Name: rs71063553
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.

rs71063553

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:114233067-114233082 (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(GC)₅ / del(GC)₄ / del(GC)₃ / d…
del(GC)₅ / del(GC)₄ / del(GC)₃ / delGCGC / delGC / dupGC / dupGCGC / dup(GC)₃ / dup(GC)₄ / dup(GC)₅ / dup(GC)₆ / dup(GC)₇
Variation Type: Indel Insertion and Deletion
Frequency: del(GC)₅=0.00000 (0/11078, ALFA)
del(GC)₄=0.00000 (0/11078, ALFA)
del(GC)₃=0.00000 (0/11078, ALFA) (+ 10 more)
delGCGC=0.00000 (0/11078, ALFA)
delGC=0.00000 (0/11078, ALFA)
dupGC=0.00000 (0/11078, ALFA)
dupGCGC=0.00000 (0/11078, ALFA)
dup(GC)₃=0.00000 (0/11078, ALFA)
dup(GC)₄=0.00000 (0/11078, ALFA)
dup(GC)₅=0.00000 (0/11078, ALFA)
dup(GC)₆=0.00000 (0/11078, ALFA)
dup(GC)₇=0.00000 (0/11078, ALFA)
delGC=0.33 (13/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZBTB16 : 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	11078	GCGCGCGCGCGCGCGC=1.00000	GCGCGC=0.00000, GCGCGCGC=0.00000, GCGCGCGCGC=0.00000, GCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00000	1.0	N/A
European	Sub	7234	GCGCGCGCGCGCGCGC=1.0000	GCGCGC=0.0000, GCGCGCGC=0.0000, GCGCGCGCGC=0.0000, GCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000	1.0	N/A
African	Sub	2492	GCGCGCGCGCGCGCGC=1.0000	GCGCGC=0.0000, GCGCGCGC=0.0000, GCGCGCGCGC=0.0000, GCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000	1.0	N/A
African Others	Sub	96	GCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
African American	Sub	2396	GCGCGCGCGCGCGCGC=1.0000	GCGCGC=0.0000, GCGCGCGC=0.0000, GCGCGCGCGC=0.0000, GCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.0000	1.0	N/A
Asian	Sub	102	GCGCGCGCGCGCGCGC=1.000	GCGCGC=0.000, GCGCGCGC=0.000, GCGCGCGCGC=0.000, GCGCGCGCGCGC=0.000, GCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.000	1.0	N/A
East Asian	Sub	82	GCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
Other Asian	Sub	20	GCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
Latin American 1	Sub	134	GCGCGCGCGCGCGCGC=1.000	GCGCGC=0.000, GCGCGCGC=0.000, GCGCGCGCGC=0.000, GCGCGCGCGCGC=0.000, GCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.000	1.0	N/A
Latin American 2	Sub	588	GCGCGCGCGCGCGCGC=1.000	GCGCGC=0.000, GCGCGCGC=0.000, GCGCGCGCGC=0.000, GCGCGCGCGCGC=0.000, GCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.000	1.0	N/A
South Asian	Sub	88	GCGCGCGCGCGCGCGC=1.00	GCGCGC=0.00, GCGCGCGC=0.00, GCGCGCGCGC=0.00, GCGCGCGCGCGC=0.00, GCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.00	1.0	N/A
Other	Sub	440	GCGCGCGCGCGCGCGC=1.000	GCGCGC=0.000, GCGCGCGC=0.000, GCGCGCGCGC=0.000, GCGCGCGCGCGC=0.000, GCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGC=0.000, GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC=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	11078	(GC)₈=1.00000	del(GC)₅=0.00000, del(GC)₄=0.00000, del(GC)₃=0.00000, delGCGC=0.00000, delGC=0.00000, dupGC=0.00000, dupGCGC=0.00000, dup(GC)₃=0.00000, dup(GC)₄=0.00000, dup(GC)₅=0.00000, dup(GC)₆=0.00000, dup(GC)₇=0.00000
