Name: rs781912833
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.

rs781912833

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:102186596-102186604 (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)₄ / delTT / delT / dupT / du…
del(T)₄ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₄=0.00000 (0/11660, ALFA)
delTT=0.00000 (0/11660, ALFA)
delT=0.00000 (0/11660, ALFA) (+ 5 more)
dupT=0.00000 (0/11660, ALFA)
dupTT=0.00000 (0/11660, ALFA)
dupTTT=0.00000 (0/11660, ALFA)
dup(T)₄=0.00000 (0/11660, ALFA)
dupTT=0.131 (78/594, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CUX1 : 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	HWEP
Total	Global	11660	TTTTTTTTT=1.00000	TTTTT=0.00000, TTTTTTT=0.00000, TTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	8004	TTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2498	TTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	92	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	2406	TTTTTTTTT=1.0000	TTTTT=0.0000, TTTTTTT=0.0000, TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	102	TTTTTTTTT=1.000	TTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	76	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	26	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	108	TTTTTTTTT=1.000	TTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	484	TTTTTTTTT=1.000	TTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	78	TTTTTTTTT=1.00	TTTTT=0.00, TTTTTTT=0.00, TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	386	TTTTTTTTT=1.000	TTTTT=0.000, TTTTTTT=0.000, TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=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	11660	(T)₉=1.00000	del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000
Allele Frequency Aggregator	European	Sub	8004	(T)₉=1.0000	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
Allele Frequency Aggregator	African	Sub	2498	(T)₉=1.0000	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
Allele Frequency Aggregator	Latin American 2	Sub	484	(T)₉=1.000	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
Allele Frequency Aggregator	Other	Sub	386	(T)₉=1.000	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
Allele Frequency Aggregator	Latin American 1	Sub	108	(T)₉=1.000	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
Allele Frequency Aggregator	Asian	Sub	102	(T)₉=1.000	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
Allele Frequency Aggregator	South Asian	Sub	78	(T)₉=1.00	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
Northern Sweden	ACPOP	Study-wide	594	- No frequency provided	dupTT=0.131

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.102186601_102186604del
GRCh38.p14 chr 7	NC_000007.14:g.102186603_102186604del
GRCh38.p14 chr 7	NC_000007.14:g.102186604del
GRCh38.p14 chr 7	NC_000007.14:g.102186604dup
GRCh38.p14 chr 7	NC_000007.14:g.102186603_102186604dup
GRCh38.p14 chr 7	NC_000007.14:g.102186602_102186604dup
GRCh38.p14 chr 7	NC_000007.14:g.102186601_102186604dup
GRCh37.p13 chr 7	NC_000007.13:g.101829881_101829884del
GRCh37.p13 chr 7	NC_000007.13:g.101829883_101829884del
GRCh37.p13 chr 7	NC_000007.13:g.101829884del
GRCh37.p13 chr 7	NC_000007.13:g.101829884dup
GRCh37.p13 chr 7	NC_000007.13:g.101829883_101829884dup
GRCh37.p13 chr 7	NC_000007.13:g.101829882_101829884dup
GRCh37.p13 chr 7	NC_000007.13:g.101829881_101829884dup
