Name: rs35330393
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.

rs35330393

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:14531900-14531916 (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
Variation Type: Indel Insertion and Deletion
Frequency: delAAA=0.00000 (0/10408, ALFA)
delAA=0.00000 (0/10408, ALFA)
delA=0.00000 (0/10408, ALFA) (+ 4 more)
dupA=0.00000 (0/10408, ALFA)
dupAA=0.00000 (0/10408, ALFA)
delA=0.026 (14/544, NorthernSweden)
delA=0.17 (7/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PARN : Intron Variant
LOC107984865 : Non Coding Transcript 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	HWEP
Total	Global	10408	AAAAAAAAAAAAAAAAA=1.00000	AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAAAAAA=0.00000	1.0	N/A
European	Sub	6542	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	2544	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African Others	Sub	92	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	2452	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
Asian	Sub	108	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
East Asian	Sub	84	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	138	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	572	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	90	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	414	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000	1.0	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	10408	(A)₁₇=1.00000	delAAA=0.00000, delAA=0.00000, delA=0.00000, dupA=0.00000, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	6542	(A)₁₇=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	2544	(A)₁₇=1.0000	delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	572	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	414	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	108	(A)₁₇=1.000	delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	90	(A)₁₇=1.00	delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Northern Sweden	ACPOP	Study-wide	544	(A)₁₇=0.974	delA=0.026
The Danish reference pan genome	Danish	Study-wide	40	(A)₁₇=0.82	delA=0.17

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 16	NC_000016.10:g.14531914_14531916del
GRCh38.p14 chr 16	NC_000016.10:g.14531915_14531916del
GRCh38.p14 chr 16	NC_000016.10:g.14531916del
GRCh38.p14 chr 16	NC_000016.10:g.14531916dup
GRCh38.p14 chr 16	NC_000016.10:g.14531915_14531916dup
GRCh37.p13 chr 16	NC_000016.9:g.14625771_14625773del
GRCh37.p13 chr 16	NC_000016.9:g.14625772_14625773del
GRCh37.p13 chr 16	NC_000016.9:g.14625773del
GRCh37.p13 chr 16	NC_000016.9:g.14625773dup
GRCh37.p13 chr 16	NC_000016.9:g.14625772_14625773dup
A RefSeqGene (LRG_1286)	NG_042871.1:g.103370_103372del
A RefSeqGene (LRG_1286)	NG_042871.1:g.103371_103372del
A RefSeqGene (LRG_1286)	NG_042871.1:g.103372del
A RefSeqGene (LRG_1286)	NG_042871.1:g.103372dup
A RefSeqGene (LRG_1286)	NG_042871.1:g.103371_103372dup
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.104771_104773del
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.104772_104773del
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.104773del
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.104773dup
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.104772_104773dup

Gene: PARN, poly(A)-specific ribonuclease (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PARN transcript variant 2	NM_001134477.3:c.1297+201… NM_001134477.3:c.1297+20119_1297+20121del	N/A	Intron Variant
PARN transcript variant 3	NM_001242992.2:c.1342+201… NM_001242992.2:c.1342+20119_1342+20121del	N/A	Intron Variant
PARN transcript variant 1	NM_002582.4:c.1480+20119_… NM_002582.4:c.1480+20119_1480+20121del	N/A	Intron Variant
PARN transcript variant X1	XM_047434181.1:c.1480+201… XM_047434181.1:c.1480+20119_1480+20121del	N/A	Intron Variant
PARN transcript variant X2	XM_047434182.1:c.1480+201… XM_047434182.1:c.1480+20119_1480+20121del	N/A	Intron Variant
PARN transcript variant X6	XM_047434183.1:c.1297+201… XM_047434183.1:c.1297+20119_1297+20121del	N/A	Intron Variant
PARN transcript variant X7	XM_047434184.1:c.1297+201… XM_047434184.1:c.1297+20119_1297+20121del	N/A	Intron Variant
PARN transcript variant X9	XM_011522514.3:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X10	XM_047434185.1:c.	N/A	Genic Downstream Transcript Variant
PARN transcript variant X3	XR_007064881.1:n.	N/A	Intron Variant
PARN transcript variant X4	XR_007064882.1:n.	N/A	Intron Variant
PARN transcript variant X5	XR_007064883.1:n.	N/A	Intron Variant
PARN transcript variant X8	XR_007064884.1:n.	N/A	Intron Variant

