Name: rs150142146
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.

rs150142146

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:196062218-196062231 (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: delAAA / delAA / delA / dupA / dup…
delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₆ / dup(A)₈
Variation Type: Indel Insertion and Deletion
Frequency: delA=0.1263 (1244/9853, ALFA)
delA=0.337 (198/588, NorthernSweden)
delA=0.38 (15/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TFRC : 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	9853	AAAAAAAAAAAAAA=0.8731	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.1263, AAAAAAAAAAAAAAA=0.0006, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.786979	0.039878	0.173143	32
European	Sub	7384	AAAAAAAAAAAAAA=0.8310	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.1682, AAAAAAAAAAAAAAA=0.0008, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	0.71611	0.053246	0.230644	32
African	Sub	1738	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	72	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	1666	AAAAAAAAAAAAAA=1.0000	AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	102	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	80	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	64	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	290	AAAAAAAAAAAAAA=1.000	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	50	AAAAAAAAAAAAAA=1.00	AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	225	AAAAAAAAAAAAAA=0.991	AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.009, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000	0.982143	0.0	0.017857	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	9853	(A)₁₄=0.8731	delAAA=0.0000, delAA=0.0000, delA=0.1263, dupA=0.0006, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	7384	(A)₁₄=0.8310	delAAA=0.0000, delAA=0.0000, delA=0.1682, dupA=0.0008, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	1738	(A)₁₄=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	290	(A)₁₄=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	225	(A)₁₄=0.991	delAAA=0.000, delAA=0.000, delA=0.009, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Asian	Sub	102	(A)₁₄=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	64	(A)₁₄=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(A)₁₄=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Northern Sweden	ACPOP	Study-wide	588	(A)₁₄=0.663	delA=0.337
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₄=0.62	delA=0.38

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.196062229_196062231del
GRCh38.p14 chr 3	NC_000003.12:g.196062230_196062231del
GRCh38.p14 chr 3	NC_000003.12:g.196062231del
GRCh38.p14 chr 3	NC_000003.12:g.196062231dup
GRCh38.p14 chr 3	NC_000003.12:g.196062230_196062231dup
GRCh38.p14 chr 3	NC_000003.12:g.196062229_196062231dup
GRCh38.p14 chr 3	NC_000003.12:g.196062226_196062231dup
GRCh38.p14 chr 3	NC_000003.12:g.196062224_196062231dup
GRCh37.p13 chr 3	NC_000003.11:g.195789100_195789102del
GRCh37.p13 chr 3	NC_000003.11:g.195789101_195789102del
GRCh37.p13 chr 3	NC_000003.11:g.195789102del
GRCh37.p13 chr 3	NC_000003.11:g.195789102dup
GRCh37.p13 chr 3	NC_000003.11:g.195789101_195789102dup
GRCh37.p13 chr 3	NC_000003.11:g.195789100_195789102dup
GRCh37.p13 chr 3	NC_000003.11:g.195789097_195789102dup
GRCh37.p13 chr 3	NC_000003.11:g.195789095_195789102dup
TFRC RefSeqGene	NG_046395.1:g.24942_24944del
TFRC RefSeqGene	NG_046395.1:g.24943_24944del
TFRC RefSeqGene	NG_046395.1:g.24944del
TFRC RefSeqGene	NG_046395.1:g.24944dup
TFRC RefSeqGene	NG_046395.1:g.24943_24944dup
TFRC RefSeqGene	NG_046395.1:g.24942_24944dup
TFRC RefSeqGene	NG_046395.1:g.24939_24944dup
TFRC RefSeqGene	NG_046395.1:g.24937_24944dup