Allele Frequency Aggregator	European	Sub	7234	(GC)₈=1.0000	del(GC)₅=0.0000, del(GC)₄=0.0000, del(GC)₃=0.0000, delGCGC=0.0000, delGC=0.0000, dupGC=0.0000, dupGCGC=0.0000, dup(GC)₃=0.0000, dup(GC)₄=0.0000, dup(GC)₅=0.0000, dup(GC)₆=0.0000, dup(GC)₇=0.0000
Allele Frequency Aggregator	African	Sub	2492	(GC)₈=1.0000	del(GC)₅=0.0000, del(GC)₄=0.0000, del(GC)₃=0.0000, delGCGC=0.0000, delGC=0.0000, dupGC=0.0000, dupGCGC=0.0000, dup(GC)₃=0.0000, dup(GC)₄=0.0000, dup(GC)₅=0.0000, dup(GC)₆=0.0000, dup(GC)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	588	(GC)₈=1.000	del(GC)₅=0.000, del(GC)₄=0.000, del(GC)₃=0.000, delGCGC=0.000, delGC=0.000, dupGC=0.000, dupGCGC=0.000, dup(GC)₃=0.000, dup(GC)₄=0.000, dup(GC)₅=0.000, dup(GC)₆=0.000, dup(GC)₇=0.000
Allele Frequency Aggregator	Other	Sub	440	(GC)₈=1.000	del(GC)₅=0.000, del(GC)₄=0.000, del(GC)₃=0.000, delGCGC=0.000, delGC=0.000, dupGC=0.000, dupGCGC=0.000, dup(GC)₃=0.000, dup(GC)₄=0.000, dup(GC)₅=0.000, dup(GC)₆=0.000, dup(GC)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	134	(GC)₈=1.000	del(GC)₅=0.000, del(GC)₄=0.000, del(GC)₃=0.000, delGCGC=0.000, delGC=0.000, dupGC=0.000, dupGCGC=0.000, dup(GC)₃=0.000, dup(GC)₄=0.000, dup(GC)₅=0.000, dup(GC)₆=0.000, dup(GC)₇=0.000
Allele Frequency Aggregator	Asian	Sub	102	(GC)₈=1.000	del(GC)₅=0.000, del(GC)₄=0.000, del(GC)₃=0.000, delGCGC=0.000, delGC=0.000, dupGC=0.000, dupGCGC=0.000, dup(GC)₃=0.000, dup(GC)₄=0.000, dup(GC)₅=0.000, dup(GC)₆=0.000, dup(GC)₇=0.000
Allele Frequency Aggregator	South Asian	Sub	88	(GC)₈=1.00	del(GC)₅=0.00, del(GC)₄=0.00, del(GC)₃=0.00, delGCGC=0.00, delGC=0.00, dupGC=0.00, dupGCGC=0.00, dup(GC)₃=0.00, dup(GC)₄=0.00, dup(GC)₅=0.00, dup(GC)₆=0.00, dup(GC)₇=0.00
The Danish reference pan genome	Danish	Study-wide	40	(GC)₈=0.68	delGC=0.33

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 11	NC_000011.10:g.114233067GC[3]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[4]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[5]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[6]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[7]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[9]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[10]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[11]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[12]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[13]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[14]
GRCh38.p14 chr 11	NC_000011.10:g.114233067GC[15]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[3]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[4]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[5]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[6]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[7]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[9]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[10]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[11]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[12]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[13]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[14]
