Name: rs145797278
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.

rs145797278

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:14463839-14463850 (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: delGGG / delGG / delG / dupG / dup…
delGGG / delGG / delG / dupG / dupGG / dupGGG
Variation Type: Indel Insertion and Deletion
Frequency: delGG=0.0000 (0/5176, ALFA)
delG=0.0000 (0/5176, ALFA)
dupG=0.0000 (0/5176, ALFA) (+ 4 more)
dupGG=0.0000 (0/5176, ALFA)
dupGGG=0.0000 (0/5176, ALFA)
delG=0.1174 (588/5008, 1000G)
dupG=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PARN : 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	5176	GGGGGGGGGGGG=1.0000	GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
European	Sub	2306	GGGGGGGGGGGG=1.0000	GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
African	Sub	2232	GGGGGGGGGGGG=1.0000	GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
African Others	Sub	96	GGGGGGGGGGGG=1.00	GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
African American	Sub	2136	GGGGGGGGGGGG=1.0000	GGGGGGGGGG=0.0000, GGGGGGGGGGG=0.0000, GGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGG=0.0000, GGGGGGGGGGGGGGG=0.0000	1.0	N/A
Asian	Sub	60	GGGGGGGGGGGG=1.00	GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
East Asian	Sub	42	GGGGGGGGGGGG=1.00	GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Other Asian	Sub	18	GGGGGGGGGGGG=1.00	GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 1	Sub	56	GGGGGGGGGGGG=1.00	GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Latin American 2	Sub	282	GGGGGGGGGGGG=1.000	GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=0.000	1.0	N/A
South Asian	Sub	24	GGGGGGGGGGGG=1.00	GGGGGGGGGG=0.00, GGGGGGGGGGG=0.00, GGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGG=0.00, GGGGGGGGGGGGGGG=0.00	1.0	N/A
Other	Sub	216	GGGGGGGGGGGG=1.000	GGGGGGGGGG=0.000, GGGGGGGGGGG=0.000, GGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGG=0.000, GGGGGGGGGGGGGGG=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	5176	(G)₁₂=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	European	Sub	2306	(G)₁₂=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	African	Sub	2232	(G)₁₂=1.0000	delGG=0.0000, delG=0.0000, dupG=0.0000, dupGG=0.0000, dupGGG=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	282	(G)₁₂=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Other	Sub	216	(G)₁₂=1.000	delGG=0.000, delG=0.000, dupG=0.000, dupGG=0.000, dupGGG=0.000
Allele Frequency Aggregator	Asian	Sub	60	(G)₁₂=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	Latin American 1	Sub	56	(G)₁₂=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(G)₁₂=1.00	delGG=0.00, delG=0.00, dupG=0.00, dupGG=0.00, dupGGG=0.00
1000Genomes	Global	Study-wide	5008	(G)₁₂=0.8826	delG=0.1174
1000Genomes	African	Sub	1322	(G)₁₂=0.9236	delG=0.0764
1000Genomes	East Asian	Sub	1008	(G)₁₂=0.7252	delG=0.2748
1000Genomes	Europe	Sub	1006	(G)₁₂=0.9573	delG=0.0427
1000Genomes	South Asian	Sub	978	(G)₁₂=0.893	delG=0.107
1000Genomes	American	Sub	694	(G)₁₂=0.911	delG=0.089
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupG=0.20

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 16	NC_000016.10:g.14463848_14463850del
GRCh38.p14 chr 16	NC_000016.10:g.14463849_14463850del
GRCh38.p14 chr 16	NC_000016.10:g.14463850del
GRCh38.p14 chr 16	NC_000016.10:g.14463850dup
GRCh38.p14 chr 16	NC_000016.10:g.14463849_14463850dup
GRCh38.p14 chr 16	NC_000016.10:g.14463848_14463850dup
GRCh37.p13 chr 16	NC_000016.9:g.14557705_14557707del
GRCh37.p13 chr 16	NC_000016.9:g.14557706_14557707del
GRCh37.p13 chr 16	NC_000016.9:g.14557707del
GRCh37.p13 chr 16	NC_000016.9:g.14557707dup
GRCh37.p13 chr 16	NC_000016.9:g.14557706_14557707dup
GRCh37.p13 chr 16	NC_000016.9:g.14557705_14557707dup
A RefSeqGene (LRG_1286)	NG_042871.1:g.171431_171433del
A RefSeqGene (LRG_1286)	NG_042871.1:g.171432_171433del
A RefSeqGene (LRG_1286)	NG_042871.1:g.171433del
A RefSeqGene (LRG_1286)	NG_042871.1:g.171433dup
A RefSeqGene (LRG_1286)	NG_042871.1:g.171432_171433dup
A RefSeqGene (LRG_1286)	NG_042871.1:g.171431_171433dup
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.36705_36707del
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.36706_36707del
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.36707del
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.36707dup
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.36706_36707dup
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.36705_36707dup

