Name: rs35136338
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.

rs35136338

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr13:44157551-44157571 (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(CA)₄ / delCACA / delCA / dupCA…
del(CA)₄ / delCACA / delCA / dupCA / dupCACA / dup(CA)₃ / dup(CA)₄
Variation Type: Indel Insertion and Deletion
Frequency: (AC)₁₀A=0.3883 (2419/6230, ALFA)
dupCA=0.4878 (2443/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SMIM2 : Intron Variant
SMIM2-IT1 : 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	6230	ACACACACACACACACACACA=0.3883	ACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.5894, ACACACACACACACACACACACACA=0.0223, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000	0.313508	0.509073	0.177419	32
European	Sub	4658	ACACACACACACACACACACA=0.1831	ACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.7870, ACACACACACACACACACACACACA=0.0298, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000	0.06895	0.690868	0.240183	32
African	Sub	1380	ACACACACACACACACACACA=1.0000	ACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	68	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1312	ACACACACACACACACACACA=1.0000	ACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACACACA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	48	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	44	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	ACACACACACACACACACACA=1.0	ACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	22	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	42	ACACACACACACACACACACA=1.00	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	ACACACACACACACACACACA=1.0	ACACACACACACA=0.0, ACACACACACACACACA=0.0, ACACACACACACACACACA=0.0, ACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACA=0.0, ACACACACACACACACACACACACACACA=0.0	1.0	0.0	0.0	N/A
Other	Sub	76	ACACACACACACACACACACA=0.92	ACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.08, ACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACACACA=0.00	0.894737	0.052632	0.052632	9

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	6230	(AC)₁₀A=0.3883	del(CA)₄=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.5894, dupCACA=0.0223, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	European	Sub	4658	(AC)₁₀A=0.1831	del(CA)₄=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.7870, dupCACA=0.0298, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	African	Sub	1380	(AC)₁₀A=1.0000	del(CA)₄=0.0000, delCACA=0.0000, delCA=0.0000, dupCA=0.0000, dupCACA=0.0000, dup(CA)₃=0.0000, dup(CA)₄=0.0000
Allele Frequency Aggregator	Other	Sub	76	(AC)₁₀A=0.92	del(CA)₄=0.00, delCACA=0.00, delCA=0.00, dupCA=0.08, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	Asian	Sub	48	(AC)₁₀A=1.00	del(CA)₄=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	Latin American 2	Sub	42	(AC)₁₀A=1.00	del(CA)₄=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(AC)₁₀A=1.00	del(CA)₄=0.00, delCACA=0.00, delCA=0.00, dupCA=0.00, dupCACA=0.00, dup(CA)₃=0.00, dup(CA)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(AC)₁₀A=1.0	del(CA)₄=0.0, delCACA=0.0, delCA=0.0, dupCA=0.0, dupCACA=0.0, dup(CA)₃=0.0, dup(CA)₄=0.0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupCA=0.4878
1000Genomes	African	Sub	1322	- No frequency provided	dupCA=0.2254
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupCA=0.2857
1000Genomes	Europe	Sub	1006	- No frequency provided	dupCA=0.7326
1000Genomes	South Asian	Sub	978	- No frequency provided	dupCA=0.648
1000Genomes	American	Sub	694	- No frequency provided	dupCA=0.700

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.44157552CA[6]
GRCh38.p14 chr 13	NC_000013.11:g.44157552CA[8]
GRCh38.p14 chr 13	NC_000013.11:g.44157552CA[9]
GRCh38.p14 chr 13	NC_000013.11:g.44157552CA[11]
GRCh38.p14 chr 13	NC_000013.11:g.44157552CA[12]
GRCh38.p14 chr 13	NC_000013.11:g.44157552CA[13]
GRCh38.p14 chr 13	NC_000013.11:g.44157552CA[14]
GRCh37.p13 chr 13	NC_000013.10:g.44731688CA[6]
GRCh37.p13 chr 13	NC_000013.10:g.44731688CA[8]
GRCh37.p13 chr 13	NC_000013.10:g.44731688CA[9]
GRCh37.p13 chr 13	NC_000013.10:g.44731688CA[11]
GRCh37.p13 chr 13	NC_000013.10:g.44731688CA[12]
GRCh37.p13 chr 13	NC_000013.10:g.44731688CA[13]
GRCh37.p13 chr 13	NC_000013.10:g.44731688CA[14]

