Name: rs570396556
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.

rs570396556

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:21496212-21496228 (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)₆ / del(A)₄ / delAAA / delAA…
del(A)₆ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₆=0.0000 (0/6096, ALFA)
delAA=0.0000 (0/6096, ALFA)
delA=0.0000 (0/6096, ALFA) (+ 6 more)
dupA=0.0000 (0/6096, ALFA)
dupAA=0.0000 (0/6096, ALFA)
dupAAA=0.0000 (0/6096, ALFA)
dup(A)₄=0.0000 (0/6096, ALFA)
delA=0.0901 (451/5008, 1000G)
dupA=0.30 (12/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TOX4 : 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	6096	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	3910	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	1380	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	58	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	1322	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	56	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	48	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	8	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	66	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	410	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	48	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	226	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=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
Allele Frequency Aggregator	Total	Global	6096	(A)₁₇=1.0000	del(A)₆=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	European	Sub	3910	(A)₁₇=1.0000	del(A)₆=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	African	Sub	1380	(A)₁₇=1.0000	del(A)₆=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	410	(A)₁₇=1.000	del(A)₆=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	226	(A)₁₇=1.000	del(A)₆=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	Latin American 1	Sub	66	(A)₁₇=1.00	del(A)₆=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)₁₇=1.00	del(A)₆=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	48	(A)₁₇=1.00	del(A)₆=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)₁₇=0.9099	delA=0.0901
1000Genomes	African	Sub	1322	(A)₁₇=0.8699	delA=0.1301
1000Genomes	East Asian	Sub	1008	(A)₁₇=0.8909	delA=0.1091
1000Genomes	Europe	Sub	1006	(A)₁₇=0.9324	delA=0.0676
1000Genomes	South Asian	Sub	978	(A)₁₇=0.947	delA=0.053
1000Genomes	American	Sub	694	(A)₁₇=0.929	delA=0.071
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.30

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 14	NC_000014.9:g.21496223_21496228del
GRCh38.p14 chr 14	NC_000014.9:g.21496225_21496228del
GRCh38.p14 chr 14	NC_000014.9:g.21496226_21496228del
GRCh38.p14 chr 14	NC_000014.9:g.21496227_21496228del
GRCh38.p14 chr 14	NC_000014.9:g.21496228del
GRCh38.p14 chr 14	NC_000014.9:g.21496228dup
GRCh38.p14 chr 14	NC_000014.9:g.21496227_21496228dup
GRCh38.p14 chr 14	NC_000014.9:g.21496226_21496228dup
GRCh38.p14 chr 14	NC_000014.9:g.21496225_21496228dup
GRCh37.p13 chr 14	NC_000014.8:g.21964381_21964386del
GRCh37.p13 chr 14	NC_000014.8:g.21964383_21964386del
GRCh37.p13 chr 14	NC_000014.8:g.21964384_21964386del
GRCh37.p13 chr 14	NC_000014.8:g.21964385_21964386del
GRCh37.p13 chr 14	NC_000014.8:g.21964386del
GRCh37.p13 chr 14	NC_000014.8:g.21964386dup
GRCh37.p13 chr 14	NC_000014.8:g.21964385_21964386dup
GRCh37.p13 chr 14	NC_000014.8:g.21964384_21964386dup
GRCh37.p13 chr 14	NC_000014.8:g.21964383_21964386dup

