Name: rs3214645
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.

rs3214645

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:75418699-75418707 (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
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.2892 (1591/5502, ALFA)
dupTT=0.2171 (1087/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SMIM21 : Intron Variant
LOC105372200 : 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	5502	TTTTTTTTT=0.4947	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.2159, TTTTTTTTTTT=0.2892, TTTTTTTTTTTT=0.0002	0.481797	0.163823	0.35438	32
European	Sub	5292	TTTTTTTTT=0.4756	TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.2241, TTTTTTTTTTT=0.3001, TTTTTTTTTTTT=0.0002	0.450755	0.173414	0.375831	30
African	Sub	126	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	8	TTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	118	TTTTTTTTT=1.000	TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTT=0	TTTTTTT=0, TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTT=0	TTTTTTT=0, TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTT=0	TTTTTTT=0, TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	12	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	44	TTTTTTTTT=1.00	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	TTTTTTTTT=1.0	TTTTTTT=0.0, TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	24	TTTTTTTTT=0.79	TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.08, TTTTTTTTTTT=0.12, TTTTTTTTTTTT=0.00	0.8	0.1	0.1	2

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	5502	(T)₉=0.4947	delTT=0.0000, delT=0.0000, dupT=0.2159, dupTT=0.2892, dupTTT=0.0002
Allele Frequency Aggregator	European	Sub	5292	(T)₉=0.4756	delTT=0.0000, delT=0.0000, dupT=0.2241, dupTT=0.3001, dupTTT=0.0002
Allele Frequency Aggregator	African	Sub	126	(T)₉=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000
Allele Frequency Aggregator	Latin American 2	Sub	44	(T)₉=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	Other	Sub	24	(T)₉=0.79	delTT=0.00, delT=0.00, dupT=0.08, dupTT=0.12, dupTTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₉=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(T)₉=1.0	delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0
Allele Frequency Aggregator	Asian	Sub	0	(T)₉=0	delTT=0, delT=0, dupT=0, dupTT=0, dupTTT=0
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.5855, dupTT=0.2171, dupTTT=0.0008
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.7216, dupTT=0.0802, dupTTT=0.0000
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.7837, dupTT=0.2113, dupTTT=0.0010
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.3231, dupTT=0.3479, dupTTT=0.0020
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.539, dupTT=0.267, dupTTT=0.001
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.484, dupTT=0.226, dupTTT=0.000

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 18	NC_000018.10:g.75418706_75418707del
GRCh38.p14 chr 18	NC_000018.10:g.75418707del
GRCh38.p14 chr 18	NC_000018.10:g.75418707dup
GRCh38.p14 chr 18	NC_000018.10:g.75418706_75418707dup
GRCh38.p14 chr 18	NC_000018.10:g.75418705_75418707dup
GRCh37.p13 chr 18	NC_000018.9:g.73130661_73130662del
GRCh37.p13 chr 18	NC_000018.9:g.73130662del
GRCh37.p13 chr 18	NC_000018.9:g.73130662dup
GRCh37.p13 chr 18	NC_000018.9:g.73130661_73130662dup
GRCh37.p13 chr 18	NC_000018.9:g.73130660_73130662dup

Gene: SMIM21, small integral membrane protein 21 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SMIM21 transcript variant 1	NM_001037331.3:c.260+86_2… NM_001037331.3:c.260+86_260+87del	N/A	Intron Variant
SMIM21 transcript variant 2	NM_001303482.2:c.260+86_2… NM_001303482.2:c.260+86_260+87del	N/A	Intron Variant

Gene: LOC105372200, uncharacterized LOC105372200 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC105372200 transcript variant X4	XR_007066471.1:n.	N/A	Intron Variant
LOC105372200 transcript variant X1	XR_935634.4:n.	N/A	Intron Variant
LOC105372200 transcript variant X2	XR_935635.4:n.	N/A	Intron Variant
LOC105372200 transcript variant X3	XR_935636.3: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	(T)₉=	delTT	delT	dupT	dupTT	dupTTT
GRCh38.p14 chr 18	NC_000018.10:g.75418699_75418707=	NC_000018.10:g.75418706_75418707del	NC_000018.10:g.75418707del	NC_000018.10:g.75418707dup	NC_000018.10:g.75418706_75418707dup	NC_000018.10:g.75418705_75418707dup
GRCh37.p13 chr 18	NC_000018.9:g.73130654_73130662=	NC_000018.9:g.73130661_73130662del	NC_000018.9:g.73130662del	NC_000018.9:g.73130662dup	NC_000018.9:g.73130661_73130662dup	NC_000018.9:g.73130660_73130662dup
SMIM21 transcript	NM_001037331.2:c.260+87=	NM_001037331.2:c.260+86_260+87del	NM_001037331.2:c.260+87del	NM_001037331.2:c.260+87dup	NM_001037331.2:c.260+86_260+87dup	NM_001037331.2:c.260+85_260+87dup
SMIM21 transcript variant 1	NM_001037331.3:c.260+87=	NM_001037331.3:c.260+86_260+87del	NM_001037331.3:c.260+87del	NM_001037331.3:c.260+87dup	NM_001037331.3:c.260+86_260+87dup	NM_001037331.3:c.260+85_260+87dup
SMIM21 transcript variant 2	NM_001303482.2:c.260+87=	NM_001303482.2:c.260+86_260+87del	NM_001303482.2:c.260+87del	NM_001303482.2:c.260+87dup	NM_001303482.2:c.260+86_260+87dup	NM_001303482.2:c.260+85_260+87dup

