Name: rs34252093
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.

rs34252093

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:6475680-6475697 (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)₈ / del(T)₅ / del(T)₄ / delT…
del(T)₈ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1494 (1129/7557, ALFA)
dup(T)₄=0.0020 (10/5008, 1000G)
(T)₁₈=0.42 (17/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TRIM3 : 2KB Upstream 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	7557	TTTTTTTTTTTTTTTTTT=0.8477	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.1494, TTTTTTTTTTTTTTTTTTTT=0.0029, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.790474	0.086433	0.123093	32
European	Sub	6429	TTTTTTTTTTTTTTTTTT=0.8213	TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.1753, TTTTTTTTTTTTTTTTTTTT=0.0034, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	0.753861	0.101796	0.144343	32
African	Sub	700	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	30	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	670	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	62	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	48	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	34	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	142	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	38	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	152	TTTTTTTTTTTTTTTTTT=0.987	TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.013, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	0.973684	0.0	0.026316	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	7557	(T)₁₈=0.8477	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1494, dupTT=0.0029, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	6429	(T)₁₈=0.8213	del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1753, dupTT=0.0034, dupTTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	700	(T)₁₈=1.000	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	152	(T)₁₈=0.987	del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.013, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 2	Sub	142	(T)₁₈=1.000	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	62	(T)₁₈=1.00	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
Allele Frequency Aggregator	South Asian	Sub	38	(T)₁₈=1.00	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
Allele Frequency Aggregator	Latin American 1	Sub	34	(T)₁₈=1.00	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
1000Genomes	Global	Study-wide	5008	- No frequency provided	dup(T)₄=0.0020
1000Genomes	African	Sub	1322	- No frequency provided	dup(T)₄=0.0061
1000Genomes	East Asian	Sub	1008	- No frequency provided	dup(T)₄=0.0000
1000Genomes	Europe	Sub	1006	- No frequency provided	dup(T)₄=0.0010
1000Genomes	South Asian	Sub	978	- No frequency provided	dup(T)₄=0.000
1000Genomes	American	Sub	694	- No frequency provided	dup(T)₄=0.001
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.57

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.6475690_6475697del
GRCh38.p14 chr 11	NC_000011.10:g.6475693_6475697del
GRCh38.p14 chr 11	NC_000011.10:g.6475694_6475697del
GRCh38.p14 chr 11	NC_000011.10:g.6475695_6475697del
GRCh38.p14 chr 11	NC_000011.10:g.6475696_6475697del
GRCh38.p14 chr 11	NC_000011.10:g.6475697del
GRCh38.p14 chr 11	NC_000011.10:g.6475697dup
GRCh38.p14 chr 11	NC_000011.10:g.6475696_6475697dup
GRCh38.p14 chr 11	NC_000011.10:g.6475695_6475697dup
GRCh38.p14 chr 11	NC_000011.10:g.6475694_6475697dup
GRCh38.p14 chr 11	NC_000011.10:g.6475693_6475697dup
GRCh37.p13 chr 11	NC_000011.9:g.6496920_6496927del
GRCh37.p13 chr 11	NC_000011.9:g.6496923_6496927del
GRCh37.p13 chr 11	NC_000011.9:g.6496924_6496927del
GRCh37.p13 chr 11	NC_000011.9:g.6496925_6496927del
GRCh37.p13 chr 11	NC_000011.9:g.6496926_6496927del
GRCh37.p13 chr 11	NC_000011.9:g.6496927del
GRCh37.p13 chr 11	NC_000011.9:g.6496927dup
GRCh37.p13 chr 11	NC_000011.9:g.6496926_6496927dup
GRCh37.p13 chr 11	NC_000011.9:g.6496925_6496927dup
GRCh37.p13 chr 11	NC_000011.9:g.6496924_6496927dup
GRCh37.p13 chr 11	NC_000011.9:g.6496923_6496927dup

Gene: TRIM3, tripartite motif containing 3 (minus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