Gene: SMIM2, small integral membrane protein 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SMIM2 transcript	NM_024058.3:c.253+3033GT[… NM_024058.3:c.253+3033GT[6]	N/A	Intron Variant

Gene: SMIM2-IT1, SMIM2 intronic transcript 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SMIM2-IT1 transcript	NR_046843.1: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	(AC)₁₀A=	del(CA)₄	delCACA	delCA	dupCA	dupCACA	dup(CA)₃	dup(CA)₄
GRCh38.p14 chr 13	NC_000013.11:g.44157551_44157571=	NC_000013.11:g.44157552CA[6]	NC_000013.11:g.44157552CA[8]	NC_000013.11:g.44157552CA[9]	NC_000013.11:g.44157552CA[11]	NC_000013.11:g.44157552CA[12]	NC_000013.11:g.44157552CA[13]	NC_000013.11:g.44157552CA[14]
GRCh37.p13 chr 13	NC_000013.10:g.44731687_44731707=	NC_000013.10:g.44731688CA[6]	NC_000013.10:g.44731688CA[8]	NC_000013.10:g.44731688CA[9]	NC_000013.10:g.44731688CA[11]	NC_000013.10:g.44731688CA[12]	NC_000013.10:g.44731688CA[13]	NC_000013.10:g.44731688CA[14]
SMIM2 transcript	NM_024058.2:c.253+3052=	NM_024058.2:c.253+3033GT[6]	NM_024058.2:c.253+3033GT[8]	NM_024058.2:c.253+3033GT[9]	NM_024058.2:c.253+3033GT[11]	NM_024058.2:c.253+3033GT[12]	NM_024058.2:c.253+3033GT[13]	NM_024058.2:c.253+3033GT[14]
SMIM2 transcript	NM_024058.3:c.253+3052=	NM_024058.3:c.253+3033GT[6]	NM_024058.3:c.253+3033GT[8]	NM_024058.3:c.253+3033GT[9]	NM_024058.3:c.253+3033GT[11]	NM_024058.3:c.253+3033GT[12]	NM_024058.3:c.253+3033GT[13]	NM_024058.3:c.253+3033GT[14]

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#.

