Name: rs1432072038
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.

rs1432072038

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:149084343-149084351 (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: delTATA / delTA / dupTA
Variation Type: Indel Insertion and Deletion
Frequency: delTATA=0.000004 (1/264690, TOPMED)
delTA=0.00004 (1/28240, 14KJPN)
delTATA=0.00022 (4/18518, ALFA) (+ 1 more)
dupTA=0.0005 (3/6404, 1000G_30x)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NBPF8 : Intron Variant
NBPF9 : Intron Variant
PFN1P2 : 2KB Upstream 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	HTRZ	HWEP
Total	Global	14048	ATATATATA=0.99993	ATATA=0.00000, ATATATA=0.00007, ATATATATATA=0.00000	0.999858	0.000142	0
European	Sub	9690	ATATATATA=1.0000	ATATA=0.0000, ATATATA=0.0000, ATATATATATA=0.0000	1.0	0.0	N/A
African	Sub	2896	ATATATATA=1.0000	ATATA=0.0000, ATATATA=0.0000, ATATATATATA=0.0000	1.0	0.0	N/A
African Others	Sub	114	ATATATATA=1.000	ATATA=0.000, ATATATA=0.000, ATATATATATA=0.000	1.0	0.0	N/A
African American	Sub	2782	ATATATATA=1.0000	ATATA=0.0000, ATATATA=0.0000, ATATATATATA=0.0000	1.0	0.0	N/A
Asian	Sub	112	ATATATATA=1.000	ATATA=0.000, ATATATA=0.000, ATATATATATA=0.000	1.0	0.0	N/A
East Asian	Sub	86	ATATATATA=1.00	ATATA=0.00, ATATATA=0.00, ATATATATATA=0.00	1.0	0.0	N/A
Other Asian	Sub	26	ATATATATA=1.00	ATATA=0.00, ATATATA=0.00, ATATATATATA=0.00	1.0	0.0	N/A
Latin American 1	Sub	146	ATATATATA=1.000	ATATA=0.000, ATATATA=0.000, ATATATATATA=0.000	1.0	0.0	N/A
Latin American 2	Sub	610	ATATATATA=1.000	ATATA=0.000, ATATATA=0.000, ATATATATATA=0.000	1.0	0.0	N/A
South Asian	Sub	98	ATATATATA=1.00	ATATA=0.00, ATATATA=0.00, ATATATATATA=0.00	1.0	0.0	N/A
Other	Sub	496	ATATATATA=0.998	ATATA=0.000, ATATATA=0.002, ATATATATATA=0.000	0.995968	0.004032	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
TopMed	Global	Study-wide	264690	(AT)₄A=0.999996	delTATA=0.000004
14KJPN	JAPANESE	Study-wide	28240	(AT)₄A=0.99996	delTA=0.00004
Allele Frequency Aggregator	Total	Global	18518	(AT)₄A=0.99973	delTATA=0.00022, delTA=0.00005, dupTA=0.00000
Allele Frequency Aggregator	European	Sub	14152	(AT)₄A=0.99972	delTATA=0.00028, delTA=0.00000, dupTA=0.00000
Allele Frequency Aggregator	African	Sub	2896	(AT)₄A=1.0000	delTATA=0.0000, delTA=0.0000, dupTA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	(AT)₄A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000
Allele Frequency Aggregator	Other	Sub	504	(AT)₄A=0.998	delTATA=0.000, delTA=0.002, dupTA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(AT)₄A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000
Allele Frequency Aggregator	Asian	Sub	112	(AT)₄A=1.000	delTATA=0.000, delTA=0.000, dupTA=0.000
Allele Frequency Aggregator	South Asian	Sub	98	(AT)₄A=1.00	delTATA=0.00, delTA=0.00, dupTA=0.00
1000Genomes_30x	Global	Study-wide	6404	- No frequency provided	dupTA=0.0005
1000Genomes_30x	African	Sub	1786	- No frequency provided	dupTA=0.0000
1000Genomes_30x	Europe	Sub	1266	- No frequency provided	dupTA=0.0000
1000Genomes_30x	South Asian	Sub	1202	- No frequency provided	dupTA=0.0000
1000Genomes_30x	East Asian	Sub	1170	- No frequency provided	dupTA=0.0000
1000Genomes_30x	American	Sub	980	- No frequency provided	dupTA=0.003

