Name: rs35161106
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.

rs35161106

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:37345909-37345927 (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: del(A)₇ / del(A)₆ / delAAA / delAA…
del(A)₇ / del(A)₆ / delAAA / delAA / delA / dupA / dupAA / dupAAA / ins(A)₃₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₇=0.00009 (1/11064, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NUP155 : 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	HTRZ	HWEP
Total	Global	11064	AAAAAAAAAAAAAAAAAAA=0.99991	AAAAAAAAAAAA=0.00009, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAAAA=0.00000	0.999819	0.000181	0
European	Sub	8808	AAAAAAAAAAAAAAAAAAA=0.9999	AAAAAAAAAAAA=0.0001, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	0.999773	0.000227	0
African	Sub	1030	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
African Others	Sub	28	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
African American	Sub	1002	AAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	N/A
Asian	Sub	112	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
East Asian	Sub	86	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other Asian	Sub	26	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Latin American 1	Sub	102	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
Latin American 2	Sub	558	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	N/A
South Asian	Sub	92	AAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	N/A
Other	Sub	362	AAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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	11064	(A)₁₉=0.99991	del(A)₇=0.00009, del(A)₆=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	8808	(A)₁₉=0.9999	del(A)₇=0.0001, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	1030	(A)₁₉=1.0000	del(A)₇=0.0000, del(A)₆=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	558	(A)₁₉=1.000	del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	362	(A)₁₉=1.000	del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	112	(A)₁₉=1.000	del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	102	(A)₁₉=1.000	del(A)₇=0.000, del(A)₆=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	92	(A)₁₉=1.00	del(A)₇=0.00, del(A)₆=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00

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 5	NC_000005.10:g.37345921_37345927del
GRCh38.p14 chr 5	NC_000005.10:g.37345922_37345927del
GRCh38.p14 chr 5	NC_000005.10:g.37345925_37345927del
GRCh38.p14 chr 5	NC_000005.10:g.37345926_37345927del
GRCh38.p14 chr 5	NC_000005.10:g.37345927del
GRCh38.p14 chr 5	NC_000005.10:g.37345927dup
GRCh38.p14 chr 5	NC_000005.10:g.37345926_37345927dup
GRCh38.p14 chr 5	NC_000005.10:g.37345925_37345927dup
GRCh38.p14 chr 5	NC_000005.10:g.37345927_37345928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 5	NC_000005.9:g.37346023_37346029del
GRCh37.p13 chr 5	NC_000005.9:g.37346024_37346029del
GRCh37.p13 chr 5	NC_000005.9:g.37346027_37346029del
GRCh37.p13 chr 5	NC_000005.9:g.37346028_37346029del
GRCh37.p13 chr 5	NC_000005.9:g.37346029del
GRCh37.p13 chr 5	NC_000005.9:g.37346029dup
GRCh37.p13 chr 5	NC_000005.9:g.37346028_37346029dup
GRCh37.p13 chr 5	NC_000005.9:g.37346027_37346029dup
GRCh37.p13 chr 5	NC_000005.9:g.37346029_37346030insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NUP155 RefSeqGene	NG_034131.1:g.30212_30218del
NUP155 RefSeqGene	NG_034131.1:g.30213_30218del
NUP155 RefSeqGene	NG_034131.1:g.30216_30218del
NUP155 RefSeqGene	NG_034131.1:g.30217_30218del
NUP155 RefSeqGene	NG_034131.1:g.30218del
NUP155 RefSeqGene	NG_034131.1:g.30218dup
NUP155 RefSeqGene	NG_034131.1:g.30217_30218dup
NUP155 RefSeqGene	NG_034131.1:g.30216_30218dup