57 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40313357	Mar 14, 2006 (126)
2	HGSV	ss77986323	Dec 06, 2007 (129)
3	HUMANGENOME_JCVI	ss95619039	Feb 04, 2009 (130)
4	BUSHMAN	ss193317396	Jul 04, 2010 (132)
5	BL	ss256165991	May 09, 2011 (135)
6	GMI	ss287904230	May 09, 2011 (138)
7	GMI	ss289174983	May 04, 2012 (138)
8	1000GENOMES	ss327521603	May 09, 2011 (135)
9	1000GENOMES	ss327622932	May 09, 2011 (135)
10	LUNTER	ss552287757	Apr 25, 2013 (138)
11	SSMP	ss664177658	Apr 01, 2015 (144)
12	BILGI_BIOE	ss666597506	Apr 25, 2013 (138)
13	1000GENOMES	ss1373106013	Aug 21, 2014 (142)
14	DDI	ss1536756827	Apr 01, 2015 (144)
15	SYSTEMSBIOZJU	ss2628298923	Nov 08, 2017 (151)
16	SWEGEN	ss3010952535	Nov 08, 2017 (151)
17	SWEGEN	ss3010952536	Nov 08, 2017 (151)
18	MCHAISSO	ss3063763059	Nov 08, 2017 (151)
19	MCHAISSO	ss3064594219	Nov 08, 2017 (151)
20	MCHAISSO	ss3065518217	Nov 08, 2017 (151)
21	BIOINF_KMB_FNS_UNIBA	ss3645299501	Oct 12, 2018 (152)
22	URBANLAB	ss3650024228	Oct 12, 2018 (152)
23	EVA_DECODE	ss3695207824	Jul 13, 2019 (153)
24	EVA_DECODE	ss3695207825	Jul 13, 2019 (153)
25	EVA_DECODE	ss3695207826	Jul 13, 2019 (153)
26	EVA_DECODE	ss3695207827	Jul 13, 2019 (153)
27	ACPOP	ss3739710714	Jul 13, 2019 (153)
28	ACPOP	ss3739710715	Jul 13, 2019 (153)
29	PACBIO	ss3787446890	Jul 13, 2019 (153)
30	PACBIO	ss3792515038	Jul 13, 2019 (153)
31	PACBIO	ss3797398802	Jul 13, 2019 (153)
32	KHV_HUMAN_GENOMES	ss3816744429	Jul 13, 2019 (153)
33	EVA	ss3833525727	Apr 27, 2020 (154)
34	EVA	ss3840343234	Apr 27, 2020 (154)
35	EVA	ss3845828792	Apr 27, 2020 (154)
36	GNOMAD	ss4265119744	Apr 26, 2021 (155)
37	GNOMAD	ss4265119745	Apr 26, 2021 (155)
38	GNOMAD	ss4265119746	Apr 26, 2021 (155)
39	GNOMAD	ss4265119747	Apr 26, 2021 (155)
40	GNOMAD	ss4265119749	Apr 26, 2021 (155)
41	GNOMAD	ss4265119750	Apr 26, 2021 (155)
42	GNOMAD	ss4265119751	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5209805827	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5209805828	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5209805829	Apr 26, 2021 (155)
46	1000G_HIGH_COVERAGE	ss5293588547	Oct 16, 2022 (156)
47	1000G_HIGH_COVERAGE	ss5293588549	Oct 16, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5293588550	Oct 16, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5293588551	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5487966306	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5487966307	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5761625998	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5761625999	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5761626000	Oct 16, 2022 (156)
55	EVA	ss5839418176	Oct 16, 2022 (156)
56	EVA	ss5839418177	Oct 16, 2022 (156)
57	EVA	ss5850711784	Oct 16, 2022 (156)
58	1000Genomes	NC_000013.10 - 44731687	Oct 12, 2018 (152)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429510914 (NC_000013.11:44157550::AC 85562/138532) Row 429510915 (NC_000013.11:44157550::ACAC 3711/138506) Row 429510916 (NC_000013.11:44157550::ACACAC 5/138568)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429510914 (NC_000013.11:44157550::AC 85562/138532) Row 429510915 (NC_000013.11:44157550::ACAC 3711/138506) Row 429510916 (NC_000013.11:44157550::ACACAC 5/138568)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429510914 (NC_000013.11:44157550::AC 85562/138532) Row 429510915 (NC_000013.11:44157550::ACAC 3711/138506) Row 429510916 (NC_000013.11:44157550::ACACAC 5/138568)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429510914 (NC_000013.11:44157550::AC 85562/138532) Row 429510915 (NC_000013.11:44157550::ACAC 3711/138506) Row 429510916 (NC_000013.11:44157550::ACACAC 5/138568)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429510914 (NC_000013.11:44157550::AC 85562/138532) Row 429510915 (NC_000013.11:44157550::ACAC 3711/138506) Row 429510916 (NC_000013.11:44157550::ACACAC 5/138568)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429510914 (NC_000013.11:44157550::AC 85562/138532) Row 429510915 (NC_000013.11:44157550::ACAC 3711/138506) Row 429510916 (NC_000013.11:44157550::ACACAC 5/138568)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 429510914 (NC_000013.11:44157550::AC 85562/138532) Row 429510915 (NC_000013.11:44157550::ACAC 3711/138506) Row 429510916 (NC_000013.11:44157550::ACACAC 5/138568)...	-	Apr 26, 2021 (155)
66	Northern Sweden Submission ignored due to conflicting rows: Row 12995579 (NC_000013.10:44731686::AC 480/600) Row 12995580 (NC_000013.10:44731686::ACAC 9/600)	-	Jul 13, 2019 (153)
67	Northern Sweden Submission ignored due to conflicting rows: Row 12995579 (NC_000013.10:44731686::AC 480/600) Row 12995580 (NC_000013.10:44731686::ACAC 9/600)	-	Jul 13, 2019 (153)
