Name: rs766748303
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.

rs766748303

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:16797857-16797879 (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)₁₄ / del(T)₁₃ / del(T)₁₂ / d…
del(T)₁₄ / del(T)₁₃ / del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: dupTTT=0.00919 (163/17744, ALFA)
dup(T)₄=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: RSU1 : 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	17744	TTTTTTTTTTTTTTTTTTTTTTT=0.97960	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00592, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00451, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00919, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00079	0.982878	0.001388	0.015733	32
European	Sub	13496	TTTTTTTTTTTTTTTTTTTTTTT=0.97325	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00778, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00585, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.01208, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00104	0.977304	0.00184	0.020856	32
African	Sub	2838	TTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	110	TTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African American	Sub	2728	TTTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	112	TTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	86	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	26	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	138	TTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	584	TTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	96	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	480	TTTTTTTTTTTTTTTTTTTTTTT=0.998	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.002, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	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	17744	(T)₂₃=0.97960	del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00592, dupTT=0.00451, dupTTT=0.00919, dup(T)₄=0.00079
Allele Frequency Aggregator	European	Sub	13496	(T)₂₃=0.97325	del(T)₁₄=0.00000, del(T)₁₃=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00778, dupTT=0.00585, dupTTT=0.01208, dup(T)₄=0.00104
Allele Frequency Aggregator	African	Sub	2838	(T)₂₃=1.0000	del(T)₁₄=0.0000, del(T)₁₃=0.0000, del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	584	(T)₂₃=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	480	(T)₂₃=0.998	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.002, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	138	(T)₂₃=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Asian	Sub	112	(T)₂₃=1.000	del(T)₁₄=0.000, del(T)₁₃=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	South Asian	Sub	96	(T)₂₃=1.00	del(T)₁₄=0.00, del(T)₁₃=0.00, del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dup(T)₄=0.23

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.16797866_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797867_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797868_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797869_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797870_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797872_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797873_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797874_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797875_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797876_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797877_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797878_16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797879del
GRCh38.p14 chr 10	NC_000010.11:g.16797879dup
