Name: rs35174866
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.

rs35174866

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr17:75677756-75677776 (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(T)₁₂ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₂ / del(T)₁₀ / del(T)₉ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.11408 (1188/10414, ALFA)
dupT=0.1406 (704/5008, 1000G)
(T)₂₁=0.4 (3/8, KOREAN)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SAP30BP : 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	10414	TTTTTTTTTTTTTTTTTTTTT=0.85126	TTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.02727, TTTTTTTTTTTTTTTTTTTTTT=0.11408, TTTTTTTTTTTTTTTTTTTTTTT=0.00682, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00058, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.827034	0.054437	0.118529	32
European	Sub	9212	TTTTTTTTTTTTTTTTTTTTT=0.8342	TTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0287, TTTTTTTTTTTTTTTTTTTTTT=0.1287, TTTTTTTTTTTTTTTTTTTTTTT=0.0077, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.803688	0.061625	0.134687	32
African	Sub	810	TTTTTTTTTTTTTTTTTTTTT=0.978	TTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.022, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	TTTTTTTTTTTTTTTTTTTTT=0.97	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	778	TTTTTTTTTTTTTTTTTTTTT=0.978	TTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.022, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	20	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	46	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	142	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	162	TTTTTTTTTTTTTTTTTTTTT=0.975	TTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.012, TTTTTTTTTTTTTTTTTTTTTT=0.012, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.987342	0.012658	0.0	32

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	10414	(T)₂₁=0.85126	del(T)₁₂=0.00000, del(T)₉=0.00000, del(T)₇=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.02727, dupT=0.11408, dupTT=0.00682, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00058
Allele Frequency Aggregator	European	Sub	9212	(T)₂₁=0.8342	del(T)₁₂=0.0000, del(T)₉=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0287, dupT=0.1287, dupTT=0.0077, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0007
Allele Frequency Aggregator	African	Sub	810	(T)₂₁=0.978	del(T)₁₂=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.022, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	162	(T)₂₁=0.975	del(T)₁₂=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.012, dupT=0.012, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	142	(T)₂₁=1.000	del(T)₁₂=0.000, del(T)₉=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 1	Sub	46	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	22	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	20	(T)₂₁=1.00	del(T)₁₂=0.00, del(T)₉=0.00, del(T)₇=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.1406
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.1286
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.1607
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.1789
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.111
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.120
KOREAN population from KRGDB	KOREAN	Study-wide	8	- No frequency provided	dupT=0.6

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 17	NC_000017.11:g.75677765_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677767_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677768_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677770_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677772_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677773_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677774_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677775_75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677776del
GRCh38.p14 chr 17	NC_000017.11:g.75677776dup
GRCh38.p14 chr 17	NC_000017.11:g.75677775_75677776dup
GRCh38.p14 chr 17	NC_000017.11:g.75677774_75677776dup
GRCh38.p14 chr 17	NC_000017.11:g.75677773_75677776dup
GRCh38.p14 chr 17	NC_000017.11:g.75677772_75677776dup
GRCh38.p14 chr 17	NC_000017.11:g.75677771_75677776dup
GRCh37.p13 chr 17	NC_000017.10:g.73673845_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673847_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673848_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673850_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673852_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673853_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673854_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673855_73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673856del
GRCh37.p13 chr 17	NC_000017.10:g.73673856dup
GRCh37.p13 chr 17	NC_000017.10:g.73673855_73673856dup
GRCh37.p13 chr 17	NC_000017.10:g.73673854_73673856dup
GRCh37.p13 chr 17	NC_000017.10:g.73673853_73673856dup
GRCh37.p13 chr 17	NC_000017.10:g.73673852_73673856dup
GRCh37.p13 chr 17	NC_000017.10:g.73673851_73673856dup

