Name: rs71121267
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.

rs71121267

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:35119850-35119868 (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)₇ / delTT / delT /…
del(T)₈ / del(T)₇ / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.3628 (1865/5140, ALFA)
(T)₁₉=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPP2R3C : Intron Variant
PRORP : 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	5140	TTTTTTTTTTTTTTTTTTT=0.4848	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0029, TTTTTTTTTTTTTTTTTTTT=0.3628, TTTTTTTTTTTTTTTTTTTTTTTT=0.0471, TTTTTTTTTTTTTTTTTTTTT=0.0984, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0023, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.57179	0.355915	0.072295	32
European	Sub	4670	TTTTTTTTTTTTTTTTTTT=0.4338	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0032, TTTTTTTTTTTTTTTTTTTT=0.3987, TTTTTTTTTTTTTTTTTTTTTTTT=0.0516, TTTTTTTTTTTTTTTTTTTTT=0.1084, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0017, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0026, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.514908	0.403096	0.081995	32
African	Sub	306	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	288	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	6	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	14	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	88	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	54	TTTTTTTTTTTTTTTTTTT=0.93	TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.06, TTTTTTTTTTTTTTTTTTTTTTTT=0.02, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	0.961538	0.038462	0.0	14

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	5140	(T)₁₉=0.4848	del(T)₈=0.0000, delTT=0.0000, delT=0.0029, dupT=0.3628, dupTT=0.0984, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0471, dup(T)₆=0.0023, dup(T)₇=0.0016
Allele Frequency Aggregator	European	Sub	4670	(T)₁₉=0.4338	del(T)₈=0.0000, delTT=0.0000, delT=0.0032, dupT=0.3987, dupTT=0.1084, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0516, dup(T)₆=0.0026, dup(T)₇=0.0017
Allele Frequency Aggregator	African	Sub	306	(T)₁₉=1.000	del(T)₈=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	88	(T)₁₉=1.00	del(T)₈=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Other	Sub	54	(T)₁₉=0.93	del(T)₈=0.00, delTT=0.00, delT=0.00, dupT=0.06, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.02, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	14	(T)₁₉=1.00	del(T)₈=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	6	(T)₁₉=1.0	del(T)₈=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₁₉=1.0	del(T)₈=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.80

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 14	NC_000014.9:g.35119861_35119868del
GRCh38.p14 chr 14	NC_000014.9:g.35119862_35119868del
GRCh38.p14 chr 14	NC_000014.9:g.35119867_35119868del
GRCh38.p14 chr 14	NC_000014.9:g.35119868del
GRCh38.p14 chr 14	NC_000014.9:g.35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119867_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119866_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119865_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119864_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119863_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119862_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119861_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119859_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119858_35119868dup