Gene: PARN, poly(A)-specific ribonuclease (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PARN transcript variant 2	NM_001134477.3:c.1488-167… NM_001134477.3:c.1488-16760_1488-16758del	N/A	Intron Variant
PARN transcript variant 3	NM_001242992.2:c.1533-167… NM_001242992.2:c.1533-16760_1533-16758del	N/A	Intron Variant
PARN transcript variant 1	NM_002582.4:c.1671-16760_… NM_002582.4:c.1671-16760_1671-16758del	N/A	Intron Variant
PARN transcript variant X9	XM_011522514.3:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X1	XM_047434181.1:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X2	XM_047434182.1:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X6	XM_047434183.1:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X7	XM_047434184.1:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X10	XM_047434185.1:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X3	XR_007064881.1:n.	N/A	Intron Variant
PARN transcript variant X4	XR_007064882.1:n.	N/A	Intron Variant
PARN transcript variant X5	XR_007064883.1:n.	N/A	Intron Variant
PARN transcript variant X8	XR_007064884.1: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	(G)₁₂=	delGGG	delGG	delG	dupG	dupGG	dupGGG
GRCh38.p14 chr 16	NC_000016.10:g.14463839_14463850=	NC_000016.10:g.14463848_14463850del	NC_000016.10:g.14463849_14463850del	NC_000016.10:g.14463850del	NC_000016.10:g.14463850dup	NC_000016.10:g.14463849_14463850dup	NC_000016.10:g.14463848_14463850dup
GRCh37.p13 chr 16	NC_000016.9:g.14557696_14557707=	NC_000016.9:g.14557705_14557707del	NC_000016.9:g.14557706_14557707del	NC_000016.9:g.14557707del	NC_000016.9:g.14557707dup	NC_000016.9:g.14557706_14557707dup	NC_000016.9:g.14557705_14557707dup
A RefSeqGene (LRG_1286)	NG_042871.1:g.171422_171433=	NG_042871.1:g.171431_171433del	NG_042871.1:g.171432_171433del	NG_042871.1:g.171433del	NG_042871.1:g.171433dup	NG_042871.1:g.171432_171433dup	NG_042871.1:g.171431_171433dup
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.36696_36707=	NT_187607.1:g.36705_36707del	NT_187607.1:g.36706_36707del	NT_187607.1:g.36707del	NT_187607.1:g.36707dup	NT_187607.1:g.36706_36707dup	NT_187607.1:g.36705_36707dup
PARN transcript variant 2	NM_001134477.2:c.1488-16758=	NM_001134477.2:c.1488-16760_1488-16758del	NM_001134477.2:c.1488-16759_1488-16758del	NM_001134477.2:c.1488-16758del	NM_001134477.2:c.1488-16758dup	NM_001134477.2:c.1488-16759_1488-16758dup	NM_001134477.2:c.1488-16760_1488-16758dup
PARN transcript variant 2	NM_001134477.3:c.1488-16758=	NM_001134477.3:c.1488-16760_1488-16758del	NM_001134477.3:c.1488-16759_1488-16758del	NM_001134477.3:c.1488-16758del	NM_001134477.3:c.1488-16758dup	NM_001134477.3:c.1488-16759_1488-16758dup	NM_001134477.3:c.1488-16760_1488-16758dup
PARN transcript variant 3	NM_001242992.1:c.1533-16758=	NM_001242992.1:c.1533-16760_1533-16758del	NM_001242992.1:c.1533-16759_1533-16758del	NM_001242992.1:c.1533-16758del	NM_001242992.1:c.1533-16758dup	NM_001242992.1:c.1533-16759_1533-16758dup	NM_001242992.1:c.1533-16760_1533-16758dup
PARN transcript variant 3	NM_001242992.2:c.1533-16758=	NM_001242992.2:c.1533-16760_1533-16758del	NM_001242992.2:c.1533-16759_1533-16758del	NM_001242992.2:c.1533-16758del	NM_001242992.2:c.1533-16758dup	NM_001242992.2:c.1533-16759_1533-16758dup	NM_001242992.2:c.1533-16760_1533-16758dup
PARN transcript variant 1	NM_002582.3:c.1671-16758=	NM_002582.3:c.1671-16760_1671-16758del	NM_002582.3:c.1671-16759_1671-16758del	NM_002582.3:c.1671-16758del	NM_002582.3:c.1671-16758dup	NM_002582.3:c.1671-16759_1671-16758dup	NM_002582.3:c.1671-16760_1671-16758dup
PARN transcript variant 1	NM_002582.4:c.1671-16758=	NM_002582.4:c.1671-16760_1671-16758del	NM_002582.4:c.1671-16759_1671-16758del	NM_002582.4:c.1671-16758del	NM_002582.4:c.1671-16758dup	NM_002582.4:c.1671-16759_1671-16758dup	NM_002582.4:c.1671-16760_1671-16758dup
PARN transcript variant X1	XM_005255341.1:c.1146-16758=	XM_005255341.1:c.1146-16760_1146-16758del	XM_005255341.1:c.1146-16759_1146-16758del	XM_005255341.1:c.1146-16758del	XM_005255341.1:c.1146-16758dup	XM_005255341.1:c.1146-16759_1146-16758dup	XM_005255341.1:c.1146-16760_1146-16758dup

