Name: rs34114730
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.

rs34114730

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:121613072-121613089 (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)₇ / delAAA / delAA / delA / …
del(A)₇ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.2950 (1877/6362, ALFA)
delA=0.2530 (1267/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FBXO40 : 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	6362	AAAAAAAAAAAAAAAAAA=0.6096	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0765, AAAAAAAAAAAAAAAAAAA=0.2950, AAAAAAAAAAAAAAAAAAAA=0.0185, AAAAAAAAAAAAAAAAAAAAA=0.0003, AAAAAAAAAAAAAAAAAAAAAA=0.0000	0.572243	0.19924	0.228517	32
European	Sub	5474	AAAAAAAAAAAAAAAAAA=0.5466	AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0890, AAAAAAAAAAAAAAAAAAA=0.3425, AAAAAAAAAAAAAAAAAAAA=0.0216, AAAAAAAAAAAAAAAAAAAAA=0.0004, AAAAAAAAAAAAAAAAAAAAAA=0.0000	0.486276	0.239707	0.274016	32
African	Sub	562	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	36	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	526	AAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	56	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	44	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	30	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	74	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	42	AAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	124	AAAAAAAAAAAAAAAAAA=0.984	AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.016, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	0.967742	0.0	0.032258	0

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	6362	(A)₁₈=0.6096	delAAA=0.0000, delAA=0.0000, delA=0.0765, dupA=0.2950, dupAA=0.0185, dupAAA=0.0003, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	5474	(A)₁₈=0.5466	delAAA=0.0000, delAA=0.0000, delA=0.0890, dupA=0.3425, dupAA=0.0216, dupAAA=0.0004, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	562	(A)₁₈=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Other	Sub	124	(A)₁₈=0.984	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.016, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	74	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Asian	Sub	56	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
Allele Frequency Aggregator	Latin American 1	Sub	30	(A)₁₈=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₈=0.7470	delA=0.2530
1000Genomes	African	Sub	1322	(A)₁₈=0.7375	delA=0.2625
1000Genomes	East Asian	Sub	1008	(A)₁₈=0.7282	delA=0.2718
1000Genomes	Europe	Sub	1006	(A)₁₈=0.7644	delA=0.2356
1000Genomes	South Asian	Sub	978	(A)₁₈=0.760	delA=0.240
1000Genomes	American	Sub	694	(A)₁₈=0.749	delA=0.251

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 3	NC_000003.12:g.121613083_121613089del
GRCh38.p14 chr 3	NC_000003.12:g.121613087_121613089del
GRCh38.p14 chr 3	NC_000003.12:g.121613088_121613089del
GRCh38.p14 chr 3	NC_000003.12:g.121613089del
GRCh38.p14 chr 3	NC_000003.12:g.121613089dup
GRCh38.p14 chr 3	NC_000003.12:g.121613088_121613089dup
GRCh38.p14 chr 3	NC_000003.12:g.121613087_121613089dup
GRCh38.p14 chr 3	NC_000003.12:g.121613086_121613089dup
GRCh37.p13 chr 3	NC_000003.11:g.121331930_121331936del
GRCh37.p13 chr 3	NC_000003.11:g.121331934_121331936del
GRCh37.p13 chr 3	NC_000003.11:g.121331935_121331936del
GRCh37.p13 chr 3	NC_000003.11:g.121331936del
GRCh37.p13 chr 3	NC_000003.11:g.121331936dup
GRCh37.p13 chr 3	NC_000003.11:g.121331935_121331936dup
GRCh37.p13 chr 3	NC_000003.11:g.121331934_121331936dup
GRCh37.p13 chr 3	NC_000003.11:g.121331933_121331936dup