GRCh38.p14 chr 14	NC_000014.9:g.35119851_35119868dup
GRCh37.p13 chr 14	NC_000014.8:g.35589067_35589074del
GRCh37.p13 chr 14	NC_000014.8:g.35589068_35589074del
GRCh37.p13 chr 14	NC_000014.8:g.35589073_35589074del
GRCh37.p13 chr 14	NC_000014.8:g.35589074del
GRCh37.p13 chr 14	NC_000014.8:g.35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589073_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589072_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589071_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589070_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589069_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589068_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589067_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589065_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589064_35589074dup
GRCh37.p13 chr 14	NC_000014.8:g.35589057_35589074dup

Gene: PPP2R3C, protein phosphatase 2 regulatory subunit B''gamma (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPP2R3C transcript variant 2	NM_001305155.2:c.-145+204… NM_001305155.2:c.-145+2045_-145+2052del	N/A	Intron Variant
PPP2R3C transcript variant 3	NM_001305156.2:c.-145+204… NM_001305156.2:c.-145+2045_-145+2052del	N/A	Intron Variant
PPP2R3C transcript variant 1	NM_017917.4:c.58+2045_58+… NM_017917.4:c.58+2045_58+2052del	N/A	Intron Variant
PPP2R3C transcript variant 4	NR_130972.2:n.	N/A	Intron Variant
PPP2R3C transcript variant X1	XM_005267782.5:c.58+2045_… XM_005267782.5:c.58+2045_58+2052del	N/A	Intron Variant
PPP2R3C transcript variant X2	XM_024449638.2:c.-36+970_… XM_024449638.2:c.-36+970_-36+977del	N/A	Intron Variant
PPP2R3C transcript variant X4	XM_047431517.1:c.58+2045_… XM_047431517.1:c.58+2045_58+2052del	N/A	Intron Variant
PPP2R3C transcript variant X3	XM_024449639.2:c.	N/A	Genic Upstream Transcript Variant

Gene: PRORP, protein only RNase P catalytic subunit (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
PRORP transcript variant 2	NM_001256678.2:c.	N/A	N/A
PRORP transcript variant 3	NM_001256679.2:c.	N/A	N/A
PRORP transcript variant 4	NM_001256680.2:c.	N/A	N/A
PRORP transcript variant 5	NM_001256681.2:c.	N/A	N/A
PRORP transcript variant 1	NM_014672.4:c.	N/A	N/A
PRORP transcript variant X2	XM_011537410.3:c.	N/A	Upstream Transcript Variant
PRORP transcript variant X5	XM_017021836.2:c.	N/A	Upstream Transcript Variant
PRORP transcript variant X3	XM_047431992.1:c.	N/A	Upstream Transcript Variant
PRORP transcript variant X8	XM_047431996.1:c.	N/A	Upstream Transcript Variant
PRORP transcript variant X1	XM_005268237.4:c.	N/A	N/A
PRORP transcript variant X4	XM_047431993.1:c.	N/A	N/A
PRORP transcript variant X6	XM_047431994.1:c.	N/A	N/A
PRORP transcript variant X7	XM_047431995.1: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)₁₉=	del(T)₈	del(T)₇	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₀	dup(T)₁₁	dup(T)₁₈
