Name: rs397853103
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.

rs397853103

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:76423143-76423163 (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)₆ / del(T)₅ / del…
del(T)₁₂ / 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)₁₇
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.0689 (688/9982, ALFA)
delT=0.3668 (1837/5008, 1000G)
delTT=0.1858 (716/3854, ALSPAC)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ESRRB : 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	9982	TTTTTTTTTTTTTTTTTTTTT=0.9151	TTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0689, TTTTTTTTTTTTTTTTTTTTTT=0.0159, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.880148	0.014621	0.105231	32
European	Sub	8216	TTTTTTTTTTTTTTTTTTTTT=0.8970	TTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0836, TTTTTTTTTTTTTTTTTTTTTT=0.0194, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.853763	0.017871	0.128366	32
African	Sub	1132	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	42	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1090	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	48	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	32	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	66	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	258	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	50	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	212	TTTTTTTTTTTTTTTTTTTTT=0.995	TTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.005, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.990566	0.0	0.009434	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	9982	(T)₂₁=0.9151	del(T)₁₂=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0689, dupT=0.0159, dupTT=0.0000, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	8216	(T)₂₁=0.8970	del(T)₁₂=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTT=0.0000, delT=0.0836, dupT=0.0194, dupTT=0.0000, dupTTT=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	1132	(T)₂₁=1.0000	del(T)₁₂=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)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	258	(T)₂₁=1.000	del(T)₁₂=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)₅=0.000
Allele Frequency Aggregator	Other	Sub	212	(T)₂₁=0.995	del(T)₁₂=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTT=0.000, delT=0.005, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	66	(T)₂₁=1.00	del(T)₁₂=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)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(T)₂₁=1.00	del(T)₁₂=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)₅=0.00
Allele Frequency Aggregator	Asian	Sub	48	(T)₂₁=1.00	del(T)₁₂=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)₅=0.00
1000Genomes	Global	Study-wide	5008	(T)₂₁=0.6332	delT=0.3668
1000Genomes	African	Sub	1322	(T)₂₁=0.5817	delT=0.4183
1000Genomes	East Asian	Sub	1008	(T)₂₁=0.6667	delT=0.3333