Gene: LOC107984865, uncharacterized LOC107984865 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC107984865 transcript variant X1	XR_001752089.3:n.19127_19… XR_001752089.3:n.19127_19129del	N/A	Non Coding Transcript Variant
LOC107984865 transcript variant X1	XR_001752089.3:n.19128_19… XR_001752089.3:n.19128_19129del	N/A	Non Coding Transcript Variant
LOC107984865 transcript variant X1	XR_001752089.3:n.19129del	N/A	Non Coding Transcript Variant
LOC107984865 transcript variant X1	XR_001752089.3:n.19129dup	N/A	Non Coding Transcript Variant
LOC107984865 transcript variant X1	XR_001752089.3:n.19128_19… XR_001752089.3:n.19128_19129dup	N/A	Non Coding Transcript 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)₁₇=	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 16	NC_000016.10:g.14531900_14531916=	NC_000016.10:g.14531914_14531916del	NC_000016.10:g.14531915_14531916del	NC_000016.10:g.14531916del	NC_000016.10:g.14531916dup	NC_000016.10:g.14531915_14531916dup
GRCh37.p13 chr 16	NC_000016.9:g.14625757_14625773=	NC_000016.9:g.14625771_14625773del	NC_000016.9:g.14625772_14625773del	NC_000016.9:g.14625773del	NC_000016.9:g.14625773dup	NC_000016.9:g.14625772_14625773dup
A RefSeqGene (LRG_1286)	NG_042871.1:g.103356_103372=	NG_042871.1:g.103370_103372del	NG_042871.1:g.103371_103372del	NG_042871.1:g.103372del	NG_042871.1:g.103372dup	NG_042871.1:g.103371_103372dup
GRCh38.p14 chr 16 alt locus HSCHR16_1_CTG1	NT_187607.1:g.104757_104773=	NT_187607.1:g.104771_104773del	NT_187607.1:g.104772_104773del	NT_187607.1:g.104773del	NT_187607.1:g.104773dup	NT_187607.1:g.104772_104773dup
LOC107984865 transcript variant X1	XR_001752089.3:n.19113_19129=	XR_001752089.3:n.19127_19129del	XR_001752089.3:n.19128_19129del	XR_001752089.3:n.19129del	XR_001752089.3:n.19129dup	XR_001752089.3:n.19128_19129dup
LOC107984865 transcript	XR_001752089.2:n.3_4insTTTTTTTTTTTTTT	XR_001752089.2:n.3_4insTTTTTTTTTTT	XR_001752089.2:n.3_4insTTTTTTTTTTTT	XR_001752089.2:n.3_4insTTTTTTTTTTTTT	XR_001752089.2:n.3_4insTTTTTTTTTTTTTTT	XR_001752089.2:n.3_4insTTTTTTTTTTTTTTTT
LOC107984865 transcript	XR_001752089.1:n.3_4insTTTTTTTTTTTTTT	XR_001752089.1:n.3_4insTTTTTTTTTTT	XR_001752089.1:n.3_4insTTTTTTTTTTTT	XR_001752089.1:n.3_4insTTTTTTTTTTTTT	XR_001752089.1:n.3_4insTTTTTTTTTTTTTTT	XR_001752089.1:n.3_4insTTTTTTTTTTTTTTTT
LOC107984865 transcript variant X2	XR_001756351.3:n.19113_19129=	XR_001756351.3:n.19127_19129del	XR_001756351.3:n.19128_19129del	XR_001756351.3:n.19129del	XR_001756351.3:n.19129dup	XR_001756351.3:n.19128_19129dup
LOC107984865 transcript	XR_001756351.2:n.3_4insTTTTTTTTTTTTTT	XR_001756351.2:n.3_4insTTTTTTTTTTT	XR_001756351.2:n.3_4insTTTTTTTTTTTT	XR_001756351.2:n.3_4insTTTTTTTTTTTTT	XR_001756351.2:n.3_4insTTTTTTTTTTTTTTT	XR_001756351.2:n.3_4insTTTTTTTTTTTTTTTT
