Name: rs35855574
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.

rs35855574

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:8376409-8376425 (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)₅ / del(A)₄ / delAAA / delAA…
del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₇=0.4764 (2386/5008, 1000G)
del(A)₄=0.0000 (0/3510, ALFA)
delAAA=0.0000 (0/3510, ALFA) (+ 4 more)
delAA=0.0000 (0/3510, ALFA)
delA=0.0000 (0/3510, ALFA)
dupA=0.0000 (0/3510, ALFA)
dupAA=0.0000 (0/3510, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: LINC02226 : 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	3510	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	2790	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	344	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	12	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	332	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	10	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
East Asian	Sub	8	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Other Asian	Sub	2	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	34	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	178	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	24	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	130	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	(A)₁₇=0.4764	delAA=0.5236
1000Genomes	African	Sub	1322	(A)₁₇=0.4077	delAA=0.5923
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.4048	delAA=0.5952
1000Genomes	Europe	Sub	1006	(A)₁₇=0.6352	delAA=0.3648
1000Genomes	South Asian	Sub	978	(A)₁₇=0.453	delAA=0.547
1000Genomes	American	Sub	694	(A)₁₇=0.514	delAA=0.486
Allele Frequency Aggregator	Total	Global	3510	(A)₁₇=1.0000	del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	2790	(A)₁₇=1.0000	del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	344	(A)₁₇=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	178	(A)₁₇=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	130	(A)₁₇=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	34	(A)₁₇=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	24	(A)₁₇=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	10	(A)₁₇=1.0	del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0

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 5	NC_000005.10:g.8376421_8376425del
GRCh38.p14 chr 5	NC_000005.10:g.8376422_8376425del
GRCh38.p14 chr 5	NC_000005.10:g.8376423_8376425del
GRCh38.p14 chr 5	NC_000005.10:g.8376424_8376425del
GRCh38.p14 chr 5	NC_000005.10:g.8376425del
GRCh38.p14 chr 5	NC_000005.10:g.8376425dup
GRCh38.p14 chr 5	NC_000005.10:g.8376424_8376425dup
GRCh37.p13 chr 5	NC_000005.9:g.8376534_8376538del
GRCh37.p13 chr 5	NC_000005.9:g.8376535_8376538del
GRCh37.p13 chr 5	NC_000005.9:g.8376536_8376538del
GRCh37.p13 chr 5	NC_000005.9:g.8376537_8376538del
GRCh37.p13 chr 5	NC_000005.9:g.8376538del
GRCh37.p13 chr 5	NC_000005.9:g.8376538dup
GRCh37.p13 chr 5	NC_000005.9:g.8376537_8376538dup

Gene: LINC02226, long intergenic non-protein coding RNA 2226 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LINC02226 transcript	NR_039984.1: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	(A)₁₇=	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 5	NC_000005.10:g.8376409_8376425=	NC_000005.10:g.8376421_8376425del	NC_000005.10:g.8376422_8376425del	NC_000005.10:g.8376423_8376425del	NC_000005.10:g.8376424_8376425del	NC_000005.10:g.8376425del	NC_000005.10:g.8376425dup	NC_000005.10:g.8376424_8376425dup
GRCh37.p13 chr 5	NC_000005.9:g.8376522_8376538=	NC_000005.9:g.8376534_8376538del	NC_000005.9:g.8376535_8376538del	NC_000005.9:g.8376536_8376538del	NC_000005.9:g.8376537_8376538del	NC_000005.9:g.8376538del	NC_000005.9:g.8376538dup	NC_000005.9:g.8376537_8376538dup

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#.