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#.

82 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	YUSUKE	ss4475592	Jul 03, 2002 (106)
2	ABI	ss40880648	Mar 13, 2006 (126)
3	HGSV	ss81056813	Dec 16, 2007 (129)
4	HGSV	ss81097013	Dec 16, 2007 (129)
5	HGSV	ss81485961	Dec 16, 2007 (129)
6	HGSV	ss81563672	Dec 16, 2007 (129)
7	HGSV	ss81863594	Dec 16, 2007 (129)
8	HGSV	ss82738586	Dec 16, 2007 (129)
9	HGSV	ss83747867	Dec 16, 2007 (129)
10	BGI	ss104717366	Apr 25, 2013 (138)
11	BGI	ss105485952	Apr 25, 2013 (138)
12	GMI	ss155753582	Dec 01, 2009 (131)
13	GMI	ss289368428	Sep 14, 2016 (149)
14	GMI	ss289368429	May 04, 2012 (138)
15	PJP	ss294948945	May 31, 2013 (138)
16	PJP	ss294948946	May 31, 2013 (138)
17	1000GENOMES	ss327869848	May 09, 2011 (135)
18	1000GENOMES	ss328001696	May 09, 2011 (135)
19	1000GENOMES	ss328260526	May 09, 2011 (135)
20	LUNTER	ss552593700	Apr 25, 2013 (138)
21	LUNTER	ss552971090	Apr 25, 2013 (138)
22	LUNTER	ss553650195	Apr 25, 2013 (138)
23	BILGI_BIOE	ss666720189	Apr 25, 2013 (138)
24	1000GENOMES	ss1377741538	Aug 21, 2014 (142)
25	1000GENOMES	ss1377741539	Aug 21, 2014 (142)
26	1000GENOMES	ss1377741541	Aug 21, 2014 (142)
27	DDI	ss1536879191	Apr 01, 2015 (144)
28	EVA_DECODE	ss1698013753	Apr 01, 2015 (144)
29	EVA_DECODE	ss1698013754	Apr 01, 2015 (144)
30	EVA_DECODE	ss1698013755	Apr 01, 2015 (144)
31	EVA_UK10K_ALSPAC	ss1709070115	Apr 01, 2015 (144)
32	EVA_UK10K_ALSPAC	ss1709070117	Apr 01, 2015 (144)
33	EVA_UK10K_TWINSUK	ss1709070976	Apr 01, 2015 (144)
34	EVA_UK10K_TWINSUK	ss1709070977	Apr 01, 2015 (144)
35	HAMMER_LAB	ss1809146482	Sep 08, 2015 (146)
36	SWEGEN	ss3016859063	Nov 08, 2017 (151)
37	SWEGEN	ss3016859064	Nov 08, 2017 (151)
38	SWEGEN	ss3016859065	Nov 08, 2017 (151)
39	MCHAISSO	ss3063901748	Nov 08, 2017 (151)
40	BEROUKHIMLAB	ss3644429866	Oct 12, 2018 (152)
41	BIOINF_KMB_FNS_UNIBA	ss3645500279	Oct 12, 2018 (152)
42	BIOINF_KMB_FNS_UNIBA	ss3645500280	Oct 12, 2018 (152)
43	URBANLAB	ss3650837989	Oct 12, 2018 (152)
44	EVA_DECODE	ss3702065046	Jul 13, 2019 (153)
45	EVA_DECODE	ss3702065047	Jul 13, 2019 (153)
46	EVA_DECODE	ss3702065048	Jul 13, 2019 (153)
47	PACBIO	ss3788431048	Jul 13, 2019 (153)
48	PACBIO	ss3788431049	Jul 13, 2019 (153)
49	PACBIO	ss3793354820	Jul 13, 2019 (153)
50	PACBIO	ss3793354821	Jul 13, 2019 (153)
51	PACBIO	ss3798241295	Jul 13, 2019 (153)
52	PACBIO	ss3798241296	Jul 13, 2019 (153)
53	KHV_HUMAN_GENOMES	ss3820904374	Jul 13, 2019 (153)
54	KHV_HUMAN_GENOMES	ss3820904375	Jul 13, 2019 (153)
55	EVA	ss3835278625	Apr 27, 2020 (154)
56	EVA	ss3841261319	Apr 27, 2020 (154)
57	EVA	ss3846764583	Apr 27, 2020 (154)
58	KOGIC	ss3980533075	Apr 27, 2020 (154)
59	KOGIC	ss3980533076	Apr 27, 2020 (154)
60	FSA-LAB	ss3984135176	Apr 26, 2021 (155)
61	FSA-LAB	ss3984135177	Apr 26, 2021 (155)
62	GNOMAD	ss4325482412	Apr 26, 2021 (155)
63	GNOMAD	ss4325482413	Apr 26, 2021 (155)
64	GNOMAD	ss4325482414	Apr 26, 2021 (155)
65	GNOMAD	ss4325482415	Apr 26, 2021 (155)
66	TOMMO_GENOMICS	ss5226074080	Apr 26, 2021 (155)
67	TOMMO_GENOMICS	ss5226074081	Apr 26, 2021 (155)
68	TOMMO_GENOMICS	ss5226074082	Apr 26, 2021 (155)
69	1000G_HIGH_COVERAGE	ss5306002373	Oct 16, 2022 (156)
70	1000G_HIGH_COVERAGE	ss5306002374	Oct 16, 2022 (156)
71	HUGCELL_USP	ss5498707510	Oct 16, 2022 (156)
72	HUGCELL_USP	ss5498707511	Oct 16, 2022 (156)
73	EVA	ss5624081547	Oct 16, 2022 (156)
74	TOMMO_GENOMICS	ss5784120510	Oct 16, 2022 (156)
75	TOMMO_GENOMICS	ss5784120511	Oct 16, 2022 (156)
76	TOMMO_GENOMICS	ss5784120512	Oct 16, 2022 (156)
77	EVA	ss5800215884	Oct 16, 2022 (156)
