Name: rs11323501
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.

rs11323501

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:43832130-43832146 (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: del(A)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₇=0.2901 (1453/5008, 1000G)
delAA=0.0727 (280/3854, ALSPAC)
delAAA=0.000 (0/136, ALFA) (+ 4 more)
delAA=0.000 (0/136, ALFA)
delA=0.000 (0/136, ALFA)
dupA=0.000 (0/136, ALFA)
(A)₁₇=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CCDC122 : 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	136	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
European	Sub	22	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African	Sub	82	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
African American	Sub	82	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Asian	Sub	6	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	6	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	2	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	18	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	AAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Other	Sub	6	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	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
1000Genomes	Global	Study-wide	5008	(A)₁₇=0.2901	delA=0.7099
1000Genomes	African	Sub	1322	(A)₁₇=0.3555	delA=0.6445
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.3175	delA=0.6825
1000Genomes	Europe	Sub	1006	(A)₁₇=0.2058	delA=0.7942
1000Genomes	South Asian	Sub	978	(A)₁₇=0.261	delA=0.739
1000Genomes	American	Sub	694	(A)₁₇=0.290	delA=0.710
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₇=0.9273	delAA=0.0727
Allele Frequency Aggregator	Total	Global	136	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000
Allele Frequency Aggregator	African	Sub	82	(A)₁₇=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	European	Sub	22	(A)₁₇=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Latin American 2	Sub	18	(A)₁₇=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00
Allele Frequency Aggregator	Other	Sub	6	(A)₁₇=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Asian	Sub	6	(A)₁₇=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	Latin American 1	Sub	2	(A)₁₇=1.0	delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(A)₁₇=0	delAAA=0, delAA=0, delA=0, dupA=0
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₇=0.20	delA=0.80

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 13	NC_000013.11:g.43832143_43832146del
GRCh38.p14 chr 13	NC_000013.11:g.43832144_43832146del
GRCh38.p14 chr 13	NC_000013.11:g.43832145_43832146del
GRCh38.p14 chr 13	NC_000013.11:g.43832146del
GRCh38.p14 chr 13	NC_000013.11:g.43832146dup
GRCh38.p14 chr 13	NC_000013.11:g.43832145_43832146dup
GRCh38.p14 chr 13	NC_000013.11:g.43832142_43832146dup
GRCh37.p13 chr 13	NC_000013.10:g.44406279_44406282del
GRCh37.p13 chr 13	NC_000013.10:g.44406280_44406282del
GRCh37.p13 chr 13	NC_000013.10:g.44406281_44406282del
GRCh37.p13 chr 13	NC_000013.10:g.44406282del
GRCh37.p13 chr 13	NC_000013.10:g.44406282dup
GRCh37.p13 chr 13	NC_000013.10:g.44406281_44406282dup
GRCh37.p13 chr 13	NC_000013.10:g.44406278_44406282dup