LOC107984865 transcript	XR_001756351.1:n.3_4insTTTTTTTTTTTTTT	XR_001756351.1:n.3_4insTTTTTTTTTTT	XR_001756351.1:n.3_4insTTTTTTTTTTTT	XR_001756351.1:n.3_4insTTTTTTTTTTTTT	XR_001756351.1:n.3_4insTTTTTTTTTTTTTTT	XR_001756351.1:n.3_4insTTTTTTTTTTTTTTTT
PARN transcript variant 2	NM_001134477.2:c.1297+20121=	NM_001134477.2:c.1297+20119_1297+20121del	NM_001134477.2:c.1297+20120_1297+20121del	NM_001134477.2:c.1297+20121del	NM_001134477.2:c.1297+20121dup	NM_001134477.2:c.1297+20120_1297+20121dup
PARN transcript variant 2	NM_001134477.3:c.1297+20121=	NM_001134477.3:c.1297+20119_1297+20121del	NM_001134477.3:c.1297+20120_1297+20121del	NM_001134477.3:c.1297+20121del	NM_001134477.3:c.1297+20121dup	NM_001134477.3:c.1297+20120_1297+20121dup
PARN transcript variant 3	NM_001242992.1:c.1342+20121=	NM_001242992.1:c.1342+20119_1342+20121del	NM_001242992.1:c.1342+20120_1342+20121del	NM_001242992.1:c.1342+20121del	NM_001242992.1:c.1342+20121dup	NM_001242992.1:c.1342+20120_1342+20121dup
PARN transcript variant 3	NM_001242992.2:c.1342+20121=	NM_001242992.2:c.1342+20119_1342+20121del	NM_001242992.2:c.1342+20120_1342+20121del	NM_001242992.2:c.1342+20121del	NM_001242992.2:c.1342+20121dup	NM_001242992.2:c.1342+20120_1342+20121dup
PARN transcript variant 1	NM_002582.3:c.1480+20121=	NM_002582.3:c.1480+20119_1480+20121del	NM_002582.3:c.1480+20120_1480+20121del	NM_002582.3:c.1480+20121del	NM_002582.3:c.1480+20121dup	NM_002582.3:c.1480+20120_1480+20121dup
PARN transcript variant 1	NM_002582.4:c.1480+20121=	NM_002582.4:c.1480+20119_1480+20121del	NM_002582.4:c.1480+20120_1480+20121del	NM_002582.4:c.1480+20121del	NM_002582.4:c.1480+20121dup	NM_002582.4:c.1480+20120_1480+20121dup
PARN transcript variant X1	XM_005255341.1:c.955+20121=	XM_005255341.1:c.955+20119_955+20121del	XM_005255341.1:c.955+20120_955+20121del	XM_005255341.1:c.955+20121del	XM_005255341.1:c.955+20121dup	XM_005255341.1:c.955+20120_955+20121dup
PARN transcript variant X1	XM_047434181.1:c.1480+20121=	XM_047434181.1:c.1480+20119_1480+20121del	XM_047434181.1:c.1480+20120_1480+20121del	XM_047434181.1:c.1480+20121del	XM_047434181.1:c.1480+20121dup	XM_047434181.1:c.1480+20120_1480+20121dup
PARN transcript variant X2	XM_047434182.1:c.1480+20121=	XM_047434182.1:c.1480+20119_1480+20121del	XM_047434182.1:c.1480+20120_1480+20121del	XM_047434182.1:c.1480+20121del	XM_047434182.1:c.1480+20121dup	XM_047434182.1:c.1480+20120_1480+20121dup
PARN transcript variant X6	XM_047434183.1:c.1297+20121=	XM_047434183.1:c.1297+20119_1297+20121del	XM_047434183.1:c.1297+20120_1297+20121del	XM_047434183.1:c.1297+20121del	XM_047434183.1:c.1297+20121dup	XM_047434183.1:c.1297+20120_1297+20121dup
PARN transcript variant X7	XM_047434184.1:c.1297+20121=	XM_047434184.1:c.1297+20119_1297+20121del	XM_047434184.1:c.1297+20120_1297+20121del	XM_047434184.1:c.1297+20121del	XM_047434184.1:c.1297+20121dup	XM_047434184.1:c.1297+20120_1297+20121dup

