Name: rs58107096
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.

rs58107096

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:113868926-113868941 (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(A)₄ / delAAA / delAA / delA / …
del(A)₄ / delAAA / delAA / delA / dupA / dupAA
Variation Type: Indel Insertion and Deletion
Frequency: dupA=0.00095 (15/15873, ALFA)
del(A)₄=0.0012 (6/5008, 1000G)
dupA=0.33 (13/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: USP28 : 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	15873	AAAAAAAAAAAAAAAA=0.99893	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00013, AAAAAAAAAAAAAAAAA=0.00095, AAAAAAAAAAAAAAAAAA=0.00000	0.998231	0.000126	0.001642	32
European	Sub	11773	AAAAAAAAAAAAAAAA=0.99856	AAAAAAAAAAAA=0.00000, AAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAA=0.00000, AAAAAAAAAAAAAAA=0.00017, AAAAAAAAAAAAAAAAA=0.00127, AAAAAAAAAAAAAAAAAA=0.00000	0.997613	0.000171	0.002217	32
African	Sub	2694	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	108	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African American	Sub	2586	AAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	108	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	84	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	140	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	600	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	90	AAAAAAAAAAAAAAAA=1.00	AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	468	AAAAAAAAAAAAAAAA=1.000	AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=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	15873	(A)₁₆=0.99893	del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00013, dupA=0.00095, dupAA=0.00000
Allele Frequency Aggregator	European	Sub	11773	(A)₁₆=0.99856	del(A)₄=0.00000, delAAA=0.00000, delAA=0.00000, delA=0.00017, dupA=0.00127, dupAA=0.00000
Allele Frequency Aggregator	African	Sub	2694	(A)₁₆=1.0000	del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	600	(A)₁₆=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	468	(A)₁₆=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	140	(A)₁₆=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	108	(A)₁₆=1.000	del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	South Asian	Sub	90	(A)₁₆=1.00	del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
1000Genomes	Global	Study-wide	5008	(A)₁₆=0.9988	del(A)₄=0.0012
1000Genomes	African	Sub	1322	(A)₁₆=0.9992	del(A)₄=0.0008
1000Genomes	East Asian	Sub	1008	(A)₁₆=1.0000	del(A)₄=0.0000
1000Genomes	Europe	Sub	1006	(A)₁₆=1.0000	del(A)₄=0.0000
1000Genomes	South Asian	Sub	978	(A)₁₆=0.995	del(A)₄=0.005
1000Genomes	American	Sub	694	(A)₁₆=1.000	del(A)₄=0.000
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=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.113868938_113868941del
GRCh38.p14 chr 11	NC_000011.10:g.113868939_113868941del
GRCh38.p14 chr 11	NC_000011.10:g.113868940_113868941del
GRCh38.p14 chr 11	NC_000011.10:g.113868941del
GRCh38.p14 chr 11	NC_000011.10:g.113868941dup
GRCh38.p14 chr 11	NC_000011.10:g.113868940_113868941dup
GRCh37.p13 chr 11	NC_000011.9:g.113739660_113739663del
GRCh37.p13 chr 11	NC_000011.9:g.113739661_113739663del
GRCh37.p13 chr 11	NC_000011.9:g.113739662_113739663del
GRCh37.p13 chr 11	NC_000011.9:g.113739663del
GRCh37.p13 chr 11	NC_000011.9:g.113739663dup
GRCh37.p13 chr 11	NC_000011.9:g.113739662_113739663dup
USP28 RefSeqGene	NG_051668.1:g.11642_11645del
USP28 RefSeqGene	NG_051668.1:g.11643_11645del
USP28 RefSeqGene	NG_051668.1:g.11644_11645del
USP28 RefSeqGene	NG_051668.1:g.11645del
USP28 RefSeqGene	NG_051668.1:g.11645dup
USP28 RefSeqGene	NG_051668.1:g.11644_11645dup

Gene: USP28, ubiquitin specific peptidase 28 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
USP28 transcript variant 2	NM_001301029.2:c.-108+651… NM_001301029.2:c.-108+6516_-108+6519del	N/A	Intron Variant