GRCh38.p14 chr 14	NC_000014.9:g.35119850_35119868=	NC_000014.9:g.35119861_35119868del	NC_000014.9:g.35119862_35119868del	NC_000014.9:g.35119867_35119868del	NC_000014.9:g.35119868del	NC_000014.9:g.35119868dup	NC_000014.9:g.35119867_35119868dup	NC_000014.9:g.35119866_35119868dup	NC_000014.9:g.35119865_35119868dup	NC_000014.9:g.35119864_35119868dup	NC_000014.9:g.35119863_35119868dup	NC_000014.9:g.35119862_35119868dup	NC_000014.9:g.35119861_35119868dup	NC_000014.9:g.35119859_35119868dup	NC_000014.9:g.35119858_35119868dup	NC_000014.9:g.35119851_35119868dup
GRCh37.p13 chr 14	NC_000014.8:g.35589056_35589074=	NC_000014.8:g.35589067_35589074del	NC_000014.8:g.35589068_35589074del	NC_000014.8:g.35589073_35589074del	NC_000014.8:g.35589074del	NC_000014.8:g.35589074dup	NC_000014.8:g.35589073_35589074dup	NC_000014.8:g.35589072_35589074dup	NC_000014.8:g.35589071_35589074dup	NC_000014.8:g.35589070_35589074dup	NC_000014.8:g.35589069_35589074dup	NC_000014.8:g.35589068_35589074dup	NC_000014.8:g.35589067_35589074dup	NC_000014.8:g.35589065_35589074dup	NC_000014.8:g.35589064_35589074dup	NC_000014.8:g.35589057_35589074dup
PPP2R3C transcript variant 2	NM_001305155.2:c.-145+2052=	NM_001305155.2:c.-145+2045_-145+2052del	NM_001305155.2:c.-145+2046_-145+2052del	NM_001305155.2:c.-145+2051_-145+2052del	NM_001305155.2:c.-145+2052del	NM_001305155.2:c.-145+2052dup	NM_001305155.2:c.-145+2051_-145+2052dup	NM_001305155.2:c.-145+2050_-145+2052dup	NM_001305155.2:c.-145+2049_-145+2052dup	NM_001305155.2:c.-145+2048_-145+2052dup	NM_001305155.2:c.-145+2047_-145+2052dup	NM_001305155.2:c.-145+2046_-145+2052dup	NM_001305155.2:c.-145+2045_-145+2052dup	NM_001305155.2:c.-145+2043_-145+2052dup	NM_001305155.2:c.-145+2042_-145+2052dup	NM_001305155.2:c.-145+2035_-145+2052dup
PPP2R3C transcript variant 3	NM_001305156.2:c.-145+2052=	NM_001305156.2:c.-145+2045_-145+2052del	NM_001305156.2:c.-145+2046_-145+2052del	NM_001305156.2:c.-145+2051_-145+2052del	NM_001305156.2:c.-145+2052del	NM_001305156.2:c.-145+2052dup	NM_001305156.2:c.-145+2051_-145+2052dup	NM_001305156.2:c.-145+2050_-145+2052dup	NM_001305156.2:c.-145+2049_-145+2052dup	NM_001305156.2:c.-145+2048_-145+2052dup	NM_001305156.2:c.-145+2047_-145+2052dup	NM_001305156.2:c.-145+2046_-145+2052dup	NM_001305156.2:c.-145+2045_-145+2052dup	NM_001305156.2:c.-145+2043_-145+2052dup	NM_001305156.2:c.-145+2042_-145+2052dup	NM_001305156.2:c.-145+2035_-145+2052dup
PPP2R3C transcript	NM_017917.2:c.58+2052=	NM_017917.2:c.58+2045_58+2052del	NM_017917.2:c.58+2046_58+2052del	NM_017917.2:c.58+2051_58+2052del	NM_017917.2:c.58+2052del	NM_017917.2:c.58+2052dup	NM_017917.2:c.58+2051_58+2052dup	NM_017917.2:c.58+2050_58+2052dup	NM_017917.2:c.58+2049_58+2052dup	NM_017917.2:c.58+2048_58+2052dup	NM_017917.2:c.58+2047_58+2052dup	NM_017917.2:c.58+2046_58+2052dup	NM_017917.2:c.58+2045_58+2052dup	NM_017917.2:c.58+2043_58+2052dup	NM_017917.2:c.58+2042_58+2052dup	NM_017917.2:c.58+2035_58+2052dup
PPP2R3C transcript variant 1	NM_017917.4:c.58+2052=	NM_017917.4:c.58+2045_58+2052del	NM_017917.4:c.58+2046_58+2052del	NM_017917.4:c.58+2051_58+2052del	NM_017917.4:c.58+2052del	NM_017917.4:c.58+2052dup	NM_017917.4:c.58+2051_58+2052dup	NM_017917.4:c.58+2050_58+2052dup	NM_017917.4:c.58+2049_58+2052dup	NM_017917.4:c.58+2048_58+2052dup	NM_017917.4:c.58+2047_58+2052dup	NM_017917.4:c.58+2046_58+2052dup	NM_017917.4:c.58+2045_58+2052dup	NM_017917.4:c.58+2043_58+2052dup	NM_017917.4:c.58+2042_58+2052dup	NM_017917.4:c.58+2035_58+2052dup
