Name: rs533558064
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.

rs533558064

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:6593330-6593348 (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)₁₀ / del(T)₆ / del(T)₅ / del…
del(T)₁₀ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.01243 (194/15602, ALFA)
delT=0.0980 (491/5008, 1000G)
delT=0.30 (12/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: INTS15 : 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	15602	TTTTTTTTTTTTTTTTTTT=0.98648	TTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00077, TTTTTTTTTTTTTTTTTTTTT=0.01243, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00026, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00006, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.977392	0.002312	0.020295	32
European	Sub	12804	TTTTTTTTTTTTTTTTTTT=0.98360	TTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00094, TTTTTTTTTTTTTTTTTTTTT=0.01507, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00031, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00008, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.972596	0.002819	0.024585	32
African	Sub	1652	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	56	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1596	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	76	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	104	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	504	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	76	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	368	TTTTTTTTTTTTTTTTTTT=0.997	TTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	0.994565	0.0	0.005435	0

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	15602	(T)₁₉=0.98648	del(T)₁₀=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00077, dupTT=0.01243, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₆=0.00006, dup(T)₇=0.00026
Allele Frequency Aggregator	European	Sub	12804	(T)₁₉=0.98360	del(T)₁₀=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00094, dupTT=0.01507, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₆=0.00008, dup(T)₇=0.00031
Allele Frequency Aggregator	African	Sub	1652	(T)₁₉=1.0000	del(T)₁₀=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	504	(T)₁₉=1.000	del(T)₁₀=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	368	(T)₁₉=0.997	del(T)₁₀=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.003, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	104	(T)₁₉=1.000	del(T)₁₀=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Asian	Sub	94	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	76	(T)₁₉=1.00	del(T)₁₀=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₆=0.00, dup(T)₇=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₉=0.9020	delT=0.0980
1000Genomes	African	Sub	1322	(T)₁₉=0.8918	delT=0.1082
1000Genomes	East Asian	Sub	1008	(T)₁₉=0.9296	delT=0.0704
1000Genomes	Europe	Sub	1006	(T)₁₉=0.9155	delT=0.0845
1000Genomes	South Asian	Sub	978	(T)₁₉=0.893	delT=0.107
1000Genomes	American	Sub	694	(T)₁₉=0.875	delT=0.125
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₉=0.70	delT=0.30

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.6593339_6593348del
GRCh38.p14 chr 7	NC_000007.14:g.6593343_6593348del
GRCh38.p14 chr 7	NC_000007.14:g.6593344_6593348del
GRCh38.p14 chr 7	NC_000007.14:g.6593345_6593348del
GRCh38.p14 chr 7	NC_000007.14:g.6593346_6593348del
GRCh38.p14 chr 7	NC_000007.14:g.6593347_6593348del
GRCh38.p14 chr 7	NC_000007.14:g.6593348del
GRCh38.p14 chr 7	NC_000007.14:g.6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593347_6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593346_6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593345_6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593344_6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593343_6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593342_6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593341_6593348dup
GRCh38.p14 chr 7	NC_000007.14:g.6593340_6593348dup
GRCh37.p13 chr 7	NC_000007.13:g.6632970_6632979del
GRCh37.p13 chr 7	NC_000007.13:g.6632974_6632979del
GRCh37.p13 chr 7	NC_000007.13:g.6632975_6632979del
GRCh37.p13 chr 7	NC_000007.13:g.6632976_6632979del
GRCh37.p13 chr 7	NC_000007.13:g.6632977_6632979del
GRCh37.p13 chr 7	NC_000007.13:g.6632978_6632979del
GRCh37.p13 chr 7	NC_000007.13:g.6632979del
GRCh37.p13 chr 7	NC_000007.13:g.6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632978_6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632977_6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632976_6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632975_6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632974_6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632973_6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632972_6632979dup
GRCh37.p13 chr 7	NC_000007.13:g.6632971_6632979dup