Gene: FBXO40, F-box protein 40 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FBXO40 transcript	NM_016298.4:c.-30-7463_-3… NM_016298.4:c.-30-7463_-30-7457del	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)₁₈=	del(A)₇	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 3	NC_000003.12:g.121613072_121613089=	NC_000003.12:g.121613083_121613089del	NC_000003.12:g.121613087_121613089del	NC_000003.12:g.121613088_121613089del	NC_000003.12:g.121613089del	NC_000003.12:g.121613089dup	NC_000003.12:g.121613088_121613089dup	NC_000003.12:g.121613087_121613089dup	NC_000003.12:g.121613086_121613089dup
GRCh37.p13 chr 3	NC_000003.11:g.121331919_121331936=	NC_000003.11:g.121331930_121331936del	NC_000003.11:g.121331934_121331936del	NC_000003.11:g.121331935_121331936del	NC_000003.11:g.121331936del	NC_000003.11:g.121331936dup	NC_000003.11:g.121331935_121331936dup	NC_000003.11:g.121331934_121331936dup	NC_000003.11:g.121331933_121331936dup
FBXO40 transcript	NM_016298.3:c.-30-7474=	NM_016298.3:c.-30-7463_-30-7457del	NM_016298.3:c.-30-7459_-30-7457del	NM_016298.3:c.-30-7458_-30-7457del	NM_016298.3:c.-30-7457del	NM_016298.3:c.-30-7457dup	NM_016298.3:c.-30-7458_-30-7457dup	NM_016298.3:c.-30-7459_-30-7457dup	NM_016298.3:c.-30-7460_-30-7457dup
FBXO40 transcript	NM_016298.4:c.-30-7474=	NM_016298.4:c.-30-7463_-30-7457del	NM_016298.4:c.-30-7459_-30-7457del	NM_016298.4:c.-30-7458_-30-7457del	NM_016298.4:c.-30-7457del	NM_016298.4:c.-30-7457dup	NM_016298.4:c.-30-7458_-30-7457dup	NM_016298.4:c.-30-7459_-30-7457dup	NM_016298.4:c.-30-7460_-30-7457dup

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#.