Gene: CCDC122, coiled-coil domain containing 122 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CCDC122 transcript variant 2	NM_001350617.2:c.	N/A	Genic Downstream Transcript Variant
CCDC122 transcript variant 3	NM_001350618.2:c.	N/A	Genic Downstream Transcript Variant
CCDC122 transcript variant 1	NM_144974.5:c.	N/A	Genic Downstream Transcript Variant
CCDC122 transcript variant X3	XM_047430112.1:c.673-8122… XM_047430112.1:c.673-8122_673-8119del	N/A	Intron Variant
CCDC122 transcript variant X4	XM_047430113.1:c.673-8122… XM_047430113.1:c.673-8122_673-8119del	N/A	Intron Variant
CCDC122 transcript variant X1	XM_017020397.3:c.	N/A	Genic Downstream Transcript Variant
CCDC122 transcript variant X2	XM_017020398.2:c.	N/A	Genic Downstream Transcript Variant
CCDC122 transcript variant X6	XM_024449324.2:c.	N/A	Genic Downstream Transcript Variant
CCDC122 transcript variant X7	XM_024449327.2:c.	N/A	Genic Downstream Transcript Variant
CCDC122 transcript variant X5	XM_047430114.1:c.	N/A	Genic Downstream Transcript 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	(A)₁₇=	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dup(A)₅
GRCh38.p14 chr 13	NC_000013.11:g.43832130_43832146=	NC_000013.11:g.43832143_43832146del	NC_000013.11:g.43832144_43832146del	NC_000013.11:g.43832145_43832146del	NC_000013.11:g.43832146del	NC_000013.11:g.43832146dup	NC_000013.11:g.43832145_43832146dup	NC_000013.11:g.43832142_43832146dup
GRCh37.p13 chr 13	NC_000013.10:g.44406266_44406282=	NC_000013.10:g.44406279_44406282del	NC_000013.10:g.44406280_44406282del	NC_000013.10:g.44406281_44406282del	NC_000013.10:g.44406282del	NC_000013.10:g.44406282dup	NC_000013.10:g.44406281_44406282dup	NC_000013.10:g.44406278_44406282dup
CCDC122 transcript variant X3	XM_047430112.1:c.673-8119=	XM_047430112.1:c.673-8122_673-8119del	XM_047430112.1:c.673-8121_673-8119del	XM_047430112.1:c.673-8120_673-8119del	XM_047430112.1:c.673-8119del	XM_047430112.1:c.673-8119dup	XM_047430112.1:c.673-8120_673-8119dup	XM_047430112.1:c.673-8123_673-8119dup
CCDC122 transcript variant X4	XM_047430113.1:c.673-8119=	XM_047430113.1:c.673-8122_673-8119del	XM_047430113.1:c.673-8121_673-8119del	XM_047430113.1:c.673-8120_673-8119del	XM_047430113.1:c.673-8119del	XM_047430113.1:c.673-8119dup	XM_047430113.1:c.673-8120_673-8119dup	XM_047430113.1:c.673-8123_673-8119dup

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#.