Gene: SAP30BP, SAP30 binding protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SAP30BP transcript variant 3	NM_001301839.2:c.216+9140… NM_001301839.2:c.216+9140_216+9151del	N/A	Intron Variant
SAP30BP transcript variant 1	NM_001301855.2:c.264+5902… NM_001301855.2:c.264+5902_264+5913del	N/A	Intron Variant
SAP30BP transcript variant 2	NM_013260.8:c.264+5902_26… NM_013260.8:c.264+5902_264+5913del	N/A	Intron Variant
SAP30BP transcript variant 4	NR_126036.2:n.	N/A	Intron Variant
SAP30BP transcript variant 5	NR_126037.2:n.	N/A	Intron Variant
SAP30BP transcript variant X1	XM_011524693.4:c.264+5902… XM_011524693.4:c.264+5902_264+5913del	N/A	Intron Variant
SAP30BP transcript variant X2	XM_011524694.3:c.216+9140… XM_011524694.3:c.216+9140_216+9151del	N/A	Intron Variant
SAP30BP transcript variant X3	XM_047435870.1:c.-47+5902… XM_047435870.1:c.-47+5902_-47+5913del	N/A	Intron Variant
SAP30BP transcript variant X4	XM_047435871.1:c.-47+5902… XM_047435871.1:c.-47+5902_-47+5913del	N/A	Intron Variant
SAP30BP transcript variant X5	XM_047435872.1:c.264+5902… XM_047435872.1:c.264+5902_264+5913del	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	(T)₂₁=	del(T)₁₂	del(T)₁₀	del(T)₉	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆
GRCh38.p14 chr 17	NC_000017.11:g.75677756_75677776=	NC_000017.11:g.75677765_75677776del	NC_000017.11:g.75677767_75677776del	NC_000017.11:g.75677768_75677776del	NC_000017.11:g.75677770_75677776del	NC_000017.11:g.75677772_75677776del	NC_000017.11:g.75677773_75677776del	NC_000017.11:g.75677774_75677776del	NC_000017.11:g.75677775_75677776del	NC_000017.11:g.75677776del	NC_000017.11:g.75677776dup	NC_000017.11:g.75677775_75677776dup	NC_000017.11:g.75677774_75677776dup	NC_000017.11:g.75677773_75677776dup	NC_000017.11:g.75677772_75677776dup	NC_000017.11:g.75677771_75677776dup
GRCh37.p13 chr 17	NC_000017.10:g.73673836_73673856=	NC_000017.10:g.73673845_73673856del	NC_000017.10:g.73673847_73673856del	NC_000017.10:g.73673848_73673856del	NC_000017.10:g.73673850_73673856del	NC_000017.10:g.73673852_73673856del	NC_000017.10:g.73673853_73673856del	NC_000017.10:g.73673854_73673856del	NC_000017.10:g.73673855_73673856del	NC_000017.10:g.73673856del	NC_000017.10:g.73673856dup	NC_000017.10:g.73673855_73673856dup	NC_000017.10:g.73673854_73673856dup	NC_000017.10:g.73673853_73673856dup	NC_000017.10:g.73673852_73673856dup	NC_000017.10:g.73673851_73673856dup
SAP30BP transcript variant 3	NM_001301839.2:c.216+9131=	NM_001301839.2:c.216+9140_216+9151del	NM_001301839.2:c.216+9142_216+9151del	NM_001301839.2:c.216+9143_216+9151del	NM_001301839.2:c.216+9145_216+9151del	NM_001301839.2:c.216+9147_216+9151del	NM_001301839.2:c.216+9148_216+9151del	NM_001301839.2:c.216+9149_216+9151del	NM_001301839.2:c.216+9150_216+9151del	NM_001301839.2:c.216+9151del	NM_001301839.2:c.216+9151dup	NM_001301839.2:c.216+9150_216+9151dup	NM_001301839.2:c.216+9149_216+9151dup	NM_001301839.2:c.216+9148_216+9151dup	NM_001301839.2:c.216+9147_216+9151dup	NM_001301839.2:c.216+9146_216+9151dup
