Name: rs34277649
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.

rs34277649

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:4155752-4155764 (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: delTT / delT / dupT / dupTT / dupT…
delTT / delT / dupT / dupTT / dupTTT / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₃=0.2905 (1455/5008, 1000G)
(T)₁₃=0.2615 (1008/3854, ALSPAC)
(T)₁₃=0.2635 (977/3708, TWINSUK) (+ 5 more)
delTT=0.000 (0/550, ALFA)
delT=0.000 (0/550, ALFA)
dupT=0.000 (0/550, ALFA)
dupTT=0.000 (0/550, ALFA)
(T)₁₃=0.45 (18/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CREB3L3 : 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	550	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
European	Sub	506	TTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African	Sub	22	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	0	TTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0	0	0	0	N/A
African American	Sub	22	TTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	0	TTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	8	TTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	6	TTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	6	TTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.7095
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.7791
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.7669
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.6183
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.664
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.690
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	- No frequency provided	dupT=0.7385
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	- No frequency provided	dupT=0.7365
Allele Frequency Aggregator	Total	Global	550	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	European	Sub	506	(T)₁₃=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	African	Sub	22	(T)₁₃=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(T)₁₃=1.0	delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
Allele Frequency Aggregator	Latin American 2	Sub	6	(T)₁₃=1.0	delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
Allele Frequency Aggregator	Other	Sub	6	(T)₁₃=1.0	delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
Allele Frequency Aggregator	Asian	Sub	2	(T)₁₃=1.0	delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₁₃=0	delTT=0, delT=0, dupT=0, dupTT=0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.55

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 19	NC_000019.10:g.4155763_4155764del
GRCh38.p14 chr 19	NC_000019.10:g.4155764del
GRCh38.p14 chr 19	NC_000019.10:g.4155764dup
GRCh38.p14 chr 19	NC_000019.10:g.4155763_4155764dup
GRCh38.p14 chr 19	NC_000019.10:g.4155762_4155764dup
GRCh38.p14 chr 19	NC_000019.10:g.4155755_4155764dup
GRCh37.p13 chr 19	NC_000019.9:g.4155760_4155761del
GRCh37.p13 chr 19	NC_000019.9:g.4155761del
GRCh37.p13 chr 19	NC_000019.9:g.4155761dup
GRCh37.p13 chr 19	NC_000019.9:g.4155760_4155761dup
GRCh37.p13 chr 19	NC_000019.9:g.4155759_4155761dup
GRCh37.p13 chr 19	NC_000019.9:g.4155752_4155761dup