78	EVA	ss5827830703	Oct 16, 2022 (156)
79	EVA	ss5827830704	Oct 16, 2022 (156)
80	EVA	ss5848471092	Oct 16, 2022 (156)
81	EVA	ss5981017994	Oct 16, 2022 (156)
82	EVA	ss5981307054	Oct 16, 2022 (156)
83	1000Genomes	NC_000018.9 - 73130654	Oct 12, 2018 (152)
84	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41684104 (NC_000018.9:73130653::T 1173/3854) Row 41684105 (NC_000018.9:73130653::TT 1346/3854)	-	Oct 12, 2018 (152)
85	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 41684104 (NC_000018.9:73130653::T 1173/3854) Row 41684105 (NC_000018.9:73130653::TT 1346/3854)	-	Oct 12, 2018 (152)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530336123 (NC_000018.10:75418698::T 62666/139502) Row 530336124 (NC_000018.10:75418698::TT 37554/139518) Row 530336125 (NC_000018.10:75418698::TTT 11/139558)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530336123 (NC_000018.10:75418698::T 62666/139502) Row 530336124 (NC_000018.10:75418698::TT 37554/139518) Row 530336125 (NC_000018.10:75418698::TTT 11/139558)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530336123 (NC_000018.10:75418698::T 62666/139502) Row 530336124 (NC_000018.10:75418698::TT 37554/139518) Row 530336125 (NC_000018.10:75418698::TTT 11/139558)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 530336123 (NC_000018.10:75418698::T 62666/139502) Row 530336124 (NC_000018.10:75418698::TT 37554/139518) Row 530336125 (NC_000018.10:75418698::TTT 11/139558)...	-	Apr 26, 2021 (155)
90	Korean Genome Project Submission ignored due to conflicting rows: Row 36911076 (NC_000018.10:75418698::T 1376/1832) Row 36911077 (NC_000018.10:75418698::TT 440/1832)	-	Apr 27, 2020 (154)
91	Korean Genome Project Submission ignored due to conflicting rows: Row 36911076 (NC_000018.10:75418698::T 1376/1832) Row 36911077 (NC_000018.10:75418698::TT 440/1832)	-	Apr 27, 2020 (154)
92	8.3KJPN Submission ignored due to conflicting rows: Row 84043387 (NC_000018.9:73130653::T 11663/16760) Row 84043388 (NC_000018.9:73130653::TT 5032/16760) Row 84043389 (NC_000018.9:73130653::TTT 1/16760)	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 84043387 (NC_000018.9:73130653::T 11663/16760) Row 84043388 (NC_000018.9:73130653::TT 5032/16760) Row 84043389 (NC_000018.9:73130653::TTT 1/16760)	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 84043387 (NC_000018.9:73130653::T 11663/16760) Row 84043388 (NC_000018.9:73130653::TT 5032/16760) Row 84043389 (NC_000018.9:73130653::TTT 1/16760)	-	Apr 26, 2021 (155)
95	14KJPN Submission ignored due to conflicting rows: Row 117957614 (NC_000018.10:75418698::T 19658/28258) Row 117957615 (NC_000018.10:75418698::TT 8492/28258) Row 117957616 (NC_000018.10:75418698::TTT 1/28258)	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 117957614 (NC_000018.10:75418698::T 19658/28258) Row 117957615 (NC_000018.10:75418698::TT 8492/28258) Row 117957616 (NC_000018.10:75418698::TTT 1/28258)	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 117957614 (NC_000018.10:75418698::T 19658/28258) Row 117957615 (NC_000018.10:75418698::TT 8492/28258) Row 117957616 (NC_000018.10:75418698::TTT 1/28258)	-	Oct 16, 2022 (156)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41684104 (NC_000018.9:73130653::T 1117/3708) Row 41684105 (NC_000018.9:73130653::TT 1301/3708)	-	Oct 12, 2018 (152)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 41684104 (NC_000018.9:73130653::T 1117/3708) Row 41684105 (NC_000018.9:73130653::TT 1301/3708)	-	Oct 12, 2018 (152)
100	ALFA	NC_000018.10 - 75418699	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)
