Name: rs71200966
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.

rs71200966

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:16682575-16682576 (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: dupCA / insCACA / ins(CA)₃ / ins(C…
dupCA / insCACA / ins(CA)₃ / ins(CA)₄ / ins(CA)₅ / ins(CA)₆ / ins(CA)₇ / ins(CA)₈ / ins(CA)₉ / ins(CA)₁₀ / ins(CA)₁₁ / ins(CA)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: CA=0.3232 (1411/4366, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RSU1 : Intron Variant
LOC124902385 : Non Coding Transcript 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	4366	CA=0.3232	CACACACACACACA=0.1196, CACACACACACA=0.4196, CACACACACACACACA=0.0772, CACACACACA=0.0298, CACACACA=0.0195, CACACACACACACACACA=0.0112	0.229867	0.360438	0.409695	19
European	Sub	4358	CA=0.3226	CACACACACACACA=0.1198, CACACACACACA=0.4199, CACACACACACACACA=0.0773, CACACACACA=0.0298, CACACACA=0.0193, CACACACACACACACACA=0.0112	0.229624	0.361285	0.409091	19
African	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
African Others	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
African American	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
Asian	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
East Asian	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
Other Asian	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
Latin American 1	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
Latin American 2	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
South Asian	Sub	0	CA=0	CACACACACACACA=0, CACACACACACA=0, CACACACACACACACA=0, CACACACACA=0, CACACACA=0, CACACACACACACACACA=0	0	0	0	N/A
Other	Sub	8	CA=0.6	CACACACACACACA=0.0, CACACACACACA=0.2, CACACACACACACACA=0.0, CACACACACA=0.0, CACACACA=0.1, CACACACACACACACACA=0.0	0.333333	0.0	0.666667	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	4366	CA=0.3232	ins(CA)₃=0.0195, ins(CA)₄=0.0298, ins(CA)₅=0.4196, ins(CA)₆=0.1196, ins(CA)₇=0.0772, ins(CA)₈=0.0112
Allele Frequency Aggregator	European	Sub	4358	CA=0.3226	ins(CA)₃=0.0193, ins(CA)₄=0.0298, ins(CA)₅=0.4199, ins(CA)₆=0.1198, ins(CA)₇=0.0773, ins(CA)₈=0.0112
Allele Frequency Aggregator	Other	Sub	8	CA=0.6	ins(CA)₃=0.1, ins(CA)₄=0.0, ins(CA)₅=0.2, ins(CA)₆=0.0, ins(CA)₇=0.0, ins(CA)₈=0.0
Allele Frequency Aggregator	Latin American 1	Sub	0	CA=0	ins(CA)₃=0, ins(CA)₄=0, ins(CA)₅=0, ins(CA)₆=0, ins(CA)₇=0, ins(CA)₈=0
Allele Frequency Aggregator	Latin American 2	Sub	0	CA=0	ins(CA)₃=0, ins(CA)₄=0, ins(CA)₅=0, ins(CA)₆=0, ins(CA)₇=0, ins(CA)₈=0
Allele Frequency Aggregator	South Asian	Sub	0	CA=0	ins(CA)₃=0, ins(CA)₄=0, ins(CA)₅=0, ins(CA)₆=0, ins(CA)₇=0, ins(CA)₈=0
Allele Frequency Aggregator	African	Sub	0	CA=0	ins(CA)₃=0, ins(CA)₄=0, ins(CA)₅=0, ins(CA)₆=0, ins(CA)₇=0, ins(CA)₈=0
Allele Frequency Aggregator	Asian	Sub	0	CA=0	ins(CA)₃=0, ins(CA)₄=0, ins(CA)₅=0, ins(CA)₆=0, ins(CA)₇=0, ins(CA)₈=0

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 10	NC_000010.11:g.16682575_16682576dup
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[3]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[4]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[5]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[6]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[7]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[8]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[9]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[10]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[11]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[12]
GRCh38.p14 chr 10	NC_000010.11:g.16682575CA[14]
GRCh37.p13 chr 10	NC_000010.10:g.16724574_16724575dup
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[3]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[4]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[5]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[6]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[7]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[8]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[9]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[10]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[11]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[12]
GRCh37.p13 chr 10	NC_000010.10:g.16724574CA[14]