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 1	NC_000001.11:g.149084344TA[2]
GRCh38.p14 chr 1	NC_000001.11:g.149084344TA[3]
GRCh38.p14 chr 1	NC_000001.11:g.149084344TA[5]
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.5899757TA[2]
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.5899757TA[3]
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.5899757TA[5]
GRCh37.p13 chr 1	NC_000001.10:g.144612929AT[2]
GRCh37.p13 chr 1	NC_000001.10:g.144612929AT[3]
GRCh37.p13 chr 1	NC_000001.10:g.144612929AT[5]
GRCh38.p14 chr 1 novel patch HSCHR1_12_CTG3	NW_025791753.1:g.51655AT[2]
GRCh38.p14 chr 1 novel patch HSCHR1_12_CTG3	NW_025791753.1:g.51655AT[3]
GRCh38.p14 chr 1 novel patch HSCHR1_12_CTG3	NW_025791753.1:g.51655AT[5]

Gene: NBPF9, NBPF member 9 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NBPF9 transcript variant 2	NM_001037675.4:c.-194-192… NM_001037675.4:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 1	NM_001277444.2:c.-194-192… NM_001277444.2:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 3	NM_001388366.1:c.-194-192… NM_001388366.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 4	NM_001388367.1:c.-194-192… NM_001388367.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 5	NM_001388368.1:c.-194-192… NM_001388368.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 6	NM_001388369.1:c.-194-192… NM_001388369.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 7	NM_001388370.1:c.-194-192… NM_001388370.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 8	NM_001388371.1:c.-194-192… NM_001388371.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 9	NM_001388372.1:c.-194-192… NM_001388372.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 10	NM_001388373.1:c.-194-192… NM_001388373.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 11	NM_001388374.1:c.-194-192… NM_001388374.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 12	NM_001388375.1:c.-194-192… NM_001388375.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 13	NM_001388376.1:c.-195+330… NM_001388376.1:c.-195+330AT[2]	N/A	Intron Variant
NBPF9 transcript variant 14	NM_001388377.1:c.-194-192… NM_001388377.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 15	NM_001388378.1:c.-194-192… NM_001388378.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 16	NM_001388379.1:c.-194-192… NM_001388379.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 17	NM_001388381.1:c.-194-192… NM_001388381.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 18	NM_001388382.1:c.-194-192… NM_001388382.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 19	NM_001388383.1:c.-194-192… NM_001388383.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant 20	NM_001388384.1:c.-194-192… NM_001388384.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant X1	XM_047420572.1:c.-195+330… XM_047420572.1:c.-195+330AT[2]	N/A	Intron Variant
NBPF9 transcript variant X3	XM_047420578.1:c.-194-192… XM_047420578.1:c.-194-1920AT[2]	N/A	Intron Variant
NBPF9 transcript variant X2	XR_007060075.1: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	(AT)₄A=	delTATA	delTA	dupTA
GRCh38.p14 chr 1	NC_000001.11:g.149084343_149084351=	NC_000001.11:g.149084344TA[2]	NC_000001.11:g.149084344TA[3]	NC_000001.11:g.149084344TA[5]
GRCh37.p13 chr 1 fix patch HG1287_PATCH	NW_003871055.3:g.5899756_5899764=	NW_003871055.3:g.5899757TA[2]	NW_003871055.3:g.5899757TA[3]	NW_003871055.3:g.5899757TA[5]
GRCh37.p13 chr 1	NC_000001.10:g.144612928_144612936=	NC_000001.10:g.144612929AT[2]	NC_000001.10:g.144612929AT[3]	NC_000001.10:g.144612929AT[5]
GRCh38.p14 chr 1 novel patch HSCHR1_12_CTG3	NW_025791753.1:g.51654_51662=	NW_025791753.1:g.51655AT[2]	NW_025791753.1:g.51655AT[3]	NW_025791753.1:g.51655AT[5]
NBPF8 transcript variant 1	NM_001037501.5:c.-291-1912=	NM_001037501.5:c.-291-1912TA[2]	NM_001037501.5:c.-291-1912TA[3]	NM_001037501.5:c.-291-1912TA[5]
NBPF9 transcript variant 2	NM_001037675.4:c.-194-1913=	NM_001037675.4:c.-194-1920AT[2]	NM_001037675.4:c.-194-1920AT[3]	NM_001037675.4:c.-194-1920AT[5]
NBPF9 transcript variant 1	NM_001277444.2:c.-194-1913=	NM_001277444.2:c.-194-1920AT[2]	NM_001277444.2:c.-194-1920AT[3]	NM_001277444.2:c.-194-1920AT[5]
