Name: rs1398685096
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.

rs1398685096

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:74781245-74781265 (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 / dupA…
delAA / delA / dupA / dupAA / dupAAA / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: delAA=0.0000 (0/1182, ALFA)
delA=0.0000 (0/1182, ALFA)
dupA=0.0000 (0/1182, ALFA) (+ 3 more)
dupAA=0.0000 (0/1182, ALFA)
dupAAA=0.0000 (0/1182, ALFA)
dup(A)₅=0.0000 (0/1182, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NCF1 : 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	1182	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	928	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	170	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	14	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	156	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	8	AAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	32	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	28	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	1182	(A)₂₁=1.0000	delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	928	(A)₂₁=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	African	Sub	170	(A)₂₁=1.000	delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	32	(A)₂₁=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Other	Sub	28	(A)₂₁=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₂₁=1.00	delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Latin American 1	Sub	8	(A)₂₁=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₅=0.0
Allele Frequency Aggregator	Asian	Sub	2	(A)₂₁=1.0	delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dupAAA=0.0, dup(A)₅=0.0

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 7	NC_000007.14:g.74781264_74781265del
GRCh38.p14 chr 7	NC_000007.14:g.74781265del
GRCh38.p14 chr 7	NC_000007.14:g.74781265dup
GRCh38.p14 chr 7	NC_000007.14:g.74781264_74781265dup
GRCh38.p14 chr 7	NC_000007.14:g.74781263_74781265dup
GRCh38.p14 chr 7	NC_000007.14:g.74781261_74781265dup
GRCh37.p13 chr 7 fix patch HG1257_PATCH	NW_003871064.1:g.2310500_2310501del
GRCh37.p13 chr 7 fix patch HG1257_PATCH	NW_003871064.1:g.2310501del
GRCh37.p13 chr 7 fix patch HG1257_PATCH	NW_003871064.1:g.2310501dup
GRCh37.p13 chr 7 fix patch HG1257_PATCH	NW_003871064.1:g.2310500_2310501dup
GRCh37.p13 chr 7 fix patch HG1257_PATCH	NW_003871064.1:g.2310499_2310501dup
GRCh37.p13 chr 7 fix patch HG1257_PATCH	NW_003871064.1:g.2310497_2310501dup
NCF1 RefSeqGene (LRG_87)	NG_009078.2:g.12301_12302del
NCF1 RefSeqGene (LRG_87)	NG_009078.2:g.12302del
NCF1 RefSeqGene (LRG_87)	NG_009078.2:g.12302dup
NCF1 RefSeqGene (LRG_87)	NG_009078.2:g.12301_12302dup
NCF1 RefSeqGene (LRG_87)	NG_009078.2:g.12300_12302dup
NCF1 RefSeqGene (LRG_87)	NG_009078.2:g.12298_12302dup
LOC106029312 genomic region	NG_042249.1:g.47428_47429del
LOC106029312 genomic region	NG_042249.1:g.47429del
LOC106029312 genomic region	NG_042249.1:g.47429dup
LOC106029312 genomic region	NG_042249.1:g.47428_47429dup
LOC106029312 genomic region	NG_042249.1:g.47427_47429dup
LOC106029312 genomic region	NG_042249.1:g.47425_47429dup
GRCh37.p13 chr 7	NC_000007.13:g.74195611dup
GRCh37.p13 chr 7	NC_000007.13:g.74195611del
GRCh37.p13 chr 7	NC_000007.13:g.74195610_74195611dup
GRCh37.p13 chr 7	NC_000007.13:g.74195609_74195611dup
GRCh37.p13 chr 7	NC_000007.13:g.74195608_74195611dup
GRCh37.p13 chr 7	NC_000007.13:g.74195606_74195611dup