68	8.3KJPN Submission ignored due to conflicting rows: Row 67775134 (NC_000013.10:44731686::AC 3793/16760) Row 67775135 (NC_000013.10:44731686::ACAC 3/16760) Row 67775136 (NC_000013.10:44731686:ACAC: 1/16760)	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 67775134 (NC_000013.10:44731686::AC 3793/16760) Row 67775135 (NC_000013.10:44731686::ACAC 3/16760) Row 67775136 (NC_000013.10:44731686:ACAC: 1/16760)	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 67775134 (NC_000013.10:44731686::AC 3793/16760) Row 67775135 (NC_000013.10:44731686::ACAC 3/16760) Row 67775136 (NC_000013.10:44731686:ACAC: 1/16760)	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 95463102 (NC_000013.11:44157550::AC 6552/28258) Row 95463103 (NC_000013.11:44157550:AC: 8/28258) Row 95463104 (NC_000013.11:44157550::ACAC 6/28258)	-	Oct 16, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 95463102 (NC_000013.11:44157550::AC 6552/28258) Row 95463103 (NC_000013.11:44157550:AC: 8/28258) Row 95463104 (NC_000013.11:44157550::ACAC 6/28258)	-	Oct 16, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 95463102 (NC_000013.11:44157550::AC 6552/28258) Row 95463103 (NC_000013.11:44157550:AC: 8/28258) Row 95463104 (NC_000013.11:44157550::ACAC 6/28258)	-	Oct 16, 2022 (156)
74	ALFA	NC_000013.11 - 44157551	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)
rs142528067	Sep 17, 2011 (135)
rs150916282	Apr 25, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4265119751	NC_000013.11:44157550:ACACACAC:	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACA	(self)
9646997559	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACA	(self)
ss5209805829	NC_000013.10:44731686:ACAC:	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACA	(self)
ss4265119750, ss5293588551	NC_000013.11:44157550:ACAC:	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACA	(self)
9646997559	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACA	(self)
ss3695207827, ss4265119749, ss5293588549, ss5761625999	NC_000013.11:44157550:AC:	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
9646997559	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACA	(self)
ss256165991, ss327521603, ss327622932, ss552287757	NC_000013.9:43629686::AC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss289174983	NC_000013.9:43629707::CA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
60922341, ss664177658, ss666597506, ss1373106013, ss1536756827, ss2628298923, ss3010952535, ss3739710714, ss3787446890, ss3792515038, ss3797398802, ss3833525727, ss3840343234, ss5209805827, ss5839418176	NC_000013.10:44731686::AC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3063763059, ss3064594219, ss3065518217, ss3645299501, ss3650024228, ss3816744429, ss3845828792, ss4265119744, ss5293588547, ss5487966306, ss5761625998, ss5850711784	NC_000013.11:44157550::AC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
9646997559	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3695207826	NC_000013.11:44157552::AC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss40313357	NT_024524.14:25711686::AC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss95619039, ss287904230	NT_024524.14:25711707::CA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss193317396	NT_024524.15:25749444::AC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACA	(self)
ss3010952536, ss3739710715, ss5209805828, ss5839418177	NC_000013.10:44731686::ACAC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4265119745, ss5293588550, ss5487966307, ss5761626000	NC_000013.11:44157550::ACAC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
9646997559	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss3695207825	NC_000013.11:44157552::ACAC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss77986323	NT_024524.14:25711707::CACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACA	(self)
ss4265119746	NC_000013.11:44157550::ACACAC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
9646997559	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss3695207824	NC_000013.11:44157552::ACACAC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACACA	(self)
ss4265119747	NC_000013.11:44157550::ACACACAC	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(self)
9646997559	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	NC_000013.11:44157550:ACACACACACAC… NC_000013.11:44157550:ACACACACACACACACACACA:ACACACACACACACACACACACACACACA	(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 rs35136338

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35136338