Name: rs11303145
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.

rs11303145

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr18:12355209-12355223 (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: delAA / delA / dupA / dupAA / insA…
delAA / delA / dupA / dupAA / insAACTCTTACAATTAAAC(A)₁₁CCC(A)₂₄
Variation Type: Indel Insertion and Deletion
Frequency: (A)₁₅=0.4374 (2499/5713, ALFA)
delA=0.3736 (1871/5008, 1000G)
(A)₁₅=0.1866 (719/3854, ALSPAC) (+ 3 more)
(A)₁₅=0.1764 (654/3708, TWINSUK)
(A)₁₅=0.301 (176/584, NorthernSweden)
(A)₁₅=0.35 (14/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: AFG3L2 : 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	5713	AAAAAAAAAAAAAAA=0.4374	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.5626, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.295582	0.421108	0.28331	32
European	Sub	4771	AAAAAAAAAAAAAAA=0.3278	AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.6722, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.157917	0.50315	0.338933	32
African	Sub	736	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	34	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	702	AAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	20	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	16	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	14	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	98	AAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	4	AAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other	Sub	70	AAAAAAAAAAAAAAA=0.90	AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.10, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	0.885714	0.085714	0.028571	14

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	5713	(A)₁₅=0.4374	delAA=0.0000, delA=0.5626, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	4771	(A)₁₅=0.3278	delAA=0.0000, delA=0.6722, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	736	(A)₁₅=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	98	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Other	Sub	70	(A)₁₅=0.90	delAA=0.00, delA=0.10, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Asian	Sub	20	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(A)₁₅=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	4	(A)₁₅=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0
1000Genomes	Global	Study-wide	5008	(A)₁₅=0.6264	delA=0.3736
1000Genomes	African	Sub	1322	(A)₁₅=0.6989	delA=0.3011
1000Genomes	East Asian	Sub	1008	(A)₁₅=0.6359	delA=0.3641
1000Genomes	Europe	Sub	1006	(A)₁₅=0.5557	delA=0.4443
1000Genomes	South Asian	Sub	978	(A)₁₅=0.559	delA=0.441
1000Genomes	American	Sub	694	(A)₁₅=0.671	delA=0.329
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(A)₁₅=0.1866	delA=0.8134
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	(A)₁₅=0.1764	delA=0.8236
Northern Sweden	ACPOP	Study-wide	584	(A)₁₅=0.301	delA=0.699
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₅=0.35	delA=0.65

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.12355222_12355223del
GRCh38.p14 chr 18	NC_000018.10:g.12355223del
GRCh38.p14 chr 18	NC_000018.10:g.12355223dup
GRCh38.p14 chr 18	NC_000018.10:g.12355222_12355223dup
GRCh38.p14 chr 18	NC_000018.10:g.12355209_12355223A[17]CT[2]TACAATTAAACAAAAAAAAAAACCCAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 18	NC_000018.9:g.12355221_12355222del
GRCh37.p13 chr 18	NC_000018.9:g.12355222del
GRCh37.p13 chr 18	NC_000018.9:g.12355222dup
GRCh37.p13 chr 18	NC_000018.9:g.12355221_12355222dup
GRCh37.p13 chr 18	NC_000018.9:g.12355208_12355222A[17]CT[2]TACAATTAAACAAAAAAAAAAACCCAAAAAAAAAAAAAAAAAAAAAAAA[1]
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.27067_27068del
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.27068del
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.27068dup
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.27067_27068dup
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.27054_27068T[24]GGGTTTTTTTTTTTGTTTAATTGTAAGAGTTTTTTTTTTTTTTTTT[1]