TRIM3 transcript variant 4	NM_001248006.2:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant 5	NM_001248007.2:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant 1	NM_006458.4:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant 2	NM_033278.4:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant X4	XM_017017098.3:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant X3	XM_024448328.2:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant X1	XM_047426257.1:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant X2	XM_047426258.1:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant X6	XM_047426261.1:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant X7	XM_047426262.1:c.	N/A	Upstream Transcript Variant
TRIM3 transcript variant X5	XM_047426259.1:c.	N/A	N/A

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)₁₈=	del(T)₈	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅
GRCh38.p14 chr 11	NC_000011.10:g.6475680_6475697=	NC_000011.10:g.6475690_6475697del	NC_000011.10:g.6475693_6475697del	NC_000011.10:g.6475694_6475697del	NC_000011.10:g.6475695_6475697del	NC_000011.10:g.6475696_6475697del	NC_000011.10:g.6475697del	NC_000011.10:g.6475697dup	NC_000011.10:g.6475696_6475697dup	NC_000011.10:g.6475695_6475697dup	NC_000011.10:g.6475694_6475697dup	NC_000011.10:g.6475693_6475697dup
GRCh37.p13 chr 11	NC_000011.9:g.6496910_6496927=	NC_000011.9:g.6496920_6496927del	NC_000011.9:g.6496923_6496927del	NC_000011.9:g.6496924_6496927del	NC_000011.9:g.6496925_6496927del	NC_000011.9:g.6496926_6496927del	NC_000011.9:g.6496927del	NC_000011.9:g.6496927dup	NC_000011.9:g.6496926_6496927dup	NC_000011.9:g.6496925_6496927dup	NC_000011.9:g.6496924_6496927dup	NC_000011.9:g.6496923_6496927dup
ARFIP2 transcript variant 2	NM_012402.4:c.1416_1433=	NM_012402.4:c.1426_1433del	NM_012402.4:c.1429_1433del	NM_012402.4:c.1430_1433del	NM_012402.4:c.1431_1433del	NM_012402.4:c.1432_1433del	NM_012402.4:c.*1433del	NM_012402.4:c.*1433dup	NM_012402.4:c.1432_1433dup	NM_012402.4:c.1431_1433dup	NM_012402.4:c.1430_1433dup	NM_012402.4:c.1429_1433dup
ARFIP2 transcript variant 2	NM_012402.3:c.1416_1433=	NM_012402.3:c.1426_1433del	NM_012402.3:c.1429_1433del	NM_012402.3:c.1430_1433del	NM_012402.3:c.1431_1433del	NM_012402.3:c.1432_1433del	NM_012402.3:c.*1433del	NM_012402.3:c.*1433dup	NM_012402.3:c.1432_1433dup	NM_012402.3:c.1431_1433dup	NM_012402.3:c.1430_1433dup	NM_012402.3:c.1429_1433dup
ARFIP2 transcript variant 1	NM_001242854.2:c.1416_1433=	NM_001242854.2:c.1426_1433del	NM_001242854.2:c.1429_1433del	NM_001242854.2:c.1430_1433del	NM_001242854.2:c.1431_1433del	NM_001242854.2:c.1432_1433del	NM_001242854.2:c.*1433del	NM_001242854.2:c.*1433dup	NM_001242854.2:c.1432_1433dup	NM_001242854.2:c.1431_1433dup	NM_001242854.2:c.1430_1433dup	NM_001242854.2:c.1429_1433dup
ARFIP2 transcript variant 3	NM_001242855.2:c.1416_1433=	NM_001242855.2:c.1426_1433del	NM_001242855.2:c.1429_1433del	NM_001242855.2:c.1430_1433del	NM_001242855.2:c.1431_1433del	NM_001242855.2:c.1432_1433del	NM_001242855.2:c.*1433del	NM_001242855.2:c.*1433dup	NM_001242855.2:c.1432_1433dup	NM_001242855.2:c.1431_1433dup	NM_001242855.2:c.1430_1433dup	NM_001242855.2:c.1429_1433dup
ARFIP2 transcript variant 4	NM_001242856.2:c.1416_1433=	NM_001242856.2:c.1426_1433del	NM_001242856.2:c.1429_1433del	NM_001242856.2:c.1430_1433del	NM_001242856.2:c.1431_1433del	NM_001242856.2:c.1432_1433del	NM_001242856.2:c.*1433del	NM_001242856.2:c.*1433dup	NM_001242856.2:c.1432_1433dup	NM_001242856.2:c.1431_1433dup	NM_001242856.2:c.1430_1433dup	NM_001242856.2:c.1429_1433dup
ARFIP2 transcript variant 1	NM_001242854.1:c.1416_1433=	NM_001242854.1:c.1426_1433del	NM_001242854.1:c.1429_1433del	NM_001242854.1:c.1430_1433del	NM_001242854.1:c.1431_1433del	NM_001242854.1:c.1432_1433del	NM_001242854.1:c.*1433del	NM_001242854.1:c.*1433dup	NM_001242854.1:c.1432_1433dup	NM_001242854.1:c.1431_1433dup	NM_001242854.1:c.1430_1433dup	NM_001242854.1:c.1429_1433dup
ARFIP2 transcript variant 22	NR_164826.1:n.2770_2787=	NR_164826.1:n.2780_2787del	NR_164826.1:n.2783_2787del	NR_164826.1:n.2784_2787del	NR_164826.1:n.2785_2787del	NR_164826.1:n.2786_2787del	NR_164826.1:n.2787del	NR_164826.1:n.2787dup	NR_164826.1:n.2786_2787dup	NR_164826.1:n.2785_2787dup	NR_164826.1:n.2784_2787dup	NR_164826.1:n.2783_2787dup