Gene: TOX4, TOX high mobility group box family member 4 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TOX4 transcript variant 2	NM_001303523.2:c.1737-323… NM_001303523.2:c.1737-323_1737-318del	N/A	Intron Variant
TOX4 transcript variant 1	NM_014828.4:c.1806-323_18… NM_014828.4:c.1806-323_1806-318del	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)₆	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄
GRCh38.p14 chr 14	NC_000014.9:g.21496212_21496228=	NC_000014.9:g.21496223_21496228del	NC_000014.9:g.21496225_21496228del	NC_000014.9:g.21496226_21496228del	NC_000014.9:g.21496227_21496228del	NC_000014.9:g.21496228del	NC_000014.9:g.21496228dup	NC_000014.9:g.21496227_21496228dup	NC_000014.9:g.21496226_21496228dup	NC_000014.9:g.21496225_21496228dup
GRCh37.p13 chr 14	NC_000014.8:g.21964370_21964386=	NC_000014.8:g.21964381_21964386del	NC_000014.8:g.21964383_21964386del	NC_000014.8:g.21964384_21964386del	NC_000014.8:g.21964385_21964386del	NC_000014.8:g.21964386del	NC_000014.8:g.21964386dup	NC_000014.8:g.21964385_21964386dup	NC_000014.8:g.21964384_21964386dup	NC_000014.8:g.21964383_21964386dup
TOX4 transcript variant 2	NM_001303523.2:c.1737-334=	NM_001303523.2:c.1737-323_1737-318del	NM_001303523.2:c.1737-321_1737-318del	NM_001303523.2:c.1737-320_1737-318del	NM_001303523.2:c.1737-319_1737-318del	NM_001303523.2:c.1737-318del	NM_001303523.2:c.1737-318dup	NM_001303523.2:c.1737-319_1737-318dup	NM_001303523.2:c.1737-320_1737-318dup	NM_001303523.2:c.1737-321_1737-318dup
TOX4 transcript	NM_014828.2:c.1806-334=	NM_014828.2:c.1806-323_1806-318del	NM_014828.2:c.1806-321_1806-318del	NM_014828.2:c.1806-320_1806-318del	NM_014828.2:c.1806-319_1806-318del	NM_014828.2:c.1806-318del	NM_014828.2:c.1806-318dup	NM_014828.2:c.1806-319_1806-318dup	NM_014828.2:c.1806-320_1806-318dup	NM_014828.2:c.1806-321_1806-318dup
TOX4 transcript variant 1	NM_014828.4:c.1806-334=	NM_014828.4:c.1806-323_1806-318del	NM_014828.4:c.1806-321_1806-318del	NM_014828.4:c.1806-320_1806-318del	NM_014828.4:c.1806-319_1806-318del	NM_014828.4:c.1806-318del	NM_014828.4:c.1806-318dup	NM_014828.4:c.1806-319_1806-318dup	NM_014828.4:c.1806-320_1806-318dup	NM_014828.4:c.1806-321_1806-318dup
TOX4 transcript variant X1	XM_005268245.1:c.1728-334=	XM_005268245.1:c.1728-323_1728-318del	XM_005268245.1:c.1728-321_1728-318del	XM_005268245.1:c.1728-320_1728-318del	XM_005268245.1:c.1728-319_1728-318del	XM_005268245.1:c.1728-318del	XM_005268245.1:c.1728-318dup	XM_005268245.1:c.1728-319_1728-318dup	XM_005268245.1:c.1728-320_1728-318dup	XM_005268245.1:c.1728-321_1728-318dup

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#.