PPP2R3C transcript variant X1	XM_005267782.1:c.58+2052=	XM_005267782.1:c.58+2045_58+2052del	XM_005267782.1:c.58+2046_58+2052del	XM_005267782.1:c.58+2051_58+2052del	XM_005267782.1:c.58+2052del	XM_005267782.1:c.58+2052dup	XM_005267782.1:c.58+2051_58+2052dup	XM_005267782.1:c.58+2050_58+2052dup	XM_005267782.1:c.58+2049_58+2052dup	XM_005267782.1:c.58+2048_58+2052dup	XM_005267782.1:c.58+2047_58+2052dup	XM_005267782.1:c.58+2046_58+2052dup	XM_005267782.1:c.58+2045_58+2052dup	XM_005267782.1:c.58+2043_58+2052dup	XM_005267782.1:c.58+2042_58+2052dup	XM_005267782.1:c.58+2035_58+2052dup
PPP2R3C transcript variant X1	XM_005267782.5:c.58+2052=	XM_005267782.5:c.58+2045_58+2052del	XM_005267782.5:c.58+2046_58+2052del	XM_005267782.5:c.58+2051_58+2052del	XM_005267782.5:c.58+2052del	XM_005267782.5:c.58+2052dup	XM_005267782.5:c.58+2051_58+2052dup	XM_005267782.5:c.58+2050_58+2052dup	XM_005267782.5:c.58+2049_58+2052dup	XM_005267782.5:c.58+2048_58+2052dup	XM_005267782.5:c.58+2047_58+2052dup	XM_005267782.5:c.58+2046_58+2052dup	XM_005267782.5:c.58+2045_58+2052dup	XM_005267782.5:c.58+2043_58+2052dup	XM_005267782.5:c.58+2042_58+2052dup	XM_005267782.5:c.58+2035_58+2052dup
PPP2R3C transcript variant X2	XM_005267783.1:c.58+2052=	XM_005267783.1:c.58+2045_58+2052del	XM_005267783.1:c.58+2046_58+2052del	XM_005267783.1:c.58+2051_58+2052del	XM_005267783.1:c.58+2052del	XM_005267783.1:c.58+2052dup	XM_005267783.1:c.58+2051_58+2052dup	XM_005267783.1:c.58+2050_58+2052dup	XM_005267783.1:c.58+2049_58+2052dup	XM_005267783.1:c.58+2048_58+2052dup	XM_005267783.1:c.58+2047_58+2052dup	XM_005267783.1:c.58+2046_58+2052dup	XM_005267783.1:c.58+2045_58+2052dup	XM_005267783.1:c.58+2043_58+2052dup	XM_005267783.1:c.58+2042_58+2052dup	XM_005267783.1:c.58+2035_58+2052dup
PPP2R3C transcript variant X3	XM_005267784.1:c.-145+2052=	XM_005267784.1:c.-145+2045_-145+2052del	XM_005267784.1:c.-145+2046_-145+2052del	XM_005267784.1:c.-145+2051_-145+2052del	XM_005267784.1:c.-145+2052del	XM_005267784.1:c.-145+2052dup	XM_005267784.1:c.-145+2051_-145+2052dup	XM_005267784.1:c.-145+2050_-145+2052dup	XM_005267784.1:c.-145+2049_-145+2052dup	XM_005267784.1:c.-145+2048_-145+2052dup	XM_005267784.1:c.-145+2047_-145+2052dup	XM_005267784.1:c.-145+2046_-145+2052dup	XM_005267784.1:c.-145+2045_-145+2052dup	XM_005267784.1:c.-145+2043_-145+2052dup	XM_005267784.1:c.-145+2042_-145+2052dup	XM_005267784.1:c.-145+2035_-145+2052dup
PPP2R3C transcript variant X4	XM_005267785.1:c.58+2052=	XM_005267785.1:c.58+2045_58+2052del	XM_005267785.1:c.58+2046_58+2052del	XM_005267785.1:c.58+2051_58+2052del	XM_005267785.1:c.58+2052del	XM_005267785.1:c.58+2052dup	XM_005267785.1:c.58+2051_58+2052dup	XM_005267785.1:c.58+2050_58+2052dup	XM_005267785.1:c.58+2049_58+2052dup	XM_005267785.1:c.58+2048_58+2052dup	XM_005267785.1:c.58+2047_58+2052dup	XM_005267785.1:c.58+2046_58+2052dup	XM_005267785.1:c.58+2045_58+2052dup	XM_005267785.1:c.58+2043_58+2052dup	XM_005267785.1:c.58+2042_58+2052dup	XM_005267785.1:c.58+2035_58+2052dup
PPP2R3C transcript variant X2	XM_024449638.2:c.-36+977=	XM_024449638.2:c.-36+970_-36+977del	XM_024449638.2:c.-36+971_-36+977del	XM_024449638.2:c.-36+976_-36+977del	XM_024449638.2:c.-36+977del	XM_024449638.2:c.-36+977dup	XM_024449638.2:c.-36+976_-36+977dup	XM_024449638.2:c.-36+975_-36+977dup	XM_024449638.2:c.-36+974_-36+977dup	XM_024449638.2:c.-36+973_-36+977dup	XM_024449638.2:c.-36+972_-36+977dup	XM_024449638.2:c.-36+971_-36+977dup	XM_024449638.2:c.-36+970_-36+977dup	XM_024449638.2:c.-36+968_-36+977dup	XM_024449638.2:c.-36+967_-36+977dup	XM_024449638.2:c.-36+960_-36+977dup