ARFIP2 transcript variant 16	NM_001376561.1:c.1626_1643=	NM_001376561.1:c.1636_1643del	NM_001376561.1:c.1639_1643del	NM_001376561.1:c.1640_1643del	NM_001376561.1:c.1641_1643del	NM_001376561.1:c.1642_1643del	NM_001376561.1:c.*1643del	NM_001376561.1:c.*1643dup	NM_001376561.1:c.1642_1643dup	NM_001376561.1:c.1641_1643dup	NM_001376561.1:c.1640_1643dup	NM_001376561.1:c.1639_1643dup
ARFIP2 transcript variant 12	NR_163424.1:n.2659_2676=	NR_163424.1:n.2669_2676del	NR_163424.1:n.2672_2676del	NR_163424.1:n.2673_2676del	NR_163424.1:n.2674_2676del	NR_163424.1:n.2675_2676del	NR_163424.1:n.2676del	NR_163424.1:n.2676dup	NR_163424.1:n.2675_2676dup	NR_163424.1:n.2674_2676dup	NR_163424.1:n.2673_2676dup	NR_163424.1:n.2672_2676dup
ARFIP2 transcript variant 6	NM_001370408.1:c.1416_1433=	NM_001370408.1:c.1426_1433del	NM_001370408.1:c.1429_1433del	NM_001370408.1:c.1430_1433del	NM_001370408.1:c.1431_1433del	NM_001370408.1:c.1432_1433del	NM_001370408.1:c.*1433del	NM_001370408.1:c.*1433dup	NM_001370408.1:c.1432_1433dup	NM_001370408.1:c.1431_1433dup	NM_001370408.1:c.1430_1433dup	NM_001370408.1:c.1429_1433dup
ARFIP2 transcript variant 17	NM_001376562.1:c.1416_1433=	NM_001376562.1:c.1426_1433del	NM_001376562.1:c.1429_1433del	NM_001376562.1:c.1430_1433del	NM_001376562.1:c.1431_1433del	NM_001376562.1:c.1432_1433del	NM_001376562.1:c.*1433del	NM_001376562.1:c.*1433dup	NM_001376562.1:c.1432_1433dup	NM_001376562.1:c.1431_1433dup	NM_001376562.1:c.1430_1433dup	NM_001376562.1:c.1429_1433dup
ARFIP2 transcript variant 3	NM_001242855.1:c.1416_1433=	NM_001242855.1:c.1426_1433del	NM_001242855.1:c.1429_1433del	NM_001242855.1:c.1430_1433del	NM_001242855.1:c.1431_1433del	NM_001242855.1:c.1432_1433del	NM_001242855.1:c.*1433del	NM_001242855.1:c.*1433dup	NM_001242855.1:c.1432_1433dup	NM_001242855.1:c.1431_1433dup	NM_001242855.1:c.1430_1433dup	NM_001242855.1:c.1429_1433dup
ARFIP2 transcript variant 13	NM_001376558.1:c.1416_1433=	NM_001376558.1:c.1426_1433del	NM_001376558.1:c.1429_1433del	NM_001376558.1:c.1430_1433del	NM_001376558.1:c.1431_1433del	NM_001376558.1:c.1432_1433del	NM_001376558.1:c.*1433del	NM_001376558.1:c.*1433dup	NM_001376558.1:c.1432_1433dup	NM_001376558.1:c.1431_1433dup	NM_001376558.1:c.1430_1433dup	NM_001376558.1:c.1429_1433dup
ARFIP2 transcript variant 14	NM_001376559.1:c.1416_1433=	NM_001376559.1:c.1426_1433del	NM_001376559.1:c.1429_1433del	NM_001376559.1:c.1430_1433del	NM_001376559.1:c.1431_1433del	NM_001376559.1:c.1432_1433del	NM_001376559.1:c.*1433del	NM_001376559.1:c.*1433dup	NM_001376559.1:c.1432_1433dup	NM_001376559.1:c.1431_1433dup	NM_001376559.1:c.1430_1433dup	NM_001376559.1:c.1429_1433dup
ARFIP2 transcript variant 15	NM_001376560.1:c.1416_1433=	NM_001376560.1:c.1426_1433del	NM_001376560.1:c.1429_1433del	NM_001376560.1:c.1430_1433del	NM_001376560.1:c.1431_1433del	NM_001376560.1:c.1432_1433del	NM_001376560.1:c.*1433del	NM_001376560.1:c.*1433dup	NM_001376560.1:c.1432_1433dup	NM_001376560.1:c.1431_1433dup	NM_001376560.1:c.1430_1433dup	NM_001376560.1:c.1429_1433dup
ARFIP2 transcript variant 7	NM_001370409.1:c.1416_1433=	NM_001370409.1:c.1426_1433del	NM_001370409.1:c.1429_1433del	NM_001370409.1:c.1430_1433del	NM_001370409.1:c.1431_1433del	NM_001370409.1:c.1432_1433del	NM_001370409.1:c.*1433del	NM_001370409.1:c.*1433dup	NM_001370409.1:c.1432_1433dup	NM_001370409.1:c.1431_1433dup	NM_001370409.1:c.1430_1433dup	NM_001370409.1:c.1429_1433dup
ARFIP2 transcript variant 18	NM_001376563.1:c.1416_1433=	NM_001376563.1:c.1426_1433del	NM_001376563.1:c.1429_1433del	NM_001376563.1:c.1430_1433del	NM_001376563.1:c.1431_1433del	NM_001376563.1:c.1432_1433del	NM_001376563.1:c.*1433del	NM_001376563.1:c.*1433dup	NM_001376563.1:c.1432_1433dup	NM_001376563.1:c.1431_1433dup	NM_001376563.1:c.1430_1433dup	NM_001376563.1:c.1429_1433dup
ARFIP2 transcript variant 5	NM_001370406.1:c.1416_1433=	NM_001370406.1:c.1426_1433del	NM_001370406.1:c.1429_1433del	NM_001370406.1:c.1430_1433del	NM_001370406.1:c.1431_1433del	NM_001370406.1:c.1432_1433del	NM_001370406.1:c.*1433del	NM_001370406.1:c.*1433dup	NM_001370406.1:c.1432_1433dup	NM_001370406.1:c.1431_1433dup	NM_001370406.1:c.1430_1433dup	NM_001370406.1:c.1429_1433dup