USP28 transcript variant 3	NM_001346252.4:c.57+6516_… NM_001346252.4:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 4	NM_001346253.2:c.57+6516_… NM_001346253.2:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 5	NM_001346254.2:c.57+6516_… NM_001346254.2:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 6	NM_001346255.2:c.48+5588_… NM_001346255.2:c.48+5588_48+5591del	N/A	Intron Variant
USP28 transcript variant 7	NM_001346257.2:c.57+6516_… NM_001346257.2:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 8	NM_001346258.2:c.57+6516_… NM_001346258.2:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 9	NM_001346259.2:c.57+6516_… NM_001346259.2:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 10	NM_001346260.2:c.-108+651… NM_001346260.2:c.-108+6516_-108+6519del	N/A	Intron Variant
USP28 transcript variant 11	NM_001346261.2:c.-108+651… NM_001346261.2:c.-108+6516_-108+6519del	N/A	Intron Variant
USP28 transcript variant 12	NM_001346262.2:c.-186+651… NM_001346262.2:c.-186+6516_-186+6519del	N/A	Intron Variant
USP28 transcript variant 13	NM_001346263.2:c.-731+651… NM_001346263.2:c.-731+6516_-731+6519del	N/A	Intron Variant
USP28 transcript variant 14	NM_001346264.2:c.-792+651… NM_001346264.2:c.-792+6516_-792+6519del	N/A	Intron Variant
USP28 transcript variant 15	NM_001346265.2:c.-1077+65… NM_001346265.2:c.-1077+6516_-1077+6519del	N/A	Intron Variant
USP28 transcript variant 16	NM_001346267.2:c.-792+651… NM_001346267.2:c.-792+6516_-792+6519del	N/A	Intron Variant
USP28 transcript variant 17	NM_001346268.2:c.-581+651… NM_001346268.2:c.-581+6516_-581+6519del	N/A	Intron Variant
USP28 transcript variant 18	NM_001346269.2:c.-866+651… NM_001346269.2:c.-866+6516_-866+6519del	N/A	Intron Variant
USP28 transcript variant 19	NM_001346270.2:c.-1077+55… NM_001346270.2:c.-1077+5588_-1077+5591del	N/A	Intron Variant
USP28 transcript variant 20	NM_001346271.2:c.-1077+65… NM_001346271.2:c.-1077+6516_-1077+6519del	N/A	Intron Variant
USP28 transcript variant 21	NM_001346272.2:c.-869+651… NM_001346272.2:c.-869+6516_-869+6519del	N/A	Intron Variant
USP28 transcript variant 22	NM_001346273.2:c.57+6516_… NM_001346273.2:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 23	NM_001400784.1:c.57+6516_… NM_001400784.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 24	NM_001400785.1:c.57+6516_… NM_001400785.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 25	NM_001400786.1:c.57+6516_… NM_001400786.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 26	NM_001400787.1:c.57+6516_… NM_001400787.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 27	NM_001400788.1:c.57+6516_… NM_001400788.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 28	NM_001400789.1:c.57+6516_… NM_001400789.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 29	NM_001400790.1:c.57+6516_… NM_001400790.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 30	NM_001400791.1:c.57+6516_… NM_001400791.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 31	NM_001400792.1:c.57+6516_… NM_001400792.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 32	NM_001400793.1:c.57+6516_… NM_001400793.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 33	NM_001400794.1:c.57+6516_… NM_001400794.1:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 34	NM_001400795.1:c.48+5588_… NM_001400795.1:c.48+5588_48+5591del	N/A	Intron Variant
USP28 transcript variant 35	NM_001400796.1:c.48+5588_… NM_001400796.1:c.48+5588_48+5591del	N/A	Intron Variant
USP28 transcript variant 36	NM_001400797.1:c.48+5588_… NM_001400797.1:c.48+5588_48+5591del	N/A	Intron Variant
USP28 transcript variant 37	NM_001400799.1:c.-108+651… NM_001400799.1:c.-108+6516_-108+6519del	N/A	Intron Variant
USP28 transcript variant 38	NM_001400800.1:c.-186+651… NM_001400800.1:c.-186+6516_-186+6519del	N/A	Intron Variant