GRCh38.p14 chr 10	NC_000010.11:g.16797878_16797879dup
GRCh38.p14 chr 10	NC_000010.11:g.16797877_16797879dup
GRCh38.p14 chr 10	NC_000010.11:g.16797876_16797879dup
GRCh38.p14 chr 10	NC_000010.11:g.16797875_16797879dup
GRCh38.p14 chr 10	NC_000010.11:g.16797874_16797879dup
GRCh38.p14 chr 10	NC_000010.11:g.16797873_16797879dup
GRCh38.p14 chr 10	NC_000010.11:g.16797872_16797879dup
GRCh37.p13 chr 10	NC_000010.10:g.16839865_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839866_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839867_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839868_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839869_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839871_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839872_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839873_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839874_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839875_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839876_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839877_16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839878del
GRCh37.p13 chr 10	NC_000010.10:g.16839878dup
GRCh37.p13 chr 10	NC_000010.10:g.16839877_16839878dup
GRCh37.p13 chr 10	NC_000010.10:g.16839876_16839878dup
GRCh37.p13 chr 10	NC_000010.10:g.16839875_16839878dup
GRCh37.p13 chr 10	NC_000010.10:g.16839874_16839878dup
GRCh37.p13 chr 10	NC_000010.10:g.16839873_16839878dup
GRCh37.p13 chr 10	NC_000010.10:g.16839872_16839878dup
GRCh37.p13 chr 10	NC_000010.10:g.16839871_16839878dup

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

Molecule type	Change	Amino acid[Codon]	SO Term
RSU1 transcript variant 1	NM_012425.4:c.110-15786_1… NM_012425.4:c.110-15786_110-15773del	N/A	Intron Variant
RSU1 transcript variant 2	NM_152724.3:c.-50-15786_-… NM_152724.3:c.-50-15786_-50-15773del	N/A	Intron Variant
RSU1 transcript variant X1	XM_047425617.1:c.110-1578… XM_047425617.1:c.110-15786_110-15773del	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)₂₃=	del(T)₁₄	del(T)₁₃	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈
GRCh38.p14 chr 10	NC_000010.11:g.16797857_16797879=	NC_000010.11:g.16797866_16797879del	NC_000010.11:g.16797867_16797879del	NC_000010.11:g.16797868_16797879del	NC_000010.11:g.16797869_16797879del	NC_000010.11:g.16797870_16797879del	NC_000010.11:g.16797872_16797879del	NC_000010.11:g.16797873_16797879del	NC_000010.11:g.16797874_16797879del	NC_000010.11:g.16797875_16797879del	NC_000010.11:g.16797876_16797879del	NC_000010.11:g.16797877_16797879del	NC_000010.11:g.16797878_16797879del	NC_000010.11:g.16797879del	NC_000010.11:g.16797879dup	NC_000010.11:g.16797878_16797879dup	NC_000010.11:g.16797877_16797879dup	NC_000010.11:g.16797876_16797879dup	NC_000010.11:g.16797875_16797879dup	NC_000010.11:g.16797874_16797879dup	NC_000010.11:g.16797873_16797879dup	NC_000010.11:g.16797872_16797879dup
GRCh37.p13 chr 10	NC_000010.10:g.16839856_16839878=	NC_000010.10:g.16839865_16839878del	NC_000010.10:g.16839866_16839878del	NC_000010.10:g.16839867_16839878del	NC_000010.10:g.16839868_16839878del	NC_000010.10:g.16839869_16839878del	NC_000010.10:g.16839871_16839878del	NC_000010.10:g.16839872_16839878del	NC_000010.10:g.16839873_16839878del	NC_000010.10:g.16839874_16839878del	NC_000010.10:g.16839875_16839878del	NC_000010.10:g.16839876_16839878del	NC_000010.10:g.16839877_16839878del	NC_000010.10:g.16839878del	NC_000010.10:g.16839878dup	NC_000010.10:g.16839877_16839878dup	NC_000010.10:g.16839876_16839878dup	NC_000010.10:g.16839875_16839878dup	NC_000010.10:g.16839874_16839878dup	NC_000010.10:g.16839873_16839878dup	NC_000010.10:g.16839872_16839878dup	NC_000010.10:g.16839871_16839878dup