ARFIP2 transcript variant 10	NM_001370413.1:c.1416_1433=	NM_001370413.1:c.1426_1433del	NM_001370413.1:c.1429_1433del	NM_001370413.1:c.1430_1433del	NM_001370413.1:c.1431_1433del	NM_001370413.1:c.1432_1433del	NM_001370413.1:c.*1433del	NM_001370413.1:c.*1433dup	NM_001370413.1:c.1432_1433dup	NM_001370413.1:c.1431_1433dup	NM_001370413.1:c.1430_1433dup	NM_001370413.1:c.1429_1433dup
ARFIP2 transcript variant 8	NM_001370411.1:c.1416_1433=	NM_001370411.1:c.1426_1433del	NM_001370411.1:c.1429_1433del	NM_001370411.1:c.1430_1433del	NM_001370411.1:c.1431_1433del	NM_001370411.1:c.1432_1433del	NM_001370411.1:c.*1433del	NM_001370411.1:c.*1433dup	NM_001370411.1:c.1432_1433dup	NM_001370411.1:c.1431_1433dup	NM_001370411.1:c.1430_1433dup	NM_001370411.1:c.1429_1433dup
ARFIP2 transcript variant 9	NM_001370412.1:c.1416_1433=	NM_001370412.1:c.1426_1433del	NM_001370412.1:c.1429_1433del	NM_001370412.1:c.1430_1433del	NM_001370412.1:c.1431_1433del	NM_001370412.1:c.1432_1433del	NM_001370412.1:c.*1433del	NM_001370412.1:c.*1433dup	NM_001370412.1:c.1432_1433dup	NM_001370412.1:c.1431_1433dup	NM_001370412.1:c.1430_1433dup	NM_001370412.1:c.1429_1433dup
ARFIP2 transcript variant 4	NM_001242856.1:c.1416_1433=	NM_001242856.1:c.1426_1433del	NM_001242856.1:c.1429_1433del	NM_001242856.1:c.1430_1433del	NM_001242856.1:c.1431_1433del	NM_001242856.1:c.1432_1433del	NM_001242856.1:c.*1433del	NM_001242856.1:c.*1433dup	NM_001242856.1:c.1432_1433dup	NM_001242856.1:c.1431_1433dup	NM_001242856.1:c.1430_1433dup	NM_001242856.1:c.1429_1433dup
ARFIP2 transcript variant 20	NR_164825.1:n.2464_2481=	NR_164825.1:n.2474_2481del	NR_164825.1:n.2477_2481del	NR_164825.1:n.2478_2481del	NR_164825.1:n.2479_2481del	NR_164825.1:n.2480_2481del	NR_164825.1:n.2481del	NR_164825.1:n.2481dup	NR_164825.1:n.2480_2481dup	NR_164825.1:n.2479_2481dup	NR_164825.1:n.2478_2481dup	NR_164825.1:n.2477_2481dup
ARFIP2 transcript variant 19	NM_001376564.1:c.1416_1433=	NM_001376564.1:c.1426_1433del	NM_001376564.1:c.1429_1433del	NM_001376564.1:c.1430_1433del	NM_001376564.1:c.1431_1433del	NM_001376564.1:c.1432_1433del	NM_001376564.1:c.*1433del	NM_001376564.1:c.*1433dup	NM_001376564.1:c.1432_1433dup	NM_001376564.1:c.1431_1433dup	NM_001376564.1:c.1430_1433dup	NM_001376564.1:c.1429_1433dup
ARFIP2 transcript variant 11	NR_163423.1:n.2424_2441=	NR_163423.1:n.2434_2441del	NR_163423.1:n.2437_2441del	NR_163423.1:n.2438_2441del	NR_163423.1:n.2439_2441del	NR_163423.1:n.2440_2441del	NR_163423.1:n.2441del	NR_163423.1:n.2441dup	NR_163423.1:n.2440_2441dup	NR_163423.1:n.2439_2441dup	NR_163423.1:n.2438_2441dup	NR_163423.1:n.2437_2441dup

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#.

44 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40027341	Dec 03, 2013 (138)
2	ABI	ss40075298	Dec 03, 2013 (142)
3	HGSV	ss80808485	Dec 04, 2013 (138)
4	PJP	ss294687180	May 09, 2011 (137)
5	PJP	ss294687181	May 09, 2011 (134)
6	1000GENOMES	ss1370474262	Aug 21, 2014 (142)
7	EVA_GENOME_DK	ss1574300172	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1706984185	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1706984186	Apr 01, 2015 (144)
10	EVA_UK10K_TWINSUK	ss1706984187	Apr 01, 2015 (144)
11	EVA_UK10K_TWINSUK	ss1706984190	Apr 01, 2015 (144)
12	SWEGEN	ss3007541039	Nov 08, 2017 (151)
13	SWEGEN	ss3007541040	Nov 08, 2017 (151)
14	EVA	ss3832459011	Apr 26, 2020 (154)
15	KOGIC	ss3969139703	Apr 26, 2020 (154)
16	KOGIC	ss3969139704	Apr 26, 2020 (154)
17	KOGIC	ss3969139705	Apr 26, 2020 (154)
18	GNOMAD	ss4229465098	Apr 26, 2021 (155)
19	GNOMAD	ss4229465099	Apr 26, 2021 (155)
20	GNOMAD	ss4229465100	Apr 26, 2021 (155)
21	GNOMAD	ss4229465101	Apr 26, 2021 (155)
22	GNOMAD	ss4229465102	Apr 26, 2021 (155)
23	GNOMAD	ss4229465103	Apr 26, 2021 (155)
24	GNOMAD	ss4229465104	Apr 26, 2021 (155)
25	GNOMAD	ss4229465105	Apr 26, 2021 (155)
26	GNOMAD	ss4229465106	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5200534342	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5200534343	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5200534344	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5200534345	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5286286516	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5286286517	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5286286518	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5286286519	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5481601545	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5481601546	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5481601547	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5481601548	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5747246293	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5747246294	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5747246295	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5747246296	Oct 16, 2022 (156)