NBPF9 transcript variant 3	NM_001388366.1:c.-194-1913=	NM_001388366.1:c.-194-1920AT[2]	NM_001388366.1:c.-194-1920AT[3]	NM_001388366.1:c.-194-1920AT[5]
NBPF9 transcript variant 4	NM_001388367.1:c.-194-1913=	NM_001388367.1:c.-194-1920AT[2]	NM_001388367.1:c.-194-1920AT[3]	NM_001388367.1:c.-194-1920AT[5]
NBPF9 transcript variant 5	NM_001388368.1:c.-194-1913=	NM_001388368.1:c.-194-1920AT[2]	NM_001388368.1:c.-194-1920AT[3]	NM_001388368.1:c.-194-1920AT[5]
NBPF9 transcript variant 6	NM_001388369.1:c.-194-1913=	NM_001388369.1:c.-194-1920AT[2]	NM_001388369.1:c.-194-1920AT[3]	NM_001388369.1:c.-194-1920AT[5]
NBPF9 transcript variant 7	NM_001388370.1:c.-194-1913=	NM_001388370.1:c.-194-1920AT[2]	NM_001388370.1:c.-194-1920AT[3]	NM_001388370.1:c.-194-1920AT[5]
NBPF9 transcript variant 8	NM_001388371.1:c.-194-1913=	NM_001388371.1:c.-194-1920AT[2]	NM_001388371.1:c.-194-1920AT[3]	NM_001388371.1:c.-194-1920AT[5]
NBPF9 transcript variant 9	NM_001388372.1:c.-194-1913=	NM_001388372.1:c.-194-1920AT[2]	NM_001388372.1:c.-194-1920AT[3]	NM_001388372.1:c.-194-1920AT[5]
NBPF9 transcript variant 10	NM_001388373.1:c.-194-1913=	NM_001388373.1:c.-194-1920AT[2]	NM_001388373.1:c.-194-1920AT[3]	NM_001388373.1:c.-194-1920AT[5]
NBPF9 transcript variant 11	NM_001388374.1:c.-194-1913=	NM_001388374.1:c.-194-1920AT[2]	NM_001388374.1:c.-194-1920AT[3]	NM_001388374.1:c.-194-1920AT[5]
NBPF9 transcript variant 12	NM_001388375.1:c.-194-1913=	NM_001388375.1:c.-194-1920AT[2]	NM_001388375.1:c.-194-1920AT[3]	NM_001388375.1:c.-194-1920AT[5]
NBPF9 transcript variant 13	NM_001388376.1:c.-195+337=	NM_001388376.1:c.-195+330AT[2]	NM_001388376.1:c.-195+330AT[3]	NM_001388376.1:c.-195+330AT[5]
NBPF9 transcript variant 14	NM_001388377.1:c.-194-1913=	NM_001388377.1:c.-194-1920AT[2]	NM_001388377.1:c.-194-1920AT[3]	NM_001388377.1:c.-194-1920AT[5]
NBPF9 transcript variant 15	NM_001388378.1:c.-194-1913=	NM_001388378.1:c.-194-1920AT[2]	NM_001388378.1:c.-194-1920AT[3]	NM_001388378.1:c.-194-1920AT[5]
NBPF9 transcript variant 16	NM_001388379.1:c.-194-1913=	NM_001388379.1:c.-194-1920AT[2]	NM_001388379.1:c.-194-1920AT[3]	NM_001388379.1:c.-194-1920AT[5]
NBPF9 transcript variant 17	NM_001388381.1:c.-194-1913=	NM_001388381.1:c.-194-1920AT[2]	NM_001388381.1:c.-194-1920AT[3]	NM_001388381.1:c.-194-1920AT[5]
NBPF9 transcript variant 18	NM_001388382.1:c.-194-1913=	NM_001388382.1:c.-194-1920AT[2]	NM_001388382.1:c.-194-1920AT[3]	NM_001388382.1:c.-194-1920AT[5]
NBPF9 transcript variant 19	NM_001388383.1:c.-194-1913=	NM_001388383.1:c.-194-1920AT[2]	NM_001388383.1:c.-194-1920AT[3]	NM_001388383.1:c.-194-1920AT[5]
NBPF9 transcript variant 20	NM_001388384.1:c.-194-1913=	NM_001388384.1:c.-194-1920AT[2]	NM_001388384.1:c.-194-1920AT[3]	NM_001388384.1:c.-194-1920AT[5]
LOC101929455 transcript variant X1	XM_005272508.1:c.386-2168=	XM_005272508.1:c.386-2168TA[2]	XM_005272508.1:c.386-2168TA[3]	XM_005272508.1:c.386-2168TA[5]
LOC101929455 transcript variant X2	XM_005272509.1:c.386-2168=	XM_005272509.1:c.386-2168TA[2]	XM_005272509.1:c.386-2168TA[3]	XM_005272509.1:c.386-2168TA[5]
LOC101929455 transcript variant X3	XM_005272510.1:c.386-2168=	XM_005272510.1:c.386-2168TA[2]	XM_005272510.1:c.386-2168TA[3]	XM_005272510.1:c.386-2168TA[5]
LOC101929455 transcript variant X4	XM_005272511.1:c.128-2168=	XM_005272511.1:c.128-2168TA[2]	XM_005272511.1:c.128-2168TA[3]	XM_005272511.1:c.128-2168TA[5]
LOC101929455 transcript variant X5	XM_005272512.1:c.-194-1912=	XM_005272512.1:c.-194-1912TA[2]	XM_005272512.1:c.-194-1912TA[3]	XM_005272512.1:c.-194-1912TA[5]
LOC101929455 transcript variant X6	XM_005272513.1:c.-189-1912=	XM_005272513.1:c.-189-1912TA[2]	XM_005272513.1:c.-189-1912TA[3]	XM_005272513.1:c.-189-1912TA[5]
NBPF9 transcript variant X1	XM_005277393.1:c.-189-1913=	XM_005277393.1:c.-189-1920AT[2]	XM_005277393.1:c.-189-1920AT[3]	XM_005277393.1:c.-189-1920AT[5]
NBPF9 transcript variant X1	XM_047420572.1:c.-195+337=	XM_047420572.1:c.-195+330AT[2]	XM_047420572.1:c.-195+330AT[3]	XM_047420572.1:c.-195+330AT[5]
NBPF9 transcript variant X3	XM_047420578.1:c.-194-1913=	XM_047420578.1:c.-194-1920AT[2]	XM_047420578.1:c.-194-1920AT[3]	XM_047420578.1:c.-194-1920AT[5]