37 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81588273	Oct 12, 2018 (152)
2	1000GENOMES	ss1373798035	Aug 21, 2014 (142)
3	EVA_GENOME_DK	ss1574722752	Apr 01, 2015 (144)
4	SWEGEN	ss3011843034	Nov 08, 2017 (151)
5	EVA_DECODE	ss3696247199	Jul 13, 2019 (153)
6	EVA_DECODE	ss3696247200	Jul 13, 2019 (153)
7	EVA_DECODE	ss3696247201	Jul 13, 2019 (153)
8	EVA_DECODE	ss3696247202	Jul 13, 2019 (153)
9	EVA_DECODE	ss3696247203	Jul 13, 2019 (153)
10	KHV_HUMAN_GENOMES	ss3817389377	Jul 13, 2019 (153)
11	EVA	ss3833803170	Apr 27, 2020 (154)
12	EVA	ss3845981121	Apr 27, 2020 (154)
13	GNOMAD	ss4274261079	Apr 26, 2021 (155)
14	GNOMAD	ss4274261080	Apr 26, 2021 (155)
15	GNOMAD	ss4274261081	Apr 26, 2021 (155)
16	GNOMAD	ss4274261082	Apr 26, 2021 (155)
17	GNOMAD	ss4274261083	Apr 26, 2021 (155)
18	GNOMAD	ss4274261084	Apr 26, 2021 (155)
19	GNOMAD	ss4274261085	Apr 26, 2021 (155)
20	GNOMAD	ss4274261086	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5212247902	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5212247903	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5212247904	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5212247905	Apr 26, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5295453958	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5295453959	Oct 16, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5295453960	Oct 16, 2022 (156)
28	1000G_HIGH_COVERAGE	ss5295453961	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5489590664	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5489590665	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5489590666	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5489590667	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5764768375	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5764768376	Oct 16, 2022 (156)
35	TOMMO_GENOMICS	ss5764768377	Oct 16, 2022 (156)
36	TOMMO_GENOMICS	ss5764768378	Oct 16, 2022 (156)
37	EVA	ss5850941055	Oct 16, 2022 (156)
38	1000Genomes	NC_000014.8 - 21964370	Oct 12, 2018 (152)
39	The Danish reference pan genome	NC_000014.8 - 21964370	Apr 27, 2020 (154)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 444841628 (NC_000014.9:21496211::A 30647/88826) Row 444841629 (NC_000014.9:21496211::AA 1240/89170) Row 444841630 (NC_000014.9:21496211::AAA 91/89240)...	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 70217209 (NC_000014.8:21964369::A 2928/16730) Row 70217210 (NC_000014.8:21964369:A: 251/16730) Row 70217211 (NC_000014.8:21964369:AA: 3/16730)...	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 70217209 (NC_000014.8:21964369::A 2928/16730) Row 70217210 (NC_000014.8:21964369:A: 251/16730) Row 70217211 (NC_000014.8:21964369:AA: 3/16730)...	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 70217209 (NC_000014.8:21964369::A 2928/16730) Row 70217210 (NC_000014.8:21964369:A: 251/16730) Row 70217211 (NC_000014.8:21964369:AA: 3/16730)...	-	Apr 26, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 70217209 (NC_000014.8:21964369::A 2928/16730) Row 70217210 (NC_000014.8:21964369:A: 251/16730) Row 70217211 (NC_000014.8:21964369:AA: 3/16730)...	-	Apr 26, 2021 (155)
52	14KJPN Submission ignored due to conflicting rows: Row 98605479 (NC_000014.9:21496211::A 4920/28230) Row 98605480 (NC_000014.9:21496211:A: 408/28230) Row 98605481 (NC_000014.9:21496211:AA: 4/28230)...	-	Oct 16, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 98605479 (NC_000014.9:21496211::A 4920/28230) Row 98605480 (NC_000014.9:21496211:A: 408/28230) Row 98605481 (NC_000014.9:21496211:AA: 4/28230)...	-	Oct 16, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 98605479 (NC_000014.9:21496211::A 4920/28230) Row 98605480 (NC_000014.9:21496211:A: 408/28230) Row 98605481 (NC_000014.9:21496211:AA: 4/28230)...	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 98605479 (NC_000014.9:21496211::A 4920/28230) Row 98605480 (NC_000014.9:21496211:A: 408/28230) Row 98605481 (NC_000014.9:21496211:AA: 4/28230)...	-	Oct 16, 2022 (156)
56	ALFA	NC_000014.9 - 21496212	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
4251231805	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4274261086	NC_000014.9:21496211:AAAA:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3696247203, ss4274261085	NC_000014.9:21496211:AAA:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5212247904	NC_000014.8:21964369:AA:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4274261084, ss5489590667, ss5764768377	NC_000014.9:21496211:AA:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
4251231805	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3696247202	NC_000014.9:21496212:AA:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
63077793, ss1373798035, ss3011843034, ss5212247903	NC_000014.8:21964369:A:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3817389377, ss4274261083, ss5295453961, ss5489590664, ss5764768376	NC_000014.9:21496211:A:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
4251231805	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3696247201	NC_000014.9:21496213:A:	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
436386, ss1574722752, ss3833803170, ss5212247902	NC_000014.8:21964369::A	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3845981121, ss4274261079, ss5295453958, ss5489590665, ss5764768375, ss5850941055	NC_000014.9:21496211::A	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
4251231805	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3696247200	NC_000014.9:21496214::A	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss81588273	NT_026437.12:2964386::A	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5212247905	NC_000014.8:21964369::AA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4274261080, ss5295453959, ss5489590666, ss5764768378	NC_000014.9:21496211::AA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
4251231805	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3696247199	NC_000014.9:21496214::AA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4274261081, ss5295453960	NC_000014.9:21496211::AAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
4251231805	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4274261082	NC_000014.9:21496211::AAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
4251231805	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000014.9:21496211:AAAAAAAAAAAAA… NC_000014.9:21496211:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(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 rs570396556

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

rs570396556