Gene: INTS15, integrator complex subunit 15 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
INTS15 transcript variant 2	NM_001303039.2:c.358-1096… NM_001303039.2:c.358-1096_358-1087del	N/A	Intron Variant
INTS15 transcript variant 1	NM_024067.4:c.415-1096_41… NM_024067.4:c.415-1096_415-1087del	N/A	Intron Variant
INTS15 transcript variant X1	XM_005249845.6:c.415-1096… XM_005249845.6:c.415-1096_415-1087del	N/A	Intron Variant
INTS15 transcript variant X2	XM_011515518.4:c.415-1096… XM_011515518.4:c.415-1096_415-1087del	N/A	Intron Variant
INTS15 transcript variant X3	XM_017012614.3:c.85-1096_… XM_017012614.3:c.85-1096_85-1087del	N/A	Intron Variant
INTS15 transcript variant X5	XM_047420833.1:c.415-1096… XM_047420833.1:c.415-1096_415-1087del	N/A	Intron Variant
INTS15 transcript variant X4	XR_926946.4:n.	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₁₉=	del(T)₁₀	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉
GRCh38.p14 chr 7	NC_000007.14:g.6593330_6593348=	NC_000007.14:g.6593339_6593348del	NC_000007.14:g.6593343_6593348del	NC_000007.14:g.6593344_6593348del	NC_000007.14:g.6593345_6593348del	NC_000007.14:g.6593346_6593348del	NC_000007.14:g.6593347_6593348del	NC_000007.14:g.6593348del	NC_000007.14:g.6593348dup	NC_000007.14:g.6593347_6593348dup	NC_000007.14:g.6593346_6593348dup	NC_000007.14:g.6593345_6593348dup	NC_000007.14:g.6593344_6593348dup	NC_000007.14:g.6593343_6593348dup	NC_000007.14:g.6593342_6593348dup	NC_000007.14:g.6593341_6593348dup	NC_000007.14:g.6593340_6593348dup
GRCh37.p13 chr 7	NC_000007.13:g.6632961_6632979=	NC_000007.13:g.6632970_6632979del	NC_000007.13:g.6632974_6632979del	NC_000007.13:g.6632975_6632979del	NC_000007.13:g.6632976_6632979del	NC_000007.13:g.6632977_6632979del	NC_000007.13:g.6632978_6632979del	NC_000007.13:g.6632979del	NC_000007.13:g.6632979dup	NC_000007.13:g.6632978_6632979dup	NC_000007.13:g.6632977_6632979dup	NC_000007.13:g.6632976_6632979dup	NC_000007.13:g.6632975_6632979dup	NC_000007.13:g.6632974_6632979dup	NC_000007.13:g.6632973_6632979dup	NC_000007.13:g.6632972_6632979dup	NC_000007.13:g.6632971_6632979dup
INTS15 transcript variant 2	NM_001303039.2:c.358-1105=	NM_001303039.2:c.358-1096_358-1087del	NM_001303039.2:c.358-1092_358-1087del	NM_001303039.2:c.358-1091_358-1087del	NM_001303039.2:c.358-1090_358-1087del	NM_001303039.2:c.358-1089_358-1087del	NM_001303039.2:c.358-1088_358-1087del	NM_001303039.2:c.358-1087del	NM_001303039.2:c.358-1087dup	NM_001303039.2:c.358-1088_358-1087dup	NM_001303039.2:c.358-1089_358-1087dup	NM_001303039.2:c.358-1090_358-1087dup	NM_001303039.2:c.358-1091_358-1087dup	NM_001303039.2:c.358-1092_358-1087dup	NM_001303039.2:c.358-1093_358-1087dup	NM_001303039.2:c.358-1094_358-1087dup	NM_001303039.2:c.358-1095_358-1087dup
C7orf26 transcript	NM_024067.2:c.415-1105=	NM_024067.2:c.415-1096_415-1087del	NM_024067.2:c.415-1092_415-1087del	NM_024067.2:c.415-1091_415-1087del	NM_024067.2:c.415-1090_415-1087del	NM_024067.2:c.415-1089_415-1087del	NM_024067.2:c.415-1088_415-1087del	NM_024067.2:c.415-1087del	NM_024067.2:c.415-1087dup	NM_024067.2:c.415-1088_415-1087dup	NM_024067.2:c.415-1089_415-1087dup	NM_024067.2:c.415-1090_415-1087dup	NM_024067.2:c.415-1091_415-1087dup	NM_024067.2:c.415-1092_415-1087dup	NM_024067.2:c.415-1093_415-1087dup	NM_024067.2:c.415-1094_415-1087dup	NM_024067.2:c.415-1095_415-1087dup
INTS15 transcript variant 1	NM_024067.4:c.415-1105=	NM_024067.4:c.415-1096_415-1087del	NM_024067.4:c.415-1092_415-1087del	NM_024067.4:c.415-1091_415-1087del	NM_024067.4:c.415-1090_415-1087del	NM_024067.4:c.415-1089_415-1087del	NM_024067.4:c.415-1088_415-1087del	NM_024067.4:c.415-1087del	NM_024067.4:c.415-1087dup	NM_024067.4:c.415-1088_415-1087dup	NM_024067.4:c.415-1089_415-1087dup	NM_024067.4:c.415-1090_415-1087dup	NM_024067.4:c.415-1091_415-1087dup	NM_024067.4:c.415-1092_415-1087dup	NM_024067.4:c.415-1093_415-1087dup	NM_024067.4:c.415-1094_415-1087dup	NM_024067.4:c.415-1095_415-1087dup