PPP2R3C transcript variant X4	XM_047431517.1:c.58+2052=	XM_047431517.1:c.58+2045_58+2052del	XM_047431517.1:c.58+2046_58+2052del	XM_047431517.1:c.58+2051_58+2052del	XM_047431517.1:c.58+2052del	XM_047431517.1:c.58+2052dup	XM_047431517.1:c.58+2051_58+2052dup	XM_047431517.1:c.58+2050_58+2052dup	XM_047431517.1:c.58+2049_58+2052dup	XM_047431517.1:c.58+2048_58+2052dup	XM_047431517.1:c.58+2047_58+2052dup	XM_047431517.1:c.58+2046_58+2052dup	XM_047431517.1:c.58+2045_58+2052dup	XM_047431517.1:c.58+2043_58+2052dup	XM_047431517.1:c.58+2042_58+2052dup	XM_047431517.1:c.58+2035_58+2052dup

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#.

54 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95637783	Dec 05, 2013 (138)
2	PJP	ss294826947	May 09, 2011 (137)
3	PJP	ss294826948	May 09, 2011 (135)
4	SSMP	ss664221147	Apr 01, 2015 (144)
5	EVA_GENOME_DK	ss1574739337	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1708009345	Apr 01, 2015 (144)
7	EVA_UK10K_ALSPAC	ss1708009348	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1708009399	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1708009402	Apr 01, 2015 (144)
10	SWEGEN	ss3012004532	Nov 08, 2017 (151)
11	URBANLAB	ss3650180092	Oct 12, 2018 (152)
12	EVA_DECODE	ss3696442553	Jul 13, 2019 (153)
13	EVA_DECODE	ss3696442554	Jul 13, 2019 (153)
14	EVA_DECODE	ss3696442555	Jul 13, 2019 (153)
15	EVA_DECODE	ss3696442556	Jul 13, 2019 (153)
16	EVA_DECODE	ss3696442557	Jul 13, 2019 (153)
17	PACBIO	ss3792675962	Jul 13, 2019 (153)
18	PACBIO	ss3792675963	Jul 13, 2019 (153)
19	PACBIO	ss3797560063	Jul 13, 2019 (153)
20	PACBIO	ss3797560064	Jul 13, 2019 (153)
21	EVA	ss3833855214	Apr 27, 2020 (154)
22	GNOMAD	ss4275945628	Apr 27, 2021 (155)
23	GNOMAD	ss4275945630	Apr 27, 2021 (155)
24	GNOMAD	ss4275945632	Apr 27, 2021 (155)
25	GNOMAD	ss4275945633	Apr 27, 2021 (155)
26	GNOMAD	ss4275945634	Apr 27, 2021 (155)
27	GNOMAD	ss4275945635	Apr 27, 2021 (155)
28	GNOMAD	ss4275945636	Apr 27, 2021 (155)
29	GNOMAD	ss4275945637	Apr 27, 2021 (155)
30	GNOMAD	ss4275945638	Apr 27, 2021 (155)
31	GNOMAD	ss4275945639	Apr 27, 2021 (155)
32	GNOMAD	ss4275945640	Apr 27, 2021 (155)
33	GNOMAD	ss4275945642	Apr 27, 2021 (155)
34	GNOMAD	ss4275945643	Apr 27, 2021 (155)
35	GNOMAD	ss4275945644	Apr 27, 2021 (155)
36	GNOMAD	ss4275945645	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5212688958	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5212688959	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5212688960	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5212688961	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5212688962	Apr 27, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5295797333	Oct 16, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5295797334	Oct 16, 2022 (156)
44	HUGCELL_USP	ss5489895825	Oct 16, 2022 (156)
45	HUGCELL_USP	ss5489895826	Oct 16, 2022 (156)
46	HUGCELL_USP	ss5489895827	Oct 16, 2022 (156)
47	HUGCELL_USP	ss5489895828	Oct 16, 2022 (156)
48	TOMMO_GENOMICS	ss5765337014	Oct 16, 2022 (156)
49	TOMMO_GENOMICS	ss5765337015	Oct 16, 2022 (156)
50	TOMMO_GENOMICS	ss5765337016	Oct 16, 2022 (156)
51	TOMMO_GENOMICS	ss5765337017	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5765337019	Oct 16, 2022 (156)
53	EVA	ss5840940197	Oct 16, 2022 (156)