50 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41908496	Mar 13, 2006 (137)
2	ABI	ss42093153	Mar 13, 2006 (126)
3	HUMANGENOME_JCVI	ss95330019	Feb 04, 2009 (130)
4	GMI	ss288409690	May 04, 2012 (137)
5	PJP	ss295122411	Jan 10, 2018 (151)
6	PJP	ss295122412	May 09, 2011 (135)
7	SSIP	ss947096167	Jan 10, 2018 (151)
8	1000GENOMES	ss1370892608	Aug 21, 2014 (142)
9	EVA_UK10K_ALSPAC	ss1703799474	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1703799476	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1703799697	Apr 01, 2015 (144)
12	EVA_UK10K_TWINSUK	ss1703799699	Apr 01, 2015 (144)
13	SWEGEN	ss2993086303	Nov 08, 2017 (151)
14	URBANLAB	ss3647511305	Oct 12, 2018 (152)
15	EVA_DECODE	ss3710158665	Jul 13, 2019 (153)
16	EVA_DECODE	ss3710158666	Jul 13, 2019 (153)
17	EVA_DECODE	ss3710158667	Jul 13, 2019 (153)
18	EVA_DECODE	ss3710158668	Jul 13, 2019 (153)
19	ACPOP	ss3730292623	Jul 13, 2019 (153)
20	ACPOP	ss3730292624	Jul 13, 2019 (153)
21	ACPOP	ss3730292625	Jul 13, 2019 (153)
22	PACBIO	ss3789942165	Jul 13, 2019 (153)
23	PACBIO	ss3789942166	Jul 13, 2019 (153)
24	PACBIO	ss3794816615	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3803743290	Jul 13, 2019 (153)
26	EVA	ss3828041319	Apr 25, 2020 (154)
27	EVA	ss3837452616	Apr 25, 2020 (154)
28	GNOMAD	ss4079663180	Apr 27, 2021 (155)
29	GNOMAD	ss4079663181	Apr 27, 2021 (155)
30	GNOMAD	ss4079663182	Apr 27, 2021 (155)
31	GNOMAD	ss4079663183	Apr 27, 2021 (155)
32	GNOMAD	ss4079663184	Apr 27, 2021 (155)
33	GNOMAD	ss4079663185	Apr 27, 2021 (155)
34	GNOMAD	ss4079663186	Apr 27, 2021 (155)
35	TOMMO_GENOMICS	ss5161280316	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5161280317	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5161280318	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5161280319	Apr 27, 2021 (155)
39	1000G_HIGH_COVERAGE	ss5255795119	Oct 12, 2022 (156)
40	1000G_HIGH_COVERAGE	ss5255795120	Oct 12, 2022 (156)
41	1000G_HIGH_COVERAGE	ss5255795121	Oct 12, 2022 (156)
42	HUGCELL_USP	ss5454965204	Oct 12, 2022 (156)
43	HUGCELL_USP	ss5454965205	Oct 12, 2022 (156)
44	HUGCELL_USP	ss5454965206	Oct 12, 2022 (156)
45	TOMMO_GENOMICS	ss5694064203	Oct 12, 2022 (156)
46	TOMMO_GENOMICS	ss5694064204	Oct 12, 2022 (156)
47	TOMMO_GENOMICS	ss5694064205	Oct 12, 2022 (156)
48	TOMMO_GENOMICS	ss5694064206	Oct 12, 2022 (156)
49	EVA	ss5826391409	Oct 12, 2022 (156)
50	EVA	ss5826391410	Oct 12, 2022 (156)
51	1000Genomes	NC_000003.11 - 121331919	Oct 12, 2018 (152)
52	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 9547721 (NC_000003.11:121331918::A 1930/3854) Row 9547722 (NC_000003.11:121331918::AA 256/3854)	-	Oct 12, 2018 (152)
53	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 9547721 (NC_000003.11:121331918::A 1930/3854) Row 9547722 (NC_000003.11:121331918::AA 256/3854)	-	Oct 12, 2018 (152)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121881904 (NC_000003.12:121613071::A 54293/119032) Row 121881905 (NC_000003.12:121613071::AA 3342/119116) Row 121881906 (NC_000003.12:121613071::AAA 25/119204)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121881904 (NC_000003.12:121613071::A 54293/119032) Row 121881905 (NC_000003.12:121613071::AA 3342/119116) Row 121881906 (NC_000003.12:121613071::AAA 25/119204)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121881904 (NC_000003.12:121613071::A 54293/119032) Row 121881905 (NC_000003.12:121613071::AA 3342/119116) Row 121881906 (NC_000003.12:121613071::AAA 25/119204)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121881904 (NC_000003.12:121613071::A 54293/119032) Row 121881905 (NC_000003.12:121613071::AA 3342/119116) Row 121881906 (NC_000003.12:121613071::AAA 25/119204)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121881904 (NC_000003.12:121613071::A 54293/119032) Row 121881905 (NC_000003.12:121613071::AA 3342/119116) Row 121881906 (NC_000003.12:121613071::AAA 25/119204)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121881904 (NC_000003.12:121613071::A 54293/119032) Row 121881905 (NC_000003.12:121613071::AA 3342/119116) Row 121881906 (NC_000003.12:121613071::AAA 25/119204)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 121881904 (NC_000003.12:121613071::A 54293/119032) Row 121881905 (NC_000003.12:121613071::AA 3342/119116) Row 121881906 (NC_000003.12:121613071::AAA 25/119204)...	-	Apr 27, 2021 (155)
61	Northern Sweden Submission ignored due to conflicting rows: Row 3577488 (NC_000003.11:121331918::A 253/576) Row 3577489 (NC_000003.11:121331918:A: 43/576) Row 3577490 (NC_000003.11:121331918::AA 15/576)	-	Jul 13, 2019 (153)
62	Northern Sweden Submission ignored due to conflicting rows: Row 3577488 (NC_000003.11:121331918::A 253/576) Row 3577489 (NC_000003.11:121331918:A: 43/576) Row 3577490 (NC_000003.11:121331918::AA 15/576)	-	Jul 13, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 3577488 (NC_000003.11:121331918::A 253/576) Row 3577489 (NC_000003.11:121331918:A: 43/576) Row 3577490 (NC_000003.11:121331918::AA 15/576)	-	Jul 13, 2019 (153)