1000Genomes	Europe	Sub	1006	(T)₂₁=0.6491	delT=0.3509
1000Genomes	South Asian	Sub	978	(T)₂₁=0.666	delT=0.334
1000Genomes	American	Sub	694	(T)₂₁=0.614	delT=0.386
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	(T)₂₁=0.8142	delTT=0.1858

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 14	NC_000014.9:g.76423152_76423163del
GRCh38.p14 chr 14	NC_000014.9:g.76423158_76423163del
GRCh38.p14 chr 14	NC_000014.9:g.76423159_76423163del
GRCh38.p14 chr 14	NC_000014.9:g.76423160_76423163del
GRCh38.p14 chr 14	NC_000014.9:g.76423161_76423163del
GRCh38.p14 chr 14	NC_000014.9:g.76423162_76423163del
GRCh38.p14 chr 14	NC_000014.9:g.76423163del
GRCh38.p14 chr 14	NC_000014.9:g.76423163dup
GRCh38.p14 chr 14	NC_000014.9:g.76423162_76423163dup
GRCh38.p14 chr 14	NC_000014.9:g.76423161_76423163dup
GRCh38.p14 chr 14	NC_000014.9:g.76423160_76423163dup
GRCh38.p14 chr 14	NC_000014.9:g.76423159_76423163dup
GRCh38.p14 chr 14	NC_000014.9:g.76423158_76423163dup
GRCh38.p14 chr 14	NC_000014.9:g.76423147_76423163dup
GRCh37.p13 chr 14	NC_000014.8:g.76889495_76889506del
GRCh37.p13 chr 14	NC_000014.8:g.76889501_76889506del
GRCh37.p13 chr 14	NC_000014.8:g.76889502_76889506del
GRCh37.p13 chr 14	NC_000014.8:g.76889503_76889506del
GRCh37.p13 chr 14	NC_000014.8:g.76889504_76889506del
GRCh37.p13 chr 14	NC_000014.8:g.76889505_76889506del
GRCh37.p13 chr 14	NC_000014.8:g.76889506del
GRCh37.p13 chr 14	NC_000014.8:g.76889506dup
GRCh37.p13 chr 14	NC_000014.8:g.76889505_76889506dup
GRCh37.p13 chr 14	NC_000014.8:g.76889504_76889506dup
GRCh37.p13 chr 14	NC_000014.8:g.76889503_76889506dup
GRCh37.p13 chr 14	NC_000014.8:g.76889502_76889506dup
GRCh37.p13 chr 14	NC_000014.8:g.76889501_76889506dup
GRCh37.p13 chr 14	NC_000014.8:g.76889490_76889506dup
ESRRB RefSeqGene	NG_012278.2:g.56806_56817del
ESRRB RefSeqGene	NG_012278.2:g.56812_56817del
ESRRB RefSeqGene	NG_012278.2:g.56813_56817del
ESRRB RefSeqGene	NG_012278.2:g.56814_56817del
ESRRB RefSeqGene	NG_012278.2:g.56815_56817del
ESRRB RefSeqGene	NG_012278.2:g.56816_56817del
ESRRB RefSeqGene	NG_012278.2:g.56817del
ESRRB RefSeqGene	NG_012278.2:g.56817dup
ESRRB RefSeqGene	NG_012278.2:g.56816_56817dup
ESRRB RefSeqGene	NG_012278.2:g.56815_56817dup
ESRRB RefSeqGene	NG_012278.2:g.56814_56817dup
ESRRB RefSeqGene	NG_012278.2:g.56813_56817dup
ESRRB RefSeqGene	NG_012278.2:g.56812_56817dup
ESRRB RefSeqGene	NG_012278.2:g.56801_56817dup

Gene: ESRRB, estrogen related receptor beta (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ESRRB transcript variant 2	NM_001379180.1:c.51-16189… NM_001379180.1:c.51-16189_51-16178del	N/A	Intron Variant
ESRRB transcript variant 1	NM_004452.4:c.-14+15556_-… NM_004452.4:c.-14+15556_-14+15567del	N/A	Intron Variant
ESRRB transcript variant X1	XM_011536547.3:c.51-16189… XM_011536547.3:c.51-16189_51-16178del	N/A	Intron Variant
ESRRB transcript variant X3	XM_011536550.3:c.-14+1555… XM_011536550.3:c.-14+15556_-14+15567del	N/A	Intron Variant
ESRRB transcript variant X4	XM_011536553.3:c.51-16189… XM_011536553.3:c.51-16189_51-16178del	N/A	Intron Variant