USP28 transcript variant 39	NM_001400801.1:c.-627+651… NM_001400801.1:c.-627+6516_-627+6519del	N/A	Intron Variant
USP28 transcript variant 40	NM_001400802.1:c.-792+651… NM_001400802.1:c.-792+6516_-792+6519del	N/A	Intron Variant
USP28 transcript variant 41	NM_001400803.1:c.-731+651… NM_001400803.1:c.-731+6516_-731+6519del	N/A	Intron Variant
USP28 transcript variant 42	NM_001400804.1:c.-731+558… NM_001400804.1:c.-731+5588_-731+5591del	N/A	Intron Variant
USP28 transcript variant 43	NM_001400805.1:c.-623+651… NM_001400805.1:c.-623+6516_-623+6519del	N/A	Intron Variant
USP28 transcript variant 44	NM_001400806.1:c.-1077+65… NM_001400806.1:c.-1077+6516_-1077+6519del	N/A	Intron Variant
USP28 transcript variant 45	NM_001400807.1:c.-108+651… NM_001400807.1:c.-108+6516_-108+6519del	N/A	Intron Variant
USP28 transcript variant 46	NM_001400809.1:c.-108+651… NM_001400809.1:c.-108+6516_-108+6519del	N/A	Intron Variant
USP28 transcript variant 47	NM_001400810.1:c.-108+651… NM_001400810.1:c.-108+6516_-108+6519del	N/A	Intron Variant
USP28 transcript variant 48	NM_001400811.1:c.-705+558… NM_001400811.1:c.-705+5588_-705+5591del	N/A	Intron Variant
USP28 transcript variant 49	NM_001400812.1:c.-1387+65… NM_001400812.1:c.-1387+6516_-1387+6519del	N/A	Intron Variant
USP28 transcript variant 50	NM_001400813.1:c.-520+651… NM_001400813.1:c.-520+6516_-520+6519del	N/A	Intron Variant
USP28 transcript variant 1	NM_020886.4:c.57+6516_57+… NM_020886.4:c.57+6516_57+6519del	N/A	Intron Variant
USP28 transcript variant 51	NR_174609.1:n.	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	(A)₁₆=	del(A)₄	delAAA	delAA	delA	dupA	dupAA
GRCh38.p14 chr 11	NC_000011.10:g.113868926_113868941=	NC_000011.10:g.113868938_113868941del	NC_000011.10:g.113868939_113868941del	NC_000011.10:g.113868940_113868941del	NC_000011.10:g.113868941del	NC_000011.10:g.113868941dup	NC_000011.10:g.113868940_113868941dup
GRCh37.p13 chr 11	NC_000011.9:g.113739648_113739663=	NC_000011.9:g.113739660_113739663del	NC_000011.9:g.113739661_113739663del	NC_000011.9:g.113739662_113739663del	NC_000011.9:g.113739663del	NC_000011.9:g.113739663dup	NC_000011.9:g.113739662_113739663dup
USP28 RefSeqGene	NG_051668.1:g.11630_11645=	NG_051668.1:g.11642_11645del	NG_051668.1:g.11643_11645del	NG_051668.1:g.11644_11645del	NG_051668.1:g.11645del	NG_051668.1:g.11645dup	NG_051668.1:g.11644_11645dup
USP28 transcript variant 2	NM_001301029.2:c.-108+6519=	NM_001301029.2:c.-108+6516_-108+6519del	NM_001301029.2:c.-108+6517_-108+6519del	NM_001301029.2:c.-108+6518_-108+6519del	NM_001301029.2:c.-108+6519del	NM_001301029.2:c.-108+6519dup	NM_001301029.2:c.-108+6518_-108+6519dup
USP28 transcript variant 3	NM_001346252.4:c.57+6519=	NM_001346252.4:c.57+6516_57+6519del	NM_001346252.4:c.57+6517_57+6519del	NM_001346252.4:c.57+6518_57+6519del	NM_001346252.4:c.57+6519del	NM_001346252.4:c.57+6519dup	NM_001346252.4:c.57+6518_57+6519dup
USP28 transcript variant 4	NM_001346253.2:c.57+6519=	NM_001346253.2:c.57+6516_57+6519del	NM_001346253.2:c.57+6517_57+6519del	NM_001346253.2:c.57+6518_57+6519del	NM_001346253.2:c.57+6519del	NM_001346253.2:c.57+6519dup	NM_001346253.2:c.57+6518_57+6519dup
USP28 transcript variant 5	NM_001346254.2:c.57+6519=	NM_001346254.2:c.57+6516_57+6519del	NM_001346254.2:c.57+6517_57+6519del	NM_001346254.2:c.57+6518_57+6519del	NM_001346254.2:c.57+6519del	NM_001346254.2:c.57+6519dup	NM_001346254.2:c.57+6518_57+6519dup
USP28 transcript variant 6	NM_001346255.2:c.48+5591=	NM_001346255.2:c.48+5588_48+5591del	NM_001346255.2:c.48+5589_48+5591del	NM_001346255.2:c.48+5590_48+5591del	NM_001346255.2:c.48+5591del	NM_001346255.2:c.48+5591dup	NM_001346255.2:c.48+5590_48+5591dup
USP28 transcript variant 7	NM_001346257.2:c.57+6519=	NM_001346257.2:c.57+6516_57+6519del	NM_001346257.2:c.57+6517_57+6519del	NM_001346257.2:c.57+6518_57+6519del	NM_001346257.2:c.57+6519del	NM_001346257.2:c.57+6519dup	NM_001346257.2:c.57+6518_57+6519dup