NUP155 RefSeqGene	NG_034131.1:g.30218_30219insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: NUP155, nucleoporin 155 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NUP155 transcript variant 3	NM_001278312.2:c.995+2590… NM_001278312.2:c.995+2590_995+2596del	N/A	Intron Variant
NUP155 transcript variant 2	NM_004298.4:c.818+2590_81… NM_004298.4:c.818+2590_818+2596del	N/A	Intron Variant
NUP155 transcript variant 1	NM_153485.3:c.995+2590_99… NM_153485.3:c.995+2590_995+2596del	N/A	Intron Variant
NUP155 transcript variant X2	XM_011514165.4:c.995+2590… XM_011514165.4:c.995+2590_995+2596del	N/A	Intron Variant
NUP155 transcript variant X1	XM_047417934.1:c.995+2590… XM_047417934.1:c.995+2590_995+2596del	N/A	Intron Variant
NUP155 transcript variant X3	XM_047417935.1:c.995+2590… XM_047417935.1:c.995+2590_995+2596del	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)₁₉=	del(A)₇	del(A)₆	delAAA	delAA	delA	dupA	dupAA	dupAAA	ins(A)₃₅
GRCh38.p14 chr 5	NC_000005.10:g.37345909_37345927=	NC_000005.10:g.37345921_37345927del	NC_000005.10:g.37345922_37345927del	NC_000005.10:g.37345925_37345927del	NC_000005.10:g.37345926_37345927del	NC_000005.10:g.37345927del	NC_000005.10:g.37345927dup	NC_000005.10:g.37345926_37345927dup	NC_000005.10:g.37345925_37345927dup	NC_000005.10:g.37345927_37345928insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 5	NC_000005.9:g.37346011_37346029=	NC_000005.9:g.37346023_37346029del	NC_000005.9:g.37346024_37346029del	NC_000005.9:g.37346027_37346029del	NC_000005.9:g.37346028_37346029del	NC_000005.9:g.37346029del	NC_000005.9:g.37346029dup	NC_000005.9:g.37346028_37346029dup	NC_000005.9:g.37346027_37346029dup	NC_000005.9:g.37346029_37346030insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NUP155 RefSeqGene	NG_034131.1:g.30200_30218=	NG_034131.1:g.30212_30218del	NG_034131.1:g.30213_30218del	NG_034131.1:g.30216_30218del	NG_034131.1:g.30217_30218del	NG_034131.1:g.30218del	NG_034131.1:g.30218dup	NG_034131.1:g.30217_30218dup	NG_034131.1:g.30216_30218dup	NG_034131.1:g.30218_30219insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant 3	NM_001278312.1:c.995+2596=	NM_001278312.1:c.995+2590_995+2596del	NM_001278312.1:c.995+2591_995+2596del	NM_001278312.1:c.995+2594_995+2596del	NM_001278312.1:c.995+2595_995+2596del	NM_001278312.1:c.995+2596del	NM_001278312.1:c.995+2596dup	NM_001278312.1:c.995+2595_995+2596dup	NM_001278312.1:c.995+2594_995+2596dup	NM_001278312.1:c.995+2596_995+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant 3	NM_001278312.2:c.995+2596=	NM_001278312.2:c.995+2590_995+2596del	NM_001278312.2:c.995+2591_995+2596del	NM_001278312.2:c.995+2594_995+2596del	NM_001278312.2:c.995+2595_995+2596del	NM_001278312.2:c.995+2596del	NM_001278312.2:c.995+2596dup	NM_001278312.2:c.995+2595_995+2596dup	NM_001278312.2:c.995+2594_995+2596dup	NM_001278312.2:c.995+2596_995+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant 2	NM_004298.3:c.818+2596=	NM_004298.3:c.818+2590_818+2596del	NM_004298.3:c.818+2591_818+2596del	NM_004298.3:c.818+2594_818+2596del	NM_004298.3:c.818+2595_818+2596del	NM_004298.3:c.818+2596del	NM_004298.3:c.818+2596dup	NM_004298.3:c.818+2595_818+2596dup	NM_004298.3:c.818+2594_818+2596dup	NM_004298.3:c.818+2596_818+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant 2	NM_004298.4:c.818+2596=	NM_004298.4:c.818+2590_818+2596del	NM_004298.4:c.818+2591_818+2596del	NM_004298.4:c.818+2594_818+2596del	NM_004298.4:c.818+2595_818+2596del	NM_004298.4:c.818+2596del	NM_004298.4:c.818+2596dup	NM_004298.4:c.818+2595_818+2596dup	NM_004298.4:c.818+2594_818+2596dup	NM_004298.4:c.818+2596_818+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant 1	NM_153485.2:c.995+2596=	NM_153485.2:c.995+2590_995+2596del	NM_153485.2:c.995+2591_995+2596del	