ESRRB transcript variant X5	XM_011536554.3:c.51-16189… XM_011536554.3:c.51-16189_51-16178del	N/A	Intron Variant
ESRRB transcript variant X6	XM_024449508.2:c.51-16189… XM_024449508.2:c.51-16189_51-16178del	N/A	Intron Variant
ESRRB transcript variant X2	XM_047431079.1:c.-14+1555… XM_047431079.1:c.-14+15556_-14+15567del	N/A	Intron Variant
ESRRB transcript variant X7	XM_047431080.1:c.3-16189_… XM_047431080.1:c.3-16189_3-16178del	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)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₁₇
GRCh38.p14 chr 14	NC_000014.9:g.76423143_76423163=	NC_000014.9:g.76423152_76423163del	NC_000014.9:g.76423158_76423163del	NC_000014.9:g.76423159_76423163del	NC_000014.9:g.76423160_76423163del	NC_000014.9:g.76423161_76423163del	NC_000014.9:g.76423162_76423163del	NC_000014.9:g.76423163del	NC_000014.9:g.76423163dup	NC_000014.9:g.76423162_76423163dup	NC_000014.9:g.76423161_76423163dup	NC_000014.9:g.76423160_76423163dup	NC_000014.9:g.76423159_76423163dup	NC_000014.9:g.76423158_76423163dup	NC_000014.9:g.76423147_76423163dup
GRCh37.p13 chr 14	NC_000014.8:g.76889486_76889506=	NC_000014.8:g.76889495_76889506del	NC_000014.8:g.76889501_76889506del	NC_000014.8:g.76889502_76889506del	NC_000014.8:g.76889503_76889506del	NC_000014.8:g.76889504_76889506del	NC_000014.8:g.76889505_76889506del	NC_000014.8:g.76889506del	NC_000014.8:g.76889506dup	NC_000014.8:g.76889505_76889506dup	NC_000014.8:g.76889504_76889506dup	NC_000014.8:g.76889503_76889506dup	NC_000014.8:g.76889502_76889506dup	NC_000014.8:g.76889501_76889506dup	NC_000014.8:g.76889490_76889506dup
ESRRB RefSeqGene	NG_012278.2:g.56797_56817=	NG_012278.2:g.56806_56817del	NG_012278.2:g.56812_56817del	NG_012278.2:g.56813_56817del	NG_012278.2:g.56814_56817del	NG_012278.2:g.56815_56817del	NG_012278.2:g.56816_56817del	NG_012278.2:g.56817del	NG_012278.2:g.56817dup	NG_012278.2:g.56816_56817dup	NG_012278.2:g.56815_56817dup	NG_012278.2:g.56814_56817dup	NG_012278.2:g.56813_56817dup	NG_012278.2:g.56812_56817dup	NG_012278.2:g.56801_56817dup
ESRRB transcript variant 2	NM_001379180.1:c.51-16198=	NM_001379180.1:c.51-16189_51-16178del	NM_001379180.1:c.51-16183_51-16178del	NM_001379180.1:c.51-16182_51-16178del	NM_001379180.1:c.51-16181_51-16178del	NM_001379180.1:c.51-16180_51-16178del	NM_001379180.1:c.51-16179_51-16178del	NM_001379180.1:c.51-16178del	NM_001379180.1:c.51-16178dup	NM_001379180.1:c.51-16179_51-16178dup	NM_001379180.1:c.51-16180_51-16178dup	NM_001379180.1:c.51-16181_51-16178dup	NM_001379180.1:c.51-16182_51-16178dup	NM_001379180.1:c.51-16183_51-16178dup	NM_001379180.1:c.51-16194_51-16178dup
ESRRB transcript	NM_004452.3:c.-14+15547=	NM_004452.3:c.-14+15556_-14+15567del	NM_004452.3:c.-14+15562_-14+15567del	NM_004452.3:c.-14+15563_-14+15567del	NM_004452.3:c.-14+15564_-14+15567del	NM_004452.3:c.-14+15565_-14+15567del	NM_004452.3:c.-14+15566_-14+15567del	NM_004452.3:c.-14+15567del	NM_004452.3:c.-14+15567dup	NM_004452.3:c.-14+15566_-14+15567dup	NM_004452.3:c.-14+15565_-14+15567dup	NM_004452.3:c.-14+15564_-14+15567dup	NM_004452.3:c.-14+15563_-14+15567dup	NM_004452.3:c.-14+15562_-14+15567dup	NM_004452.3:c.-14+15551_-14+15567dup