54	EVA	ss5840940198	Oct 16, 2022 (156)
55	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35266279 (NC_000014.8:35589055::TT 2209/3854) Row 35266280 (NC_000014.8:35589055::TTT 1056/3854)	-	Oct 12, 2018 (152)
56	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 35266279 (NC_000014.8:35589055::TT 2209/3854) Row 35266280 (NC_000014.8:35589055::TTT 1056/3854)	-	Oct 12, 2018 (152)
57	The Danish reference pan genome	NC_000014.8 - 35589056	Apr 27, 2020 (154)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 447659757 (NC_000014.9:35119849::T 56892/107462) Row 447659759 (NC_000014.9:35119849::TT 20178/107608) Row 447659761 (NC_000014.9:35119849::TTT 240/107834)...	-	Apr 27, 2021 (155)
73	8.3KJPN Submission ignored due to conflicting rows: Row 70658265 (NC_000014.8:35589055::T 5561/16110) Row 70658266 (NC_000014.8:35589055::TT 4505/16110) Row 70658267 (NC_000014.8:35589055::TTTTT 383/16110)...	-	Apr 27, 2021 (155)
74	8.3KJPN Submission ignored due to conflicting rows: Row 70658265 (NC_000014.8:35589055::T 5561/16110) Row 70658266 (NC_000014.8:35589055::TT 4505/16110) Row 70658267 (NC_000014.8:35589055::TTTTT 383/16110)...	-	Apr 27, 2021 (155)
75	8.3KJPN Submission ignored due to conflicting rows: Row 70658265 (NC_000014.8:35589055::T 5561/16110) Row 70658266 (NC_000014.8:35589055::TT 4505/16110) Row 70658267 (NC_000014.8:35589055::TTTTT 383/16110)...	-	Apr 27, 2021 (155)
76	8.3KJPN Submission ignored due to conflicting rows: Row 70658265 (NC_000014.8:35589055::T 5561/16110) Row 70658266 (NC_000014.8:35589055::TT 4505/16110) Row 70658267 (NC_000014.8:35589055::TTTTT 383/16110)...	-	Apr 27, 2021 (155)
77	8.3KJPN Submission ignored due to conflicting rows: Row 70658265 (NC_000014.8:35589055::T 5561/16110) Row 70658266 (NC_000014.8:35589055::TT 4505/16110) Row 70658267 (NC_000014.8:35589055::TTTTT 383/16110)...	-	Apr 27, 2021 (155)
78	14KJPN Submission ignored due to conflicting rows: Row 99174118 (NC_000014.9:35119849::TT 8954/28134) Row 99174119 (NC_000014.9:35119849::TTTTT 714/28134) Row 99174120 (NC_000014.9:35119849::T 10721/28134)...	-	Oct 16, 2022 (156)
79	14KJPN Submission ignored due to conflicting rows: Row 99174118 (NC_000014.9:35119849::TT 8954/28134) Row 99174119 (NC_000014.9:35119849::TTTTT 714/28134) Row 99174120 (NC_000014.9:35119849::T 10721/28134)...	-	Oct 16, 2022 (156)
80	14KJPN Submission ignored due to conflicting rows: Row 99174118 (NC_000014.9:35119849::TT 8954/28134) Row 99174119 (NC_000014.9:35119849::TTTTT 714/28134) Row 99174120 (NC_000014.9:35119849::T 10721/28134)...	-	Oct 16, 2022 (156)
81	14KJPN Submission ignored due to conflicting rows: Row 99174118 (NC_000014.9:35119849::TT 8954/28134) Row 99174119 (NC_000014.9:35119849::TTTTT 714/28134) Row 99174120 (NC_000014.9:35119849::T 10721/28134)...	-	Oct 16, 2022 (156)
82	14KJPN Submission ignored due to conflicting rows: Row 99174118 (NC_000014.9:35119849::TT 8954/28134) Row 99174119 (NC_000014.9:35119849::TTTTT 714/28134) Row 99174120 (NC_000014.9:35119849::T 10721/28134)...	-	Oct 16, 2022 (156)
83	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35266279 (NC_000014.8:35589055::TT 2123/3708) Row 35266280 (NC_000014.8:35589055::TTT 1012/3708)	-	Oct 12, 2018 (152)
84	UK 10K study - Twins Submission ignored due to conflicting rows: Row 35266279 (NC_000014.8:35589055::TT 2123/3708) Row 35266280 (NC_000014.8:35589055::TTT 1012/3708)	-	Oct 12, 2018 (152)