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375698_375701del
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375700_375701del
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375701del
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375701dup
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375700_375701dup
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375699_375701dup
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375698_375701dup
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110931_110934del
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110933_110934del
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110934del
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110934dup
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110933_110934dup
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110932_110934dup
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110931_110934dup

Gene: CUX1, cut like homeobox 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CUX1 transcript variant 4	NM_001202543.2:c.1051-321… NM_001202543.2:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant 5	NM_001202544.3:c.1003-321… NM_001202544.3:c.1003-3212_1003-3209del	N/A	Intron Variant
CUX1 transcript variant 6	NM_001202545.3:c.913-3212… NM_001202545.3:c.913-3212_913-3209del	N/A	Intron Variant
CUX1 transcript variant 7	NM_001202546.3:c.934-3212… NM_001202546.3:c.934-3212_934-3209del	N/A	Intron Variant
CUX1 transcript variant 2	NM_001913.5:c.1051-3212_1… NM_001913.5:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant 3	NM_181500.4:c.1045-3212_1… NM_181500.4:c.1045-3212_1045-3209del	N/A	Intron Variant
CUX1 transcript variant 1	NM_181552.4:c.1018-3212_1… NM_181552.4:c.1018-3212_1018-3209del	N/A	Intron Variant
CUX1 transcript variant X1	XM_005250150.4:c.1018-321… XM_005250150.4:c.1018-3212_1018-3209del	N/A	Intron Variant
CUX1 transcript variant X18	XM_005250154.4:c.1018-321… XM_005250154.4:c.1018-3212_1018-3209del	N/A	Intron Variant
CUX1 transcript variant X4	XM_006715854.3:c.1018-321… XM_006715854.3:c.1018-3212_1018-3209del	N/A	Intron Variant
CUX1 transcript variant X13	XM_011515825.3:c.1051-321… XM_011515825.3:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant X12	XM_017011760.3:c.1045-321… XM_017011760.3:c.1045-3212_1045-3209del	N/A	Intron Variant
CUX1 transcript variant X8	XM_024446668.2:c.1012-321… XM_024446668.2:c.1012-3212_1012-3209del	N/A	Intron Variant
CUX1 transcript variant X2	XM_047419906.1:c.1012-321… XM_047419906.1:c.1012-3212_1012-3209del	N/A	Intron Variant
CUX1 transcript variant X3	XM_047419907.1:c.1012-321… XM_047419907.1:c.1012-3212_1012-3209del	N/A	Intron Variant
CUX1 transcript variant X5	XM_047419908.1:c.1051-321… XM_047419908.1:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant X6	XM_047419909.1:c.1045-321… XM_047419909.1:c.1045-3212_1045-3209del	N/A	Intron Variant
CUX1 transcript variant X7	XM_047419910.1:c.1045-321… XM_047419910.1:c.1045-3212_1045-3209del	N/A	Intron Variant
CUX1 transcript variant X9	XM_047419911.1:c.1012-321… XM_047419911.1:c.1012-3212_1012-3209del	N/A	Intron Variant
CUX1 transcript variant X10	XM_047419912.1:c.1051-321… XM_047419912.1:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant X11	XM_047419913.1:c.1051-321… XM_047419913.1:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant X14	XM_047419914.1:c.1051-321… XM_047419914.1:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant X15	XM_047419915.1:c.1045-321… XM_047419915.1:c.1045-3212_1045-3209del	N/A	Intron Variant