ESRRB transcript variant 1	NM_004452.4:c.-14+15547=	NM_004452.4:c.-14+15556_-14+15567del	NM_004452.4:c.-14+15562_-14+15567del	NM_004452.4:c.-14+15563_-14+15567del	NM_004452.4:c.-14+15564_-14+15567del	NM_004452.4:c.-14+15565_-14+15567del	NM_004452.4:c.-14+15566_-14+15567del	NM_004452.4:c.-14+15567del	NM_004452.4:c.-14+15567dup	NM_004452.4:c.-14+15566_-14+15567dup	NM_004452.4:c.-14+15565_-14+15567dup	NM_004452.4:c.-14+15564_-14+15567dup	NM_004452.4:c.-14+15563_-14+15567dup	NM_004452.4:c.-14+15562_-14+15567dup	NM_004452.4:c.-14+15551_-14+15567dup
ESRRB transcript variant X1	XM_005267403.1:c.51-16198=	XM_005267403.1:c.51-16189_51-16178del	XM_005267403.1:c.51-16183_51-16178del	XM_005267403.1:c.51-16182_51-16178del	XM_005267403.1:c.51-16181_51-16178del	XM_005267403.1:c.51-16180_51-16178del	XM_005267403.1:c.51-16179_51-16178del	XM_005267403.1:c.51-16178del	XM_005267403.1:c.51-16178dup	XM_005267403.1:c.51-16179_51-16178dup	XM_005267403.1:c.51-16180_51-16178dup	XM_005267403.1:c.51-16181_51-16178dup	XM_005267403.1:c.51-16182_51-16178dup	XM_005267403.1:c.51-16183_51-16178dup	XM_005267403.1:c.51-16194_51-16178dup
ESRRB transcript variant X2	XM_005267404.1:c.51-16198=	XM_005267404.1:c.51-16189_51-16178del	XM_005267404.1:c.51-16183_51-16178del	XM_005267404.1:c.51-16182_51-16178del	XM_005267404.1:c.51-16181_51-16178del	XM_005267404.1:c.51-16180_51-16178del	XM_005267404.1:c.51-16179_51-16178del	XM_005267404.1:c.51-16178del	XM_005267404.1:c.51-16178dup	XM_005267404.1:c.51-16179_51-16178dup	XM_005267404.1:c.51-16180_51-16178dup	XM_005267404.1:c.51-16181_51-16178dup	XM_005267404.1:c.51-16182_51-16178dup	XM_005267404.1:c.51-16183_51-16178dup	XM_005267404.1:c.51-16194_51-16178dup
ESRRB transcript variant X1	XM_011536547.3:c.51-16198=	XM_011536547.3:c.51-16189_51-16178del	XM_011536547.3:c.51-16183_51-16178del	XM_011536547.3:c.51-16182_51-16178del	XM_011536547.3:c.51-16181_51-16178del	XM_011536547.3:c.51-16180_51-16178del	XM_011536547.3:c.51-16179_51-16178del	XM_011536547.3:c.51-16178del	XM_011536547.3:c.51-16178dup	XM_011536547.3:c.51-16179_51-16178dup	XM_011536547.3:c.51-16180_51-16178dup	XM_011536547.3:c.51-16181_51-16178dup	XM_011536547.3:c.51-16182_51-16178dup	XM_011536547.3:c.51-16183_51-16178dup	XM_011536547.3:c.51-16194_51-16178dup
ESRRB transcript variant X3	XM_011536550.3:c.-14+15547=	XM_011536550.3:c.-14+15556_-14+15567del	XM_011536550.3:c.-14+15562_-14+15567del	XM_011536550.3:c.-14+15563_-14+15567del	XM_011536550.3:c.-14+15564_-14+15567del	XM_011536550.3:c.-14+15565_-14+15567del	XM_011536550.3:c.-14+15566_-14+15567del	XM_011536550.3:c.-14+15567del	XM_011536550.3:c.-14+15567dup	XM_011536550.3:c.-14+15566_-14+15567dup	XM_011536550.3:c.-14+15565_-14+15567dup	XM_011536550.3:c.-14+15564_-14+15567dup	XM_011536550.3:c.-14+15563_-14+15567dup	XM_011536550.3:c.-14+15562_-14+15567dup	XM_011536550.3:c.-14+15551_-14+15567dup