Gene: AFG3L2, AFG3 like matrix AAA peptidase subunit 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
AFG3L2 transcript	NM_006796.3:c.1164+1484_1… NM_006796.3:c.1164+1484_1164+1485del	N/A	Intron Variant
AFG3L2 transcript variant X1	XM_011525601.4:c.1164+148… XM_011525601.4:c.1164+1484_1164+1485del	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)₁₅=	delAA	delA	dupA	dupAA	insAACTCTTACAATTAAAC(A)₁₁CCC(A)₂₄
GRCh38.p14 chr 18	NC_000018.10:g.12355209_12355223=	NC_000018.10:g.12355222_12355223del	NC_000018.10:g.12355223del	NC_000018.10:g.12355223dup	NC_000018.10:g.12355222_12355223dup	NC_000018.10:g.12355209_12355223A[17]CT[2]TACAATTAAACAAAAAAAAAAACCCAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 18	NC_000018.9:g.12355208_12355222=	NC_000018.9:g.12355221_12355222del	NC_000018.9:g.12355222del	NC_000018.9:g.12355222dup	NC_000018.9:g.12355221_12355222dup	NC_000018.9:g.12355208_12355222A[17]CT[2]TACAATTAAACAAAAAAAAAAACCCAAAAAAAAAAAAAAAAAAAAAAAA[1]
AFG3L2 RefSeqGene (LRG_666)	NG_023361.1:g.27054_27068=	NG_023361.1:g.27067_27068del	NG_023361.1:g.27068del	NG_023361.1:g.27068dup	NG_023361.1:g.27067_27068dup	NG_023361.1:g.27054_27068T[24]GGGTTTTTTTTTTTGTTTAATTGTAAGAGTTTTTTTTTTTTTTTTT[1]
AFG3L2 transcript	NM_006796.2:c.1164+1485=	NM_006796.2:c.1164+1484_1164+1485del	NM_006796.2:c.1164+1485del	NM_006796.2:c.1164+1485dup	NM_006796.2:c.1164+1484_1164+1485dup	NM_006796.2:c.1164+1485_1164+1486insTTTTTTTTTTTTTTTTTTTTTTTTGGGTTTTTTTTTTTGTTTAATTGTAAGAGTT
AFG3L2 transcript	NM_006796.3:c.1164+1485=	NM_006796.3:c.1164+1484_1164+1485del	NM_006796.3:c.1164+1485del	NM_006796.3:c.1164+1485dup	NM_006796.3:c.1164+1484_1164+1485dup	NM_006796.3:c.1164+1485_1164+1486insTTTTTTTTTTTTTTTTTTTTTTTTGGGTTTTTTTTTTTGTTTAATTGTAAGAGTT
AFG3L2 transcript variant X1	XM_011525601.4:c.1164+1485=	XM_011525601.4:c.1164+1484_1164+1485del	XM_011525601.4:c.1164+1485del	XM_011525601.4:c.1164+1485dup	XM_011525601.4:c.1164+1484_1164+1485dup	XM_011525601.4:c.1164+1485_1164+1486insTTTTTTTTTTTTTTTTTTTTTTTTGGGTTTTTTTTTTTGTTTAATTGTAAGAGTT