USP28 transcript variant 8	NM_001346258.2:c.57+6519=	NM_001346258.2:c.57+6516_57+6519del	NM_001346258.2:c.57+6517_57+6519del	NM_001346258.2:c.57+6518_57+6519del	NM_001346258.2:c.57+6519del	NM_001346258.2:c.57+6519dup	NM_001346258.2:c.57+6518_57+6519dup
USP28 transcript variant 9	NM_001346259.2:c.57+6519=	NM_001346259.2:c.57+6516_57+6519del	NM_001346259.2:c.57+6517_57+6519del	NM_001346259.2:c.57+6518_57+6519del	NM_001346259.2:c.57+6519del	NM_001346259.2:c.57+6519dup	NM_001346259.2:c.57+6518_57+6519dup
USP28 transcript variant 10	NM_001346260.2:c.-108+6519=	NM_001346260.2:c.-108+6516_-108+6519del	NM_001346260.2:c.-108+6517_-108+6519del	NM_001346260.2:c.-108+6518_-108+6519del	NM_001346260.2:c.-108+6519del	NM_001346260.2:c.-108+6519dup	NM_001346260.2:c.-108+6518_-108+6519dup
USP28 transcript variant 11	NM_001346261.2:c.-108+6519=	NM_001346261.2:c.-108+6516_-108+6519del	NM_001346261.2:c.-108+6517_-108+6519del	NM_001346261.2:c.-108+6518_-108+6519del	NM_001346261.2:c.-108+6519del	NM_001346261.2:c.-108+6519dup	NM_001346261.2:c.-108+6518_-108+6519dup
USP28 transcript variant 12	NM_001346262.2:c.-186+6519=	NM_001346262.2:c.-186+6516_-186+6519del	NM_001346262.2:c.-186+6517_-186+6519del	NM_001346262.2:c.-186+6518_-186+6519del	NM_001346262.2:c.-186+6519del	NM_001346262.2:c.-186+6519dup	NM_001346262.2:c.-186+6518_-186+6519dup
USP28 transcript variant 13	NM_001346263.2:c.-731+6519=	NM_001346263.2:c.-731+6516_-731+6519del	NM_001346263.2:c.-731+6517_-731+6519del	NM_001346263.2:c.-731+6518_-731+6519del	NM_001346263.2:c.-731+6519del	NM_001346263.2:c.-731+6519dup	NM_001346263.2:c.-731+6518_-731+6519dup
USP28 transcript variant 14	NM_001346264.2:c.-792+6519=	NM_001346264.2:c.-792+6516_-792+6519del	NM_001346264.2:c.-792+6517_-792+6519del	NM_001346264.2:c.-792+6518_-792+6519del	NM_001346264.2:c.-792+6519del	NM_001346264.2:c.-792+6519dup	NM_001346264.2:c.-792+6518_-792+6519dup
USP28 transcript variant 15	NM_001346265.2:c.-1077+6519=	NM_001346265.2:c.-1077+6516_-1077+6519del	NM_001346265.2:c.-1077+6517_-1077+6519del	NM_001346265.2:c.-1077+6518_-1077+6519del	NM_001346265.2:c.-1077+6519del	NM_001346265.2:c.-1077+6519dup	NM_001346265.2:c.-1077+6518_-1077+6519dup
USP28 transcript variant 16	NM_001346267.2:c.-792+6519=	NM_001346267.2:c.-792+6516_-792+6519del	NM_001346267.2:c.-792+6517_-792+6519del	NM_001346267.2:c.-792+6518_-792+6519del	NM_001346267.2:c.-792+6519del	NM_001346267.2:c.-792+6519dup	NM_001346267.2:c.-792+6518_-792+6519dup
USP28 transcript variant 17	NM_001346268.2:c.-581+6519=	NM_001346268.2:c.-581+6516_-581+6519del	NM_001346268.2:c.-581+6517_-581+6519del	NM_001346268.2:c.-581+6518_-581+6519del	NM_001346268.2:c.-581+6519del	NM_001346268.2:c.-581+6519dup	NM_001346268.2:c.-581+6518_-581+6519dup
USP28 transcript variant 18	NM_001346269.2:c.-866+6519=	NM_001346269.2:c.-866+6516_-866+6519del	NM_001346269.2:c.-866+6517_-866+6519del	NM_001346269.2:c.-866+6518_-866+6519del	NM_001346269.2:c.-866+6519del	NM_001346269.2:c.-866+6519dup	NM_001346269.2:c.-866+6518_-866+6519dup
USP28 transcript variant 19	NM_001346270.2:c.-1077+5591=	NM_001346270.2:c.-1077+5588_-1077+5591del	NM_001346270.2:c.-1077+5589_-1077+5591del	NM_001346270.2:c.-1077+5590_-1077+5591del	NM_001346270.2:c.-1077+5591del	NM_001346270.2:c.-1077+5591dup	NM_001346270.2:c.-1077+5590_-1077+5591dup
USP28 transcript variant 20	NM_001346271.2:c.-1077+6519=	NM_001346271.2:c.-1077+6516_-1077+6519del	NM_001346271.2:c.-1077+6517_-1077+6519del	NM_001346271.2:c.-1077+6518_-1077+6519del	NM_001346271.2:c.-1077+6519del	NM_001346271.2:c.-1077+6519dup	NM_001346271.2:c.-1077+6518_-1077+6519dup
USP28 transcript variant 21	NM_001346272.2:c.-869+6519=	NM_001346272.2:c.-869+6516_-869+6519del	NM_001346272.2:c.-869+6517_-869+6519del	NM_001346272.2:c.-869+6518_-869+6519del	NM_001346272.2:c.-869+6519del	NM_001346272.2:c.-869+6519dup	NM_001346272.2:c.-869+6518_-869+6519dup