SAP30BP transcript variant 1	NM_001301855.2:c.264+5893=	NM_001301855.2:c.264+5902_264+5913del	NM_001301855.2:c.264+5904_264+5913del	NM_001301855.2:c.264+5905_264+5913del	NM_001301855.2:c.264+5907_264+5913del	NM_001301855.2:c.264+5909_264+5913del	NM_001301855.2:c.264+5910_264+5913del	NM_001301855.2:c.264+5911_264+5913del	NM_001301855.2:c.264+5912_264+5913del	NM_001301855.2:c.264+5913del	NM_001301855.2:c.264+5913dup	NM_001301855.2:c.264+5912_264+5913dup	NM_001301855.2:c.264+5911_264+5913dup	NM_001301855.2:c.264+5910_264+5913dup	NM_001301855.2:c.264+5909_264+5913dup	NM_001301855.2:c.264+5908_264+5913dup
SAP30BP transcript	NM_013260.6:c.264+5893=	NM_013260.6:c.264+5902_264+5913del	NM_013260.6:c.264+5904_264+5913del	NM_013260.6:c.264+5905_264+5913del	NM_013260.6:c.264+5907_264+5913del	NM_013260.6:c.264+5909_264+5913del	NM_013260.6:c.264+5910_264+5913del	NM_013260.6:c.264+5911_264+5913del	NM_013260.6:c.264+5912_264+5913del	NM_013260.6:c.264+5913del	NM_013260.6:c.264+5913dup	NM_013260.6:c.264+5912_264+5913dup	NM_013260.6:c.264+5911_264+5913dup	NM_013260.6:c.264+5910_264+5913dup	NM_013260.6:c.264+5909_264+5913dup	NM_013260.6:c.264+5908_264+5913dup
SAP30BP transcript variant 2	NM_013260.8:c.264+5893=	NM_013260.8:c.264+5902_264+5913del	NM_013260.8:c.264+5904_264+5913del	NM_013260.8:c.264+5905_264+5913del	NM_013260.8:c.264+5907_264+5913del	NM_013260.8:c.264+5909_264+5913del	NM_013260.8:c.264+5910_264+5913del	NM_013260.8:c.264+5911_264+5913del	NM_013260.8:c.264+5912_264+5913del	NM_013260.8:c.264+5913del	NM_013260.8:c.264+5913dup	NM_013260.8:c.264+5912_264+5913dup	NM_013260.8:c.264+5911_264+5913dup	NM_013260.8:c.264+5910_264+5913dup	NM_013260.8:c.264+5909_264+5913dup	NM_013260.8:c.264+5908_264+5913dup
SAP30BP transcript variant X1	XM_005257256.1:c.216+9131=	XM_005257256.1:c.216+9140_216+9151del	XM_005257256.1:c.216+9142_216+9151del	XM_005257256.1:c.216+9143_216+9151del	XM_005257256.1:c.216+9145_216+9151del	XM_005257256.1:c.216+9147_216+9151del	XM_005257256.1:c.216+9148_216+9151del	XM_005257256.1:c.216+9149_216+9151del	XM_005257256.1:c.216+9150_216+9151del	XM_005257256.1:c.216+9151del	XM_005257256.1:c.216+9151dup	XM_005257256.1:c.216+9150_216+9151dup	XM_005257256.1:c.216+9149_216+9151dup	XM_005257256.1:c.216+9148_216+9151dup	XM_005257256.1:c.216+9147_216+9151dup	XM_005257256.1:c.216+9146_216+9151dup
SAP30BP transcript variant X3	XM_005257258.1:c.264+5893=	XM_005257258.1:c.264+5902_264+5913del	XM_005257258.1:c.264+5904_264+5913del	XM_005257258.1:c.264+5905_264+5913del	XM_005257258.1:c.264+5907_264+5913del	XM_005257258.1:c.264+5909_264+5913del	XM_005257258.1:c.264+5910_264+5913del	XM_005257258.1:c.264+5911_264+5913del	XM_005257258.1:c.264+5912_264+5913del	XM_005257258.1:c.264+5913del	XM_005257258.1:c.264+5913dup	XM_005257258.1:c.264+5912_264+5913dup	XM_005257258.1:c.264+5911_264+5913dup	XM_005257258.1:c.264+5910_264+5913dup	XM_005257258.1:c.264+5909_264+5913dup	XM_005257258.1:c.264+5908_264+5913dup