CUX1 transcript variant X16	XM_047419916.1:c.1051-321… XM_047419916.1:c.1051-3212_1051-3209del	N/A	Intron Variant
CUX1 transcript variant X17	XM_047419917.1:c.1051-321… XM_047419917.1:c.1051-3212_1051-3209del	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)₉=	del(T)₄	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄
GRCh38.p14 chr 7	NC_000007.14:g.102186596_102186604=	NC_000007.14:g.102186601_102186604del	NC_000007.14:g.102186603_102186604del	NC_000007.14:g.102186604del	NC_000007.14:g.102186604dup	NC_000007.14:g.102186603_102186604dup	NC_000007.14:g.102186602_102186604dup	NC_000007.14:g.102186601_102186604dup
GRCh37.p13 chr 7	NC_000007.13:g.101829876_101829884=	NC_000007.13:g.101829881_101829884del	NC_000007.13:g.101829883_101829884del	NC_000007.13:g.101829884del	NC_000007.13:g.101829884dup	NC_000007.13:g.101829883_101829884dup	NC_000007.13:g.101829882_101829884dup	NC_000007.13:g.101829881_101829884dup
CUX1 RefSeqGene (LRG_1123)	NG_029476.2:g.375693_375701=	NG_029476.2:g.375698_375701del	NG_029476.2:g.375700_375701del	NG_029476.2:g.375701del	NG_029476.2:g.375701dup	NG_029476.2:g.375700_375701dup	NG_029476.2:g.375699_375701dup	NG_029476.2:g.375698_375701dup
GRCh37.p13 chr 7 fix patch HG115_PATCH	NW_003571037.1:g.110926_110934=	NW_003571037.1:g.110931_110934del	NW_003571037.1:g.110933_110934del	NW_003571037.1:g.110934del	NW_003571037.1:g.110934dup	NW_003571037.1:g.110933_110934dup	NW_003571037.1:g.110932_110934dup	NW_003571037.1:g.110931_110934dup
CUX1 transcript variant 4	NM_001202543.1:c.1051-3217=	NM_001202543.1:c.1051-3212_1051-3209del	NM_001202543.1:c.1051-3210_1051-3209del	NM_001202543.1:c.1051-3209del	NM_001202543.1:c.1051-3209dup	NM_001202543.1:c.1051-3210_1051-3209dup	NM_001202543.1:c.1051-3211_1051-3209dup	NM_001202543.1:c.1051-3212_1051-3209dup
CUX1 transcript variant 4	NM_001202543.2:c.1051-3217=	NM_001202543.2:c.1051-3212_1051-3209del	NM_001202543.2:c.1051-3210_1051-3209del	NM_001202543.2:c.1051-3209del	NM_001202543.2:c.1051-3209dup	NM_001202543.2:c.1051-3210_1051-3209dup	NM_001202543.2:c.1051-3211_1051-3209dup	NM_001202543.2:c.1051-3212_1051-3209dup
CUX1 transcript variant 5	NM_001202544.1:c.1003-3217=	NM_001202544.1:c.1003-3212_1003-3209del	NM_001202544.1:c.1003-3210_1003-3209del	NM_001202544.1:c.1003-3209del	NM_001202544.1:c.1003-3209dup	NM_001202544.1:c.1003-3210_1003-3209dup	NM_001202544.1:c.1003-3211_1003-3209dup	NM_001202544.1:c.1003-3212_1003-3209dup
CUX1 transcript variant 5	NM_001202544.3:c.1003-3217=	NM_001202544.3:c.1003-3212_1003-3209del	NM_001202544.3:c.1003-3210_1003-3209del	NM_001202544.3:c.1003-3209del	NM_001202544.3:c.1003-3209dup	NM_001202544.3:c.1003-3210_1003-3209dup	NM_001202544.3:c.1003-3211_1003-3209dup	NM_001202544.3:c.1003-3212_1003-3209dup
CUX1 transcript variant 6	NM_001202545.1:c.913-3217=	NM_001202545.1:c.913-3212_913-3209del	NM_001202545.1:c.913-3210_913-3209del	NM_001202545.1:c.913-3209del	NM_001202545.1:c.913-3209dup	NM_001202545.1:c.913-3210_913-3209dup	NM_001202545.1:c.913-3211_913-3209dup	NM_001202545.1:c.913-3212_913-3209dup
CUX1 transcript variant 6	NM_001202545.3:c.913-3217=	NM_001202545.3:c.913-3212_913-3209del	NM_001202545.3:c.913-3210_913-3209del	NM_001202545.3:c.913-3209del	NM_001202545.3:c.913-3209dup	NM_001202545.3:c.913-3210_913-3209dup	NM_001202545.3:c.913-3211_913-3209dup	NM_001202545.3:c.913-3212_913-3209dup