53 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DEVINE_LAB	ss15201644	Mar 15, 2016 (147)
2	ABI	ss40357111	Mar 15, 2006 (137)
3	HGSV	ss77942415	Sep 08, 2015 (146)
4	HGSV	ss80937328	Sep 08, 2015 (146)
5	HUMANGENOME_JCVI	ss95618970	Dec 05, 2013 (138)
6	GMI	ss287904189	May 09, 2011 (137)
7	GMI	ss289174821	May 04, 2012 (137)
8	PJP	ss294795048	May 09, 2011 (137)
9	PJP	ss294795049	May 09, 2011 (134)
10	BILGI_BIOE	ss666597421	Apr 25, 2013 (138)
11	SSIP	ss947313666	Aug 21, 2014 (142)
12	1000GENOMES	ss1373103317	Aug 21, 2014 (142)
13	EVA_GENOME_DK	ss1574632093	Apr 01, 2015 (144)
14	EVA_UK10K_ALSPAC	ss1707767953	Apr 01, 2015 (144)
15	EVA_UK10K_TWINSUK	ss1707768329	Apr 01, 2015 (144)
16	EVA_UK10K_TWINSUK	ss1710599840	Apr 01, 2015 (144)
17	EVA_UK10K_ALSPAC	ss1710599866	Apr 01, 2015 (144)
18	SWEGEN	ss3010948916	Nov 08, 2017 (151)
19	MCHAISSO	ss3063762971	Nov 08, 2017 (151)
20	MCHAISSO	ss3064594111	Nov 08, 2017 (151)
21	MCHAISSO	ss3065518102	Nov 08, 2017 (151)
22	EVA_DECODE	ss3695203491	Jul 13, 2019 (153)
23	EVA_DECODE	ss3695203492	Jul 13, 2019 (153)
24	EVA_DECODE	ss3695203493	Jul 13, 2019 (153)
25	ACPOP	ss3739708719	Jul 13, 2019 (153)
26	ACPOP	ss3739708720	Jul 13, 2019 (153)
27	PACBIO	ss3787446237	Jul 13, 2019 (153)
28	PACBIO	ss3797398234	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3816741831	Jul 13, 2019 (153)
30	EVA	ss3833524508	Apr 27, 2020 (154)
31	GNOMAD	ss4265082629	Apr 26, 2021 (155)
32	GNOMAD	ss4265082630	Apr 26, 2021 (155)
33	GNOMAD	ss4265082631	Apr 26, 2021 (155)
34	GNOMAD	ss4265082632	Apr 26, 2021 (155)
35	GNOMAD	ss4265082633	Apr 26, 2021 (155)
36	GNOMAD	ss4265082634	Apr 26, 2021 (155)
37	GNOMAD	ss4265082635	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5209795744	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5209795745	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5209795746	Apr 26, 2021 (155)
41	1000G_HIGH_COVERAGE	ss5293581235	Oct 17, 2022 (156)
42	1000G_HIGH_COVERAGE	ss5293581236	Oct 17, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5293581237	Oct 17, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5293581238	Oct 17, 2022 (156)
45	HUGCELL_USP	ss5487959681	Oct 17, 2022 (156)
46	HUGCELL_USP	ss5487959682	Oct 17, 2022 (156)
47	HUGCELL_USP	ss5487959683	Oct 17, 2022 (156)
48	TOMMO_GENOMICS	ss5761613018	Oct 17, 2022 (156)
49	TOMMO_GENOMICS	ss5761613019	Oct 17, 2022 (156)
50	TOMMO_GENOMICS	ss5761613020	Oct 17, 2022 (156)
51	EVA	ss5839415016	Oct 17, 2022 (156)
52	EVA	ss5839415017	Oct 17, 2022 (156)
53	EVA	ss5924932890	Oct 17, 2022 (156)
54	1000Genomes	NC_000013.10 - 44406266	Oct 12, 2018 (152)
55	The Avon Longitudinal Study of Parents and Children	NC_000013.10 - 44406266	Oct 12, 2018 (152)
56	The Danish reference pan genome	NC_000013.10 - 44406266	Apr 27, 2020 (154)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429449273 (NC_000013.11:43832129::A 88/107292) Row 429449274 (NC_000013.11:43832129::AA 5/107306) Row 429449275 (NC_000013.11:43832129::AAAAA 2/107308)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429449273 (NC_000013.11:43832129::A 88/107292) Row 429449274 (NC_000013.11:43832129::AA 5/107306) Row 429449275 (NC_000013.11:43832129::AAAAA 2/107308)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429449273 (NC_000013.11:43832129::A 88/107292) Row 429449274 (NC_000013.11:43832129::AA 5/107306) Row 429449275 (NC_000013.11:43832129::AAAAA 2/107308)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429449273 (NC_000013.11:43832129::A 88/107292) Row 429449274 (NC_000013.11:43832129::AA 5/107306) Row 429449275 (NC_000013.11:43832129::AAAAA 2/107308)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429449273 (NC_000013.11:43832129::A 88/107292) Row 429449274 (NC_000013.11:43832129::AA 5/107306) Row 429449275 (NC_000013.11:43832129::AAAAA 2/107308)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429449273 (NC_000013.11:43832129::A 88/107292) Row 429449274 (NC_000013.11:43832129::AA 5/107306) Row 429449275 (NC_000013.11:43832129::AAAAA 2/107308)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429449273 (NC_000013.11:43832129::A 88/107292) Row 429449274 (NC_000013.11:43832129::AA 5/107306) Row 429449275 (NC_000013.11:43832129::AAAAA 2/107308)...	-	Apr 26, 2021 (155)
64	Northern Sweden Submission ignored due to conflicting rows: Row 12993584 (NC_000013.10:44406265:A: 351/540) Row 12993585 (NC_000013.10:44406265:AA: 22/540)	-	Jul 13, 2019 (153)
65	Northern Sweden Submission ignored due to conflicting rows: Row 12993584 (NC_000013.10:44406265:A: 351/540) Row 12993585 (NC_000013.10:44406265:AA: 22/540)	-	Jul 13, 2019 (153)
66	8.3KJPN Submission ignored due to conflicting rows: Row 67765051 (NC_000013.10:44406265:A: 12824/16756) Row 67765052 (NC_000013.10:44406265:AA: 1030/16756) Row 67765053 (NC_000013.10:44406265::A 68/16756)	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 67765051 (NC_000013.10:44406265:A: 12824/16756) Row 67765052 (NC_000013.10:44406265:AA: 1030/16756) Row 67765053 (NC_000013.10:44406265::A 68/16756)	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 67765051 (NC_000013.10:44406265:A: 12824/16756) Row 67765052 (NC_000013.10:44406265:AA: 1030/16756) Row 67765053 (NC_000013.10:44406265::A 68/16756)	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 95450122 (NC_000013.11:43832129:A: 21680/28258) Row 95450123 (NC_000013.11:43832129:AA: 1744/28258) Row 95450124 (NC_000013.11:43832129::A 116/28258)	-	Oct 17, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 95450122 (NC_000013.11:43832129:A: 21680/28258) Row 95450123 (NC_000013.11:43832129:AA: 1744/28258) Row 95450124 (NC_000013.11:43832129::A 116/28258)	-	Oct 17, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 95450122 (NC_000013.11:43832129:A: 21680/28258) Row 95450123 (NC_000013.11:43832129:AA: 1744/28258) Row 95450124 (NC_000013.11:43832129::A 116/28258)	-	Oct 17, 2022 (156)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 33838582 (NC_000013.10:44406266:A: 3416/3708) Row 33838583 (NC_000013.10:44406265:AA: 286/3708)	-	Apr 27, 2020 (154)
73	UK 10K study - Twins	-	Oct 12, 2018 (152)
74	ALFA	NC_000013.11 - 43832130	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).