RSU1 transcript variant 1	NM_012425.3:c.110-15773=	NM_012425.3:c.110-15786_110-15773del	NM_012425.3:c.110-15785_110-15773del	NM_012425.3:c.110-15784_110-15773del	NM_012425.3:c.110-15783_110-15773del	NM_012425.3:c.110-15782_110-15773del	NM_012425.3:c.110-15780_110-15773del	NM_012425.3:c.110-15779_110-15773del	NM_012425.3:c.110-15778_110-15773del	NM_012425.3:c.110-15777_110-15773del	NM_012425.3:c.110-15776_110-15773del	NM_012425.3:c.110-15775_110-15773del	NM_012425.3:c.110-15774_110-15773del	NM_012425.3:c.110-15773del	NM_012425.3:c.110-15773dup	NM_012425.3:c.110-15774_110-15773dup	NM_012425.3:c.110-15775_110-15773dup	NM_012425.3:c.110-15776_110-15773dup	NM_012425.3:c.110-15777_110-15773dup	NM_012425.3:c.110-15778_110-15773dup	NM_012425.3:c.110-15779_110-15773dup	NM_012425.3:c.110-15780_110-15773dup
RSU1 transcript variant 1	NM_012425.4:c.110-15773=	NM_012425.4:c.110-15786_110-15773del	NM_012425.4:c.110-15785_110-15773del	NM_012425.4:c.110-15784_110-15773del	NM_012425.4:c.110-15783_110-15773del	NM_012425.4:c.110-15782_110-15773del	NM_012425.4:c.110-15780_110-15773del	NM_012425.4:c.110-15779_110-15773del	NM_012425.4:c.110-15778_110-15773del	NM_012425.4:c.110-15777_110-15773del	NM_012425.4:c.110-15776_110-15773del	NM_012425.4:c.110-15775_110-15773del	NM_012425.4:c.110-15774_110-15773del	NM_012425.4:c.110-15773del	NM_012425.4:c.110-15773dup	NM_012425.4:c.110-15774_110-15773dup	NM_012425.4:c.110-15775_110-15773dup	NM_012425.4:c.110-15776_110-15773dup	NM_012425.4:c.110-15777_110-15773dup	NM_012425.4:c.110-15778_110-15773dup	NM_012425.4:c.110-15779_110-15773dup	NM_012425.4:c.110-15780_110-15773dup
RSU1 transcript variant 2	NM_152724.2:c.-50-15773=	NM_152724.2:c.-50-15786_-50-15773del	NM_152724.2:c.-50-15785_-50-15773del	NM_152724.2:c.-50-15784_-50-15773del	NM_152724.2:c.-50-15783_-50-15773del	NM_152724.2:c.-50-15782_-50-15773del	NM_152724.2:c.-50-15780_-50-15773del	NM_152724.2:c.-50-15779_-50-15773del	NM_152724.2:c.-50-15778_-50-15773del	NM_152724.2:c.-50-15777_-50-15773del	NM_152724.2:c.-50-15776_-50-15773del	NM_152724.2:c.-50-15775_-50-15773del	NM_152724.2:c.-50-15774_-50-15773del	NM_152724.2:c.-50-15773del	NM_152724.2:c.-50-15773dup	NM_152724.2:c.-50-15774_-50-15773dup	NM_152724.2:c.-50-15775_-50-15773dup	NM_152724.2:c.-50-15776_-50-15773dup	NM_152724.2:c.-50-15777_-50-15773dup	NM_152724.2:c.-50-15778_-50-15773dup	NM_152724.2:c.-50-15779_-50-15773dup	NM_152724.2:c.-50-15780_-50-15773dup
RSU1 transcript variant 2	NM_152724.3:c.-50-15773=	NM_152724.3:c.-50-15786_-50-15773del	NM_152724.3:c.-50-15785_-50-15773del	NM_152724.3:c.-50-15784_-50-15773del	NM_152724.3:c.-50-15783_-50-15773del	NM_152724.3:c.-50-15782_-50-15773del	NM_152724.3:c.-50-15780_-50-15773del	NM_152724.3:c.-50-15779_-50-15773del	NM_152724.3:c.-50-15778_-50-15773del	NM_152724.3:c.-50-15777_-50-15773del	NM_152724.3:c.-50-15776_-50-15773del	NM_152724.3:c.-50-15775_-50-15773del	NM_152724.3:c.-50-15774_-50-15773del	NM_152724.3:c.-50-15773del	NM_152724.3:c.-50-15773dup	NM_152724.3:c.-50-15774_-50-15773dup	NM_152724.3:c.-50-15775_-50-15773dup	NM_152724.3:c.-50-15776_-50-15773dup	NM_152724.3:c.-50-15777_-50-15773dup	NM_152724.3:c.-50-15778_-50-15773dup	NM_152724.3:c.-50-15779_-50-15773dup	NM_152724.3:c.-50-15780_-50-15773dup