Gene: RSU1, Ras suppressor protein 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
RSU1 transcript variant 1	NM_012425.4:c.731+12447_7… NM_012425.4:c.731+12447_731+12448dup	N/A	Intron Variant
RSU1 transcript variant 2	NM_152724.3:c.572+12447_5… NM_152724.3:c.572+12447_572+12448dup	N/A	Intron Variant
RSU1 transcript variant X1	XM_047425617.1:c.598+6996… XM_047425617.1:c.598+69963_598+69964dup	N/A	Intron Variant

Gene: LOC124902385, uncharacterized LOC124902385 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
LOC124902385 transcript	XR_007062073.1:n.4918_491… XR_007062073.1:n.4918_4919dup	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[3]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[4]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[5]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[6]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[7]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[8]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[9]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[1… XR_007062073.1:n.4918TG[10]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[1… XR_007062073.1:n.4918TG[11]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[1… XR_007062073.1:n.4918TG[12]	N/A	Non Coding Transcript Variant
LOC124902385 transcript	XR_007062073.1:n.4918TG[1… XR_007062073.1:n.4918TG[14]	N/A	Non Coding 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	CA=	dupCA	insCACA	ins(CA)₃	ins(CA)₄	ins(CA)₅	ins(CA)₆	ins(CA)₇	ins(CA)₈	ins(CA)₉	ins(CA)₁₀	ins(CA)₁₁	ins(CA)₁₃
GRCh38.p14 chr 10	NC_000010.11:g.16682575_16682576=	NC_000010.11:g.16682575_16682576dup	NC_000010.11:g.16682575CA[3]	NC_000010.11:g.16682575CA[4]	NC_000010.11:g.16682575CA[5]	NC_000010.11:g.16682575CA[6]	NC_000010.11:g.16682575CA[7]	NC_000010.11:g.16682575CA[8]	NC_000010.11:g.16682575CA[9]	NC_000010.11:g.16682575CA[10]	NC_000010.11:g.16682575CA[11]	NC_000010.11:g.16682575CA[12]	NC_000010.11:g.16682575CA[14]
GRCh37.p13 chr 10	NC_000010.10:g.16724574_16724575=	NC_000010.10:g.16724574_16724575dup	NC_000010.10:g.16724574CA[3]	NC_000010.10:g.16724574CA[4]	NC_000010.10:g.16724574CA[5]	NC_000010.10:g.16724574CA[6]	NC_000010.10:g.16724574CA[7]	NC_000010.10:g.16724574CA[8]	NC_000010.10:g.16724574CA[9]	NC_000010.10:g.16724574CA[10]	NC_000010.10:g.16724574CA[11]	NC_000010.10:g.16724574CA[12]	NC_000010.10:g.16724574CA[14]
LOC124902385 transcript	XR_007062073.1:n.4918_4919=	XR_007062073.1:n.4918_4919dup	XR_007062073.1:n.4918TG[3]	XR_007062073.1:n.4918TG[4]	XR_007062073.1:n.4918TG[5]	XR_007062073.1:n.4918TG[6]	XR_007062073.1:n.4918TG[7]	XR_007062073.1:n.4918TG[8]	XR_007062073.1:n.4918TG[9]	XR_007062073.1:n.4918TG[10]	XR_007062073.1:n.4918TG[11]	XR_007062073.1:n.4918TG[12]	XR_007062073.1:n.4918TG[14]
RSU1 transcript variant 1	NM_012425.3:c.731+12448=	NM_012425.3:c.731+12447_731+12448dup	NM_012425.3:c.731+12448_731+12449insTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTGTGTG	NM_012425.3:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTGTGTGTGTG
RSU1 transcript variant 1	NM_012425.4:c.731+12448=	NM_012425.4:c.731+12447_731+12448dup	NM_012425.4:c.731+12448_731+12449insTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTGTGTG	NM_012425.4:c.731+12448_731+12449insTGTGTGTGTGTGTGTGTGTGTGTGTG
RSU1 transcript variant 2	NM_152724.2:c.572+12448=	NM_152724.2:c.572+12447_572+12448dup	NM_152724.2:c.572+12448_572+12449insTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTGTGTG	NM_152724.2:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTGTGTGTGTG
RSU1 transcript variant 2	NM_152724.3:c.572+12448=	NM_152724.3:c.572+12447_572+12448dup	NM_152724.3:c.572+12448_572+12449insTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTGTGTG	NM_152724.3:c.572+12448_572+12449insTGTGTGTGTGTGTGTGTGTGTGTGTG
RSU1 transcript variant X1	XM_005252552.1:c.598+69964=	XM_005252552.1:c.598+69963_598+69964dup	XM_005252552.1:c.598+69964_598+69965insTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTGTGTG	XM_005252552.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTGTGTGTGTG
RSU1 transcript variant X2	XM_005252553.1:c.680+12448=	XM_005252553.1:c.680+12447_680+12448dup	XM_005252553.1:c.680+12448_680+12449insTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTGTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTGTGTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTGTGTGTGTGTGTG	XM_005252553.1:c.680+12448_680+12449insTGTGTGTGTGTGTGTGTGTGTGTGTG
RSU1 transcript variant X1	XM_047425617.1:c.598+69964=	XM_047425617.1:c.598+69963_598+69964dup	XM_047425617.1:c.598+69964_598+69965insTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTGTGTG	XM_047425617.1:c.598+69964_598+69965insTGTGTGTGTGTGTGTGTGTGTGTGTG