USP28 transcript variant 22	NM_001346273.2:c.57+6519=	NM_001346273.2:c.57+6516_57+6519del	NM_001346273.2:c.57+6517_57+6519del	NM_001346273.2:c.57+6518_57+6519del	NM_001346273.2:c.57+6519del	NM_001346273.2:c.57+6519dup	NM_001346273.2:c.57+6518_57+6519dup
USP28 transcript variant 23	NM_001400784.1:c.57+6519=	NM_001400784.1:c.57+6516_57+6519del	NM_001400784.1:c.57+6517_57+6519del	NM_001400784.1:c.57+6518_57+6519del	NM_001400784.1:c.57+6519del	NM_001400784.1:c.57+6519dup	NM_001400784.1:c.57+6518_57+6519dup
USP28 transcript variant 24	NM_001400785.1:c.57+6519=	NM_001400785.1:c.57+6516_57+6519del	NM_001400785.1:c.57+6517_57+6519del	NM_001400785.1:c.57+6518_57+6519del	NM_001400785.1:c.57+6519del	NM_001400785.1:c.57+6519dup	NM_001400785.1:c.57+6518_57+6519dup
USP28 transcript variant 25	NM_001400786.1:c.57+6519=	NM_001400786.1:c.57+6516_57+6519del	NM_001400786.1:c.57+6517_57+6519del	NM_001400786.1:c.57+6518_57+6519del	NM_001400786.1:c.57+6519del	NM_001400786.1:c.57+6519dup	NM_001400786.1:c.57+6518_57+6519dup
USP28 transcript variant 26	NM_001400787.1:c.57+6519=	NM_001400787.1:c.57+6516_57+6519del	NM_001400787.1:c.57+6517_57+6519del	NM_001400787.1:c.57+6518_57+6519del	NM_001400787.1:c.57+6519del	NM_001400787.1:c.57+6519dup	NM_001400787.1:c.57+6518_57+6519dup
USP28 transcript variant 27	NM_001400788.1:c.57+6519=	NM_001400788.1:c.57+6516_57+6519del	NM_001400788.1:c.57+6517_57+6519del	NM_001400788.1:c.57+6518_57+6519del	NM_001400788.1:c.57+6519del	NM_001400788.1:c.57+6519dup	NM_001400788.1:c.57+6518_57+6519dup
USP28 transcript variant 28	NM_001400789.1:c.57+6519=	NM_001400789.1:c.57+6516_57+6519del	NM_001400789.1:c.57+6517_57+6519del	NM_001400789.1:c.57+6518_57+6519del	NM_001400789.1:c.57+6519del	NM_001400789.1:c.57+6519dup	NM_001400789.1:c.57+6518_57+6519dup
USP28 transcript variant 29	NM_001400790.1:c.57+6519=	NM_001400790.1:c.57+6516_57+6519del	NM_001400790.1:c.57+6517_57+6519del	NM_001400790.1:c.57+6518_57+6519del	NM_001400790.1:c.57+6519del	NM_001400790.1:c.57+6519dup	NM_001400790.1:c.57+6518_57+6519dup
USP28 transcript variant 30	NM_001400791.1:c.57+6519=	NM_001400791.1:c.57+6516_57+6519del	NM_001400791.1:c.57+6517_57+6519del	NM_001400791.1:c.57+6518_57+6519del	NM_001400791.1:c.57+6519del	NM_001400791.1:c.57+6519dup	NM_001400791.1:c.57+6518_57+6519dup
USP28 transcript variant 31	NM_001400792.1:c.57+6519=	NM_001400792.1:c.57+6516_57+6519del	NM_001400792.1:c.57+6517_57+6519del	NM_001400792.1:c.57+6518_57+6519del	NM_001400792.1:c.57+6519del	NM_001400792.1:c.57+6519dup	NM_001400792.1:c.57+6518_57+6519dup
USP28 transcript variant 32	NM_001400793.1:c.57+6519=	NM_001400793.1:c.57+6516_57+6519del	NM_001400793.1:c.57+6517_57+6519del	NM_001400793.1:c.57+6518_57+6519del	NM_001400793.1:c.57+6519del	NM_001400793.1:c.57+6519dup	NM_001400793.1:c.57+6518_57+6519dup
USP28 transcript variant 33	NM_001400794.1:c.57+6519=	NM_001400794.1:c.57+6516_57+6519del	NM_001400794.1:c.57+6517_57+6519del	NM_001400794.1:c.57+6518_57+6519del	NM_001400794.1:c.57+6519del	NM_001400794.1:c.57+6519dup	NM_001400794.1:c.57+6518_57+6519dup
USP28 transcript variant 34	NM_001400795.1:c.48+5591=	NM_001400795.1:c.48+5588_48+5591del	NM_001400795.1:c.48+5589_48+5591del	NM_001400795.1:c.48+5590_48+5591del	NM_001400795.1:c.48+5591del	NM_001400795.1:c.48+5591dup	NM_001400795.1:c.48+5590_48+5591dup
USP28 transcript variant 35	NM_001400796.1:c.48+5591=	NM_001400796.1:c.48+5588_48+5591del	NM_001400796.1:c.48+5589_48+5591del	NM_001400796.1:c.48+5590_48+5591del	NM_001400796.1:c.48+5591del	NM_001400796.1:c.48+5591dup	NM_001400796.1:c.48+5590_48+5591dup
USP28 transcript variant 36	NM_001400797.1:c.48+5591=	NM_001400797.1:c.48+5588_48+5591del	NM_001400797.1:c.48+5589_48+5591del	NM_001400797.1:c.48+5590_48+5591del	NM_001400797.1:c.48+5591del	NM_001400797.1:c.48+5591dup	NM_001400797.1:c.48+5590_48+5591dup