CUX1 transcript variant 7	NM_001202546.1:c.934-3217=	NM_001202546.1:c.934-3212_934-3209del	NM_001202546.1:c.934-3210_934-3209del	NM_001202546.1:c.934-3209del	NM_001202546.1:c.934-3209dup	NM_001202546.1:c.934-3210_934-3209dup	NM_001202546.1:c.934-3211_934-3209dup	NM_001202546.1:c.934-3212_934-3209dup
CUX1 transcript variant 7	NM_001202546.3:c.934-3217=	NM_001202546.3:c.934-3212_934-3209del	NM_001202546.3:c.934-3210_934-3209del	NM_001202546.3:c.934-3209del	NM_001202546.3:c.934-3209dup	NM_001202546.3:c.934-3210_934-3209dup	NM_001202546.3:c.934-3211_934-3209dup	NM_001202546.3:c.934-3212_934-3209dup
CUX1 transcript variant 2	NM_001913.3:c.1051-3217=	NM_001913.3:c.1051-3212_1051-3209del	NM_001913.3:c.1051-3210_1051-3209del	NM_001913.3:c.1051-3209del	NM_001913.3:c.1051-3209dup	NM_001913.3:c.1051-3210_1051-3209dup	NM_001913.3:c.1051-3211_1051-3209dup	NM_001913.3:c.1051-3212_1051-3209dup
CUX1 transcript variant 2	NM_001913.5:c.1051-3217=	NM_001913.5:c.1051-3212_1051-3209del	NM_001913.5:c.1051-3210_1051-3209del	NM_001913.5:c.1051-3209del	NM_001913.5:c.1051-3209dup	NM_001913.5:c.1051-3210_1051-3209dup	NM_001913.5:c.1051-3211_1051-3209dup	NM_001913.5:c.1051-3212_1051-3209dup
CUX1 transcript variant 3	NM_181500.2:c.1045-3217=	NM_181500.2:c.1045-3212_1045-3209del	NM_181500.2:c.1045-3210_1045-3209del	NM_181500.2:c.1045-3209del	NM_181500.2:c.1045-3209dup	NM_181500.2:c.1045-3210_1045-3209dup	NM_181500.2:c.1045-3211_1045-3209dup	NM_181500.2:c.1045-3212_1045-3209dup
CUX1 transcript variant 3	NM_181500.4:c.1045-3217=	NM_181500.4:c.1045-3212_1045-3209del	NM_181500.4:c.1045-3210_1045-3209del	NM_181500.4:c.1045-3209del	NM_181500.4:c.1045-3209dup	NM_181500.4:c.1045-3210_1045-3209dup	NM_181500.4:c.1045-3211_1045-3209dup	NM_181500.4:c.1045-3212_1045-3209dup
CUX1 transcript variant 1	NM_181552.3:c.1018-3217=	NM_181552.3:c.1018-3212_1018-3209del	NM_181552.3:c.1018-3210_1018-3209del	NM_181552.3:c.1018-3209del	NM_181552.3:c.1018-3209dup	NM_181552.3:c.1018-3210_1018-3209dup	NM_181552.3:c.1018-3211_1018-3209dup	NM_181552.3:c.1018-3212_1018-3209dup
CUX1 transcript variant 1	NM_181552.4:c.1018-3217=	NM_181552.4:c.1018-3212_1018-3209del	NM_181552.4:c.1018-3210_1018-3209del	NM_181552.4:c.1018-3209del	NM_181552.4:c.1018-3209dup	NM_181552.4:c.1018-3210_1018-3209dup	NM_181552.4:c.1018-3211_1018-3209dup	NM_181552.4:c.1018-3212_1018-3209dup
CUX1 transcript variant X1	XM_005250150.1:c.1318-3217=	XM_005250150.1:c.1318-3212_1318-3209del	XM_005250150.1:c.1318-3210_1318-3209del	XM_005250150.1:c.1318-3209del	XM_005250150.1:c.1318-3209dup	XM_005250150.1:c.1318-3210_1318-3209dup	XM_005250150.1:c.1318-3211_1318-3209dup	XM_005250150.1:c.1318-3212_1318-3209dup
CUX1 transcript variant X1	XM_005250150.4:c.1018-3217=	XM_005250150.4:c.1018-3212_1018-3209del	XM_005250150.4:c.1018-3210_1018-3209del	XM_005250150.4:c.1018-3209del	XM_005250150.4:c.1018-3209dup	XM_005250150.4:c.1018-3210_1018-3209dup	XM_005250150.4:c.1018-3211_1018-3209dup	XM_005250150.4:c.1018-3212_1018-3209dup
CUX1 transcript variant X2	XM_005250151.1:c.1312-3217=	XM_005250151.1:c.1312-3212_1312-3209del	XM_005250151.1:c.1312-3210_1312-3209del	XM_005250151.1:c.1312-3209del	XM_005250151.1:c.1312-3209dup	XM_005250151.1:c.1312-3210_1312-3209dup	XM_005250151.1:c.1312-3211_1312-3209dup	XM_005250151.1:c.1312-3212_1312-3209dup