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

48 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss77920619	Sep 08, 2015 (146)
2	HGSV	ss77931727	Sep 08, 2015 (146)
3	HGSV	ss81944649	Sep 08, 2015 (146)
4	BL	ss256191947	May 09, 2011 (137)
5	GMI	ss289347987	May 04, 2012 (137)
6	SSMP	ss664384711	Apr 01, 2015 (144)
7	BILGI_BIOE	ss666705004	Apr 25, 2013 (138)
8	1000GENOMES	ss1377201836	Aug 21, 2014 (142)
9	EVA_GENOME_DK	ss1575118775	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1708911034	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1708911211	Apr 01, 2015 (144)
12	SYSTEMSBIOZJU	ss2629129314	Nov 08, 2017 (151)
13	SWEGEN	ss3016180178	Nov 08, 2017 (151)
14	MCHAISSO	ss3063884478	Nov 08, 2017 (151)
15	MCHAISSO	ss3064728942	Nov 08, 2017 (151)
16	MCHAISSO	ss3065672444	Nov 08, 2017 (151)
17	BIOINF_KMB_FNS_UNIBA	ss3645475998	Oct 12, 2018 (152)
18	URBANLAB	ss3650744252	Oct 12, 2018 (152)
19	EVA_DECODE	ss3701247714	Jul 13, 2019 (153)
20	EVA_DECODE	ss3701247715	Jul 13, 2019 (153)
21	ACPOP	ss3742366579	Jul 13, 2019 (153)
22	PACBIO	ss3788317570	Jul 13, 2019 (153)
23	PACBIO	ss3793257343	Jul 13, 2019 (153)
24	PACBIO	ss3798143571	Jul 13, 2019 (153)
25	KHV_HUMAN_GENOMES	ss3820403862	Jul 13, 2019 (153)
26	EVA	ss3835068639	Apr 27, 2020 (154)
27	EVA	ss3846648759	Apr 27, 2020 (154)
28	KOGIC	ss3979634782	Apr 27, 2020 (154)
29	KOGIC	ss3979634783	Apr 27, 2020 (154)
30	KOGIC	ss3979634784	Apr 27, 2020 (154)
31	GNOMAD	ss4318347731	Apr 26, 2021 (155)
32	GNOMAD	ss4318347732	Apr 26, 2021 (155)
33	GNOMAD	ss4318347733	Apr 26, 2021 (155)
34	GNOMAD	ss4318347734	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5224226400	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5224226401	Apr 26, 2021 (155)
37	1000G_HIGH_COVERAGE	ss5304522048	Oct 16, 2022 (156)
38	1000G_HIGH_COVERAGE	ss5304522049	Oct 16, 2022 (156)
39	1000G_HIGH_COVERAGE	ss5304522050	Oct 16, 2022 (156)
40	HUGCELL_USP	ss5497418179	Oct 16, 2022 (156)
41	HUGCELL_USP	ss5497418180	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5781013227	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5781013228	Oct 16, 2022 (156)
44	TOMMO_GENOMICS	ss5781013229	Oct 16, 2022 (156)
45	EVA	ss5827260397	Oct 16, 2022 (156)
46	EVA	ss5851971688	Oct 16, 2022 (156)
47	EVA	ss5873253426	Oct 16, 2022 (156)
48	EVA	ss5952279899	Oct 16, 2022 (156)
49	1000Genomes	NC_000018.9 - 12355208	Oct 12, 2018 (152)
50	The Avon Longitudinal Study of Parents and Children	NC_000018.9 - 12355208	Oct 12, 2018 (152)
51	The Danish reference pan genome	NC_000018.9 - 12355208	Apr 27, 2020 (154)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518381311 (NC_000018.10:12355208::A 323/127700) Row 518381312 (NC_000018.10:12355208::AA 1/127714) Row 518381313 (NC_000018.10:12355208::AAAAAAAAAAAAAAAAACTCTTACAATTAAACAAAAAAAAAAACCCAAAAAAAAA 1/127716)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518381311 (NC_000018.10:12355208::A 323/127700) Row 518381312 (NC_000018.10:12355208::AA 1/127714) Row 518381313 (NC_000018.10:12355208::AAAAAAAAAAAAAAAAACTCTTACAATTAAACAAAAAAAAAAACCCAAAAAAAAA 1/127716)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518381311 (NC_000018.10:12355208::A 323/127700) Row 518381312 (NC_000018.10:12355208::AA 1/127714) Row 518381313 (NC_000018.10:12355208::AAAAAAAAAAAAAAAAACTCTTACAATTAAACAAAAAAAAAAACCCAAAAAAAAA 1/127716)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518381311 (NC_000018.10:12355208::A 323/127700) Row 518381312 (NC_000018.10:12355208::AA 1/127714) Row 518381313 (NC_000018.10:12355208::AAAAAAAAAAAAAAAAACTCTTACAATTAAACAAAAAAAAAAACCCAAAAAAAAA 1/127716)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 518381311 (NC_000018.10:12355208::A 323/127700) Row 518381312 (NC_000018.10:12355208::AA 1/127714) Row 518381313 (NC_000018.10:12355208::AAAAAAAAAAAAAAAAACTCTTACAATTAAACAAAAAAAAAAACCCAAAAAAAAA 1/127716)...	-	Apr 26, 2021 (155)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 36012783 (NC_000018.10:12355209:A: 970/1830) Row 36012784 (NC_000018.10:12355208:AA: 26/1830) Row 36012785 (NC_000018.10:12355210::A 23/1830)	-	Apr 27, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 36012783 (NC_000018.10:12355209:A: 970/1830) Row 36012784 (NC_000018.10:12355208:AA: 26/1830) Row 36012785 (NC_000018.10:12355210::A 23/1830)	-	Apr 27, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 36012783 (NC_000018.10:12355209:A: 970/1830) Row 36012784 (NC_000018.10:12355208:AA: 26/1830) Row 36012785 (NC_000018.10:12355210::A 23/1830)	-	Apr 27, 2020 (154)