43	EVA	ss5836215676	Oct 16, 2022 (156)
44	EVA	ss5836215677	Oct 16, 2022 (156)
45	1000Genomes	NC_000011.9 - 6496910	Oct 12, 2018 (152)
46	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29136477 (NC_000011.9:6496909::T 1688/3854) Row 29136478 (NC_000011.9:6496909::TT 296/3854)	-	Oct 12, 2018 (152)
47	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 29136477 (NC_000011.9:6496909::T 1688/3854) Row 29136478 (NC_000011.9:6496909::TT 296/3854)	-	Oct 12, 2018 (152)
48	The Danish reference pan genome	NC_000011.9 - 6496910	Apr 26, 2020 (154)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 370392355 (NC_000011.10:6475679::T 44361/104374) Row 370392356 (NC_000011.10:6475679::TT 1526/104376) Row 370392357 (NC_000011.10:6475679::TTT 760/104422)...	-	Apr 26, 2021 (155)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 25517704 (NC_000011.10:6475680::T 504/1824) Row 25517705 (NC_000011.10:6475679:T: 168/1824) Row 25517706 (NC_000011.10:6475680::TT 35/1824)	-	Apr 26, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 25517704 (NC_000011.10:6475680::T 504/1824) Row 25517705 (NC_000011.10:6475679:T: 168/1824) Row 25517706 (NC_000011.10:6475680::TT 35/1824)	-	Apr 26, 2020 (154)
61	Korean Genome Project Submission ignored due to conflicting rows: Row 25517704 (NC_000011.10:6475680::T 504/1824) Row 25517705 (NC_000011.10:6475679:T: 168/1824) Row 25517706 (NC_000011.10:6475680::TT 35/1824)	-	Apr 26, 2020 (154)
62	8.3KJPN Submission ignored due to conflicting rows: Row 58503649 (NC_000011.9:6496909::T 3369/16628) Row 58503650 (NC_000011.9:6496909::TT 20/16628) Row 58503651 (NC_000011.9:6496909:T: 22/16628)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 58503649 (NC_000011.9:6496909::T 3369/16628) Row 58503650 (NC_000011.9:6496909::TT 20/16628) Row 58503651 (NC_000011.9:6496909:T: 22/16628)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 58503649 (NC_000011.9:6496909::T 3369/16628) Row 58503650 (NC_000011.9:6496909::TT 20/16628) Row 58503651 (NC_000011.9:6496909:T: 22/16628)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 58503649 (NC_000011.9:6496909::T 3369/16628) Row 58503650 (NC_000011.9:6496909::TT 20/16628) Row 58503651 (NC_000011.9:6496909:T: 22/16628)...	-	Apr 26, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 81083397 (NC_000011.10:6475679::T 6157/28222) Row 81083398 (NC_000011.10:6475679::TT 25/28222) Row 81083399 (NC_000011.10:6475679:T: 45/28222)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 81083397 (NC_000011.10:6475679::T 6157/28222) Row 81083398 (NC_000011.10:6475679::TT 25/28222) Row 81083399 (NC_000011.10:6475679:T: 45/28222)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 81083397 (NC_000011.10:6475679::T 6157/28222) Row 81083398 (NC_000011.10:6475679::TT 25/28222) Row 81083399 (NC_000011.10:6475679:T: 45/28222)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 81083397 (NC_000011.10:6475679::T 6157/28222) Row 81083398 (NC_000011.10:6475679::TT 25/28222) Row 81083399 (NC_000011.10:6475679:T: 45/28222)...	-	Oct 16, 2022 (156)
70	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29136477 (NC_000011.9:6496909::T 1641/3708) Row 29136478 (NC_000011.9:6496909::TT 276/3708)	-	Oct 12, 2018 (152)
71	UK 10K study - Twins Submission ignored due to conflicting rows: Row 29136477 (NC_000011.9:6496909::T 1641/3708) Row 29136478 (NC_000011.9:6496909::TT 276/3708)	-	Oct 12, 2018 (152)
72	ALFA	NC_000011.10 - 6475680	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)
rs59542046	May 25, 2008 (130)
rs72248591	May 11, 2012 (137)
rs144308296	May 11, 2012 (137)