ESRRB transcript variant X4	XM_011536553.3:c.51-16198=	XM_011536553.3:c.51-16189_51-16178del	XM_011536553.3:c.51-16183_51-16178del	XM_011536553.3:c.51-16182_51-16178del	XM_011536553.3:c.51-16181_51-16178del	XM_011536553.3:c.51-16180_51-16178del	XM_011536553.3:c.51-16179_51-16178del	XM_011536553.3:c.51-16178del	XM_011536553.3:c.51-16178dup	XM_011536553.3:c.51-16179_51-16178dup	XM_011536553.3:c.51-16180_51-16178dup	XM_011536553.3:c.51-16181_51-16178dup	XM_011536553.3:c.51-16182_51-16178dup	XM_011536553.3:c.51-16183_51-16178dup	XM_011536553.3:c.51-16194_51-16178dup
ESRRB transcript variant X5	XM_011536554.3:c.51-16198=	XM_011536554.3:c.51-16189_51-16178del	XM_011536554.3:c.51-16183_51-16178del	XM_011536554.3:c.51-16182_51-16178del	XM_011536554.3:c.51-16181_51-16178del	XM_011536554.3:c.51-16180_51-16178del	XM_011536554.3:c.51-16179_51-16178del	XM_011536554.3:c.51-16178del	XM_011536554.3:c.51-16178dup	XM_011536554.3:c.51-16179_51-16178dup	XM_011536554.3:c.51-16180_51-16178dup	XM_011536554.3:c.51-16181_51-16178dup	XM_011536554.3:c.51-16182_51-16178dup	XM_011536554.3:c.51-16183_51-16178dup	XM_011536554.3:c.51-16194_51-16178dup
ESRRB transcript variant X6	XM_024449508.2:c.51-16198=	XM_024449508.2:c.51-16189_51-16178del	XM_024449508.2:c.51-16183_51-16178del	XM_024449508.2:c.51-16182_51-16178del	XM_024449508.2:c.51-16181_51-16178del	XM_024449508.2:c.51-16180_51-16178del	XM_024449508.2:c.51-16179_51-16178del	XM_024449508.2:c.51-16178del	XM_024449508.2:c.51-16178dup	XM_024449508.2:c.51-16179_51-16178dup	XM_024449508.2:c.51-16180_51-16178dup	XM_024449508.2:c.51-16181_51-16178dup	XM_024449508.2:c.51-16182_51-16178dup	XM_024449508.2:c.51-16183_51-16178dup	XM_024449508.2:c.51-16194_51-16178dup
ESRRB transcript variant X2	XM_047431079.1:c.-14+15547=	XM_047431079.1:c.-14+15556_-14+15567del	XM_047431079.1:c.-14+15562_-14+15567del	XM_047431079.1:c.-14+15563_-14+15567del	XM_047431079.1:c.-14+15564_-14+15567del	XM_047431079.1:c.-14+15565_-14+15567del	XM_047431079.1:c.-14+15566_-14+15567del	XM_047431079.1:c.-14+15567del	XM_047431079.1:c.-14+15567dup	XM_047431079.1:c.-14+15566_-14+15567dup	XM_047431079.1:c.-14+15565_-14+15567dup	XM_047431079.1:c.-14+15564_-14+15567dup	XM_047431079.1:c.-14+15563_-14+15567dup	XM_047431079.1:c.-14+15562_-14+15567dup	XM_047431079.1:c.-14+15551_-14+15567dup
ESRRB transcript variant X7	XM_047431080.1:c.3-16198=	XM_047431080.1:c.3-16189_3-16178del	XM_047431080.1:c.3-16183_3-16178del	XM_047431080.1:c.3-16182_3-16178del	XM_047431080.1:c.3-16181_3-16178del	XM_047431080.1:c.3-16180_3-16178del	XM_047431080.1:c.3-16179_3-16178del	XM_047431080.1:c.3-16178del	XM_047431080.1:c.3-16178dup	XM_047431080.1:c.3-16179_3-16178dup	XM_047431080.1:c.3-16180_3-16178dup	XM_047431080.1:c.3-16181_3-16178dup	XM_047431080.1:c.3-16182_3-16178dup	XM_047431080.1:c.3-16183_3-16178dup	XM_047431080.1:c.3-16194_3-16178dup

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#.