Gene: CREB3L3, cAMP responsive element binding protein 3 like 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CREB3L3 transcript variant 2	NM_001271995.2:c.156+736_… NM_001271995.2:c.156+736_156+737del	N/A	Intron Variant
CREB3L3 transcript variant 3	NM_001271996.2:c.156+736_… NM_001271996.2:c.156+736_156+737del	N/A	Intron Variant
CREB3L3 transcript variant 4	NM_001271997.2:c.156+736_… NM_001271997.2:c.156+736_156+737del	N/A	Intron Variant
CREB3L3 transcript variant 1	NM_032607.3:c.156+736_156… NM_032607.3:c.156+736_156+737del	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	(T)₁₃=	delTT	delT	dupT	dupTT	dupTTT	dup(T)₁₀
GRCh38.p14 chr 19	NC_000019.10:g.4155752_4155764=	NC_000019.10:g.4155763_4155764del	NC_000019.10:g.4155764del	NC_000019.10:g.4155764dup	NC_000019.10:g.4155763_4155764dup	NC_000019.10:g.4155762_4155764dup	NC_000019.10:g.4155755_4155764dup
GRCh37.p13 chr 19	NC_000019.9:g.4155749_4155761=	NC_000019.9:g.4155760_4155761del	NC_000019.9:g.4155761del	NC_000019.9:g.4155761dup	NC_000019.9:g.4155760_4155761dup	NC_000019.9:g.4155759_4155761dup	NC_000019.9:g.4155752_4155761dup
CREB3L3 transcript variant 2	NM_001271995.1:c.156+725=	NM_001271995.1:c.156+736_156+737del	NM_001271995.1:c.156+737del	NM_001271995.1:c.156+737dup	NM_001271995.1:c.156+736_156+737dup	NM_001271995.1:c.156+735_156+737dup	NM_001271995.1:c.156+728_156+737dup
CREB3L3 transcript variant 2	NM_001271995.2:c.156+725=	NM_001271995.2:c.156+736_156+737del	NM_001271995.2:c.156+737del	NM_001271995.2:c.156+737dup	NM_001271995.2:c.156+736_156+737dup	NM_001271995.2:c.156+735_156+737dup	NM_001271995.2:c.156+728_156+737dup
CREB3L3 transcript variant 3	NM_001271996.1:c.156+725=	NM_001271996.1:c.156+736_156+737del	NM_001271996.1:c.156+737del	NM_001271996.1:c.156+737dup	NM_001271996.1:c.156+736_156+737dup	NM_001271996.1:c.156+735_156+737dup	NM_001271996.1:c.156+728_156+737dup
CREB3L3 transcript variant 3	NM_001271996.2:c.156+725=	NM_001271996.2:c.156+736_156+737del	NM_001271996.2:c.156+737del	NM_001271996.2:c.156+737dup	NM_001271996.2:c.156+736_156+737dup	NM_001271996.2:c.156+735_156+737dup	NM_001271996.2:c.156+728_156+737dup
CREB3L3 transcript variant 4	NM_001271997.1:c.156+725=	NM_001271997.1:c.156+736_156+737del	NM_001271997.1:c.156+737del	NM_001271997.1:c.156+737dup	NM_001271997.1:c.156+736_156+737dup	NM_001271997.1:c.156+735_156+737dup	NM_001271997.1:c.156+728_156+737dup
CREB3L3 transcript variant 4	NM_001271997.2:c.156+725=	NM_001271997.2:c.156+736_156+737del	NM_001271997.2:c.156+737del	NM_001271997.2:c.156+737dup	NM_001271997.2:c.156+736_156+737dup	NM_001271997.2:c.156+735_156+737dup	NM_001271997.2:c.156+728_156+737dup
CREB3L3 transcript variant 1	NM_032607.2:c.156+725=	NM_032607.2:c.156+736_156+737del	NM_032607.2:c.156+737del	NM_032607.2:c.156+737dup	NM_032607.2:c.156+736_156+737dup	NM_032607.2:c.156+735_156+737dup	NM_032607.2:c.156+728_156+737dup
CREB3L3 transcript variant 1	NM_032607.3:c.156+725=	NM_032607.3:c.156+736_156+737del	NM_032607.3:c.156+737del	NM_032607.3:c.156+737dup	NM_032607.3:c.156+736_156+737dup	NM_032607.3:c.156+735_156+737dup	NM_032607.3:c.156+728_156+737dup
CREB3L3 transcript variant X1	XM_005259661.1:c.156+725=	XM_005259661.1:c.156+736_156+737del	XM_005259661.1:c.156+737del	XM_005259661.1:c.156+737dup	XM_005259661.1:c.156+736_156+737dup	XM_005259661.1:c.156+735_156+737dup	XM_005259661.1:c.156+728_156+737dup

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#.