rs397849718	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5200534345	NC_000011.9:6496909:TTTTTTTT:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5747246296	NC_000011.10:6475679:TTTTTTTT:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT
ss4229465106	NC_000011.10:6475679:TTTTT:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4229465105	NC_000011.10:6475679:TTTT:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4229465104	NC_000011.10:6475679:TTT:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4229465103	NC_000011.10:6475679:TT:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss294687181	NC_000011.8:6453502:T:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5200534344	NC_000011.9:6496909:T:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3969139704, ss5286286518, ss5481601547, ss5747246295	NC_000011.10:6475679:T:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss40075298	NT_009237.18:6436926:T:	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss294687180	NC_000011.8:6453486::T	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
277246, ss1574300172, ss1706984185, ss1706984187, ss3007541039, ss3832459011, ss5200534342, ss5836215676	NC_000011.9:6496909::T	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4229465098, ss5286286516, ss5481601545, ss5747246293	NC_000011.10:6475679::T	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3969139703	NC_000011.10:6475680::T	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss40027341, ss80808485	NT_009237.18:6436927::T	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss1706984186, ss1706984190, ss3007541040, ss5200534343, ss5836215677	NC_000011.9:6496909::TT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4229465099, ss5286286517, ss5481601546, ss5747246294	NC_000011.10:6475679::TT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3969139705	NC_000011.10:6475680::TT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4229465100, ss5286286519, ss5481601548	NC_000011.10:6475679::TTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
52458855, ss1370474262	NC_000011.9:6496909::TTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229465101	NC_000011.10:6475679::TTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
8949772336	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4229465102	NC_000011.10:6475679::TTTTT	NC_000011.10:6475679:TTTTTTTTTTTTT… NC_000011.10:6475679:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(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 rs34252093

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

Placement	(T)₁₈=	del(T)₈	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅
GRCh38.p14 chr 11	NC_000011.10:g.6475680_6475697=	NC_000011.10:g.6475690_6475697del	NC_000011.10:g.6475693_6475697del	NC_000011.10:g.6475694_6475697del	NC_000011.10:g.6475695_6475697del	NC_000011.10:g.6475696_6475697del	NC_000011.10:g.6475697del	NC_000011.10:g.6475697dup	NC_000011.10:g.6475696_6475697dup	NC_000011.10:g.6475695_6475697dup	NC_000011.10:g.6475694_6475697dup	NC_000011.10:g.6475693_6475697dup
GRCh37.p13 chr 11	NC_000011.9:g.6496910_6496927=	NC_000011.9:g.6496920_6496927del	NC_000011.9:g.6496923_6496927del	NC_000011.9:g.6496924_6496927del	NC_000011.9:g.6496925_6496927del	NC_000011.9:g.6496926_6496927del	NC_000011.9:g.6496927del	NC_000011.9:g.6496927dup	NC_000011.9:g.6496926_6496927dup	NC_000011.9:g.6496925_6496927dup	NC_000011.9:g.6496924_6496927dup	NC_000011.9:g.6496923_6496927dup
ARFIP2 transcript variant 2	NM_012402.4:c.1416_1433=	NM_012402.4:c.1426_1433del	NM_012402.4:c.1429_1433del	NM_012402.4:c.1430_1433del	NM_012402.4:c.1431_1433del	NM_012402.4:c.1432_1433del	NM_012402.4:c.*1433del	NM_012402.4:c.*1433dup	NM_012402.4:c.1432_1433dup	NM_012402.4:c.1431_1433dup	NM_012402.4:c.1430_1433dup	NM_012402.4:c.1429_1433dup
ARFIP2 transcript variant 2	NM_012402.3:c.1416_1433=	NM_012402.3:c.1426_1433del	NM_012402.3:c.1429_1433del	NM_012402.3:c.1430_1433del	NM_012402.3:c.1431_1433del	NM_012402.3:c.1432_1433del	NM_012402.3:c.*1433del	NM_012402.3:c.*1433dup	NM_012402.3:c.1432_1433dup	NM_012402.3:c.1431_1433dup	NM_012402.3:c.1430_1433dup	NM_012402.3:c.1429_1433dup