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#.

32 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95761184	Feb 13, 2009 (130)
2	SWEGEN	ss3006014881	Jan 10, 2018 (151)
3	SWEGEN	ss3006014882	Jan 10, 2018 (151)
4	SWEGEN	ss3006014883	Jan 10, 2018 (151)
5	SWEGEN	ss3006014884	Jan 10, 2018 (151)
6	SWEGEN	ss3006014885	Jan 10, 2018 (151)
7	EVA	ss3831994777	Apr 26, 2020 (154)
8	GNOMAD	ss4213696478	Apr 26, 2021 (155)
9	GNOMAD	ss4213696479	Apr 26, 2021 (155)
10	GNOMAD	ss4213696480	Apr 26, 2021 (155)
11	GNOMAD	ss4213696481	Apr 26, 2021 (155)
12	GNOMAD	ss4213696482	Apr 26, 2021 (155)
13	GNOMAD	ss4213696483	Apr 26, 2021 (155)
14	GNOMAD	ss4213696484	Apr 26, 2021 (155)
15	GNOMAD	ss4213696485	Apr 26, 2021 (155)
16	GNOMAD	ss4213696486	Apr 26, 2021 (155)
17	GNOMAD	ss4213696487	Apr 26, 2021 (155)
18	GNOMAD	ss4213696488	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5196476395	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5196476396	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5196476397	Apr 26, 2021 (155)
22	TOMMO_GENOMICS	ss5196476398	Apr 26, 2021 (155)
23	TOMMO_GENOMICS	ss5196476399	Apr 26, 2021 (155)
24	TOMMO_GENOMICS	ss5196476400	Apr 26, 2021 (155)
25	1000G_HIGH_COVERAGE	ss5283087929	Oct 16, 2022 (156)
26	HUGCELL_USP	ss5478848478	Oct 16, 2022 (156)
27	HUGCELL_USP	ss5478848479	Oct 16, 2022 (156)
28	HUGCELL_USP	ss5478848480	Oct 16, 2022 (156)
29	HUGCELL_USP	ss5478848481	Oct 16, 2022 (156)
30	HUGCELL_USP	ss5478848482	Oct 16, 2022 (156)
31	TOMMO_GENOMICS	ss5741387215	Oct 16, 2022 (156)
32	TOMMO_GENOMICS	ss5741387216	Oct 16, 2022 (156)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344752135 (NC_000010.11:16682574::CACA 1258/127412) Row 344752136 (NC_000010.11:16682574::CACACA 6426/127254) Row 344752137 (NC_000010.11:16682574::CACACACA 6099/127212)...	-	Apr 26, 2021 (155)
44	8.3KJPN Submission ignored due to conflicting rows: Row 54445702 (NC_000010.10:16724573::CACACACACACA 3385/16616) Row 54445703 (NC_000010.10:16724573::CACACACACA 5057/16616) Row 54445704 (NC_000010.10:16724573::CACACACA 1776/16616)...	-	Apr 26, 2021 (155)
45	8.3KJPN Submission ignored due to conflicting rows: Row 54445702 (NC_000010.10:16724573::CACACACACACA 3385/16616) Row 54445703 (NC_000010.10:16724573::CACACACACA 5057/16616) Row 54445704 (NC_000010.10:16724573::CACACACA 1776/16616)...	-	Apr 26, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 54445702 (NC_000010.10:16724573::CACACACACACA 3385/16616) Row 54445703 (NC_000010.10:16724573::CACACACACA 5057/16616) Row 54445704 (NC_000010.10:16724573::CACACACA 1776/16616)...	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 54445702 (NC_000010.10:16724573::CACACACACACA 3385/16616) Row 54445703 (NC_000010.10:16724573::CACACACACA 5057/16616) Row 54445704 (NC_000010.10:16724573::CACACACA 1776/16616)...	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 54445702 (NC_000010.10:16724573::CACACACACACA 3385/16616) Row 54445703 (NC_000010.10:16724573::CACACACACA 5057/16616) Row 54445704 (NC_000010.10:16724573::CACACACA 1776/16616)...	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 54445702 (NC_000010.10:16724573::CACACACACACA 3385/16616) Row 54445703 (NC_000010.10:16724573::CACACACACA 5057/16616) Row 54445704 (NC_000010.10:16724573::CACACACA 1776/16616)...	-	Apr 26, 2021 (155)