USP28 transcript variant 37	NM_001400799.1:c.-108+6519=	NM_001400799.1:c.-108+6516_-108+6519del	NM_001400799.1:c.-108+6517_-108+6519del	NM_001400799.1:c.-108+6518_-108+6519del	NM_001400799.1:c.-108+6519del	NM_001400799.1:c.-108+6519dup	NM_001400799.1:c.-108+6518_-108+6519dup
USP28 transcript variant 38	NM_001400800.1:c.-186+6519=	NM_001400800.1:c.-186+6516_-186+6519del	NM_001400800.1:c.-186+6517_-186+6519del	NM_001400800.1:c.-186+6518_-186+6519del	NM_001400800.1:c.-186+6519del	NM_001400800.1:c.-186+6519dup	NM_001400800.1:c.-186+6518_-186+6519dup
USP28 transcript variant 39	NM_001400801.1:c.-627+6519=	NM_001400801.1:c.-627+6516_-627+6519del	NM_001400801.1:c.-627+6517_-627+6519del	NM_001400801.1:c.-627+6518_-627+6519del	NM_001400801.1:c.-627+6519del	NM_001400801.1:c.-627+6519dup	NM_001400801.1:c.-627+6518_-627+6519dup
USP28 transcript variant 40	NM_001400802.1:c.-792+6519=	NM_001400802.1:c.-792+6516_-792+6519del	NM_001400802.1:c.-792+6517_-792+6519del	NM_001400802.1:c.-792+6518_-792+6519del	NM_001400802.1:c.-792+6519del	NM_001400802.1:c.-792+6519dup	NM_001400802.1:c.-792+6518_-792+6519dup
USP28 transcript variant 41	NM_001400803.1:c.-731+6519=	NM_001400803.1:c.-731+6516_-731+6519del	NM_001400803.1:c.-731+6517_-731+6519del	NM_001400803.1:c.-731+6518_-731+6519del	NM_001400803.1:c.-731+6519del	NM_001400803.1:c.-731+6519dup	NM_001400803.1:c.-731+6518_-731+6519dup
USP28 transcript variant 42	NM_001400804.1:c.-731+5591=	NM_001400804.1:c.-731+5588_-731+5591del	NM_001400804.1:c.-731+5589_-731+5591del	NM_001400804.1:c.-731+5590_-731+5591del	NM_001400804.1:c.-731+5591del	NM_001400804.1:c.-731+5591dup	NM_001400804.1:c.-731+5590_-731+5591dup
USP28 transcript variant 43	NM_001400805.1:c.-623+6519=	NM_001400805.1:c.-623+6516_-623+6519del	NM_001400805.1:c.-623+6517_-623+6519del	NM_001400805.1:c.-623+6518_-623+6519del	NM_001400805.1:c.-623+6519del	NM_001400805.1:c.-623+6519dup	NM_001400805.1:c.-623+6518_-623+6519dup
USP28 transcript variant 44	NM_001400806.1:c.-1077+6519=	NM_001400806.1:c.-1077+6516_-1077+6519del	NM_001400806.1:c.-1077+6517_-1077+6519del	NM_001400806.1:c.-1077+6518_-1077+6519del	NM_001400806.1:c.-1077+6519del	NM_001400806.1:c.-1077+6519dup	NM_001400806.1:c.-1077+6518_-1077+6519dup
USP28 transcript variant 45	NM_001400807.1:c.-108+6519=	NM_001400807.1:c.-108+6516_-108+6519del	NM_001400807.1:c.-108+6517_-108+6519del	NM_001400807.1:c.-108+6518_-108+6519del	NM_001400807.1:c.-108+6519del	NM_001400807.1:c.-108+6519dup	NM_001400807.1:c.-108+6518_-108+6519dup
USP28 transcript variant 46	NM_001400809.1:c.-108+6519=	NM_001400809.1:c.-108+6516_-108+6519del	NM_001400809.1:c.-108+6517_-108+6519del	NM_001400809.1:c.-108+6518_-108+6519del	NM_001400809.1:c.-108+6519del	NM_001400809.1:c.-108+6519dup	NM_001400809.1:c.-108+6518_-108+6519dup
USP28 transcript variant 47	NM_001400810.1:c.-108+6519=	NM_001400810.1:c.-108+6516_-108+6519del	NM_001400810.1:c.-108+6517_-108+6519del	NM_001400810.1:c.-108+6518_-108+6519del	NM_001400810.1:c.-108+6519del	NM_001400810.1:c.-108+6519dup	NM_001400810.1:c.-108+6518_-108+6519dup
USP28 transcript variant 48	NM_001400811.1:c.-705+5591=	NM_001400811.1:c.-705+5588_-705+5591del	NM_001400811.1:c.-705+5589_-705+5591del	NM_001400811.1:c.-705+5590_-705+5591del	NM_001400811.1:c.-705+5591del	NM_001400811.1:c.-705+5591dup	NM_001400811.1:c.-705+5590_-705+5591dup
USP28 transcript variant 49	NM_001400812.1:c.-1387+6519=	NM_001400812.1:c.-1387+6516_-1387+6519del	NM_001400812.1:c.-1387+6517_-1387+6519del	NM_001400812.1:c.-1387+6518_-1387+6519del	NM_001400812.1:c.-1387+6519del	NM_001400812.1:c.-1387+6519dup	NM_001400812.1:c.-1387+6518_-1387+6519dup