43 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40493099	Dec 03, 2013 (138)
2	1000GENOMES	ss1374310478	Aug 21, 2014 (142)
3	EVA_UK10K_ALSPAC	ss1708126230	Apr 01, 2015 (144)
4	EVA_UK10K_TWINSUK	ss1708126280	Apr 01, 2015 (144)
5	EVA_UK10K_ALSPAC	ss1710644576	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1710644600	Apr 01, 2015 (144)
7	SWEGEN	ss3012482527	Nov 08, 2017 (151)
8	PACBIO	ss3787713887	Jul 13, 2019 (153)
9	PACBIO	ss3792744319	Jul 13, 2019 (153)
10	PACBIO	ss3797628716	Jul 13, 2019 (153)
11	KHV_HUMAN_GENOMES	ss3817860973	Jul 13, 2019 (153)
12	EVA	ss3834008148	Apr 27, 2020 (154)
13	KOGIC	ss3975278144	Apr 27, 2020 (154)
14	KOGIC	ss3975278145	Apr 27, 2020 (154)
15	KOGIC	ss3975278146	Apr 27, 2020 (154)
16	KOGIC	ss3975278147	Apr 27, 2020 (154)
17	GNOMAD	ss4281025053	Apr 26, 2021 (155)
18	GNOMAD	ss4281025054	Apr 26, 2021 (155)
19	GNOMAD	ss4281025055	Apr 26, 2021 (155)
20	GNOMAD	ss4281025056	Apr 26, 2021 (155)
21	GNOMAD	ss4281025057	Apr 26, 2021 (155)
22	GNOMAD	ss4281025058	Apr 26, 2021 (155)
23	GNOMAD	ss4281025059	Apr 26, 2021 (155)
24	GNOMAD	ss4281025060	Apr 26, 2021 (155)
25	GNOMAD	ss4281025061	Apr 26, 2021 (155)
26	GNOMAD	ss4281025062	Apr 26, 2021 (155)
27	GNOMAD	ss4281025063	Apr 26, 2021 (155)
28	TOPMED	ss4976589701	Apr 26, 2021 (155)
29	TOPMED	ss4976589702	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5214012113	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5214012114	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5214012115	Apr 26, 2021 (155)
33	1000G_HIGH_COVERAGE	ss5296826489	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5296826490	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5296826491	Oct 16, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5296826492	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5490811961	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5490811962	Oct 16, 2022 (156)
39	HUGCELL_USP	ss5490811963	Oct 16, 2022 (156)
40	SANFORD_IMAGENETICS	ss5656561138	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5767043860	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5767043861	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5767043862	Oct 16, 2022 (156)
44	1000Genomes	NC_000014.8 - 76889486	Oct 12, 2018 (152)
45	The Avon Longitudinal Study of Parents and Children	NC_000014.8 - 76889486	Oct 12, 2018 (152)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 456162311 (NC_000014.9:76423142::T 2995/103996) Row 456162312 (NC_000014.9:76423142::TT 1331/103994) Row 456162313 (NC_000014.9:76423142::TTT 32/104012)...	-	Apr 26, 2021 (155)
57	Korean Genome Project Submission ignored due to conflicting rows: Row 31656145 (NC_000014.9:76423143:T: 632/1830) Row 31656146 (NC_000014.9:76423144::TT 22/1830) Row 31656147 (NC_000014.9:76423142:TT: 101/1830)...	-	Apr 27, 2020 (154)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 31656145 (NC_000014.9:76423143:T: 632/1830) Row 31656146 (NC_000014.9:76423144::TT 22/1830) Row 31656147 (NC_000014.9:76423142:TT: 101/1830)...	-	Apr 27, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 31656145 (NC_000014.9:76423143:T: 632/1830) Row 31656146 (NC_000014.9:76423144::TT 22/1830) Row 31656147 (NC_000014.9:76423142:TT: 101/1830)...	-	Apr 27, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 31656145 (NC_000014.9:76423143:T: 632/1830) Row 31656146 (NC_000014.9:76423144::TT 22/1830) Row 31656147 (NC_000014.9:76423142:TT: 101/1830)...	-	Apr 27, 2020 (154)
