Name: rs1162270732
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.

rs1162270732

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr20:13224842-13224863 (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)₁₂ / del(T)₁₁ / del(T)₁₀ / d…
del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₃ / dup(T)₁₈
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₁=0.000011 (3/264690, TOPMED)
delT=0.04699 (505/10748, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: TASP1 : Intron Variant
ISM1 : 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	10748	TTTTTTTTTTTTTTTTTTTTTT=0.90873	TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.02186, TTTTTTTTTTTTTTTTTTTTT=0.04699, TTTTTTTTTTTTTTTTTTTTTTT=0.00633, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00261, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.01200, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00149	0.916142	0.003249	0.080609	3
European	Sub	8608	TTTTTTTTTTTTTTTTTTTTTT=0.8864	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0273, TTTTTTTTTTTTTTTTTTTTT=0.0586, TTTTTTTTTTTTTTTTTTTTTTT=0.0077, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0033, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0150, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0019	0.893154	0.004149	0.102697	1
African	Sub	1148	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	46	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1102	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	82	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	64	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	96	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	466	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	290	TTTTTTTTTTTTTTTTTTTTTT=0.990	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTTTT=0.007, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.993056	0.0	0.006944	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
TopMed	Global	Study-wide	264690	(T)₂₂=0.999989	del(T)₁₁=0.000011
Allele Frequency Aggregator	Total	Global	10748	(T)₂₂=0.90873	del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.02186, delT=0.04699, dupT=0.00633, dupTT=0.00000, dupTTT=0.00261, dup(T)₄=0.01200, dup(T)₈=0.00149
Allele Frequency Aggregator	European	Sub	8608	(T)₂₂=0.8864	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0273, delT=0.0586, dupT=0.0077, dupTT=0.0000, dupTTT=0.0033, dup(T)₄=0.0150, dup(T)₈=0.0019
Allele Frequency Aggregator	African	Sub	1148	(T)₂₂=1.0000	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	466	(T)₂₂=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₆=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, dup(T)₈=0.000
Allele Frequency Aggregator	Other	Sub	290	(T)₂₂=0.990	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.003, dupT=0.007, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Latin American 1	Sub	96	(T)₂₂=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₆=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, dup(T)₈=0.00
Allele Frequency Aggregator	Asian	Sub	82	(T)₂₂=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₆=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, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(T)₂₂=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₆=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, dup(T)₈=0.00

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 20	NC_000020.11:g.13224852_13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224853_13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224854_13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224858_13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224860_13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224861_13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224862_13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224863del
GRCh38.p14 chr 20	NC_000020.11:g.13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224862_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224861_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224860_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224859_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224858_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224857_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224856_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224855_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224854_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224853_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224851_13224863dup
GRCh38.p14 chr 20	NC_000020.11:g.13224846_13224863dup
GRCh37.p13 chr 20	NC_000020.10:g.13205499_13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205500_13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205501_13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205505_13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205507_13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205508_13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205509_13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205510del
GRCh37.p13 chr 20	NC_000020.10:g.13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205509_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205508_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205507_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205506_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205505_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205504_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205503_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205502_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205501_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205500_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205498_13205510dup
GRCh37.p13 chr 20	NC_000020.10:g.13205493_13205510dup

Gene: ISM1, isthmin 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ISM1 transcript	NM_080826.2:c.138+2938_13… NM_080826.2:c.138+2938_138+2949del	N/A	Intron Variant
ISM1 transcript variant X1	XM_017027680.2:c.138+2938… XM_017027680.2:c.138+2938_138+2949del	N/A	Intron Variant