85	ALFA	NC_000014.9 - 35119850	Apr 27, 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)
rs147162928	Sep 17, 2011 (135)
rs149625837	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3012004532	NC_000014.8:35589055:TTTTTTTT:	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3696442553, ss4275945645	NC_000014.9:35119849:TTTTTTTT:	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4275945644	NC_000014.9:35119849:TTTTTTT:	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4275945643	NC_000014.9:35119849:TT:	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4275945642, ss5489895825	NC_000014.9:35119849:T:	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss294826948	NC_000014.7:34658825::T	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
442696, ss664221147, ss1574739337, ss3792675962, ss3797560063, ss5212688958	NC_000014.8:35589055::T	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3650180092, ss4275945628, ss5295797333, ss5489895826, ss5765337016	NC_000014.9:35119849::T	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3696442554	NC_000014.9:35119857::T	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss95637783	NT_026437.12:16589074::T	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss294826947	NC_000014.7:34658807::TT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1708009345, ss1708009399, ss3792675963, ss3797560064, ss3833855214, ss5212688959, ss5840940197	NC_000014.8:35589055::TT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945630, ss5489895827, ss5765337014	NC_000014.9:35119849::TT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3696442555	NC_000014.9:35119857::TT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss1708009348, ss1708009402, ss5212688962, ss5840940198	NC_000014.8:35589055::TTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945632, ss5765337019	NC_000014.9:35119849::TTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696442556	NC_000014.9:35119857::TTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945633	NC_000014.9:35119849::TTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5212688960	NC_000014.8:35589055::TTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945634, ss5295797334, ss5489895828, ss5765337015	NC_000014.9:35119849::TTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696442557	NC_000014.9:35119857::TTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5212688961	NC_000014.8:35589055::TTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945635, ss5765337017	NC_000014.9:35119849::TTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945636	NC_000014.9:35119849::TTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11718972480	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945637	NC_000014.9:35119849::TTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945638	NC_000014.9:35119849::TTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945639	NC_000014.9:35119849::TTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4275945640	NC_000014.9:35119849::TTTTTTTTTTTT… NC_000014.9:35119849::TTTTTTTTTTTTTTTTTT	NC_000014.9:35119849:TTTTTTTTTTTTT… NC_000014.9:35119849:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs71121267

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

rs71121267