C7orf26 transcript variant X1	XM_005249845.1:c.415-1105=	XM_005249845.1:c.415-1096_415-1087del	XM_005249845.1:c.415-1092_415-1087del	XM_005249845.1:c.415-1091_415-1087del	XM_005249845.1:c.415-1090_415-1087del	XM_005249845.1:c.415-1089_415-1087del	XM_005249845.1:c.415-1088_415-1087del	XM_005249845.1:c.415-1087del	XM_005249845.1:c.415-1087dup	XM_005249845.1:c.415-1088_415-1087dup	XM_005249845.1:c.415-1089_415-1087dup	XM_005249845.1:c.415-1090_415-1087dup	XM_005249845.1:c.415-1091_415-1087dup	XM_005249845.1:c.415-1092_415-1087dup	XM_005249845.1:c.415-1093_415-1087dup	XM_005249845.1:c.415-1094_415-1087dup	XM_005249845.1:c.415-1095_415-1087dup
INTS15 transcript variant X1	XM_005249845.6:c.415-1105=	XM_005249845.6:c.415-1096_415-1087del	XM_005249845.6:c.415-1092_415-1087del	XM_005249845.6:c.415-1091_415-1087del	XM_005249845.6:c.415-1090_415-1087del	XM_005249845.6:c.415-1089_415-1087del	XM_005249845.6:c.415-1088_415-1087del	XM_005249845.6:c.415-1087del	XM_005249845.6:c.415-1087dup	XM_005249845.6:c.415-1088_415-1087dup	XM_005249845.6:c.415-1089_415-1087dup	XM_005249845.6:c.415-1090_415-1087dup	XM_005249845.6:c.415-1091_415-1087dup	XM_005249845.6:c.415-1092_415-1087dup	XM_005249845.6:c.415-1093_415-1087dup	XM_005249845.6:c.415-1094_415-1087dup	XM_005249845.6:c.415-1095_415-1087dup
C7orf26 transcript variant X2	XM_005249846.1:c.358-1105=	XM_005249846.1:c.358-1096_358-1087del	XM_005249846.1:c.358-1092_358-1087del	XM_005249846.1:c.358-1091_358-1087del	XM_005249846.1:c.358-1090_358-1087del	XM_005249846.1:c.358-1089_358-1087del	XM_005249846.1:c.358-1088_358-1087del	XM_005249846.1:c.358-1087del	XM_005249846.1:c.358-1087dup	XM_005249846.1:c.358-1088_358-1087dup	XM_005249846.1:c.358-1089_358-1087dup	XM_005249846.1:c.358-1090_358-1087dup	XM_005249846.1:c.358-1091_358-1087dup	XM_005249846.1:c.358-1092_358-1087dup	XM_005249846.1:c.358-1093_358-1087dup	XM_005249846.1:c.358-1094_358-1087dup	XM_005249846.1:c.358-1095_358-1087dup
INTS15 transcript variant X2	XM_011515518.4:c.415-1105=	XM_011515518.4:c.415-1096_415-1087del	XM_011515518.4:c.415-1092_415-1087del	XM_011515518.4:c.415-1091_415-1087del	XM_011515518.4:c.415-1090_415-1087del	XM_011515518.4:c.415-1089_415-1087del	XM_011515518.4:c.415-1088_415-1087del	XM_011515518.4:c.415-1087del	XM_011515518.4:c.415-1087dup	XM_011515518.4:c.415-1088_415-1087dup	XM_011515518.4:c.415-1089_415-1087dup	XM_011515518.4:c.415-1090_415-1087dup	XM_011515518.4:c.415-1091_415-1087dup	XM_011515518.4:c.415-1092_415-1087dup	XM_011515518.4:c.415-1093_415-1087dup	XM_011515518.4:c.415-1094_415-1087dup	XM_011515518.4:c.415-1095_415-1087dup
INTS15 transcript variant X3	XM_017012614.3:c.85-1105=	XM_017012614.3:c.85-1096_85-1087del	XM_017012614.3:c.85-1092_85-1087del	XM_017012614.3:c.85-1091_85-1087del	XM_017012614.3:c.85-1090_85-1087del	XM_017012614.3:c.85-1089_85-1087del	XM_017012614.3:c.85-1088_85-1087del	XM_017012614.3:c.85-1087del	XM_017012614.3:c.85-1087dup	XM_017012614.3:c.85-1088_85-1087dup	XM_017012614.3:c.85-1089_85-1087dup	XM_017012614.3:c.85-1090_85-1087dup	XM_017012614.3:c.85-1091_85-1087dup	XM_017012614.3:c.85-1092_85-1087dup	XM_017012614.3:c.85-1093_85-1087dup	XM_017012614.3:c.85-1094_85-1087dup	XM_017012614.3:c.85-1095_85-1087dup
INTS15 transcript variant X5	XM_047420833.1:c.415-1105=	XM_047420833.1:c.415-1096_415-1087del	XM_047420833.1:c.415-1092_415-1087del	XM_047420833.1:c.415-1091_415-1087del	XM_047420833.1:c.415-1090_415-1087del	XM_047420833.1:c.415-1089_415-1087del	XM_047420833.1:c.415-1088_415-1087del	XM_047420833.1:c.415-1087del	XM_047420833.1:c.415-1087dup	XM_047420833.1:c.415-1088_415-1087dup	XM_047420833.1:c.415-1089_415-1087dup	XM_047420833.1:c.415-1090_415-1087dup	XM_047420833.1:c.415-1091_415-1087dup	XM_047420833.1:c.415-1092_415-1087dup	XM_047420833.1:c.415-1093_415-1087dup	XM_047420833.1:c.415-1094_415-1087dup	XM_047420833.1:c.415-1095_415-1087dup

