	NM_052873.2:c.147+10305_147+10306insATATATATA	NM_052873.2:c.147+10305_147+10306insATATATATATATATATATA	NM_052873.2:c.147+10305_147+10306insATATATATATATATATATATA	NM_052873.2:c.147+10305_147+10306insATATATATATATATATATATATA	NM_052873.2:c.147+10305_147+10306insGTATATATA
IFT43 transcript variant 1	NM_052873.3:c.147+10306=	NM_052873.3:c.147+10305_147+10306insA	NM_052873.3:c.147+10305_147+10306insATA	NM_052873.3:c.147+10305_147+10306insATATA	NM_052873.3:c.147+10305_147+10306insATATATA	NM_052873.3:c.147+10305_147+10306insATATATATA	NM_052873.3:c.147+10305_147+10306insATATATATATATATATATA	NM_052873.3:c.147+10305_147+10306insATATATATATATATATATATA	NM_052873.3:c.147+10305_147+10306insATATATATATATATATATATATA	NM_052873.3:c.147+10305_147+10306insGTATATATA
IFT43 transcript variant X1	XM_005267296.1:c.84+10306=	XM_005267296.1:c.84+10305_84+10306insA	XM_005267296.1:c.84+10305_84+10306insATA	XM_005267296.1:c.84+10305_84+10306insATATA	XM_005267296.1:c.84+10305_84+10306insATATATA	XM_005267296.1:c.84+10305_84+10306insATATATATA	XM_005267296.1:c.84+10305_84+10306insATATATATATATATATATA	XM_005267296.1:c.84+10305_84+10306insATATATATATATATATATATA	XM_005267296.1:c.84+10305_84+10306insATATATATATATATATATATATA	XM_005267296.1:c.84+10305_84+10306insGTATATATA
IFT43 transcript variant X2	XM_005267297.1:c.84+10306=	XM_005267297.1:c.84+10305_84+10306insA	XM_005267297.1:c.84+10305_84+10306insATA	XM_005267297.1:c.84+10305_84+10306insATATA	XM_005267297.1:c.84+10305_84+10306insATATATA	XM_005267297.1:c.84+10305_84+10306insATATATATA	XM_005267297.1:c.84+10305_84+10306insATATATATATATATATATA	XM_005267297.1:c.84+10305_84+10306insATATATATATATATATATATA	XM_005267297.1:c.84+10305_84+10306insATATATATATATATATATATATA	XM_005267297.1:c.84+10305_84+10306insGTATATATA

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#.