NM_153485.2:c.995+2594_995+2596del	NM_153485.2:c.995+2595_995+2596del	NM_153485.2:c.995+2596del	NM_153485.2:c.995+2596dup	NM_153485.2:c.995+2595_995+2596dup	NM_153485.2:c.995+2594_995+2596dup	NM_153485.2:c.995+2596_995+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant 1	NM_153485.3:c.995+2596=	NM_153485.3:c.995+2590_995+2596del	NM_153485.3:c.995+2591_995+2596del	NM_153485.3:c.995+2594_995+2596del	NM_153485.3:c.995+2595_995+2596del	NM_153485.3:c.995+2596del	NM_153485.3:c.995+2596dup	NM_153485.3:c.995+2595_995+2596dup	NM_153485.3:c.995+2594_995+2596dup	NM_153485.3:c.995+2596_995+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant X2	XM_011514165.4:c.995+2596=	XM_011514165.4:c.995+2590_995+2596del	XM_011514165.4:c.995+2591_995+2596del	XM_011514165.4:c.995+2594_995+2596del	XM_011514165.4:c.995+2595_995+2596del	XM_011514165.4:c.995+2596del	XM_011514165.4:c.995+2596dup	XM_011514165.4:c.995+2595_995+2596dup	XM_011514165.4:c.995+2594_995+2596dup	XM_011514165.4:c.995+2596_995+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant X1	XM_047417934.1:c.995+2596=	XM_047417934.1:c.995+2590_995+2596del	XM_047417934.1:c.995+2591_995+2596del	XM_047417934.1:c.995+2594_995+2596del	XM_047417934.1:c.995+2595_995+2596del	XM_047417934.1:c.995+2596del	XM_047417934.1:c.995+2596dup	XM_047417934.1:c.995+2595_995+2596dup	XM_047417934.1:c.995+2594_995+2596dup	XM_047417934.1:c.995+2596_995+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NUP155 transcript variant X3	XM_047417935.1:c.995+2596=	XM_047417935.1:c.995+2590_995+2596del	XM_047417935.1:c.995+2591_995+2596del	XM_047417935.1:c.995+2594_995+2596del	XM_047417935.1:c.995+2595_995+2596del	XM_047417935.1:c.995+2596del	XM_047417935.1:c.995+2596dup	XM_047417935.1:c.995+2595_995+2596dup	XM_047417935.1:c.995+2594_995+2596dup	XM_047417935.1:c.995+2596_995+2597insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

28 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42470676	Mar 14, 2006 (126)
2	MCHAISSO	ss3066013021	Nov 08, 2017 (151)
3	ACPOP	ss3732264689	Jul 13, 2019 (153)
4	ACPOP	ss3732264690	Jul 13, 2019 (153)
5	EVA	ss3829196968	Apr 26, 2020 (154)
6	KOGIC	ss3956446040	Apr 26, 2020 (154)
7	KOGIC	ss3956446041	Apr 26, 2020 (154)
8	KOGIC	ss3956446042	Apr 26, 2020 (154)
9	GNOMAD	ss4102623081	Apr 26, 2021 (155)
10	GNOMAD	ss4102623082	Apr 26, 2021 (155)
11	GNOMAD	ss4102623083	Apr 26, 2021 (155)
12	GNOMAD	ss4102623084	Apr 26, 2021 (155)
13	GNOMAD	ss4102623085	Apr 26, 2021 (155)
14	GNOMAD	ss4102623086	Apr 26, 2021 (155)
15	GNOMAD	ss4102623087	Apr 26, 2021 (155)
16	GNOMAD	ss4102623088	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5171255297	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5171255298	Apr 26, 2021 (155)
19	1000G_HIGH_COVERAGE	ss5263567476	Oct 17, 2022 (156)
20	1000G_HIGH_COVERAGE	ss5263567477	Oct 17, 2022 (156)
21	1000G_HIGH_COVERAGE	ss5263567478	Oct 17, 2022 (156)
22	1000G_HIGH_COVERAGE	ss5263567479	Oct 17, 2022 (156)
23	HUGCELL_USP	ss5461834023	Oct 17, 2022 (156)
24	HUGCELL_USP	ss5461834024	Oct 17, 2022 (156)
25	HUGCELL_USP	ss5461834025	Oct 17, 2022 (156)
26	HUGCELL_USP	ss5461834026	Oct 17, 2022 (156)
27	TOMMO_GENOMICS	ss5707167747	Oct 17, 2022 (156)
28	TOMMO_GENOMICS	ss5707167748	Oct 17, 2022 (156)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 185521719 (NC_000005.10:37345908::A 3489/62290) Row 185521720 (NC_000005.10:37345908::AA 19/62600) Row 185521721 (NC_000005.10:37345908::AAA 1/62678)...	-	Apr 26, 2021 (155)
37	Korean Genome Project Submission ignored due to conflicting rows: Row 12824041 (NC_000005.10:37345908:A: 138/1740) Row 12824042 (NC_000005.10:37345909::A 228/1740) Row 12824043 (NC_000005.10:37345909::AA 21/1740)	-	Apr 26, 2020 (154)