CUX1 transcript variant X3	XM_005250152.1:c.1270-3217=	XM_005250152.1:c.1270-3212_1270-3209del	XM_005250152.1:c.1270-3210_1270-3209del	XM_005250152.1:c.1270-3209del	XM_005250152.1:c.1270-3209dup	XM_005250152.1:c.1270-3210_1270-3209dup	XM_005250152.1:c.1270-3211_1270-3209dup	XM_005250152.1:c.1270-3212_1270-3209dup
CUX1 transcript variant X4	XM_005250153.1:c.1003-3217=	XM_005250153.1:c.1003-3212_1003-3209del	XM_005250153.1:c.1003-3210_1003-3209del	XM_005250153.1:c.1003-3209del	XM_005250153.1:c.1003-3209dup	XM_005250153.1:c.1003-3210_1003-3209dup	XM_005250153.1:c.1003-3211_1003-3209dup	XM_005250153.1:c.1003-3212_1003-3209dup
CUX1 transcript variant X5	XM_005250154.1:c.1318-3217=	XM_005250154.1:c.1318-3212_1318-3209del	XM_005250154.1:c.1318-3210_1318-3209del	XM_005250154.1:c.1318-3209del	XM_005250154.1:c.1318-3209dup	XM_005250154.1:c.1318-3210_1318-3209dup	XM_005250154.1:c.1318-3211_1318-3209dup	XM_005250154.1:c.1318-3212_1318-3209dup
CUX1 transcript variant X18	XM_005250154.4:c.1018-3217=	XM_005250154.4:c.1018-3212_1018-3209del	XM_005250154.4:c.1018-3210_1018-3209del	XM_005250154.4:c.1018-3209del	XM_005250154.4:c.1018-3209dup	XM_005250154.4:c.1018-3210_1018-3209dup	XM_005250154.4:c.1018-3211_1018-3209dup	XM_005250154.4:c.1018-3212_1018-3209dup
CUX1 transcript variant X6	XM_005250155.1:c.1093-3217=	XM_005250155.1:c.1093-3212_1093-3209del	XM_005250155.1:c.1093-3210_1093-3209del	XM_005250155.1:c.1093-3209del	XM_005250155.1:c.1093-3209dup	XM_005250155.1:c.1093-3210_1093-3209dup	XM_005250155.1:c.1093-3211_1093-3209dup	XM_005250155.1:c.1093-3212_1093-3209dup
CUX1 transcript variant X4	XM_006715854.3:c.1018-3217=	XM_006715854.3:c.1018-3212_1018-3209del	XM_006715854.3:c.1018-3210_1018-3209del	XM_006715854.3:c.1018-3209del	XM_006715854.3:c.1018-3209dup	XM_006715854.3:c.1018-3210_1018-3209dup	XM_006715854.3:c.1018-3211_1018-3209dup	XM_006715854.3:c.1018-3212_1018-3209dup
CUX1 transcript variant X13	XM_011515825.3:c.1051-3217=	XM_011515825.3:c.1051-3212_1051-3209del	XM_011515825.3:c.1051-3210_1051-3209del	XM_011515825.3:c.1051-3209del	XM_011515825.3:c.1051-3209dup	XM_011515825.3:c.1051-3210_1051-3209dup	XM_011515825.3:c.1051-3211_1051-3209dup	XM_011515825.3:c.1051-3212_1051-3209dup
CUX1 transcript variant X12	XM_017011760.3:c.1045-3217=	XM_017011760.3:c.1045-3212_1045-3209del	XM_017011760.3:c.1045-3210_1045-3209del	XM_017011760.3:c.1045-3209del	XM_017011760.3:c.1045-3209dup	XM_017011760.3:c.1045-3210_1045-3209dup	XM_017011760.3:c.1045-3211_1045-3209dup	XM_017011760.3:c.1045-3212_1045-3209dup
CUX1 transcript variant X8	XM_024446668.2:c.1012-3217=	XM_024446668.2:c.1012-3212_1012-3209del	XM_024446668.2:c.1012-3210_1012-3209del	XM_024446668.2:c.1012-3209del	XM_024446668.2:c.1012-3209dup	XM_024446668.2:c.1012-3210_1012-3209dup	XM_024446668.2:c.1012-3211_1012-3209dup	XM_024446668.2:c.1012-3212_1012-3209dup
CUX1 transcript variant X2	XM_047419906.1:c.1012-3217=	XM_047419906.1:c.1012-3212_1012-3209del	XM_047419906.1:c.1012-3210_1012-3209del	XM_047419906.1:c.1012-3209del	XM_047419906.1:c.1012-3209dup	XM_047419906.1:c.1012-3210_1012-3209dup	XM_047419906.1:c.1012-3211_1012-3209dup	XM_047419906.1:c.1012-3212_1012-3209dup
CUX1 transcript variant X3	XM_047419907.1:c.1012-3217=	XM_047419907.1:c.1012-3212_1012-3209del	XM_047419907.1:c.1012-3210_1012-3209del	XM_047419907.1:c.1012-3209del	XM_047419907.1:c.1012-3209dup	XM_047419907.1:c.1012-3210_1012-3209dup	XM_047419907.1:c.1012-3211_1012-3209dup	XM_047419907.1:c.1012-3212_1012-3209dup