64	8.3KJPN Submission ignored due to conflicting rows: Row 19249623 (NC_000003.11:121331918::A 2928/16740) Row 19249624 (NC_000003.11:121331918:A: 1372/16740) Row 19249625 (NC_000003.11:121331918::AA 378/16740)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 19249623 (NC_000003.11:121331918::A 2928/16740) Row 19249624 (NC_000003.11:121331918:A: 1372/16740) Row 19249625 (NC_000003.11:121331918::AA 378/16740)...	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 19249623 (NC_000003.11:121331918::A 2928/16740) Row 19249624 (NC_000003.11:121331918:A: 1372/16740) Row 19249625 (NC_000003.11:121331918::AA 378/16740)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 19249623 (NC_000003.11:121331918::A 2928/16740) Row 19249624 (NC_000003.11:121331918:A: 1372/16740) Row 19249625 (NC_000003.11:121331918::AA 378/16740)...	-	Apr 27, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 27901307 (NC_000003.12:121613071::A 4799/28254) Row 27901308 (NC_000003.12:121613071:A: 2398/28254) Row 27901309 (NC_000003.12:121613071::AA 571/28254)...	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 27901307 (NC_000003.12:121613071::A 4799/28254) Row 27901308 (NC_000003.12:121613071:A: 2398/28254) Row 27901309 (NC_000003.12:121613071::AA 571/28254)...	-	Oct 12, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 27901307 (NC_000003.12:121613071::A 4799/28254) Row 27901308 (NC_000003.12:121613071:A: 2398/28254) Row 27901309 (NC_000003.12:121613071::AA 571/28254)...	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 27901307 (NC_000003.12:121613071::A 4799/28254) Row 27901308 (NC_000003.12:121613071:A: 2398/28254) Row 27901309 (NC_000003.12:121613071::AA 571/28254)...	-	Oct 12, 2022 (156)
72	UK 10K study - Twins Submission ignored due to conflicting rows: Row 9547721 (NC_000003.11:121331918::A 1880/3708) Row 9547722 (NC_000003.11:121331918::AA 222/3708)	-	Oct 12, 2018 (152)
73	UK 10K study - Twins Submission ignored due to conflicting rows: Row 9547721 (NC_000003.11:121331918::A 1880/3708) Row 9547722 (NC_000003.11:121331918::AA 222/3708)	-	Oct 12, 2018 (152)
74	ALFA	NC_000003.12 - 121613072	Apr 27, 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)
rs34117334	May 11, 2012 (137)
rs71884531	May 11, 2012 (137)
rs72411700	May 11, 2012 (137)
rs149608077	Sep 17, 2011 (135)
rs66893060	Feb 26, 2009 (130)
rs569925395	Jul 01, 2015 (144)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4079663186	NC_000003.12:121613071:AAAAAAA:	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4079663185	NC_000003.12:121613071:AAA:	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
13962964985	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3710158668, ss4079663184	NC_000003.12:121613071:AA:	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
13962964985	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss288409690	NC_000003.10:122814608:A:	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
17141693, ss1370892608, ss2993086303, ss3730292624, ss3837452616, ss5161280317	NC_000003.11:121331918:A:	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3647511305, ss3803743290, ss4079663183, ss5255795119, ss5454965204, ss5694064204	NC_000003.12:121613071:A:	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
13962964985	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3710158667	NC_000003.12:121613072:A:	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss295122411	NC_000003.10:122814609::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss295122412	NC_000003.10:122814626::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1703799474, ss1703799697, ss3730292623, ss3789942165, ss3828041319, ss5161280316, ss5826391409	NC_000003.11:121331918::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss947096167	NC_000003.11:121331919::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4079663180, ss5255795121, ss5454965205, ss5694064203	NC_000003.12:121613071::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
13962964985	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3710158666	NC_000003.12:121613073::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss41908496	NT_005612.16:27827081::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss42093153, ss95330019	NT_005612.16:27827082::A	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss1703799476, ss1703799699, ss3730292625, ss3789942166, ss3794816615, ss5161280318, ss5826391410	NC_000003.11:121331918::AA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4079663181, ss5255795120, ss5454965206, ss5694064205	NC_000003.12:121613071::AA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
13962964985	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3710158665	NC_000003.12:121613073::AA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5161280319	NC_000003.11:121331918::AAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4079663182, ss5694064206	NC_000003.12:121613071::AAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
13962964985	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
13962964985	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3403795031	NC_000003.12:121613071::AAAA	NC_000003.12:121613071:AAAAAAAAAAA… NC_000003.12:121613071:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs34114730

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

rs34114730