40 SubSNP, 14 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41001989	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95945190	Dec 05, 2013 (138)
3	BL	ss256189088	May 09, 2011 (138)
4	GMI	ss289372957	May 04, 2012 (137)
5	SSMP	ss664443887	Apr 01, 2015 (144)
6	BILGI_BIOE	ss666722521	Apr 25, 2013 (138)
7	1000GENOMES	ss1377872026	Aug 21, 2014 (142)
8	EVA_GENOME_DK	ss1575222849	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1709099189	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1709099193	Apr 01, 2015 (144)
11	SYSTEMSBIOZJU	ss2629264302	Nov 08, 2017 (151)
12	SWEGEN	ss3017000948	Nov 08, 2017 (151)
13	BIOINF_KMB_FNS_UNIBA	ss3645504909	Oct 12, 2018 (152)
14	URBANLAB	ss3650856505	Oct 12, 2018 (152)
15	EVA_DECODE	ss3702232872	Jul 13, 2019 (153)
16	EVA_DECODE	ss3702232873	Jul 13, 2019 (153)
17	EVA_DECODE	ss3702232874	Jul 13, 2019 (153)
18	PACBIO	ss3793374730	Jul 13, 2019 (153)
19	PACBIO	ss3798261308	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3821002464	Jul 13, 2019 (153)
21	EVA	ss3835322085	Apr 27, 2020 (154)
22	EVA	ss3841283334	Apr 27, 2020 (154)
23	EVA	ss3846787337	Apr 27, 2020 (154)
24	GNOMAD	ss4326753496	Apr 26, 2021 (155)
25	GNOMAD	ss4326753497	Apr 26, 2021 (155)
26	GNOMAD	ss4326753498	Apr 26, 2021 (155)
27	GNOMAD	ss4326753499	Apr 26, 2021 (155)
28	GNOMAD	ss4326753500	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5226473400	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5226473401	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5306297270	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5306297271	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5498954388	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5784660298	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5784660299	Oct 16, 2022 (156)
36	EVA	ss5840179732	Oct 16, 2022 (156)
37	EVA	ss5840179733	Oct 16, 2022 (156)
38	EVA	ss5852182777	Oct 16, 2022 (156)
39	EVA	ss5927094927	Oct 16, 2022 (156)
40	EVA	ss5953297545	Oct 16, 2022 (156)
41	1000Genomes	NC_000019.9 - 4155749	Oct 12, 2018 (152)
42	The Avon Longitudinal Study of Parents and Children	NC_000019.9 - 4155749	Oct 12, 2018 (152)
43	The Danish reference pan genome	NC_000019.9 - 4155749	Apr 27, 2020 (154)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532576488 (NC_000019.10:4155751::T 99016/125266) Row 532576489 (NC_000019.10:4155751::TT 251/125182) Row 532576490 (NC_000019.10:4155751::TTT 4/125314)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532576488 (NC_000019.10:4155751::T 99016/125266) Row 532576489 (NC_000019.10:4155751::TT 251/125182) Row 532576490 (NC_000019.10:4155751::TTT 4/125314)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532576488 (NC_000019.10:4155751::T 99016/125266) Row 532576489 (NC_000019.10:4155751::TT 251/125182) Row 532576490 (NC_000019.10:4155751::TTT 4/125314)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532576488 (NC_000019.10:4155751::T 99016/125266) Row 532576489 (NC_000019.10:4155751::TT 251/125182) Row 532576490 (NC_000019.10:4155751::TTT 4/125314)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 532576488 (NC_000019.10:4155751::T 99016/125266) Row 532576489 (NC_000019.10:4155751::TT 251/125182) Row 532576490 (NC_000019.10:4155751::TTT 4/125314)...	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 84442707 (NC_000019.9:4155748::T 14024/16342) Row 84442708 (NC_000019.9:4155748::TT 24/16342)	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 84442707 (NC_000019.9:4155748::T 14024/16342) Row 84442708 (NC_000019.9:4155748::TT 24/16342)	-	Apr 26, 2021 (155)
51	14KJPN Submission ignored due to conflicting rows: Row 118497402 (NC_000019.10:4155751::T 20609/24758) Row 118497403 (NC_000019.10:4155751::TT 27/24758)	-	Oct 16, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 118497402 (NC_000019.10:4155751::T 20609/24758) Row 118497403 (NC_000019.10:4155751::TT 27/24758)	-	Oct 16, 2022 (156)
53	UK 10K study - Twins	NC_000019.9 - 4155749	Oct 12, 2018 (152)
54	ALFA	NC_000019.10 - 4155752	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)
rs142201928	May 15, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4326753500	NC_000019.10:4155751:TT:	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
12040133247	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3017000948	NC_000019.9:4155748:T:	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4326753499	NC_000019.10:4155751:T:	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
12040133247	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss256189088	NC_000019.8:4106748::T	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss289372957	NC_000019.8:4106761::T	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
75518514, 41851916, 616007, 41851916, ss664443887, ss666722521, ss1377872026, ss1575222849, ss1709099189, ss1709099193, ss2629264302, ss3793374730, ss3798261308, ss3835322085, ss3841283334, ss5226473400, ss5840179732, ss5953297545	NC_000019.9:4155748::T	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3645504909, ss3650856505, ss3702232872, ss3821002464, ss3846787337, ss4326753496, ss5306297270, ss5498954388, ss5784660298, ss5852182777, ss5927094927	NC_000019.10:4155751::T	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
12040133247	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss41001989, ss95945190	NT_011255.14:4095761::T	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss5226473401, ss5840179733	NC_000019.9:4155748::TT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3702232873, ss4326753497, ss5306297271, ss5784660299	NC_000019.10:4155751::TT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
12040133247	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4326753498	NC_000019.10:4155751::TTT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3702232874	NC_000019.10:4155751::TTTTTTTTTT	NC_000019.10:4155751:TTTTTTTTTTTTT… NC_000019.10:4155751:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(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 rs34277649

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

rs34277649