61	8.3KJPN Submission ignored due to conflicting rows: Row 71981420 (NC_000014.8:76889485:T: 4999/16688) Row 71981421 (NC_000014.8:76889485::T 189/16688) Row 71981422 (NC_000014.8:76889485:TT: 24/16688)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 71981420 (NC_000014.8:76889485:T: 4999/16688) Row 71981421 (NC_000014.8:76889485::T 189/16688) Row 71981422 (NC_000014.8:76889485:TT: 24/16688)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 71981420 (NC_000014.8:76889485:T: 4999/16688) Row 71981421 (NC_000014.8:76889485::T 189/16688) Row 71981422 (NC_000014.8:76889485:TT: 24/16688)	-	Apr 26, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 100880964 (NC_000014.9:76423142:T: 9381/28254) Row 100880965 (NC_000014.9:76423142::T 343/28254) Row 100880966 (NC_000014.9:76423142:TT: 30/28254)	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 100880964 (NC_000014.9:76423142:T: 9381/28254) Row 100880965 (NC_000014.9:76423142::T 343/28254) Row 100880966 (NC_000014.9:76423142:TT: 30/28254)	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 100880964 (NC_000014.9:76423142:T: 9381/28254) Row 100880965 (NC_000014.9:76423142::T 343/28254) Row 100880966 (NC_000014.9:76423142:TT: 30/28254)	-	Oct 16, 2022 (156)
67	TopMed Submission ignored due to conflicting rows: Row 192135360 (NC_000014.9:76423142:TTTT: 3/264690) Row 192135361 (NC_000014.9:76423142:TTTTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
68	TopMed Submission ignored due to conflicting rows: Row 192135360 (NC_000014.9:76423142:TTTT: 3/264690) Row 192135361 (NC_000014.9:76423142:TTTTTTTTTTTT: 1/264690)	-	Apr 26, 2021 (155)
69	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35953498 (NC_000014.8:76889486:T: 1097/3708) Row 35953499 (NC_000014.8:76889485:TT: 698/3708)	-	Apr 27, 2020 (154)
70	UK 10K study - Twins	-	Oct 12, 2018 (152)
71	ALFA	NC_000014.9 - 76423143	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
ss4281025063, ss4976589702	NC_000014.9:76423142:TTTTTTTTTTTT:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4976589701	NC_000014.9:76423142:TTTT:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4281025062	NC_000014.9:76423142:TTT:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
35953499, ss1708126230, ss1708126280, ss3012482527, ss3787713887, ss5214012115	NC_000014.8:76889485:TT:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3975278146, ss4281025061, ss5296826492, ss5490811963, ss5767043862	NC_000014.9:76423142:TT:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
64697347, ss1374310478, ss3792744319, ss3797628716, ss3834008148, ss5214012113, ss5656561138	NC_000014.8:76889485:T:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1710644576, ss1710644600	NC_000014.8:76889486:T:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3817860973, ss4281025060, ss5296826489, ss5490811961, ss5767043860	NC_000014.9:76423142:T:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3975278144	NC_000014.9:76423143:T:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss40493099	NT_026437.12:57889485:T:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5214012114	NC_000014.8:76889485::T	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4281025053, ss5296826491, ss5490811962, ss5767043861	NC_000014.9:76423142::T	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3975278147	NC_000014.9:76423144::T	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4281025054, ss5296826490	NC_000014.9:76423142::TT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3975278145	NC_000014.9:76423144::TT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4281025055	NC_000014.9:76423142::TTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4281025056	NC_000014.9:76423142::TTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4281025057	NC_000014.9:76423142::TTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4390420	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4281025058	NC_000014.9:76423142::TTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4281025059	NC_000014.9:76423142::TTTTTTTTTTTT… NC_000014.9:76423142::TTTTTTTTTTTTTTTTT	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3215681210	NC_000014.9:76423142:TTTTT:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
ss3215681211	NC_000014.9:76423142:TTTTTT:	NC_000014.9:76423142:TTTTTTTTTTTTT… NC_000014.9:76423142:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

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

No publications for rs397853103

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

rs397853103