17 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3697014667	Jul 13, 2019 (153)
2	EVA_DECODE	ss3697014668	Jul 13, 2019 (153)
3	GNOMAD	ss4280975231	Apr 26, 2021 (155)
4	GNOMAD	ss4280975232	Apr 26, 2021 (155)
5	GNOMAD	ss4280975233	Apr 26, 2021 (155)
6	GNOMAD	ss4280975234	Apr 26, 2021 (155)
7	GNOMAD	ss4280975235	Apr 26, 2021 (155)
8	GNOMAD	ss4280975236	Apr 26, 2021 (155)
9	GNOMAD	ss4280975237	Apr 26, 2021 (155)
10	GNOMAD	ss4280975238	Apr 26, 2021 (155)
11	TOMMO_GENOMICS	ss5213998847	Apr 26, 2021 (155)
12	TOMMO_GENOMICS	ss5213998848	Apr 26, 2021 (155)
13	TOMMO_GENOMICS	ss5213998849	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5213998850	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5767026761	Oct 16, 2022 (156)
16	TOMMO_GENOMICS	ss5767026762	Oct 16, 2022 (156)
17	TOMMO_GENOMICS	ss5767026763	Oct 16, 2022 (156)
18	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
19	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
20	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
21	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
22	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
23	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456076741 (NC_000014.9:75999282::A 136/24460) Row 456076742 (NC_000014.9:75999282::ATA 26/24610) Row 456076743 (NC_000014.9:75999282::ATATA 58/24586)...	-	Apr 26, 2021 (155)
26	8.3KJPN Submission ignored due to conflicting rows: Row 71968154 (NC_000014.8:76465625::A 142/12984) Row 71968155 (NC_000014.8:76465625::ATA 22/12984) Row 71968156 (NC_000014.8:76465625::ATATA 30/12984)...	-	Apr 26, 2021 (155)
27	8.3KJPN Submission ignored due to conflicting rows: Row 71968154 (NC_000014.8:76465625::A 142/12984) Row 71968155 (NC_000014.8:76465625::ATA 22/12984) Row 71968156 (NC_000014.8:76465625::ATATA 30/12984)...	-	Apr 26, 2021 (155)
28	8.3KJPN Submission ignored due to conflicting rows: Row 71968154 (NC_000014.8:76465625::A 142/12984) Row 71968155 (NC_000014.8:76465625::ATA 22/12984) Row 71968156 (NC_000014.8:76465625::ATATA 30/12984)...	-	Apr 26, 2021 (155)
29	8.3KJPN Submission ignored due to conflicting rows: Row 71968154 (NC_000014.8:76465625::A 142/12984) Row 71968155 (NC_000014.8:76465625::ATA 22/12984) Row 71968156 (NC_000014.8:76465625::ATATA 30/12984)...	-	Apr 26, 2021 (155)
30	14KJPN Submission ignored due to conflicting rows: Row 100863865 (NC_000014.9:75999282::ATA 35/25920) Row 100863866 (NC_000014.9:75999282::A 134/25920) Row 100863867 (NC_000014.9:75999282::ATATA 42/25920)	-	Oct 16, 2022 (156)
31	14KJPN Submission ignored due to conflicting rows: Row 100863865 (NC_000014.9:75999282::ATA 35/25920) Row 100863866 (NC_000014.9:75999282::A 134/25920) Row 100863867 (NC_000014.9:75999282::ATATA 42/25920)	-	Oct 16, 2022 (156)
32	14KJPN Submission ignored due to conflicting rows: Row 100863865 (NC_000014.9:75999282::ATA 35/25920) Row 100863866 (NC_000014.9:75999282::A 134/25920) Row 100863867 (NC_000014.9:75999282::ATATA 42/25920)	-	Oct 16, 2022 (156)
33	ALFA	NC_000014.9 - 75999283	Apr 26, 2021 (155)

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
ss5213998847	NC_000014.8:76465625::A	NC_000014.9:75999282::A	(self)
1515755313, ss3697014667, ss4280975231, ss5767026762	NC_000014.9:75999282::A	NC_000014.9:75999282::A	(self)
ss5213998848	NC_000014.8:76465625::ATA	NC_000014.9:75999282::ATA	(self)
1515755313, ss3697014668, ss4280975232, ss5767026761	NC_000014.9:75999282::ATA	NC_000014.9:75999282::ATA	(self)
ss5213998849	NC_000014.8:76465625::ATATA	NC_000014.9:75999282::ATATA	(self)
1515755313, ss4280975233, ss5767026763	NC_000014.9:75999282::ATATA	NC_000014.9:75999282::ATATA	(self)
ss5213998850	NC_000014.8:76465625::ATATATA	NC_000014.9:75999282::ATATATA	(self)
ss4280975234	NC_000014.9:75999282::ATATATA	NC_000014.9:75999282::ATATATA	(self)
ss4280975235	NC_000014.9:75999282::ATATATATA	NC_000014.9:75999282::ATATATATA	(self)
ss4280975236	NC_000014.9:75999282::ATATATATATAT… NC_000014.9:75999282::ATATATATATATATATATA	NC_000014.9:75999282::ATATATATATAT… NC_000014.9:75999282::ATATATATATATATATATA	(self)
ss4280975237	NC_000014.9:75999282::ATATATATATAT… NC_000014.9:75999282::ATATATATATATATATATATA	NC_000014.9:75999282::ATATATATATAT… NC_000014.9:75999282::ATATATATATATATATATATA	(self)
ss4280975238	NC_000014.9:75999282::ATATATATATAT… NC_000014.9:75999282::ATATATATATATATATATATATA	NC_000014.9:75999282::ATATATATATAT… NC_000014.9:75999282::ATATATATATATATATATATATA	(self)
1515755313	NC_000014.9:75999282::GTATATATA	NC_000014.9:75999282::GTATATATA	(self)

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

No publications for rs1491301918

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.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491301918