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#.

31 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BL	ss256162365	May 09, 2011 (134)
2	SSMP	ss664302379	Apr 01, 2015 (144)
3	1000GENOMES	ss1375598811	Aug 21, 2014 (142)
4	EVA_GENOME_DK	ss1574930344	Apr 01, 2015 (144)
5	SWEGEN	ss3014134514	Nov 08, 2017 (151)
6	EVA_DECODE	ss3698925098	Jul 13, 2019 (153)
7	EVA_DECODE	ss3698925099	Jul 13, 2019 (153)
8	EVA_DECODE	ss3698925100	Jul 13, 2019 (153)
9	PACBIO	ss3787992507	Jul 13, 2019 (153)
10	PACBIO	ss3792984113	Jul 13, 2019 (153)
11	PACBIO	ss3797869097	Jul 13, 2019 (153)
12	KHV_HUMAN_GENOMES	ss3819035582	Jul 13, 2019 (153)
13	EVA	ss3834497452	Apr 27, 2020 (154)
14	GNOMAD	ss4297583769	Apr 26, 2021 (155)
15	GNOMAD	ss4297583770	Apr 26, 2021 (155)
16	GNOMAD	ss4297583771	Apr 26, 2021 (155)
17	GNOMAD	ss4297583776	Apr 26, 2021 (155)
18	GNOMAD	ss4297583777	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5218611529	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5218611530	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5218611531	Apr 26, 2021 (155)
22	1000G_HIGH_COVERAGE	ss5300284321	Oct 17, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5300284322	Oct 17, 2022 (156)
24	HUGCELL_USP	ss5493798326	Oct 17, 2022 (156)
25	HUGCELL_USP	ss5493798327	Oct 17, 2022 (156)
26	TOMMO_GENOMICS	ss5773146828	Oct 17, 2022 (156)
27	TOMMO_GENOMICS	ss5773146829	Oct 17, 2022 (156)
28	TOMMO_GENOMICS	ss5773146830	Oct 17, 2022 (156)
29	EVA	ss5846163182	Oct 17, 2022 (156)
30	EVA	ss5846163183	Oct 17, 2022 (156)
31	EVA	ss5851510318	Oct 17, 2022 (156)
32	1000Genomes	NC_000016.9 - 14557696	Oct 12, 2018 (152)
33	The Danish reference pan genome	NC_000016.9 - 14557696	Apr 27, 2020 (154)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484033755 (NC_000016.10:14463838::G 21245/87022) Row 484033756 (NC_000016.10:14463838::GG 142/87626) Row 484033757 (NC_000016.10:14463838::GGG 11/87662)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484033755 (NC_000016.10:14463838::G 21245/87022) Row 484033756 (NC_000016.10:14463838::GG 142/87626) Row 484033757 (NC_000016.10:14463838::GGG 11/87662)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484033755 (NC_000016.10:14463838::G 21245/87022) Row 484033756 (NC_000016.10:14463838::GG 142/87626) Row 484033757 (NC_000016.10:14463838::GGG 11/87662)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484033755 (NC_000016.10:14463838::G 21245/87022) Row 484033756 (NC_000016.10:14463838::GG 142/87626) Row 484033757 (NC_000016.10:14463838::GGG 11/87662)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484033755 (NC_000016.10:14463838::G 21245/87022) Row 484033756 (NC_000016.10:14463838::GG 142/87626) Row 484033757 (NC_000016.10:14463838::GGG 11/87662)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484033755 (NC_000016.10:14463838::G 21245/87022) Row 484033756 (NC_000016.10:14463838::GG 142/87626) Row 484033757 (NC_000016.10:14463838::GGG 11/87662)...	-	Apr 26, 2021 (155)
40	8.3KJPN Submission ignored due to conflicting rows: Row 76580836 (NC_000016.9:14557695:G: 4468/16744) Row 76580837 (NC_000016.9:14557695::G 96/16744) Row 76580838 (NC_000016.9:14557695:GG: 13/16744)	-	Apr 26, 2021 (155)