50	14KJPN Submission ignored due to conflicting rows: Row 75224319 (NC_000010.11:16682574::CACACACA 17764/27664) Row 75224320 (NC_000010.11:16682574::CACA 5156/27664)	-	Oct 16, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 75224319 (NC_000010.11:16682574::CACACACA 17764/27664) Row 75224320 (NC_000010.11:16682574::CACA 5156/27664)	-	Oct 16, 2022 (156)
52	ALFA	NC_000010.11 - 16682575	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
ss95761184	NT_008705.16:16664575::CA	NC_000010.11:16682574:CA:CACA	(self)
ss4213696478, ss5741387216	NC_000010.11:16682574::CACA	NC_000010.11:16682574:CA:CACACA	(self)
ss3006014885, ss5196476399	NC_000010.10:16724573::CACACA	NC_000010.11:16682574:CA:CACACACA	(self)
ss4213696479, ss5478848482	NC_000010.11:16682574::CACACA	NC_000010.11:16682574:CA:CACACACA	(self)
4571332427	NC_000010.11:16682574:CA:CACACACA	NC_000010.11:16682574:CA:CACACACA	(self)
ss3006014883, ss5196476397	NC_000010.10:16724573::CACACACA	NC_000010.11:16682574:CA:CACACACACA	(self)
ss4213696480, ss5478848481, ss5741387215	NC_000010.11:16682574::CACACACA	NC_000010.11:16682574:CA:CACACACACA	(self)
4571332427	NC_000010.11:16682574:CA:CACACACACA	NC_000010.11:16682574:CA:CACACACACA	(self)
ss3006014881, ss3831994777, ss5196476396	NC_000010.10:16724573::CACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACA	(self)
ss4213696481, ss5283087929, ss5478848478	NC_000010.11:16682574::CACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACA	(self)
4571332427	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACA	(self)
ss3006014882, ss5196476395	NC_000010.10:16724573::CACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACA	(self)
ss4213696482, ss5478848479	NC_000010.11:16682574::CACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACA	(self)
4571332427	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACA	(self)
ss3006014884, ss5196476398	NC_000010.10:16724573::CACACACACAC… NC_000010.10:16724573::CACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACA	(self)
ss4213696483, ss5478848480	NC_000010.11:16682574::CACACACACAC… NC_000010.11:16682574::CACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACA	(self)
4571332427	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACA	(self)
ss5196476400	NC_000010.10:16724573::CACACACACAC… NC_000010.10:16724573::CACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACA	(self)
ss4213696484	NC_000010.11:16682574::CACACACACAC… NC_000010.11:16682574::CACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACA	(self)
4571332427	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACA	(self)
ss4213696485	NC_000010.11:16682574::CACACACACAC… NC_000010.11:16682574::CACACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACACA	(self)
ss4213696486	NC_000010.11:16682574::CACACACACAC… NC_000010.11:16682574::CACACACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACACACA	(self)
ss4213696487	NC_000010.11:16682574::CACACACACAC… NC_000010.11:16682574::CACACACACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACACACACA	(self)
ss4213696488	NC_000010.11:16682574::CACACACACAC… NC_000010.11:16682574::CACACACACACACACACACACACACA	NC_000010.11:16682574:CA:CACACACAC… NC_000010.11:16682574:CA:CACACACACACACACACACACACACACA	(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 rs71200966

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).
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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs71200966