Gene: NCF1, neutrophil cytosolic factor 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NCF1 transcript	NM_000265.7:c.451+429_451… NM_000265.7:c.451+429_451+430del	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)₂₁=	delAA	delA	dupA	dupAA	dupAAA	dup(A)₅
GRCh38.p14 chr 7	NC_000007.14:g.74781245_74781265=	NC_000007.14:g.74781264_74781265del	NC_000007.14:g.74781265del	NC_000007.14:g.74781265dup	NC_000007.14:g.74781264_74781265dup	NC_000007.14:g.74781263_74781265dup	NC_000007.14:g.74781261_74781265dup
GRCh37.p13 chr 7 fix patch HG1257_PATCH	NW_003871064.1:g.2310481_2310501=	NW_003871064.1:g.2310500_2310501del	NW_003871064.1:g.2310501del	NW_003871064.1:g.2310501dup	NW_003871064.1:g.2310500_2310501dup	NW_003871064.1:g.2310499_2310501dup	NW_003871064.1:g.2310497_2310501dup
NCF1 RefSeqGene (LRG_87)	NG_009078.2:g.12282_12302=	NG_009078.2:g.12301_12302del	NG_009078.2:g.12302del	NG_009078.2:g.12302dup	NG_009078.2:g.12301_12302dup	NG_009078.2:g.12300_12302dup	NG_009078.2:g.12298_12302dup
LOC106029312 genomic region	NG_042249.1:g.47409_47429=	NG_042249.1:g.47428_47429del	NG_042249.1:g.47429del	NG_042249.1:g.47429dup	NG_042249.1:g.47428_47429dup	NG_042249.1:g.47427_47429dup	NG_042249.1:g.47425_47429dup
GRCh37.p13 chr 7	NC_000007.13:g.74195611dup	NC_000007.13:g.74195611del	NC_000007.13:g.74195592_74195611=	NC_000007.13:g.74195610_74195611dup	NC_000007.13:g.74195609_74195611dup	NC_000007.13:g.74195608_74195611dup	NC_000007.13:g.74195606_74195611dup
NCF1 transcript	NM_000265.5:c.451+430dup	NM_000265.5:c.451+430del	NM_000265.5:c.451+411=	NM_000265.5:c.451+429_451+430dup	NM_000265.5:c.451+428_451+430dup	NM_000265.5:c.451+427_451+430dup	NM_000265.5:c.451+425_451+430dup
NCF1 transcript	NM_000265.7:c.451+410=	NM_000265.7:c.451+429_451+430del	NM_000265.7:c.451+430del	NM_000265.7:c.451+430dup	NM_000265.7:c.451+429_451+430dup	NM_000265.7:c.451+428_451+430dup	NM_000265.7:c.451+426_451+430dup
NCF1 transcript variant X1	XM_005250543.1:c.451+430dup	XM_005250543.1:c.451+430del	XM_005250543.1:c.451+411=	XM_005250543.1:c.451+429_451+430dup	XM_005250543.1:c.451+428_451+430dup	XM_005250543.1:c.451+427_451+430dup	XM_005250543.1:c.451+425_451+430dup
NCF1 transcript variant X2	XM_005250544.1:c.451+430dup	XM_005250544.1:c.451+430del	XM_005250544.1:c.451+411=	XM_005250544.1:c.451+429_451+430dup	XM_005250544.1:c.451+428_451+430dup	XM_005250544.1:c.451+427_451+430dup	XM_005250544.1:c.451+425_451+430dup
NCF1 transcript variant X1	XM_005277608.1:c.451+410=	XM_005277608.1:c.451+429_451+430del	XM_005277608.1:c.451+430del	XM_005277608.1:c.451+430dup	XM_005277608.1:c.451+429_451+430dup	XM_005277608.1:c.451+428_451+430dup	XM_005277608.1:c.451+426_451+430dup
NCF1 transcript variant X2	XM_005277609.1:c.451+410=	XM_005277609.1:c.451+429_451+430del	XM_005277609.1:c.451+430del	XM_005277609.1:c.451+430dup	XM_005277609.1:c.451+429_451+430dup	XM_005277609.1:c.451+428_451+430dup	XM_005277609.1:c.451+426_451+430dup

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#.