ARFIP2 transcript variant 1	NM_001242854.2:c.1416_1433=	NM_001242854.2:c.1426_1433del	NM_001242854.2:c.1429_1433del	NM_001242854.2:c.1430_1433del	NM_001242854.2:c.1431_1433del	NM_001242854.2:c.1432_1433del	NM_001242854.2:c.*1433del	NM_001242854.2:c.*1433dup	NM_001242854.2:c.1432_1433dup	NM_001242854.2:c.1431_1433dup	NM_001242854.2:c.1430_1433dup	NM_001242854.2:c.1429_1433dup
ARFIP2 transcript variant 3	NM_001242855.2:c.1416_1433=	NM_001242855.2:c.1426_1433del	NM_001242855.2:c.1429_1433del	NM_001242855.2:c.1430_1433del	NM_001242855.2:c.1431_1433del	NM_001242855.2:c.1432_1433del	NM_001242855.2:c.*1433del	NM_001242855.2:c.*1433dup	NM_001242855.2:c.1432_1433dup	NM_001242855.2:c.1431_1433dup	NM_001242855.2:c.1430_1433dup	NM_001242855.2:c.1429_1433dup
ARFIP2 transcript variant 4	NM_001242856.2:c.1416_1433=	NM_001242856.2:c.1426_1433del	NM_001242856.2:c.1429_1433del	NM_001242856.2:c.1430_1433del	NM_001242856.2:c.1431_1433del	NM_001242856.2:c.1432_1433del	NM_001242856.2:c.*1433del	NM_001242856.2:c.*1433dup	NM_001242856.2:c.1432_1433dup	NM_001242856.2:c.1431_1433dup	NM_001242856.2:c.1430_1433dup	NM_001242856.2:c.1429_1433dup
ARFIP2 transcript variant 1	NM_001242854.1:c.1416_1433=	NM_001242854.1:c.1426_1433del	NM_001242854.1:c.1429_1433del	NM_001242854.1:c.1430_1433del	NM_001242854.1:c.1431_1433del	NM_001242854.1:c.1432_1433del	NM_001242854.1:c.*1433del	NM_001242854.1:c.*1433dup	NM_001242854.1:c.1432_1433dup	NM_001242854.1:c.1431_1433dup	NM_001242854.1:c.1430_1433dup	NM_001242854.1:c.1429_1433dup
ARFIP2 transcript variant 22	NR_164826.1:n.2770_2787=	NR_164826.1:n.2780_2787del	NR_164826.1:n.2783_2787del	NR_164826.1:n.2784_2787del	NR_164826.1:n.2785_2787del	NR_164826.1:n.2786_2787del	NR_164826.1:n.2787del	NR_164826.1:n.2787dup	NR_164826.1:n.2786_2787dup	NR_164826.1:n.2785_2787dup	NR_164826.1:n.2784_2787dup	NR_164826.1:n.2783_2787dup
ARFIP2 transcript variant 16	NM_001376561.1:c.1626_1643=	NM_001376561.1:c.1636_1643del	NM_001376561.1:c.1639_1643del	NM_001376561.1:c.1640_1643del	NM_001376561.1:c.1641_1643del	NM_001376561.1:c.1642_1643del	NM_001376561.1:c.*1643del	NM_001376561.1:c.*1643dup	NM_001376561.1:c.1642_1643dup	NM_001376561.1:c.1641_1643dup	NM_001376561.1:c.1640_1643dup	NM_001376561.1:c.1639_1643dup
ARFIP2 transcript variant 12	NR_163424.1:n.2659_2676=	NR_163424.1:n.2669_2676del	NR_163424.1:n.2672_2676del	NR_163424.1:n.2673_2676del	NR_163424.1:n.2674_2676del	NR_163424.1:n.2675_2676del	NR_163424.1:n.2676del	NR_163424.1:n.2676dup	NR_163424.1:n.2675_2676dup	NR_163424.1:n.2674_2676dup	NR_163424.1:n.2673_2676dup	NR_163424.1:n.2672_2676dup
ARFIP2 transcript variant 6	NM_001370408.1:c.1416_1433=	NM_001370408.1:c.1426_1433del	NM_001370408.1:c.1429_1433del	NM_001370408.1:c.1430_1433del	NM_001370408.1:c.1431_1433del	NM_001370408.1:c.1432_1433del	NM_001370408.1:c.*1433del	NM_001370408.1:c.*1433dup	NM_001370408.1:c.1432_1433dup	NM_001370408.1:c.1431_1433dup	NM_001370408.1:c.1430_1433dup	NM_001370408.1:c.1429_1433dup
ARFIP2 transcript variant 17	NM_001376562.1:c.1416_1433=	NM_001376562.1:c.1426_1433del	NM_001376562.1:c.1429_1433del	NM_001376562.1:c.1430_1433del	NM_001376562.1:c.1431_1433del	NM_001376562.1:c.1432_1433del	NM_001376562.1:c.*1433del	NM_001376562.1:c.*1433dup	NM_001376562.1:c.1432_1433dup	NM_001376562.1:c.1431_1433dup	NM_001376562.1:c.1430_1433dup	NM_001376562.1:c.1429_1433dup
ARFIP2 transcript variant 3	NM_001242855.1:c.1416_1433=	NM_001242855.1:c.1426_1433del	NM_001242855.1:c.1429_1433del	NM_001242855.1:c.1430_1433del	NM_001242855.1:c.1431_1433del	NM_001242855.1:c.1432_1433del	NM_001242855.1:c.*1433del	NM_001242855.1:c.*1433dup	NM_001242855.1:c.1432_1433dup	NM_001242855.1:c.1431_1433dup	NM_001242855.1:c.1430_1433dup	NM_001242855.1:c.1429_1433dup
ARFIP2 transcript variant 13	NM_001376558.1:c.1416_1433=	NM_001376558.1:c.1426_1433del	NM_001376558.1:c.1429_1433del	NM_001376558.1:c.1430_1433del	NM_001376558.1:c.1431_1433del	NM_001376558.1:c.1432_1433del	NM_001376558.1:c.*1433del	NM_001376558.1:c.*1433dup	NM_001376558.1:c.1432_1433dup	NM_001376558.1:c.1431_1433dup	NM_001376558.1:c.1430_1433dup	NM_001376558.1:c.1429_1433dup
ARFIP2 transcript variant 14	NM_001376559.1:c.1416_1433=	NM_001376559.1:c.1426_1433del	NM_001376559.1:c.1429_1433del	NM_001376559.1:c.1430_1433del	NM_001376559.1:c.1431_1433del	NM_001376559.1:c.1432_1433del	NM_001376559.1:c.*1433del	NM_001376559.1:c.*1433dup	NM_001376559.1:c.1432_1433dup	NM_001376559.1:c.1431_1433dup	NM_001376559.1:c.1430_1433dup	NM_001376559.1:c.1429_1433dup