Gene: TFRC, transferrin receptor (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TFRC transcript variant 2	NM_001128148.3:c.1468+362… NM_001128148.3:c.1468+362_1468+364del	N/A	Intron Variant
TFRC transcript variant 3	NM_001313965.2:c.1225+362… NM_001313965.2:c.1225+362_1225+364del	N/A	Intron Variant
TFRC transcript variant 4	NM_001313966.2:c.622+362_… NM_001313966.2:c.622+362_622+364del	N/A	Intron Variant
TFRC transcript variant 1	NM_003234.4:c.1468+362_14… NM_003234.4:c.1468+362_1468+364del	N/A	Intron Variant
TFRC transcript variant X1	XM_047448786.1:c.622+362_… XM_047448786.1:c.622+362_622+364del	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)₁₄=	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₆	dup(A)₈
GRCh38.p14 chr 3	NC_000003.12:g.196062218_196062231=	NC_000003.12:g.196062229_196062231del	NC_000003.12:g.196062230_196062231del	NC_000003.12:g.196062231del	NC_000003.12:g.196062231dup	NC_000003.12:g.196062230_196062231dup	NC_000003.12:g.196062229_196062231dup	NC_000003.12:g.196062226_196062231dup	NC_000003.12:g.196062224_196062231dup
GRCh37.p13 chr 3	NC_000003.11:g.195789089_195789102=	NC_000003.11:g.195789100_195789102del	NC_000003.11:g.195789101_195789102del	NC_000003.11:g.195789102del	NC_000003.11:g.195789102dup	NC_000003.11:g.195789101_195789102dup	NC_000003.11:g.195789100_195789102dup	NC_000003.11:g.195789097_195789102dup	NC_000003.11:g.195789095_195789102dup
TFRC RefSeqGene	NG_046395.1:g.24931_24944=	NG_046395.1:g.24942_24944del	NG_046395.1:g.24943_24944del	NG_046395.1:g.24944del	NG_046395.1:g.24944dup	NG_046395.1:g.24943_24944dup	NG_046395.1:g.24942_24944dup	NG_046395.1:g.24939_24944dup	NG_046395.1:g.24937_24944dup
TFRC transcript variant 2	NM_001128148.1:c.1468+364=	NM_001128148.1:c.1468+362_1468+364del	NM_001128148.1:c.1468+363_1468+364del	NM_001128148.1:c.1468+364del	NM_001128148.1:c.1468+364dup	NM_001128148.1:c.1468+363_1468+364dup	NM_001128148.1:c.1468+362_1468+364dup	NM_001128148.1:c.1468+359_1468+364dup	NM_001128148.1:c.1468+357_1468+364dup
TFRC transcript variant 2	NM_001128148.3:c.1468+364=	NM_001128148.3:c.1468+362_1468+364del	NM_001128148.3:c.1468+363_1468+364del	NM_001128148.3:c.1468+364del	NM_001128148.3:c.1468+364dup	NM_001128148.3:c.1468+363_1468+364dup	NM_001128148.3:c.1468+362_1468+364dup	NM_001128148.3:c.1468+359_1468+364dup	NM_001128148.3:c.1468+357_1468+364dup
TFRC transcript variant 3	NM_001313965.2:c.1225+364=	NM_001313965.2:c.1225+362_1225+364del	NM_001313965.2:c.1225+363_1225+364del	NM_001313965.2:c.1225+364del	NM_001313965.2:c.1225+364dup	NM_001313965.2:c.1225+363_1225+364dup	NM_001313965.2:c.1225+362_1225+364dup	NM_001313965.2:c.1225+359_1225+364dup	NM_001313965.2:c.1225+357_1225+364dup
TFRC transcript variant 4	NM_001313966.2:c.622+364=	NM_001313966.2:c.622+362_622+364del	NM_001313966.2:c.622+363_622+364del	NM_001313966.2:c.622+364del	NM_001313966.2:c.622+364dup	NM_001313966.2:c.622+363_622+364dup	NM_001313966.2:c.622+362_622+364dup	NM_001313966.2:c.622+359_622+364dup	NM_001313966.2:c.622+357_622+364dup
TFRC transcript variant 1	NM_003234.2:c.1468+364=	NM_003234.2:c.1468+362_1468+364del	NM_003234.2:c.1468+363_1468+364del	NM_003234.2:c.1468+364del	NM_003234.2:c.1468+364dup	NM_003234.2:c.1468+363_1468+364dup	NM_003234.2:c.1468+362_1468+364dup	NM_003234.2:c.1468+359_1468+364dup	NM_003234.2:c.1468+357_1468+364dup
TFRC transcript variant 1	NM_003234.4:c.1468+364=	NM_003234.4:c.1468+362_1468+364del	NM_003234.4:c.1468+363_1468+364del	NM_003234.4:c.1468+364del	NM_003234.4:c.1468+364dup	NM_003234.4:c.1468+363_1468+364dup	NM_003234.4:c.1468+362_1468+364dup	NM_003234.4:c.1468+359_1468+364dup	NM_003234.4:c.1468+357_1468+364dup
TFRC transcript variant X1	XM_047448786.1:c.622+364=	XM_047448786.1:c.622+362_622+364del	XM_047448786.1:c.622+363_622+364del	XM_047448786.1:c.622+364del	XM_047448786.1:c.622+364dup	XM_047448786.1:c.622+363_622+364dup	XM_047448786.1:c.622+362_622+364dup	XM_047448786.1:c.622+359_622+364dup	XM_047448786.1:c.622+357_622+364dup

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#.