Associated ID	History Updated (Build)
rs11326843	May 11, 2012 (137)
rs35436014	May 11, 2012 (137)
rs59424685	May 25, 2008 (130)
rs71716466	May 11, 2012 (137)
rs377403030	May 13, 2013 (138)
rs869194256	Jul 19, 2016 (147)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4265082635	NC_000013.11:43832129:AAAA:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3695203493, ss4265082634, ss5293581237	NC_000013.11:43832129:AAA:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
9932176683	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
33838583, ss1707767953, ss1707768329, ss3010948916, ss3739708720, ss5209795745, ss5839415017	NC_000013.10:44406265:AA:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4265082633, ss5293581236, ss5487959681, ss5761613019	NC_000013.11:43832129:AA:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
9932176683	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3695203492	NC_000013.11:43832130:AA:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss289174821, ss294795048	NC_000013.9:43304265:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss77942415, ss80937328, ss294795049	NC_000013.9:43304281:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
60913466, 402103, ss666597421, ss1373103317, ss1574632093, ss3739708719, ss3787446237, ss3797398234, ss3833524508, ss5209795744, ss5839415016	NC_000013.10:44406265:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss947313666, ss1710599840, ss1710599866	NC_000013.10:44406266:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3063762971, ss3064594111, ss3065518102, ss3816741831, ss4265082632, ss5293581235, ss5487959682, ss5761613018, ss5924932890	NC_000013.11:43832129:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
9932176683	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3695203491	NC_000013.11:43832131:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss40357111, ss287904189	NT_024524.14:25386265:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss15201644, ss95618970	NT_024524.14:25386281:A:	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5209795746	NC_000013.10:44406265::A	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4265082629, ss5293581238, ss5487959683, ss5761613020	NC_000013.11:43832129::A	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
9932176683	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4265082630	NC_000013.11:43832129::AA	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4265082631	NC_000013.11:43832129::AAAAA	NC_000013.11:43832129:AAAAAAAAAAAA… NC_000013.11:43832129:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(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 rs11323501

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

rs11323501