RSU1 transcript variant X1	XM_005252552.1:c.110-15773=	XM_005252552.1:c.110-15786_110-15773del	XM_005252552.1:c.110-15785_110-15773del	XM_005252552.1:c.110-15784_110-15773del	XM_005252552.1:c.110-15783_110-15773del	XM_005252552.1:c.110-15782_110-15773del	XM_005252552.1:c.110-15780_110-15773del	XM_005252552.1:c.110-15779_110-15773del	XM_005252552.1:c.110-15778_110-15773del	XM_005252552.1:c.110-15777_110-15773del	XM_005252552.1:c.110-15776_110-15773del	XM_005252552.1:c.110-15775_110-15773del	XM_005252552.1:c.110-15774_110-15773del	XM_005252552.1:c.110-15773del	XM_005252552.1:c.110-15773dup	XM_005252552.1:c.110-15774_110-15773dup	XM_005252552.1:c.110-15775_110-15773dup	XM_005252552.1:c.110-15776_110-15773dup	XM_005252552.1:c.110-15777_110-15773dup	XM_005252552.1:c.110-15778_110-15773dup	XM_005252552.1:c.110-15779_110-15773dup	XM_005252552.1:c.110-15780_110-15773dup
RSU1 transcript variant X2	XM_005252553.1:c.109+19116=	XM_005252553.1:c.109+19103_109+19116del	XM_005252553.1:c.109+19104_109+19116del	XM_005252553.1:c.109+19105_109+19116del	XM_005252553.1:c.109+19106_109+19116del	XM_005252553.1:c.109+19107_109+19116del	XM_005252553.1:c.109+19109_109+19116del	XM_005252553.1:c.109+19110_109+19116del	XM_005252553.1:c.109+19111_109+19116del	XM_005252553.1:c.109+19112_109+19116del	XM_005252553.1:c.109+19113_109+19116del	XM_005252553.1:c.109+19114_109+19116del	XM_005252553.1:c.109+19115_109+19116del	XM_005252553.1:c.109+19116del	XM_005252553.1:c.109+19116dup	XM_005252553.1:c.109+19115_109+19116dup	XM_005252553.1:c.109+19114_109+19116dup	XM_005252553.1:c.109+19113_109+19116dup	XM_005252553.1:c.109+19112_109+19116dup	XM_005252553.1:c.109+19111_109+19116dup	XM_005252553.1:c.109+19110_109+19116dup	XM_005252553.1:c.109+19109_109+19116dup
RSU1 transcript variant X1	XM_047425617.1:c.110-15773=	XM_047425617.1:c.110-15786_110-15773del	XM_047425617.1:c.110-15785_110-15773del	XM_047425617.1:c.110-15784_110-15773del	XM_047425617.1:c.110-15783_110-15773del	XM_047425617.1:c.110-15782_110-15773del	XM_047425617.1:c.110-15780_110-15773del	XM_047425617.1:c.110-15779_110-15773del	XM_047425617.1:c.110-15778_110-15773del	XM_047425617.1:c.110-15777_110-15773del	XM_047425617.1:c.110-15776_110-15773del	XM_047425617.1:c.110-15775_110-15773del	XM_047425617.1:c.110-15774_110-15773del	XM_047425617.1:c.110-15773del	XM_047425617.1:c.110-15773dup	XM_047425617.1:c.110-15774_110-15773dup	XM_047425617.1:c.110-15775_110-15773dup	XM_047425617.1:c.110-15776_110-15773dup	XM_047425617.1:c.110-15777_110-15773dup	XM_047425617.1:c.110-15778_110-15773dup	XM_047425617.1:c.110-15779_110-15773dup	XM_047425617.1:c.110-15780_110-15773dup

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#.

40 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_GENOME_DK	ss1574155150	Apr 01, 2015 (144)
2	SWEGEN	ss3006016459	Nov 08, 2017 (151)
3	EVA_DECODE	ss3689379462	Jul 13, 2019 (153)
4	EVA_DECODE	ss3689379466	Jul 13, 2019 (153)
5	EVA_DECODE	ss3689379472	Jul 13, 2019 (153)
6	EVA_DECODE	ss3689379476	Jul 13, 2019 (153)
7	KOGIC	ss3967298029	Apr 26, 2020 (154)
8	KOGIC	ss3967298030	Apr 26, 2020 (154)
9	KOGIC	ss3967298031	Apr 26, 2020 (154)
10	GNOMAD	ss4213713338	Apr 26, 2021 (155)
11	GNOMAD	ss4213713347	Apr 26, 2021 (155)
12	GNOMAD	ss4213713348	Apr 26, 2021 (155)
13	GNOMAD	ss4213713349	Apr 26, 2021 (155)
14	GNOMAD	ss4213713350	Apr 26, 2021 (155)
15	GNOMAD	ss4213713351	Apr 26, 2021 (155)
16	GNOMAD	ss4213713352	Apr 26, 2021 (155)
17	GNOMAD	ss4213713353	Apr 26, 2021 (155)
18	GNOMAD	ss4213713354	Apr 26, 2021 (155)
19	GNOMAD	ss4213713355	Apr 26, 2021 (155)
20	GNOMAD	ss4213713356	Apr 26, 2021 (155)
21	GNOMAD	ss4213713357	Apr 26, 2021 (155)
22	GNOMAD	ss4213713358	Apr 26, 2021 (155)
23	GNOMAD	ss4213713359	Apr 26, 2021 (155)
24	GNOMAD	ss4213713360	Apr 26, 2021 (155)
25	GNOMAD	ss4213713361	Apr 26, 2021 (155)
26	TOPMED	ss4844012041	Apr 26, 2021 (155)
27	TOPMED	ss4844012042	Apr 26, 2021 (155)
28	TOPMED	ss4844012043	Apr 26, 2021 (155)
29	TOPMED	ss4844012044	Apr 26, 2021 (155)
30	TOPMED	ss4844012045	Apr 26, 2021 (155)