GRCh37.p13 chr 11	NC_000011.9:g.114103789GC[15]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[3]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[4]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[5]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[6]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[7]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[9]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[10]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[11]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[12]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[13]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[14]
ZBTB16 RefSeqGene	NG_012140.2:g.178492GC[15]

Gene: ZBTB16, zinc finger and BTB domain containing 16 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZBTB16 transcript variant 2	NM_001018011.3:c.1454-910… NM_001018011.3:c.1454-9100GC[3]	N/A	Intron Variant
ZBTB16 transcript variant 3	NM_001354750.2:c.1454-910… NM_001354750.2:c.1454-9100GC[3]	N/A	Intron Variant
ZBTB16 transcript variant 4	NM_001354751.2:c.1454-910… NM_001354751.2:c.1454-9100GC[3]	N/A	Intron Variant
ZBTB16 transcript variant 5	NM_001354752.1:c.1367-910… NM_001354752.1:c.1367-9100GC[3]	N/A	Intron Variant
ZBTB16 transcript variant 1	NM_006006.6:c.1454-9100GC… NM_006006.6:c.1454-9100GC[3]	N/A	Intron Variant
ZBTB16 transcript variant X1	XM_005271658.6:c.	N/A	Genic Downstream Transcript Variant
ZBTB16 transcript variant X2	XM_047427563.1:c.	N/A	Genic Downstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(GC)₈=	del(GC)₅	del(GC)₄	del(GC)₃	delGCGC	delGC	dupGC	dupGCGC	dup(GC)₃	dup(GC)₄	dup(GC)₅	dup(GC)₆	dup(GC)₇
GRCh38.p14 chr 11	NC_000011.10:g.114233067_114233082=	NC_000011.10:g.114233067GC[3]	NC_000011.10:g.114233067GC[4]	NC_000011.10:g.114233067GC[5]	NC_000011.10:g.114233067GC[6]	NC_000011.10:g.114233067GC[7]	NC_000011.10:g.114233067GC[9]	NC_000011.10:g.114233067GC[10]	NC_000011.10:g.114233067GC[11]	NC_000011.10:g.114233067GC[12]	NC_000011.10:g.114233067GC[13]	NC_000011.10:g.114233067GC[14]	NC_000011.10:g.114233067GC[15]
GRCh37.p13 chr 11	NC_000011.9:g.114103789_114103804=	NC_000011.9:g.114103789GC[3]	NC_000011.9:g.114103789GC[4]	NC_000011.9:g.114103789GC[5]	NC_000011.9:g.114103789GC[6]	NC_000011.9:g.114103789GC[7]	NC_000011.9:g.114103789GC[9]	NC_000011.9:g.114103789GC[10]	NC_000011.9:g.114103789GC[11]	NC_000011.9:g.114103789GC[12]	NC_000011.9:g.114103789GC[13]	NC_000011.9:g.114103789GC[14]	NC_000011.9:g.114103789GC[15]
ZBTB16 RefSeqGene	NG_012140.2:g.178492_178507=	NG_012140.2:g.178492GC[3]	NG_012140.2:g.178492GC[4]	NG_012140.2:g.178492GC[5]	NG_012140.2:g.178492GC[6]	NG_012140.2:g.178492GC[7]	NG_012140.2:g.178492GC[9]	NG_012140.2:g.178492GC[10]	NG_012140.2:g.178492GC[11]	NG_012140.2:g.178492GC[12]	NG_012140.2:g.178492GC[13]	NG_012140.2:g.178492GC[14]	NG_012140.2:g.178492GC[15]
ZBTB16 transcript variant 2	NM_001018011.1:c.1454-9100=	NM_001018011.1:c.1454-9100GC[3]	NM_001018011.1:c.1454-9100GC[4]	NM_001018011.1:c.1454-9100GC[5]	NM_001018011.1:c.1454-9100GC[6]	NM_001018011.1:c.1454-9100GC[7]	NM_001018011.1:c.1454-9100GC[9]	NM_001018011.1:c.1454-9100GC[10]	NM_001018011.1:c.1454-9100GC[11]	NM_001018011.1:c.1454-9100GC[12]	NM_001018011.1:c.1454-9100GC[13]	NM_001018011.1:c.1454-9100GC[14]	NM_001018011.1:c.1454-9100GC[15]