Gene: TASP1, taspase 1 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
TASP1 transcript variant 2	NM_001323602.2:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant 3	NM_001323603.2:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant 4	NM_001323604.2:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant 1	NM_017714.3:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant 5	NR_136628.2:n.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant 6	NR_136629.2:n.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant 7	NR_136630.2:n.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant 8	NR_136631.2:n.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X12	XM_017027929.3:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X14	XM_017027931.3:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X1	XM_047440267.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X2	XM_047440268.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X4	XM_047440269.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X6	XM_047440270.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X7	XM_047440271.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X8	XM_047440272.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X9	XM_047440273.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X10	XM_047440274.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X11	XM_047440275.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X13	XM_047440276.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X15	XM_047440277.1:c.	N/A	Genic Downstream Transcript Variant
TASP1 transcript variant X5	XR_001754319.3:n.	N/A	Intron Variant
TASP1 transcript variant X3	XR_007067463.1:n.	N/A	Genic Downstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₂=	del(T)₁₂	del(T)₁₁	del(T)₁₀	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₃	dup(T)₁₈
GRCh38.p14 chr 20	NC_000020.11:g.13224842_13224863=	NC_000020.11:g.13224852_13224863del	NC_000020.11:g.13224853_13224863del	NC_000020.11:g.13224854_13224863del	NC_000020.11:g.13224858_13224863del	NC_000020.11:g.13224860_13224863del	NC_000020.11:g.13224861_13224863del	NC_000020.11:g.13224862_13224863del	NC_000020.11:g.13224863del	NC_000020.11:g.13224863dup	NC_000020.11:g.13224862_13224863dup	NC_000020.11:g.13224861_13224863dup	NC_000020.11:g.13224860_13224863dup	NC_000020.11:g.13224859_13224863dup	NC_000020.11:g.13224858_13224863dup	NC_000020.11:g.13224857_13224863dup	NC_000020.11:g.13224856_13224863dup	NC_000020.11:g.13224855_13224863dup	NC_000020.11:g.13224854_13224863dup	NC_000020.11:g.13224853_13224863dup	NC_000020.11:g.13224851_13224863dup	NC_000020.11:g.13224846_13224863dup
GRCh37.p13 chr 20	NC_000020.10:g.13205489_13205510=	NC_000020.10:g.13205499_13205510del	NC_000020.10:g.13205500_13205510del	NC_000020.10:g.13205501_13205510del	NC_000020.10:g.13205505_13205510del	NC_000020.10:g.13205507_13205510del	NC_000020.10:g.13205508_13205510del	NC_000020.10:g.13205509_13205510del	NC_000020.10:g.13205510del	NC_000020.10:g.13205510dup	NC_000020.10:g.13205509_13205510dup	NC_000020.10:g.13205508_13205510dup	NC_000020.10:g.13205507_13205510dup	NC_000020.10:g.13205506_13205510dup	NC_000020.10:g.13205505_13205510dup	NC_000020.10:g.13205504_13205510dup	NC_000020.10:g.13205503_13205510dup	NC_000020.10:g.13205502_13205510dup	NC_000020.10:g.13205501_13205510dup	NC_000020.10:g.13205500_13205510dup	NC_000020.10:g.13205498_13205510dup	NC_000020.10:g.13205493_13205510dup
ISM1 transcript	NM_080826.1:c.138+2928=	NM_080826.1:c.138+2938_138+2949del	NM_080826.1:c.138+2939_138+2949del	NM_080826.1:c.138+2940_138+2949del	NM_080826.1:c.138+2944_138+2949del	NM_080826.1:c.138+2946_138+2949del	NM_080826.1:c.138+2947_138+2949del	NM_080826.1:c.138+2948_138+2949del	NM_080826.1:c.138+2949del	NM_080826.1:c.138+2949dup	NM_080826.1:c.138+2948_138+2949dup	NM_080826.1:c.138+2947_138+2949dup	NM_080826.1:c.138+2946_138+2949dup	NM_080826.1:c.138+2945_138+2949dup	NM_080826.1:c.138+2944_138+2949dup	NM_080826.1:c.138+2943_138+2949dup	NM_080826.1:c.138+2942_138+2949dup	NM_080826.1:c.138+2941_138+2949dup	NM_080826.1:c.138+2940_138+2949dup	NM_080826.1:c.138+2939_138+2949dup	NM_080826.1:c.138+2937_138+2949dup	NM_080826.1:c.138+2932_138+2949dup
ISM1 transcript	NM_080826.2:c.138+2928=	NM_080826.2:c.138+2938_138+2949del	NM_080826.2:c.138+2939_138+2949del	NM_080826.2:c.138+2940_138+2949del	NM_080826.2:c.138+2944_138+2949del	NM_080826.2:c.138+2946_138+2949del	NM_080826.2:c.138+2947_138+2949del	NM_080826.2:c.138+2948_138+2949del	NM_080826.2:c.138+2949del	NM_080826.2:c.138+2949dup	NM_080826.2:c.138+2948_138+2949dup	NM_080826.2:c.138+2947_138+2949dup	NM_080826.2:c.138+2946_138+2949dup	NM_080826.2:c.138+2945_138+2949dup	NM_080826.2:c.138+2944_138+2949dup	NM_080826.2:c.138+2943_138+2949dup	NM_080826.2:c.138+2942_138+2949dup	NM_080826.2:c.138+2941_138+2949dup	NM_080826.2:c.138+2940_138+2949dup	NM_080826.2:c.138+2939_138+2949dup	NM_080826.2:c.138+2937_138+2949dup	NM_080826.2:c.138+2932_138+2949dup
ISM1 transcript variant X1	XM_017027680.2:c.138+2928=	XM_017027680.2:c.138+2938_138+2949del	XM_017027680.2:c.138+2939_138+2949del	XM_017027680.2:c.138+2940_138+2949del	XM_017027680.2:c.138+2944_138+2949del	XM_017027680.2:c.138+2946_138+2949del	XM_017027680.2:c.138+2947_138+2949del	XM_017027680.2:c.138+2948_138+2949del	XM_017027680.2:c.138+2949del	XM_017027680.2:c.138+2949dup	XM_017027680.2:c.138+2948_138+2949dup	XM_017027680.2:c.138+2947_138+2949dup	XM_017027680.2:c.138+2946_138+2949dup	XM_017027680.2:c.138+2945_138+2949dup	XM_017027680.2:c.138+2944_138+2949dup	XM_017027680.2:c.138+2943_138+2949dup	XM_017027680.2:c.138+2942_138+2949dup	XM_017027680.2:c.138+2941_138+2949dup	XM_017027680.2:c.138+2940_138+2949dup	XM_017027680.2:c.138+2939_138+2949dup	XM_017027680.2:c.138+2937_138+2949dup	XM_017027680.2:c.138+2932_138+2949dup