SAP30BP transcript variant X1	XM_011524693.4:c.264+5893=	XM_011524693.4:c.264+5902_264+5913del	XM_011524693.4:c.264+5904_264+5913del	XM_011524693.4:c.264+5905_264+5913del	XM_011524693.4:c.264+5907_264+5913del	XM_011524693.4:c.264+5909_264+5913del	XM_011524693.4:c.264+5910_264+5913del	XM_011524693.4:c.264+5911_264+5913del	XM_011524693.4:c.264+5912_264+5913del	XM_011524693.4:c.264+5913del	XM_011524693.4:c.264+5913dup	XM_011524693.4:c.264+5912_264+5913dup	XM_011524693.4:c.264+5911_264+5913dup	XM_011524693.4:c.264+5910_264+5913dup	XM_011524693.4:c.264+5909_264+5913dup	XM_011524693.4:c.264+5908_264+5913dup
SAP30BP transcript variant X2	XM_011524694.3:c.216+9131=	XM_011524694.3:c.216+9140_216+9151del	XM_011524694.3:c.216+9142_216+9151del	XM_011524694.3:c.216+9143_216+9151del	XM_011524694.3:c.216+9145_216+9151del	XM_011524694.3:c.216+9147_216+9151del	XM_011524694.3:c.216+9148_216+9151del	XM_011524694.3:c.216+9149_216+9151del	XM_011524694.3:c.216+9150_216+9151del	XM_011524694.3:c.216+9151del	XM_011524694.3:c.216+9151dup	XM_011524694.3:c.216+9150_216+9151dup	XM_011524694.3:c.216+9149_216+9151dup	XM_011524694.3:c.216+9148_216+9151dup	XM_011524694.3:c.216+9147_216+9151dup	XM_011524694.3:c.216+9146_216+9151dup
SAP30BP transcript variant X3	XM_047435870.1:c.-47+5893=	XM_047435870.1:c.-47+5902_-47+5913del	XM_047435870.1:c.-47+5904_-47+5913del	XM_047435870.1:c.-47+5905_-47+5913del	XM_047435870.1:c.-47+5907_-47+5913del	XM_047435870.1:c.-47+5909_-47+5913del	XM_047435870.1:c.-47+5910_-47+5913del	XM_047435870.1:c.-47+5911_-47+5913del	XM_047435870.1:c.-47+5912_-47+5913del	XM_047435870.1:c.-47+5913del	XM_047435870.1:c.-47+5913dup	XM_047435870.1:c.-47+5912_-47+5913dup	XM_047435870.1:c.-47+5911_-47+5913dup	XM_047435870.1:c.-47+5910_-47+5913dup	XM_047435870.1:c.-47+5909_-47+5913dup	XM_047435870.1:c.-47+5908_-47+5913dup
SAP30BP transcript variant X4	XM_047435871.1:c.-47+5893=	XM_047435871.1:c.-47+5902_-47+5913del	XM_047435871.1:c.-47+5904_-47+5913del	XM_047435871.1:c.-47+5905_-47+5913del	XM_047435871.1:c.-47+5907_-47+5913del	XM_047435871.1:c.-47+5909_-47+5913del	XM_047435871.1:c.-47+5910_-47+5913del	XM_047435871.1:c.-47+5911_-47+5913del	XM_047435871.1:c.-47+5912_-47+5913del	XM_047435871.1:c.-47+5913del	XM_047435871.1:c.-47+5913dup	XM_047435871.1:c.-47+5912_-47+5913dup	XM_047435871.1:c.-47+5911_-47+5913dup	XM_047435871.1:c.-47+5910_-47+5913dup	XM_047435871.1:c.-47+5909_-47+5913dup	XM_047435871.1:c.-47+5908_-47+5913dup
SAP30BP transcript variant X5	XM_047435872.1:c.264+5893=	XM_047435872.1:c.264+5902_264+5913del	XM_047435872.1:c.264+5904_264+5913del	XM_047435872.1:c.264+5905_264+5913del	XM_047435872.1:c.264+5907_264+5913del	XM_047435872.1:c.264+5909_264+5913del	XM_047435872.1:c.264+5910_264+5913del	XM_047435872.1:c.264+5911_264+5913del	XM_047435872.1:c.264+5912_264+5913del	XM_047435872.1:c.264+5913del	XM_047435872.1:c.264+5913dup	XM_047435872.1:c.264+5912_264+5913dup	XM_047435872.1:c.264+5911_264+5913dup	XM_047435872.1:c.264+5910_264+5913dup	XM_047435872.1:c.264+5909_264+5913dup	XM_047435872.1:c.264+5908_264+5913dup