ZBTB16 transcript variant 2	NM_001018011.3:c.1454-9100=	NM_001018011.3:c.1454-9100GC[3]	NM_001018011.3:c.1454-9100GC[4]	NM_001018011.3:c.1454-9100GC[5]	NM_001018011.3:c.1454-9100GC[6]	NM_001018011.3:c.1454-9100GC[7]	NM_001018011.3:c.1454-9100GC[9]	NM_001018011.3:c.1454-9100GC[10]	NM_001018011.3:c.1454-9100GC[11]	NM_001018011.3:c.1454-9100GC[12]	NM_001018011.3:c.1454-9100GC[13]	NM_001018011.3:c.1454-9100GC[14]	NM_001018011.3:c.1454-9100GC[15]
ZBTB16 transcript variant 3	NM_001354750.2:c.1454-9100=	NM_001354750.2:c.1454-9100GC[3]	NM_001354750.2:c.1454-9100GC[4]	NM_001354750.2:c.1454-9100GC[5]	NM_001354750.2:c.1454-9100GC[6]	NM_001354750.2:c.1454-9100GC[7]	NM_001354750.2:c.1454-9100GC[9]	NM_001354750.2:c.1454-9100GC[10]	NM_001354750.2:c.1454-9100GC[11]	NM_001354750.2:c.1454-9100GC[12]	NM_001354750.2:c.1454-9100GC[13]	NM_001354750.2:c.1454-9100GC[14]	NM_001354750.2:c.1454-9100GC[15]
ZBTB16 transcript variant 4	NM_001354751.2:c.1454-9100=	NM_001354751.2:c.1454-9100GC[3]	NM_001354751.2:c.1454-9100GC[4]	NM_001354751.2:c.1454-9100GC[5]	NM_001354751.2:c.1454-9100GC[6]	NM_001354751.2:c.1454-9100GC[7]	NM_001354751.2:c.1454-9100GC[9]	NM_001354751.2:c.1454-9100GC[10]	NM_001354751.2:c.1454-9100GC[11]	NM_001354751.2:c.1454-9100GC[12]	NM_001354751.2:c.1454-9100GC[13]	NM_001354751.2:c.1454-9100GC[14]	NM_001354751.2:c.1454-9100GC[15]
ZBTB16 transcript variant 5	NM_001354752.1:c.1367-9100=	NM_001354752.1:c.1367-9100GC[3]	NM_001354752.1:c.1367-9100GC[4]	NM_001354752.1:c.1367-9100GC[5]	NM_001354752.1:c.1367-9100GC[6]	NM_001354752.1:c.1367-9100GC[7]	NM_001354752.1:c.1367-9100GC[9]	NM_001354752.1:c.1367-9100GC[10]	NM_001354752.1:c.1367-9100GC[11]	NM_001354752.1:c.1367-9100GC[12]	NM_001354752.1:c.1367-9100GC[13]	NM_001354752.1:c.1367-9100GC[14]	NM_001354752.1:c.1367-9100GC[15]
ZBTB16 transcript variant 1	NM_006006.4:c.1454-9100=	NM_006006.4:c.1454-9100GC[3]	NM_006006.4:c.1454-9100GC[4]	NM_006006.4:c.1454-9100GC[5]	NM_006006.4:c.1454-9100GC[6]	NM_006006.4:c.1454-9100GC[7]	NM_006006.4:c.1454-9100GC[9]	NM_006006.4:c.1454-9100GC[10]	NM_006006.4:c.1454-9100GC[11]	NM_006006.4:c.1454-9100GC[12]	NM_006006.4:c.1454-9100GC[13]	NM_006006.4:c.1454-9100GC[14]	NM_006006.4:c.1454-9100GC[15]
ZBTB16 transcript variant 1	NM_006006.6:c.1454-9100=	NM_006006.6:c.1454-9100GC[3]	NM_006006.6:c.1454-9100GC[4]	NM_006006.6:c.1454-9100GC[5]	NM_006006.6:c.1454-9100GC[6]	NM_006006.6:c.1454-9100GC[7]	NM_006006.6:c.1454-9100GC[9]	NM_006006.6:c.1454-9100GC[10]	NM_006006.6:c.1454-9100GC[11]	NM_006006.6:c.1454-9100GC[12]	NM_006006.6:c.1454-9100GC[13]	NM_006006.6:c.1454-9100GC[14]	NM_006006.6:c.1454-9100GC[15]
ZBTB16 transcript variant X1	XM_005271657.1:c.1454-9100=	XM_005271657.1:c.1454-9100GC[3]	XM_005271657.1:c.1454-9100GC[4]	XM_005271657.1:c.1454-9100GC[5]	XM_005271657.1:c.1454-9100GC[6]	XM_005271657.1:c.1454-9100GC[7]	XM_005271657.1:c.1454-9100GC[9]	XM_005271657.1:c.1454-9100GC[10]	XM_005271657.1:c.1454-9100GC[11]	XM_005271657.1:c.1454-9100GC[12]	XM_005271657.1:c.1454-9100GC[13]	XM_005271657.1:c.1454-9100GC[14]	XM_005271657.1:c.1454-9100GC[15]

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#.