CUX1 transcript variant X5	XM_047419908.1:c.1051-3217=	XM_047419908.1:c.1051-3212_1051-3209del	XM_047419908.1:c.1051-3210_1051-3209del	XM_047419908.1:c.1051-3209del	XM_047419908.1:c.1051-3209dup	XM_047419908.1:c.1051-3210_1051-3209dup	XM_047419908.1:c.1051-3211_1051-3209dup	XM_047419908.1:c.1051-3212_1051-3209dup
CUX1 transcript variant X6	XM_047419909.1:c.1045-3217=	XM_047419909.1:c.1045-3212_1045-3209del	XM_047419909.1:c.1045-3210_1045-3209del	XM_047419909.1:c.1045-3209del	XM_047419909.1:c.1045-3209dup	XM_047419909.1:c.1045-3210_1045-3209dup	XM_047419909.1:c.1045-3211_1045-3209dup	XM_047419909.1:c.1045-3212_1045-3209dup
CUX1 transcript variant X7	XM_047419910.1:c.1045-3217=	XM_047419910.1:c.1045-3212_1045-3209del	XM_047419910.1:c.1045-3210_1045-3209del	XM_047419910.1:c.1045-3209del	XM_047419910.1:c.1045-3209dup	XM_047419910.1:c.1045-3210_1045-3209dup	XM_047419910.1:c.1045-3211_1045-3209dup	XM_047419910.1:c.1045-3212_1045-3209dup
CUX1 transcript variant X9	XM_047419911.1:c.1012-3217=	XM_047419911.1:c.1012-3212_1012-3209del	XM_047419911.1:c.1012-3210_1012-3209del	XM_047419911.1:c.1012-3209del	XM_047419911.1:c.1012-3209dup	XM_047419911.1:c.1012-3210_1012-3209dup	XM_047419911.1:c.1012-3211_1012-3209dup	XM_047419911.1:c.1012-3212_1012-3209dup
CUX1 transcript variant X10	XM_047419912.1:c.1051-3217=	XM_047419912.1:c.1051-3212_1051-3209del	XM_047419912.1:c.1051-3210_1051-3209del	XM_047419912.1:c.1051-3209del	XM_047419912.1:c.1051-3209dup	XM_047419912.1:c.1051-3210_1051-3209dup	XM_047419912.1:c.1051-3211_1051-3209dup	XM_047419912.1:c.1051-3212_1051-3209dup
CUX1 transcript variant X11	XM_047419913.1:c.1051-3217=	XM_047419913.1:c.1051-3212_1051-3209del	XM_047419913.1:c.1051-3210_1051-3209del	XM_047419913.1:c.1051-3209del	XM_047419913.1:c.1051-3209dup	XM_047419913.1:c.1051-3210_1051-3209dup	XM_047419913.1:c.1051-3211_1051-3209dup	XM_047419913.1:c.1051-3212_1051-3209dup
CUX1 transcript variant X14	XM_047419914.1:c.1051-3217=	XM_047419914.1:c.1051-3212_1051-3209del	XM_047419914.1:c.1051-3210_1051-3209del	XM_047419914.1:c.1051-3209del	XM_047419914.1:c.1051-3209dup	XM_047419914.1:c.1051-3210_1051-3209dup	XM_047419914.1:c.1051-3211_1051-3209dup	XM_047419914.1:c.1051-3212_1051-3209dup
CUX1 transcript variant X15	XM_047419915.1:c.1045-3217=	XM_047419915.1:c.1045-3212_1045-3209del	XM_047419915.1:c.1045-3210_1045-3209del	XM_047419915.1:c.1045-3209del	XM_047419915.1:c.1045-3209dup	XM_047419915.1:c.1045-3210_1045-3209dup	XM_047419915.1:c.1045-3211_1045-3209dup	XM_047419915.1:c.1045-3212_1045-3209dup
CUX1 transcript variant X16	XM_047419916.1:c.1051-3217=	XM_047419916.1:c.1051-3212_1051-3209del	XM_047419916.1:c.1051-3210_1051-3209del	XM_047419916.1:c.1051-3209del	XM_047419916.1:c.1051-3209dup	XM_047419916.1:c.1051-3210_1051-3209dup	XM_047419916.1:c.1051-3211_1051-3209dup	XM_047419916.1:c.1051-3212_1051-3209dup
CUX1 transcript variant X17	XM_047419917.1:c.1051-3217=	XM_047419917.1:c.1051-3212_1051-3209del	XM_047419917.1:c.1051-3210_1051-3209del	XM_047419917.1:c.1051-3209del	XM_047419917.1:c.1051-3209dup	XM_047419917.1:c.1051-3210_1051-3209dup	XM_047419917.1:c.1051-3211_1051-3209dup	XM_047419917.1:c.1051-3212_1051-3209dup

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#.