48 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42410482	Mar 15, 2006 (126)
2	HGSV	ss80110173	Dec 14, 2007 (130)
3	BUSHMAN	ss193785981	Mar 15, 2016 (147)
4	BILGI_BIOE	ss666298678	Apr 25, 2013 (138)
5	1000GENOMES	ss1373407307	Aug 21, 2014 (142)
6	HAMMER_LAB	ss1803030589	Sep 08, 2015 (146)
7	EVA_DECODE	ss3714069379	Jul 13, 2019 (153)
8	EVA_DECODE	ss3714069380	Jul 13, 2019 (153)
9	EVA_DECODE	ss3714069381	Jul 13, 2019 (153)
10	EVA_DECODE	ss3714069382	Jul 13, 2019 (153)
11	EVA_DECODE	ss3714069383	Jul 13, 2019 (153)
12	EVA_DECODE	ss3714069384	Jul 13, 2019 (153)
13	ACPOP	ss3732072832	Jul 13, 2019 (153)
14	ACPOP	ss3732072833	Jul 13, 2019 (153)
15	PACBIO	ss3785018605	Jul 13, 2019 (153)
16	PACBIO	ss3790437366	Jul 13, 2019 (153)
17	PACBIO	ss3790437367	Jul 13, 2019 (153)
18	PACBIO	ss3795313904	Jul 13, 2019 (153)
19	PACBIO	ss3795313905	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3806210926	Jul 13, 2019 (153)
21	EVA	ss3829085126	Apr 26, 2020 (154)
22	EVA	ss3838004845	Apr 26, 2020 (154)
23	EVA	ss3843444510	Apr 26, 2020 (154)
24	GNOMAD	ss4098981029	Apr 26, 2021 (155)
25	GNOMAD	ss4098981030	Apr 26, 2021 (155)
26	GNOMAD	ss4098981031	Apr 26, 2021 (155)
27	GNOMAD	ss4098981032	Apr 26, 2021 (155)
28	GNOMAD	ss4098981033	Apr 26, 2021 (155)
29	GNOMAD	ss4098981034	Apr 26, 2021 (155)
30	GNOMAD	ss4098981035	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5170301358	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5170301359	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5170301360	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5170301361	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5262814276	Oct 13, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5262814277	Oct 13, 2022 (156)
37	1000G_HIGH_COVERAGE	ss5262814279	Oct 13, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5262814280	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5461165980	Oct 13, 2022 (156)
40	HUGCELL_USP	ss5461165981	Oct 13, 2022 (156)
41	HUGCELL_USP	ss5461165983	Oct 13, 2022 (156)
42	HUGCELL_USP	ss5461165984	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5705952611	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5705952612	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5705952614	Oct 13, 2022 (156)
46	TOMMO_GENOMICS	ss5705952615	Oct 13, 2022 (156)
47	EVA	ss5834494357	Oct 13, 2022 (156)
48	EVA	ss5834494358	Oct 13, 2022 (156)
49	1000Genomes	NC_000005.9 - 8376522	Oct 12, 2018 (152)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179409185 (NC_000005.10:8376408::A 236/99716) Row 179409186 (NC_000005.10:8376408::AA 3/99836) Row 179409187 (NC_000005.10:8376408:A: 6418/99722)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179409185 (NC_000005.10:8376408::A 236/99716) Row 179409186 (NC_000005.10:8376408::AA 3/99836) Row 179409187 (NC_000005.10:8376408:A: 6418/99722)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179409185 (NC_000005.10:8376408::A 236/99716) Row 179409186 (NC_000005.10:8376408::AA 3/99836) Row 179409187 (NC_000005.10:8376408:A: 6418/99722)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179409185 (NC_000005.10:8376408::A 236/99716) Row 179409186 (NC_000005.10:8376408::AA 3/99836) Row 179409187 (NC_000005.10:8376408:A: 6418/99722)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179409185 (NC_000005.10:8376408::A 236/99716) Row 179409186 (NC_000005.10:8376408::AA 3/99836) Row 179409187 (NC_000005.10:8376408:A: 6418/99722)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179409185 (NC_000005.10:8376408::A 236/99716) Row 179409186 (NC_000005.10:8376408::AA 3/99836) Row 179409187 (NC_000005.10:8376408:A: 6418/99722)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 179409185 (NC_000005.10:8376408::A 236/99716) Row 179409186 (NC_000005.10:8376408::AA 3/99836) Row 179409187 (NC_000005.10:8376408:A: 6418/99722)...	-	Apr 26, 2021 (155)
57	Northern Sweden Submission ignored due to conflicting rows: Row 5357697 (NC_000005.9:8376521:AA: 131/542) Row 5357698 (NC_000005.9:8376521:A: 7/542)	-	Jul 13, 2019 (153)
58	Northern Sweden Submission ignored due to conflicting rows: Row 5357697 (NC_000005.9:8376521:AA: 131/542) Row 5357698 (NC_000005.9:8376521:A: 7/542)	-	Jul 13, 2019 (153)