59 SubSNP, 36 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95580876	Feb 13, 2009 (130)
2	1000GENOMES	ss327473181	May 09, 2011 (134)
3	LUNTER	ss552434877	Apr 25, 2013 (138)
4	EVA_GENOME_DK	ss1574419306	Apr 01, 2015 (144)
5	URBANLAB	ss3649709350	Oct 12, 2018 (152)
6	EVA_DECODE	ss3692638945	Jul 13, 2019 (153)
7	EVA_DECODE	ss3692638946	Jul 13, 2019 (153)
8	EVA_DECODE	ss3692638947	Jul 13, 2019 (153)
9	EVA_DECODE	ss3692638948	Jul 13, 2019 (153)
10	EVA_DECODE	ss3692638949	Jul 13, 2019 (153)
11	EVA_DECODE	ss3692638950	Jul 13, 2019 (153)
12	ACPOP	ss3738557684	Jul 13, 2019 (153)
13	ACPOP	ss3738557685	Jul 13, 2019 (153)
14	ACPOP	ss3738557686	Jul 13, 2019 (153)
15	ACPOP	ss3738557688	Jul 13, 2019 (153)
16	PACBIO	ss3787073192	Jul 13, 2019 (153)
17	KHV_HUMAN_GENOMES	ss3815167336	Jul 13, 2019 (153)
18	EVA	ss3832849255	Apr 26, 2020 (154)
19	KOGIC	ss3970788575	Apr 26, 2020 (154)
20	KOGIC	ss3970788576	Apr 26, 2020 (154)
21	KOGIC	ss3970788577	Apr 26, 2020 (154)
22	KOGIC	ss3970788578	Apr 26, 2020 (154)
23	KOGIC	ss3970788579	Apr 26, 2020 (154)
24	KOGIC	ss3970788580	Apr 26, 2020 (154)
25	GNOMAD	ss4242928620	Apr 26, 2021 (155)
26	GNOMAD	ss4242928621	Apr 26, 2021 (155)
27	GNOMAD	ss4242928622	Apr 26, 2021 (155)
28	GNOMAD	ss4242928623	Apr 26, 2021 (155)
29	GNOMAD	ss4242928627	Apr 26, 2021 (155)
30	GNOMAD	ss4242928628	Apr 26, 2021 (155)
31	GNOMAD	ss4242928629	Apr 26, 2021 (155)
32	GNOMAD	ss4242928630	Apr 26, 2021 (155)
33	GNOMAD	ss4242928631	Apr 26, 2021 (155)
34	GNOMAD	ss4242928632	Apr 26, 2021 (155)
35	GNOMAD	ss4242928633	Apr 26, 2021 (155)
36	GNOMAD	ss4242928634	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5203980591	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5203980592	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5203980593	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5203980594	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5203980595	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5203980596	Apr 26, 2021 (155)
43	1000G_HIGH_COVERAGE	ss5288973335	Oct 16, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5288973336	Oct 16, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5288973337	Oct 16, 2022 (156)
46	1000G_HIGH_COVERAGE	ss5288973338	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5483955740	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5483955741	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5483955742	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5483955743	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5752454814	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5752454815	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5752454816	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5752454817	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5752454818	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5752454819	Oct 16, 2022 (156)
57	EVA	ss5837257508	Oct 16, 2022 (156)
58	EVA	ss5837257509	Oct 16, 2022 (156)
59	EVA	ss5837257510	Oct 16, 2022 (156)
60	The Danish reference pan genome	NC_000011.9 - 114103789	Apr 26, 2020 (154)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392558634 (NC_000011.10:114233066::GC 1634/87540) Row 392558635 (NC_000011.10:114233066::GCGC 456/87756) Row 392558636 (NC_000011.10:114233066::GCGCGC 361/87766)...	-	Apr 26, 2021 (155)
73	Korean Genome Project Submission ignored due to conflicting rows: Row 27166576 (NC_000011.10:114233068:GCGC: 287/1702) Row 27166577 (NC_000011.10:114233070:GC: 173/1702) Row 27166578 (NC_000011.10:114233066:GCGCGC: 175/1702)...	-	Apr 26, 2020 (154)
74	Korean Genome Project Submission ignored due to conflicting rows: Row 27166576 (NC_000011.10:114233068:GCGC: 287/1702) Row 27166577 (NC_000011.10:114233070:GC: 173/1702) Row 27166578 (NC_000011.10:114233066:GCGCGC: 175/1702)...	-	Apr 26, 2020 (154)
75	Korean Genome Project Submission ignored due to conflicting rows: Row 27166576 (NC_000011.10:114233068:GCGC: 287/1702) Row 27166577 (NC_000011.10:114233070:GC: 173/1702) Row 27166578 (NC_000011.10:114233066:GCGCGC: 175/1702)...	-	Apr 26, 2020 (154)