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#.

45 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss3017901680	Nov 08, 2017 (151)
2	MCHAISSO	ss3064847267	Jan 10, 2018 (151)
3	PACBIO	ss3793504835	Jul 13, 2019 (153)
4	PACBIO	ss3793504836	Jul 13, 2019 (153)
5	PACBIO	ss3798391999	Jul 13, 2019 (153)
6	PACBIO	ss3798392000	Jul 13, 2019 (153)
7	GNOMAD	ss4335425434	Apr 26, 2021 (155)
8	GNOMAD	ss4335425435	Apr 26, 2021 (155)
9	GNOMAD	ss4335425436	Apr 26, 2021 (155)
10	GNOMAD	ss4335425437	Apr 26, 2021 (155)
11	GNOMAD	ss4335425438	Apr 26, 2021 (155)
12	GNOMAD	ss4335425439	Apr 26, 2021 (155)
13	GNOMAD	ss4335425440	Apr 26, 2021 (155)
14	GNOMAD	ss4335425441	Apr 26, 2021 (155)
15	GNOMAD	ss4335425442	Apr 26, 2021 (155)
16	GNOMAD	ss4335425443	Apr 26, 2021 (155)
17	GNOMAD	ss4335425444	Apr 26, 2021 (155)
18	GNOMAD	ss4335425445	Apr 26, 2021 (155)
19	GNOMAD	ss4335425447	Apr 26, 2021 (155)
20	GNOMAD	ss4335425448	Apr 26, 2021 (155)
21	GNOMAD	ss4335425449	Apr 26, 2021 (155)
22	GNOMAD	ss4335425450	Apr 26, 2021 (155)
23	GNOMAD	ss4335425451	Apr 26, 2021 (155)
24	GNOMAD	ss4335425452	Apr 26, 2021 (155)
25	GNOMAD	ss4335425453	Apr 26, 2021 (155)
26	TOPMED	ss5083002603	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5228932275	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5228932276	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5228932277	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5228932278	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5228932279	Apr 26, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5308158257	Oct 13, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5308158258	Oct 13, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5308158259	Oct 13, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5308158260	Oct 13, 2022 (156)
36	HUGCELL_USP	ss5500551640	Oct 13, 2022 (156)
37	HUGCELL_USP	ss5500551641	Oct 13, 2022 (156)
38	HUGCELL_USP	ss5500551642	Oct 13, 2022 (156)
39	HUGCELL_USP	ss5500551643	Oct 13, 2022 (156)
40	SANFORD_IMAGENETICS	ss5662907113	Oct 13, 2022 (156)
41	TOMMO_GENOMICS	ss5787944908	Oct 13, 2022 (156)
42	TOMMO_GENOMICS	ss5787944909	Oct 13, 2022 (156)
43	TOMMO_GENOMICS	ss5787944910	Oct 13, 2022 (156)
44	TOMMO_GENOMICS	ss5787944911	Oct 13, 2022 (156)
45	TOMMO_GENOMICS	ss5787944912	Oct 13, 2022 (156)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 547082094 (NC_000020.11:13224841::T 1773/98472) Row 547082095 (NC_000020.11:13224841::TT 352/98494) Row 547082096 (NC_000020.11:13224841::TTT 243/98434)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 86901582 (NC_000020.10:13205488:TT: 1074/16632) Row 86901583 (NC_000020.10:13205488:T: 2283/16632) Row 86901584 (NC_000020.10:13205488::TTT 32/16632)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 86901582 (NC_000020.10:13205488:TT: 1074/16632) Row 86901583 (NC_000020.10:13205488:T: 2283/16632) Row 86901584 (NC_000020.10:13205488::TTT 32/16632)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 86901582 (NC_000020.10:13205488:TT: 1074/16632) Row 86901583 (NC_000020.10:13205488:T: 2283/16632) Row 86901584 (NC_000020.10:13205488::TTT 32/16632)...	-	Apr 26, 2021 (155)
69	8.3KJPN Submission ignored due to conflicting rows: Row 86901582 (NC_000020.10:13205488:TT: 1074/16632) Row 86901583 (NC_000020.10:13205488:T: 2283/16632) Row 86901584 (NC_000020.10:13205488::TTT 32/16632)...	-	Apr 26, 2021 (155)
70	8.3KJPN Submission ignored due to conflicting rows: Row 86901582 (NC_000020.10:13205488:TT: 1074/16632) Row 86901583 (NC_000020.10:13205488:T: 2283/16632) Row 86901584 (NC_000020.10:13205488::TTT 32/16632)...	-	Apr 26, 2021 (155)
71	14KJPN Submission ignored due to conflicting rows: Row 121782012 (NC_000020.11:13224841:T: 4556/28126) Row 121782013 (NC_000020.11:13224841:TT: 2173/28126) Row 121782014 (NC_000020.11:13224841::T 103/28126)...	-	Oct 13, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 121782012 (NC_000020.11:13224841:T: 4556/28126) Row 121782013 (NC_000020.11:13224841:TT: 2173/28126) Row 121782014 (NC_000020.11:13224841::T 103/28126)...	-	Oct 13, 2022 (156)