31	TOPMED	ss4844012046	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5196480955	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5196480957	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5196480960	Apr 26, 2021 (155)
35	1000G_HIGH_COVERAGE	ss5283091411	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5478851809	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5478851810	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5741393031	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5741393033	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5741393034	Oct 16, 2022 (156)
41	The Danish reference pan genome	NC_000010.10 - 16839856	Apr 26, 2020 (154)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 344781003 (NC_000010.11:16797856::TT 658/96046) Row 344781012 (NC_000010.11:16797856::TTTT 145/96082) Row 344781013 (NC_000010.11:16797856::TTTTT 28/96104)...	-	Apr 26, 2021 (155)
58	Korean Genome Project Submission ignored due to conflicting rows: Row 23676030 (NC_000010.11:16797869::T 116/1810) Row 23676031 (NC_000010.11:16797868:T: 68/1810) Row 23676032 (NC_000010.11:16797856:TTTTTTTTTTTTT: 5/1810)	-	Apr 26, 2020 (154)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 23676030 (NC_000010.11:16797869::T 116/1810) Row 23676031 (NC_000010.11:16797868:T: 68/1810) Row 23676032 (NC_000010.11:16797856:TTTTTTTTTTTTT: 5/1810)	-	Apr 26, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 23676030 (NC_000010.11:16797869::T 116/1810) Row 23676031 (NC_000010.11:16797868:T: 68/1810) Row 23676032 (NC_000010.11:16797856:TTTTTTTTTTTTT: 5/1810)	-	Apr 26, 2020 (154)
61	8.3KJPN Submission ignored due to conflicting rows: Row 54450262 (NC_000010.10:16839855::T 71/16202) Row 54450264 (NC_000010.10:16839855:TTTTTTTTTTTTT: 92/16202) Row 54450267 (NC_000010.10:16839855:TTTTTTT: 2/16202)	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 54450262 (NC_000010.10:16839855::T 71/16202) Row 54450264 (NC_000010.10:16839855:TTTTTTTTTTTTT: 92/16202) Row 54450267 (NC_000010.10:16839855:TTTTTTT: 2/16202)	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 54450262 (NC_000010.10:16839855::T 71/16202) Row 54450264 (NC_000010.10:16839855:TTTTTTTTTTTTT: 92/16202) Row 54450267 (NC_000010.10:16839855:TTTTTTT: 2/16202)	-	Apr 26, 2021 (155)
64	14KJPN Submission ignored due to conflicting rows: Row 75230135 (NC_000010.11:16797856::T 154/28178) Row 75230137 (NC_000010.11:16797856:TTTTTTTTTTTTT: 169/28178) Row 75230138 (NC_000010.11:16797856:T: 17/28178)	-	Oct 16, 2022 (156)
65	14KJPN Submission ignored due to conflicting rows: Row 75230135 (NC_000010.11:16797856::T 154/28178) Row 75230137 (NC_000010.11:16797856:TTTTTTTTTTTTT: 169/28178) Row 75230138 (NC_000010.11:16797856:T: 17/28178)	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 75230135 (NC_000010.11:16797856::T 154/28178) Row 75230137 (NC_000010.11:16797856:TTTTTTTTTTTTT: 169/28178) Row 75230138 (NC_000010.11:16797856:T: 17/28178)	-	Oct 16, 2022 (156)
67	TopMed Submission ignored due to conflicting rows: Row 59557696 (NC_000010.11:16797856:TTTTT: 3/264690) Row 59557697 (NC_000010.11:16797856:TTTTTTT: 10/264690) Row 59557698 (NC_000010.11:16797856:TTTTTTTT: 2/264690)...	-	Apr 26, 2021 (155)
68	TopMed Submission ignored due to conflicting rows: Row 59557696 (NC_000010.11:16797856:TTTTT: 3/264690) Row 59557697 (NC_000010.11:16797856:TTTTTTT: 10/264690) Row 59557698 (NC_000010.11:16797856:TTTTTTTT: 2/264690)...	-	Apr 26, 2021 (155)
69	TopMed Submission ignored due to conflicting rows: Row 59557696 (NC_000010.11:16797856:TTTTT: 3/264690) Row 59557697 (NC_000010.11:16797856:TTTTTTT: 10/264690) Row 59557698 (NC_000010.11:16797856:TTTTTTTT: 2/264690)...	-	Apr 26, 2021 (155)