76	Korean Genome Project Submission ignored due to conflicting rows: Row 27166576 (NC_000011.10:114233068:GCGC: 287/1702) Row 27166577 (NC_000011.10:114233070:GC: 173/1702) Row 27166578 (NC_000011.10:114233066:GCGCGC: 175/1702)...	-	Apr 26, 2020 (154)
77	Korean Genome Project Submission ignored due to conflicting rows: Row 27166576 (NC_000011.10:114233068:GCGC: 287/1702) Row 27166577 (NC_000011.10:114233070:GC: 173/1702) Row 27166578 (NC_000011.10:114233066:GCGCGC: 175/1702)...	-	Apr 26, 2020 (154)
78	Korean Genome Project Submission ignored due to conflicting rows: Row 27166576 (NC_000011.10:114233068:GCGC: 287/1702) Row 27166577 (NC_000011.10:114233070:GC: 173/1702) Row 27166578 (NC_000011.10:114233066:GCGCGC: 175/1702)...	-	Apr 26, 2020 (154)
79	Northern Sweden Submission ignored due to conflicting rows: Row 11842549 (NC_000011.9:114103788:GCGC: 128/510) Row 11842550 (NC_000011.9:114103788:GCGCGC: 27/510) Row 11842551 (NC_000011.9:114103788:GC: 59/510)...	-	Jul 13, 2019 (153)
80	Northern Sweden Submission ignored due to conflicting rows: Row 11842549 (NC_000011.9:114103788:GCGC: 128/510) Row 11842550 (NC_000011.9:114103788:GCGCGC: 27/510) Row 11842551 (NC_000011.9:114103788:GC: 59/510)...	-	Jul 13, 2019 (153)
81	Northern Sweden Submission ignored due to conflicting rows: Row 11842549 (NC_000011.9:114103788:GCGC: 128/510) Row 11842550 (NC_000011.9:114103788:GCGCGC: 27/510) Row 11842551 (NC_000011.9:114103788:GC: 59/510)...	-	Jul 13, 2019 (153)
82	Northern Sweden Submission ignored due to conflicting rows: Row 11842549 (NC_000011.9:114103788:GCGC: 128/510) Row 11842550 (NC_000011.9:114103788:GCGCGC: 27/510) Row 11842551 (NC_000011.9:114103788:GC: 59/510)...	-	Jul 13, 2019 (153)
83	8.3KJPN Submission ignored due to conflicting rows: Row 61949898 (NC_000011.9:114103788:GCGC: 1784/15088) Row 61949899 (NC_000011.9:114103788:GCGCGC: 1371/15088) Row 61949900 (NC_000011.9:114103788:GC: 1635/15088)...	-	Apr 26, 2021 (155)
84	8.3KJPN Submission ignored due to conflicting rows: Row 61949898 (NC_000011.9:114103788:GCGC: 1784/15088) Row 61949899 (NC_000011.9:114103788:GCGCGC: 1371/15088) Row 61949900 (NC_000011.9:114103788:GC: 1635/15088)...	-	Apr 26, 2021 (155)
85	8.3KJPN Submission ignored due to conflicting rows: Row 61949898 (NC_000011.9:114103788:GCGC: 1784/15088) Row 61949899 (NC_000011.9:114103788:GCGCGC: 1371/15088) Row 61949900 (NC_000011.9:114103788:GC: 1635/15088)...	-	Apr 26, 2021 (155)
86	8.3KJPN Submission ignored due to conflicting rows: Row 61949898 (NC_000011.9:114103788:GCGC: 1784/15088) Row 61949899 (NC_000011.9:114103788:GCGCGC: 1371/15088) Row 61949900 (NC_000011.9:114103788:GC: 1635/15088)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 61949898 (NC_000011.9:114103788:GCGC: 1784/15088) Row 61949899 (NC_000011.9:114103788:GCGCGC: 1371/15088) Row 61949900 (NC_000011.9:114103788:GC: 1635/15088)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 61949898 (NC_000011.9:114103788:GCGC: 1784/15088) Row 61949899 (NC_000011.9:114103788:GCGCGC: 1371/15088) Row 61949900 (NC_000011.9:114103788:GC: 1635/15088)...	-	Apr 26, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 86291918 (NC_000011.10:114233066:GCGC: 3475/26988) Row 86291919 (NC_000011.10:114233066::GCGCGC 136/26988) Row 86291920 (NC_000011.10:114233066::GCGCGCGC 606/26988)...	-	Oct 16, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 86291918 (NC_000011.10:114233066:GCGC: 3475/26988) Row 86291919 (NC_000011.10:114233066::GCGCGC 136/26988) Row 86291920 (NC_000011.10:114233066::GCGCGCGC 606/26988)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 86291918 (NC_000011.10:114233066:GCGC: 3475/26988) Row 86291919 (NC_000011.10:114233066::GCGCGC 136/26988) Row 86291920 (NC_000011.10:114233066::GCGCGCGC 606/26988)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 86291918 (NC_000011.10:114233066:GCGC: 3475/26988) Row 86291919 (NC_000011.10:114233066::GCGCGC 136/26988) Row 86291920 (NC_000011.10:114233066::GCGCGCGC 606/26988)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 86291918 (NC_000011.10:114233066:GCGC: 3475/26988) Row 86291919 (NC_000011.10:114233066::GCGCGC 136/26988) Row 86291920 (NC_000011.10:114233066::GCGCGCGC 606/26988)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 86291918 (NC_000011.10:114233066:GCGC: 3475/26988) Row 86291919 (NC_000011.10:114233066::GCGCGC 136/26988) Row 86291920 (NC_000011.10:114233066::GCGCGCGC 606/26988)...	-	Oct 16, 2022 (156)