rs72583288	Feb 26, 2009 (130)
rs201700120	Apr 25, 2013 (138)
rs141792598	Sep 17, 2011 (135)
rs146626551	Oct 04, 2011 (135)
rs386365405	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4325482415	NC_000018.10:75418698:TT:	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTT	(self)
14030520915	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTT	(self)
14030520915	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTT	(self)
ss289368428, ss327869848, ss328260526, ss552971090, ss553650195, ss1698013753	NC_000018.8:71259641::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
ss294948946	NC_000018.8:71259648::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
ss289368429	NC_000018.8:71259650::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
75194436, ss666720189, ss1377741538, ss1536879191, ss1709070115, ss1709070976, ss1809146482, ss3016859063, ss3644429866, ss3788431049, ss3793354820, ss3798241295, ss3835278625, ss5226074080, ss5624081547, ss5800215884, ss5827830704, ss5981307054	NC_000018.9:73130653::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
ss3645500279, ss3650837989, ss3702065046, ss3820904375, ss3980533075, ss4325482412, ss5306002373, ss5498707510, ss5784120510	NC_000018.10:75418698::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
14030520915	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
ss4475592, ss40880648, ss155753582	NT_025028.14:20921517::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
ss104717366, ss105485952	NT_025028.14:20921525::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
ss81863594, ss82738586, ss83747867	NT_025028.14:20921526::T	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTT	(self)
ss289368428, ss328001696, ss552593700, ss1698013754	NC_000018.8:71259641::TT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	(self)
ss294948945	NC_000018.8:71259642::TT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	(self)
75194436, ss1377741539, ss1709070117, ss1709070977, ss3016859064, ss3788431048, ss3793354821, ss3798241296, ss3841261319, ss3984135176, ss5226074081, ss5827830703, ss5981017994	NC_000018.9:73130653::TT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	(self)
ss3984135177, ss5848471092	NC_000018.9:73130662::TT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	(self)
ss3063901748, ss3645500280, ss3702065047, ss3820904374, ss3846764583, ss3980533076, ss4325482413, ss5306002374, ss5498707511, ss5784120511	NC_000018.10:75418698::TT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	(self)
14030520915	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	(self)
ss81056813, ss81097013, ss81485961, ss81563672	NT_025028.14:20921526::TT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTT	(self)
ss1698013755	NC_000018.8:71259641::TTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTTT	(self)
75194436, ss1377741541, ss3016859065, ss5226074082	NC_000018.9:73130653::TTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTTT	(self)
ss3702065048, ss4325482414, ss5784120512	NC_000018.10:75418698::TTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTTT	(self)
14030520915	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTTT	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3284493466	NC_000018.10:75418698:T:	NC_000018.10:75418698:TTTTTTTTT:TT… NC_000018.10:75418698:TTTTTTTTT:TTTTTTTT

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

No publications for rs3214645

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

rs3214645