34 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81718632	Oct 12, 2018 (152)
2	GMI	ss288861900	Oct 12, 2018 (152)
3	DDI	ss1536557814	Apr 09, 2015 (144)
4	BIOINF_KMB_FNS_UNIBA	ss3646047724	Oct 12, 2018 (152)
5	EVA_DECODE	ss3720339538	Jul 13, 2019 (153)
6	EVA_DECODE	ss3720339541	Jul 13, 2019 (153)
7	EVA_DECODE	ss3720339542	Jul 13, 2019 (153)
8	EVA_DECODE	ss3720339543	Jul 13, 2019 (153)
9	ACPOP	ss3734917808	Jul 13, 2019 (153)
10	PACBIO	ss3785910662	Jul 13, 2019 (153)
11	PACBIO	ss3791197216	Jul 13, 2019 (153)
12	PACBIO	ss3796077268	Jul 13, 2019 (153)
13	EVA	ss3830731362	Apr 26, 2020 (154)
14	KOGIC	ss3962236868	Apr 26, 2020 (154)
15	KOGIC	ss3962236869	Apr 26, 2020 (154)
16	KOGIC	ss3962236870	Apr 26, 2020 (154)
17	GNOMAD	ss4169737626	Apr 26, 2021 (155)
18	GNOMAD	ss4169737631	Apr 26, 2021 (155)
19	GNOMAD	ss4169737632	Apr 26, 2021 (155)
20	GNOMAD	ss4169737633	Apr 26, 2021 (155)
21	GNOMAD	ss4169737635	Apr 26, 2021 (155)
22	GNOMAD	ss4169737636	Apr 26, 2021 (155)
23	TOPMED	ss4757180560	Apr 26, 2021 (155)
24	TOPMED	ss4757180561	Apr 26, 2021 (155)
25	TOMMO_GENOMICS	ss5184754721	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5184754723	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5184754724	Apr 26, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5274099823	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5471060065	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5471060067	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5471060068	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5725503942	Oct 16, 2022 (156)
33	TOMMO_GENOMICS	ss5725503944	Oct 16, 2022 (156)
34	TOMMO_GENOMICS	ss5725503945	Oct 16, 2022 (156)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271190540 (NC_000007.14:102186595::T 1987/118166) Row 271190545 (NC_000007.14:102186595::TT 12058/118042) Row 271190546 (NC_000007.14:102186595::TTT 35/118182)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271190540 (NC_000007.14:102186595::T 1987/118166) Row 271190545 (NC_000007.14:102186595::TT 12058/118042) Row 271190546 (NC_000007.14:102186595::TTT 35/118182)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271190540 (NC_000007.14:102186595::T 1987/118166) Row 271190545 (NC_000007.14:102186595::TT 12058/118042) Row 271190546 (NC_000007.14:102186595::TTT 35/118182)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271190540 (NC_000007.14:102186595::T 1987/118166) Row 271190545 (NC_000007.14:102186595::TT 12058/118042) Row 271190546 (NC_000007.14:102186595::TTT 35/118182)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271190540 (NC_000007.14:102186595::T 1987/118166) Row 271190545 (NC_000007.14:102186595::TT 12058/118042) Row 271190546 (NC_000007.14:102186595::TTT 35/118182)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 271190540 (NC_000007.14:102186595::T 1987/118166) Row 271190545 (NC_000007.14:102186595::TT 12058/118042) Row 271190546 (NC_000007.14:102186595::TTT 35/118182)...	-	Apr 26, 2021 (155)
41	Korean Genome Project Submission ignored due to conflicting rows: Row 18614869 (NC_000007.14:102186597::TT 54/1830) Row 18614870 (NC_000007.14:102186597::T 4/1830) Row 18614871 (NC_000007.14:102186596:T: 1/1830)	-	Apr 26, 2020 (154)
42	Korean Genome Project Submission ignored due to conflicting rows: Row 18614869 (NC_000007.14:102186597::TT 54/1830) Row 18614870 (NC_000007.14:102186597::T 4/1830) Row 18614871 (NC_000007.14:102186596:T: 1/1830)	-	Apr 26, 2020 (154)
43	Korean Genome Project Submission ignored due to conflicting rows: Row 18614869 (NC_000007.14:102186597::TT 54/1830) Row 18614870 (NC_000007.14:102186597::T 4/1830) Row 18614871 (NC_000007.14:102186596:T: 1/1830)	-	Apr 26, 2020 (154)
44	Northern Sweden	NC_000007.13 - 101829876	Jul 13, 2019 (153)