95	ALFA	NC_000011.10 - 114233067	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs71911782	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4242928634	NC_000011.10:114233066:GCGCGCGCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGC	(self)
ss4242928633	NC_000011.10:114233066:GCGCGCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGC	(self)
ss552434877	NC_000011.8:113608998:GCGCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGC	(self)
ss3738557685, ss3832849255, ss5203980592, ss5837257510	NC_000011.9:114103788:GCGCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGC	(self)
ss3649709350, ss3692638950, ss3970788577, ss4242928632, ss5288973338, ss5483955742, ss5752454818	NC_000011.10:114233066:GCGCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGC	(self)
ss95580876	NT_033899.8:17666210:GCGCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGC	(self)
ss327473181	NC_000011.8:113608998:GCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
ss3738557684, ss5203980591, ss5837257508	NC_000011.9:114103788:GCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
ss3815167336, ss4242928631, ss5288973335, ss5483955743, ss5752454814	NC_000011.10:114233066:GCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
ss3692638949, ss3970788575	NC_000011.10:114233068:GCGC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGC	(self)
322211, ss1574419306, ss3738557686, ss3787073192, ss5203980593, ss5837257509	NC_000011.9:114103788:GC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	(self)
ss4242928630, ss5288973336, ss5483955741, ss5752454819	NC_000011.10:114233066:GC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	(self)
ss3692638948, ss3970788576	NC_000011.10:114233070:GC:	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGC	(self)
ss3738557688	NC_000011.9:114103788::GC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGC	(self)
ss4242928620, ss5288973337, ss5483955740	NC_000011.10:114233066::GC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGC	(self)
ss3692638947	NC_000011.10:114233072::GC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGC	(self)
ss4242928621	NC_000011.10:114233066::GCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	(self)
ss3692638946	NC_000011.10:114233072::GCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGC	(self)
ss5203980594	NC_000011.9:114103788::GCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	(self)
ss4242928622, ss5752454815	NC_000011.10:114233066::GCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	(self)
ss3692638945, ss3970788579	NC_000011.10:114233072::GCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGC	(self)
ss5203980596	NC_000011.9:114103788::GCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGC	(self)
ss4242928623, ss5752454816	NC_000011.10:114233066::GCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGC	(self)
ss3970788578	NC_000011.10:114233072::GCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGC	(self)
ss5203980595	NC_000011.9:114103788::GCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGC	(self)
ss4242928627, ss5752454817	NC_000011.10:114233066::GCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGC	(self)
ss3970788580	NC_000011.10:114233072::GCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGC	(self)
ss4242928628	NC_000011.10:114233066::GCGCGCGCGC… NC_000011.10:114233066::GCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGCGC	(self)
ss4242928629	NC_000011.10:114233066::GCGCGCGCGC… NC_000011.10:114233066::GCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC	(self)
941467992	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC	NC_000011.10:114233066:GCGCGCGCGCG… NC_000011.10:114233066:GCGCGCGCGCGCGCGC:GCGCGCGCGCGCGCGCGCGCGCGCGCGCGC	(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 rs71063553

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
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71063553