59	8.3KJPN Submission ignored due to conflicting rows: Row 28270665 (NC_000005.9:8376521:AA: 6780/16738) Row 28270666 (NC_000005.9:8376521:A: 2557/16738) Row 28270667 (NC_000005.9:8376521:AAA: 9/16738)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 28270665 (NC_000005.9:8376521:AA: 6780/16738) Row 28270666 (NC_000005.9:8376521:A: 2557/16738) Row 28270667 (NC_000005.9:8376521:AAA: 9/16738)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 28270665 (NC_000005.9:8376521:AA: 6780/16738) Row 28270666 (NC_000005.9:8376521:A: 2557/16738) Row 28270667 (NC_000005.9:8376521:AAA: 9/16738)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 28270665 (NC_000005.9:8376521:AA: 6780/16738) Row 28270666 (NC_000005.9:8376521:A: 2557/16738) Row 28270667 (NC_000005.9:8376521:AAA: 9/16738)...	-	Apr 26, 2021 (155)
63	14KJPN Submission ignored due to conflicting rows: Row 39789715 (NC_000005.10:8376408:AA: 11644/28254) Row 39789716 (NC_000005.10:8376408:A: 4369/28254) Row 39789718 (NC_000005.10:8376408:AAA: 14/28254)...	-	Oct 13, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 39789715 (NC_000005.10:8376408:AA: 11644/28254) Row 39789716 (NC_000005.10:8376408:A: 4369/28254) Row 39789718 (NC_000005.10:8376408:AAA: 14/28254)...	-	Oct 13, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 39789715 (NC_000005.10:8376408:AA: 11644/28254) Row 39789716 (NC_000005.10:8376408:A: 4369/28254) Row 39789718 (NC_000005.10:8376408:AAA: 14/28254)...	-	Oct 13, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 39789715 (NC_000005.10:8376408:AA: 11644/28254) Row 39789716 (NC_000005.10:8376408:A: 4369/28254) Row 39789718 (NC_000005.10:8376408:AAA: 14/28254)...	-	Oct 13, 2022 (156)
67	ALFA	NC_000005.10 - 8376409	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)
rs57643268	May 23, 2008 (130)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3714069384, ss4098981035	NC_000005.10:8376408:AAAAA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4098981034	NC_000005.10:8376408:AAAA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
386440534	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3714069383	NC_000005.10:8376409:AAAA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3829085126, ss5170301360, ss5834494358	NC_000005.9:8376521:AAA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4098981033, ss5262814279, ss5461165984, ss5705952614	NC_000005.10:8376408:AAA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
386440534	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3714069382	NC_000005.10:8376410:AAA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss80110173	NC_000005.8:8429536:AA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
25384779, ss666298678, ss1373407307, ss1803030589, ss3732072832, ss3785018605, ss3790437366, ss3795313904, ss3838004845, ss5170301358, ss5834494357	NC_000005.9:8376521:AA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3806210926, ss3843444510, ss4098981032, ss5262814277, ss5461165980, ss5705952611	NC_000005.10:8376408:AA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
386440534	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3714069381	NC_000005.10:8376411:AA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss193785981	NT_006576.16:8366521:AA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss42410482	NT_006576.16:8366536:AA:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3732072833, ss3790437367, ss3795313905, ss5170301359	NC_000005.9:8376521:A:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4098981031, ss5262814276, ss5461165981, ss5705952612	NC_000005.10:8376408:A:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
386440534	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3714069380	NC_000005.10:8376412:A:	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss5170301361	NC_000005.9:8376521::A	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4098981029, ss5262814280, ss5461165983, ss5705952615	NC_000005.10:8376408::A	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
386440534	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3714069379	NC_000005.10:8376413::A	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4098981030	NC_000005.10:8376408::AA	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
386440534	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000005.10:8376408:AAAAAAAAAAAAA… NC_000005.10:8376408:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(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 rs35855574

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

rs35855574