70	TopMed Submission ignored due to conflicting rows: Row 59557696 (NC_000010.11:16797856:TTTTT: 3/264690) Row 59557697 (NC_000010.11:16797856:TTTTTTT: 10/264690) Row 59557698 (NC_000010.11:16797856:TTTTTTTT: 2/264690)...	-	Apr 26, 2021 (155)
71	TopMed Submission ignored due to conflicting rows: Row 59557696 (NC_000010.11:16797856:TTTTT: 3/264690) Row 59557697 (NC_000010.11:16797856:TTTTTTT: 10/264690) Row 59557698 (NC_000010.11:16797856:TTTTTTTT: 2/264690)...	-	Apr 26, 2021 (155)
72	TopMed Submission ignored due to conflicting rows: Row 59557696 (NC_000010.11:16797856:TTTTT: 3/264690) Row 59557697 (NC_000010.11:16797856:TTTTTTT: 10/264690) Row 59557698 (NC_000010.11:16797856:TTTTTTTT: 2/264690)...	-	Apr 26, 2021 (155)
73	ALFA	NC_000010.11 - 16797857	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
ss4844012046	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss5196480957	NC_000010.10:16839855:TTTTTTTTTTTT… NC_000010.10:16839855:TTTTTTTTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3967298031, ss4213713361, ss5741393033	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4213713360, ss4844012045	NC_000010.11:16797856:TTTTTTTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4844012044	NC_000010.11:16797856:TTTTTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4213713359, ss4844012043	NC_000010.11:16797856:TTTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss5196480960	NC_000010.10:16839855:TTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4213713358, ss4844012042	NC_000010.11:16797856:TTTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4213713357	NC_000010.11:16797856:TTTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4213713356, ss4844012041	NC_000010.11:16797856:TTTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4213713355	NC_000010.11:16797856:TTTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4213713354	NC_000010.11:16797856:TTT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4213713353	NC_000010.11:16797856:TT:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4213713352, ss5478851809, ss5741393034	NC_000010.11:16797856:T:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3967298030	NC_000010.11:16797868:T:	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3006016459, ss5196480955	NC_000010.10:16839855::T	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5283091411, ss5478851810, ss5741393031	NC_000010.11:16797856::T	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3689379472	NC_000010.11:16797858::T	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3967298029	NC_000010.11:16797869::T	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4213713338	NC_000010.11:16797856::TT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3689379466	NC_000010.11:16797857::TT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3689379476	NC_000010.11:16797860::TT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
223973, ss1574155150	NC_000010.10:16839855::TTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3689379462, ss4213713347	NC_000010.11:16797856::TTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
9322365372	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4213713348	NC_000010.11:16797856::TTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4213713349	NC_000010.11:16797856::TTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4213713350	NC_000010.11:16797856::TTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4213713351	NC_000010.11:16797856::TTTTTTTT	NC_000010.11:16797856:TTTTTTTTTTTT… NC_000010.11:16797856:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs766748303

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

rs766748303