35 SubSNP, 12 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193717124	Oct 12, 2018 (152)
2	GMI	ss287741050	May 09, 2011 (134)
3	GMI	ss288471546	May 04, 2012 (137)
4	BILGI_BIOE	ss666242236	Apr 25, 2013 (138)
5	EVA_GENOME_DK	ss1576137079	Apr 01, 2015 (144)
6	HAMMER_LAB	ss1800744530	Sep 08, 2015 (146)
7	SWEGEN	ss2993934162	Nov 08, 2017 (151)
8	MCHAISSO	ss3064948869	Nov 08, 2017 (151)
9	EVA_DECODE	ss3711175176	Jul 13, 2019 (153)
10	EVA_DECODE	ss3711175177	Jul 13, 2019 (153)
11	EVA_DECODE	ss3711175178	Jul 13, 2019 (153)
12	EVA_DECODE	ss3711175179	Jul 13, 2019 (153)
13	EVA_DECODE	ss3711175180	Jul 13, 2019 (153)
14	ACPOP	ss3730750728	Jul 13, 2019 (153)
15	PACBIO	ss3784586986	Jul 13, 2019 (153)
16	EVA	ss3828311716	Apr 25, 2020 (154)
17	EVA	ss3837587598	Apr 25, 2020 (154)
18	EVA	ss3843020804	Apr 25, 2020 (154)
19	GNOMAD	ss4088705919	Apr 26, 2021 (155)
20	GNOMAD	ss4088705920	Apr 26, 2021 (155)
21	GNOMAD	ss4088705921	Apr 26, 2021 (155)
22	GNOMAD	ss4088705922	Apr 26, 2021 (155)
23	GNOMAD	ss4088705923	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5163653481	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5163653482	Apr 26, 2021 (155)
26	1000G_HIGH_COVERAGE	ss5257626038	Oct 13, 2022 (156)
27	1000G_HIGH_COVERAGE	ss5257626039	Oct 13, 2022 (156)
28	HUGCELL_USP	ss5456603328	Oct 13, 2022 (156)
29	HUGCELL_USP	ss5456603329	Oct 13, 2022 (156)
30	HUGCELL_USP	ss5456603330	Oct 13, 2022 (156)
31	TOMMO_GENOMICS	ss5697139807	Oct 13, 2022 (156)
32	TOMMO_GENOMICS	ss5697139808	Oct 13, 2022 (156)
33	YY_MCH	ss5804648361	Oct 13, 2022 (156)
34	EVA	ss5827101799	Oct 13, 2022 (156)
35	EVA	ss5854034886	Oct 13, 2022 (156)
36	The Danish reference pan genome	NC_000003.11 - 195789089	Apr 25, 2020 (154)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137028545 (NC_000003.12:196062217::A 416/124618) Row 137028546 (NC_000003.12:196062217::AA 1/124684) Row 137028547 (NC_000003.12:196062217::AAAAAA 1/124686)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137028545 (NC_000003.12:196062217::A 416/124618) Row 137028546 (NC_000003.12:196062217::AA 1/124684) Row 137028547 (NC_000003.12:196062217::AAAAAA 1/124686)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137028545 (NC_000003.12:196062217::A 416/124618) Row 137028546 (NC_000003.12:196062217::AA 1/124684) Row 137028547 (NC_000003.12:196062217::AAAAAA 1/124686)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137028545 (NC_000003.12:196062217::A 416/124618) Row 137028546 (NC_000003.12:196062217::AA 1/124684) Row 137028547 (NC_000003.12:196062217::AAAAAA 1/124686)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 137028545 (NC_000003.12:196062217::A 416/124618) Row 137028546 (NC_000003.12:196062217::AA 1/124684) Row 137028547 (NC_000003.12:196062217::AAAAAA 1/124686)...	-	Apr 26, 2021 (155)
42	Northern Sweden	NC_000003.11 - 195789089	Jul 13, 2019 (153)
43	8.3KJPN Submission ignored due to conflicting rows: Row 21622788 (NC_000003.11:195789088:A: 1520/16758) Row 21622789 (NC_000003.11:195789088::A 10/16758)	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 21622788 (NC_000003.11:195789088:A: 1520/16758) Row 21622789 (NC_000003.11:195789088::A 10/16758)	-	Apr 26, 2021 (155)
45	14KJPN Submission ignored due to conflicting rows: Row 30976911 (NC_000003.12:196062217:A: 2569/28258) Row 30976912 (NC_000003.12:196062217::A 14/28258)	-	Oct 13, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 30976911 (NC_000003.12:196062217:A: 2569/28258) Row 30976912 (NC_000003.12:196062217::A 14/28258)	-	Oct 13, 2022 (156)
47	ALFA	NC_000003.12 - 196062218	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
ss3711175180	NC_000003.12:196062217:AAA:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
5923057551	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4088705923, ss5456603330	NC_000003.12:196062217:AA:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
5923057551	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss3711175179	NC_000003.12:196062218:AA:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss288471546	NC_000003.10:197273485:A:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
884925, 4035593, ss666242236, ss1576137079, ss1800744530, ss2993934162, ss3730750728, ss3784586986, ss3828311716, ss3837587598, ss5163653481, ss5827101799	NC_000003.11:195789088:A:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3064948869, ss3843020804, ss4088705922, ss5257626038, ss5456603328, ss5697139807, ss5804648361, ss5854034886	NC_000003.12:196062217:A:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
5923057551	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss3711175178	NC_000003.12:196062219:A:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss287741050	NT_029928.13:1741837:A:	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5163653482	NC_000003.11:195789088::A	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4088705919, ss5257626039, ss5456603329, ss5697139808	NC_000003.12:196062217::A	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5923057551	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3711175177	NC_000003.12:196062220::A	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss193717124	NT_005612.17:102356643::A	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4088705920	NC_000003.12:196062217::AA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5923057551	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5923057551	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4088705921	NC_000003.12:196062217::AAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3711175176	NC_000003.12:196062220::AAAAAAAA	NC_000003.12:196062217:AAAAAAAAAAA… NC_000003.12:196062217:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(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 rs150142146

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

rs150142146