45	8.3KJPN Submission ignored due to conflicting rows: Row 42724028 (NC_000007.13:101829875::TT 350/16758) Row 42724030 (NC_000007.13:101829875::T 49/16758) Row 42724031 (NC_000007.13:101829875:T: 5/16758)	-	Apr 26, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 42724028 (NC_000007.13:101829875::TT 350/16758) Row 42724030 (NC_000007.13:101829875::T 49/16758) Row 42724031 (NC_000007.13:101829875:T: 5/16758)	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 42724028 (NC_000007.13:101829875::TT 350/16758) Row 42724030 (NC_000007.13:101829875::T 49/16758) Row 42724031 (NC_000007.13:101829875:T: 5/16758)	-	Apr 26, 2021 (155)
48	14KJPN Submission ignored due to conflicting rows: Row 59341046 (NC_000007.14:102186595::TT 578/28258) Row 59341048 (NC_000007.14:102186595::T 75/28258) Row 59341049 (NC_000007.14:102186595:T: 8/28258)	-	Oct 16, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 59341046 (NC_000007.14:102186595::TT 578/28258) Row 59341048 (NC_000007.14:102186595::T 75/28258) Row 59341049 (NC_000007.14:102186595:T: 8/28258)	-	Oct 16, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 59341046 (NC_000007.14:102186595::TT 578/28258) Row 59341048 (NC_000007.14:102186595::T 75/28258) Row 59341049 (NC_000007.14:102186595:T: 8/28258)	-	Oct 16, 2022 (156)
51	TopMed Submission ignored due to conflicting rows: Row 594558119 (NC_000007.14:102186595:T: 958/264690) Row 594558120 (NC_000007.14:102186595:TT: 23/264690)	-	Apr 26, 2021 (155)
52	TopMed Submission ignored due to conflicting rows: Row 594558119 (NC_000007.14:102186595:T: 958/264690) Row 594558120 (NC_000007.14:102186595:TT: 23/264690)	-	Apr 26, 2021 (155)
53	ALFA	NC_000007.14 - 102186596	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
1828171913	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTT	(self)
ss3720339538, ss4169737636, ss4757180561	NC_000007.14:102186595:TT:	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTT	(self)
1828171913	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTT	(self)
ss5184754724	NC_000007.13:101829875:T:	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTT	(self)
ss4169737635, ss4757180560, ss5471060068, ss5725503945	NC_000007.14:102186595:T:	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTT	(self)
1828171913	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTT	(self)
ss3962236870	NC_000007.14:102186596:T:	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTT	(self)
ss288861900	NC_000007.12:101616604::T	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTT	(self)
ss5184754723	NC_000007.13:101829875::T	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTT	(self)
ss3646047724, ss4169737626, ss5471060067, ss5725503944	NC_000007.14:102186595::T	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTT	(self)
1828171913	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTT	(self)
ss3720339541, ss3962236869	NC_000007.14:102186597::T	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTT	(self)
ss81718632	NT_007933.15:39862727::T	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTT	(self)
8202673, ss1536557814, ss3734917808, ss3785910662, ss3791197216, ss3796077268, ss3830731362, ss5184754721	NC_000007.13:101829875::TT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTT	(self)
ss4169737631, ss5274099823, ss5471060065, ss5725503942	NC_000007.14:102186595::TT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTT	(self)
1828171913	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTT	(self)
ss3720339542, ss3962236868	NC_000007.14:102186597::TT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTT	(self)
ss4169737632	NC_000007.14:102186595::TTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTTT	(self)
1828171913	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTTT	(self)
ss3720339543	NC_000007.14:102186597::TTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTTT	(self)
ss4169737633	NC_000007.14:102186595::TTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTTTT	(self)
1828171913	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2465750700	NC_000007.13:101829875:TT:	NC_000007.14:102186595:TTTTTTTTT:T… NC_000007.14:102186595:TTTTTTTTT:TTTTTTT

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

No publications for rs781912833

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

rs781912833