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#.

9 SubSNP, 7 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	GNOMAD	ss4003004185	Apr 27, 2021 (155)
2	GNOMAD	ss4003004187	Apr 27, 2021 (155)
3	GNOMAD	ss4003004188	Apr 27, 2021 (155)
4	TOPMED	ss4467066064	Apr 27, 2021 (155)
5	1000G_HIGH_COVERAGE	ss5244167003	Oct 12, 2022 (156)
6	HUGCELL_USP	ss5444787719	Oct 12, 2022 (156)
7	1000G_HIGH_COVERAGE	ss5517433420	Oct 12, 2022 (156)
8	TOMMO_GENOMICS	ss5673438789	Oct 12, 2022 (156)
9	YY_MCH	ss5801230726	Oct 12, 2022 (156)
10	1000Genomes_30x	NC_000001.11 - 149084343	Oct 12, 2022 (156)
11	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25984895 (NC_000001.11:149084342::AT 36/135880) Row 25984897 (NC_000001.11:149084342:AT: 5/135880) Row 25984898 (NC_000001.11:149084342:ATAT: 0/135880)	-	Apr 27, 2021 (155)
12	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25984895 (NC_000001.11:149084342::AT 36/135880) Row 25984897 (NC_000001.11:149084342:AT: 5/135880) Row 25984898 (NC_000001.11:149084342:ATAT: 0/135880)	-	Apr 27, 2021 (155)
13	gnomAD - Genomes Submission ignored due to conflicting rows: Row 25984895 (NC_000001.11:149084342::AT 36/135880) Row 25984897 (NC_000001.11:149084342:AT: 5/135880) Row 25984898 (NC_000001.11:149084342:ATAT: 0/135880)	-	Apr 27, 2021 (155)
14	14KJPN	NC_000001.11 - 149084343	Oct 12, 2022 (156)
15	TopMed	NC_000001.11 - 149084343	Apr 27, 2021 (155)
16	ALFA	NC_000001.11 - 149084343	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
30672399, ss4003004188, ss4467066064, ss5801230726	NC_000001.11:149084342:ATAT:	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATA	(self)
13776404022	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATA	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATA	(self)
7275893, ss4003004187, ss5673438789	NC_000001.11:149084342:AT:	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATATA	(self)
13776404022	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATATA	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATATA	(self)
4959355, ss4003004185, ss5244167003, ss5444787719, ss5517433420	NC_000001.11:149084342::AT	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATATATATA	(self)
13776404022	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATATATATA	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATATATATA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
4099592, ss5146130285	NC_000001.10:144612927:TA:	NC_000001.11:149084342:ATATATATA:A… NC_000001.11:149084342:ATATATATA:ATATATA	rs1661005216

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

No publications for rs1432072038

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
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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

rs1432072038