ARFIP2 transcript variant 15	NM_001376560.1:c.1416_1433=	NM_001376560.1:c.1426_1433del	NM_001376560.1:c.1429_1433del	NM_001376560.1:c.1430_1433del	NM_001376560.1:c.1431_1433del	NM_001376560.1:c.1432_1433del	NM_001376560.1:c.*1433del	NM_001376560.1:c.*1433dup	NM_001376560.1:c.1432_1433dup	NM_001376560.1:c.1431_1433dup	NM_001376560.1:c.1430_1433dup	NM_001376560.1:c.1429_1433dup
ARFIP2 transcript variant 7	NM_001370409.1:c.1416_1433=	NM_001370409.1:c.1426_1433del	NM_001370409.1:c.1429_1433del	NM_001370409.1:c.1430_1433del	NM_001370409.1:c.1431_1433del	NM_001370409.1:c.1432_1433del	NM_001370409.1:c.*1433del	NM_001370409.1:c.*1433dup	NM_001370409.1:c.1432_1433dup	NM_001370409.1:c.1431_1433dup	NM_001370409.1:c.1430_1433dup	NM_001370409.1:c.1429_1433dup
ARFIP2 transcript variant 18	NM_001376563.1:c.1416_1433=	NM_001376563.1:c.1426_1433del	NM_001376563.1:c.1429_1433del	NM_001376563.1:c.1430_1433del	NM_001376563.1:c.1431_1433del	NM_001376563.1:c.1432_1433del	NM_001376563.1:c.*1433del	NM_001376563.1:c.*1433dup	NM_001376563.1:c.1432_1433dup	NM_001376563.1:c.1431_1433dup	NM_001376563.1:c.1430_1433dup	NM_001376563.1:c.1429_1433dup
ARFIP2 transcript variant 5	NM_001370406.1:c.1416_1433=	NM_001370406.1:c.1426_1433del	NM_001370406.1:c.1429_1433del	NM_001370406.1:c.1430_1433del	NM_001370406.1:c.1431_1433del	NM_001370406.1:c.1432_1433del	NM_001370406.1:c.*1433del	NM_001370406.1:c.*1433dup	NM_001370406.1:c.1432_1433dup	NM_001370406.1:c.1431_1433dup	NM_001370406.1:c.1430_1433dup	NM_001370406.1:c.1429_1433dup
ARFIP2 transcript variant 10	NM_001370413.1:c.1416_1433=	NM_001370413.1:c.1426_1433del	NM_001370413.1:c.1429_1433del	NM_001370413.1:c.1430_1433del	NM_001370413.1:c.1431_1433del	NM_001370413.1:c.1432_1433del	NM_001370413.1:c.*1433del	NM_001370413.1:c.*1433dup	NM_001370413.1:c.1432_1433dup	NM_001370413.1:c.1431_1433dup	NM_001370413.1:c.1430_1433dup	NM_001370413.1:c.1429_1433dup
ARFIP2 transcript variant 8	NM_001370411.1:c.1416_1433=	NM_001370411.1:c.1426_1433del	NM_001370411.1:c.1429_1433del	NM_001370411.1:c.1430_1433del	NM_001370411.1:c.1431_1433del	NM_001370411.1:c.1432_1433del	NM_001370411.1:c.*1433del	NM_001370411.1:c.*1433dup	NM_001370411.1:c.1432_1433dup	NM_001370411.1:c.1431_1433dup	NM_001370411.1:c.1430_1433dup	NM_001370411.1:c.1429_1433dup
ARFIP2 transcript variant 9	NM_001370412.1:c.1416_1433=	NM_001370412.1:c.1426_1433del	NM_001370412.1:c.1429_1433del	NM_001370412.1:c.1430_1433del	NM_001370412.1:c.1431_1433del	NM_001370412.1:c.1432_1433del	NM_001370412.1:c.*1433del	NM_001370412.1:c.*1433dup	NM_001370412.1:c.1432_1433dup	NM_001370412.1:c.1431_1433dup	NM_001370412.1:c.1430_1433dup	NM_001370412.1:c.1429_1433dup
ARFIP2 transcript variant 4	NM_001242856.1:c.1416_1433=	NM_001242856.1:c.1426_1433del	NM_001242856.1:c.1429_1433del	NM_001242856.1:c.1430_1433del	NM_001242856.1:c.1431_1433del	NM_001242856.1:c.1432_1433del	NM_001242856.1:c.*1433del	NM_001242856.1:c.*1433dup	NM_001242856.1:c.1432_1433dup	NM_001242856.1:c.1431_1433dup	NM_001242856.1:c.1430_1433dup	NM_001242856.1:c.1429_1433dup
ARFIP2 transcript variant 20	NR_164825.1:n.2464_2481=	NR_164825.1:n.2474_2481del	NR_164825.1:n.2477_2481del	NR_164825.1:n.2478_2481del	NR_164825.1:n.2479_2481del	NR_164825.1:n.2480_2481del	NR_164825.1:n.2481del	NR_164825.1:n.2481dup	NR_164825.1:n.2480_2481dup	NR_164825.1:n.2479_2481dup	NR_164825.1:n.2478_2481dup	NR_164825.1:n.2477_2481dup
ARFIP2 transcript variant 19	NM_001376564.1:c.1416_1433=	NM_001376564.1:c.1426_1433del	NM_001376564.1:c.1429_1433del	NM_001376564.1:c.1430_1433del	NM_001376564.1:c.1431_1433del	NM_001376564.1:c.1432_1433del	NM_001376564.1:c.*1433del	NM_001376564.1:c.*1433dup	NM_001376564.1:c.1432_1433dup	NM_001376564.1:c.1431_1433dup	NM_001376564.1:c.1430_1433dup	NM_001376564.1:c.1429_1433dup
ARFIP2 transcript variant 11	NR_163423.1:n.2424_2441=	NR_163423.1:n.2434_2441del	NR_163423.1:n.2437_2441del	NR_163423.1:n.2438_2441del	NR_163423.1:n.2439_2441del	NR_163423.1:n.2440_2441del	NR_163423.1:n.2441del	NR_163423.1:n.2441dup	NR_163423.1:n.2440_2441dup	NR_163423.1:n.2439_2441dup	NR_163423.1:n.2438_2441dup	NR_163423.1:n.2437_2441dup

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34252093