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#.

36 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40837264	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss95701194	Oct 12, 2018 (152)
3	PJP	ss294924096	May 31, 2013 (138)
4	PJP	ss294924097	Oct 12, 2018 (152)
5	1000GENOMES	ss1376958914	Aug 21, 2014 (142)
6	SWEGEN	ss3015910558	Nov 08, 2017 (151)
7	KHV_HUMAN_GENOMES	ss3820203658	Jul 13, 2019 (153)
8	EVA	ss3834980230	Apr 27, 2020 (154)
9	KRGDB	ss3936000184	Apr 27, 2020 (154)
10	GNOMAD	ss4315733014	Apr 27, 2021 (155)
11	GNOMAD	ss4315733015	Apr 27, 2021 (155)
12	GNOMAD	ss4315733016	Apr 27, 2021 (155)
13	GNOMAD	ss4315733017	Apr 27, 2021 (155)
14	GNOMAD	ss4315733019	Apr 27, 2021 (155)
15	GNOMAD	ss4315733020	Apr 27, 2021 (155)
16	GNOMAD	ss4315733021	Apr 27, 2021 (155)
17	GNOMAD	ss4315733022	Apr 27, 2021 (155)
18	GNOMAD	ss4315733023	Apr 27, 2021 (155)
19	GNOMAD	ss4315733024	Apr 27, 2021 (155)
20	TOMMO_GENOMICS	ss5223498214	Apr 27, 2021 (155)
21	TOMMO_GENOMICS	ss5223498215	Apr 27, 2021 (155)
22	TOMMO_GENOMICS	ss5223498216	Apr 27, 2021 (155)
23	1000G_HIGH_COVERAGE	ss5303949701	Oct 16, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5303949702	Oct 16, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5303949703	Oct 16, 2022 (156)
26	1000G_HIGH_COVERAGE	ss5303949704	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5496913127	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5496913128	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5496913129	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5496913130	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5780048901	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5780048902	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5780048903	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5780048905	Oct 16, 2022 (156)
35	EVA	ss5834293922	Oct 16, 2022 (156)
36	EVA	ss5851898047	Oct 16, 2022 (156)
37	1000Genomes	NC_000017.10 - 73673836	Oct 12, 2018 (152)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 513998009 (NC_000017.11:75677755::T 35650/109776) Row 513998010 (NC_000017.11:75677755::TT 1129/109850) Row 513998011 (NC_000017.11:75677755::TTT 4/109872)...	-	Apr 27, 2021 (155)
48	KOREAN population from KRGDB	NC_000017.10 - 73673836	Apr 27, 2020 (154)
49	8.3KJPN Submission ignored due to conflicting rows: Row 81467521 (NC_000017.10:73673835::T 8601/16592) Row 81467522 (NC_000017.10:73673835:T: 699/16592) Row 81467523 (NC_000017.10:73673835::TT 63/16592)	-	Apr 27, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 81467521 (NC_000017.10:73673835::T 8601/16592) Row 81467522 (NC_000017.10:73673835:T: 699/16592) Row 81467523 (NC_000017.10:73673835::TT 63/16592)	-	Apr 27, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 81467521 (NC_000017.10:73673835::T 8601/16592) Row 81467522 (NC_000017.10:73673835:T: 699/16592) Row 81467523 (NC_000017.10:73673835::TT 63/16592)	-	Apr 27, 2021 (155)
52	14KJPN Submission ignored due to conflicting rows: Row 113886005 (NC_000017.11:75677755::T 14549/28092) Row 113886006 (NC_000017.11:75677755:T: 1192/28092) Row 113886007 (NC_000017.11:75677755::TT 86/28092)...	-	Oct 16, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 113886005 (NC_000017.11:75677755::T 14549/28092) Row 113886006 (NC_000017.11:75677755:T: 1192/28092) Row 113886007 (NC_000017.11:75677755::TT 86/28092)...	-	Oct 16, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 113886005 (NC_000017.11:75677755::T 14549/28092) Row 113886006 (NC_000017.11:75677755:T: 1192/28092) Row 113886007 (NC_000017.11:75677755::TT 86/28092)...	-	Oct 16, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 113886005 (NC_000017.11:75677755::T 14549/28092) Row 113886006 (NC_000017.11:75677755:T: 1192/28092) Row 113886007 (NC_000017.11:75677755::TT 86/28092)...	-	Oct 16, 2022 (156)
56	ALFA	NC_000017.11 - 75677756	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
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3015910558	NC_000017.10:73673835:TTTTTTTTTT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4315733024	NC_000017.11:75677755:TTTTTTTTT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4315733023	NC_000017.11:75677755:TTTTT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4315733022	NC_000017.11:75677755:TTTT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4315733021	NC_000017.11:75677755:TTT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5834293922	NC_000017.10:73673835:TT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT
ss4315733020, ss5303949704, ss5496913127	NC_000017.11:75677755:TT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5223498215	NC_000017.10:73673835:T:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4315733019, ss5303949701, ss5496913128, ss5780048902	NC_000017.11:75677755:T:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294924096	NC_000017.9:71185431::T	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss294924097	NC_000017.9:71185451::T	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
72837484, 43177578, ss1376958914, ss3834980230, ss3936000184, ss5223498214	NC_000017.10:73673835::T	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3820203658, ss4315733014, ss5303949702, ss5496913129, ss5780048901, ss5851898047	NC_000017.11:75677755::T	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss40837264	NT_010783.15:38947987::T	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss95701194	NT_010783.15:38948008::T	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5223498216	NC_000017.10:73673835::TT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4315733015, ss5303949703, ss5496913130, ss5780048903	NC_000017.11:75677755::TT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4315733016	NC_000017.11:75677755::TTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4315733017, ss5780048905	NC_000017.11:75677755::TTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
5607350858	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3268914311	NC_000017.11:75677755::TTTT	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
ss3268914320	NC_000017.11:75677755:TTTTTTTTTTTT:	NC_000017.11:75677755:TTTTTTTTTTTT… NC_000017.11:75677755:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT

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

No publications for rs35174866

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

rs35174866