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#.

42 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SSIP	ss947188545	Aug 21, 2014 (142)
2	1000GENOMES	ss1376711496	Aug 21, 2014 (142)
3	EVA_GENOME_DK	ss1576932979	Apr 01, 2015 (144)
4	SWEGEN	ss3000546588	Nov 08, 2017 (151)
5	SWEGEN	ss3000546589	Nov 08, 2017 (151)
6	SWEGEN	ss3000546590	Nov 08, 2017 (151)
7	KHV_HUMAN_GENOMES	ss3809289738	Jul 13, 2019 (153)
8	EVA	ss3830385446	Apr 26, 2020 (154)
9	GNOMAD	ss4157566168	Apr 26, 2021 (155)
10	GNOMAD	ss4157566169	Apr 26, 2021 (155)
11	GNOMAD	ss4157566170	Apr 26, 2021 (155)
12	GNOMAD	ss4157566171	Apr 26, 2021 (155)
13	GNOMAD	ss4157566172	Apr 26, 2021 (155)
14	GNOMAD	ss4157566173	Apr 26, 2021 (155)
15	GNOMAD	ss4157566174	Apr 26, 2021 (155)
16	GNOMAD	ss4157566175	Apr 26, 2021 (155)
17	GNOMAD	ss4157566176	Apr 26, 2021 (155)
18	GNOMAD	ss4157566178	Apr 26, 2021 (155)
19	GNOMAD	ss4157566179	Apr 26, 2021 (155)
20	GNOMAD	ss4157566180	Apr 26, 2021 (155)
21	GNOMAD	ss4157566181	Apr 26, 2021 (155)
22	GNOMAD	ss4157566182	Apr 26, 2021 (155)
23	TOPMED	ss4733953020	Apr 26, 2021 (155)
24	TOPMED	ss4733953021	Apr 26, 2021 (155)
25	TOPMED	ss4733953022	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5181604859	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5181604860	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5181604861	Apr 26, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5271656212	Oct 13, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5271656213	Oct 13, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5271656214	Oct 13, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5271656215	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5271656216	Oct 13, 2022 (156)
34	HUGCELL_USP	ss5468961645	Oct 13, 2022 (156)
35	HUGCELL_USP	ss5468961646	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5468961647	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5468961648	Oct 13, 2022 (156)
38	TOMMO_GENOMICS	ss5721001699	Oct 13, 2022 (156)
39	TOMMO_GENOMICS	ss5721001700	Oct 13, 2022 (156)
40	TOMMO_GENOMICS	ss5721001701	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5721001703	Oct 13, 2022 (156)
42	EVA	ss5855739558	Oct 13, 2022 (156)
43	1000Genomes	NC_000007.13 - 6632961	Oct 12, 2018 (152)
44	The Danish reference pan genome	NC_000007.13 - 6632961	Apr 26, 2020 (154)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 251528651 (NC_000007.14:6593329::T 1887/120140) Row 251528652 (NC_000007.14:6593329::TT 13711/120086) Row 251528653 (NC_000007.14:6593329::TTT 582/120156)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 39574166 (NC_000007.13:6632960::T 70/16752) Row 39574167 (NC_000007.13:6632960::TT 275/16752) Row 39574168 (NC_000007.13:6632960:T: 16/16752)	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 39574166 (NC_000007.13:6632960::T 70/16752) Row 39574167 (NC_000007.13:6632960::TT 275/16752) Row 39574168 (NC_000007.13:6632960:T: 16/16752)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 39574166 (NC_000007.13:6632960::T 70/16752) Row 39574167 (NC_000007.13:6632960::TT 275/16752) Row 39574168 (NC_000007.13:6632960:T: 16/16752)	-	Apr 26, 2021 (155)
63	14KJPN Submission ignored due to conflicting rows: Row 54838803 (NC_000007.14:6593329::TT 547/28258) Row 54838804 (NC_000007.14:6593329::T 115/28258) Row 54838805 (NC_000007.14:6593329:T: 27/28258)...	-	Oct 13, 2022 (156)