60	Northern Sweden	NC_000018.9 - 12355208	Jul 13, 2019 (153)
61	8.3KJPN Submission ignored due to conflicting rows: Row 82195707 (NC_000018.9:12355207:A: 9578/16756) Row 82195708 (NC_000018.9:12355207::A 27/16756)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 82195707 (NC_000018.9:12355207:A: 9578/16756) Row 82195708 (NC_000018.9:12355207::A 27/16756)	-	Apr 26, 2021 (155)
63	14KJPN Submission ignored due to conflicting rows: Row 114850331 (NC_000018.10:12355208:A: 15082/27724) Row 114850332 (NC_000018.10:12355208:AA: 22/27724) Row 114850333 (NC_000018.10:12355208::A 35/27724)	-	Oct 16, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 114850331 (NC_000018.10:12355208:A: 15082/27724) Row 114850332 (NC_000018.10:12355208:AA: 22/27724) Row 114850333 (NC_000018.10:12355208::A 35/27724)	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 114850331 (NC_000018.10:12355208:A: 15082/27724) Row 114850332 (NC_000018.10:12355208:AA: 22/27724) Row 114850333 (NC_000018.10:12355208::A 35/27724)	-	Oct 16, 2022 (156)
66	UK 10K study - Twins	NC_000018.9 - 12355208	Oct 12, 2018 (152)
67	ALFA	NC_000018.10 - 12355209	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)
rs56272731	May 11, 2012 (137)
rs59502093	May 25, 2008 (130)
rs139562626	May 11, 2012 (137)
rs374876816	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3701247715, ss3979634783, ss4318347734, ss5304522050, ss5781013228	NC_000018.10:12355208:AA:	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
169170512	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss256191947, ss289347987	NC_000018.8:12345207:A:	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss77920619, ss77931727, ss81944649	NC_000018.8:12345221:A:	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
73486546, 40719571, 585939, 15651444, 40719571, ss664384711, ss666705004, ss1377201836, ss1575118775, ss1708911034, ss1708911211, ss2629129314, ss3016180178, ss3742366579, ss3788317570, ss3793257343, ss3798143571, ss3835068639, ss5224226400, ss5827260397, ss5952279899	NC_000018.9:12355207:A:	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3063884478, ss3064728942, ss3065672444, ss3645475998, ss3650744252, ss3820403862, ss3846648759, ss4318347733, ss5304522048, ss5497418179, ss5781013227, ss5851971688, ss5873253426	NC_000018.10:12355208:A:	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
169170512	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3701247714, ss3979634782	NC_000018.10:12355209:A:	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss5224226401	NC_000018.9:12355207::A	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4318347731, ss5304522049, ss5497418180, ss5781013229	NC_000018.10:12355208::A	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
169170512	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3979634784	NC_000018.10:12355210::A	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4318347732	NC_000018.10:12355208::AA	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
169170512	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
	NC_000018.10:12355208::AAAAAAAAAAA… NC_000018.10:12355208::AAAAAAAAAAAAAAAAACTCTTACAATTAAACAAAAAAAAAAACCCAAAAAAAAA	NC_000018.10:12355208:AAAAAAAAAAAA… NC_000018.10:12355208:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAACTCTTACAATTAAACAAAAAAAAAAACCCAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs11303145

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

rs11303145