USP28 transcript variant 50	NM_001400813.1:c.-520+6519=	NM_001400813.1:c.-520+6516_-520+6519del	NM_001400813.1:c.-520+6517_-520+6519del	NM_001400813.1:c.-520+6518_-520+6519del	NM_001400813.1:c.-520+6519del	NM_001400813.1:c.-520+6519dup	NM_001400813.1:c.-520+6518_-520+6519dup
USP28 transcript	NM_020886.2:c.57+6519=	NM_020886.2:c.57+6516_57+6519del	NM_020886.2:c.57+6517_57+6519del	NM_020886.2:c.57+6518_57+6519del	NM_020886.2:c.57+6519del	NM_020886.2:c.57+6519dup	NM_020886.2:c.57+6518_57+6519dup
USP28 transcript variant 1	NM_020886.4:c.57+6519=	NM_020886.4:c.57+6516_57+6519del	NM_020886.4:c.57+6517_57+6519del	NM_020886.4:c.57+6518_57+6519del	NM_020886.4:c.57+6519del	NM_020886.4:c.57+6519dup	NM_020886.4:c.57+6518_57+6519dup
USP28 transcript variant X1	XM_005271630.1:c.57+6519=	XM_005271630.1:c.57+6516_57+6519del	XM_005271630.1:c.57+6517_57+6519del	XM_005271630.1:c.57+6518_57+6519del	XM_005271630.1:c.57+6519del	XM_005271630.1:c.57+6519dup	XM_005271630.1:c.57+6518_57+6519dup
USP28 transcript variant X2	XM_005271631.1:c.57+6519=	XM_005271631.1:c.57+6516_57+6519del	XM_005271631.1:c.57+6517_57+6519del	XM_005271631.1:c.57+6518_57+6519del	XM_005271631.1:c.57+6519del	XM_005271631.1:c.57+6519dup	XM_005271631.1:c.57+6518_57+6519dup
USP28 transcript variant X3	XM_005271632.1:c.48+5591=	XM_005271632.1:c.48+5588_48+5591del	XM_005271632.1:c.48+5589_48+5591del	XM_005271632.1:c.48+5590_48+5591del	XM_005271632.1:c.48+5591del	XM_005271632.1:c.48+5591dup	XM_005271632.1:c.48+5590_48+5591dup
USP28 transcript variant X4	XM_005271633.1:c.-10+5837=	XM_005271633.1:c.-10+5834_-10+5837del	XM_005271633.1:c.-10+5835_-10+5837del	XM_005271633.1:c.-10+5836_-10+5837del	XM_005271633.1:c.-10+5837del	XM_005271633.1:c.-10+5837dup	XM_005271633.1:c.-10+5836_-10+5837dup
USP28 transcript variant X5	XM_005271634.1:c.57+6519=	XM_005271634.1:c.57+6516_57+6519del	XM_005271634.1:c.57+6517_57+6519del	XM_005271634.1:c.57+6518_57+6519del	XM_005271634.1:c.57+6519del	XM_005271634.1:c.57+6519dup	XM_005271634.1:c.57+6518_57+6519dup
USP28 transcript variant X6	XM_005271635.1:c.169+5591=	XM_005271635.1:c.169+5588_169+5591del	XM_005271635.1:c.169+5589_169+5591del	XM_005271635.1:c.169+5590_169+5591del	XM_005271635.1:c.169+5591del	XM_005271635.1:c.169+5591dup	XM_005271635.1:c.169+5590_169+5591dup
USP28 transcript variant X7	XM_005271636.1:c.57+6519=	XM_005271636.1:c.57+6516_57+6519del	XM_005271636.1:c.57+6517_57+6519del	XM_005271636.1:c.57+6518_57+6519del	XM_005271636.1:c.57+6519del	XM_005271636.1:c.57+6519dup	XM_005271636.1:c.57+6518_57+6519dup
USP28 transcript variant X8	XM_005271637.1:c.57+6519=	XM_005271637.1:c.57+6516_57+6519del	XM_005271637.1:c.57+6517_57+6519del	XM_005271637.1:c.57+6518_57+6519del	XM_005271637.1:c.57+6519del	XM_005271637.1:c.57+6519dup	XM_005271637.1:c.57+6518_57+6519dup
USP28 transcript variant X9	XM_005271638.1:c.57+6519=	XM_005271638.1:c.57+6516_57+6519del	XM_005271638.1:c.57+6517_57+6519del	XM_005271638.1:c.57+6518_57+6519del	XM_005271638.1:c.57+6519del	XM_005271638.1:c.57+6519dup	XM_005271638.1:c.57+6518_57+6519dup
USP28 transcript variant X10	XM_005271639.1:c.57+6519=	XM_005271639.1:c.57+6516_57+6519del	XM_005271639.1:c.57+6517_57+6519del	XM_005271639.1:c.57+6518_57+6519del	XM_005271639.1:c.57+6519del	XM_005271639.1:c.57+6519dup	XM_005271639.1:c.57+6518_57+6519dup
USP28 transcript variant X11	XM_005271640.1:c.-108+6519=	XM_005271640.1:c.-108+6516_-108+6519del	XM_005271640.1:c.-108+6517_-108+6519del	XM_005271640.1:c.-108+6518_-108+6519del	XM_005271640.1:c.-108+6519del	XM_005271640.1:c.-108+6519dup	XM_005271640.1:c.-108+6518_-108+6519dup
USP28 transcript variant X12	XM_005271641.1:c.-108+6519=	XM_005271641.1:c.-108+6516_-108+6519del	XM_005271641.1:c.-108+6517_-108+6519del	XM_005271641.1:c.-108+6518_-108+6519del	XM_005271641.1:c.-108+6519del	XM_005271641.1:c.-108+6519dup	XM_005271641.1:c.-108+6518_-108+6519dup

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#.