14 SubSNP, 11 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3001428558	Oct 12, 2018 (152)
2	GNOMAD	ss4166256574	Apr 26, 2021 (155)
3	GNOMAD	ss4166256575	Apr 26, 2021 (155)
4	GNOMAD	ss4166256576	Apr 26, 2021 (155)
5	TOMMO_GENOMICS	ss5183871725	Apr 26, 2021 (155)
6	TOMMO_GENOMICS	ss5183871726	Apr 26, 2021 (155)
7	TOMMO_GENOMICS	ss5183871727	Apr 26, 2021 (155)
8	HUGCELL_USP	ss5470479361	Oct 16, 2022 (156)
9	SANFORD_IMAGENETICS	ss5643248323	Oct 16, 2022 (156)
10	TOMMO_GENOMICS	ss5724348811	Oct 16, 2022 (156)
11	TOMMO_GENOMICS	ss5724348812	Oct 16, 2022 (156)
12	TOMMO_GENOMICS	ss5724348813	Oct 16, 2022 (156)
13	TOMMO_GENOMICS	ss5724348815	Oct 16, 2022 (156)
14	YY_MCH	ss5808776338	Oct 16, 2022 (156)
15	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265633130 (NC_000007.14:74781244::A 54/11438) Row 265633131 (NC_000007.14:74781244::AA 3/11446) Row 265633132 (NC_000007.14:74781244:A: 3396/11418)	-	Apr 26, 2021 (155)
16	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265633130 (NC_000007.14:74781244::A 54/11438) Row 265633131 (NC_000007.14:74781244::AA 3/11446) Row 265633132 (NC_000007.14:74781244:A: 3396/11418)	-	Apr 26, 2021 (155)
17	gnomAD - Genomes Submission ignored due to conflicting rows: Row 265633130 (NC_000007.14:74781244::A 54/11438) Row 265633131 (NC_000007.14:74781244::AA 3/11446) Row 265633132 (NC_000007.14:74781244:A: 3396/11418)	-	Apr 26, 2021 (155)
18	8.3KJPN Submission ignored due to conflicting rows: Row 41841032 (NC_000007.13:74195591:A: 205/16426) Row 41841033 (NC_000007.13:74195591::A 96/16426) Row 41841034 (NC_000007.13:74195591::AA 4/16426)	-	Apr 26, 2021 (155)
19	8.3KJPN Submission ignored due to conflicting rows: Row 41841032 (NC_000007.13:74195591:A: 205/16426) Row 41841033 (NC_000007.13:74195591::A 96/16426) Row 41841034 (NC_000007.13:74195591::AA 4/16426)	-	Apr 26, 2021 (155)
20	8.3KJPN Submission ignored due to conflicting rows: Row 41841032 (NC_000007.13:74195591:A: 205/16426) Row 41841033 (NC_000007.13:74195591::A 96/16426) Row 41841034 (NC_000007.13:74195591::AA 4/16426)	-	Apr 26, 2021 (155)
21	14KJPN Submission ignored due to conflicting rows: Row 58185915 (NC_000007.14:74781244:A: 9060/16270) Row 58185916 (NC_000007.14:74781244::A 40/16270) Row 58185917 (NC_000007.14:74781244:AA: 534/16270)...	-	Oct 16, 2022 (156)
22	14KJPN Submission ignored due to conflicting rows: Row 58185915 (NC_000007.14:74781244:A: 9060/16270) Row 58185916 (NC_000007.14:74781244::A 40/16270) Row 58185917 (NC_000007.14:74781244:AA: 534/16270)...	-	Oct 16, 2022 (156)
23	14KJPN Submission ignored due to conflicting rows: Row 58185915 (NC_000007.14:74781244:A: 9060/16270) Row 58185916 (NC_000007.14:74781244::A 40/16270) Row 58185917 (NC_000007.14:74781244:AA: 534/16270)...	-	Oct 16, 2022 (156)
24	14KJPN Submission ignored due to conflicting rows: Row 58185915 (NC_000007.14:74781244:A: 9060/16270) Row 58185916 (NC_000007.14:74781244::A 40/16270) Row 58185917 (NC_000007.14:74781244:AA: 534/16270)...	-	Oct 16, 2022 (156)
25	ALFA	NC_000007.14 - 74781245	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
ss5724348813	NC_000007.14:74781244:AA:	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
7835319284	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5183871725	NC_000007.13:74195591:A:	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4166256576, ss5470479361, ss5724348811, ss5808776338	NC_000007.14:74781244:A:	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
7835319284	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3001428558, ss5183871726, ss5643248323	NC_000007.13:74195591::A	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4166256574, ss5724348812	NC_000007.14:74781244::A	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
7835319284	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5183871727	NC_000007.13:74195591::AA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4166256575	NC_000007.14:74781244::AA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
7835319284	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
7835319284	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss5724348815	NC_000007.14:74781244::AAAAA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
7835319284	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:74781244:AAAAAAAAAAAA… NC_000007.14:74781244:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs1398685096

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

rs1398685096