64	14KJPN Submission ignored due to conflicting rows: Row 54838803 (NC_000007.14:6593329::TT 547/28258) Row 54838804 (NC_000007.14:6593329::T 115/28258) Row 54838805 (NC_000007.14:6593329:T: 27/28258)...	-	Oct 13, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 54838803 (NC_000007.14:6593329::TT 547/28258) Row 54838804 (NC_000007.14:6593329::T 115/28258) Row 54838805 (NC_000007.14:6593329:T: 27/28258)...	-	Oct 13, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 54838803 (NC_000007.14:6593329::TT 547/28258) Row 54838804 (NC_000007.14:6593329::T 115/28258) Row 54838805 (NC_000007.14:6593329:T: 27/28258)...	-	Oct 13, 2022 (156)
67	TopMed Submission ignored due to conflicting rows: Row 571330579 (NC_000007.14:6593329:TTTTT: 1/264690) Row 571330580 (NC_000007.14:6593329:TTTTTT: 9/264690) Row 571330581 (NC_000007.14:6593329:TTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
68	TopMed Submission ignored due to conflicting rows: Row 571330579 (NC_000007.14:6593329:TTTTT: 1/264690) Row 571330580 (NC_000007.14:6593329:TTTTTT: 9/264690) Row 571330581 (NC_000007.14:6593329:TTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
69	TopMed Submission ignored due to conflicting rows: Row 571330579 (NC_000007.14:6593329:TTTTT: 1/264690) Row 571330580 (NC_000007.14:6593329:TTTTTT: 9/264690) Row 571330581 (NC_000007.14:6593329:TTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
70	ALFA	NC_000007.14 - 6593330	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
ss4733953022	NC_000007.14:6593329:TTTTTTTTTT:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4157566182, ss4733953021	NC_000007.14:6593329:TTTTTT:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4157566181, ss4733953020	NC_000007.14:6593329:TTTTT:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4157566180	NC_000007.14:6593329:TTTT:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4157566179	NC_000007.14:6593329:TTT:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4157566178	NC_000007.14:6593329:TT:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
35654083, 1129932, ss1376711496, ss1576932979, ss5181604861	NC_000007.13:6632960:T:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3809289738, ss5271656215, ss5468961645, ss5721001701, ss5855739558	NC_000007.14:6593329:T:	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3000546590, ss3830385446, ss5181604859	NC_000007.13:6632960::T	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4157566168, ss5271656214, ss5468961646, ss5721001700	NC_000007.14:6593329::T	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3000546589, ss5181604860	NC_000007.13:6632960::TT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss947188545	NC_000007.13:6632961::TT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566169, ss5271656213, ss5468961647, ss5721001699	NC_000007.14:6593329::TT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566170, ss5271656212, ss5468961648	NC_000007.14:6593329::TTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566171	NC_000007.14:6593329::TTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566172	NC_000007.14:6593329::TTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566173	NC_000007.14:6593329::TTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3000546588	NC_000007.13:6632960::TTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566174, ss5271656216, ss5721001703	NC_000007.14:6593329::TTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
3368727187	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566175	NC_000007.14:6593329::TTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4157566176	NC_000007.14:6593329::TTTTTTTTT	NC_000007.14:6593329:TTTTTTTTTTTTT… NC_000007.14:6593329:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs533558064

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

rs533558064