27 SubSNP, 15 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80065837	Dec 14, 2007 (129)
2	GMI	ss289097367	May 04, 2012 (137)
3	1000GENOMES	ss1371534550	Aug 21, 2014 (142)
4	EVA_GENOME_DK	ss1574419092	Apr 01, 2015 (144)
5	SWEGEN	ss3008808633	Nov 08, 2017 (151)
6	PACBIO	ss3787072400	Jul 13, 2019 (153)
7	EVA	ss3832847875	Apr 26, 2020 (154)
8	GNOMAD	ss4242883354	Apr 26, 2021 (155)
9	GNOMAD	ss4242883355	Apr 26, 2021 (155)
10	GNOMAD	ss4242883356	Apr 26, 2021 (155)
11	GNOMAD	ss4242883357	Apr 26, 2021 (155)
12	GNOMAD	ss4242883358	Apr 26, 2021 (155)
13	GNOMAD	ss4242883359	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5203968654	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5203968655	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5203968656	Apr 26, 2021 (155)
17	1000G_HIGH_COVERAGE	ss5288963807	Oct 16, 2022 (156)
18	1000G_HIGH_COVERAGE	ss5288963808	Oct 16, 2022 (156)
19	HUGCELL_USP	ss5483946732	Oct 16, 2022 (156)
20	HUGCELL_USP	ss5483946734	Oct 16, 2022 (156)
21	HUGCELL_USP	ss5483946735	Oct 16, 2022 (156)
22	HUGCELL_USP	ss5483946736	Oct 16, 2022 (156)
23	TOMMO_GENOMICS	ss5752439267	Oct 16, 2022 (156)
24	TOMMO_GENOMICS	ss5752439268	Oct 16, 2022 (156)
25	TOMMO_GENOMICS	ss5752439270	Oct 16, 2022 (156)
26	EVA	ss5850158289	Oct 16, 2022 (156)
27	EVA	ss5980703686	Oct 16, 2022 (156)
28	1000Genomes	NC_000011.9 - 113739648	Oct 12, 2018 (152)
29	The Danish reference pan genome	NC_000011.9 - 113739648	Apr 26, 2020 (154)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392482471 (NC_000011.10:113868925::A 1245/71340) Row 392482472 (NC_000011.10:113868925::AA 22/71474) Row 392482473 (NC_000011.10:113868925:A: 339/71420)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392482471 (NC_000011.10:113868925::A 1245/71340) Row 392482472 (NC_000011.10:113868925::AA 22/71474) Row 392482473 (NC_000011.10:113868925:A: 339/71420)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392482471 (NC_000011.10:113868925::A 1245/71340) Row 392482472 (NC_000011.10:113868925::AA 22/71474) Row 392482473 (NC_000011.10:113868925:A: 339/71420)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392482471 (NC_000011.10:113868925::A 1245/71340) Row 392482472 (NC_000011.10:113868925::AA 22/71474) Row 392482473 (NC_000011.10:113868925:A: 339/71420)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392482471 (NC_000011.10:113868925::A 1245/71340) Row 392482472 (NC_000011.10:113868925::AA 22/71474) Row 392482473 (NC_000011.10:113868925:A: 339/71420)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 392482471 (NC_000011.10:113868925::A 1245/71340) Row 392482472 (NC_000011.10:113868925::AA 22/71474) Row 392482473 (NC_000011.10:113868925:A: 339/71420)...	-	Apr 26, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 61937961 (NC_000011.9:113739647::A 99/16758) Row 61937962 (NC_000011.9:113739647:A: 29/16758) Row 61937963 (NC_000011.9:113739647::AA 2/16758)	-	Apr 26, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 61937961 (NC_000011.9:113739647::A 99/16758) Row 61937962 (NC_000011.9:113739647:A: 29/16758) Row 61937963 (NC_000011.9:113739647::AA 2/16758)	-	Apr 26, 2021 (155)
38	8.3KJPN Submission ignored due to conflicting rows: Row 61937961 (NC_000011.9:113739647::A 99/16758) Row 61937962 (NC_000011.9:113739647:A: 29/16758) Row 61937963 (NC_000011.9:113739647::AA 2/16758)	-	Apr 26, 2021 (155)
39	14KJPN Submission ignored due to conflicting rows: Row 86276371 (NC_000011.10:113868925::A 176/28256) Row 86276372 (NC_000011.10:113868925:A: 29/28256) Row 86276374 (NC_000011.10:113868925::AA 2/28256)	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 86276371 (NC_000011.10:113868925::A 176/28256) Row 86276372 (NC_000011.10:113868925:A: 29/28256) Row 86276374 (NC_000011.10:113868925::AA 2/28256)	-	Oct 16, 2022 (156)
41	14KJPN Submission ignored due to conflicting rows: Row 86276371 (NC_000011.10:113868925::A 176/28256) Row 86276372 (NC_000011.10:113868925:A: 29/28256) Row 86276374 (NC_000011.10:113868925::AA 2/28256)	-	Oct 16, 2022 (156)
42	ALFA	NC_000011.10 - 113868926	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)
rs199789546	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
55621976, ss1371534550	NC_000011.9:113739647:AAAA:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4242883359	NC_000011.10:113868925:AAAA:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
7497265183	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4242883358	NC_000011.10:113868925:AAA:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
7497265183	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss80065837	NC_000011.8:113244871:AA:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4242883357, ss5483946735	NC_000011.10:113868925:AA:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
7497265183	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss289097367	NC_000011.8:113244857:A:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3787072400, ss3832847875, ss5203968655, ss5980703686	NC_000011.9:113739647:A:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss4242883356, ss5288963808, ss5483946732, ss5752439268, ss5850158289	NC_000011.10:113868925:A:	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
7497265183	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
322075, ss1574419092, ss3008808633, ss5203968654	NC_000011.9:113739647::A	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4242883354, ss5288963807, ss5483946734, ss5752439267	NC_000011.10:113868925::A	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
7497265183	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5203968656	NC_000011.9:113739647::AA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4242883355, ss5483946736, ss5752439270	NC_000011.10:113868925::AA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
7497265183	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:113868925:AAAAAAAAAAA… NC_000011.10:113868925:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(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 rs58107096

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

rs58107096