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#.

22 SubSNP, 13 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40642690	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss96711001	Dec 05, 2013 (138)
3	EVA_GENOME_DK	ss1574930389	Apr 01, 2015 (144)
4	MCHAISSO	ss3065612281	Nov 08, 2017 (151)
5	URBANLAB	ss3650473530	Oct 12, 2018 (152)
6	EVA_DECODE	ss3698925867	Jul 13, 2019 (153)
7	EVA_DECODE	ss3698925868	Jul 13, 2019 (153)
8	EVA_DECODE	ss3698925870	Jul 13, 2019 (153)
9	ACPOP	ss3741374420	Jul 13, 2019 (153)
10	EVA	ss3834497561	Apr 27, 2020 (154)
11	GNOMAD	ss4297592351	Apr 26, 2021 (155)
12	GNOMAD	ss4297592352	Apr 26, 2021 (155)
13	GNOMAD	ss4297592353	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5218613578	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5218613579	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5218613580	Apr 26, 2021 (155)
17	1000G_HIGH_COVERAGE	ss5300285662	Oct 17, 2022 (156)
18	HUGCELL_USP	ss5493799547	Oct 17, 2022 (156)
19	HUGCELL_USP	ss5493799548	Oct 17, 2022 (156)
20	TOMMO_GENOMICS	ss5773149479	Oct 17, 2022 (156)
21	TOMMO_GENOMICS	ss5773149480	Oct 17, 2022 (156)
22	TOMMO_GENOMICS	ss5773149481	Oct 17, 2022 (156)
23	The Danish reference pan genome	NC_000016.9 - 14625757	Apr 27, 2020 (154)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484047639 (NC_000016.10:14531899::A 2940/99614) Row 484047640 (NC_000016.10:14531899::AA 47/99640) Row 484047641 (NC_000016.10:14531899:A: 5270/99546)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484047639 (NC_000016.10:14531899::A 2940/99614) Row 484047640 (NC_000016.10:14531899::AA 47/99640) Row 484047641 (NC_000016.10:14531899:A: 5270/99546)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484047639 (NC_000016.10:14531899::A 2940/99614) Row 484047640 (NC_000016.10:14531899::AA 47/99640) Row 484047641 (NC_000016.10:14531899:A: 5270/99546)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 484047639 (NC_000016.10:14531899::A 2940/99614) Row 484047640 (NC_000016.10:14531899::AA 47/99640) Row 484047641 (NC_000016.10:14531899:A: 5270/99546)...	-	Apr 26, 2021 (155)
28	Northern Sweden	NC_000016.9 - 14625757	Jul 13, 2019 (153)
29	8.3KJPN Submission ignored due to conflicting rows: Row 76582885 (NC_000016.9:14625756:A: 72/16760) Row 76582886 (NC_000016.9:14625756::A 343/16760) Row 76582887 (NC_000016.9:14625756::AA 13/16760)	-	Apr 26, 2021 (155)
30	8.3KJPN Submission ignored due to conflicting rows: Row 76582885 (NC_000016.9:14625756:A: 72/16760) Row 76582886 (NC_000016.9:14625756::A 343/16760) Row 76582887 (NC_000016.9:14625756::AA 13/16760)	-	Apr 26, 2021 (155)
31	8.3KJPN Submission ignored due to conflicting rows: Row 76582885 (NC_000016.9:14625756:A: 72/16760) Row 76582886 (NC_000016.9:14625756::A 343/16760) Row 76582887 (NC_000016.9:14625756::AA 13/16760)	-	Apr 26, 2021 (155)
32	14KJPN Submission ignored due to conflicting rows: Row 106986583 (NC_000016.10:14531899::A 595/28258) Row 106986584 (NC_000016.10:14531899:A: 87/28258) Row 106986585 (NC_000016.10:14531899::AA 26/28258)	-	Oct 17, 2022 (156)
33	14KJPN Submission ignored due to conflicting rows: Row 106986583 (NC_000016.10:14531899::A 595/28258) Row 106986584 (NC_000016.10:14531899:A: 87/28258) Row 106986585 (NC_000016.10:14531899::AA 26/28258)	-	Oct 17, 2022 (156)
34	14KJPN Submission ignored due to conflicting rows: Row 106986583 (NC_000016.10:14531899::A 595/28258) Row 106986584 (NC_000016.10:14531899:A: 87/28258) Row 106986585 (NC_000016.10:14531899::AA 26/28258)	-	Oct 17, 2022 (156)
35	ALFA	NC_000016.10 - 14531900	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)
rs71373030	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
5998332832	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss3698925870, ss4297592353	NC_000016.10:14531899:AA:	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
5998332832	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
518273, 14659285, ss1574930389, ss3741374420, ss5218613578	NC_000016.9:14625756:A:	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3065612281, ss3650473530, ss5300285662, ss5493799547, ss5773149480	NC_000016.10:14531899:A:	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
5998332832	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3698925868	NC_000016.10:14531900:A:	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss96711001	NT_010393.16:14565756:A:	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss40642690	NT_010393.16:14565772:A:	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3834497561, ss5218613579	NC_000016.9:14625756::A	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4297592351, ss5493799548, ss5773149479	NC_000016.10:14531899::A	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
5998332832	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3698925867	NC_000016.10:14531901::A	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5218613580	NC_000016.9:14625756::AA	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4297592352, ss5773149481	NC_000016.10:14531899::AA	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
5998332832	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3241156397	NC_000016.10:14531899:AAA:	NC_000016.10:14531899:AAAAAAAAAAAA… NC_000016.10:14531899:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA

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

No publications for rs35330393

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

rs35330393