73	14KJPN Submission ignored due to conflicting rows: Row 121782012 (NC_000020.11:13224841:T: 4556/28126) Row 121782013 (NC_000020.11:13224841:TT: 2173/28126) Row 121782014 (NC_000020.11:13224841::T 103/28126)...	-	Oct 13, 2022 (156)
74	14KJPN Submission ignored due to conflicting rows: Row 121782012 (NC_000020.11:13224841:T: 4556/28126) Row 121782013 (NC_000020.11:13224841:TT: 2173/28126) Row 121782014 (NC_000020.11:13224841::T 103/28126)...	-	Oct 13, 2022 (156)
75	14KJPN Submission ignored due to conflicting rows: Row 121782012 (NC_000020.11:13224841:T: 4556/28126) Row 121782013 (NC_000020.11:13224841:TT: 2173/28126) Row 121782014 (NC_000020.11:13224841::T 103/28126)...	-	Oct 13, 2022 (156)
76	TopMed	NC_000020.11 - 13224842	Apr 26, 2021 (155)
77	ALFA	NC_000020.11 - 13224842	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss3017901680	NC_000020.10:13205488:TTTTTTTTTTTT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4335425453	NC_000020.11:13224841:TTTTTTTTTTTT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
358111548, ss4335425452, ss5083002603	NC_000020.11:13224841:TTTTTTTTTTT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4335425451	NC_000020.11:13224841:TTTTTTTTTT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4335425450	NC_000020.11:13224841:TTTTTT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4335425449	NC_000020.11:13224841:TTTT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4335425448, ss5308158260	NC_000020.11:13224841:TTT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3793504835, ss3798391999, ss5228932275, ss5662907113	NC_000020.10:13205488:TT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3064847267, ss4335425447, ss5308158259, ss5500551643, ss5787944909	NC_000020.11:13224841:TT:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3793504836, ss3798392000, ss5228932276	NC_000020.10:13205488:T:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5308158257, ss5500551641, ss5787944908	NC_000020.11:13224841:T:	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5228932278	NC_000020.10:13205488::T	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425434, ss5308158258, ss5500551640, ss5787944910	NC_000020.11:13224841::T	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425435, ss5500551642, ss5787944911	NC_000020.11:13224841::TT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5228932277	NC_000020.10:13205488::TTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425436	NC_000020.11:13224841::TTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5228932279	NC_000020.10:13205488::TTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5787944912	NC_000020.11:13224841::TTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425437	NC_000020.11:13224841::TTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425438	NC_000020.11:13224841::TTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425439	NC_000020.11:13224841::TTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425440	NC_000020.11:13224841::TTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7995459610	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425441	NC_000020.11:13224841::TTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425442	NC_000020.11:13224841::TTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425443	NC_000020.11:13224841::TTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425444	NC_000020.11:13224841::TTTTTTTTTTT… NC_000020.11:13224841::TTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4335425445	NC_000020.11:13224841::TTTTTTTTTTT… NC_000020.11:13224841::TTTTTTTTTTTTTTTTTT	NC_000020.11:13224841:TTTTTTTTTTTT… NC_000020.11:13224841:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs1162270732

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

rs1162270732