41	8.3KJPN Submission ignored due to conflicting rows: Row 76580836 (NC_000016.9:14557695:G: 4468/16744) Row 76580837 (NC_000016.9:14557695::G 96/16744) Row 76580838 (NC_000016.9:14557695:GG: 13/16744)	-	Apr 26, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 76580836 (NC_000016.9:14557695:G: 4468/16744) Row 76580837 (NC_000016.9:14557695::G 96/16744) Row 76580838 (NC_000016.9:14557695:GG: 13/16744)	-	Apr 26, 2021 (155)
43	14KJPN Submission ignored due to conflicting rows: Row 106983932 (NC_000016.10:14463838:G: 7185/28250) Row 106983933 (NC_000016.10:14463838::G 212/28250) Row 106983934 (NC_000016.10:14463838:GG: 19/28250)	-	Oct 17, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 106983932 (NC_000016.10:14463838:G: 7185/28250) Row 106983933 (NC_000016.10:14463838::G 212/28250) Row 106983934 (NC_000016.10:14463838:GG: 19/28250)	-	Oct 17, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 106983932 (NC_000016.10:14463838:G: 7185/28250) Row 106983933 (NC_000016.10:14463838::G 212/28250) Row 106983934 (NC_000016.10:14463838:GG: 19/28250)	-	Oct 17, 2022 (156)
46	ALFA	NC_000016.10 - 14463839	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
ss4297583777	NC_000016.10:14463838:GGG:	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGG	(self)
ss5218611531	NC_000016.9:14557695:GG:	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGG	(self)
ss4297583776, ss5773146830	NC_000016.10:14463838:GG:	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGG	(self)
14237918092	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGG	(self)
ss256162365	NC_000016.8:14465196:G:	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGG	(self)
68697176, ss664302379, ss1375598811, ss3014134514, ss5218611529	NC_000016.9:14557695:G:	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGG	(self)
ss3698925100, ss3819035582, ss5300284322, ss5493798327, ss5773146828, ss5851510318	NC_000016.10:14463838:G:	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGG	(self)
14237918092	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGG	(self)
518245, ss1574930344, ss3787992507, ss3792984113, ss3797869097, ss3834497452, ss5218611530, ss5846163182	NC_000016.9:14557695::G	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss4297583769, ss5300284321, ss5493798326, ss5773146829	NC_000016.10:14463838::G	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
14237918092	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss3698925099	NC_000016.10:14463839::G	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGG	(self)
ss5846163183	NC_000016.9:14557695::GG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGG
ss4297583770	NC_000016.10:14463838::GG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
14237918092	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss3698925098	NC_000016.10:14463839::GG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGG	(self)
ss4297583771	NC_000016.10:14463838::GGG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGGG	(self)
14237918092	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGGG	NC_000016.10:14463838:GGGGGGGGGGGG… NC_000016.10:14463838:GGGGGGGGGGGG:GGGGGGGGGGGGGGG	(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 rs145797278

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
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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

rs145797278