38	Korean Genome Project Submission ignored due to conflicting rows: Row 12824041 (NC_000005.10:37345908:A: 138/1740) Row 12824042 (NC_000005.10:37345909::A 228/1740) Row 12824043 (NC_000005.10:37345909::AA 21/1740)	-	Apr 26, 2020 (154)
39	Korean Genome Project Submission ignored due to conflicting rows: Row 12824041 (NC_000005.10:37345908:A: 138/1740) Row 12824042 (NC_000005.10:37345909::A 228/1740) Row 12824043 (NC_000005.10:37345909::AA 21/1740)	-	Apr 26, 2020 (154)
40	Northern Sweden Submission ignored due to conflicting rows: Row 5549554 (NC_000005.9:37346010::A 12/498) Row 5549555 (NC_000005.9:37346010::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 1/498)	-	Jul 13, 2019 (153)
41	Northern Sweden Submission ignored due to conflicting rows: Row 5549554 (NC_000005.9:37346010::A 12/498) Row 5549555 (NC_000005.9:37346010::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA 1/498)	-	Jul 13, 2019 (153)
42	8.3KJPN Submission ignored due to conflicting rows: Row 29224604 (NC_000005.9:37346010:A: 89/16760) Row 29224605 (NC_000005.9:37346010::A 59/16760)	-	Apr 26, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 29224604 (NC_000005.9:37346010:A: 89/16760) Row 29224605 (NC_000005.9:37346010::A 59/16760)	-	Apr 26, 2021 (155)
44	14KJPN Submission ignored due to conflicting rows: Row 41004851 (NC_000005.10:37345908:A: 171/28258) Row 41004852 (NC_000005.10:37345908::A 91/28258)	-	Oct 17, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 41004851 (NC_000005.10:37345908:A: 171/28258) Row 41004852 (NC_000005.10:37345908::A 91/28258)	-	Oct 17, 2022 (156)
46	ALFA	NC_000005.10 - 37345909	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
ss4102623088	NC_000005.10:37345908:AAAAAAA:	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
14700897584	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4102623087	NC_000005.10:37345908:AAAAAA:	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
14700897584	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4102623086	NC_000005.10:37345908:AAA:	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
14700897584	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4102623085, ss5263567476, ss5461834024	NC_000005.10:37345908:AA:	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
14700897584	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5171255297	NC_000005.9:37346010:A:	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3066013021, ss3956446040, ss4102623084, ss5263567477, ss5461834025, ss5707167747	NC_000005.10:37345908:A:	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
14700897584	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss42470676	NT_006576.16:37336010:A:	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3732264689, ss3829196968, ss5171255298	NC_000005.9:37346010::A	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4102623081, ss5263567478, ss5461834023, ss5707167748	NC_000005.10:37345908::A	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
14700897584	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3956446041	NC_000005.10:37345909::A	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4102623082, ss5461834026	NC_000005.10:37345908::AA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
14700897584	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3956446042	NC_000005.10:37345909::AA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4102623083, ss5263567479	NC_000005.10:37345908::AAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3732264690	NC_000005.9:37346010::AAAAAAAAAAAA… NC_000005.9:37346010::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:37345908:AAAAAAAAAAAA… NC_000005.10:37345908:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs35161106

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

rs35161106